Variant report

Variant	rs1407481
Chromosome Location	chr1:168901413-168901414
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs1014249	0.83[ASN][1000 genomes]
rs10737544	0.85[ASN][1000 genomes]
rs10800396	0.81[ASN][1000 genomes]
rs10919019	0.92[ASN][1000 genomes]
rs12128029	0.84[ASN][1000 genomes]
rs1407478	0.84[ASN][1000 genomes]
rs1407480	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2900884	0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs4656169	0.93[ASN][1000 genomes]
rs4656625	0.84[ASN][1000 genomes]
rs4656626	0.94[ASN][1000 genomes]
rs4656627	0.94[ASN][1000 genomes]
rs4656628	0.94[ASN][1000 genomes]
rs6427161	0.84[ASN][1000 genomes]
rs6692447	0.85[ASN][1000 genomes]
rs67169143	0.84[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	nsv869415	chr1:168467284-169153863	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	44 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	chr1:168896400-168901600	Weak transcription	Fetal Heart	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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