| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:19192596-19192910 | Common:2; Rare:83 | ||||
| chr19:19516163-19516300 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr19:29213135-29213328 | Common:3; Rare:61 | ||||
| chr19:32971939-32972262 | Common:4; Rare:90 | ||||
| chr19:33521765-33521948 | Rare:55; Clinvar:3 | ||||
| chr19:34254525-34254594 | Rare:17 | ||||
| chr19:34365066-34365249 | Common:1; Rare:79 | ||||
| chr19:34428312-34428425 | Rare:48 | ||||
| chr19:34677552-34677717 | Common:3; Rare:44 | ||||
| chr19:35545454-35545705 | Common:4; Rare:84 | ||||
| chr19:35745397-35745698 | Rare:88 | ||||
| chr19:35757890-35758193 | Common:2; Rare:90 | ||||
| chr19:36014205-36014553 | Common:2; Rare:94 | ||||
| chr19:36114811-36114983 | Common:2; Rare:73 | ||||
| chr19:36214888-36215196 | Common:1; Rare:82 |