Variant report

Variant	rs10874405
Chromosome Location	chr1:84128045-84128046
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs10782814	0.84[ASN][1000 genomes]
rs10782815	0.92[ASN][1000 genomes]
rs10874404	0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11590582	0.97[ASN][1000 genomes]
rs11590583	0.97[ASN][1000 genomes]
rs12409454	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4379690	0.97[ASN][1000 genomes]
rs4415589	0.97[ASN][1000 genomes]
rs4548461	0.97[ASN][1000 genomes]
rs61790671	0.83[AFR][1000 genomes];0.97[AMR][1000 genomes];0.96[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs7417359	0.93[AMR][1000 genomes];0.84[EUR][1000 genomes];0.97[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:84122800-84131800	Weak transcription	Pancreas	Pancrea
2	chr1:84126400-84132000	Weak transcription	H9 Derived Neuron 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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