Variant report

Variant	rs10042178
Chromosome Location	chr5:167510519-167510520
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:167501000-167512800	Weak transcription	Placenta Amnion	Placenta Amnion
2	chr5:167501600-167514800	Weak transcription	NHEK	skin
3	chr5:167501800-167511800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr5:167504000-167511600	Weak transcription	Left Ventricle	heart
5	chr5:167504400-167512600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr5:167505200-167515400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
7	chr5:167510200-167512800	Weak transcription	Fetal Brain Male	brain
8	chr5:167510400-167511600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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