| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:74164761-74165048 | Common:1; Rare:50 | ||||
| chr10:74190091-74190409 | Common:3; Rare:57 | ||||
| chr10:75021921-75022061 | Rare:36; Clinvar (benign):1 | ||||
| chr10:75192201-75192431 | Common:3; Rare:40 | ||||
| chr10:75225617-75225829 | Rare:44 | ||||
| chr10:75233069-75233289 | Common:3; Rare:39 | ||||
| chr10:75234145-75234636 | Common:2; Rare:145 | ||||
| chr10:75294977-75295174 | Common:1; Rare:39 | ||||
| chr10:75295342-75295412 | Common:2; Rare:16 | ||||
| chr10:75359076-75359161 | Rare:8 | ||||
| chr10:75399875-75400174 | Rare:131 | ||||
| chr10:75402679-75403071 | Common:3; Rare:103 | ||||
| chr10:75403100-75403160 | Rare:12 | ||||
| chr10:75403379-75403813 | Common:1; Rare:93 | ||||
| chr10:75403840-75403959 | Rare:31 |