Variant report

Variant	rs1837295
Chromosome Location	chr13:80568672-80568673
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 30 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs10507901	0.81[ASN][1000 genomes]
rs12585712	0.85[ASN][1000 genomes]
rs1853995	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2196781	0.97[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2329144	0.87[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs2329147	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs35409297	0.99[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs3843950	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs3850060	0.90[AFR][1000 genomes];0.83[EUR][1000 genomes]
rs3861146	0.94[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3966634	0.82[ASN][1000 genomes]
rs4290373	0.91[AFR][1000 genomes];0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4306392	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4885687	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs4885688	0.89[AMR][1000 genomes];0.86[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs66994466	0.93[ASN][1000 genomes]
rs7317135	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs7333430	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs9531007	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9531009	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9545275	0.89[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9545281	0.95[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9545290	0.99[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs9545292	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9545295	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9574522	0.89[AFR][1000 genomes];0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832658	chr13:80486980-80680221	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv562417	chr13:80489814-80618915	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv900591	chr13:80512487-80613204	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv900592	chr13:80512487-80715893	Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:80561400-80569000	Weak transcription	HSMM	muscle
2	chr13:80563800-80569000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr13:80563800-80569000	Weak transcription	HSMMtube	muscle
4	chr13:80563800-80569200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
5	chr13:80564000-80569000	Weak transcription	NH-A	brain
6	chr13:80564200-80569000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr13:80564600-80569200	Weak transcription	NHLF	lung
8	chr13:80564800-80569000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr13:80564800-80569000	Weak transcription	HMEC	breast
10	chr13:80564800-80569200	Weak transcription	NHEK	skin
11	chr13:80565000-80569000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr13:80565000-80569000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr13:80565000-80569200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr13:80565000-80569200	Weak transcription	Osteobl	bone
15	chr13:80565200-80569000	Weak transcription	Hela-S3	cervix
16	chr13:80565200-80569200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr13:80565400-80569000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr13:80568000-80571800	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr13:80568400-80570200	Enhancers	NHDF-Ad	bronchial
20	chr13:80568400-80571600	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr13:80568600-80569400	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr13:80568600-80569400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr13:80568600-80569800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
24	chr13:80568600-80570200	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr13:80568600-80570200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr13:80568600-80570600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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