| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:6197739-6197827 | Common:2; Rare:26 | ||||
| chr1:6206029-6206142 | Common:1; Rare:26 | ||||
| chr1:6235895-6236186 | Common:6; Rare:122 | ||||
| chr1:6385586-6386029 | Common:1; Rare:110 | ||||
| chr1:6393275-6393544 | Common:2; Rare:94 | ||||
| chr1:6393702-6393829 | Rare:41 | ||||
| chr1:6424670-6424788 | Common:1; Rare:43 | ||||
| chr1:6477578-6477857 | Common:2; Rare:73; Clinvar (benign):1 | ||||
| chr1:6491665-6491793 | Rare:14 | ||||
| chr1:6497369-6497656 | Common:2; Rare:80 | ||||
| chr1:6599355-6599593 | Common:3; Rare:82 | ||||
| chr1:6613453-6613784 | Common:2; Rare:120 | ||||
| chr1:7784127-7784387 | Common:2; Rare:103 | ||||
| chr1:7954109-7954297 | Rare:48 | ||||
| chr1:7961446-7961791 | Common:4; Rare:119; Clinvar:3; Clinvar (benign):3 |