Variant report

Variant rs2397156
Chromosome Location chr6:54158799-54158800
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:10 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr6:54153800-54160000 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr6:54156200-54159800 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
3 chr6:54156800-54158800 Weak transcription NH-A brain
4 chr6:54157000-54158800 Weak transcription Osteobl bone
5 chr6:54157000-54159000 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr6:54157200-54164000 Weak transcription NHDF-Ad bronchial
7 chr6:54157600-54162200 Weak transcription ES-I3 Cell Line embryonic stem cell
8 chr6:54157600-54164000 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr6:54158400-54158800 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr6:54158600-54159400 Enhancers HUVEC blood vessel

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