Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22316221-22316518 | Common:2; Rare:137 | ||||
chr10:22321410-22321590 | Rare:62 | ||||
chr10:22325506-22325702 | Rare:82 | ||||
chr10:24952561-24952932 | Common:4; Rare:115 | ||||
chr10:25016438-25016685 | Common:8; Rare:98 | ||||
chr10:25016946-25017110 | Common:4; Rare:71 | ||||
chr10:26697558-26697954 | Common:3; Rare:120; Clinvar:2; Clinvar (benign):3 | ||||
chr10:27100419-27100630 | Common:4; Rare:61; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154310-27154480 | Rare:45 | ||||
chr10:27155161-27155460 | Common:7; Rare:125; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240715-27240897 | Rare:49 | ||||
chr10:27242058-27242241 | Common:1; Rare:78 | ||||
chr10:27504129-27504367 | Rare:124; Clinvar:4; Clinvar (benign):1 | ||||
chr10:28532458-28532812 | Common:5; Rare:135 | ||||
chr10:28677227-28677535 | Common:6; Rare:138 |