| ID: 127267750 | H3K4me1 hESC enhancer GRCh37_chr1:17446537-17447071 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17120042..17120576) | | |
| ID: 127267749 | H3K4me1 hESC enhancer GRCh37_chr1:17412349-17412850 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17085854..17086355) | | |
| ID: 127267748 | H3K4me1 hESC enhancer GRCh37_chr1:17356477-17356976 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17029982..17030481) | | |
| ID: 127267747 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:17342829-17343364 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17016334..17016869) | | |
| ID: 127267746 | H3K27ac hESC enhancer GRCh37_chr1:17342294-17342828 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17015799..17016333) | | |
| ID: 127267745 | H3K4me1 hESC enhancer GRCh37_chr1:17319735-17320236 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16993240..16993741) | | |
| ID: 127267744 | H3K4me1 hESC enhancer GRCh37_chr1:17305891-17306396 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16979396..16979901) | | |
| ID: 127267743 | H3K4me1 hESC enhancer GRCh37_chr1:17305383-17305890 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16978888..16979395) | | |
| ID: 127267742 | H3K4me1 hESC enhancer GRCh37_chr1:17304877-17305382 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16978382..16978887) | | |
| ID: 127267741 | H3K4me1 hESC enhancer GRCh37_chr1:17300945-17301752 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16974450..16975257) | | |
| ID: 127267740 | H3K27ac-H3K4me1 hESC enhancer GRCh37_chr1:17298533-17299510 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16972038..16973015) | | |
| ID: 124903861 | uncharacterized LOC124903861 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17111776..17113845) | | |
| ID: 105376808 | uncharacterized LOC105376808 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17135665..17138955) | | |
| ID: 105376806 | uncharacterized LOC105376806 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16975861..16977795) | | |
| ID: 23400 | ATPase cation transporting 13A2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16985958..17011928, complement) | CLN12, HSA9947, KRPPD, PARK9, SPG78 | 610513 |
| ID: 11240 | peptidyl arginine deiminase 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17066761..17119451, complement) | PAD-H19, PAD2, PDI2 | 607935 |
| ID: 9696 | ciliary rootlet coiled-coil, rootletin [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16914085..16972964) | CROCC1, ROLT, TAX1BP2 | 615776 |
| ID: 6390 | succinate dehydrogenase complex iron sulfur subunit B [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (17018722..17054032, complement) | CWS2, IP, MC2DN4, PGL4, PPGL4, SDH, SDH1, SDH2, SDHIP | 185470 |
| ID: 4237 | microfibril associated protein 2 [Homo sapiens (human)] | Chromosome 1, NC_000001.11 (16974502..16981583, complement) | MAGP, MAGP-1, MAGP1 | 156790 |