| ID: 127271115 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:201095506-201096496 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201126378..201127368) | | |
| ID: 127271114 | H3K4me1 hESC enhancer GRCh37_chr1:201084381-201084901 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201115253..201115773) | | |
| ID: 127271113 | H3K4me1 hESC enhancer GRCh37_chr1:201072987-201073503 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201103859..201104375) | | |
| ID: 127271112 | H3K4me1 hESC enhancer GRCh37_chr1:201070741-201071240 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201101613..201102112) | | |
| ID: 127271111 | H3K4me1 hESC enhancer GRCh37_chr1:201070239-201070740 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201101111..201101612) | | |
| ID: 127271110 | H3K4me1 hESC enhancer GRCh37_chr1:201031613-201032386 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201062485..201063258) | | |
| ID: 127271109 | H3K4me1 hESC enhancer GRCh37_chr1:201028065-201028818 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201058937..201059690) | | |
| ID: 127271108 | H3K4me1 hESC enhancer GRCh37_chr1:201022145-201023102 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201053017..201053974) | | |
| ID: 127271107 | H3K4me1 hESC enhancer GRCh37_chr1:201021057-201021557 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201051929..201052429) | | |
| ID: 127271106 | H3K4me1 hESC enhancer GRCh37_chr1:200991037-200991644 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201021909..201022516) | | |
| ID: 124904481 | uncharacterized LOC124904481 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201095749..201098638) | | |
| ID: 112577527 | Sharpr-MPRA regulatory region 14143 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201028561..201028855) | | |
| ID: 101929305 | uncharacterized LOC101929305 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201023949..201036676) | | |
| ID: 647219 | achaete-scute family bHLH transcription factor 5 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201113943..201127184, complement) | ASH-5, AmeloD, bHLHa47 | |
| ID: 23046 | kinesin family member 21B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (200969390..201023714, complement) | | 608322 |
| ID: 779 | calcium voltage-gated channel subunit alpha1 S [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (201039512..201112426, complement) | CACNL1A3, CCHL1A3, CMYP18, Cav1.1, DHPRM, HOKPP, HOKPP1, MHS5, TTPP1, hypoPP | 114208 |