Variant report

Variant	rs7350653
Chromosome Location	chr13:69301250-69301251
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs287380	0.86[EUR][1000 genomes]
rs287382	0.86[EUR][1000 genomes]
rs73206158	0.88[AMR][1000 genomes]
rs73206165	0.88[AMR][1000 genomes]
rs73206166	0.88[AMR][1000 genomes]
rs73206168	0.88[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs73206169	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73206170	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73206171	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73206174	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73206176	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73206182	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73206183	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73206188	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206191	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206192	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206193	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206194	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206195	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206196	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73206197	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs73206198	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs73206199	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206200	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73206201	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73207803	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73207804	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73207805	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73207807	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9317720	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9317721	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9317722	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9529406	0.88[AMR][1000 genomes]
rs9529407	0.88[AMR][1000 genomes]
rs9529411	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9529412	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9529413	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9529414	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9529419	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs9529420	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9529421	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9529422	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9529423	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9529424	0.93[EUR][1000 genomes]
rs9541483	0.82[EUR][1000 genomes]
rs9541496	0.88[AMR][1000 genomes]
rs9541497	0.88[AMR][1000 genomes]
rs9541498	0.88[AMR][1000 genomes]
rs9541499	0.88[AMR][1000 genomes]
rs9541500	0.83[AMR][1000 genomes]
rs9541501	0.88[AMR][1000 genomes]
rs9541502	0.88[AMR][1000 genomes]
rs9541503	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9541504	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9541505	1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs9541506	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9541507	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9541508	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9541509	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9541510	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9541511	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs9541513	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9541514	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9541515	0.88[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9541522	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9541525	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9541526	0.93[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9541527	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv900442	chr13:69223307-69387266	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv900444	chr13:69233599-69380036	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
3	nsv1049303	chr13:69238676-69923558	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv900446	chr13:69240180-69328753	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv562163	chr13:69240945-69302618	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv900450	chr13:69249927-69361505	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv1038918	chr13:69251052-69919763	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv541829	chr13:69251052-69919763	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv900451	chr13:69290386-69387266	Weak transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv3357726	chr13:69297551-69302049	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69289400-69301400	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr13:69297400-69301400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
3	chr13:69301200-69301600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr13:69301200-69301800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived

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