| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:17305472-17305940 | Common:5; Rare:157 | ||||
| chr19:17306019-17306200 | Rare:53 | ||||
| chr19:17306224-17306366 | Common:2; Rare:50 | ||||
| chr19:17309219-17309621 | Common:3; Rare:116 | ||||
| chr19:17336574-17336755 | Rare:43 | ||||
| chr19:17337080-17337151 | Rare:14 | ||||
| chr19:17337274-17337656 | Common:1; Rare:94; Clinvar:1 | ||||
| chr19:17338030-17338208 | Common:1; Rare:70; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr19:17405100-17405413 | Common:2; Rare:71 | ||||
| chr19:17405513-17405899 | Common:7; Rare:83 | ||||
| chr19:17405969-17406145 | Common:1; Rare:47; Clinvar:1 | ||||
| chr19:17406296-17406556 | Common:3; Rare:48 | ||||
| chr19:17419686-17420113 | Common:20; Rare:119 | ||||
| chr19:17420378-17420398 | Rare:6 | ||||
| chr19:17470178-17470550 | Common:1; Rare:110 |