| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98732410-98732504 | Rare:18 | ||||
| chr3:98732512-98732726 | Rare:38 | ||||
| chr3:99817562-99817934 | Rare:112 | ||||
| chr3:99876161-99876254 | Rare:23 | ||||
| chr3:100260690-100261036 | Rare:93 | ||||
| chr3:100334628-100334794 | Common:1; Rare:71 | ||||
| chr3:100401382-100401592 | Common:1; Rare:45 | ||||
| chr3:100492413-100492735 | Common:2; Rare:99 | ||||
| chr3:100709207-100709721 | Common:9; Rare:155; Clinvar (benign):1 | ||||
| chr3:101513122-101513328 | Common:8; Rare:43 | ||||
| chr3:101561759-101561967 | Common:2; Rare:78 | ||||
| chr3:101574045-101574267 | Common:1; Rare:78 | ||||
| chr3:101677053-101677404 | Rare:115 | ||||
| chr3:101686480-101686890 | Common:2; Rare:163 | ||||
| chr3:101724361-101724646 | Common:1; Rare:64 |