Variant report

Variant	rs3757049
Chromosome Location	chr6:69758072-69758073
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 34 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:30)

rs_ID	r²[population]
rs10455681	1.00[YRI][hapmap]
rs10455682	1.00[YRI][hapmap]
rs12665384	0.91[JPT][hapmap];1.00[YRI][hapmap]
rs12665411	0.91[JPT][hapmap];1.00[YRI][hapmap]
rs1336654	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1415032	0.83[JPT][hapmap];1.00[YRI][hapmap]
rs1572940	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1953614	0.81[EUR][1000 genomes]
rs3798971	0.86[JPT][hapmap]
rs3798982	0.91[JPT][hapmap];1.00[YRI][hapmap]
rs3798983	0.91[JPT][hapmap];1.00[YRI][hapmap]
rs3798990	0.91[JPT][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs3798995	0.91[JPT][hapmap];0.84[EUR][1000 genomes]
rs3798997	1.00[CEU][hapmap];0.90[JPT][hapmap];1.00[YRI][hapmap];0.93[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3798999	0.81[CHB][hapmap];0.91[JPT][hapmap]
rs3799000	0.91[JPT][hapmap]
rs3799019	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3799027	1.00[YRI][hapmap]
rs3799048	1.00[YRI][hapmap]
rs3823070	1.00[YRI][hapmap]
rs688606	1.00[YRI][hapmap]
rs72906776	0.82[EUR][1000 genomes]
rs779460	1.00[YRI][hapmap]
rs779463	1.00[YRI][hapmap]
rs779484	1.00[YRI][hapmap]
rs9354826	1.00[YRI][hapmap]
rs9360369	1.00[CEU][hapmap];0.95[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs9363980	0.93[AMR][1000 genomes];0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs960991	0.91[JPT][hapmap];1.00[YRI][hapmap];0.84[EUR][1000 genomes]
rs9718113	0.94[EUR][1000 genomes];0.89[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	nsv886137	chr6:69684850-70095690	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv463148	chr6:69746054-69781786	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
3	nsv603632	chr6:69746054-69781786	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv603633	chr6:69748600-69794079	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69685800-69758800	Weak transcription	Fetal Brain Male	brain
2	chr6:69720400-69758600	Weak transcription	Cortex derived primary cultured neurospheres	brain
3	chr6:69729400-69759400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
4	chr6:69753600-69794800	Weak transcription	Fetal Lung	lung
5	chr6:69756400-69769000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr6:69756600-69759600	Weak transcription	Brain Angular Gyrus	brain

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