| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:40750957-40751259 | Common:1; Rare:84 | ||||
| chr19:40778017-40778298 | Common:1; Rare:90 | ||||
| chr19:41219183-41219375 | Common:1; Rare:49 | ||||
| chr19:41262313-41262583 | Rare:47 | ||||
| chr19:41263033-41263253 | Common:3; Rare:41 | ||||
| chr19:41264985-41265102 | Common:1; Rare:25 | ||||
| chr19:41310117-41310309 | Rare:81 | ||||
| chr19:41353780-41354100 | Common:2; Rare:104 | ||||
| chr19:41363746-41363983 | Common:1; Rare:77; Clinvar:1 | ||||
| chr19:41364137-41364212 | Rare:24 | ||||
| chr19:41376213-41376546 | Rare:74 | ||||
| chr19:41397332-41397477 | Common:3; Rare:42 | ||||
| chr19:41860103-41860289 | Common:1; Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr19:41884133-41884458 | Rare:84 | ||||
| chr19:42075816-42076199 | Rare:105 |