Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:119268617-119268811 | Common:1; Rare:56 | ||||
chr5:119355825-119356021 | Common:2; Rare:50 | ||||
chr5:122774859-122775105 | Common:1; Rare:93 | ||||
chr5:122845315-122845625 | Common:3; Rare:107 | ||||
chr5:127290683-127290839 | Rare:34 | ||||
chr5:127517527-127517704 | Common:4; Rare:80 | ||||
chr5:128538222-128538378 | Common:5; Rare:53 | ||||
chr5:131170693-131171002 | Common:1; Rare:63; Clinvar (benign):1 | ||||
chr5:131635211-131635446 | Common:1; Rare:86 | ||||
chr5:131796943-131797221 | Rare:78 | ||||
chr5:132227797-132227913 | Common:2; Rare:28 | ||||
chr5:132556804-132557003 | Common:1; Rare:68; Clinvar:1 | ||||
chr5:132866493-132866694 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
chr5:132963519-132963803 | Common:1; Rare:73 | ||||
chr5:133051868-133052199 | Rare:109 |