| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38264769-38264994 | Rare:68 | ||||
| chr19:38315913-38316244 | Common:1; Rare:87 | ||||
| chr19:38647372-38647713 | Common:3; Rare:120 | ||||
| chr19:38724207-38724562 | Common:2; Rare:121; Clinvar:1; Clinvar (benign):3 | ||||
| chr19:38831726-38832061 | Common:4; Rare:110; Clinvar (benign):1 | ||||
| chr19:38852319-38852532 | Rare:49 | ||||
| chr19:38899592-38899937 | Rare:93 | ||||
| chr19:38930700-38931002 | Common:3; Rare:91; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr19:39391039-39391425 | Common:1; Rare:156 | ||||
| chr19:39406699-39406927 | Rare:92 | ||||
| chr19:39407081-39407106 | Rare:5 | ||||
| chr19:39407503-39407808 | Rare:75 | ||||
| chr19:39480731-39480888 | Common:3; Rare:87; Clinvar (pathogenic):1 | ||||
| chr19:39846294-39846468 | Common:1; Rare:79 | ||||
| chr19:39970957-39971196 | Common:3; Rare:62 |