Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54542070-54542313 | Common:2; Rare:69 | ||||
chr1:54623504-54623643 | Rare:31 | ||||
chr1:54800766-54800953 | Common:1; Rare:64 | ||||
chr1:54801141-54801403 | Common:1; Rare:62 | ||||
chr1:54887103-54887374 | Common:1; Rare:90; Clinvar:4; Clinvar (benign):1 | ||||
chr1:54980553-54980891 | Common:4; Rare:68 | ||||
chr1:55215349-55215420 | Rare:34 | ||||
chr1:56645245-56645375 | Common:1; Rare:47 | ||||
chr1:58546706-58546942 | Common:4; Rare:94 | ||||
chr1:58783757-58783868 | Common:1; Rare:32 | ||||
chr1:58783871-58784404 | Common:1; Rare:142 | ||||
chr1:59296520-59297108 | Common:14; Rare:165 | ||||
chr1:61076970-61077330 | Common:3; Rare:85 | ||||
chr1:61742342-61742551 | Rare:62 | ||||
chr1:62436253-62436364 | Common:2; Rare:36 |