Variant report

Variant rs558469773
Chromosome Location chr3:93602770-93602771
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:93581400-93611000 Weak transcription Aorta Aorta
2 chr3:93591000-93610200 Weak transcription Ovary ovary
3 chr3:93591000-93614200 Strong transcription Liver Liver
4 chr3:93594400-93610600 Weak transcription Lung lung
5 chr3:93594600-93632800 Weak transcription HepG2 liver
6 chr3:93596200-93611000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr3:93597400-93612400 Weak transcription HSMMtube muscle
8 chr3:93597400-93629200 Weak transcription Rectal Mucosa Donor 29 rectum
9 chr3:93597600-93609800 Weak transcription Fetal Intestine Small intestine
10 chr3:93597800-93628800 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
11 chr3:93598000-93603000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
12 chr3:93598600-93602800 Weak transcription Breast Myoepithelial Primary Cells Breast
13 chr3:93601200-93613200 Weak transcription Rectal Smooth Muscle rectum
14 chr3:93601800-93625200 Weak transcription Foreskin Melanocyte Primary Cells skin01 Skin
15 chr3:93601800-93627200 Weak transcription Duodenum Smooth Muscle Duodenum
16 chr3:93602000-93608400 Weak transcription Left Ventricle heart
17 chr3:93602000-93610400 Weak transcription ES-I3 Cell Line embryonic stem cell
18 chr3:93602200-93603200 ZNF genes & repeats Fetal Intestine Large intestine
19 chr3:93602600-93603400 Strong transcription Foreskin Melanocyte Primary Cells skin03 Skin

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