Variant report

Variant	rs10170488
Chromosome Location	chr2:53729659-53729660
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 52 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10165742	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10167973	0.89[ASN][1000 genomes]
rs10183446	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10183776	0.92[ASN][1000 genomes]
rs10191277	0.80[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10194030	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10194206	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10204173	0.89[ASN][1000 genomes]
rs10204330	0.91[ASN][1000 genomes]
rs10204468	0.91[ASN][1000 genomes]
rs10204470	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.85[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10206558	0.88[ASN][1000 genomes]
rs12472781	0.89[ASN][1000 genomes]
rs13394011	0.87[ASN][1000 genomes]
rs13394197	0.84[ASN][1000 genomes]
rs13394939	0.89[ASN][1000 genomes]
rs13416219	0.92[ASN][1000 genomes]
rs13420695	0.89[ASN][1000 genomes]
rs13427989	0.88[ASN][1000 genomes]
rs13429824	0.92[ASN][1000 genomes]
rs1472238	0.95[ASN][1000 genomes]
rs1565796	0.90[ASN][1000 genomes]
rs17189463	0.88[ASN][1000 genomes]
rs17268033	0.91[ASN][1000 genomes]
rs4671411	0.88[ASN][1000 genomes]
rs4672452	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4672453	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4672456	0.92[ASN][1000 genomes]
rs4672461	0.82[ASN][1000 genomes]
rs6545352	0.86[ASN][1000 genomes]
rs6742054	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6743847	0.88[ASN][1000 genomes]
rs72618655	0.88[ASN][1000 genomes]
rs7559727	0.92[ASN][1000 genomes]
rs7571640	0.93[ASN][1000 genomes]
rs7586356	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7586411	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7586468	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7586738	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7599710	0.88[ASN][1000 genomes]
rs7604056	0.88[ASN][1000 genomes]
rs7607091	0.80[ASN][1000 genomes]
rs961241	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1002145	chr2:53387912-53832213	Enhancers Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv535718	chr2:53387912-53832213	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	nsv997401	chr2:53515629-53863347	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv999571	chr2:53690538-53775723	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv1012754	chr2:53690538-53785037	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv457873	chr2:53701324-53785037	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv582009	chr2:53701324-53785037	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
8	nsv457886	chr2:53722595-53835083	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv582010	chr2:53722595-53835083	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:53718200-53737600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr2:53726400-53731400	Weak transcription	Hela-S3	cervix
3	chr2:53726400-53737000	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr2:53727400-53730800	Weak transcription	Lung	lung
5	chr2:53727600-53732800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:53728800-53732800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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