| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:10291281-10291517 | Common:1; Rare:69 | ||||
| chr19:10315924-10316108 | Common:3; Rare:93; Clinvar (benign):7 | ||||
| chr19:10333213-10333341 | Rare:44 | ||||
| chr19:10333420-10333774 | Common:1; Rare:124 | ||||
| chr19:10339387-10339504 | Rare:33 | ||||
| chr19:10339560-10339872 | Common:1; Rare:80 | ||||
| chr19:10339874-10340106 | Common:1; Rare:31 | ||||
| chr19:10380390-10381018 | Common:13; Rare:174; Clinvar:5 | ||||
| chr19:10403411-10403655 | Rare:102 | ||||
| chr19:10403806-10403932 | Rare:32 | ||||
| chr19:10430675-10430853 | Common:1; Rare:35 | ||||
| chr19:10502094-10502225 | Rare:22 | ||||
| chr19:10502293-10502466 | Common:1; Rare:40 | ||||
| chr19:10502625-10503053 | Rare:117 | ||||
| chr19:10503277-10503457 | Rare:36 |