Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:10304973-10305085 | Rare:28 | ||||
chr11:10541145-10541314 | Rare:65 | ||||
chr11:10800137-10800650 | Rare:139 | ||||
chr11:10800746-10801006 | Common:1; Rare:86 | ||||
chr11:10858030-10858231 | Common:2; Rare:56 | ||||
chr11:13277512-13277843 | Common:2; Rare:88 | ||||
chr11:18322126-18322313 | Common:3; Rare:66; Clinvar:1; Clinvar (benign):2 | ||||
chr11:18322499-18322576 | Common:2; Rare:34 | ||||
chr11:18526880-18526972 | Rare:42 | ||||
chr11:18588634-18588804 | Rare:66 | ||||
chr11:27506735-27506849 | Common:1; Rare:52 | ||||
chr11:28108134-28108398 | Common:1; Rare:76 | ||||
chr11:31369807-31369901 | Rare:29 | ||||
chr11:31509601-31509784 | Common:1; Rare:56 | ||||
chr11:33161399-33161624 | Common:5; Rare:58 |