| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:941705-941772 | Common:1; Rare:24 | ||||
| chr1:1231923-1232204 | Rare:91 | ||||
| chr1:1324624-1324816 | Common:2; Rare:104 | ||||
| chr1:1358513-1358837 | Common:2; Rare:111 | ||||
| chr1:1399307-1399610 | Common:1; Rare:136 | ||||
| chr1:1407137-1407391 | Common:1; Rare:112 | ||||
| chr1:1435606-1435746 | Rare:50 | ||||
| chr1:1615367-1615546 | Common:1; Rare:88 | ||||
| chr1:1658941-1659046 | Common:1; Rare:41 | ||||
| chr1:1724319-1724503 | Common:4; Rare:65 | ||||
| chr1:2391543-2391923 | Common:2; Rare:139 | ||||
| chr1:3624766-3625060 | Common:1; Rare:97 | ||||
| chr1:3857161-3857508 | Common:2; Rare:99 | ||||
| chr1:3900182-3900411 | Common:12; Rare:114 | ||||
| chr1:7961457-7961773 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):3 |