| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:176002254-176002407 | Common:2; Rare:61 | ||||
| chr2:177212572-177212797 | Common:2; Rare:96 | ||||
| chr2:177264630-177264830 | Common:2; Rare:64 | ||||
| chr2:177392680-177392770 | Rare:19 | ||||
| chr2:181892110-181892207 | Common:1; Rare:27 | ||||
| chr2:186486036-186486344 | Common:3; Rare:86 | ||||
| chr2:189784294-189784506 | Common:3; Rare:67; Clinvar:6; Clinvar (benign):1 | ||||
| chr2:191014133-191014340 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr2:191677858-191678140 | Common:4; Rare:78 | ||||
| chr2:196639579-196639671 | Rare:19 | ||||
| chr2:197434980-197435273 | Rare:94 | ||||
| chr2:197499807-197500131 | Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:197500171-197500430 | Common:1; Rare:108 | ||||
| chr2:200306592-200306901 | Common:2; Rare:99 | ||||
| chr2:200811319-200811572 | Common:1; Rare:77 |