Variant report

Variant	rs6444532
Chromosome Location	chr3:190999760-190999761
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:41)

rs_ID	r²[population]
rs10937468	0.83[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10937469	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10937470	0.83[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12488359	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2117542	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2117545	0.82[CEU][hapmap]
rs2124077	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2124078	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2124079	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2364375	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2572057	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2603668	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603669	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603670	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603671	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603672	0.84[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603673	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603674	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603677	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603678	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603679	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603680	0.84[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2603681	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2603683	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2603685	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2631670	0.85[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2631671	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2631672	0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4388026	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4687207	0.95[CHB][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61123810	0.85[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs61193081	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6444533	0.83[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6444534	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6444535	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6788097	0.80[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6788319	0.80[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6802677	0.86[CEU][hapmap];0.82[CHB][hapmap]
rs7633752	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7644967	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7645540	0.83[CEU][hapmap];0.95[CHB][hapmap];0.83[JPT][hapmap];0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv428100	chr3:190793797-191092633	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv931943	chr3:190860224-191321873	Weak transcription Enhancers Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	esv2757910	chr3:190867011-191279107	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	esv2759209	chr3:190867011-191279107	Weak transcription Active TSS Flanking Active TSS Enhancers Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
5	nsv878101	chr3:190891939-191059322	Enhancers Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
6	nsv428428	chr3:190936834-191215596	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv997716	chr3:190943706-191027499	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv10369	chr3:190994774-191011447	Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr3:190998400-191001600	Enhancers	Hela-S3	cervix
2	chr3:190999000-191000800	Weak transcription	Liver	Liver
3	chr3:190999600-191000000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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