Variant report

Variant rs4735428
Chromosome Location chr8:91894812-91894813
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr8:91876800-91901000 Weak transcription Aorta Aorta
2 chr8:91888400-91895800 Weak transcription Stomach Smooth Muscle stomach
3 chr8:91890400-91907600 Weak transcription iPS-15b Cell Line embryonic stem cell
4 chr8:91890600-91895400 Weak transcription HUES48 Cell Line embryonic stem cell
5 chr8:91890600-91902800 Weak transcription HUES6 Cell Line embryonic stem cell
6 chr8:91890800-91895600 Weak transcription ES-I3 Cell Line embryonic stem cell
7 chr8:91890800-91895600 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
8 chr8:91892000-91895600 Weak transcription Brain Inferior Temporal Lobe brain
9 chr8:91892600-91895600 Weak transcription Brain Angular Gyrus brain
10 chr8:91893800-91897800 Enhancers Foreskin Fibroblast Primary Cells skin01 Skin
11 chr8:91894600-91895400 Enhancers Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
12 chr8:91894800-91895000 Enhancers Foreskin Fibroblast Primary Cells skin02 Skin
13 chr8:91894800-91895000 Enhancers Brain Hippocampus Middle brain
14 chr8:91894800-91896600 Enhancers NHDF-Ad bronchial

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