Variant report

Variant rs11013023
Chromosome Location chr10:18499851-18499852
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr10:18485000-18503800 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr10:18486800-18502000 Weak transcription Fetal Stomach stomach
3 chr10:18493800-18503800 Weak transcription Fetal Brain Male brain
4 chr10:18494400-18503600 Weak transcription Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived
5 chr10:18495200-18501400 Weak transcription Stomach Smooth Muscle stomach
6 chr10:18497800-18503000 Enhancers Fetal Heart heart
7 chr10:18498600-18500000 Weak transcription Rectal Smooth Muscle rectum
8 chr10:18498600-18502800 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
9 chr10:18499000-18500200 Enhancers Fetal Intestine Small intestine
10 chr10:18499200-18500800 Weak transcription Primary hematopoietic stem cells blood
11 chr10:18499200-18501400 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
12 chr10:18499200-18511000 Weak transcription Aorta Aorta
13 chr10:18499600-18500600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
14 chr10:18499600-18500800 Enhancers Pancreatic Islets Pancreatic Islet
15 chr10:18499800-18500000 Enhancers Colon Smooth Muscle Colon
16 chr10:18499800-18500200 Enhancers Fetal Intestine Large intestine
17 chr10:18499800-18500400 Enhancers Duodenum Mucosa Duodenum

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