| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:134374467-134374783 | Common:1; Rare:88 | ||||
| chr3:134485442-134485693 | Rare:47 | ||||
| chr3:134485694-134485782 | Rare:34 | ||||
| chr3:134485957-134486275 | Common:3; Rare:111 | ||||
| chr3:134794951-134795540 | Common:2; Rare:132 | ||||
| chr3:134823756-134823852 | Rare:16 | ||||
| chr3:135965527-135965813 | Common:1; Rare:120 | ||||
| chr3:136195301-136195442 | Rare:46 | ||||
| chr3:136196255-136196360 | Rare:40 | ||||
| chr3:136196562-136196711 | Rare:43 | ||||
| chr3:136196852-136196979 | Rare:38 | ||||
| chr3:136250272-136250402 | Common:2; Rare:58; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr3:136255238-136255343 | Rare:24 | ||||
| chr3:136255768-136255921 | Rare:40; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:136752229-136752763 | Common:1; Rare:175 |