Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:160031956-160032040 | Rare:24 | ||||
chr1:160205369-160205486 | Common:1; Rare:43 | ||||
chr1:160262433-160262517 | Rare:30 | ||||
chr1:160343173-160343399 | Rare:92 | ||||
chr1:160579442-160579678 | Rare:44 | ||||
chr1:160647037-160647119 | Rare:12 | ||||
chr1:161021082-161021490 | Common:6; Rare:109 | ||||
chr1:161045860-161046042 | Common:1; Rare:46 | ||||
chr1:161118022-161118155 | Rare:69 | ||||
chr1:161132426-161132882 | Common:2; Rare:141 | ||||
chr1:161159350-161159500 | Common:2; Rare:41 | ||||
chr1:161199008-161199326 | Rare:47 | ||||
chr1:161225768-161226072 | Common:10; Rare:44 | ||||
chr1:161314212-161314417 | Common:3; Rare:76; Clinvar:7; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:161766163-161766364 | Common:3; Rare:60 |