Variant report

Variant	rs60730935
Chromosome Location	chr10:55139678-55139679
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 77 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:62)

rs_ID	r²[population]
rs10508994	0.80[EUR][1000 genomes]
rs10508995	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11003591	0.80[EUR][1000 genomes]
rs11003592	0.80[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs11003593	0.80[EUR][1000 genomes]
rs11003594	0.92[ASN][1000 genomes]
rs11003595	0.91[ASN][1000 genomes]
rs12251771	0.80[EUR][1000 genomes]
rs12266888	0.80[EUR][1000 genomes]
rs12266915	0.80[EUR][1000 genomes]
rs12411918	0.89[EUR][1000 genomes]
rs12412145	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12414765	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs12415081	0.82[EUR][1000 genomes]
rs12416448	0.82[EUR][1000 genomes]
rs12571480	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12572525	0.82[EUR][1000 genomes]
rs1909407	0.91[ASN][1000 genomes]
rs1909408	0.91[ASN][1000 genomes]
rs1909410	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1909412	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1909413	0.82[AMR][1000 genomes];0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1909414	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1909415	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1909416	0.94[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1909425	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2133469	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2133470	0.85[AFR][1000 genomes];0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2173518	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2173519	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2173520	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2173521	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2384239	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2384240	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2384241	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2384246	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs28891704	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs35133620	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4307632	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4468253	0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4614347	0.84[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4935427	0.91[ASN][1000 genomes]
rs4935430	0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4935431	0.80[ASN][1000 genomes]
rs4935432	0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4935433	0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4935434	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4935435	0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs5004996	0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs60091591	0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs61284846	0.83[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs74134539	0.80[EUR][1000 genomes]
rs74134545	0.91[ASN][1000 genomes]
rs74134546	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs74134547	0.83[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs74134548	0.81[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs74134554	0.85[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs74134556	0.90[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs74134558	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs74134567	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs74134571	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs74134573	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2752952	chr10:54900994-55497594	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1041908	chr10:55003164-55283251	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv540629	chr10:55003164-55283251	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1040943	chr10:55040577-55279797	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv540630	chr10:55040577-55279797	Weak transcription ZNF genes & repeats Flanking Active TSS Enhancers Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
6	nsv1037480	chr10:55102814-55289571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	esv3504729	chr10:55117683-55140591	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
8	esv3504840	chr10:55117689-55140609	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
9	esv3504618	chr10:55117750-55140559	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3504951	chr10:55117750-55140559	Enhancers ZNF genes & repeats Weak transcription Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	nsv8664	chr10:55118472-55141090	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
12	nsv1038412	chr10:55119013-55142163	ZNF genes & repeats Enhancers Weak transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	nsv442183	chr10:55119045-55142101	ZNF genes & repeats Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv514559	chr10:55119330-55140490	Weak transcription Enhancers ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
15	nsv524194	chr10:55137321-55146357	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55130800-55141400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr10:55139600-55140200	Enhancers	Fetal Intestine Small	intestine

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