Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:179882168-179882308 | Common:1; Rare:26 | ||||
chr1:179882527-179882822 | Rare:148; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954475-179954834 | Common:3; Rare:84 | ||||
chr1:180631861-180632169 | Common:5; Rare:112 | ||||
chr1:181088521-181088704 | Rare:62 | ||||
chr1:182391303-182391480 | Rare:36 | ||||
chr1:182391686-182392007 | Common:3; Rare:118; Clinvar:5; Clinvar (benign):3 | ||||
chr1:182604383-182604525 | Rare:30 | ||||
chr1:183635666-183636100 | Common:4; Rare:124 | ||||
chr1:184386886-184387177 | Rare:76 | ||||
chr1:184754726-184755182 | Common:1; Rare:112 | ||||
chr1:185156708-185156762 | Common:1; Rare:27 | ||||
chr1:185156906-185157297 | Common:2; Rare:109 | ||||
chr1:186375097-186375497 | Rare:115 | ||||
chr1:186375649-186375899 | Common:1; Rare:69 |