| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:5653143-5653347 | Rare:60 | ||||
| chr19:5799292-5799493 | Common:6; Rare:48 | ||||
| chr19:5828719-5828873 | Common:2; Rare:24 | ||||
| chr19:5838017-5838099 | Rare:25 | ||||
| chr19:5847934-5847981 | Common:1; Rare:9 | ||||
| chr19:6707171-6707488 | Common:2; Rare:100; Clinvar:1; Clinvar (benign):2 | ||||
| chr19:7379006-7379165 | Common:2; Rare:28 | ||||
| chr19:7391255-7391348 | Common:2; Rare:19 | ||||
| chr19:7610571-7610735 | Common:2; Rare:51 | ||||
| chr19:7623174-7623436 | Rare:80 | ||||
| chr19:10561001-10561169 | Rare:62 | ||||
| chr19:10796529-10796799 | Common:2; Rare:58 | ||||
| chr19:10805871-10805945 | Common:1; Rare:19; Clinvar (benign):3 | ||||
| chr19:10823763-10823821 | Common:1; Rare:13; Clinvar:1; Clinvar (benign):5 | ||||
| chr19:11003154-11003377 | Common:2; Rare:70; Clinvar:1; Clinvar (benign):9 |