Gene neighbors for Gene (Select 129929986) - Gene

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Name/Gene ID	Description	Location	Aliases	MIM
Select item 129929986 LOC129929986 ID: 129929986	ATAC-STARR-seq lymphoblastoid silent region 569 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31423650..31423749)
Select item 129660191 LOC129660191 ID: 129660191	ReSE screen-validated silencer GRCh37_chr1:31839312-31839494 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31366465..31366647)
Select item 127882477 LOC127882477 ID: 127882477	H3K4me1 hESC enhancer GRCh37_chr1:31907359-31908163 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31434512..31435316)
Select item 127268527 LOC127268527 ID: 127268527	H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:31897631-31898192 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31424784..31425345)
Select item 127268526 LOC127268526 ID: 127268526	H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:31897069-31897630 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31424222..31424783)
Select item 127268525 LOC127268525 ID: 127268525	H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:31887579-31888127 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31414732..31415280)
Select item 127268524 LOC127268524 ID: 127268524	H3K27ac hESC enhancer GRCh37_chr1:31885808-31886308 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31412961..31413461)
Select item 126805682 LOC126805682 ID: 126805682	P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:31943609-31944808 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31470762..31471961)
Select item 126805681 LOC126805681 ID: 126805681	P300/CBP strongly-dependent group 1 enhancer GRCh37_chr1:31926120-31927319 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31453273..31454472)
Select item 124903900 LOC124903900 ID: 124903900	uncharacterized LOC124903900 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31426410..31471476, complement)
Select item 124903892 LOC124903892 ID: 124903892	uncharacterized LOC124903892 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31374299..31377487)
Select item 122056826 LOC122056826 ID: 122056826	Sharpr-MPRA regulatory region 2178 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31394702..31394996)
Select item 122056825 LOC122056825 ID: 122056825	Sharpr-MPRA regulatory region 3310 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31376802..31377096)
Select item 122056824 LOC122056824 ID: 122056824	Sharpr-MPRA regulatory region 13821 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31373262..31373556)
Select item 110594336 LOC110594336 ID: 110594336	MS1 minisatellite repeat instability region [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31428806..31434663)
Select item 105379772 LOC105379772 ID: 105379772	uncharacterized LOC105379772 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31471118..31482156)
Select item 105378625 LOC105378625 ID: 105378625	uncharacterized LOC105378625 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31445854..31450649)
Select item 105378623 LOC105378623 ID: 105378623	uncharacterized LOC105378623 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31383577..31389830, complement)
Select item 347735 SERINC2 ID: 347735	serine incorporator 2 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31409777..31434678)	FKSG84, PRO0899, TDE2, TDE2L	614549
Select item 51538 ZCCHC17 ID: 51538	zinc finger CCHC-type containing 17 [Homo sapiens (human)]	Chromosome 1, NC_000001.11 (31297032..31364936)	HSPC251, PS1D, pNO40	619744