| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:27793633-27794066 | Common:1; Rare:107 | ||||
| chr19:36331645-36331934 | Common:2; Rare:76 | ||||
| chr19:37251704-37251942 | Common:6; Rare:61 | ||||
| chr19:38845675-38845912 | Common:1; Rare:70 | ||||
| chr19:41500614-41500732 | Rare:18 | ||||
| chr19:41981720-41982107 | Rare:85; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr19:42287190-42287447 | Common:1; Rare:84; Clinvar:2 | ||||
| chr19:42396881-42397184 | Common:1; Rare:75 | ||||
| chr19:45451545-45451718 | Rare:38 | ||||
| chr19:46428902-46429022 | Common:1; Rare:23 | ||||
| chr19:46860833-46861133 | Common:3; Rare:96 | ||||
| chr19:47324540-47324713 | Common:3; Rare:28 | ||||
| chr19:51354157-51354441 | Common:2; Rare:106; Clinvar:1; Clinvar (benign):4 | ||||
| chr19:51354761-51354990 | Common:1; Rare:37 | ||||
| chr19:52942596-52942711 | Common:1; Rare:40 |