Variant report

Variant	rs1322494
Chromosome Location	chr1:168837734-168837735
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs11577020	1.00[JPT][hapmap];0.84[EUR][1000 genomes]
rs11586213	0.80[EUR][1000 genomes]
rs12033844	0.96[EUR][1000 genomes]
rs12124802	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs12139484	0.87[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1322493	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1322496	0.96[EUR][1000 genomes]
rs1540942	0.80[EUR][1000 genomes]
rs17571933	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2065128	1.00[CHB][hapmap]
rs2104191	0.84[EUR][1000 genomes]
rs2146204	1.00[TSI][hapmap];0.80[EUR][1000 genomes]
rs2208748	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2208749	0.92[AFR][1000 genomes];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59148528	0.85[EUR][1000 genomes]
rs715007	0.94[ASN][1000 genomes]
rs72695642	0.80[EUR][1000 genomes]
rs973608	0.80[TSI][hapmap]
rs992055	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 gene(s)	inside rSNPs	diseases
2	nsv831847	chr1:168669877-168850129	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
3	nsv437258	chr1:168824111-168890420	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs1322494	POU2F1	cis	parietal	SCAN
rs1322494	CREG1	cis	cerebellum	SCAN
rs1322494	POGK	cis	cerebellum	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:168836800-168838000	Enhancers	Pancreas	Pancrea
2	chr1:168837000-168837800	Enhancers	Stomach Mucosa	stomach
3	chr1:168837000-168838800	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr1:168837400-168837800	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr1:168837600-168838000	Enhancers	Psoas Muscle	Psoas

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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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