Variant report

Variant rs72969976
Chromosome Location chr1:93465526-93465527
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:18 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr1:93451800-93466000 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
2 chr1:93459800-93466000 Weak transcription Brain Anterior Caudate brain
3 chr1:93459800-93466000 Weak transcription GM12878-XiMat blood
4 chr1:93461800-93466000 Weak transcription Pancreas Pancrea
5 chr1:93462200-93465800 Weak transcription Stomach Mucosa stomach
6 chr1:93462800-93466000 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
7 chr1:93463200-93465800 Weak transcription Brain Cingulate Gyrus brain
8 chr1:93463800-93465600 Weak transcription iPS-15b Cell Line embryonic stem cell
9 chr1:93463800-93466000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
10 chr1:93463800-93466000 Weak transcription Foreskin Keratinocyte Primary Cells skin03 Skin
11 chr1:93463800-93466000 Weak transcription Placenta Placenta
12 chr1:93463800-93467600 Weak transcription H1 BMP4 Derived Trophoblast Cultured Cells ES cell derived
13 chr1:93464800-93465800 Weak transcription H1 Cell Line embryonic stem cell
14 chr1:93464800-93466000 Weak transcription Fetal Muscle Leg muscle
15 chr1:93465200-93466000 Weak transcription Fetal Intestine Large intestine
16 chr1:93465200-93468000 Enhancers Fetal Intestine Small intestine
17 chr1:93465400-93465800 Weak transcription ES-I3 Cell Line embryonic stem cell
18 chr1:93465400-93466000 Enhancers HUES64 Cell Line embryonic stem cell

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