Variant report

Variant	rs4730966
Chromosome Location	chr7:120261959-120261960
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	chr7:120255038..120256549-chr7:120260668..120263169,2	MCF-7	breast:
2	chr7:120260960..120263312-chr7:120264903..120266573,2	K562	blood:

Extended variants
information (count: 76 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs10085878	0.95[JPT][hapmap]
rs10230753	0.95[JPT][hapmap]
rs10258480	0.95[JPT][hapmap]
rs10276390	0.81[JPT][hapmap]
rs10278347	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10953918	0.81[JPT][hapmap]
rs11980474	0.81[JPT][hapmap]
rs12530902	0.95[JPT][hapmap]
rs12531042	0.80[JPT][hapmap]
rs12531146	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12531730	0.81[JPT][hapmap]
rs12537274	1.00[JPT][hapmap]
rs12540785	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12706290	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12706291	0.91[CHB][hapmap];1.00[JPT][hapmap];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12706292	0.91[CHB][hapmap];1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs13224331	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13227896	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13241174	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs1358369	1.00[JPT][hapmap]
rs1405835	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1405836	0.95[JPT][hapmap]
rs1527653	0.95[JPT][hapmap]
rs1569089	0.86[CHB][hapmap];1.00[JPT][hapmap]
rs17132703	0.81[JPT][hapmap]
rs17142829	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1881023	1.00[JPT][hapmap]
rs1881024	0.95[JPT][hapmap]
rs1918465	1.00[CEU][hapmap];0.96[CHB][hapmap];0.95[JPT][hapmap];0.90[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1997229	0.95[JPT][hapmap]
rs2402539	0.95[JPT][hapmap]
rs3814461	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4464900	0.95[JPT][hapmap]
rs4610678	1.00[JPT][hapmap]
rs4727909	0.86[AMR][1000 genomes];0.92[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4727910	0.95[JPT][hapmap]
rs4730965	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6466752	1.00[JPT][hapmap]
rs6948806	0.81[JPT][hapmap]
rs6950967	1.00[JPT][hapmap]
rs6951226	0.95[JPT][hapmap]
rs6978175	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6979618	0.86[JPT][hapmap]
rs702415	0.81[JPT][hapmap]
rs702416	0.85[JPT][hapmap]
rs7781883	0.83[ASN][1000 genomes]
rs7790906	1.00[JPT][hapmap]
rs7791822	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap]
rs7791851	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs7798075	0.80[JPT][hapmap]
rs7808260	0.95[JPT][hapmap]
rs802332	0.85[JPT][hapmap]
rs802334	0.85[JPT][hapmap]
rs802335	0.85[JPT][hapmap]
rs802336	0.86[JPT][hapmap]
rs802339	0.84[JPT][hapmap]
rs802340	0.91[JPT][hapmap]
rs802345	0.81[JPT][hapmap]
rs802349	0.81[JPT][hapmap]
rs802352	0.81[JPT][hapmap]
rs802353	0.81[JPT][hapmap]
rs802355	0.81[JPT][hapmap]
rs802358	0.81[JPT][hapmap]
rs802360	0.81[JPT][hapmap]
rs802362	0.81[JPT][hapmap]
rs802364	0.85[JPT][hapmap]
rs802365	0.81[JPT][hapmap]
rs802367	0.85[JPT][hapmap]
rs802371	0.86[JPT][hapmap]
rs802372	0.85[JPT][hapmap]
rs802374	0.85[JPT][hapmap]
rs802377	0.85[JPT][hapmap]
rs802378	0.80[JPT][hapmap]
rs9641642	0.95[CHB][hapmap];1.00[JPT][hapmap]
rs9649423	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889117	chr7:120122040-120266458	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	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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