| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:179592596-179592678 | Rare:20 | ||||
| chr3:181713310-181713621 | Common:2; Rare:62 | ||||
| chr3:181715486-181715656 | Rare:26 | ||||
| chr3:184242652-184242867 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:184317421-184317816 | Common:2; Rare:99 | ||||
| chr3:184322368-184322677 | Rare:96; Clinvar:1 | ||||
| chr3:184322688-184322865 | Rare:57 | ||||
| chr3:184323401-184323975 | Common:3; Rare:124 | ||||
| chr3:184332708-184332963 | Rare:66 | ||||
| chr3:184710803-184710837 | Rare:5 | ||||
| chr3:185418801-185419137 | Common:2; Rare:50 | ||||
| chr3:185976102-185976414 | Common:1; Rare:50 | ||||
| chr3:185980768-185981069 | Common:1; Rare:49 | ||||
| chr3:186584184-186584521 | Common:1; Rare:61 | ||||
| chr3:187038459-187038718 | Common:2; Rare:54 |