| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:69841255-69841535 | Common:4; Rare:37 | ||||
| chr2:70086254-70086492 | Common:4; Rare:94 | ||||
| chr2:74370469-74370820 | Common:1; Rare:87; Clinvar:3; Clinvar (benign):3 | ||||
| chr2:75667816-75667970 | Common:2; Rare:29 | ||||
| chr2:85543428-85543780 | Rare:63; Clinvar (benign):1 | ||||
| chr2:96254063-96254408 | Rare:70; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:96549554-96549800 | Rare:46 | ||||
| chr2:100818382-100818591 | Rare:54 | ||||
| chr2:101004007-101004249 | Rare:55 | ||||
| chr2:104853187-104853291 | Rare:20 | ||||
| chr2:109128346-109128627 | Common:1; Rare:70 | ||||
| chr2:109130362-109130631 | Common:1; Rare:67 | ||||
| chr2:109173770-109173964 | Rare:39 | ||||
| chr2:113584044-113584098 | Rare:14 | ||||
| chr2:131682429-131682542 | Common:3; Rare:43 |