Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:96389862-96390043 | Common:1; Rare:72 | ||||
chr11:101914862-101915310 | Common:8; Rare:130 | ||||
chr11:102347158-102347244 | Common:1; Rare:24 | ||||
chr11:102452683-102452878 | Rare:59 | ||||
chr11:106077326-106077706 | Common:2; Rare:113 | ||||
chr11:108009284-108009345 | Rare:32 | ||||
chr11:108222597-108223043 | Rare:146; Clinvar:7 | ||||
chr11:111766359-111766415 | Rare:31 | ||||
chr11:111879154-111879482 | Rare:95 | ||||
chr11:111912730-111912757 | Rare:4 | ||||
chr11:111913130-111913292 | Rare:45 | ||||
chr11:111923738-111923775 | Common:1; Rare:4 | ||||
chr11:112074023-112074352 | Common:1; Rare:68 | ||||
chr11:112086720-112086917 | Rare:83; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr11:112226314-112226435 | Rare:57 |