| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:42846342-42846794 | Common:3; Rare:273 | ||||
| chr1:42943212-42943514 | Common:3; Rare:121; Clinvar:7; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr1:42958735-42959166 | Common:13; Rare:281; Clinvar:20; Clinvar (benign):13 | ||||
| chr1:43147501-43148040 | Common:21; Rare:256 | ||||
| chr1:43172180-43172440 | Common:4; Rare:270 | ||||
| chr1:43172460-43172770 | Common:22; Rare:225 | ||||
| chr1:43270390-43270770 | Rare:172 | ||||
| chr1:43270881-43271130 | Rare:73 | ||||
| chr1:43285511-43285720 | Common:4; Rare:63 | ||||
| chr1:43358526-43359148 | Common:21; Rare:464 | ||||
| chr1:43366264-43367243 | Common:8; Rare:333 | ||||
| chr1:43367570-43367858 | Common:6; Rare:129 | ||||
| chr1:43367915-43368312 | Rare:277 | ||||
| chr1:43389611-43390142 | Common:12; Rare:416; Clinvar:2 | ||||
| chr1:43530401-43531101 | Common:15; Rare:357 |