Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:218270128-218270538 | Common:5; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
chr2:218659606-218659730 | Rare:29 | ||||
chr2:218671977-218672315 | Common:2; Rare:85 | ||||
chr2:219229630-219229867 | Common:1; Rare:50 | ||||
chr2:219245424-219245505 | Rare:22 | ||||
chr2:230416121-230416245 | Rare:40 | ||||
chr2:232550555-232550713 | Rare:58 | ||||
chr2:237487146-237487276 | Common:2; Rare:32 | ||||
chr2:241315182-241315327 | Common:3; Rare:48 | ||||
chr2:241315661-241315969 | Common:4; Rare:121 | ||||
chr20:347049-347121 | Rare:21 | ||||
chr20:543688-543837 | Rare:61 | ||||
chr20:1118443-1118642 | Common:2; Rare:63 | ||||
chr20:3209439-3209508 | Rare:19 | ||||
chr20:3846737-3846885 | Rare:44 |