Variant report

Variant	rs9524284
Chromosome Location	chr13:94609509-94609510
allele	A/T
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:74)

rs_ID	r²[population]
rs10492635	0.82[CEU][hapmap]
rs1318496	1.00[YRI][hapmap]
rs1415737	0.82[CEU][hapmap]
rs1415740	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1415741	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1415742	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1415743	0.82[CEU][hapmap]
rs1556082	0.82[CEU][hapmap]
rs17253537	0.82[CEU][hapmap]
rs1832360	0.91[EUR][1000 genomes]
rs1933145	0.88[CEU][hapmap];0.91[EUR][1000 genomes]
rs1933146	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1933147	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs1933148	0.96[EUR][1000 genomes]
rs2892675	0.84[CEU][hapmap]
rs35534726	0.94[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs3904817	0.80[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4528446	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4771884	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6650320	1.00[CEU][hapmap]
rs6650321	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs72644500	0.92[ASN][1000 genomes]
rs7323264	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs7325794	1.00[CEU][hapmap];0.83[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.94[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7327560	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7985851	1.00[CEU][hapmap];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7994682	0.82[CEU][hapmap]
rs8000417	0.84[CEU][hapmap]
rs928188	0.91[CEU][hapmap];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs9284275	0.91[CEU][hapmap];0.96[EUR][1000 genomes]
rs9284276	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs9301919	0.91[CEU][hapmap];0.91[EUR][1000 genomes]
rs9301920	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs9301921	1.00[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9301926	0.82[CEU][hapmap]
rs945937	0.95[EUR][1000 genomes]
rs945938	0.93[EUR][1000 genomes]
rs9516319	0.91[CEU][hapmap];0.96[EUR][1000 genomes]
rs9516322	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9516323	0.91[CEU][hapmap];0.94[EUR][1000 genomes]
rs9516324	0.91[CEU][hapmap];0.94[EUR][1000 genomes]
rs9516325	0.91[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.84[AMR][1000 genomes];0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9516330	1.00[CHB][hapmap];0.94[JPT][hapmap];0.93[ASN][1000 genomes]
rs9516331	0.82[CEU][hapmap]
rs9524287	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9524288	0.91[EUR][1000 genomes]
rs9524290	0.91[CEU][hapmap];0.92[EUR][1000 genomes]
rs9524291	0.92[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9524292	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs9524293	0.91[CEU][hapmap];0.84[CHB][hapmap];0.89[JPT][hapmap];0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9524294	0.95[EUR][1000 genomes]
rs9524295	0.93[EUR][1000 genomes]
rs9524297	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9524298	0.91[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9524299	0.91[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9524300	0.91[CEU][hapmap];0.90[EUR][1000 genomes]
rs9524302	0.82[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9524303	0.92[CHB][hapmap];0.94[JPT][hapmap]
rs9524304	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs9524305	0.92[CHB][hapmap];1.00[JPT][hapmap]
rs9524306	0.82[CEU][hapmap];0.92[CHB][hapmap];1.00[JPT][hapmap]
rs9524309	0.85[CEU][hapmap];0.90[CHB][hapmap];0.85[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs9524310	0.93[ASN][1000 genomes]
rs9524311	0.82[CEU][hapmap]
rs9524312	0.82[CEU][hapmap]
rs9524314	0.82[CEU][hapmap]
rs9524319	0.82[CEU][hapmap]
rs9584175	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9584176	0.91[CEU][hapmap];0.94[EUR][1000 genomes]
rs9589877	0.91[CEU][hapmap];0.94[EUR][1000 genomes]
rs9589878	0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.93[ASN][1000 genomes]
rs9589882	0.82[CEU][hapmap]
rs9589883	0.82[CEU][hapmap]
rs981341	0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:7 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948714	chr13:94100104-94699435	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv933807	chr13:94187158-94845505	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1045230	chr13:94277683-94764671	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv948455	chr13:94451368-94988900	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv916640	chr13:94521959-95101443	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv533063	chr13:94560362-95101443	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1052141	chr13:94596760-94689892	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94607800-94609800	Enhancers	Fetal Stomach	stomach
2	chr13:94609000-94610200	Weak transcription	HepG2	liver
3	chr13:94609200-94618200	Weak transcription	Liver	Liver

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