Variant report

Variant	rs1926635
Chromosome Location	chr13:92982359-92982360
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:92980924..92984645-chr13:92987086..92990340,3	K562	blood:
2	chr13:92982264..92985131-chr13:93004741..93006675,2	K562	blood:
3	chr13:92981004..92983533-chr13:93023966..93025848,2	K562	blood:

Extended variants
information (count: 93 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10162003	1.00[CEU][hapmap];0.95[CHB][hapmap];0.87[JPT][hapmap];0.93[YRI][hapmap];0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11616708	0.81[EUR][1000 genomes]
rs11616739	0.81[JPT][hapmap]
rs13378505	0.91[CHB][hapmap];0.86[JPT][hapmap]
rs1887157	0.85[ASN][1000 genomes]
rs1926629	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1926631	1.00[CEU][hapmap];0.95[CHB][hapmap];0.86[JPT][hapmap]
rs1926632	0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs1926633	0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1926637	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1926638	1.00[CEU][hapmap];0.95[CHB][hapmap];0.82[JPT][hapmap];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs1926639	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1926640	0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs1926641	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs1926642	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap]
rs1926643	0.83[CHB][hapmap];0.82[JPT][hapmap];1.00[YRI][hapmap]
rs1926644	1.00[CEU][hapmap];0.91[CHB][hapmap];0.93[YRI][hapmap]
rs1926645	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.93[YRI][hapmap]
rs1926646	0.96[CEU][hapmap];0.91[CHB][hapmap];0.91[JPT][hapmap];1.00[YRI][hapmap]
rs1926647	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs1926650	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1926653	0.81[ASN][1000 genomes]
rs1926655	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs2148522	0.84[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs2182535	0.86[ASN][1000 genomes]
rs2182536	0.86[CHB][hapmap]
rs4085673	0.85[ASN][1000 genomes]
rs4338645	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4433679	0.81[CEU][hapmap]
rs4505184	0.86[EUR][1000 genomes]
rs4508310	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs4601908	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs4771856	0.95[CHB][hapmap];0.86[JPT][hapmap];0.86[ASN][1000 genomes]
rs4771857	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6492595	0.81[CEU][hapmap]
rs6492597	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6492598	0.83[EUR][1000 genomes]
rs6492599	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6492600	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs6492602	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs6492603	0.95[CHB][hapmap];0.87[JPT][hapmap];0.86[ASN][1000 genomes]
rs6492604	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6492605	0.87[CHB][hapmap]
rs716623	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs716624	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7323550	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7325201	0.87[CHB][hapmap]
rs7325768	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7327328	0.81[JPT][hapmap]
rs7330825	0.87[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7331847	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7332149	1.00[CEU][hapmap];0.83[CHB][hapmap];0.82[JPT][hapmap]
rs7332756	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[YRI][hapmap];0.95[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs7334109	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];0.93[YRI][hapmap]
rs7490525	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7981777	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7982677	0.86[CHB][hapmap]
rs7985663	0.90[EUR][1000 genomes]
rs7985916	1.00[CEU][hapmap];0.91[CHB][hapmap];0.81[JPT][hapmap];1.00[YRI][hapmap]
rs7994032	0.83[EUR][1000 genomes]
rs7996483	0.81[CEU][hapmap]
rs7996497	0.92[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7997136	1.00[CEU][hapmap];0.95[CHB][hapmap];0.81[JPT][hapmap];0.87[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7998166	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9284271	0.82[EUR][1000 genomes]
rs9301792	0.96[CEU][hapmap];0.95[CHB][hapmap];0.81[JPT][hapmap];0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9301794	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs9301797	0.91[CHB][hapmap]
rs9516060	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9516062	1.00[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];1.00[YRI][hapmap]
rs9516063	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9523630	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9584017	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs9584018	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs9584021	0.86[CHB][hapmap]
rs9584022	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs9584023	0.96[CEU][hapmap];0.91[CHB][hapmap];0.82[JPT][hapmap]
rs9584024	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs9589502	0.95[CHB][hapmap];0.87[JPT][hapmap]
rs9589504	0.95[CHB][hapmap];0.86[JPT][hapmap]
rs9589506	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap];0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9589508	0.86[CHB][hapmap]
rs9589512	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9589522	0.95[CHB][hapmap];0.91[JPT][hapmap]
rs9589523	1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[YRI][hapmap]

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	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92981600-92983000	Weak transcription	Pancreas	Pancrea

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