Variant report

Variant rs376380552
Chromosome Location chr8:11590711-11590712
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:20 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:11585000-11591000 Weak transcription Duodenum Mucosa Duodenum
2 chr8:11585600-11592400 Enhancers Liver Liver
3 chr8:11587200-11592400 Enhancers Left Ventricle heart
4 chr8:11587400-11591600 Enhancers Right Atrium heart
5 chr8:11588000-11591400 Enhancers Fetal Heart heart
6 chr8:11588400-11593200 Weak transcription HepG2 liver
7 chr8:11589600-11591200 Weak transcription Right Ventricle heart
8 chr8:11589800-11592400 Strong transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
9 chr8:11590000-11592000 Weak transcription Fetal Intestine Small intestine
10 chr8:11590200-11591600 Enhancers Stomach Mucosa stomach
11 chr8:11590200-11591800 Enhancers Brain Germinal Matrix brain
12 chr8:11590400-11591200 Bivalent Enhancer Fetal Lung lung
13 chr8:11590400-11591600 Enhancers Colon Smooth Muscle Colon
14 chr8:11590400-11591600 Enhancers Stomach Smooth Muscle stomach
15 chr8:11590400-11593800 Weak transcription Pancreas Pancrea
16 chr8:11590400-11594000 Weak transcription Gastric stomach
17 chr8:11590600-11591000 Weak transcription Ovary ovary
18 chr8:11590600-11591200 Enhancers hESC Derived CD56+ Mesoderm Cultured Cells ES cell derived
19 chr8:11590600-11591200 Weak transcription Placenta Placenta
20 chr8:11590600-11591400 Bivalent Enhancer Primary hematopoietic stem cells G-CSF-mobilized Female --

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