| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:176207449-176207713 | Common:4; Rare:187 | ||||
| chr1:177969928-177970231 | Common:2; Rare:106 | ||||
| chr1:178093470-178093930 | Common:11; Rare:208 | ||||
| chr1:178093979-178094146 | Common:2; Rare:81 | ||||
| chr1:178094340-178094740 | Common:2; Rare:244 | ||||
| chr1:178725098-178725338 | Common:20; Rare:173 | ||||
| chr1:178871025-178871227 | Rare:41 | ||||
| chr1:179025584-179026008 | Common:10; Rare:174 | ||||
| chr1:179081912-179082138 | Common:2; Rare:137 | ||||
| chr1:179229600-179229859 | Common:13; Rare:109 | ||||
| chr1:179365504-179365986 | Common:13; Rare:160 | ||||
| chr1:179881760-179882306 | Common:5; Rare:173 | ||||
| chr1:179882603-179882874 | Rare:214; Clinvar:12; Clinvar (benign):1 | ||||
| chr1:179882895-179883295 | Common:8; Rare:172; Clinvar:2; Clinvar (benign):3 | ||||
| chr1:179954332-179954583 | Common:2; Rare:59 |