Variant report

Variant rs12710327
Chromosome Location chr20:23569689-23569690
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:23 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr20:23568400-23570000 Enhancers HepG2 liver
2 chr20:23569000-23569800 Enhancers Stomach Mucosa stomach
3 chr20:23569200-23569800 Enhancers Primary monocytes fromperipheralblood blood
4 chr20:23569200-23569800 Enhancers Foreskin Keratinocyte Primary Cells skin02 Skin
5 chr20:23569200-23570000 Enhancers Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
6 chr20:23569200-23570000 Enhancers Foreskin Keratinocyte Primary Cells skin03 Skin
7 chr20:23569200-23570000 Enhancers Fetal Thymus thymus
8 chr20:23569400-23569800 Enhancers Primary hematopoietic stem cells short term culture blood
9 chr20:23569400-23569800 Enhancers Adipose Nuclei Adipose
10 chr20:23569400-23569800 Enhancers NHEK skin
11 chr20:23569600-23569800 Flanking Bivalent TSS/Enh H9 Cell Line embryonic stem cell
12 chr20:23569600-23569800 Enhancers hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
13 chr20:23569600-23569800 Flanking Bivalent TSS/Enh HUES64 Cell Line embryonic stem cell
14 chr20:23569600-23569800 Flanking Bivalent TSS/Enh iPS-15b Cell Line embryonic stem cell
15 chr20:23569600-23569800 Flanking Bivalent TSS/Enh iPS-18 Cell Line embryonic stem cell
16 chr20:23569600-23569800 Bivalent Enhancer iPS-20b Cell Line embryonic stem cell
17 chr20:23569600-23569800 Enhancers Placenta Placenta
18 chr20:23569600-23569800 Enhancers HMEC breast
19 chr20:23569600-23569800 Flanking Active TSS K562 blood
20 chr20:23569600-23570000 Active TSS ES-I3 Cell Line embryonic stem cell
21 chr20:23569600-23570000 Enhancers HUES48 Cell Line embryonic stem cell
22 chr20:23569600-23570000 Flanking Active TSS HUES6 Cell Line embryonic stem cell
23 chr20:23569600-23570000 Active TSS Primary hematopoietic stem cells G-CSF-mobilized Male --

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