Variant report

Variant	rs73316421
Chromosome Location	chr14:78911222-78911223
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:49)

rs_ID	r²[population]
rs17107366	1.00[EUR][1000 genomes]
rs17107393	1.00[EUR][1000 genomes]
rs17107411	1.00[EUR][1000 genomes]
rs17107437	1.00[EUR][1000 genomes]
rs17107516	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17107519	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17107523	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17107530	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17107594	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17107611	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2215834	1.00[EUR][1000 genomes]
rs2366154	1.00[EUR][1000 genomes]
rs3891717	1.00[EUR][1000 genomes]
rs4384537	1.00[EUR][1000 genomes]
rs4520775	1.00[EUR][1000 genomes]
rs56923572	1.00[AMR][1000 genomes]
rs58330928	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59762056	1.00[AMR][1000 genomes]
rs59819728	1.00[AMR][1000 genomes]
rs61052532	1.00[AMR][1000 genomes]
rs6574436	1.00[EUR][1000 genomes]
rs7146066	1.00[EUR][1000 genomes]
rs7148862	1.00[EUR][1000 genomes]
rs7149532	1.00[EUR][1000 genomes]
rs7149679	1.00[EUR][1000 genomes]
rs719055	1.00[EUR][1000 genomes]
rs73316040	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316042	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316045	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73316436	1.00[AMR][1000 genomes]
rs73316456	1.00[AMR][1000 genomes]
rs73316459	1.00[AMR][1000 genomes]
rs73316471	1.00[AMR][1000 genomes]
rs73316478	1.00[AMR][1000 genomes]
rs73320490	1.00[AMR][1000 genomes]
rs73320491	1.00[AMR][1000 genomes]
rs73324490	1.00[AMR][1000 genomes]
rs73327172	1.00[EUR][1000 genomes]
rs73327195	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73327200	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73329110	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73329120	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73329172	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7492592	1.00[EUR][1000 genomes]
rs759230	1.00[EUR][1000 genomes]
rs887892	1.00[EUR][1000 genomes]
rs887893	1.00[EUR][1000 genomes]
rs887894	1.00[EUR][1000 genomes]
rs887895	1.00[EUR][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	nsv832837	chr14:78766805-78946526	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
2	esv2757577	chr14:78875607-78912967	Weak transcription Enhancers ZNF genes & repeats Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	n/a
3	esv2760000	chr14:78875607-79173528	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	esv2758363	chr14:78903610-79173528	Enhancers Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:78894400-78914600	Weak transcription	GM12878-XiMat	blood
2	chr14:78907200-78928200	Weak transcription	Brain Germinal Matrix	brain

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