Variant report

Variant	rs4899847
Chromosome Location	chr14:84621025-84621026
allele	A/C
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]
rs10135627	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs12100815	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12100819	0.83[ASN][1000 genomes]
rs1381621	0.81[ASN][1000 genomes]
rs1462343	0.81[ASN][1000 genomes]
rs1564057	0.81[ASN][1000 genomes]
rs1564058	0.82[ASN][1000 genomes]
rs1676055	0.83[ASN][1000 genomes]
rs2249653	0.83[ASN][1000 genomes]
rs4899846	0.87[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4904160	0.83[ASN][1000 genomes]
rs4904161	0.83[ASN][1000 genomes]
rs4904165	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6574774	0.83[ASN][1000 genomes]
rs6574775	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7160548	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[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	nsv565376	chr14:84612088-84644822	Enhancers Weak transcription	TF binding region lncRNA	3 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	chr14:84620400-84621400	Weak transcription	Fetal Heart	heart

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

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