Variant report

Variant	rs1072508
Chromosome Location	chr1:86345486-86345487
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 69 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs1072509	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10873730	1.00[CHB][hapmap]
rs10873731	0.91[CHB][hapmap];0.83[ASN][1000 genomes]
rs11161693	0.95[CHB][hapmap]
rs11161695	0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs11161696	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11161697	0.94[CEU][hapmap];1.00[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12029238	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs12127479	0.80[ASN][1000 genomes]
rs12144570	0.94[CEU][hapmap];0.81[EUR][1000 genomes]
rs1564516	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17411495	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs186376	0.95[CHB][hapmap];0.95[JPT][hapmap];0.94[YRI][hapmap];0.89[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs1904947	1.00[CHB][hapmap]
rs2256515	0.80[ASN][1000 genomes]
rs2795038	0.80[ASN][1000 genomes]
rs2892901	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs313698	0.86[AFR][1000 genomes];0.84[ASN][1000 genomes]
rs313700	0.85[ASN][1000 genomes]
rs313701	0.95[CHB][hapmap]
rs313702	0.95[CHB][hapmap]
rs313703	0.95[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs313704	0.95[CHB][hapmap];0.95[JPT][hapmap];0.90[YRI][hapmap];0.87[AFR][1000 genomes];0.86[ASN][1000 genomes]
rs313705	0.95[CHB][hapmap]
rs313706	0.95[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.86[ASN][1000 genomes]
rs313707	0.95[CHB][hapmap]
rs313708	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs313709	0.95[CHB][hapmap]
rs313738	0.95[CHB][hapmap]
rs313740	0.91[CHB][hapmap]
rs313741	0.91[CHB][hapmap]
rs313742	0.91[CHB][hapmap]
rs313746	0.91[CHB][hapmap]
rs313747	0.88[AFR][1000 genomes];0.85[ASN][1000 genomes]
rs313748	0.85[ASN][1000 genomes]
rs313756	0.91[CHB][hapmap]
rs313757	0.95[CHB][hapmap]
rs313758	0.91[CHB][hapmap];0.95[JPT][hapmap];0.83[YRI][hapmap];0.85[ASN][1000 genomes]
rs313759	0.91[CHB][hapmap];0.95[JPT][hapmap];0.84[YRI][hapmap];0.85[ASN][1000 genomes]
rs313763	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs313764	0.80[ASN][1000 genomes]
rs313766	0.80[ASN][1000 genomes]
rs313768	0.80[ASN][1000 genomes]
rs313769	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs313770	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs313771	1.00[CHB][hapmap]
rs313773	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs313774	0.81[ASN][1000 genomes]
rs313775	1.00[CHB][hapmap];0.80[ASN][1000 genomes]
rs428475	1.00[CHB][hapmap]
rs435007	0.95[AFR][1000 genomes];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs437257	1.00[CHB][hapmap]
rs482789	0.91[CHB][hapmap]
rs537408	0.91[CHB][hapmap]
rs573444	0.86[CHB][hapmap]
rs593146	0.85[CHB][hapmap]
rs629140	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6576793	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap];0.94[YRI][hapmap];0.93[AFR][1000 genomes];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs7524286	0.95[CHB][hapmap];0.91[JPT][hapmap];0.80[ASN][1000 genomes]
rs7536101	0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs7544141	0.80[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	nsv817212	chr1:86127851-86658426	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	nsv546721	chr1:86226352-86392577	Weak transcription Strong transcription Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
3	nsv999743	chr1:86241246-86364846	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
4	nsv1011293	chr1:86270649-86416972	Enhancers Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
5	nsv546722	chr1:86278315-86891073	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	9 gene(s)	inside rSNPs	diseases
6	nsv871189	chr1:86315724-86402244	Weak transcription Strong transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases
7	esv1810714	chr1:86339811-86392577	Weak transcription Enhancers ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv823409	chr1:86342838-86352563	Strong transcription Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:86341200-86347000	Weak transcription	Fetal Lung	lung
2	chr1:86342400-86370600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr1:86344000-86347000	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr1:86345400-86345600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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