Variant report

Variant	rs571515
Chromosome Location	chr6:23638331-23638332
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs1407242	0.88[CHB][hapmap];0.82[JPT][hapmap];0.93[ASN][1000 genomes]
rs2145771	0.92[ASN][1000 genomes]
rs4712770	0.91[ASN][1000 genomes]
rs475625	0.87[CHB][hapmap];0.81[JPT][hapmap]
rs492593	0.90[ASN][1000 genomes]
rs500694	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs505304	0.88[CHB][hapmap];0.92[ASN][1000 genomes]
rs510023	0.82[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs527469	0.88[CHB][hapmap];0.82[JPT][hapmap];0.86[MEX][hapmap];0.88[ASN][1000 genomes]
rs527583	0.88[ASN][1000 genomes]
rs541250	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs574440	0.80[AFR][1000 genomes];0.90[ASN][1000 genomes]
rs576816	0.89[ASW][hapmap];0.88[CHB][hapmap];0.94[LWK][hapmap];0.86[MEX][hapmap];0.84[AFR][1000 genomes];0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1029930	chr6:23481989-24289948	Enhancers Flanking Active TSS Strong transcription Bivalent Enhancer Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv830608	chr6:23558655-23644405	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv883478	chr6:23615399-23659465	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
4	nsv462656	chr6:23629281-23721032	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a
5	nsv601125	chr6:23629281-23721032	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	n/a

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs571515	FKSG83	cis	parietal	SCAN

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:23635200-23639600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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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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