ID: 129664277 | ReSE screen-validated silencer GRCh37_chr18:76816919-76817092 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79056919..79057092) | | |
ID: 127889706 | H3K4me1 hESC enhancer GRCh37_chr18:76819471-76819970 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79059471..79059970) | | |
ID: 127889705 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:76753804-76754785 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78993804..78994785) | | |
ID: 127889704 | NANOG hESC enhancer GRCh37_chr18:76744863-76745377 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78984863..78985377) | | |
ID: 127889703 | OCT4-NANOG hESC enhancer GRCh37_chr18:76743410-76744168 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78983410..78984168) | | |
ID: 127889702 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr18:76741235-76742064 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78981235..78982064) | | |
ID: 127889701 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:76736667-76737380 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78976667..78977380) | | |
ID: 127889700 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr18:76732815-76733411 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78972815..78973411) | | |
ID: 127889699 | H3K4me1 hESC enhancer GRCh37_chr18:76732217-76732814 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78972217..78972814) | | |
ID: 127889698 | H3K4me1 hESC enhancer GRCh37_chr18:76707071-76707585 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78947071..78947585) | | |
ID: 127889697 | H3K4me1 hESC enhancer GRCh37_chr18:76695174-76696141 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78935174..78936141) | | |
ID: 127889696 | H3K4me1 hESC enhancer GRCh37_chr18:76694205-76695173 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78934205..78935173) | | |
ID: 126862829 | BRD4-independent group 4 enhancer GRCh37_chr18:76766909-76768108 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79006909..79008108) | | |
ID: 105372225 | uncharacterized LOC105372225 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79001397..79064040, complement) | | |
ID: 645321 | long intergenic non-protein coding RNA 1896 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78976555..78979691, complement) | | |
ID: 374868 | ATPase phospholipid transporting 9B (putative) [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (79069394..79378283) | ATPASEP, ATPIIB, HUSSY-20, NEO1L, hMMR1 | 614446 |
ID: 27164 | spalt like transcription factor 3 [Homo sapiens (human)] | Chromosome 18, NC_000018.10 (78979818..78998969) | ZNF796 | 605079 |