| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74529120-74529381 | Rare:94 | ||||
| chr2:74529392-74529536 | Common:1; Rare:55; Clinvar (benign):2 | ||||
| chr2:74529611-74530059 | Rare:148; Clinvar:4; Clinvar (benign):1 | ||||
| chr2:74530465-74530627 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74548794-74549175 | Rare:95 | ||||
| chr2:74549408-74549750 | Rare:82 | ||||
| chr2:74554003-74554197 | Rare:40 | ||||
| chr2:74654046-74654461 | Common:2; Rare:149 | ||||
| chr2:74833794-74834150 | Common:1; Rare:108 | ||||
| chr2:74834794-74835065 | Rare:72 | ||||
| chr2:74835133-74835333 | Rare:50 | ||||
| chr2:74835485-74835663 | Common:3; Rare:55 | ||||
| chr2:74958280-74958725 | Common:6; Rare:141 | ||||
| chr2:74958840-74959045 | Rare:79 | ||||
| chr2:75199497-75199604 | Rare:14 |