Variant report

Variant	rs987449
Chromosome Location	chr7:14493460-14493461
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 64 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:60)

rs_ID	r²[population]
rs10236653	0.89[CEU][hapmap];0.86[GIH][hapmap];0.91[MEX][hapmap];0.83[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10237359	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10245826	0.87[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10260522	0.88[CEU][hapmap]
rs10266998	0.83[EUR][1000 genomes]
rs10274270	0.89[CEU][hapmap]
rs10274418	0.87[CEU][hapmap]
rs10274552	0.82[CEU][hapmap];0.84[GIH][hapmap]
rs10499442	1.00[CEU][hapmap];0.90[EUR][1000 genomes]
rs10950530	0.81[EUR][1000 genomes]
rs11505395	0.89[CEU][hapmap]
rs11505396	0.85[CEU][hapmap]
rs11767890	0.96[CEU][hapmap];0.84[EUR][1000 genomes]
rs11767969	0.84[CEU][hapmap];0.80[EUR][1000 genomes]
rs11771647	0.85[CEU][hapmap];0.85[GIH][hapmap];0.81[EUR][1000 genomes]
rs11980816	0.93[ASW][hapmap];0.82[CEU][hapmap];0.87[GIH][hapmap];0.81[YRI][hapmap]
rs12669548	0.86[ASW][hapmap];0.96[CEU][hapmap];0.95[GIH][hapmap];0.82[LWK][hapmap];0.91[MEX][hapmap];0.81[MKK][hapmap];0.81[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs12674261	1.00[CEU][hapmap];0.98[GIH][hapmap];0.83[MEX][hapmap];0.86[TSI][hapmap];0.83[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs12699617	0.88[CEU][hapmap]
rs12699622	1.00[CEU][hapmap];0.93[GIH][hapmap];0.84[TSI][hapmap];0.90[EUR][1000 genomes]
rs12699626	0.85[CEU][hapmap];0.80[EUR][1000 genomes]
rs12699635	0.81[CEU][hapmap]
rs12699641	0.88[CEU][hapmap]
rs13221160	0.82[EUR][1000 genomes]
rs13232496	0.85[CEU][hapmap]
rs13236153	0.82[CEU][hapmap]
rs1431521	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1431528	0.96[CEU][hapmap];0.98[GIH][hapmap];0.87[MEX][hapmap];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs1431532	0.84[CEU][hapmap]
rs1560576	0.92[CEU][hapmap]
rs182034	0.82[GIH][hapmap]
rs1835675	0.94[AFR][1000 genomes];0.93[AMR][1000 genomes];0.92[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1897300	0.96[CEU][hapmap];0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs196751	1.00[ASW][hapmap];0.96[CEU][hapmap];0.81[CHB][hapmap];1.00[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.84[LWK][hapmap];0.91[MEX][hapmap];0.87[TSI][hapmap];0.84[YRI][hapmap];0.87[AFR][1000 genomes];0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs196757	0.88[CEU][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1991685	1.00[CEU][hapmap];0.98[GIH][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs2052980	0.85[CEU][hapmap]
rs2357960	0.89[CEU][hapmap];0.80[GIH][hapmap];0.84[TSI][hapmap]
rs3823843	1.00[CEU][hapmap];0.98[GIH][hapmap];0.87[MEX][hapmap];0.89[TSI][hapmap];0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4370419	1.00[CEU][hapmap]
rs4721335	0.80[CEU][hapmap]
rs4721343	0.82[CEU][hapmap]
rs4721345	0.85[CEU][hapmap]
rs6461104	1.00[ASW][hapmap];1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[CHD][hapmap];0.98[GIH][hapmap];0.82[JPT][hapmap];1.00[MEX][hapmap];0.95[TSI][hapmap];0.81[YRI][hapmap];0.82[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6958607	0.85[CEU][hapmap]
rs6958691	0.92[CEU][hapmap]
rs6979012	0.85[CEU][hapmap]
rs6979330	0.85[CEU][hapmap]
rs6980167	0.85[CEU][hapmap]
rs7777633	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7783571	0.90[EUR][1000 genomes]
rs7794432	0.90[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7794969	0.83[EUR][1000 genomes]
rs7800703	0.96[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7801624	0.81[EUR][1000 genomes]
rs7802759	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs7807072	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];1.00[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9639203	0.80[GIH][hapmap]
rs9690425	0.81[CEU][hapmap]
rs987448	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv949033	chr7:14086106-14860323	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv915603	chr7:14443884-14624268	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	esv1848567	chr7:14464118-14579801	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv887707	chr7:14471682-14576163	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	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
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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