| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:36418621-36418712 | Rare:28 | ||||
| chr19:36528230-36528322 | Common:1; Rare:25 | ||||
| chr19:36573247-36573439 | Common:3; Rare:60 | ||||
| chr19:36605244-36605324 | Common:2; Rare:19 | ||||
| chr19:36687435-36687624 | Common:2; Rare:58 | ||||
| chr19:37317635-37317917 | Common:6; Rare:76 | ||||
| chr19:37469262-37469388 | Common:2; Rare:37 | ||||
| chr19:38264345-38264585 | Common:5; Rare:62 | ||||
| chr19:38264791-38264924 | Rare:45 | ||||
| chr19:38618847-38619266 | Common:4; Rare:124 | ||||
| chr19:38831765-38832047 | Common:4; Rare:82; Clinvar (benign):1 | ||||
| chr19:38930738-38931005 | Common:3; Rare:73; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:39391020-39391418 | Common:1; Rare:158 | ||||
| chr19:39406706-39406847 | Rare:53 | ||||
| chr19:39846307-39846468 | Common:1; Rare:75 |