Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:79006662-79006862 | Common:1; Rare:67 | ||||
chr1:83999104-83999280 | Common:1; Rare:53 | ||||
chr1:84077844-84078141 | Common:3; Rare:113 | ||||
chr1:84506550-84506714 | Common:3; Rare:31 | ||||
chr1:84574416-84574585 | Common:1; Rare:51 | ||||
chr1:84690418-84690730 | Rare:102 | ||||
chr1:84996892-84997182 | Common:7; Rare:80 | ||||
chr1:85048439-85048603 | Common:2; Rare:38 | ||||
chr1:85259623-85259856 | Common:4; Rare:89 | ||||
chr1:85276288-85276774 | Common:7; Rare:147; Clinvar (benign):3 | ||||
chr1:85464577-85464704 | Common:3; Rare:31 | ||||
chr1:85578112-85578236 | Rare:22 | ||||
chr1:85578242-85578390 | Common:1; Rare:24 | ||||
chr1:85708310-85708518 | Common:2; Rare:75 | ||||
chr1:86704460-86704928 | Common:3; Rare:174 |