| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:178450731-178450897 | Rare:56 | ||||
| chr2:178451074-178451366 | Common:6; Rare:86; Clinvar:4; Clinvar (benign):3 | ||||
| chr2:178478464-178478659 | Common:1; Rare:55 | ||||
| chr2:178480196-178480372 | Common:1; Rare:53 | ||||
| chr2:180980268-180980545 | Common:1; Rare:86 | ||||
| chr2:180980872-180980967 | Rare:16 | ||||
| chr2:181457237-181457662 | Common:2; Rare:157 | ||||
| chr2:181891665-181892275 | Common:6; Rare:239 | ||||
| chr2:182715935-182716483 | Common:3; Rare:179 | ||||
| chr2:182716812-182717033 | Common:1; Rare:46 | ||||
| chr2:183038416-183038704 | Common:4; Rare:87 | ||||
| chr2:183078680-183078806 | Rare:26 | ||||
| chr2:183124269-183124460 | Common:2; Rare:68 | ||||
| chr2:186485978-186486455 | Common:3; Rare:137 | ||||
| chr2:186505153-186505520 | Rare:63 |