Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:99732121-99732275 | Rare:45; Clinvar:3 | ||||
chr10:100912708-100913028 | Common:1; Rare:97 | ||||
chr10:100987445-100987557 | Rare:45 | ||||
chr10:101588217-101588329 | Rare:47 | ||||
chr10:102714271-102714627 | Common:2; Rare:119 | ||||
chr10:103396419-103396655 | Rare:84 | ||||
chr10:110919294-110919616 | Common:7; Rare:79 | ||||
chr10:112446898-112447273 | Common:3; Rare:90 | ||||
chr10:119080780-119080968 | Common:1; Rare:84 | ||||
chr10:122879525-122879753 | Common:4; Rare:57 | ||||
chr10:125719514-125719709 | Rare:59 | ||||
chr10:125823207-125823552 | Common:1; Rare:109; Clinvar:1; Clinvar (benign):1 | ||||
chr10:132331853-132332182 | Common:12; Rare:87 | ||||
chr10:133308844-133308964 | Rare:55 | ||||
chr11:777471-777602 | Rare:58 |