| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:98593173-98593343 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:98593590-98593847 | Common:2; Rare:94 | ||||
| chr3:98732571-98732713 | Rare:29 | ||||
| chr3:99817570-99817920 | Rare:101 | ||||
| chr3:100260731-100261031 | Rare:78 | ||||
| chr3:100334655-100334786 | Common:1; Rare:57 | ||||
| chr3:100401367-100401539 | Common:1; Rare:40 | ||||
| chr3:100709236-100709677 | Common:6; Rare:137; Clinvar (benign):1 | ||||
| chr3:101561743-101561938 | Common:2; Rare:68 | ||||
| chr3:101574045-101574276 | Common:1; Rare:81 | ||||
| chr3:101677096-101677181 | Rare:37 | ||||
| chr3:101686642-101686906 | Common:2; Rare:104 | ||||
| chr3:101849713-101850143 | Rare:114 | ||||
| chr3:101850568-101850727 | Rare:34 | ||||
| chr3:108091018-108091335 | Common:1; Rare:89 |