| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:115658801-115659177 | Common:3; Rare:92 | ||||
| chr3:115784590-115784692 | Common:1; Rare:35 | ||||
| chr3:116038602-116038745 | Rare:19 | ||||
| chr3:118782868-118782953 | Rare:15 | ||||
| chr3:118809988-118810086 | Common:2; Rare:19 | ||||
| chr3:119292792-119292965 | Common:1; Rare:23 | ||||
| chr3:119294877-119295297 | Common:4; Rare:102; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:119295529-119295641 | Rare:31 | ||||
| chr3:119321513-119321766 | Common:3; Rare:48 | ||||
| chr3:119322647-119322781 | Rare:33 | ||||
| chr3:119322857-119323631 | Common:6; Rare:174 | ||||
| chr3:119408716-119408783 | Rare:11 | ||||
| chr3:119550171-119550205 | Rare:4 | ||||
| chr3:119550764-119550869 | Common:2; Rare:10 | ||||
| chr3:119553806-119553992 | Rare:31 |