Variant report

Variant rs67941180
Chromosome Location chr5:127908636-127908637
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr5:127903800-127908800 Weak transcription Placenta Amnion Placenta Amnion
2 chr5:127904000-127908800 Weak transcription Placenta Placenta
3 chr5:127907200-127910600 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
4 chr5:127907400-127911000 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
5 chr5:127907600-127908800 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
6 chr5:127907600-127910200 Enhancers Muscle Satellite Cultured Cells --
7 chr5:127907800-127908800 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
8 chr5:127907800-127910400 Enhancers NHEK skin
9 chr5:127907800-127911000 Enhancers A549 lung
10 chr5:127908000-127908800 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr5:127908000-127910600 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
12 chr5:127908400-127910800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
13 chr5:127908600-127910400 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
14 chr5:127908600-127910400 Enhancers HMEC breast

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