| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:128091056-128091343 | Common:8; Rare:97 | ||||
| chr2:130181571-130181760 | Common:2; Rare:84 | ||||
| chr2:130342121-130342279 | Rare:65; Clinvar:1 | ||||
| chr2:130342642-130342935 | Common:5; Rare:92 | ||||
| chr2:131493045-131493097 | Common:1; Rare:13 | ||||
| chr2:134918588-134918898 | Common:1; Rare:130 | ||||
| chr2:135531172-135531502 | Common:1; Rare:66 | ||||
| chr2:144513791-144513954 | Rare:43 | ||||
| chr2:144514819-144514937 | Rare:19 | ||||
| chr2:144517454-144517610 | Rare:34 | ||||
| chr2:144518134-144518203 | Common:1; Rare:14 | ||||
| chr2:144520311-144520528 | Common:4; Rare:40; Clinvar (benign):1 | ||||
| chr2:148020694-148021100 | Common:2; Rare:93; Clinvar (benign):2 | ||||
| chr2:148021565-148021625 | Rare:14 | ||||
| chr2:149587685-149588032 | Common:1; Rare:91; Clinvar:1 |