Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:125496127-125496527 | Rare:149 | ||||
chr11:125569112-125569562 | Common:9; Rare:482 | ||||
chr11:125569581-125570020 | Common:2; Rare:168 | ||||
chr11:125591546-125592045 | Common:10; Rare:193 | ||||
chr11:125592273-125592937 | Common:42; Rare:1060; Clinvar (benign):1 | ||||
chr11:125593066-125593598 | Common:3; Rare:257 | ||||
chr11:125624698-125625098 | Rare:71 | ||||
chr11:125625470-125626060 | Common:16; Rare:836 | ||||
chr11:125626080-125626590 | Common:7; Rare:359 | ||||
chr11:125626497-125626908 | Common:1; Rare:190 | ||||
chr11:125887360-125888470 | Common:13; Rare:711 | ||||
chr11:125902921-125903410 | Common:5; Rare:136 | ||||
chr11:126210971-126211371 | Common:2; Rare:210 | ||||
chr11:126211437-126211882 | Common:3; Rare:716 | ||||
chr11:126268374-126268774 | Common:5; Rare:150 |