| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:118710069-118710212 | Rare:36 | ||||
| chr6:118893918-118894309 | Common:3; Rare:117 | ||||
| chr6:119349691-119349909 | Common:2; Rare:73 | ||||
| chr6:121334444-121334534 | Common:2; Rare:39 | ||||
| chr6:121435568-121435785 | Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:122471699-122472048 | Common:4; Rare:116 | ||||
| chr6:122788836-122789187 | Rare:56 | ||||
| chr6:122789343-122789466 | Common:1; Rare:55 | ||||
| chr6:124962869-124963219 | Common:1; Rare:127 | ||||
| chr6:124963527-124963744 | Rare:37 | ||||
| chr6:125301688-125301780 | Common:2; Rare:35 | ||||
| chr6:125301824-125302202 | Common:8; Rare:111 | ||||
| chr6:125781059-125781202 | Rare:25 | ||||
| chr6:125790822-125791050 | Common:2; Rare:71 | ||||
| chr6:125919041-125919350 | Rare:70 |