Variant report

Variant rs3856995
Chromosome Location chr4:160365961-160365962
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr4:160350600-160367800 Weak transcription HSMM muscle
2 chr4:160357600-160367000 Weak transcription NH-A brain
3 chr4:160362800-160366800 Weak transcription Cortex derived primary cultured neurospheres brain
4 chr4:160364200-160368000 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr4:160364400-160367600 Weak transcription NHEK skin
6 chr4:160364600-160367400 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
7 chr4:160364800-160368000 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
8 chr4:160365400-160366200 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
9 chr4:160365400-160366200 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
10 chr4:160365400-160366200 Enhancers Left Ventricle heart
11 chr4:160365600-160366800 Weak transcription Fetal Lung lung
12 chr4:160365600-160367000 Weak transcription NHLF lung
13 chr4:160365800-160366400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
14 chr4:160365800-160366400 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
15 chr4:160365800-160366400 Enhancers HMEC breast
16 chr4:160365800-160367000 Weak transcription Fetal Stomach stomach

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