Variant report

Variant	rs66831722
Chromosome Location	chr3:25148054-25148055
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs1587426	0.89[ASN][1000 genomes]
rs1603983	0.85[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs1603984	0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1603985	1.00[ASN][1000 genomes]
rs1603986	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs34850898	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs4858705	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6550949	0.93[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6550950	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6763490	0.82[EUR][1000 genomes]
rs6778399	0.82[EUR][1000 genomes]
rs7622091	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs9826164	0.86[ASN][1000 genomes]
rs9877729	0.82[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:25147600-25152200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr3:25147800-25157600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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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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