| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:37231542-37231720 | Common:4; Rare:104; Clinvar (benign):3 | ||||
| chr2:37344513-37344759 | Common:2; Rare:83 | ||||
| chr2:38602877-38603005 | Common:1; Rare:51 | ||||
| chr2:38875886-38876055 | Common:1; Rare:63 | ||||
| chr2:39437078-39437453 | Common:4; Rare:134 | ||||
| chr2:43595957-43596205 | Common:1; Rare:90 | ||||
| chr2:44361479-44361986 | Common:3; Rare:160 | ||||
| chr2:46073692-46073910 | Rare:44 | ||||
| chr2:46297675-46297816 | Rare:55; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:46617012-46617255 | Common:6; Rare:102 | ||||
| chr2:46915724-46916122 | Common:4; Rare:128; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:46941684-46941785 | Common:2; Rare:40; Clinvar (benign):1 | ||||
| chr2:47176439-47176569 | Rare:93; Clinvar (benign):5 | ||||
| chr2:48440631-48440857 | Common:7; Rare:111 | ||||
| chr2:53767740-53767881 | Common:2; Rare:53 |