Variant report

Variant rs2392611
Chromosome Location chr7:38976398-38976399
allele A/G
Outlinks Ensembl   UCSC
Chromatin state (count:12 , 50 per page) page: 1
No. Chromosome Location Chromatin state Cell line Tissue
1 chr7:38969800-38977400 Weak transcription ES-I3 Cell Line embryonic stem cell
2 chr7:38969800-38977800 Weak transcription H9 Derived Neuronal Progenitor Cultured Cells ES cell derived
3 chr7:38970200-38977000 Weak transcription H9 Derived Neuron Cultured Cells ES cell derived
4 chr7:38970200-38977000 Weak transcription HUVEC blood vessel
5 chr7:38972600-38977200 Weak transcription HUES48 Cell Line embryonic stem cell
6 chr7:38972600-38977400 Weak transcription Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells embryonic stem cell
7 chr7:38972600-38978000 Weak transcription HUES6 Cell Line embryonic stem cell
8 chr7:38972600-38978000 Weak transcription iPS-20b Cell Line embryonic stem cell
9 chr7:38972600-38978000 Weak transcription Fetal Brain Female brain
10 chr7:38972600-38987200 Weak transcription Aorta Aorta
11 chr7:38974400-38978200 Weak transcription H1 Derived Neuronal Progenitor Cultured Cells ES cell derived
12 chr7:38975800-38976400 Enhancers Fetal Brain Male brain

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