Variant report

Variant rs1933014
Chromosome Location chr9:85173575-85173576
allele G/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:85167200-85174600 Weak transcription Gastric stomach
2 chr9:85169200-85173800 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
3 chr9:85169200-85173800 Weak transcription HUES6 Cell Line embryonic stem cell
4 chr9:85170000-85176800 Enhancers HepG2 liver
5 chr9:85170800-85177000 Enhancers Stomach Mucosa stomach
6 chr9:85171000-85173800 Weak transcription hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
7 chr9:85172000-85176000 Enhancers Liver Liver
8 chr9:85172200-85173800 Weak transcription Fetal Kidney kidney
9 chr9:85172200-85174800 Weak transcription Pancreas Pancrea
10 chr9:85172800-85173800 Weak transcription Fetal Lung lung
11 chr9:85173200-85175200 Enhancers Pancreatic Islets Pancreatic Islet
12 chr9:85173200-85175800 Enhancers Fetal Intestine Large intestine
13 chr9:85173400-85175000 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
14 chr9:85173400-85175400 Weak transcription Fetal Thymus thymus
15 chr9:85173400-85175600 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr9:85173400-85175800 Enhancers Fetal Adrenal Gland Adrenal Gland
17 chr9:85173400-85175800 Enhancers Fetal Intestine Small intestine

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