| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116279505-116279662 | Common:2; Rare:53 | ||||
| chr6:116279667-116280098 | Common:2; Rare:147 | ||||
| chr6:116571187-116571593 | Common:3; Rare:115 | ||||
| chr6:116877130-116877284 | Common:3; Rare:55 | ||||
| chr6:117602176-117602247 | Rare:32 | ||||
| chr6:117602278-117602363 | Rare:26 | ||||
| chr6:117602423-117602633 | Common:4; Rare:59 | ||||
| chr6:117675305-117675505 | Common:3; Rare:54 | ||||
| chr6:118548234-118548344 | Common:2; Rare:26; Clinvar:2; Clinvar (benign):2 | ||||
| chr6:118893853-118894225 | Common:6; Rare:107 | ||||
| chr6:118934958-118935071 | Common:4; Rare:36 | ||||
| chr6:119349249-119349413 | Common:2; Rare:27 | ||||
| chr6:119349677-119349930 | Common:2; Rare:84 | ||||
| chr6:121334426-121334531 | Common:3; Rare:46 | ||||
| chr6:121334683-121334792 | Common:1; Rare:17 |