Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:69087973-69088214 | Rare:51 | ||||
chr10:69801624-69801942 | Common:2; Rare:81 | ||||
chr10:70132768-70132936 | Rare:43 | ||||
chr10:70170425-70170670 | Common:4; Rare:83 | ||||
chr10:70404074-70404439 | Rare:122 | ||||
chr10:70815701-70816021 | Common:1; Rare:98 | ||||
chr10:71773490-71773745 | Common:3; Rare:74 | ||||
chr10:71819463-71819902 | Common:1; Rare:173; Clinvar:5; Clinvar (benign):4 | ||||
chr10:71964194-71964565 | Common:4; Rare:100; Clinvar:1; Clinvar (benign):3 | ||||
chr10:72216227-72216530 | Common:3; Rare:91 | ||||
chr10:72273699-72273947 | Rare:68 | ||||
chr10:73096772-73097028 | Common:3; Rare:78 | ||||
chr10:73110291-73110536 | Rare:45 | ||||
chr10:73167965-73168290 | Rare:85 | ||||
chr10:73252559-73252789 | Common:2; Rare:66; Clinvar:5; Clinvar (benign):2 |