| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:23806883-23807283 | Common:3; Rare:127 | ||||
| chr3:23915748-23916561 | Common:4; Rare:243 | ||||
| chr3:23916804-23917230 | Rare:156 | ||||
| chr3:23945089-23945362 | Common:7; Rare:103 | ||||
| chr3:23945807-23946564 | Common:13; Rare:477 | ||||
| chr3:24494600-24494990 | Rare:82; Clinvar:1 | ||||
| chr3:25428102-25428370 | Rare:59 | ||||
| chr3:25663508-25664585 | Common:12; Rare:447 | ||||
| chr3:25664833-25665132 | Common:4; Rare:95 | ||||
| chr3:25783363-25783669 | Common:2; Rare:102; Clinvar (benign):3 | ||||
| chr3:25789960-25790119 | Common:4; Rare:62 | ||||
| chr3:26622554-26622954 | Rare:104 | ||||
| chr3:27369320-27369620 | Rare:66 | ||||
| chr3:27484381-27484738 | Common:3; Rare:119 | ||||
| chr3:28241396-28241672 | Common:1; Rare:94 |