| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:129449706-129450284 | Common:4; Rare:227 | ||||
| chr3:129461015-129461415 | Rare:142; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr3:129461358-129461758 | Common:3; Rare:62 | ||||
| chr3:129461760-129462200 | Common:2; Rare:68 | ||||
| chr3:129462384-129462784 | Common:2; Rare:89 | ||||
| chr3:129481782-129481906 | Rare:21 | ||||
| chr3:129578371-129578771 | Common:4; Rare:146 | ||||
| chr3:129606617-129607070 | Common:13; Rare:324 | ||||
| chr3:129607080-129607450 | Common:1; Rare:73 | ||||
| chr3:129892380-129893018 | Common:1; Rare:186 | ||||
| chr3:129893022-129893422 | Common:5; Rare:102 | ||||
| chr3:129893358-129893520 | Rare:74 | ||||
| chr3:129893536-129893981 | Rare:983 | ||||
| chr3:130093656-130095015 | Common:34; Rare:1101 | ||||
| chr3:130345280-130346090 | Common:28; Rare:366 |