Variant report

Variant	rs61952268
Chromosome Location	chr13:65254881-65254882
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:68)

rs_ID	r²[population]
rs10507715	0.93[EUR][1000 genomes]
rs1158557	0.82[EUR][1000 genomes]
rs11839758	0.93[EUR][1000 genomes]
rs11840161	0.93[EUR][1000 genomes]
rs11842717	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12586097	0.92[EUR][1000 genomes]
rs1390517	0.91[EUR][1000 genomes]
rs1496147	0.92[EUR][1000 genomes]
rs1496148	0.92[EUR][1000 genomes]
rs17089984	0.93[EUR][1000 genomes]
rs17090038	0.93[EUR][1000 genomes]
rs17090280	0.91[EUR][1000 genomes]
rs1826792	0.90[EUR][1000 genomes]
rs2006947	0.93[EUR][1000 genomes]
rs2050560	0.93[EUR][1000 genomes]
rs2132464	0.89[EUR][1000 genomes]
rs2324721	0.93[EUR][1000 genomes]
rs2875418	0.93[EUR][1000 genomes]
rs4144393	0.90[EUR][1000 genomes]
rs4144394	0.90[EUR][1000 genomes]
rs4433690	0.92[EUR][1000 genomes]
rs61950065	0.93[EUR][1000 genomes]
rs61950066	0.93[EUR][1000 genomes]
rs61950067	0.93[EUR][1000 genomes]
rs61950093	0.89[EUR][1000 genomes]
rs61950094	0.90[EUR][1000 genomes]
rs61952265	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs61952266	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6562367	0.95[EUR][1000 genomes]
rs6562370	0.91[EUR][1000 genomes]
rs7320529	0.92[EUR][1000 genomes]
rs7322177	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7322256	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7324521	0.83[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7330428	0.91[EUR][1000 genomes]
rs7334582	0.93[EUR][1000 genomes]
rs74090037	0.90[EUR][1000 genomes]
rs74090042	0.93[EUR][1000 genomes]
rs7983133	0.89[EUR][1000 genomes]
rs7992247	0.93[EUR][1000 genomes]
rs7993657	0.93[EUR][1000 genomes]
rs7994548	0.90[EUR][1000 genomes]
rs7994586	0.89[EUR][1000 genomes]
rs7995538	0.89[EUR][1000 genomes]
rs8001295	0.89[EUR][1000 genomes]
rs903807	0.90[EUR][1000 genomes]
rs9285251	0.93[EUR][1000 genomes]
rs9317441	0.93[EUR][1000 genomes]
rs9564185	0.91[EUR][1000 genomes]
rs9564186	0.91[EUR][1000 genomes]
rs9564189	0.86[EUR][1000 genomes]
rs9564190	0.91[EUR][1000 genomes]
rs9564191	0.90[EUR][1000 genomes]
rs9571256	0.91[EUR][1000 genomes]
rs9571257	0.89[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs9571258	0.93[EUR][1000 genomes]
rs9571259	0.92[EUR][1000 genomes]
rs9571260	0.91[EUR][1000 genomes]
rs9571265	0.91[EUR][1000 genomes]
rs9571266	0.92[EUR][1000 genomes]
rs9571267	0.92[EUR][1000 genomes]
rs9571268	0.90[EUR][1000 genomes]
rs9571269	0.91[EUR][1000 genomes]
rs9571270	0.91[EUR][1000 genomes]
rs9571271	0.91[EUR][1000 genomes]
rs9571272	0.89[EUR][1000 genomes]
rs9571273	0.91[EUR][1000 genomes]
rs9571275	0.90[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv455914	chr13:64432922-65368490	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv561965	chr13:64432922-65368490	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv3367739	chr13:64805577-65549276	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv900359	chr13:65182365-65321033	ZNF genes & repeats Enhancers Weak transcription Active TSS Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
5	nsv561969	chr13:65215262-65297794	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
6	nsv1038150	chr13:65224379-65354892	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS	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	chr13:65250000-65263000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr13:65250400-65262800	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr13:65250400-65263200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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