Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:63594204-63594384 | Common:2; Rare:41 | ||||
chr1:64965934-64966181 | Common:1; Rare:67 | ||||
chr1:64966428-64966724 | Common:2; Rare:113 | ||||
chr1:65148043-65148209 | Common:4; Rare:37 | ||||
chr1:65148705-65149002 | Common:3; Rare:85 | ||||
chr1:65254277-65254572 | Common:2; Rare:107 | ||||
chr1:65420120-65420530 | Common:3; Rare:90 | ||||
chr1:65420541-65421045 | Common:5; Rare:134; Clinvar:2; Clinvar (benign):1 | ||||
chr1:65792748-65793143 | Common:2; Rare:96 | ||||
chr1:66331468-66331768 | Common:1; Rare:46 | ||||
chr1:66331770-66331846 | Rare:21 | ||||
chr1:66332105-66332307 | Rare:40 | ||||
chr1:66332309-66332359 | Rare:8 | ||||
chr1:66332382-66332458 | Rare:27 | ||||
chr1:66924754-66925076 | Common:2; Rare:136 |