| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:99817555-99817920 | Rare:107 | ||||
| chr3:99876136-99876254 | Rare:29 | ||||
| chr3:100260699-100261067 | Rare:110 | ||||
| chr3:100334624-100334786 | Common:1; Rare:68 | ||||
| chr3:100401064-100401207 | Rare:43 | ||||
| chr3:100401367-100401652 | Common:2; Rare:61 | ||||
| chr3:100492129-100492206 | Rare:25 | ||||
| chr3:100492402-100492869 | Common:11; Rare:124 | ||||
| chr3:100709207-100709721 | Common:9; Rare:155; Clinvar (benign):1 | ||||
| chr3:101513115-101513325 | Common:8; Rare:42 | ||||
| chr3:101561740-101561991 | Common:2; Rare:89 | ||||
| chr3:101573972-101574242 | Rare:98 | ||||
| chr3:101677074-101677411 | Rare:108 | ||||
| chr3:101685816-101686025 | Common:3; Rare:56 | ||||
| chr3:101686480-101686875 | Common:2; Rare:158 |