| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73071322-73071501 | Common:1; Rare:58 | ||||
| chr2:73071689-73071870 | Common:2; Rare:72 | ||||
| chr2:73233193-73233468 | Common:1; Rare:75 | ||||
| chr2:73234195-73234368 | Common:2; Rare:55 | ||||
| chr2:73385729-73386059 | Common:4; Rare:167; Clinvar:16; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr2:73737250-73737473 | Common:2; Rare:68 | ||||
| chr2:73828804-73829047 | Common:1; Rare:59 | ||||
| chr2:73926722-73927019 | Common:2; Rare:150; Clinvar:10; Clinvar (benign):3 | ||||
| chr2:74147830-74148150 | Common:3; Rare:84; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178798-74179065 | Common:3; Rare:83 | ||||
| chr2:74391793-74392140 | Common:2; Rare:164 | ||||
| chr2:74421576-74421776 | Rare:66 | ||||
| chr2:74440487-74440805 | Rare:85 | ||||
| chr2:74454884-74455123 | Rare:69 | ||||
| chr2:74465354-74465461 | Common:1; Rare:29 |