Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:17201612-17201671 | Common:1; Rare:31 | ||||
chr10:17228891-17229026 | Common:3; Rare:33 | ||||
chr10:17230526-17230710 | Rare:79; Clinvar:1 | ||||
chr10:17643898-17644283 | Common:2; Rare:114 | ||||
chr10:18651540-18651738 | Common:1; Rare:82 | ||||
chr10:19816279-19816464 | Common:5; Rare:32 | ||||
chr10:19816510-19816638 | Common:1; Rare:36 | ||||
chr10:22321410-22321595 | Rare:63 | ||||
chr10:24466457-24466533 | Rare:10 | ||||
chr10:27154323-27154480 | Rare:42 | ||||
chr10:27155197-27155423 | Common:7; Rare:100; Clinvar:3; Clinvar (benign):7 | ||||
chr10:27240740-27240886 | Rare:40 | ||||
chr10:27242095-27242221 | Common:1; Rare:48 | ||||
chr10:28532442-28532780 | Common:5; Rare:123 | ||||
chr10:30059529-30059722 | Rare:70 |