| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:941705-941772 | Not yet | Common:1; Rare:24 | 88 | ||
| chr1:1231923-1232204 | Not yet | Rare:91 | 308 | ||
| chr1:1324624-1324816 | Not yet | Common:2; Rare:104 | 256 | ||
| chr1:1358513-1358837 | Not yet | Common:2; Rare:111 | 308 | ||
| chr1:1399307-1399610 | Not yet | Common:1; Rare:136 | 290 | ||
| chr1:1407137-1407391 | Not yet | Common:1; Rare:112 | 284 | ||
| chr1:1435606-1435746 | Not yet | Rare:50 | 104 | ||
| chr1:1615367-1615546 | Not yet | Common:1; Rare:88 | 214 | ||
| chr1:1658941-1659046 | Not yet | Common:1; Rare:41 | 246 | ||
| chr1:1724319-1724503 | Not yet | Common:4; Rare:65 | 337 | ||
| chr1:2391543-2391923 | Not yet | Common:2; Rare:139 | 310 | ||
| chr1:3624766-3625060 | Not yet | Common:1; Rare:97 | 284 | ||
| chr1:3857161-3857508 | Not yet | Common:2; Rare:99 | 345 | ||
| chr1:3900182-3900411 | Not yet | Common:12; Rare:114 | 269 | ||
| chr1:7961457-7961773 | Not yet | Common:4; Rare:108; Clinvar:2; Clinvar (benign):3 | 282 |