| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:93495760-93496160 | Common:8; Rare:71 | ||||
| chr10:93496342-93496727 | Common:5; Rare:95 | ||||
| chr10:93496851-93496876 | Rare:4 | ||||
| chr10:93701889-93702112 | Rare:37 | ||||
| chr10:93702161-93702194 | Common:1; Rare:7 | ||||
| chr10:93702345-93703128 | Common:9; Rare:201 | ||||
| chr10:93893842-93894067 | Common:1; Rare:87 | ||||
| chr10:94362625-94362681 | Rare:13 | ||||
| chr10:94362815-94363129 | Common:5; Rare:125 | ||||
| chr10:94545291-94545354 | Rare:8 | ||||
| chr10:94545391-94545524 | Rare:28 | ||||
| chr10:94545630-94545922 | Common:4; Rare:99 | ||||
| chr10:95561328-95561625 | Common:4; Rare:94 | ||||
| chr10:95656611-95656740 | Common:1; Rare:43; Clinvar:4; Clinvar (benign):2 | ||||
| chr10:95656794-95656943 | Rare:32 |