| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:39834074-39834491 | Common:3; Rare:114 | ||||
| chr19:39840244-39840515 | Common:1; Rare:80 | ||||
| chr19:39846307-39846470 | Common:1; Rare:76 | ||||
| chr19:39970961-39971254 | Common:2; Rare:80 | ||||
| chr19:39979607-39980145 | Rare:110 | ||||
| chr19:39996925-39997113 | Common:5; Rare:61 | ||||
| chr19:40056157-40056293 | Rare:19 | ||||
| chr19:40284893-40285208 | Common:1; Rare:98 | ||||
| chr19:40285209-40285474 | Common:1; Rare:89 | ||||
| chr19:40348329-40348794 | Common:4; Rare:144 | ||||
| chr19:40377794-40378139 | Common:2; Rare:119; Clinvar (benign):1 | ||||
| chr19:40425881-40426127 | Common:1; Rare:85 | ||||
| chr19:40444225-40444476 | Common:3; Rare:82 | ||||
| chr19:40465689-40466084 | Common:3; Rare:121 | ||||
| chr19:40716861-40717160 | Common:1; Rare:99 |