| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:633430-633835 | Common:48; Rare:820 | ||||
| chr19:634097-634497 | Common:2; Rare:83 | ||||
| chr19:639576-639994 | Common:28; Rare:590 | ||||
| chr19:663113-663573 | Common:18; Rare:725 | ||||
| chr19:679816-680230 | Common:8; Rare:148 | ||||
| chr19:680310-680831 | Common:16; Rare:883 | ||||
| chr19:694928-695328 | Common:7; Rare:127; Clinvar (benign):1 | ||||
| chr19:695236-695740 | Common:13; Rare:326 | ||||
| chr19:708650-709149 | Common:17; Rare:374 | ||||
| chr19:796711-797535 | Common:6; Rare:1121 | ||||
| chr19:797610-798127 | Common:28; Rare:1169 | ||||
| chr19:798042-799090 | Common:15; Rare:443 | ||||
| chr19:799092-799768 | Common:15; Rare:474 | ||||
| chr19:804569-804969 | Common:4; Rare:220 | ||||
| chr19:821146-822420 | Common:16; Rare:801 |