Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:87818207-87818293 | Rare:28 | ||||
chr10:90921120-90921495 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
chr10:91633056-91633230 | Common:1; Rare:55 | ||||
chr10:97445990-97446217 | Rare:58 | ||||
chr10:99732078-99732314 | Rare:84; Clinvar:3 | ||||
chr10:100987459-100987555 | Rare:37 | ||||
chr10:101588195-101588328 | Rare:52 | ||||
chr10:103396451-103396686 | Rare:84 | ||||
chr10:110919295-110919619 | Common:7; Rare:80 | ||||
chr10:112446938-112447246 | Common:2; Rare:70 | ||||
chr10:119080777-119080923 | Rare:57 | ||||
chr10:119178792-119178940 | Common:3; Rare:56 | ||||
chr10:122954202-122954484 | Rare:104 | ||||
chr10:125719466-125719716 | Rare:78 | ||||
chr10:125823200-125823560 | Common:1; Rare:118; Clinvar:1; Clinvar (benign):1 |