Variant report

Variant	rs11715442
Chromosome Location	chr3:59945810-59945811
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 19 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11707548	0.98[ASN][1000 genomes]
rs11707783	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11711589	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11921436	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1879996	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs212034	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2366964	0.90[ASN][1000 genomes]
rs2630189	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2630191	0.90[EUR][1000 genomes]
rs2736796	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs2736802	0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs3772475	0.90[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs6446097	0.90[ASN][1000 genomes]
rs7629424	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs9819930	0.82[AFR][1000 genomes];0.83[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9881070	0.83[AMR][1000 genomes];0.96[EUR][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	chr3:59945600-59946400	Enhancers	Primary T helper cells fromperipheralblood	blood
7	chr3:59945600-59946400	Weak transcription	Dnd41	blood
8	chr3:59945800-59946400	Enhancers	Primary T helper cells PMA-I stimulated	--

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

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