| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40403685-40403803 | Common:1; Rare:54; Clinvar:3; Clinvar (benign):3 | ||||
| chr19:40404215-40404345 | Rare:30 | ||||
| chr19:40420821-40420905 | Common:1; Rare:20 | ||||
| chr19:40420975-40421138 | Common:2; Rare:31 | ||||
| chr19:40421179-40421436 | Common:2; Rare:61 | ||||
| chr19:40425084-40425394 | Common:2; Rare:58 | ||||
| chr19:40433363-40433414 | Common:1; Rare:7 | ||||
| chr19:40433775-40433833 | Rare:7 | ||||
| chr19:40434033-40434128 | Common:1; Rare:27 | ||||
| chr19:40434198-40434247 | Common:1; Rare:4 | ||||
| chr19:40602218-40602280 | Rare:8 | ||||
| chr19:40602447-40602619 | Rare:46 | ||||
| chr19:40603306-40603478 | Common:1; Rare:25 | ||||
| chr19:40603596-40603726 | Rare:18 | ||||
| chr19:40603872-40604242 | Rare:83 |