Variant report

Variant	rs10492635
Chromosome Location	chr13:94699435-94699436
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 65 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs1318496	0.91[CEU][hapmap]
rs1415736	0.91[CEU][hapmap];0.83[CHB][hapmap];0.88[GIH][hapmap]
rs1415737	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs1415743	1.00[CEU][hapmap]
rs1556082	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs17253537	1.00[CEU][hapmap];0.83[CHB][hapmap];0.89[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1933146	0.82[CEU][hapmap];0.83[CHB][hapmap]
rs1933147	0.82[CEU][hapmap]
rs2021983	0.91[CEU][hapmap];0.85[EUR][1000 genomes]
rs2225228	0.81[AMR][1000 genomes]
rs2225229	0.81[AMR][1000 genomes]
rs6492685	0.91[CEU][hapmap];0.83[CHB][hapmap]
rs6650320	0.82[CEU][hapmap]
rs6650321	0.82[CEU][hapmap]
rs7323264	0.82[CEU][hapmap]
rs7325794	0.82[CEU][hapmap]
rs7985851	0.82[CEU][hapmap]
rs7994682	1.00[CEU][hapmap]
rs9284275	0.83[CHB][hapmap]
rs9284276	0.82[CEU][hapmap]
rs9301919	0.82[CHB][hapmap]
rs9301920	0.82[CEU][hapmap];0.83[CHB][hapmap];0.81[GIH][hapmap]
rs9301921	0.82[CEU][hapmap]
rs9301926	1.00[CEU][hapmap]
rs9301927	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs9301928	0.82[AMR][1000 genomes]
rs9516319	0.83[CHB][hapmap]
rs9516323	0.83[CHB][hapmap]
rs9516324	0.82[CHB][hapmap]
rs9516331	1.00[CEU][hapmap]
rs9516334	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9516335	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9524284	0.82[CEU][hapmap]
rs9524290	0.83[CHB][hapmap]
rs9524292	0.82[CEU][hapmap]
rs9524302	1.00[CEU][hapmap]
rs9524305	0.91[CEU][hapmap]
rs9524306	1.00[CEU][hapmap]
rs9524309	1.00[CEU][hapmap]
rs9524311	1.00[CEU][hapmap]
rs9524312	1.00[CEU][hapmap];0.83[CHB][hapmap]
rs9524313	0.90[CEU][hapmap]
rs9524314	1.00[CEU][hapmap]
rs9524316	1.00[CEU][hapmap];0.85[CHB][hapmap];0.81[EUR][1000 genomes]
rs9524317	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.89[AMR][1000 genomes];0.88[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9524318	1.00[CEU][hapmap];0.81[CHB][hapmap];0.89[JPT][hapmap];0.90[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9524319	1.00[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.97[TSI][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9556348	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9561490	0.91[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.93[TSI][hapmap];0.90[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9561491	0.91[CEU][hapmap];0.83[CHB][hapmap];0.95[JPT][hapmap];0.97[TSI][hapmap];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9584176	0.88[CHB][hapmap];0.84[JPT][hapmap]
rs9589877	0.83[CHB][hapmap]
rs9589878	1.00[CEU][hapmap]
rs9589880	0.91[CEU][hapmap]
rs9589881	0.91[CEU][hapmap]
rs9589882	1.00[CEU][hapmap];0.80[CHB][hapmap]
rs9589883	1.00[CEU][hapmap]
rs9589884	0.81[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	nsv430599	chr13:94699399-94934930	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	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	chr13:94698800-94702800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:94699400-94700200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:94699400-94708600	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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