| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34424739-34425194 | Common:3; Rare:117; Clinvar (benign):6 | ||||
| chr6:34425993-34426195 | Common:5; Rare:82; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696768-34696988 | Common:1; Rare:52 | ||||
| chr6:34757330-34757558 | Common:1; Rare:68 | ||||
| chr6:35058108-35058304 | Rare:39 | ||||
| chr6:35214212-35214385 | Common:1; Rare:46 | ||||
| chr6:35921054-35921261 | Common:1; Rare:88 | ||||
| chr6:36442915-36443083 | Common:2; Rare:68 | ||||
| chr6:36547379-36547559 | Common:1; Rare:88 | ||||
| chr6:36594172-36594468 | Common:5; Rare:109 | ||||
| chr6:36678626-36678721 | Rare:31 | ||||
| chr6:36874775-36874889 | Rare:44 | ||||
| chr6:36875008-36875168 | Common:1; Rare:22 | ||||
| chr6:36885646-36886011 | Common:5; Rare:101 | ||||
| chr6:37257606-37257806 | Rare:49 |