Variant report

Variant	rs7332149
Chromosome Location	chr13:93018191-93018192
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	chr13:93012828..93015636-chr13:93017565..93019548,2	K562	blood:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10162003	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1887156	0.81[JPT][hapmap]
rs1926624	0.81[JPT][hapmap]
rs1926629	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap]
rs1926631	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap]
rs1926633	0.87[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1926635	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1926637	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1926638	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[YRI][hapmap];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1926639	1.00[CEU][hapmap];0.82[CHB][hapmap];0.86[JPT][hapmap];0.82[YRI][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1926641	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1926642	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs1926643	0.81[CHB][hapmap];1.00[JPT][hapmap]
rs1926644	1.00[CEU][hapmap];0.90[CHB][hapmap];0.95[JPT][hapmap]
rs1926645	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1926646	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1926647	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs1926650	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap]
rs2148522	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2182536	0.85[CHB][hapmap];0.86[JPT][hapmap]
rs35520935	0.85[ASN][1000 genomes]
rs35801347	0.85[ASN][1000 genomes]
rs4338645	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4362255	0.85[ASN][1000 genomes]
rs4505184	0.83[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4508310	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap]
rs4771857	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6492597	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap]
rs6492599	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap]
rs6492600	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap]
rs6492602	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs6492604	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs6492605	0.86[CHB][hapmap]
rs716623	1.00[CEU][hapmap];0.81[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs716624	1.00[CEU][hapmap];0.82[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7323550	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7325201	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs7325768	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7330825	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7331847	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7332756	0.93[CEU][hapmap];0.86[CHB][hapmap];0.83[JPT][hapmap];0.91[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs7334109	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7490525	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7981777	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7982677	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs7985663	0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7985916	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap]
rs7996497	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7997136	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7998166	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap]
rs9301792	0.96[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9516060	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap]
rs9516062	1.00[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs9516063	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap]
rs9523630	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9584021	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs9584023	0.96[CEU][hapmap];0.91[CHB][hapmap];1.00[JPT][hapmap]
rs9589506	1.00[CEU][hapmap];0.83[CHB][hapmap];0.83[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9589508	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs9589512	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9589523	0.81[CHB][hapmap];0.85[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2756005	chr13:92584199-93080799	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	esv2753357	chr13:92903199-93026399	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1036835	chr13:92953101-93039812	Enhancers ZNF genes & repeats Weak transcription Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
4	nsv1050788	chr13:92953101-93045491	Enhancers Active TSS Weak transcription ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv1051394	chr13:92959102-93049128	Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1037815	chr13:92959102-93052008	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv456068	chr13:92961151-93038913	Enhancers Weak transcription ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv562727	chr13:92961151-93038913	Weak transcription Enhancers Active TSS ZNF genes & repeats	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv900903	chr13:92999147-93043373	Enhancers ZNF genes & repeats Active TSS Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
10	nsv976254	chr13:93007578-93034690	Active TSS Enhancers 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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