Variant report

Variant	rs6771866
Chromosome Location	chr3:151424408-151424409
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs17204613	0.84[EUR][1000 genomes]
rs17204620	0.84[EUR][1000 genomes]
rs17283171	0.84[EUR][1000 genomes]
rs62274178	0.82[AMR][1000 genomes]
rs62274180	0.82[AMR][1000 genomes]
rs62274181	1.00[AFR][1000 genomes];0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs62274196	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs62274201	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs62274203	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs62274205	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes]
rs7639000	0.82[EUR][1000 genomes]
rs7653191	0.82[AMR][1000 genomes];0.81[EUR][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv995048	chr3:151114074-151560019	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	12 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	chr3:151424400-151425200	Enhancers	Dnd41	blood

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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