| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:52685833-52686101 | Common:2; Rare:108 | ||||
| chr3:52705487-52706172 | Common:5; Rare:204 | ||||
| chr3:55480871-55481002 | Rare:33; Clinvar (benign):1 | ||||
| chr3:55481006-55481088 | Rare:14 | ||||
| chr3:55487187-55487621 | Rare:102; Clinvar:7; Clinvar (benign):1 | ||||
| chr3:57227604-57227787 | Common:1; Rare:60 | ||||
| chr3:57597272-57597667 | Common:4; Rare:123 | ||||
| chr3:58433792-58434049 | Common:2; Rare:93; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:62318825-62319058 | Common:1; Rare:98 | ||||
| chr3:64018668-64018919 | Common:2; Rare:73 | ||||
| chr3:67654557-67654778 | Common:2; Rare:88 | ||||
| chr3:69013236-69013451 | Common:1; Rare:56 | ||||
| chr3:69013590-69013838 | Common:1; Rare:78 | ||||
| chr3:69080354-69080459 | Rare:44 | ||||
| chr3:73624933-73625112 | Common:4; Rare:46 |