| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:7553801-7553842 | Rare:3 | ||||
| chr6:7571350-7572072 | Common:5; Rare:190; Clinvar:11; Clinvar (benign):17; Clinvar (pathogenic):2 | ||||
| chr6:13710779-13710987 | Rare:82 | ||||
| chr6:13794170-13794398 | Common:1; Rare:36 | ||||
| chr6:16436666-16436786 | Common:1; Rare:23 | ||||
| chr6:16760055-16760203 | Rare:52 | ||||
| chr6:21595864-21596016 | Rare:57 | ||||
| chr6:25992577-25992738 | Rare:40 | ||||
| chr6:26122976-26123202 | Common:3; Rare:68 | ||||
| chr6:26157079-26157125 | Common:1; Rare:28 | ||||
| chr6:26521775-26522070 | Common:1; Rare:58 | ||||
| chr6:27019791-27019955 | Common:1; Rare:36 | ||||
| chr6:28136771-28136922 | Common:1; Rare:52 | ||||
| chr6:28923360-28923407 | Common:1; Rare:15 | ||||
| chr6:29752581-29752667 | Common:1; Rare:9 |