Variant report

Variant rs2366111
Chromosome Location chr2:210483861-210483862
allele C/T
Outlinks Ensembl   UCSC
Chromatin state (count:15 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210476600-210493600 Weak transcription Aorta Aorta
2 chr2:210479200-210484600 Weak transcription Fetal Brain Male brain
3 chr2:210480000-210493200 Weak transcription Brain Germinal Matrix brain
4 chr2:210481000-210484400 Weak transcription Cortex derived primary cultured neurospheres brain
5 chr2:210481000-210486400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
6 chr2:210481000-210493400 Weak transcription Pancreas Pancrea
7 chr2:210481000-210500400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
8 chr2:210481200-210484200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
9 chr2:210481400-210493600 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
10 chr2:210481600-210484600 Weak transcription iPS-20b Cell Line embryonic stem cell
11 chr2:210481600-210487800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
12 chr2:210482400-210484400 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
13 chr2:210482600-210484400 Weak transcription hESC Derived CD184+ Endoderm Cultured Cells ES cell derived
14 chr2:210483400-210484400 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
15 chr2:210483800-210485000 Enhancers HUVEC blood vessel

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