Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122954185-122954499 | Rare:116 | ||||
chr10:123008791-123009023 | Common:5; Rare:63; Clinvar:4; Clinvar (benign):5 | ||||
chr10:125719460-125719727 | Rare:86 | ||||
chr10:125823200-125823585 | Common:1; Rare:132; Clinvar:1; Clinvar (benign):1 | ||||
chr10:126905107-126905465 | Common:2; Rare:123 | ||||
chr10:129466883-129467282 | Common:5; Rare:165; Clinvar:1 | ||||
chr10:131981904-131982154 | Common:1; Rare:91 | ||||
chr10:132331795-132332166 | Common:16; Rare:120 | ||||
chr10:133308835-133309004 | Common:1; Rare:78 | ||||
chr11:207343-207720 | Common:8; Rare:129 | ||||
chr11:208688-208857 | Rare:69 | ||||
chr11:236333-236491 | Common:6; Rare:45 | ||||
chr11:236924-237044 | Common:1; Rare:47 | ||||
chr11:307579-308435 | Common:33; Rare:231 | ||||
chr11:504446-504518 | Common:1; Rare:22 |