Variant report

Variant	rs72656534
Chromosome Location	chr8:63870205-63870206
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:18)

rs_ID	r²[population]
rs10093652	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10096151	0.81[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs11786957	0.84[EUR][1000 genomes]
rs11995525	0.84[EUR][1000 genomes]
rs16929916	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16929920	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs16929982	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs16930023	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs16930077	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs2736683	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs58909118	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs61056009	0.82[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs61594679	0.85[EUR][1000 genomes]
rs72656522	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72656527	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs72658314	0.88[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs72658324	0.88[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7834288	0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018879	chr8:63281724-63937632	Enhancers Weak transcription Flanking Bivalent TSS/Enh Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
2	nsv1033527	chr8:63673915-64073735	Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
3	nsv890963	chr8:63846472-63885100	Strong transcription Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv890964	chr8:63848556-63898146	Enhancers Bivalent Enhancer Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
5	nsv611447	chr8:63867493-63883593	Weak transcription Strong transcription Enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63859600-63877800	Weak transcription	Cortex derived primary cultured neurospheres	brain
2	chr8:63868600-63895800	Weak transcription	Fetal Brain Female	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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