| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73234217-73234368 | Common:1; Rare:49 | ||||
| chr2:73385609-73386090 | Common:4; Rare:223; Clinvar:17; Clinvar (benign):9; Clinvar (pathogenic):1 | ||||
| chr2:73386118-73386329 | Common:1; Rare:79; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:73737237-73737498 | Common:2; Rare:83 | ||||
| chr2:73828804-73829057 | Common:2; Rare:60 | ||||
| chr2:73926701-73927051 | Common:2; Rare:165; Clinvar:11; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr2:74147830-74148165 | Common:3; Rare:88; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178772-74179026 | Common:2; Rare:68 | ||||
| chr2:74198424-74198679 | Rare:111 | ||||
| chr2:74391793-74392143 | Common:2; Rare:165 | ||||
| chr2:74421571-74421781 | Rare:71 | ||||
| chr2:74440425-74440642 | Rare:59 | ||||
| chr2:74454863-74455138 | Rare:75 | ||||
| chr2:74458100-74458509 | Common:1; Rare:125 | ||||
| chr2:74465354-74465449 | Rare:25 |