| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:158713797-158713987 | Common:2; Rare:48 | ||||
| chr3:169765038-169765211 | Rare:74; Clinvar:2; Clinvar (pathogenic):2 | ||||
| chr3:183267686-183267924 | Rare:32 | ||||
| chr3:183268196-183268264 | Rare:6 | ||||
| chr3:187740035-187740139 | Rare:20 | ||||
| chr3:187742258-187742416 | Common:1; Rare:28 | ||||
| chr3:193825155-193825421 | Common:2; Rare:40 | ||||
| chr3:194322096-194322322 | Common:3; Rare:40 | ||||
| chr3:194322776-194322875 | Common:3; Rare:21 | ||||
| chr3:194583866-194584020 | Common:10; Rare:56 | ||||
| chr3:195761546-195761842 | Common:1; Rare:69 | ||||
| chr3:195880057-195880073 | Rare:4 | ||||
| chr3:197516624-197516785 | Common:1; Rare:29 | ||||
| chr3:197627837-197627984 | Common:5; Rare:51 | ||||
| chr3:197850500-197850811 | Common:1; Rare:60 |