Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:576431-576531 | Rare:40 | ||||
chr11:695772-695827 | Rare:22 | ||||
chr11:747279-747514 | Rare:98; Clinvar:2; Clinvar (benign):1 | ||||
chr11:777458-777611 | Common:1; Rare:67 | ||||
chr11:809715-810038 | Common:2; Rare:136 | ||||
chr11:832814-833020 | Common:7; Rare:68 | ||||
chr11:842487-842978 | Common:8; Rare:202 | ||||
chr11:1309588-1309839 | Common:1; Rare:108 | ||||
chr11:1834212-1834428 | Rare:49 | ||||
chr11:2992232-2992522 | Common:2; Rare:112 | ||||
chr11:3840905-3841079 | Rare:76 | ||||
chr11:3855551-3855711 | Common:2; Rare:32 | ||||
chr11:4094571-4094877 | Common:2; Rare:83 | ||||
chr11:4393665-4393803 | Rare:32 | ||||
chr11:4608171-4608405 | Common:1; Rare:64 |