| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35775647-35775812 | Common:1; Rare:48 | ||||
| chr19:35899294-35899501 | Common:4; Rare:31 | ||||
| chr19:35899702-35900031 | Common:2; Rare:91 | ||||
| chr19:35900342-35900752 | Common:1; Rare:93 | ||||
| chr19:35902395-35902586 | Common:1; Rare:34 | ||||
| chr19:35994955-35995492 | Common:1; Rare:159; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:35995656-35995864 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr19:36014156-36014587 | Common:2; Rare:119 | ||||
| chr19:36032846-36032996 | Common:1; Rare:45 | ||||
| chr19:36053981-36054246 | Rare:99 | ||||
| chr19:36054248-36054653 | Common:3; Rare:111 | ||||
| chr19:36054710-36055063 | Common:2; Rare:126; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:36114788-36115003 | Common:2; Rare:86 | ||||
| chr19:36115135-36115593 | Common:4; Rare:142 | ||||
| chr19:36115640-36115841 | Rare:53 |