Variant report

Variant	rs10224582
Chromosome Location	chr7:78659092-78659093
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	chr7:78656805..78659401-chr7:78662080..78664588,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:59)

rs_ID	r²[population]
rs1006818	0.95[CHB][hapmap];0.80[JPT][hapmap]
rs10215372	0.81[ASN][1000 genomes]
rs10226001	0.91[CEU][hapmap];0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs10231279	1.00[CEU][hapmap]
rs10240536	0.95[CEU][hapmap];0.81[YRI][hapmap]
rs11769552	0.90[CHB][hapmap];0.82[ASN][1000 genomes]
rs12113491	0.90[CHB][hapmap]
rs12536821	0.91[CEU][hapmap];0.95[CHB][hapmap];0.82[ASN][1000 genomes]
rs12536843	0.81[ASN][1000 genomes]
rs12537793	0.82[CEU][hapmap]
rs12538053	0.80[ASN][1000 genomes]
rs12539532	0.91[CEU][hapmap];0.95[CHB][hapmap]
rs12540352	0.84[CEU][hapmap];0.90[CHB][hapmap]
rs12540925	0.84[CEU][hapmap];0.91[CHB][hapmap]
rs17151881	0.91[CHB][hapmap];0.95[JPT][hapmap]
rs2006635	0.89[CHB][hapmap]
rs2079955	0.83[ASN][1000 genomes]
rs2098180	0.87[CEU][hapmap];0.91[CHB][hapmap];0.83[ASN][1000 genomes]
rs2098181	0.84[ASN][1000 genomes]
rs2109713	0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs2159687	0.91[CEU][hapmap];0.90[CHB][hapmap]
rs2191726	0.83[ASN][1000 genomes]
rs2191727	0.83[ASN][1000 genomes]
rs2191728	0.83[ASN][1000 genomes]
rs2191730	0.82[CHB][hapmap];0.81[JPT][hapmap]
rs2280607	0.95[CHB][hapmap]
rs2280608	0.81[ASN][1000 genomes]
rs2363930	0.83[ASN][1000 genomes]
rs2363931	0.83[ASN][1000 genomes]
rs28572181	0.84[ASN][1000 genomes]
rs28716458	0.82[ASN][1000 genomes]
rs34086589	0.80[ASN][1000 genomes]
rs4727794	0.83[CEU][hapmap];0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs4727796	0.91[CEU][hapmap];0.90[CHB][hapmap];0.84[ASN][1000 genomes]
rs4730597	0.88[CEU][hapmap];0.95[CHB][hapmap]
rs4730599	0.95[CHB][hapmap];0.80[ASN][1000 genomes]
rs4730601	0.90[CHB][hapmap];0.80[ASN][1000 genomes]
rs4730619	0.87[CEU][hapmap];0.95[CHB][hapmap];0.83[ASN][1000 genomes]
rs5004248	0.88[CEU][hapmap];0.91[CHB][hapmap]
rs6466471	0.81[ASN][1000 genomes]
rs6466477	0.83[ASN][1000 genomes]
rs6946707	0.80[CHB][hapmap];0.81[JPT][hapmap]
rs6952133	0.82[ASN][1000 genomes]
rs6954088	0.83[CEU][hapmap];0.95[JPT][hapmap]
rs6958348	0.82[EUR][1000 genomes]
rs6962482	0.87[CEU][hapmap];0.95[JPT][hapmap]
rs6964007	0.91[CEU][hapmap];0.95[CHB][hapmap]
rs727652	0.91[CHB][hapmap]
rs7778014	0.83[EUR][1000 genomes]
rs7779315	0.91[CHB][hapmap]
rs7781812	0.81[ASN][1000 genomes]
rs7789063	0.91[CHB][hapmap]
rs7791770	0.80[ASN][1000 genomes]
rs7792974	0.91[CEU][hapmap];0.90[CHB][hapmap];0.80[ASN][1000 genomes]
rs7797398	0.81[ASN][1000 genomes]
rs7799032	0.81[ASN][1000 genomes]
rs7805367	0.90[CHB][hapmap]
rs984312	0.91[CEU][hapmap];0.95[CHB][hapmap];0.82[ASN][1000 genomes]
rs985175	0.87[CEU][hapmap];0.85[CHB][hapmap];0.91[JPT][hapmap];0.86[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[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	nsv464598	chr7:78492642-79483480	Weak transcription Enhancers Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS 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	15 gene(s)	inside rSNPs	diseases
2	nsv607659	chr7:78492642-79483480	Enhancers Bivalent/Poised TSS Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	nsv482826	chr7:78548319-78717605	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv471642	chr7:78548320-78717605	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1029799	chr7:78608097-79061737	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
6	nsv831040	chr7:78623195-78831998	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv521257	chr7:78632489-78662425	Enhancers ZNF genes & repeats Weak transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv607660	chr7:78644077-78666050	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
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