| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:1103794-1104116 | Common:4; Rare:135 | ||||
| chr19:1105374-1105703 | Common:2; Rare:157; Clinvar (pathogenic):1 | ||||
| chr19:1260935-1261173 | Common:3; Rare:79 | ||||
| chr19:1269057-1269406 | Common:2; Rare:134 | ||||
| chr19:1354827-1355008 | Rare:75 | ||||
| chr19:1605390-1605631 | Common:3; Rare:95 | ||||
| chr19:2269251-2269597 | Common:2; Rare:147 | ||||
| chr19:2328559-2328712 | Common:2; Rare:74 | ||||
| chr19:2475862-2476130 | Common:1; Rare:83 | ||||
| chr19:2783250-2783584 | Common:1; Rare:105 | ||||
| chr19:2785266-2785545 | Common:5; Rare:83 | ||||
| chr19:3359329-3359637 | Common:2; Rare:100 | ||||
| chr19:3971021-3971354 | Common:1; Rare:122 | ||||
| chr19:3982805-3983292 | Common:5; Rare:175; Clinvar:1; Clinvar (benign):6 | ||||
| chr19:4182532-4182698 | Common:1; Rare:60 |