Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:925679-926004 | Common:3; Rare:140 | ||||
chr11:942937-943085 | Common:1; Rare:35 | ||||
chr11:1309213-1309973 | Common:4; Rare:246 | ||||
chr11:1309988-1310524 | Common:4; Rare:122 | ||||
chr11:1389635-1389917 | Common:2; Rare:60 | ||||
chr11:1559097-1559351 | Common:1; Rare:64 | ||||
chr11:1559458-1559702 | Common:3; Rare:46 | ||||
chr11:1572006-1572136 | Rare:43 | ||||
chr11:1572217-1572531 | Common:2; Rare:93 | ||||
chr11:1750197-1750259 | Rare:15 | ||||
chr11:1762595-1762670 | Rare:18 | ||||
chr11:1763512-1763571 | Rare:16 | ||||
chr11:1763853-1764139 | Common:3; Rare:127; Clinvar:5; Clinvar (benign):6 | ||||
chr11:1830738-1830842 | Rare:26 | ||||
chr11:1834248-1834493 | Rare:56 |