Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr21:44801738-44801870 | Rare:62 | ||||
chr21:44873631-44874040 | Common:8; Rare:163 | ||||
chr21:44939877-44940056 | Common:2; Rare:50 | ||||
chr21:45287869-45288091 | Common:6; Rare:88 | ||||
chr21:45404913-45405178 | Common:12; Rare:163 | ||||
chr21:45981502-45981814 | Common:23; Rare:72; Clinvar (benign):2 | ||||
chr21:46097534-46097855 | Common:8; Rare:85 | ||||
chr21:46286230-46286402 | Common:4; Rare:64 | ||||
chr21:46323792-46324213 | Common:2; Rare:159; Clinvar:3; Clinvar (benign):1 | ||||
chr22:17159167-17159368 | Common:6; Rare:90 | ||||
chr22:17628595-17628860 | Common:2; Rare:81 | ||||
chr22:18077840-18078032 | Common:3; Rare:63; Clinvar:3; Clinvar (benign):2 | ||||
chr22:19447694-19447761 | Common:1; Rare:28 | ||||
chr22:19479100-19479466 | Common:4; Rare:134 | ||||
chr22:19479693-19479936 | Common:3; Rare:55 |