| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40750472-40750814 | Common:3; Rare:83 | ||||
| chr19:40751041-40751304 | Common:3; Rare:83 | ||||
| chr19:40777934-40778262 | Common:1; Rare:92 | ||||
| chr19:41218697-41218989 | Common:8; Rare:62 | ||||
| chr19:41219089-41219098 | Rare:1 | ||||
| chr19:41219115-41219436 | Common:1; Rare:87 | ||||
| chr19:41262315-41262595 | Rare:50 | ||||
| chr19:41264932-41265110 | Common:2; Rare:38 | ||||
| chr19:41310133-41310279 | Rare:60 | ||||
| chr19:41363795-41363992 | Common:1; Rare:70; Clinvar:1 | ||||
| chr19:41364080-41364309 | Common:1; Rare:70; Clinvar:2 | ||||
| chr19:41397318-41397520 | Common:4; Rare:54 | ||||
| chr19:41397566-41397830 | Common:7; Rare:90; Clinvar (benign):4 | ||||
| chr19:41860059-41860287 | Common:1; Rare:90; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41959279-41959459 | Common:1; Rare:58 |