Variant report

Variant	rs3810844
Chromosome Location	chr4:147830499-147830500
allele	C/T
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:13)

rs_ID	r²[population]
rs13104820	0.82[ASW][hapmap];0.83[LWK][hapmap];0.81[MEX][hapmap];0.88[YRI][hapmap];0.81[AFR][1000 genomes]
rs13120245	0.86[MEX][hapmap]
rs13138511	0.90[AFR][1000 genomes];0.89[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs1816596	0.82[ASW][hapmap];0.91[GIH][hapmap];0.83[LWK][hapmap];0.87[MKK][hapmap];0.88[TSI][hapmap];0.88[YRI][hapmap];0.84[AFR][1000 genomes];0.80[EUR][1000 genomes]
rs34431124	0.88[AFR][1000 genomes]
rs34470581	0.95[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs34764961	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs35168292	0.88[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs3827595	0.86[MEX][hapmap]
rs62328057	0.93[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7664149	0.86[MEX][hapmap]
rs984695	0.83[AMR][1000 genomes]
rs984696	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:147830400-147830600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin

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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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