Variant report

Variant rs1146595
Chromosome Location chr1:76237095-76237096
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:13 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:76221200-76238400 Weak transcription Brain Cingulate Gyrus brain
2 chr1:76227400-76249800 Weak transcription Primary B cells from peripheral blood blood
3 chr1:76227800-76239600 Weak transcription GM12878-XiMat blood
4 chr1:76232800-76243200 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
5 chr1:76234000-76241000 Weak transcription Muscle Satellite Cultured Cells --
6 chr1:76234600-76237600 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr1:76234600-76237600 Weak transcription NHEK skin
8 chr1:76234600-76237800 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
9 chr1:76234600-76241200 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:76236400-76237200 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr1:76236600-76237200 Enhancers iPS-18 Cell Line embryonic stem cell
12 chr1:76236600-76238000 Enhancers HUES48 Cell Line embryonic stem cell
13 chr1:76237000-76237200 Enhancers H1 Cell Line embryonic stem cell

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