Variant report

Variant	rs10264249
Chromosome Location	chr7:83474495-83474496
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs10224301	0.85[EUR][1000 genomes]
rs10231380	0.83[EUR][1000 genomes]
rs10245587	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10248473	0.82[AFR][1000 genomes];0.86[EUR][1000 genomes]
rs10248603	0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10248941	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10251914	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10253119	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10254040	0.85[EUR][1000 genomes]
rs10270310	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs10275692	0.84[EUR][1000 genomes]
rs1474450	0.88[EUR][1000 genomes]
rs1474451	0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1474452	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1526498	0.84[EUR][1000 genomes]
rs17148226	0.83[EUR][1000 genomes]
rs1990427	0.87[EUR][1000 genomes]
rs2177910	0.87[EUR][1000 genomes]
rs28669930	0.87[EUR][1000 genomes]
rs4732523	0.87[EUR][1000 genomes]
rs6467968	0.89[EUR][1000 genomes]
rs6467969	0.89[EUR][1000 genomes]
rs6942612	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6965648	0.97[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6977444	0.95[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7778838	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7802095	0.85[EUR][1000 genomes]
rs7803071	0.85[EUR][1000 genomes]
rs7803495	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7803725	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9690506	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9692445	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888617	chr7:83352427-83479375	Flanking Active TSS ZNF genes & repeats Enhancers Bivalent Enhancer Weak transcription Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv607707	chr7:83381032-83646816	Weak transcription Enhancers Strong transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv1020865	chr7:83393101-83504439	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
4	nsv1017260	chr7:83393101-83506643	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
5	nsv888619	chr7:83452312-83549032	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv888620	chr7:83459908-83593805	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv1794884	chr7:83468908-83489827	Enhancers Weak transcription ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:83460400-83478800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr7:83464200-83474800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr7:83474200-83474600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell

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