Variant report

Variant	rs7744024
Chromosome Location	chr6:118528493-118528494
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs11153725	0.87[MEX][hapmap]
rs12202829	0.86[CHB][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs1413845	1.00[CEU][hapmap];0.85[CHB][hapmap];0.88[CHD][hapmap];1.00[GIH][hapmap];0.81[JPT][hapmap];0.92[MEX][hapmap];0.98[TSI][hapmap];0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1413846	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.98[TSI][hapmap];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs205915	0.86[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs205916	0.83[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs2105020	0.86[CHB][hapmap];0.81[JPT][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2356077	0.83[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs281869	0.96[MEX][hapmap]
rs2883849	0.87[MEX][hapmap]
rs58826473	0.83[AMR][1000 genomes]
rs6569006	0.82[ASN][1000 genomes]
rs6936121	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.89[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.89[TSI][hapmap];0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7766406	0.88[AMR][1000 genomes];1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9374723	0.83[ASN][1000 genomes]
rs9387565	0.82[CHB][hapmap];0.82[JPT][hapmap];0.83[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs9398485	0.86[CHB][hapmap];0.86[CHD][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.83[AMR][1000 genomes];0.87[ASN][1000 genomes]
rs9481770	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv530526	chr6:118027339-118718476	Weak transcription Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
2	nsv428153	chr6:118430517-118586974	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1030089	chr6:118436482-118604516	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv538427	chr6:118436482-118604516	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:118525600-118529400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:118526800-118532400	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:118528400-118529000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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