| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:35748239-35748629 | Common:3; Rare:111 | ||||
| chr19:35757009-35757066 | Rare:16 | ||||
| chr19:35757934-35758218 | Common:2; Rare:88 | ||||
| chr19:35899710-35899870 | Common:1; Rare:50 | ||||
| chr19:35900538-35900684 | Rare:33 | ||||
| chr19:35908242-35908317 | Rare:20; Clinvar:2 | ||||
| chr19:36014183-36014517 | Common:2; Rare:95 | ||||
| chr19:36032810-36032921 | Common:2; Rare:29 | ||||
| chr19:36054155-36054176 | Rare:10 | ||||
| chr19:36054187-36054361 | Rare:64 | ||||
| chr19:36054368-36054588 | Common:3; Rare:60 | ||||
| chr19:36054745-36055054 | Common:2; Rare:110; Clinvar:4; Clinvar (benign):1 | ||||
| chr19:36114769-36115011 | Common:2; Rare:97 | ||||
| chr19:36115674-36115793 | Rare:31 | ||||
| chr19:36139832-36140087 | Rare:78 |