Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23778275-23778476 | Common:9; Rare:108 | ||||
chr1:23800745-23800932 | Common:1; Rare:59 | ||||
chr1:23825411-23825534 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959607-23959901 | Common:2; Rare:81 | ||||
chr1:23960053-23960095 | Rare:17 | ||||
chr1:23980251-23980605 | Common:1; Rare:111 | ||||
chr1:24642985-24643346 | Common:2; Rare:110 | ||||
chr1:25232442-25232622 | Rare:76 | ||||
chr1:25247076-25247125 | Rare:11 | ||||
chr1:25247449-25247591 | Common:1; Rare:44 | ||||
chr1:25338236-25338440 | Common:1; Rare:72 | ||||
chr1:25819821-25820013 | Common:4; Rare:61 | ||||
chr1:25859362-25859580 | Common:3; Rare:90 | ||||
chr1:25906397-25906588 | Rare:74 | ||||
chr1:26279953-26280185 | Rare:132 |