| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:48872214-48872467 | Common:4; Rare:174 | ||||
| chr19:48896160-48896500 | Common:3; Rare:93 | ||||
| chr19:48900157-48900432 | Common:3; Rare:156 | ||||
| chr19:48918751-48919320 | Common:10; Rare:344 | ||||
| chr19:48933460-48933890 | Common:9; Rare:199 | ||||
| chr19:48954643-48954935 | Common:1; Rare:179 | ||||
| chr19:48955061-48955461 | Common:3; Rare:181 | ||||
| chr19:48964880-48965833 | Common:3; Rare:373; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):12 | ||||
| chr19:48993247-48993590 | Common:6; Rare:272; Clinvar:5; Clinvar (benign):4 | ||||
| chr19:48993602-48993913 | Common:9; Rare:132 | ||||
| chr19:49085116-49085594 | Common:6; Rare:373 | ||||
| chr19:49114140-49114440 | Common:6; Rare:120 | ||||
| chr19:49118930-49119520 | Common:2; Rare:360 | ||||
| chr19:49128029-49128284 | Common:4; Rare:133 | ||||
| chr19:49149538-49150299 | Common:2; Rare:232 |