Variant report

Variant	rs7195958
Chromosome Location	chr16:72036577-72036578
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:71916441..71919299-chr16:72035111..72037347,2	MCF-7	breast:
2	chr16:72027985..72030147-chr16:72034897..72037159,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000182149	Chromatin interaction
ENSG00000102984	Chromatin interaction

Extended variants
information (count: 34 )
Associated
traits (count: 12 )

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10048111	0.80[ASN][1000 genomes]
rs1035559	0.87[ASW][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.82[JPT][hapmap];0.83[LWK][hapmap];0.81[MEX][hapmap];0.93[YRI][hapmap];0.88[AFR][1000 genomes];0.80[AMR][1000 genomes];0.88[ASN][1000 genomes]
rs1035560	0.89[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11642993	0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs11648003	0.90[ASN][1000 genomes]
rs11864188	0.82[ASN][1000 genomes]
rs11864453	0.94[CHB][hapmap];0.94[JPT][hapmap];0.86[ASN][1000 genomes]
rs12599952	0.81[ASN][1000 genomes]
rs12708928	0.81[CHD][hapmap]
rs2012817	0.91[AFR][1000 genomes];0.88[ASN][1000 genomes]
rs2074627	0.81[CHD][hapmap]
rs2278027	0.92[ASN][1000 genomes]
rs3213420	0.80[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs3213422	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4788454	0.88[ASW][hapmap];0.88[CHD][hapmap];0.96[LWK][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs4788597	0.91[CHD][hapmap];0.84[JPT][hapmap];0.88[ASN][1000 genomes]
rs4788598	0.84[JPT][hapmap];0.88[ASN][1000 genomes]
rs4788600	0.94[ASW][hapmap];0.88[CHD][hapmap];0.84[JPT][hapmap];0.93[YRI][hapmap];0.88[ASN][1000 genomes]
rs7185215	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs7185407	0.81[ASW][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.83[GIH][hapmap];0.94[JPT][hapmap];0.81[MEX][hapmap];0.86[YRI][hapmap];0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs7186207	1.00[CEU][hapmap];0.88[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.87[MKK][hapmap];0.98[TSI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7201491	0.81[AFR][1000 genomes];0.81[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs752434	0.86[ASN][1000 genomes]
rs8051239	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8051882	0.81[CHD][hapmap]
rs929866	0.84[CHB][hapmap];0.91[CHD][hapmap];0.88[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	nsv948468	chr16:71727571-72651914	Enhancers Weak transcription Strong transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	89 gene(s)	inside rSNPs	diseases
2	nsv1056439	chr16:71916498-72051144	Strong transcription Weak transcription ZNF genes & repeats Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv1055854	chr16:71922144-72082886	Strong transcription Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
4	nsv833273	chr16:71971805-72152854	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	31 gene(s)	inside rSNPs	diseases
5	esv2758430	chr16:71976344-72274347	Weak transcription Strong transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
6	esv2758654	chr16:71976344-72274347	Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Active TSS Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
7	nsv428329	chr16:71976344-72274347	Strong transcription Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
8	nsv906894	chr16:72013539-72046211	Weak transcription Enhancers Active TSS Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	12 gene(s)	inside rSNPs	n/a

mRNA abundance (count:12)

SNP	Gene	Cis/trans	Tissue	Source
rs7195958	ZFP90	cis	parietal	SCAN
rs7195958	DHODH	cis	cerebellum	SCAN
rs7195958	HPR	cis	parietal	SCAN
rs7195958	DHODH	cis	Adipose Subcutaneous	GTEx
rs7195958	HP	cis	parietal	SCAN
rs7195958	DHX38	cis	lymphoblastoid	seeQTL
rs7195958	HPR	cis	cerebellum	SCAN
rs7195958	DHODH	cis	parietal	SCAN
rs7195958	DHODH	cis	Artery Aorta	GTEx
rs7195958	DHODH	cis	Artery Tibial	GTEx
rs7195958	DHODH	cis	Nerve Tibial	GTEx
rs7195958	DHODH	cis	Esophagus Muscularis	GTEx

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:72035000-72037800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr16:72035800-72037000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr16:72036000-72036600	Enhancers	HepG2	liver
4	chr16:72036400-72041800	Weak transcription	Primary monocytes fromperipheralblood	blood

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