| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:12730831-12731700 | Common:5; Rare:370 | ||||
| chr19:12734131-12734531 | Rare:99 | ||||
| chr19:12734463-12735031 | Common:8; Rare:677 | ||||
| chr19:12736803-12737599 | Common:12; Rare:639 | ||||
| chr19:12775423-12775823 | Common:12; Rare:406 | ||||
| chr19:12777507-12777907 | Common:3; Rare:80 | ||||
| chr19:12777952-12778352 | Common:1; Rare:76 | ||||
| chr19:12778270-12778981 | Common:4; Rare:344 | ||||
| chr19:12791204-12791996 | Common:4; Rare:539 | ||||
| chr19:12792180-12792350 | Common:4; Rare:74 | ||||
| chr19:12792413-12793502 | Common:9; Rare:353 | ||||
| chr19:12800195-12800479 | Common:2; Rare:86 | ||||
| chr19:12801115-12801515 | Common:3; Rare:195 | ||||
| chr19:12801699-12802512 | Common:5; Rare:591 | ||||
| chr19:12806332-12806732 | Common:8; Rare:329; Clinvar:7; Clinvar (benign):5 |