Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:23559837-23560063 | Common:1; Rare:68 | ||||
chr1:23691654-23691826 | Common:3; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
chr1:23778281-23778596 | Common:10; Rare:130 | ||||
chr1:23825369-23825537 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr1:23868285-23868454 | Common:3; Rare:48; Clinvar:1; Clinvar (benign):2 | ||||
chr1:23959070-23959126 | Rare:12 | ||||
chr1:23959532-23959922 | Common:5; Rare:98 | ||||
chr1:23980189-23980497 | Rare:79 | ||||
chr1:24108408-24108713 | Rare:106 | ||||
chr1:24415633-24415829 | Common:1; Rare:55 | ||||
chr1:24642966-24643335 | Common:2; Rare:115 | ||||
chr1:25232442-25232662 | Rare:89 | ||||
chr1:25247445-25247606 | Common:2; Rare:51 | ||||
chr1:25338214-25338447 | Common:1; Rare:80 | ||||
chr1:25819858-25820029 | Common:3; Rare:54 |