| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:13150218-13150445 | Common:1; Rare:76 | ||||
| chr19:13747684-13747949 | Common:1; Rare:102 | ||||
| chr19:13764391-13764718 | Common:5; Rare:109 | ||||
| chr19:13906032-13906416 | Rare:86 | ||||
| chr19:13906422-13906465 | Rare:9; Clinvar:2 | ||||
| chr19:13906764-13907075 | Common:1; Rare:48 | ||||
| chr19:13923346-13923720 | Common:1; Rare:120; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:14072459-14072840 | Common:3; Rare:102 | ||||
| chr19:14136847-14137197 | Common:2; Rare:70 | ||||
| chr19:14160669-14160950 | Common:1; Rare:91 | ||||
| chr19:14440192-14440282 | Rare:21 | ||||
| chr19:14496050-14496373 | Common:6; Rare:134 | ||||
| chr19:14529290-14529677 | Common:1; Rare:171 | ||||
| chr19:14690044-14690103 | Rare:17 | ||||
| chr19:15125128-15125219 | Rare:18 |