| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:110567381-110567804 | Common:2; Rare:129; Clinvar:2; Clinvar (benign):5 | ||||
| chr10:110871582-110872016 | Rare:141 | ||||
| chr10:110918937-110918953 | Rare:3 | ||||
| chr10:110919133-110919636 | Common:8; Rare:133 | ||||
| chr10:112446731-112447334 | Common:3; Rare:148 | ||||
| chr10:112950044-112950373 | Common:3; Rare:67 | ||||
| chr10:112950971-112951256 | Common:2; Rare:73 | ||||
| chr10:113552715-113553188 | Common:2; Rare:102; Clinvar:3; Clinvar (benign):2 | ||||
| chr10:113854320-113854974 | Common:1; Rare:153 | ||||
| chr10:116272144-116272453 | Common:2; Rare:69 | ||||
| chr10:117005062-117005476 | Common:2; Rare:124 | ||||
| chr10:117374210-117374345 | Rare:40 | ||||
| chr10:118046670-118047011 | Common:4; Rare:107 | ||||
| chr10:118754930-118755292 | Common:1; Rare:119 | ||||
| chr10:119080772-119080979 | Common:1; Rare:91 |