Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:318279-318680 | Rare:36 | ||||
chr11:319534-319789 | Common:1; Rare:71 | ||||
chr11:319863-320152 | Common:1; Rare:86 | ||||
chr11:325895-326050 | Common:2; Rare:37 | ||||
chr11:356337-356578 | Common:9; Rare:63 | ||||
chr11:498020-498233 | Rare:65 | ||||
chr11:532681-532945 | Common:5; Rare:80; Clinvar:11; Clinvar (benign):10 | ||||
chr11:697221-697379 | Common:2; Rare:30 | ||||
chr11:762848-762919 | Common:1; Rare:14 | ||||
chr11:912720-912838 | Rare:23 | ||||
chr11:1995912-1996091 | Rare:49 | ||||
chr11:2377998-2378136 | Common:3; Rare:38 | ||||
chr11:3100438-3100550 | Common:2; Rare:16 | ||||
chr11:3778965-3779158 | Common:1; Rare:60 | ||||
chr11:3839268-3839405 | Common:1; Rare:22 |