| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:38618806-38619270 | Common:4; Rare:134 | ||||
| chr19:38647367-38647748 | Common:3; Rare:132 | ||||
| chr19:38831762-38831980 | Common:4; Rare:76; Clinvar (benign):1 | ||||
| chr19:38849259-38849453 | Rare:77 | ||||
| chr19:38849884-38850144 | Common:1; Rare:102 | ||||
| chr19:38850354-38850715 | Common:1; Rare:120 | ||||
| chr19:38851876-38852140 | Common:2; Rare:98 | ||||
| chr19:38899578-38899980 | Rare:112 | ||||
| chr19:38930706-38930996 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):3 | ||||
| chr19:38975351-38975528 | Common:1; Rare:28 | ||||
| chr19:38975600-38975910 | Common:1; Rare:69 | ||||
| chr19:39125551-39125847 | Rare:80 | ||||
| chr19:39341919-39342297 | Common:1; Rare:103 | ||||
| chr19:39391032-39391449 | Common:1; Rare:171 | ||||
| chr19:39406683-39406850 | Rare:56 |