Variant report

Variant	rs12470132
Chromosome Location	chr2:11167956-11167957
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10173572	0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13027949	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2084924	0.83[ASN][1000 genomes]
rs3951237	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4668707	0.90[ASN][1000 genomes]
rs4668711	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669679	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4669681	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4669682	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6432164	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs994303	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][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	nsv833392	chr2:11054580-11235239	Weak transcription Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:11161800-11168600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr2:11163000-11168800	Weak transcription	Right Atrium	heart
3	chr2:11164800-11171200	Weak transcription	Pancreas	Pancrea
4	chr2:11165000-11170000	Weak transcription	Fetal Lung	lung
5	chr2:11167600-11168800	Weak transcription	ES-UCSF4 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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