Variant report

Variant rs11029172
Chromosome Location chr11:26110311-26110312
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26101400-26112600 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
2 chr11:26109200-26110600 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
3 chr11:26109200-26110600 Enhancers Hela-S3 cervix
4 chr11:26109200-26111200 Enhancers Primary B cells from cord blood blood
5 chr11:26109200-26111800 Enhancers Primary B cells from peripheral blood blood
6 chr11:26109400-26110600 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
7 chr11:26109400-26110600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
8 chr11:26109400-26110800 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
9 chr11:26109400-26111400 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
10 chr11:26109600-26110400 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
11 chr11:26109600-26110400 Enhancers NHDF-Ad bronchial
12 chr11:26109800-26110600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr11:26109800-26110600 Enhancers GM12878-XiMat blood
14 chr11:26109800-26110800 Weak transcription Foreskin Melanocyte Primary Cells skin03 Skin

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