Variant report

Variant rs73018956
Chromosome Location chr3:155723579-155723580
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:17 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr3:155723000-155723800 Enhancers ES-UCSF4 Cell Line embryonic stem cell
2 chr3:155723000-155724000 Enhancers iPS-18 Cell Line embryonic stem cell
3 chr3:155723000-155724000 Enhancers Ganglion Eminence derived primary cultured neurospheres brain
4 chr3:155723000-155724200 Enhancers HUES48 Cell Line embryonic stem cell
5 chr3:155723000-155724200 Enhancers HUES6 Cell Line embryonic stem cell
6 chr3:155723000-155724200 Enhancers HUES64 Cell Line embryonic stem cell
7 chr3:155723000-155724200 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr3:155723000-155724800 Enhancers Fetal Intestine Large intestine
9 chr3:155723000-155724800 Enhancers Fetal Intestine Small intestine
10 chr3:155723200-155723600 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
11 chr3:155723400-155723600 Flanking Active TSS HepG2 liver
12 chr3:155723400-155723800 Enhancers ES-WA7 Cell Line embryonic stem cell
13 chr3:155723400-155723800 Flanking Active TSS iPS-20b Cell Line embryonic stem cell
14 chr3:155723400-155723800 Enhancers Foreskin Melanocyte Primary Cells skin03 Skin
15 chr3:155723400-155724000 Enhancers ES-I3 Cell Line embryonic stem cell
16 chr3:155723400-155724000 Enhancers H9 Derived Neuron Cultured Cells ES cell derived
17 chr3:155723400-155724000 Enhancers Liver Liver

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