Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87818158-87818248 | Rare:33 | ||||
chr10:97426116-97426291 | Common:2; Rare:71 | ||||
chr10:97445985-97446225 | Rare:60 | ||||
chr10:99430657-99430940 | Common:3; Rare:63 | ||||
chr10:99732093-99732275 | Rare:56; Clinvar:3 | ||||
chr10:100987457-100987535 | Rare:38 | ||||
chr10:101588163-101588329 | Rare:70 | ||||
chr10:103396411-103396664 | Rare:90 | ||||
chr10:110919326-110919616 | Common:7; Rare:75 | ||||
chr10:112446904-112447256 | Common:3; Rare:85 | ||||
chr10:119080777-119080920 | Rare:56 | ||||
chr10:119892528-119892765 | Common:3; Rare:88 | ||||
chr10:122954202-122954476 | Rare:101 | ||||
chr10:125823205-125823553 | Common:1; Rare:111; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905302-126905458 | Rare:60 |