Variant report

Variant	rs563456199
Chromosome Location	chr6:5804337-5804338
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 1 )
Associated
traits (count: 0)

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv970074	chr6:5804160-5811421	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5804000-5804800	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
2	chr6:5804200-5804400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:5804200-5804800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr6:5804200-5804800	Enhancers	Fetal Thymus	thymus
5	chr6:5804200-5805000	ZNF genes & repeats	Aorta	Aorta

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

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