Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:36386415-36386815 | Rare:109 | ||||
chr1:36401019-36401297 | Common:3; Rare:105 | ||||
chr1:39158674-39158916 | Common:2; Rare:103 | ||||
chr1:39214110-39214660 | Rare:119 | ||||
chr1:40758688-40759085 | Rare:96 | ||||
chr1:40919520-40919850 | Common:9; Rare:135 | ||||
chr1:42929630-42930065 | Common:4; Rare:201; Clinvar:13; Clinvar (benign):30; Clinvar (pathogenic):11 | ||||
chr1:42961349-42961562 | Common:4; Rare:63 | ||||
chr1:42980410-42980810 | Rare:130 | ||||
chr1:42990810-42991100 | Common:3; Rare:81 | ||||
chr1:43007419-43007840 | Common:12; Rare:232 | ||||
chr1:43008340-43008680 | Rare:98 | ||||
chr1:43008700-43009140 | Common:2; Rare:157 | ||||
chr1:43031653-43032101 | Common:5; Rare:169 | ||||
chr1:43034110-43034680 | Common:4; Rare:119 |