| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:99141429-99141791 | Common:2; Rare:127 | ||||
| chr2:99154766-99155181 | Common:7; Rare:151; Clinvar (benign):3 | ||||
| chr2:99155449-99155539 | Common:1; Rare:27 | ||||
| chr2:99180939-99181274 | Common:2; Rare:102 | ||||
| chr2:99181366-99181489 | Rare:34 | ||||
| chr2:99335920-99336426 | Common:2; Rare:139 | ||||
| chr2:99337138-99337518 | Common:1; Rare:113 | ||||
| chr2:99337840-99337864 | Rare:4 | ||||
| chr2:99489901-99490396 | Common:2; Rare:193 | ||||
| chr2:100142455-100142710 | Common:4; Rare:44 | ||||
| chr2:100417317-100417680 | Rare:106 | ||||
| chr2:100562612-100563061 | Common:5; Rare:130 | ||||
| chr2:100563088-100563431 | Common:2; Rare:101 | ||||
| chr2:100924754-100924902 | Common:1; Rare:20 | ||||
| chr2:101002083-101002409 | Rare:113 |