Variant report

Variant rs12996265
Chromosome Location chr2:210486167-210486168
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:16 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr2:210476600-210493600 Weak transcription Aorta Aorta
2 chr2:210480000-210493200 Weak transcription Brain Germinal Matrix brain
3 chr2:210481000-210486400 Weak transcription Ganglion Eminence derived primary cultured neurospheres brain
4 chr2:210481000-210493400 Weak transcription Pancreas Pancrea
5 chr2:210481000-210500400 Weak transcription Foreskin Keratinocyte Primary Cells skin02 Skin
6 chr2:210481400-210493600 Strong transcription H9 Derived Neuron Cultured Cells ES cell derived
7 chr2:210481600-210487800 Weak transcription iPS DF 6.9 Cell Line embryonic stem cell
8 chr2:210484400-210486800 Strong transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
9 chr2:210484600-210497200 Weak transcription hESC Derived CD56+ Ectoderm Cultured Cells ES cell derived
10 chr2:210484800-210492800 Weak transcription Fetal Brain Male brain
11 chr2:210484800-210496000 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr2:210485000-210489000 Weak transcription ES-WA7 Cell Line embryonic stem cell
13 chr2:210485200-210487000 Weak transcription HUES64 Cell Line embryonic stem cell
14 chr2:210485400-210486400 Weak transcription Cortex derived primary cultured neurospheres brain
15 chr2:210485400-210486400 Weak transcription Pancreatic Islets Pancreatic Islet
16 chr2:210485400-210494400 Weak transcription Fetal Brain Female brain

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