| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:40505971-40506115 | Rare:29 | ||||
| chr3:40524828-40525013 | Common:1; Rare:52 | ||||
| chr3:42581913-42582143 | Common:3; Rare:69 | ||||
| chr3:42582256-42582333 | Rare:22 | ||||
| chr3:42600297-42600749 | Common:3; Rare:175 | ||||
| chr3:42701480-42701696 | Common:1; Rare:39 | ||||
| chr3:42702573-42702896 | Rare:73 | ||||
| chr3:42719077-42719417 | Common:23; Rare:33 | ||||
| chr3:42804272-42804657 | Common:2; Rare:104 | ||||
| chr3:43286449-43286637 | Common:2; Rare:87 | ||||
| chr3:43690817-43690993 | Common:3; Rare:95; Clinvar:7; Clinvar (benign):2 | ||||
| chr3:44338339-44338807 | Common:8; Rare:154 | ||||
| chr3:44477646-44477750 | Common:1; Rare:18 | ||||
| chr3:44624888-44625095 | Common:2; Rare:61 | ||||
| chr3:44761583-44761794 | Common:3; Rare:77 |