| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40609896-40610355 | Common:20; Rare:260 | ||||
| chr19:40613225-40613460 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:40613373-40613773 | Rare:144; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:40613700-40614308 | Common:14; Rare:686; Clinvar:9; Clinvar (benign):10 | ||||
| chr19:40614523-40614923 | Common:5; Rare:110 | ||||
| chr19:40623820-40624342 | Common:8; Rare:348; Clinvar:3; Clinvar (benign):13 | ||||
| chr19:40689565-40689965 | Common:2; Rare:95 | ||||
| chr19:40690573-40691240 | Common:12; Rare:454 | ||||
| chr19:40691177-40691910 | Common:13; Rare:247 | ||||
| chr19:40714946-40716288 | Common:31; Rare:773 | ||||
| chr19:40716676-40717128 | Common:9; Rare:516 | ||||
| chr19:40717275-40718144 | Common:3; Rare:540 | ||||
| chr19:40718536-40719197 | Common:3; Rare:229 | ||||
| chr19:40748911-40749343 | Common:4; Rare:138 | ||||
| chr19:40749420-40750063 | Common:20; Rare:519 |