| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48965144-48965314 | Rare:44 | ||||
| chr19:48965525-48966097 | Common:2; Rare:348; Clinvar:7; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr19:48993281-48993608 | Common:3; Rare:136; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:48993731-48993930 | Common:5; Rare:61 | ||||
| chr19:49056112-49056314 | Common:2; Rare:111 | ||||
| chr19:49064699-49065182 | Rare:212 | ||||
| chr19:49085109-49085524 | Common:3; Rare:169 | ||||
| chr19:49114140-49114540 | Common:6; Rare:98 | ||||
| chr19:49114910-49115240 | Common:2; Rare:89 | ||||
| chr19:49128029-49128315 | Common:2; Rare:79 | ||||
| chr19:49142920-49143187 | Common:4; Rare:59 | ||||
| chr19:49149331-49149545 | Common:1; Rare:77 | ||||
| chr19:49149733-49149986 | Common:1; Rare:52 | ||||
| chr19:49155381-49155628 | Common:1; Rare:45 | ||||
| chr19:49157592-49157880 | Common:3; Rare:97; Clinvar:2; Clinvar (benign):2 |