| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48645466-48646790 | Common:6; Rare:485 | ||||
| chr19:48738662-48739190 | Common:3; Rare:266 | ||||
| chr19:48755320-48755630 | Common:2; Rare:77 | ||||
| chr19:48810854-48811237 | Rare:260 | ||||
| chr19:48835694-48836499 | Common:4; Rare:288 | ||||
| chr19:48867860-48868290 | Common:14; Rare:158 | ||||
| chr19:48868527-48868665 | Rare:21 | ||||
| chr19:48872187-48872541 | Common:6; Rare:282 | ||||
| chr19:48899989-48900415 | Common:3; Rare:261 | ||||
| chr19:48933508-48933732 | Common:8; Rare:121 | ||||
| chr19:48954610-48954995 | Common:1; Rare:305 | ||||
| chr19:48955066-48955480 | Common:3; Rare:222 | ||||
| chr19:48965012-48965468 | Common:2; Rare:286; Clinvar:3; Clinvar (pathogenic):12 | ||||
| chr19:48965554-48965954 | Common:1; Rare:245; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr19:48993155-48993610 | Common:12; Rare:535; Clinvar:9; Clinvar (benign):9 |