Variant report

Variant rs12341726
Chromosome Location chr9:93849810-93849811
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:11 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr9:93846600-93850200 Enhancers Primary monocytes fromperipheralblood blood
2 chr9:93847600-93850000 Enhancers Monocytes-CD14+_RO01746 blood
3 chr9:93847800-93855600 Weak transcription iPS DF 19.11 Cell Line embryonic stem cell
4 chr9:93848200-93851600 Weak transcription HepG2 liver
5 chr9:93848200-93852200 Weak transcription Primary hematopoietic stem cells G-CSF-mobilized Female --
6 chr9:93849000-93850000 Enhancers IMR90 fetal lung fibroblasts Cell Line lung
7 chr9:93849600-93850000 ZNF genes & repeats Fetal Intestine Small intestine
8 chr9:93849800-93850000 Enhancers Psoas Muscle Psoas
9 chr9:93849800-93851800 Weak transcription Adipose Derived Mesenchymal Stem Cell Cultured Cells ES cell derived
10 chr9:93849800-93852000 Weak transcription Foreskin Fibroblast Primary Cells skin01 Skin
11 chr9:93849800-93852200 Weak transcription Skeletal Muscle Female skeletal muscle

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