Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23959641-23959916 | Common:2; Rare:73 | ||||
chr1:23980189-23980486 | Rare:76 | ||||
chr1:24415540-24415835 | Common:2; Rare:78 | ||||
chr1:24642949-24643335 | Common:2; Rare:123 | ||||
chr1:24745273-24745622 | Common:2; Rare:121 | ||||
chr1:25232442-25232657 | Rare:87 | ||||
chr1:25247445-25247639 | Common:2; Rare:69 | ||||
chr1:25337833-25337934 | Rare:14 | ||||
chr1:25338188-25338492 | Common:2; Rare:101 | ||||
chr1:25819878-25820225 | Common:4; Rare:103 | ||||
chr1:26279953-26280201 | Rare:138 | ||||
chr1:26280479-26280875 | Common:3; Rare:97 | ||||
chr1:26432112-26432404 | Common:4; Rare:79; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26695762-26696047 | Common:1; Rare:88 | ||||
chr1:26787671-26788214 | Common:3; Rare:161; Clinvar:2; Clinvar (benign):2 |