| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:41325473-41325621 | Common:1; Rare:32 | ||||
| chr19:41325990-41326137 | Rare:36 | ||||
| chr19:41326514-41326613 | Common:2; Rare:12 | ||||
| chr19:41327345-41327752 | Common:4; Rare:106 | ||||
| chr19:41327831-41327982 | Common:2; Rare:34 | ||||
| chr19:41331510-41332021 | Common:3; Rare:82 | ||||
| chr19:41351584-41351777 | Common:2; Rare:35 | ||||
| chr19:41352385-41352997 | Common:3; Rare:155; Clinvar (benign):1 | ||||
| chr19:41361090-41361362 | Rare:37 | ||||
| chr19:41379167-41379256 | Common:4; Rare:14 | ||||
| chr19:41396290-41396454 | Common:1; Rare:34 | ||||
| chr19:41398903-41399038 | Common:1; Rare:24 | ||||
| chr19:41454194-41454387 | Rare:27 | ||||
| chr19:41454472-41454724 | Common:2; Rare:42 | ||||
| chr19:41477462-41477782 | Common:1; Rare:64 |