| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:18571665-18571891 | Common:2; Rare:96 | ||||
| chr19:18919344-18919740 | Common:2; Rare:139 | ||||
| chr19:19033482-19033734 | Common:2; Rare:74 | ||||
| chr19:19170212-19170410 | Common:2; Rare:44 | ||||
| chr19:19192110-19192205 | Common:1; Rare:34 | ||||
| chr19:19320478-19320802 | Common:4; Rare:109 | ||||
| chr19:19516157-19516331 | Rare:103; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:19643575-19643736 | Common:3; Rare:52 | ||||
| chr19:19668714-19668849 | Common:1; Rare:38 | ||||
| chr19:19821717-19821894 | Common:1; Rare:58 | ||||
| chr19:19900801-19900982 | Common:1; Rare:47 | ||||
| chr19:20167038-20167226 | Common:2; Rare:70 | ||||
| chr19:20565752-20565959 | Rare:56 | ||||
| chr19:20923103-20923317 | Rare:57 | ||||
| chr19:21020350-21020688 | Common:4; Rare:71 |