Variant report

Variant	rs34001515
Chromosome Location	chr4:91025850-91025851
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 80 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs10516857	0.81[EUR][1000 genomes]
rs10516858	0.92[CEU][hapmap];0.90[TSI][hapmap];0.88[EUR][1000 genomes]
rs10516860	0.82[EUR][1000 genomes]
rs10516862	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10516864	0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11732065	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[YRI][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12500465	0.81[EUR][1000 genomes]
rs12639636	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs12642395	0.88[EUR][1000 genomes]
rs12642404	0.88[EUR][1000 genomes]
rs12647171	0.83[EUR][1000 genomes]
rs12647266	0.83[EUR][1000 genomes]
rs12648872	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12649987	0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12650363	0.83[EUR][1000 genomes]
rs12651123	0.91[CEU][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs13103611	0.88[CEU][hapmap];0.94[CHB][hapmap];0.96[CHD][hapmap];0.86[GIH][hapmap];1.00[JPT][hapmap]
rs13104940	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs13107286	0.83[EUR][1000 genomes]
rs13108338	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs13113863	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs13119778	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13120745	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13121853	0.88[EUR][1000 genomes]
rs13124133	0.82[EUR][1000 genomes]
rs13131070	0.88[EUR][1000 genomes]
rs13131903	0.80[EUR][1000 genomes]
rs13132515	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs13132730	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13148977	0.81[EUR][1000 genomes]
rs13149395	0.87[EUR][1000 genomes]
rs13150124	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs13151441	0.82[EUR][1000 genomes]
rs1443796	0.82[EUR][1000 genomes]
rs1562034	0.82[EUR][1000 genomes]
rs17204072	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];1.00[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17204198	0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17205805	0.96[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.82[LWK][hapmap];0.82[MKK][hapmap];0.97[TSI][hapmap];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs17808648	0.88[EUR][1000 genomes]
rs17808829	0.88[CEU][hapmap];0.83[TSI][hapmap];0.82[EUR][1000 genomes]
rs1812076	0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1835521	0.87[ASW][hapmap];0.96[CEU][hapmap];1.00[CHB][hapmap];0.96[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.92[LWK][hapmap];0.98[MKK][hapmap];1.00[TSI][hapmap];0.82[YRI][hapmap];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1982293	0.88[EUR][1000 genomes]
rs2120372	0.83[EUR][1000 genomes]
rs2120375	0.80[EUR][1000 genomes]
rs34064092	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs34146382	0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34243515	0.86[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34343229	0.88[EUR][1000 genomes]
rs34886505	0.86[EUR][1000 genomes]
rs35197902	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs36047807	0.93[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs55663876	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs55686873	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62312738	0.80[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs62312743	0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs62313888	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62313890	0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6532212	0.81[EUR][1000 genomes]
rs6814978	0.82[EUR][1000 genomes]
rs6819755	0.82[EUR][1000 genomes]
rs6830014	0.82[CEU][hapmap];0.88[EUR][1000 genomes]
rs6837222	0.83[EUR][1000 genomes]
rs723992	0.83[TSI][hapmap];0.81[EUR][1000 genomes]
rs72659470	0.83[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7438673	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7660182	0.88[EUR][1000 genomes]
rs7661577	0.81[EUR][1000 genomes]
rs7672024	0.83[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7677884	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7677966	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs7685355	0.81[EUR][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	nsv1012406	chr4:90167781-91166787	Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Enhancers Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv949454	chr4:90272120-91156917	Flanking Bivalent TSS/Enh Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
3	nsv470053	chr4:90879613-91439573	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
4	nsv879537	chr4:90883047-91165346	Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
5	nsv931074	chr4:90970476-91753697	Enhancers Strong transcription Bivalent/Poised TSS Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv830006	chr4:90971656-91186340	Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
7	nsv879538	chr4:90993172-91080308	Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases
8	nsv879539	chr4:91015463-91065352	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent/Poised TSS Active TSS Bivalent Enhancer Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:91024400-91030200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived

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