| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74482127-74482385 | Rare:95 | ||||
| chr2:74482546-74482811 | Rare:98 | ||||
| chr2:74482843-74483129 | Common:1; Rare:103 | ||||
| chr2:74483154-74483411 | Common:2; Rare:95 | ||||
| chr2:74502481-74502718 | Rare:62 | ||||
| chr2:74502993-74503209 | Common:1; Rare:45 | ||||
| chr2:74503211-74503520 | Rare:83 | ||||
| chr2:74507253-74507894 | Common:1; Rare:175 | ||||
| chr2:74529111-74529307 | Common:1; Rare:66 | ||||
| chr2:74529382-74529501 | Common:2; Rare:43; Clinvar (benign):2 | ||||
| chr2:74529572-74530202 | Rare:202; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:74530453-74530557 | Common:1; Rare:24; Clinvar (benign):1 | ||||
| chr2:74530686-74531051 | Rare:79; Clinvar:2 | ||||
| chr2:74548813-74549166 | Rare:92 | ||||
| chr2:74549359-74549735 | Rare:94 |