Variant report

Variant rs12472667
Chromosome Location chr2:171629063-171629064
allele C/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:171628400-171629400 Enhancers Breast Myoepithelial Primary Cells Breast
2 chr2:171628400-171629400 Enhancers Brain Anterior Caudate brain
3 chr2:171628600-171629400 Enhancers Cortex derived primary cultured neurospheres brain
4 chr2:171628600-171629400 Flanking Active TSS K562 blood
5 chr2:171628800-171629800 Enhancers H1 Cell Line embryonic stem cell
6 chr2:171628800-171632600 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
7 chr2:171628800-171634000 Weak transcription Breast variant Human Mammary Epithelial Cells (vHMEC) Breast
8 chr2:171629000-171629200 Enhancers ES-I3 Cell Line embryonic stem cell
9 chr2:171629000-171629400 Weak transcription H1 BMP4 Derived Mesendoderm Cultured Cells ES cell derived
10 chr2:171629000-171629400 Active TSS HUES6 Cell Line embryonic stem cell
11 chr2:171629000-171629400 Active TSS iPS-20b Cell Line embryonic stem cell
12 chr2:171629000-171629400 Flanking Active TSS Ganglion Eminence derived primary cultured neurospheres brain
13 chr2:171629000-171629400 Enhancers NHEK skin
14 chr2:171629000-171629800 Active TSS hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
15 chr2:171629000-171629800 Enhancers HUES64 Cell Line embryonic stem cell
16 chr2:171629000-171634000 Weak transcription HUES48 Cell Line embryonic stem cell

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