Variant report

Variant	rs34685895
Chromosome Location	chr8:63203304-63203305
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:18)

rs_ID	r²[population]
rs1104845	0.95[AMR][1000 genomes]
rs1104848	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12907101	1.00[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs17819216	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17819222	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17819228	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34146683	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs34247233	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs34755247	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35299498	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35472570	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs35734155	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs35941636	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs36132540	0.90[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7182185	1.00[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs72732242	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs8033157	0.90[AMR][1000 genomes]
rs933997	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1019143	chr8:63142202-63390820	Bivalent/Poised TSS Weak transcription Flanking Active TSS Bivalent Enhancer Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	esv2757277	chr8:63156123-63260182	Active TSS Flanking Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
3	esv2759621	chr8:63156123-63260182	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Weak transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	2 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	chr8:63191000-63209200	Weak transcription	Cortex derived primary cultured neurospheres	brain

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Input of quick search could be:

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

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