Variant report

Variant	rs924803
Chromosome Location	chr2:125402320-125402321
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 81 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs10165603	0.81[CEU][hapmap]
rs10184472	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs10196022	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10202655	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs10202736	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs10206545	0.93[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs10207721	0.86[ASN][1000 genomes]
rs11123056	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11674701	0.85[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs11675141	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11676952	0.86[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs11686268	0.92[CEU][hapmap];0.92[CHB][hapmap];0.95[JPT][hapmap]
rs12470814	0.86[ASN][1000 genomes]
rs12473998	0.86[ASN][1000 genomes]
rs12995183	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs13003103	0.84[ASN][1000 genomes]
rs13011609	0.93[ASN][1000 genomes]
rs1394141	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1394142	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1394143	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1394146	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1454133	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs1504015	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.87[ASN][1000 genomes]
rs1504022	0.82[CEU][hapmap]
rs1504023	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1587788	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1587789	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs1604806	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs17392807	1.00[YRI][hapmap]
rs1902004	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs2174251	1.00[YRI][hapmap]
rs2174252	1.00[YRI][hapmap]
rs2219107	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4588196	1.00[YRI][hapmap]
rs4848249	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4848250	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4848251	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4848252	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4848257	0.85[ASN][1000 genomes]
rs4848947	0.93[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs4848949	0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4848950	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4848953	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4848956	1.00[CHB][hapmap];0.94[JPT][hapmap];0.87[YRI][hapmap]
rs4848957	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs4848959	0.94[ASN][1000 genomes]
rs4848960	0.94[ASN][1000 genomes]
rs6541966	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs6707181	0.96[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6707400	0.92[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs6707412	0.94[ASN][1000 genomes]
rs6712020	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.85[ASN][1000 genomes]
rs6720324	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6721614	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs6727845	0.92[CEU][hapmap];1.00[CHB][hapmap];0.94[JPT][hapmap]
rs6739364	0.89[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs6743015	0.93[ASN][1000 genomes]
rs6745271	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6750530	0.86[ASN][1000 genomes]
rs6751507	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6754751	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs727179	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs727180	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7560341	0.92[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7564755	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs7586683	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7599608	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap]
rs7599787	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7605511	0.93[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs768318	1.00[YRI][hapmap]
rs768319	0.87[YRI][hapmap]
rs924802	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs936028	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs936029	0.89[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs963189	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap]
rs963190	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap]
rs9646915	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs9646916	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.94[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv834357	chr2:125258157-125421507	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
2	nsv834359	chr2:125367872-125536022	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island	1 gene(s)	inside rSNPs	diseases
3	nsv428727	chr2:125372897-125512949	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island	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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