Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:118988545-118988755 | Common:1; Rare:70 | ||||
chr5:119070880-119071149 | Common:2; Rare:85 | ||||
chr5:119268573-119268840 | Common:1; Rare:72 | ||||
chr5:119355825-119356057 | Common:3; Rare:61 | ||||
chr5:121961850-121962035 | Common:2; Rare:67 | ||||
chr5:122077109-122077257 | Common:1; Rare:25 | ||||
chr5:122077486-122077717 | Common:1; Rare:97; Clinvar (benign):4 | ||||
chr5:122078239-122078547 | Common:1; Rare:70 | ||||
chr5:122774918-122775110 | Rare:73 | ||||
chr5:122845516-122845621 | Common:3; Rare:40 | ||||
chr5:123036615-123036954 | Common:2; Rare:86 | ||||
chr5:123511928-123512161 | Common:1; Rare:80 | ||||
chr5:126595192-126595345 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):8 | ||||
chr5:128538195-128538525 | Common:8; Rare:92 | ||||
chr5:129094467-129094760 | Common:3; Rare:119 |