Variant report

Variant rs7996733
Chromosome Location chr13:51580114-51580115
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr13:51575400-51580200 Weak transcription Duodenum Smooth Muscle Duodenum
2 chr13:51577800-51580200 Enhancers Brain Germinal Matrix brain
3 chr13:51577800-51581000 Enhancers Fetal Muscle Leg muscle
4 chr13:51578200-51580200 Enhancers Fetal Muscle Trunk muscle
5 chr13:51578200-51581800 Enhancers Fetal Intestine Large intestine
6 chr13:51578800-51580200 Enhancers HUES6 Cell Line embryonic stem cell
7 chr13:51578800-51581800 Enhancers Fetal Intestine Small intestine
8 chr13:51579000-51580400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
9 chr13:51579200-51581200 Enhancers HSMMtube muscle
10 chr13:51579400-51580400 Enhancers HepG2 liver
11 chr13:51579400-51581600 Bivalent Enhancer Foreskin Fibroblast Primary Cells skin01 Skin
12 chr13:51579400-51583800 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Male --
13 chr13:51579600-51580600 Weak transcription Fetal Stomach stomach
14 chr13:51579600-51581000 Enhancers Duodenum Mucosa Duodenum
15 chr13:51579600-51581400 Enhancers Muscle Satellite Cultured Cells --
16 chr13:51579800-51581200 Enhancers Aorta Aorta
17 chr13:51580000-51580200 Flanking Active TSS Mesenchymal Stem Cell Derived Adipocyte Cultured Cells ES cell derived

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