Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:74732966-74733344 | Common:6; Rare:131 | ||||
chr1:75724308-75724598 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):3 | ||||
chr1:77219385-77219520 | Rare:62 | ||||
chr1:77887959-77888419 | Common:26; Rare:204 | ||||
chr1:77888424-77888758 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77979020-77979291 | Common:2; Rare:92 | ||||
chr1:77979452-77979553 | Common:1; Rare:28 | ||||
chr1:78004547-78005001 | Common:4; Rare:99 | ||||
chr1:78045694-78045995 | Rare:66 | ||||
chr1:83999096-83999468 | Common:7; Rare:109 | ||||
chr1:84077943-84078311 | Common:3; Rare:112 | ||||
chr1:84574388-84574601 | Common:1; Rare:64 | ||||
chr1:84690405-84690668 | Rare:84 | ||||
chr1:85048439-85048618 | Common:2; Rare:39 | ||||
chr1:85276432-85276774 | Common:5; Rare:103 |