| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:148644012-148644204 | Common:1; Rare:32 | ||||
| chr2:148644375-148644836 | Rare:339 | ||||
| chr2:148644820-148645100 | Common:2; Rare:125 | ||||
| chr2:148645108-148646188 | Common:4; Rare:885 | ||||
| chr2:149586736-149587715 | Common:19; Rare:635; Clinvar:4; Clinvar (benign):19 | ||||
| chr2:149587650-149588050 | Common:5; Rare:401; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:151260938-151261526 | Common:16; Rare:353 | ||||
| chr2:151261680-151262350 | Common:14; Rare:283 | ||||
| chr2:151289157-151290230 | Common:13; Rare:662 | ||||
| chr2:151290405-151290747 | Common:2; Rare:54 | ||||
| chr2:151409376-151411290 | Common:40; Rare:1887 | ||||
| chr2:151827809-151828209 | Common:6; Rare:136 | ||||
| chr2:151828334-151828809 | Common:20; Rare:740 | ||||
| chr2:152175230-152176300 | Common:14; Rare:1169 | ||||
| chr2:152334873-152335273 | Common:2; Rare:212 |