| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:116371619-116371840 | Common:2; Rare:53 | ||||
| chr6:116386621-116386763 | Rare:28 | ||||
| chr6:116431117-116431436 | Common:1; Rare:65; Clinvar (benign):2 | ||||
| chr6:117527783-117527801 | Rare:2 | ||||
| chr6:117569300-117569577 | Rare:44 | ||||
| chr6:117697000-117697015 | Common:1; Rare:1 | ||||
| chr6:117704013-117704060 | Rare:12 | ||||
| chr6:118475321-118475340 | Rare:1 | ||||
| chr6:118481896-118482024 | Common:2; Rare:28 | ||||
| chr6:119185872-119186060 | Common:3; Rare:33 | ||||
| chr6:119221277-119221414 | Common:2; Rare:26 | ||||
| chr6:119350594-119350645 | Rare:12 | ||||
| chr6:121124844-121124992 | Common:2; Rare:21 | ||||
| chr6:121437226-121437391 | Common:6; Rare:39 | ||||
| chr6:122415941-122416180 | Common:4; Rare:42 |