| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:174999220-174999580 | Common:11; Rare:448 | ||||
| chr1:174999525-175000160 | Common:20; Rare:1137 | ||||
| chr1:175000327-175000727 | Common:2; Rare:91 | ||||
| chr1:175014418-175015456 | Common:9; Rare:377; Clinvar (pathogenic):3 | ||||
| chr1:175022956-175023733 | Common:7; Rare:559 | ||||
| chr1:175192143-175192543 | Common:2; Rare:72 | ||||
| chr1:175192698-175192901 | Common:7; Rare:249 | ||||
| chr1:175192940-175193360 | Common:11; Rare:194 | ||||
| chr1:176205573-176205973 | Common:2; Rare:86 | ||||
| chr1:176206060-176206761 | Common:3; Rare:586 | ||||
| chr1:176206720-176208128 | Common:44; Rare:1833 | ||||
| chr1:177032382-177032782 | Common:1; Rare:185 | ||||
| chr1:178093460-178093970 | Common:19; Rare:356 | ||||
| chr1:178724988-178725388 | Common:59; Rare:524 | ||||
| chr1:178725802-178725908 | Rare:23 |