| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7868703-7869079 | Common:2; Rare:86 | ||||
| chr19:7871380-7871590 | Rare:42 | ||||
| chr19:7871610-7871930 | Rare:106 | ||||
| chr19:7918981-7919277 | Common:2; Rare:71 | ||||
| chr19:8050599-8050916 | Common:3; Rare:82 | ||||
| chr19:8154430-8154840 | Common:7; Rare:88 | ||||
| chr19:8155007-8155121 | Rare:27 | ||||
| chr19:8161249-8161490 | Common:3; Rare:50 | ||||
| chr19:8268803-8269159 | Common:5; Rare:99 | ||||
| chr19:8355747-8355850 | Rare:13 | ||||
| chr19:8362022-8362271 | Common:1; Rare:52 | ||||
| chr19:8506219-8506330 | Common:1; Rare:22 | ||||
| chr19:8525844-8526041 | Rare:40 | ||||
| chr19:8552828-8553034 | Rare:43 | ||||
| chr19:8580868-8581000 | Rare:39; Clinvar:2; Clinvar (benign):1 |