| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12643946-12644034 | Rare:19 | ||||
| chr19:12675259-12675566 | Common:2; Rare:74 | ||||
| chr19:12793558-12793720 | Common:3; Rare:38 | ||||
| chr19:13167579-13167722 | Rare:40 | ||||
| chr19:13839259-13839262 | |||||
| chr19:13840812-13840896 | Common:1; Rare:16 | ||||
| chr19:13912375-13912563 | Common:1; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:13926629-13926732 | Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
| chr19:14074226-14074549 | Common:1; Rare:75 | ||||
| chr19:14409699-14409763 | Rare:24 | ||||
| chr19:15120073-15120090 | Rare:2 | ||||
| chr19:15399500-15399688 | Rare:42 | ||||
| chr19:15697003-15697354 | Common:6; Rare:103 | ||||
| chr19:18309739-18310104 | Common:1; Rare:107 | ||||
| chr19:18319671-18319995 | Rare:64 |