Variant report

Variant rs568868901
Chromosome Location chr2:180414609-180414610
allele -/T
Outlinks Ensembl   UCSC
Chromatin state (count:14 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:180408400-180423400 Weak transcription H1 Derived Mesenchymal Stem Cells ES cell derived
2 chr2:180408800-180415600 Weak transcription Fetal Brain Female brain
3 chr2:180410000-180415400 Weak transcription Liver Liver
4 chr2:180410200-180415400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
5 chr2:180410600-180416200 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
6 chr2:180413800-180416200 Bivalent Enhancer iPS-18 Cell Line embryonic stem cell
7 chr2:180414000-180416200 Enhancers iPS-15b Cell Line embryonic stem cell
8 chr2:180414000-180416400 Enhancers HUES64 Cell Line embryonic stem cell
9 chr2:180414000-180416800 Enhancers HepG2 liver
10 chr2:180414200-180416600 Enhancers iPS-20b Cell Line embryonic stem cell
11 chr2:180414200-180417000 Enhancers HUES6 Cell Line embryonic stem cell
12 chr2:180414400-180415000 Enhancers ES-UCSF4 Cell Line embryonic stem cell
13 chr2:180414600-180415000 Flanking Active TSS HUES48 Cell Line embryonic stem cell
14 chr2:180414600-180415400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived

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