| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:34392302-34392456 | Rare:66 | ||||
| chr6:34424753-34425173 | Common:3; Rare:110; Clinvar (benign):6 | ||||
| chr6:34426003-34426146 | Common:4; Rare:67; Clinvar:1; Clinvar (benign):8 | ||||
| chr6:34696728-34696966 | Common:1; Rare:55 | ||||
| chr6:34757293-34757559 | Common:1; Rare:75 | ||||
| chr6:34887956-34888092 | Common:1; Rare:39 | ||||
| chr6:35259405-35259772 | Common:3; Rare:114 | ||||
| chr6:35921042-35921261 | Common:1; Rare:92 | ||||
| chr6:36442854-36443083 | Common:2; Rare:89 | ||||
| chr6:36547278-36547593 | Common:1; Rare:128 | ||||
| chr6:36594140-36594393 | Common:4; Rare:100 | ||||
| chr6:36676409-36676508 | Common:2; Rare:14 | ||||
| chr6:36678415-36678823 | Common:1; Rare:100 | ||||
| chr6:36874775-36874882 | Rare:43 | ||||
| chr6:36874961-36875153 | Common:1; Rare:30 |