Variant report

Variant	rs17691869
Chromosome Location	chr3:179631621-179631622
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10049363	0.95[YRI][hapmap]
rs12171276	0.93[CEU][hapmap];0.82[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12487519	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs12488582	0.94[EUR][1000 genomes]
rs13083814	0.87[EUR][1000 genomes]
rs13085715	0.94[EUR][1000 genomes]
rs13091962	0.95[EUR][1000 genomes]
rs13097749	0.93[EUR][1000 genomes]
rs13325663	0.94[YRI][hapmap];0.84[AFR][1000 genomes]
rs1404272	0.87[CEU][hapmap]
rs16830886	0.84[AFR][1000 genomes]
rs17691629	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs17692126	0.86[CEU][hapmap]
rs28651290	0.97[EUR][1000 genomes]
rs34446871	1.00[CEU][hapmap];0.97[EUR][1000 genomes]
rs34849178	0.90[EUR][1000 genomes]
rs62291649	1.00[EUR][1000 genomes]
rs67980618	0.92[EUR][1000 genomes]
rs9822592	1.00[CEU][hapmap];0.89[YRI][hapmap];0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv829807	chr3:179527567-179745153	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv829808	chr3:179574614-179754321	Strong transcription Bivalent/Poised TSS Enhancers Weak transcription Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:179624800-179639000	Weak transcription	Brain Substantia Nigra	brain
2	chr3:179627400-179632000	Weak transcription	Dnd41	blood
3	chr3:179629200-179631800	Weak transcription	Brain Hippocampus Middle	brain
4	chr3:179630000-179638800	Weak transcription	Brain Angular Gyrus	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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