| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:87504773-87504966 | Common:1; Rare:95 | ||||
| chr10:87658937-87659184 | Common:5; Rare:34 | ||||
| chr10:87659576-87659946 | Common:7; Rare:97 | ||||
| chr10:87659957-87659997 | Rare:8 | ||||
| chr10:87660003-87660200 | Common:2; Rare:60 | ||||
| chr10:87660908-87660969 | Rare:9 | ||||
| chr10:87815358-87815400 | Rare:11 | ||||
| chr10:87817784-87818399 | Common:2; Rare:182 | ||||
| chr10:87862003-87862616 | Common:2; Rare:278; Clinvar:1 | ||||
| chr10:87862717-87862895 | Common:1; Rare:43 | ||||
| chr10:87864132-87864538 | Common:1; Rare:123; Clinvar:18; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr10:88880150-88880557 | Common:1; Rare:91 | ||||
| chr10:88990491-88990861 | Common:5; Rare:103; Clinvar (benign):5 | ||||
| chr10:88991285-88991442 | Common:2; Rare:30 | ||||
| chr10:89251761-89252113 | Common:3; Rare:91; Clinvar:5 |