| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:117602423-117602683 | Common:4; Rare:69 | ||||
| chr6:117675298-117675505 | Common:3; Rare:56 | ||||
| chr6:118548271-118548350 | Common:1; Rare:15; Clinvar:1; Clinvar (benign):1 | ||||
| chr6:118651466-118651754 | Common:5; Rare:91 | ||||
| chr6:118893908-118894313 | Common:3; Rare:123 | ||||
| chr6:119349705-119349974 | Common:3; Rare:101 | ||||
| chr6:121334442-121334579 | Common:3; Rare:56 | ||||
| chr6:121334687-121334791 | Common:1; Rare:16 | ||||
| chr6:122399351-122399758 | Common:6; Rare:152 | ||||
| chr6:122471701-122471950 | Common:4; Rare:90 | ||||
| chr6:122789098-122789410 | Common:2; Rare:87 | ||||
| chr6:122789491-122789819 | Common:1; Rare:84 | ||||
| chr6:124962856-124962979 | Rare:42 | ||||
| chr6:124963088-124963384 | Common:2; Rare:89 | ||||
| chr6:125154060-125154271 | Rare:38 |