| ID: 127895792 | NANOG-H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:29663849-29664720 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29267860..29268731) | | |
| ID: 127895791 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:29656440-29657293 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29260451..29261304) | | |
| ID: 127895790 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:29655585-29656439 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29259596..29260450) | | |
| ID: 127895789 | H3K4me1 hESC enhancer GRCh37_chr22:29630135-29630635 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29234146..29234646) | | |
| ID: 127895788 | H3K4me1 hESC enhancer GRCh37_chr22:29629634-29630134 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29233645..29234145) | | |
| ID: 127895787 | H3K4me1 hESC enhancer GRCh37_chr22:29619669-29620170 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29223680..29224181) | | |
| ID: 127895786 | H3K4me1 hESC enhancer GRCh37_chr22:29614189-29614768 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29218200..29218779) | | |
| ID: 127895785 | H3K4me1 hESC enhancer GRCh37_chr22:29613609-29614188 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29217620..29218199) | | |
| ID: 127895784 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr22:29612449-29613028 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29216460..29217039) | | |
| ID: 127895783 | H3K4me1 hESC enhancer GRCh37_chr22:29611869-29612448 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29215880..29216459) | | |
| ID: 127895782 | H3K4me1 hESC enhancer GRCh37_chr22:29611289-29611868 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29215300..29215879) | | |
| ID: 127895781 | H3K4me1 hESC enhancer GRCh37_chr22:29610708-29611288 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29214719..29215299) | | |
| ID: 124905099 | uncharacterized LOC124905099 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29216327..29219811) | | |
| ID: 116309129 | CRISPRi-validated cis-regulatory element chr22.1165 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29195471..29196309) | | |
| ID: 112695076 | Sharpr-MPRA regulatory region 4816 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29197121..29197415) | | |
| ID: 105372985 | uncharacterized LOC105372985 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29223408..29225830, complement) | | |
| ID: 101929638 | uncharacterized LOC101929638 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29180263..29205832, complement) | | |
| ID: 129080 | EMI domain containing 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29205896..29259597) | EMI5, EMU1 | 608926 |
| ID: 25807 | rhomboid domain containing 3 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29259852..29268163, complement) | C22orf3, HS984G1A, PTAG | |
| ID: 2130 | EWS RNA binding protein 1 [Homo sapiens (human)] | Chromosome 22, NC_000022.11 (29268268..29300521) | EWS, EWS-FLI1, bK984G1.4 | 133450 |