| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:195040795-195041098 | Common:2; Rare:60 | ||||
| chr3:195068050-195068610 | Common:20; Rare:212 | ||||
| chr3:195102527-195102920 | Common:5; Rare:131 | ||||
| chr3:195540343-195540722 | Common:2; Rare:100 | ||||
| chr3:195546317-195546527 | Common:1; Rare:22 | ||||
| chr3:195657879-195658129 | Common:13; Rare:42 | ||||
| chr3:195847050-195847420 | Common:3; Rare:94 | ||||
| chr3:195954515-195954618 | Common:2; Rare:14 | ||||
| chr3:195990220-195990429 | Rare:49 | ||||
| chr3:196075050-196075580 | Common:8; Rare:272; Clinvar (pathogenic):2 | ||||
| chr3:196108381-196108692 | Common:12; Rare:119 | ||||
| chr3:196110410-196110710 | Common:3; Rare:95 | ||||
| chr3:196135810-196136380 | Common:2; Rare:154 | ||||
| chr3:196138530-196138636 | Rare:14 | ||||
| chr3:196138560-196139020 | Common:1; Rare:73 |