| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12782934-12783030 | Rare:26 | ||||
| chr19:12789838-12790166 | Common:1; Rare:67 | ||||
| chr19:12790307-12790425 | Rare:22 | ||||
| chr19:12793390-12793833 | Common:4; Rare:99 | ||||
| chr19:12793854-12794223 | Rare:76 | ||||
| chr19:12839040-12839076 | Rare:2 | ||||
| chr19:12867634-12867776 | Common:1; Rare:58 | ||||
| chr19:12880506-12880908 | Common:1; Rare:105 | ||||
| chr19:12885088-12885393 | Rare:77; Clinvar (pathogenic):2 | ||||
| chr19:12885572-12885674 | Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
| chr19:12885874-12885927 | Common:2; Rare:24; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:12913027-12913282 | Rare:60 | ||||
| chr19:12937450-12937548 | Common:1; Rare:11 | ||||
| chr19:12965777-12965803 | |||||
| chr19:12983565-12983758 | Rare:59 |