Variant report

Variant	rs7775911
Chromosome Location	chr6:5804717-5804718
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 2 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:1)

rs_ID	r²[population]
rs73720252	1.00[EUR][1000 genomes]

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:6 , 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	chr6:5804200-5804800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr6:5804200-5804800	Enhancers	Fetal Thymus	thymus
4	chr6:5804200-5805000	ZNF genes & repeats	Aorta	Aorta
5	chr6:5804400-5807200	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr6:5804600-5804800	ZNF genes & repeats	Pancreas	Pancrea

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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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