| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:142147140-142147300 | Rare:63 | ||||
| chr6:143060413-143060494 | Rare:18 | ||||
| chr6:143060742-143060919 | Common:7; Rare:61 | ||||
| chr6:143450660-143450921 | Common:1; Rare:100; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143511670-143511924 | Common:4; Rare:52 | ||||
| chr6:145814718-145814925 | Common:1; Rare:98 | ||||
| chr6:149546010-149546159 | Rare:63 | ||||
| chr6:149648664-149648817 | Common:1; Rare:52 | ||||
| chr6:149718058-149718193 | Common:3; Rare:49 | ||||
| chr6:149746491-149746617 | Common:2; Rare:62 | ||||
| chr6:149749589-149749835 | Rare:120 | ||||
| chr6:151391503-151391853 | Common:3; Rare:101 | ||||
| chr6:151452047-151452540 | Common:4; Rare:174 | ||||
| chr6:152302003-152302236 | Rare:75; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:152983021-152983315 | Common:2; Rare:93 |