Variant report

Variant rs538494
Chromosome Location chr11:86849091-86849092
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr11:86809000-86876000 Weak transcription Left Ventricle heart
2 chr11:86833400-86849400 Weak transcription Primary hematopoietic stem cells blood
3 chr11:86834600-86849800 Weak transcription Primary B cells from cord blood blood
4 chr11:86836200-86853000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
5 chr11:86836800-86877200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr11:86837200-86852600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr11:86839600-86850400 Weak transcription Fetal Lung lung
8 chr11:86840000-86849800 Weak transcription HepG2 liver
9 chr11:86843200-86850200 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
10 chr11:86846600-86849800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
11 chr11:86847200-86853200 Weak transcription ES-UCSF4 Cell Line embryonic stem cell
12 chr11:86847800-86849600 Enhancers Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
13 chr11:86847800-86851200 ZNF genes & repeats hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr11:86848400-86849400 Weak transcription Adipose Nuclei Adipose
15 chr11:86848600-86849800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin

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