| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:112254337-112254658 | Rare:59 | ||||
| chr6:112254692-112254908 | Rare:39 | ||||
| chr6:116100695-116100920 | Common:1; Rare:88 | ||||
| chr6:116254017-116254246 | Common:5; Rare:71 | ||||
| chr6:116279099-116279474 | Common:3; Rare:148 | ||||
| chr6:116279505-116279592 | Rare:27 | ||||
| chr6:116279817-116280143 | Common:3; Rare:108 | ||||
| chr6:116461335-116461383 | Common:1; Rare:7 | ||||
| chr6:116571159-116571605 | Common:3; Rare:130 | ||||
| chr6:116680806-116681303 | Common:4; Rare:140 | ||||
| chr6:117602414-117602660 | Common:4; Rare:67 | ||||
| chr6:117675318-117675498 | Common:3; Rare:49 | ||||
| chr6:118547994-118548344 | Common:2; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:118651497-118651754 | Common:4; Rare:85 | ||||
| chr6:118893835-118894313 | Common:10; Rare:142 |