| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:33454415-33454620 | Rare:53 | ||||
| chr6:33711654-33711876 | Common:2; Rare:93; Clinvar (benign):1 | ||||
| chr6:34236749-34236906 | Common:3; Rare:65 | ||||
| chr6:34249092-34249408 | Common:2; Rare:74 | ||||
| chr6:34392274-34392678 | Rare:153 | ||||
| chr6:34696679-34696980 | Common:1; Rare:67 | ||||
| chr6:34757325-34757554 | Common:1; Rare:66 | ||||
| chr6:34887949-34888146 | Common:1; Rare:46 | ||||
| chr6:35258738-35258960 | Rare:30 | ||||
| chr6:35259250-35259797 | Common:3; Rare:168 | ||||
| chr6:35468228-35468447 | Common:3; Rare:77 | ||||
| chr6:35688809-35689140 | Common:1; Rare:114 | ||||
| chr6:35728026-35728245 | Rare:43 | ||||
| chr6:35797284-35797377 | Common:2; Rare:32 | ||||
| chr6:35921042-35921171 | Rare:66 |