Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:145098154-145098339 | Rare:65 | ||||
chr4:182144418-182144691 | Common:3; Rare:85 | ||||
chr4:183659132-183659317 | Common:1; Rare:53 | ||||
chr4:184649442-184649756 | Common:4; Rare:101 | ||||
chr4:185425922-185426014 | Rare:30 | ||||
chr5:218134-218353 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):4 | ||||
chr5:612163-612351 | Rare:74 | ||||
chr5:892676-892949 | Common:5; Rare:96 | ||||
chr5:1799791-1799979 | Common:4; Rare:90 | ||||
chr5:1801300-1801432 | Common:4; Rare:57; Clinvar:1; Clinvar (benign):1 | ||||
chr5:7869010-7869200 | Common:2; Rare:94; Clinvar (benign):1 | ||||
chr5:10353600-10353896 | Common:3; Rare:106 | ||||
chr5:16465715-16465895 | Rare:32 | ||||
chr5:31532070-31532315 | Common:1; Rare:65 | ||||
chr5:34915493-34915741 | Common:1; Rare:56 |