Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:125823192-125823573 | Common:1; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
chr10:125823648-125823699 | Rare:13 | ||||
chr10:126905302-126905468 | Rare:64 | ||||
chr10:132331786-132332193 | Common:17; Rare:132 | ||||
chr10:133308829-133308994 | Rare:76 | ||||
chr11:207338-207719 | Common:8; Rare:129 | ||||
chr11:208638-208855 | Rare:81 | ||||
chr11:236919-237059 | Common:1; Rare:55 | ||||
chr11:320721-321012 | Common:10; Rare:91; Clinvar:1 | ||||
chr11:560710-561003 | Common:5; Rare:137 | ||||
chr11:576413-576519 | Rare:43 | ||||
chr11:695621-695817 | Rare:50 | ||||
chr11:777465-777607 | Common:1; Rare:62 | ||||
chr11:809783-810037 | Common:2; Rare:115 | ||||
chr11:832881-833018 | Common:7; Rare:50 |