Variant report

Variant	rs826786
Chromosome Location	chr7:147047213-147047214
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:147045457..147047946-chr7:147059907..147061995,2	K562	blood:

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:65)

rs_ID	r²[population]
rs1018991	0.82[GIH][hapmap]
rs10228191	1.00[CEU][hapmap];0.91[JPT][hapmap]
rs10236330	0.85[JPT][hapmap]
rs10239550	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10264424	1.00[CEU][hapmap];0.91[JPT][hapmap];0.80[EUR][1000 genomes]
rs10265626	0.87[CEU][hapmap];0.91[JPT][hapmap]
rs10267232	0.82[GIH][hapmap]
rs12112534	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1304809	1.00[JPT][hapmap]
rs13230403	0.95[JPT][hapmap]
rs1479841	0.91[JPT][hapmap]
rs1479842	0.82[CHD][hapmap];0.90[JPT][hapmap]
rs1479847	0.80[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1528532	0.85[CEU][hapmap];0.84[JPT][hapmap]
rs1585815	1.00[CEU][hapmap];0.82[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1842275	0.91[JPT][hapmap];0.86[ASN][1000 genomes]
rs2620438	0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2620472	0.84[CHD][hapmap];0.90[JPT][hapmap]
rs2620475	0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs2692131	0.90[JPT][hapmap]
rs2697452	1.00[JPT][hapmap]
rs2697453	0.91[JPT][hapmap]
rs2697457	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap]
rs6464815	0.89[GIH][hapmap];0.90[JPT][hapmap]
rs700293	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.94[MEX][hapmap];0.94[TSI][hapmap]
rs700296	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];0.94[CHD][hapmap];1.00[GIH][hapmap];0.95[JPT][hapmap];1.00[LWK][hapmap];0.93[MEX][hapmap];0.90[MKK][hapmap];1.00[TSI][hapmap];0.91[YRI][hapmap]
rs700298	1.00[CEU][hapmap];0.89[JPT][hapmap]
rs700299	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap]
rs700300	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap]
rs700301	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap]
rs700306	1.00[CEU][hapmap];0.89[CHB][hapmap];0.91[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs700308	1.00[ASW][hapmap];0.88[CHB][hapmap];0.91[CHD][hapmap];0.93[GIH][hapmap];0.84[JPT][hapmap];0.94[TSI][hapmap]
rs700311	0.84[CHB][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs700312	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs700313	1.00[CEU][hapmap];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7778880	0.82[GIH][hapmap]
rs7803992	0.82[YRI][hapmap]
rs826641	0.90[JPT][hapmap]
rs826642	1.00[CEU][hapmap];0.86[JPT][hapmap]
rs826645	0.83[CHD][hapmap];1.00[JPT][hapmap]
rs826646	0.83[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs826647	1.00[CEU][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs826649	0.89[JPT][hapmap]
rs826650	1.00[CEU][hapmap];0.91[JPT][hapmap];0.82[EUR][1000 genomes]
rs826651	1.00[CEU][hapmap];0.83[CHD][hapmap];0.90[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.82[EUR][1000 genomes]
rs826652	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap]
rs826655	1.00[ASW][hapmap];0.89[CEU][hapmap];0.82[CHB][hapmap];0.88[CHD][hapmap];0.96[GIH][hapmap];0.90[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs826656	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826657	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826658	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs826659	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826660	1.00[ASW][hapmap];1.00[CEU][hapmap];0.82[CHB][hapmap];0.88[CHD][hapmap];0.93[GIH][hapmap];1.00[JPT][hapmap];0.87[MEX][hapmap];0.94[TSI][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826661	1.00[CEU][hapmap];0.81[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826662	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826663	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826664	0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs826788	0.89[JPT][hapmap]
rs826790	0.82[CHD][hapmap]
rs826793	0.91[JPT][hapmap]
rs826802	0.81[CHD][hapmap]
rs826812	1.00[CEU][hapmap];0.89[CHB][hapmap];1.00[JPT][hapmap];0.85[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs826813	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs826814	1.00[CEU][hapmap];0.82[CHB][hapmap];0.91[JPT][hapmap];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs826823	0.88[CHB][hapmap];0.91[CHD][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs872713	1.00[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv933033	chr7:146720301-147081560	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
2	nsv1033898	chr7:146721499-147081768	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	5 gene(s)	inside rSNPs	diseases
3	nsv931005	chr7:146730472-147381257	Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1033398	chr7:146989035-147101573	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
5	nsv465192	chr7:147001077-147086045	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
6	nsv608943	chr7:147001077-147086045	Weak transcription Enhancers	TF binding region CpG island Chromatin interactive region miRNA	1 gene(s)	inside rSNPs	n/a
7	nsv526693	chr7:147011388-147054250	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
8	nsv1018715	chr7:147012067-147052280	Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	n/a
9	esv3332464	chr7:147044819-147049817	Inactive region	Chromatin interactive region	n/a	n/a	n/a

No data

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

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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