| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:125823200-125823615 | Common:1; Rare:148; Clinvar:1; Clinvar (benign):1 | ||||
| chr10:125896478-125896591 | Rare:4 | ||||
| chr10:126905283-126905473 | Rare:73 | ||||
| chr10:128047421-128047659 | Common:4; Rare:79 | ||||
| chr10:130136312-130136474 | Common:6; Rare:67 | ||||
| chr10:132331810-132332240 | Common:14; Rare:144 | ||||
| chr10:133308811-133309013 | Common:1; Rare:96 | ||||
| chr11:207317-207719 | Common:8; Rare:135 | ||||
| chr11:208654-208857 | Rare:78 | ||||
| chr11:236324-236513 | Common:6; Rare:60 | ||||
| chr11:236913-237052 | Common:1; Rare:54 | ||||
| chr11:288812-289128 | Common:2; Rare:83 | ||||
| chr11:320707-320932 | Common:5; Rare:85; Clinvar:1 | ||||
| chr11:506728-506994 | Common:3; Rare:89 | ||||
| chr11:507169-507505 | Common:4; Rare:110 |