Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:33440624-33441108 | Common:7; Rare:137 | ||||
chr5:34915472-34915741 | Common:1; Rare:65 | ||||
chr5:36151881-36152195 | Rare:100 | ||||
chr5:36876544-36876922 | Common:1; Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
chr5:37379059-37379360 | Common:3; Rare:69 | ||||
chr5:38557236-38557259 | Rare:5 | ||||
chr5:39074346-39074528 | Common:1; Rare:86 | ||||
chr5:39424941-39425308 | Common:3; Rare:74 | ||||
chr5:40755906-40756114 | Rare:59 | ||||
chr5:40798158-40798303 | Rare:58 | ||||
chr5:43067351-43067384 | Rare:7 | ||||
chr5:43067438-43067708 | Rare:47 | ||||
chr5:43121369-43121648 | Common:1; Rare:107 | ||||
chr5:43313364-43313657 | Common:3; Rare:80 | ||||
chr5:43483837-43483970 | Common:1; Rare:46 |