Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:22321411-22321600 | Rare:63 | ||||
chr10:22325577-22325671 | Rare:50 | ||||
chr10:24466428-24466560 | Rare:25 | ||||
chr10:24722730-24722836 | Rare:35 | ||||
chr10:24952074-24952384 | Common:2; Rare:57 | ||||
chr10:24952567-24952941 | Common:4; Rare:112 | ||||
chr10:25016434-25016667 | Common:8; Rare:86 | ||||
chr10:25016971-25017095 | Common:4; Rare:53 | ||||
chr10:26697626-26697877 | Common:2; Rare:77; Clinvar:2; Clinvar (benign):3 | ||||
chr10:26860859-26861384 | Common:7; Rare:140 | ||||
chr10:27100403-27100582 | Common:3; Rare:55; Clinvar:4; Clinvar (benign):2 | ||||
chr10:27154315-27154480 | Rare:43 | ||||
chr10:27155165-27155448 | Common:7; Rare:119; Clinvar:5; Clinvar (benign):7 | ||||
chr10:27240478-27240893 | Common:2; Rare:119 | ||||
chr10:27242058-27242241 | Common:1; Rare:78 |