Variant report

Variant rs7107869
Chromosome Location chr11:26643186-26643187
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:26641600-26644800 Enhancers HMEC breast
2 chr11:26642000-26645000 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
3 chr11:26642000-26645200 Enhancers NHEK skin
4 chr11:26642200-26643200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr11:26642200-26643200 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr11:26642200-26643600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr11:26642200-26643800 Enhancers Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
8 chr11:26642200-26644800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr11:26642200-26644800 Enhancers NHDF-Ad bronchial
10 chr11:26642200-26645000 Enhancers Muscle Satellite Cultured Cells --
11 chr11:26642200-26645000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr11:26642200-26645000 Enhancers Placenta Amnion Placenta Amnion
13 chr11:26642200-26645200 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr11:26642200-26645200 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
15 chr11:26642200-26645200 Enhancers Hela-S3 cervix
16 chr11:26642600-26643200 Enhancers NH-A brain
17 chr11:26642800-26643600 Enhancers A549 lung
18 chr11:26643000-26643600 Weak transcription Fetal Intestine Small intestine
19 chr11:26643000-26644400 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin

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