Variant report

Variant rs11915601
Chromosome Location chr3:155723889-155723890
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:155723000-155724000 Enhancers iPS-18 Cell Line embryonic stem cell
2 chr3:155723000-155724000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
3 chr3:155723000-155724200 Enhancers HUES48 Cell Line embryonic stem cell
4 chr3:155723000-155724200 Enhancers HUES6 Cell Line embryonic stem cell
5 chr3:155723000-155724200 Enhancers HUES64 Cell Line embryonic stem cell
6 chr3:155723000-155724200 Enhancers iPS-15b Cell Line embryonic stem cell
7 chr3:155723000-155724800 Enhancers Fetal Intestine Large intestine
8 chr3:155723000-155724800 Enhancers Fetal Intestine Small intestine
9 chr3:155723400-155724000 Enhancers ES-I3 Cell Line embryonic stem cell
10 chr3:155723400-155724000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
11 chr3:155723400-155724000 Enhancers Liver Liver
12 chr3:155723600-155724000 Enhancers H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
13 chr3:155723600-155724200 Enhancers hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
14 chr3:155723800-155724000 Flanking Active TSS HepG2 liver
15 chr3:155723800-155724200 Enhancers iPS-20b Cell Line embryonic stem cell
16 chr3:155723800-155724200 Enhancers Pancreatic Islets Pancreatic Islet

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