Variant report

Variant	rs6467666
Chromosome Location	chr7:136168540-136168541
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10237752	0.82[EUR][1000 genomes]
rs10246158	0.82[EUR][1000 genomes]
rs10262287	0.82[EUR][1000 genomes]
rs10277668	0.82[EUR][1000 genomes]
rs10281253	0.82[EUR][1000 genomes]
rs1030338	0.85[EUR][1000 genomes]
rs10480518	0.82[EUR][1000 genomes]
rs1364746	0.82[EUR][1000 genomes]
rs1364747	0.82[EUR][1000 genomes]
rs2350171	0.82[EUR][1000 genomes]
rs34332130	0.82[EUR][1000 genomes]
rs4728400	0.82[EUR][1000 genomes]
rs6949586	0.82[EUR][1000 genomes]
rs73453454	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][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	nsv518439	chr7:136134265-136452082	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	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	chr7:136163600-136169000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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

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