| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123701436-123701648 | Common:1; Rare:67; Clinvar:7 | ||||
| chr3:125375221-125375426 | Rare:60 | ||||
| chr3:126084103-126084281 | Common:1; Rare:75 | ||||
| chr3:127672808-127673014 | Common:3; Rare:99 | ||||
| chr3:127823169-127823340 | Common:3; Rare:34 | ||||
| chr3:128052178-128052532 | Common:2; Rare:122 | ||||
| chr3:128153383-128153496 | Rare:34 | ||||
| chr3:128650556-128650738 | Rare:66 | ||||
| chr3:128725975-128726189 | Common:1; Rare:60; Clinvar:2 | ||||
| chr3:128879408-128879694 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129183814-129184079 | Common:2; Rare:89 | ||||
| chr3:129315874-129316109 | Common:2; Rare:58 | ||||
| chr3:129316254-129316377 | Common:1; Rare:46 | ||||
| chr3:129439829-129440234 | Common:1; Rare:123; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:129893545-129893866 | Rare:129 |