Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:53946261-53946518 | Common:2; Rare:90 | ||||
chr1:54053184-54053678 | Common:6; Rare:163 | ||||
chr1:54199988-54200218 | Rare:56 | ||||
chr1:54887013-54887109 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
chr1:55215323-55215426 | Rare:44 | ||||
chr1:56645245-56645384 | Common:1; Rare:53 | ||||
chr1:59296508-59296854 | Common:12; Rare:93 | ||||
chr1:61742346-61742471 | Rare:33 | ||||
chr1:62688251-62688533 | Common:1; Rare:109; Clinvar:1 | ||||
chr1:62784047-62784180 | Rare:50 | ||||
chr1:63523161-63523581 | Common:3; Rare:115 | ||||
chr1:63593621-63593691 | Rare:37; Clinvar (pathogenic):1 | ||||
chr1:64841247-64841462 | Rare:53 | ||||
chr1:66533386-66533826 | Common:2; Rare:75 | ||||
chr1:66533837-66534190 | Common:2; Rare:88 |