Variant report

Variant	rs57156345
Chromosome Location	chr7:109144544-109144545
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs12533306	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12705597	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs12705605	0.82[ASN][1000 genomes]
rs13232439	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1528540	0.88[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4596584	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6968264	0.87[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7801496	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs7802842	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023379	chr7:109003574-109355234	Weak transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv608079	chr7:109098364-109862289	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:109141000-109145800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

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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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