| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:101686480-101686887 | Common:2; Rare:162 | ||||
| chr3:101724525-101724694 | Rare:59 | ||||
| chr3:101779100-101779259 | Common:3; Rare:51 | ||||
| chr3:101779411-101779686 | Common:1; Rare:64 | ||||
| chr3:105366779-105366934 | Common:1; Rare:40 | ||||
| chr3:105868822-105869228 | Common:8; Rare:138 | ||||
| chr3:107522810-107523060 | Common:1; Rare:61 | ||||
| chr3:108222318-108222611 | Common:3; Rare:89 | ||||
| chr3:108589371-108589945 | Common:3; Rare:177 | ||||
| chr3:111071551-111071811 | Common:1; Rare:84 | ||||
| chr3:111541958-111542262 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:111674527-111674745 | Rare:70 | ||||
| chr3:111859206-111859292 | Common:2; Rare:17 | ||||
| chr3:111859396-111859873 | Common:2; Rare:146 | ||||
| chr3:111978891-111979064 | Common:2; Rare:57 |