| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:10292905-10293020 | Common:1; Rare:26 | ||||
| chr3:11154364-11154538 | Common:3; Rare:44 | ||||
| chr3:11225875-11226004 | Rare:16 | ||||
| chr3:11582332-11582439 | Rare:30 | ||||
| chr3:11719419-11719593 | Rare:56 | ||||
| chr3:11846843-11846996 | Common:1; Rare:42 | ||||
| chr3:12158708-12158959 | Rare:113 | ||||
| chr3:12158963-12159055 | Rare:32 | ||||
| chr3:12287781-12288003 | Common:6; Rare:39 | ||||
| chr3:12288936-12289092 | Common:1; Rare:33 | ||||
| chr3:12351240-12351528 | Rare:38 | ||||
| chr3:12556914-12557175 | Common:5; Rare:91 | ||||
| chr3:12663495-12663817 | Common:7; Rare:93; Clinvar:1 | ||||
| chr3:12663821-12663913 | Rare:25; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:12663934-12664300 | Common:2; Rare:102; Clinvar:3; Clinvar (benign):8 |