Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:124916737-124916920 | Common:2; Rare:64 | ||||
chr10:124989678-124989916 | Rare:60 | ||||
chr10:130110466-130110569 | Common:2; Rare:34 | ||||
chr10:132633241-132633472 | Common:2; Rare:41 | ||||
chr11:319836-320171 | Common:3; Rare:102 | ||||
chr11:840479-840522 | Rare:22 | ||||
chr11:1227141-1227392 | Common:2; Rare:72; Clinvar (benign):1 | ||||
chr11:1995874-1996167 | Common:1; Rare:83 | ||||
chr11:3156401-3156504 | Common:2; Rare:19 | ||||
chr11:3159168-3159451 | Common:1; Rare:62 | ||||
chr11:8709125-8709380 | Rare:36 | ||||
chr11:9758150-9758356 | Rare:56 | ||||
chr11:10606392-10606662 | Rare:43 | ||||
chr11:12086691-12086871 | Common:2; Rare:31 | ||||
chr11:16996366-16996655 | Rare:54 |