| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74440428-74440642 | Rare:59 | ||||
| chr2:74441854-74442026 | Common:2; Rare:37 | ||||
| chr2:74458100-74458498 | Common:1; Rare:119 | ||||
| chr2:74459493-74459957 | Rare:132 | ||||
| chr2:74465329-74465459 | Common:1; Rare:34; Clinvar:1 | ||||
| chr2:74482840-74483106 | Common:1; Rare:90 | ||||
| chr2:74502491-74502632 | Rare:35 | ||||
| chr2:74507321-74507454 | Rare:43 | ||||
| chr2:74507659-74507729 | Rare:17 | ||||
| chr2:74529579-74530036 | Rare:148; Clinvar:5; Clinvar (benign):1 | ||||
| chr2:74554512-74554755 | Common:1; Rare:79 | ||||
| chr2:74654112-74654285 | Rare:43 | ||||
| chr2:74833854-74834212 | Rare:107 | ||||
| chr2:74835141-74835325 | Rare:49 | ||||
| chr2:74958332-74958677 | Common:5; Rare:102 |