Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:21345493-21345674 | Rare:66 | ||||
chr1:21782976-21783279 | Common:2; Rare:109 | ||||
chr1:22052381-22052742 | Common:4; Rare:102 | ||||
chr1:23019285-23019503 | Rare:63 | ||||
chr1:23344219-23344554 | Common:2; Rare:113 | ||||
chr1:23559444-23559648 | Common:1; Rare:88 | ||||
chr1:23691739-23691858 | Common:2; Rare:60; Clinvar:2; Clinvar (benign):2 | ||||
chr1:23743269-23743533 | Rare:97 | ||||
chr1:23778281-23778639 | Common:10; Rare:138 | ||||
chr1:23791805-23791979 | Rare:32 | ||||
chr1:23825411-23825545 | Common:2; Rare:43; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:23959496-23959986 | Common:5; Rare:115 | ||||
chr1:23980214-23980604 | Common:1; Rare:114 | ||||
chr1:24187232-24187444 | Common:6; Rare:61 | ||||
chr1:24642885-24643329 | Common:2; Rare:147 |