| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:2164533-2165374 | Common:10; Rare:532 | ||||
| chr19:2235670-2236329 | Common:2; Rare:263 | ||||
| chr19:2269636-2269868 | Common:7; Rare:170 | ||||
| chr19:2270074-2270310 | Common:4; Rare:73 | ||||
| chr19:2328390-2328719 | Common:4; Rare:231 | ||||
| chr19:2427010-2427270 | Common:7; Rare:120 | ||||
| chr19:2427531-2427684 | Common:2; Rare:67 | ||||
| chr19:2434260-2434780 | Common:1; Rare:165; Clinvar:2; Clinvar (benign):2 | ||||
| chr19:2456887-2457104 | Rare:119; Clinvar:2 | ||||
| chr19:2475859-2476132 | Common:2; Rare:167 | ||||
| chr19:2783220-2783605 | Common:1; Rare:204 | ||||
| chr19:2819705-2819999 | Common:5; Rare:80 | ||||
| chr19:2841189-2841543 | Common:4; Rare:215 | ||||
| chr19:2900631-2900991 | Common:20; Rare:284 | ||||
| chr19:2944850-2945218 | Common:6; Rare:128 |