| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127294073-127294219 | Common:2; Rare:56; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387227-127387437 | Common:4; Rare:74 | ||||
| chr2:127387891-127388256 | Common:10; Rare:159 | ||||
| chr2:127526312-127526598 | Common:2; Rare:107 | ||||
| chr2:127526803-127526963 | Rare:27 | ||||
| chr2:127619808-127620065 | Rare:47 | ||||
| chr2:127650529-127650792 | Common:5; Rare:73 | ||||
| chr2:127675063-127675414 | Common:4; Rare:59 | ||||
| chr2:127675526-127675629 | Rare:22 | ||||
| chr2:127811099-127811259 | Rare:52 | ||||
| chr2:127858112-127858219 | Common:1; Rare:51 | ||||
| chr2:127885828-127885991 | Rare:44 | ||||
| chr2:127886209-127886479 | Common:1; Rare:65 | ||||
| chr2:128028016-128028388 | Common:1; Rare:105 | ||||
| chr2:128091031-128091355 | Common:8; Rare:105 |