| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40777921-40778280 | Common:1; Rare:98 | ||||
| chr19:41262363-41262583 | Rare:39 | ||||
| chr19:41363795-41364005 | Common:1; Rare:76; Clinvar:1 | ||||
| chr19:41364128-41364219 | Rare:31 | ||||
| chr19:41397329-41397426 | Common:2; Rare:33 | ||||
| chr19:41439531-41439672 | Common:1; Rare:41 | ||||
| chr19:41861010-41861209 | Rare:63; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:42075810-42076199 | Rare:110 | ||||
| chr19:42132402-42132646 | Rare:49 | ||||
| chr19:42220128-42220354 | Common:2; Rare:62 | ||||
| chr19:42302421-42302503 | Rare:17 | ||||
| chr19:43575477-43575827 | Common:2; Rare:91 | ||||
| chr19:43596127-43596450 | Common:2; Rare:100 | ||||
| chr19:43619572-43619664 | Common:1; Rare:30 | ||||
| chr19:43901790-43901866 | Rare:17 |