Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:161339685-161339818 | Rare:14 | ||||
chr2:162172055-162172329 | Rare:52 | ||||
chr2:162192361-162192405 | Rare:9 | ||||
chr2:162192516-162192727 | Common:1; Rare:44 | ||||
chr2:162192884-162192978 | Rare:18 | ||||
chr2:162197295-162197416 | Rare:27 | ||||
chr2:162236411-162236425 | Rare:3 | ||||
chr2:166204108-166204411 | Common:1; Rare:97; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:166213095-166213196 | Rare:16 | ||||
chr2:166274851-166275134 | Common:1; Rare:45 | ||||
chr2:166275166-166275307 | Common:1; Rare:22 | ||||
chr2:166297969-166298178 | Common:2; Rare:40 | ||||
chr2:166300281-166300643 | Rare:63 | ||||
chr2:169570454-169570715 | Common:2; Rare:43 | ||||
chr2:169810919-169811319 | Rare:108 |