Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:217920907-217921095 | Common:3; Rare:37 | ||||
chr2:217930008-217930132 | Common:1; Rare:19 | ||||
chr2:217957249-217957379 | Common:3; Rare:23 | ||||
chr2:217966015-217966332 | Common:11; Rare:97 | ||||
chr2:218402453-218402714 | Common:1; Rare:90 | ||||
chr2:219417426-219417482 | Rare:8 | ||||
chr2:226796892-226797060 | Rare:57; Clinvar (pathogenic):1 | ||||
chr2:231199302-231199457 | Rare:25 | ||||
chr2:238728152-238728347 | Common:2; Rare:40 | ||||
chr20:3668965-3669234 | Common:5; Rare:65; Clinvar (benign):1 | ||||
chr20:3804793-3804853 | Rare:23 | ||||
chr20:3808165-3808358 | Common:3; Rare:39 | ||||
chr20:4822395-4822552 | Common:2; Rare:31 | ||||
chr20:4822647-4822776 | Rare:33 | ||||
chr20:17570692-17570945 | Common:1; Rare:51 |