| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:94062930-94063052 | Rare:33 | ||||
| chr3:98593571-98593855 | Common:2; Rare:103 | ||||
| chr3:98901125-98901165 | Common:1; Rare:16 | ||||
| chr3:98901638-98902024 | Common:1; Rare:148 | ||||
| chr3:99638386-99638630 | Common:1; Rare:59 | ||||
| chr3:99817568-99817972 | Rare:125 | ||||
| chr3:100260666-100261056 | Rare:114 | ||||
| chr3:100334692-100334780 | Common:1; Rare:42 | ||||
| chr3:100401336-100401555 | Common:1; Rare:56 | ||||
| chr3:100709229-100709748 | Common:6; Rare:155; Clinvar (benign):1 | ||||
| chr3:108589429-108589722 | Common:3; Rare:71 | ||||
| chr3:111859567-111859861 | Rare:95 | ||||
| chr3:112561532-112561709 | Rare:71 | ||||
| chr3:112561866-112562078 | Common:1; Rare:65 | ||||
| chr3:113745988-113746310 | Common:2; Rare:112 |