| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35900438-35900744 | Common:1; Rare:72 | ||||
| chr19:35902403-35902583 | Common:1; Rare:32 | ||||
| chr19:35908543-35908549 | |||||
| chr19:35994970-35995251 | Common:1; Rare:73; Clinvar (benign):1 | ||||
| chr19:35995397-35995467 | Rare:22; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr19:36014160-36014580 | Common:2; Rare:118 | ||||
| chr19:36053976-36054342 | Rare:130 | ||||
| chr19:36054369-36054620 | Common:3; Rare:67 | ||||
| chr19:36054709-36055050 | Common:1; Rare:121; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:36114779-36114986 | Common:2; Rare:83 | ||||
| chr19:36115155-36115583 | Common:4; Rare:137 | ||||
| chr19:36115630-36115802 | Rare:46 | ||||
| chr19:36139487-36139581 | Common:1; Rare:24 | ||||
| chr19:36139816-36140188 | Common:1; Rare:111 | ||||
| chr19:36141168-36141322 | Common:1; Rare:69 |