Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:33324860-33325026 | Common:4; Rare:64 | ||||
chr21:33479884-33480147 | Rare:89 | ||||
chr21:33542805-33543090 | Common:3; Rare:104 | ||||
chr21:36060508-36060574 | Common:1; Rare:20 | ||||
chr21:36134961-36135110 | Rare:38 | ||||
chr21:37073003-37073444 | Common:5; Rare:159 | ||||
chr21:39445775-39445896 | Common:1; Rare:41 | ||||
chr21:42879522-42879665 | Common:3; Rare:49 | ||||
chr21:42893179-42893356 | Common:1; Rare:67 | ||||
chr21:44873626-44874050 | Common:8; Rare:170 | ||||
chr21:44939871-44940053 | Common:2; Rare:52 | ||||
chr21:45287879-45288052 | Common:5; Rare:64 | ||||
chr21:45404878-45405197 | Common:12; Rare:181 | ||||
chr21:45405528-45405860 | Common:3; Rare:104 | ||||
chr21:45981496-45981827 | Common:23; Rare:79; Clinvar (benign):2 |