| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:127106918-127107306 | Common:1; Rare:117; Clinvar:9; Clinvar (benign):2 | ||||
| chr2:127294077-127294212 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr2:127387931-127388250 | Common:9; Rare:137 | ||||
| chr2:127645752-127646060 | Common:2; Rare:67 | ||||
| chr2:127650531-127650658 | Common:5; Rare:29 | ||||
| chr2:127811121-127811287 | Common:1; Rare:60 | ||||
| chr2:127858096-127858202 | Common:1; Rare:60 | ||||
| chr2:127885932-127885972 | Rare:5 | ||||
| chr2:128091057-128091342 | Common:8; Rare:96 | ||||
| chr2:130181564-130181796 | Common:3; Rare:100 | ||||
| chr2:130182126-130182374 | Common:2; Rare:100 | ||||
| chr2:130342123-130342253 | Rare:54; Clinvar:1 | ||||
| chr2:130342292-130342346 | Common:1; Rare:11 | ||||
| chr2:130342692-130342935 | Common:3; Rare:80 | ||||
| chr2:130755367-130755557 | Common:1; Rare:45 |