| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38852311-38852367 | Rare:18 | ||||
| chr19:38899503-38900180 | Rare:192 | ||||
| chr19:38930471-38930556 | Common:1; Rare:37; Clinvar (benign):1 | ||||
| chr19:38930708-38931085 | Common:4; Rare:108; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975642-38975796 | Common:1; Rare:33 | ||||
| chr19:39032234-39032605 | Common:7; Rare:69 | ||||
| chr19:39125558-39125877 | Common:1; Rare:80 | ||||
| chr19:39390642-39390748 | Rare:18 | ||||
| chr19:39390850-39390925 | Rare:31 | ||||
| chr19:39390991-39391438 | Common:1; Rare:173 | ||||
| chr19:39406701-39406852 | Rare:57 | ||||
| chr19:39413405-39413573 | Common:1; Rare:53 | ||||
| chr19:39435527-39436225 | Common:9; Rare:283 | ||||
| chr19:39445436-39445962 | Common:3; Rare:157 | ||||
| chr19:39480556-39480961 | Common:3; Rare:178; Clinvar (pathogenic):1 |