ID: 129663769 | ReSE screen-validated silencer GRCh37_chr16:15149302-15149486 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15055445..15055629) | | |
ID: 129663768 | ReSE screen-validated silencer GRCh37_chr16:15106867-15106972 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15013010..15013115) | | |
ID: 129390770 | MPRA-validated peak2507 silencer [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15062169..15062369) | | |
ID: 127883266 | H3K4me1 hESC enhancer GRCh37_chr16:15243079-15243774 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15149222..15149917) | | |
ID: 127883265 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:15240089-15241062 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15146232..15147205) | | |
ID: 127883264 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:15231552-15232159 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15137695..15138302) | | |
ID: 127883263 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:15122498-15123030 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15028641..15029173) | | |
ID: 127883262 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:15121593-15122216 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15027736..15028359) | | |
ID: 127883261 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr16:15120969-15121592 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15027112..15027735) | | |
ID: 127883260 | H3K27ac hESC enhancer GRCh37_chr16:15110265-15110764 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15016408..15016907) | | |
ID: 127883259 | H3K27ac hESC enhancer GRCh37_chr16:15109763-15110264 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15015906..15016407) | | |
ID: 127883258 | H3K27ac hESC enhancer GRCh37_chr16:15068201-15068964 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (14974344..14975107) | | |
ID: 127883257 | H3K4me1 hESC enhancer GRCh37_chr16:15041723-15042222 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (14947866..14948365) | | |
ID: 127883256 | H3K4me1 hESC enhancer GRCh37_chr16:15041221-15041722 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (14947364..14947865) | | |
ID: 125146418 | Sharpr-MPRA regulatory region 4661 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (14973892..14974186) | | |
ID: 112340378 | Sharpr-MPRA regulatory region 13846 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15094252..15094546) | | |
ID: 112340377 | Sharpr-MPRA regulatory region 1947 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15025212..15025506) | | |
ID: 109951030 | PKD1P3-NPIPA1 readthrough [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (14911762..14952060) | | |
ID: 105376752 | nuclear pore complex interacting protein family, member A9 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (18358090..18376839, complement) | | |
ID: 105371096 | uncharacterized LOC105371096 [Homo sapiens (human)] | Chromosome 16, NC_000016.10 (15181238..15190527) | | |