| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:11231574-11231680 | Common:1; Rare:13 | ||||
| chr19:12672995-12673240 | Rare:85 | ||||
| chr19:13836279-13836407 | Rare:28 | ||||
| chr19:13839160-13839374 | Common:1; Rare:42 | ||||
| chr19:13839620-13839835 | Rare:53 | ||||
| chr19:13840556-13840897 | Common:1; Rare:77 | ||||
| chr19:13841485-13841699 | Common:1; Rare:46 | ||||
| chr19:13841762-13841780 | Rare:2 | ||||
| chr19:14409699-14409766 | Rare:25 | ||||
| chr19:14565950-14566083 | Common:1; Rare:54 | ||||
| chr19:15049895-15049998 | Common:2; Rare:14 | ||||
| chr19:15050263-15050580 | Common:13; Rare:39 | ||||
| chr19:15053469-15053853 | Common:1; Rare:144 | ||||
| chr19:15185256-15185702 | Common:1; Rare:131; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr19:15191803-15192058 | Common:1; Rare:85; Clinvar (benign):2; Clinvar (pathogenic):1 |