Variant report

Variant	rs11707816
Chromosome Location	chr3:59946469-59946470
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs1038517	1.00[ASW][hapmap]
rs10510821	1.00[CEU][hapmap];0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs11708404	1.00[YRI][hapmap];0.85[AFR][1000 genomes]
rs11715559	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs1580457	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs17031569	0.87[ASW][hapmap];1.00[CEU][hapmap];0.85[GIH][hapmap];0.91[LWK][hapmap];0.82[MEX][hapmap];0.97[MKK][hapmap];1.00[TSI][hapmap];0.86[YRI][hapmap];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17061546	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs17061598	1.00[CEU][hapmap];0.85[YRI][hapmap];0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs212020	0.82[MEX][hapmap]
rs2687898	0.95[EUR][1000 genomes]
rs2736814	1.00[MEX][hapmap]
rs3772460	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.82[MEX][hapmap];0.95[MKK][hapmap];0.93[TSI][hapmap];0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3821477	0.88[CHB][hapmap];1.00[CHD][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs57077895	0.89[ASN][1000 genomes]
rs7626013	1.00[ASW][hapmap];1.00[CEU][hapmap];0.85[GIH][hapmap];1.00[LWK][hapmap];0.82[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.93[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs974035	1.00[ASW][hapmap];0.87[LWK][hapmap];0.82[MEX][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs9815985	0.97[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	nsv428085	chr3:59782509-60070116	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1014983	chr3:59884024-60558331	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv590387	chr3:59890976-60481459	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:59941200-59947600	Strong transcription	Primary T cells from cord blood	blood
2	chr3:59943200-59964400	Weak transcription	Primary T cells fromperipheralblood	blood
3	chr3:59943400-59946600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
4	chr3:59943400-59951600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
5	chr3:59943800-59959600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
6	chr3:59946400-59948000	Strong transcription	Dnd41	blood
7	chr3:59946400-59951600	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr3:59946400-59958200	Weak transcription	Primary T helper cells fromperipheralblood	blood

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

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