Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:28088565-28088793 | Common:3; Rare:76 | ||||
chr1:28232994-28233082 | Common:1; Rare:29 | ||||
chr1:28505823-28506050 | Common:2; Rare:89 | ||||
chr1:28552847-28553113 | Common:2; Rare:99 | ||||
chr1:28643016-28643163 | Rare:62 | ||||
chr1:28736698-28737010 | Common:2; Rare:103 | ||||
chr1:28886777-28887138 | Common:4; Rare:90 | ||||
chr1:31296744-31297086 | Common:5; Rare:112 | ||||
chr1:32072845-32072942 | Rare:24 | ||||
chr1:32200412-32200685 | Rare:53 | ||||
chr1:32291961-32292156 | Rare:71 | ||||
chr1:32650916-32651307 | Common:2; Rare:149 | ||||
chr1:32817257-32817686 | Rare:117; Clinvar:5; Clinvar (benign):1 | ||||
chr1:33080992-33081165 | Common:2; Rare:43 | ||||
chr1:34985235-34985368 | Common:1; Rare:53 |