Variant report

Variant	rs36046455
Chromosome Location	chr10:55463891-55463892
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 72 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:48)

rs_ID	r²[population]
rs11003685	0.80[EUR][1000 genomes]
rs11003692	0.81[EUR][1000 genomes]
rs11003693	0.80[EUR][1000 genomes]
rs11003695	0.82[EUR][1000 genomes]
rs11003696	0.84[EUR][1000 genomes]
rs11003697	0.83[EUR][1000 genomes]
rs11003699	0.84[EUR][1000 genomes]
rs11003701	0.83[EUR][1000 genomes]
rs11003702	0.83[EUR][1000 genomes]
rs11003704	0.82[EUR][1000 genomes]
rs11003706	0.80[EUR][1000 genomes]
rs11003714	0.81[EUR][1000 genomes]
rs11003715	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11003723	0.87[EUR][1000 genomes]
rs11003725	0.84[EUR][1000 genomes]
rs11003768	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11003769	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs11003781	0.99[EUR][1000 genomes]
rs11492404	0.82[EUR][1000 genomes]
rs12355362	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12769841	0.80[EUR][1000 genomes]
rs12772474	0.82[EUR][1000 genomes]
rs1489832	0.82[EUR][1000 genomes]
rs16937596	0.82[EUR][1000 genomes]
rs16937607	0.84[EUR][1000 genomes]
rs16937609	0.83[EUR][1000 genomes]
rs17343	0.83[EUR][1000 genomes]
rs17344	0.82[EUR][1000 genomes]
rs17345	0.81[EUR][1000 genomes]
rs17346	0.84[EUR][1000 genomes]
rs17696599	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs34684767	0.81[EUR][1000 genomes]
rs351853	0.82[EUR][1000 genomes]
rs35895688	0.82[EUR][1000 genomes]
rs35957518	0.87[EUR][1000 genomes]
rs370415	0.80[EUR][1000 genomes]
rs386402	0.80[EUR][1000 genomes]
rs56282513	0.82[EUR][1000 genomes]
rs61859175	0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7083485	0.83[EUR][1000 genomes]
rs7092924	0.83[EUR][1000 genomes]
rs7093101	0.83[EUR][1000 genomes]
rs7098115	0.84[EUR][1000 genomes]
rs7098708	0.83[EUR][1000 genomes]
rs767605	0.84[EUR][1000 genomes]
rs7898956	0.83[EUR][1000 genomes]
rs7900645	0.82[EUR][1000 genomes]
rs9733895	0.82[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:24 , 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	nsv1044282	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv540631	chr10:55186501-55516392	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv1043501	chr10:55186701-55516253	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv540632	chr10:55186701-55516253	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv1050323	chr10:55190079-55546575	Weak transcription ZNF genes & repeats Enhancers Active TSS Strong transcription Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
7	esv2757386	chr10:55357136-55531037	Enhancers Weak transcription Strong transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	esv2759753	chr10:55357136-55586930	Enhancers Flanking Active TSS Active TSS Weak transcription ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	esv2758220	chr10:55360612-55586930	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv1847684	chr10:55371601-55638740	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	esv1842975	chr10:55378668-55736655	ZNF genes & repeats Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1043179	chr10:55379719-55463942	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
13	esv34353	chr10:55383168-55479314	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
14	nsv895410	chr10:55385962-55577022	Active TSS Enhancers ZNF genes & repeats Flanking Active TSS Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
15	esv2755263	chr10:55394094-55546994	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv895415	chr10:55395380-55473976	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
17	nsv895416	chr10:55395380-55539954	Enhancers Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv895420	chr10:55408854-55473976	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	Chromatin interactive region	n/a	inside rSNPs	diseases
19	nsv895421	chr10:55408854-55539954	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
20	nsv428556	chr10:55413202-55586930	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
21	nsv895424	chr10:55423964-55473976	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv895425	chr10:55423964-55539954	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
23	esv1815412	chr10:55446058-55522899	ZNF genes & repeats Enhancers Weak transcription Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
24	esv1824167	chr10:55454152-55522899	Weak transcription Active TSS Enhancers ZNF genes & repeats	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:55463400-55468000	Weak transcription	Fetal Heart	heart

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