| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40777921-40778280 | Common:1; Rare:98 | ||||
| chr19:41262336-41262565 | Rare:44 | ||||
| chr19:41363795-41363983 | Common:1; Rare:69; Clinvar:1 | ||||
| chr19:41364137-41364317 | Rare:55 | ||||
| chr19:41397332-41397658 | Common:5; Rare:90 | ||||
| chr19:41860865-41861209 | Common:2; Rare:103; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:41959276-41959448 | Common:1; Rare:58 | ||||
| chr19:42075805-42076199 | Rare:112 | ||||
| chr19:42232671-42232758 | Common:1; Rare:14 | ||||
| chr19:42302305-42302656 | Rare:104 | ||||
| chr19:42302766-42303093 | Common:7; Rare:60 | ||||
| chr19:42442897-42443236 | Common:3; Rare:48 | ||||
| chr19:43504116-43504343 | Common:5; Rare:70 | ||||
| chr19:43596121-43596442 | Common:2; Rare:99 | ||||
| chr19:43619571-43619818 | Common:3; Rare:80 |