| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:7851456-7851730 | Common:1; Rare:56 | ||||
| chr19:7903536-7903941 | Rare:135 | ||||
| chr19:7920243-7920375 | Rare:61 | ||||
| chr19:7943621-7944017 | Rare:116 | ||||
| chr19:7973860-7974168 | Rare:80 | ||||
| chr19:8005530-8005829 | Common:1; Rare:107 | ||||
| chr19:8321308-8321703 | Common:2; Rare:159 | ||||
| chr19:8364037-8364158 | Common:1; Rare:32 | ||||
| chr19:8390077-8390455 | Common:2; Rare:109 | ||||
| chr19:8444784-8445144 | Common:4; Rare:155; Clinvar (benign):1 | ||||
| chr19:8445491-8445745 | Common:3; Rare:98 | ||||
| chr19:8514129-8514202 | Common:1; Rare:24 | ||||
| chr19:8526376-8526490 | Rare:43; Clinvar (benign):1 | ||||
| chr19:8577422-8577731 | Common:4; Rare:52 | ||||
| chr19:8698406-8698436 | Rare:11 |