Variant report

Variant rs13284299
Chromosome Location chr9:116862427-116862428
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:19 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:116861200-116862600 Flanking Active TSS HepG2 liver
2 chr9:116861600-116862600 Enhancers H1 Derived Mesenchymal Stem Cells ES cell derived
3 chr9:116861600-116862600 Enhancers ES-UCSF4 Cell Line embryonic stem cell
4 chr9:116861600-116862600 Enhancers Pancreas Pancrea
5 chr9:116861800-116862600 Bivalent Enhancer H1 Cell Line embryonic stem cell
6 chr9:116861800-116862600 Bivalent Enhancer hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
7 chr9:116861800-116862600 Enhancers iPS DF 6.9 Cell Line embryonic stem cell
8 chr9:116861800-116863400 Enhancers Fetal Kidney kidney
9 chr9:116861800-116863400 Enhancers A549 lung
10 chr9:116861800-116863800 Enhancers Liver Liver
11 chr9:116862000-116862800 Enhancers Fetal Intestine Large intestine
12 chr9:116862000-116863000 Enhancers Fetal Intestine Small intestine
13 chr9:116862200-116862600 Bivalent Enhancer H9 Cell Line embryonic stem cell
14 chr9:116862200-116863000 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Female --
15 chr9:116862200-116863600 Enhancers HUVEC blood vessel
16 chr9:116862400-116862600 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
17 chr9:116862400-116862800 Bivalent Enhancer Primary hematopoietic stem cells short term culture blood
18 chr9:116862400-116863200 Enhancers Primary hematopoietic stem cells G-CSF-mobilized Male --
19 chr9:116862400-116864200 Enhancers Pancreatic Islets Pancreatic Islet

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