Variant report

Variant rs6811709
Chromosome Location chr4:81208879-81208880
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:81190600-81223800 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr4:81196800-81211400 Strong transcription NH-A brain
3 chr4:81200000-81216600 Weak transcription HMEC breast
4 chr4:81202200-81226200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
5 chr4:81206800-81210600 Genic enhancers NHDF-Ad bronchial
6 chr4:81206800-81222800 Weak transcription Foreskin Fibroblast Primary Cells skin02 Skin
7 chr4:81207000-81209000 Genic enhancers Foreskin Fibroblast Primary Cells skin01 Skin
8 chr4:81207000-81210200 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
9 chr4:81207800-81210000 Strong transcription Muscle Satellite Cultured Cells --
10 chr4:81207800-81210400 Strong transcription HSMM muscle
11 chr4:81207800-81212000 Strong transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr4:81208000-81209000 Enhancers Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
13 chr4:81208000-81211600 Weak transcription IMR90 fetal lung fibroblasts Cell Line lung
14 chr4:81208000-81216200 Weak transcription NHLF lung
15 chr4:81208200-81210000 Strong transcription Bone Marrow Derived Cultured Mesenchymal Stem Cells Bone marrow
16 chr4:81208800-81209000 Enhancers Fetal Heart heart
17 chr4:81208800-81211600 Strong transcription Osteobl bone

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