Variant report

Variant rs4367113
Chromosome Location chr3:134287975-134287976
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:134269800-134296600 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
2 chr3:134272000-134289800 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
3 chr3:134279400-134288600 Weak transcription HSMMtube muscle
4 chr3:134281200-134288400 Weak transcription Duodenum Mucosa Duodenum
5 chr3:134281600-134297600 Weak transcription Gastric stomach
6 chr3:134283400-134288000 Weak transcription Brain Hippocampus Middle brain
7 chr3:134283400-134297200 Weak transcription Brain Angular Gyrus brain
8 chr3:134284400-134292200 Weak transcription Primary T cells from cord blood blood
9 chr3:134286600-134288000 Weak transcription Fetal Kidney kidney
10 chr3:134287200-134288800 ZNF genes & repeats H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
11 chr3:134287400-134288400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
12 chr3:134287800-134288000 Strong transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
13 chr3:134287800-134288000 ZNF genes & repeats Breast Myoepithelial Primary Cells Breast
14 chr3:134287800-134288200 ZNF genes & repeats Primary hematopoietic stem cells short term culture blood
15 chr3:134287800-134288800 ZNF genes & repeats H1 Cell Line embryonic stem cell

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