| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17337957-17338370 | Common:4; Rare:309; Clinvar (benign):13; Clinvar (pathogenic):3 | ||||
| chr19:17403812-17404506 | Common:8; Rare:257 | ||||
| chr19:17405011-17405411 | Common:2; Rare:96 | ||||
| chr19:17405369-17406711 | Common:49; Rare:789; Clinvar:1 | ||||
| chr19:17418784-17419650 | Common:11; Rare:215 | ||||
| chr19:17419560-17420300 | Common:133; Rare:987 | ||||
| chr19:17448070-17448500 | Common:1; Rare:96 | ||||
| chr19:17448549-17448949 | Common:1; Rare:202 | ||||
| chr19:17469710-17470090 | Common:4; Rare:141 | ||||
| chr19:17470100-17470563 | Common:4; Rare:222 | ||||
| chr19:17470537-17470937 | Common:9; Rare:189 | ||||
| chr19:17489024-17489424 | Common:12; Rare:327 | ||||
| chr19:17511280-17512550 | Common:29; Rare:1700 | ||||
| chr19:17523239-17523656 | Common:3; Rare:278 | ||||
| chr19:17539644-17540115 | Common:6; Rare:264 |