| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:119178773-119178941 | Common:3; Rare:70 | ||||
| chr10:119207558-119207571 | Rare:3 | ||||
| chr10:119542593-119542796 | Common:4; Rare:55 | ||||
| chr10:119596438-119596546 | Rare:40 | ||||
| chr10:119596631-119596755 | Common:1; Rare:32 | ||||
| chr10:119596911-119597284 | Common:2; Rare:102 | ||||
| chr10:119651209-119651848 | Common:7; Rare:223; Clinvar:9; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
| chr10:119872814-119872991 | Common:4; Rare:68 | ||||
| chr10:119892521-119892942 | Common:4; Rare:159 | ||||
| chr10:120851207-120851515 | Common:6; Rare:111 | ||||
| chr10:121927842-121928075 | Common:2; Rare:92 | ||||
| chr10:121959398-121959548 | Rare:36 | ||||
| chr10:121974163-121974479 | Common:3; Rare:55 | ||||
| chr10:121974731-121974891 | Common:1; Rare:52 | ||||
| chr10:121975125-121975375 | Common:1; Rare:52 |