| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr14:105419691-105419843 | Common:1; Rare:30 | ||||
| chr14:105486888-105486915 | Rare:6 | ||||
| chr14:105487024-105487233 | Common:1; Rare:59 | ||||
| chr14:105487633-105487833 | Common:1; Rare:62 | ||||
| chr14:105489822-105489921 | Rare:17 | ||||
| chr14:105490692-105491345 | Common:1; Rare:190 | ||||
| chr14:105491628-105491732 | Common:1; Rare:50 | ||||
| chr14:105528483-105528595 | Rare:22 | ||||
| chr15:22786153-22786230 | Rare:17 | ||||
| chr15:22786461-22786809 | Rare:121; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr15:22838364-22838770 | Common:3; Rare:147 | ||||
| chr15:22980306-22980539 | Rare:86 | ||||
| chr15:23038874-23039152 | Common:5; Rare:78 | ||||
| chr15:23039482-23039802 | Common:1; Rare:136 | ||||
| chr15:23565507-23565710 | Common:2; Rare:64 |