Variant report

Variant	rs16903085
Chromosome Location	chr5:36491074-36491075
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:36488200-36494000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
2	chr5:36490200-36492400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr5:36490400-36491200	Enhancers	HMEC	breast
4	chr5:36490400-36491200	Enhancers	NHEK	skin
5	chr5:36490400-36495800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr5:36490600-36491400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr5:36490600-36492400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
8	chr5:36490600-36493200	Weak transcription	HSMM	muscle
9	chr5:36490800-36491800	Weak transcription	Hela-S3	cervix
10	chr5:36490800-36492400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	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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