Variant report

Variant	rs1254531
Chromosome Location	chr10:44579062-44579063
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]
rs11238840	1.00[ASN][1000 genomes]
rs1254530	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs182075	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs182076	0.86[ASN][1000 genomes]
rs187900	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs187901	0.86[ASN][1000 genomes]
rs1938557	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs268312	0.86[ASN][1000 genomes]
rs268313	0.86[ASN][1000 genomes]
rs268319	0.86[ASN][1000 genomes]
rs268321	0.84[ASN][1000 genomes]
rs268322	0.84[ASN][1000 genomes]
rs931225	0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:44576600-44579800	Enhancers	Pancreas	Pancrea
2	chr10:44579000-44580200	Enhancers	Fetal Heart	heart
3	chr10:44579000-44582000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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