ID: 127274201 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:98963419-98963930 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98346956..98347467) | | |
ID: 127274200 | OCT4-NANOG-H3K27ac hESC enhancer GRCh37_chr2:98950857-98951787 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98334394..98335324) | | |
ID: 127274199 | NANOG hESC enhancer GRCh37_chr2:98933593-98934329 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98317130..98317866) | | |
ID: 127274198 | H3K4me1 hESC enhancer GRCh37_chr2:98896664-98897164 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98280201..98280701) | | |
ID: 127274197 | NANOG hESC enhancer GRCh37_chr2:98808643-98809198 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98192180..98192735) | | |
ID: 127274196 | H3K4me1 hESC enhancer GRCh37_chr2:98779443-98779989 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98162980..98163526) | | |
ID: 127274195 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:98748819-98749404 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98132356..98132941) | | |
ID: 127274194 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr2:98748232-98748818 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98131769..98132355) | | |
ID: 127274193 | NANOG-H3K27ac hESC enhancer GRCh37_chr2:98746447-98747273 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98129984..98130810) | | |
ID: 127274192 | H3K4me1 hESC enhancer GRCh37_chr2:98733965-98734464 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98117502..98118001) | | |
ID: 127274191 | H3K4me1 hESC enhancer GRCh37_chr2:98733463-98733964 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98117000..98117501) | | |
ID: 127274190 | H3K4me1 hESC enhancer GRCh37_chr2:98703859-98704359 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98087396..98087896) | | |
ID: 127274189 | H3K4me1 hESC enhancer GRCh37_chr2:98703358-98703858 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98086895..98087395) | | |
ID: 127274188 | H3K27ac hESC enhancer GRCh37_chr2:98664273-98664773 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98047810..98048310) | | |
ID: 126806278 | P300/CBP strongly-dependent group 1 enhancer GRCh37_chr2:98750133-98751332 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98133670..98134869) | | |
ID: 126806277 | CDK7 strongly-dependent group 2 enhancer GRCh37_chr2:98670618-98671817 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98054155..98055354) | | |
ID: 122817712 | Sharpr-MPRA regulatory region 9320 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98128546..98128840) | | |
ID: 105373501 | uncharacterized LOC105373501 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98045236..98052399, complement) | | |
ID: 200403 | von Willebrand factor A domain containing 3B [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98087167..98330616) | SCAR22 | 614884 |
ID: 1261 | cyclic nucleotide gated channel subunit alpha 3 [Homo sapiens (human)] | Chromosome 2, NC_000002.12 (98346456..98398601) | ACHM2, CCNC1, CCNCa, CCNCalpha, CNCG3, CNG3 | 600053 |