Variant report

Variant	rs12591658
Chromosome Location	chr15:74139953-74139954
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11632590	0.87[EUR][1000 genomes]
rs11635478	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1452388	0.94[EUR][1000 genomes]
rs1452390	0.98[EUR][1000 genomes]
rs1452391	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2127016	0.87[EUR][1000 genomes]
rs2127017	0.87[EUR][1000 genomes]
rs2415232	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2415233	0.97[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs28493876	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35192808	0.89[EUR][1000 genomes]
rs35809461	0.91[EUR][1000 genomes]
rs55841941	0.91[EUR][1000 genomes]
rs56047016	0.90[EUR][1000 genomes]
rs896591	0.97[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	nsv1043335	chr15:74078689-74241186	Weak transcription Flanking Active TSS Strong transcription Enhancers Bivalent Enhancer Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74132400-74146600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:74134400-74140800	Weak transcription	Fetal Brain Male	brain
3	chr15:74137000-74141600	Weak transcription	Pancreas	Pancrea

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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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