Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66925196-66925503 | Common:2; Rare:96 | ||||
chr1:67429993-67430102 | Rare:39 | ||||
chr1:67430136-67430311 | Rare:54 | ||||
chr1:70205542-70205764 | Rare:72 | ||||
chr1:70354680-70354827 | Rare:51 | ||||
chr1:71080979-71081359 | Rare:106 | ||||
chr1:74198148-74198338 | Common:2; Rare:108 | ||||
chr1:74732994-74733277 | Common:5; Rare:91 | ||||
chr1:75732697-75732920 | Common:1; Rare:69; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):7 | ||||
chr1:77759711-77759865 | Common:2; Rare:64 | ||||
chr1:77888079-77888395 | Common:1; Rare:75 | ||||
chr1:77888429-77888758 | Common:1; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr1:77979012-77979233 | Common:2; Rare:83 | ||||
chr1:77979405-77979537 | Common:1; Rare:32 | ||||
chr1:78004552-78004883 | Common:3; Rare:81 |