| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:72273620-72274020 | Common:1; Rare:100 | ||||
| chr3:73600650-73600907 | Common:2; Rare:48 | ||||
| chr3:73623413-73624243 | Common:8; Rare:288 | ||||
| chr3:75435053-75435369 | Common:3; Rare:114 | ||||
| chr3:75481583-75481983 | Common:3; Rare:139 | ||||
| chr3:75641030-75641370 | Rare:59 | ||||
| chr3:75658652-75658774 | Rare:16 | ||||
| chr3:75672510-75672870 | Rare:5 | ||||
| chr3:76539920-76540270 | Common:7; Rare:54 | ||||
| chr3:77051874-77052376 | Rare:150 | ||||
| chr3:78035380-78035750 | Common:2; Rare:80 | ||||
| chr3:78176859-78177259 | Common:1; Rare:94 | ||||
| chr3:78986357-78986757 | Rare:90 | ||||
| chr3:81451154-81451554 | Common:1; Rare:119 | ||||
| chr3:81761188-81761435 | Common:2; Rare:99; Clinvar (benign):4; Clinvar (pathogenic):1 |