Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:193105378-193105523 | Common:3; Rare:60 | ||||
chr1:193186605-193186687 | Rare:16 | ||||
chr1:197146539-197146808 | Common:1; Rare:57; Clinvar:4; Clinvar (benign):1 | ||||
chr1:200409996-200410234 | Rare:74 | ||||
chr1:200620698-200620891 | Common:1; Rare:52 | ||||
chr1:200669380-200669572 | Common:2; Rare:57 | ||||
chr1:200669937-200670126 | Common:1; Rare:44 | ||||
chr1:201888415-201888696 | Common:2; Rare:63 | ||||
chr1:201946452-201946793 | Common:2; Rare:55 | ||||
chr1:202341894-202342146 | Common:1; Rare:65 | ||||
chr1:202958228-202958462 | Common:3; Rare:71 | ||||
chr1:203007231-203007460 | Common:2; Rare:94 | ||||
chr1:203626664-203626989 | Common:1; Rare:65 | ||||
chr1:204411785-204412070 | Common:5; Rare:91 | ||||
chr1:204516288-204516473 | Common:1; Rare:53 |