| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:6739129-6739286 | Common:1; Rare:21 | ||||
| chr19:6740627-6741112 | Common:1; Rare:126 | ||||
| chr19:7395022-7395188 | Common:4; Rare:52 | ||||
| chr19:7629523-7629848 | Common:5; Rare:117; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr19:7636996-7637143 | Common:2; Rare:50; Clinvar (benign):1 | ||||
| chr19:7920151-7920360 | Rare:72 | ||||
| chr19:7925441-7925746 | Common:2; Rare:80 | ||||
| chr19:7943630-7943990 | Rare:101 | ||||
| chr19:8308291-8308637 | Common:2; Rare:112 | ||||
| chr19:8321340-8321703 | Common:2; Rare:142 | ||||
| chr19:8364030-8364153 | Common:1; Rare:34 | ||||
| chr19:8390068-8390412 | Common:1; Rare:97 | ||||
| chr19:8390413-8390452 | Common:1; Rare:10 | ||||
| chr19:8444800-8445092 | Common:3; Rare:130; Clinvar (benign):1 | ||||
| chr19:8514121-8514222 | Common:2; Rare:32 |