Variant report

Variant	rs11119225
Chromosome Location	chr1:209297240-209297241
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 8 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs1174557	1.00[ASN][1000 genomes]
rs1174558	1.00[ASN][1000 genomes]
rs1174561	1.00[ASN][1000 genomes]
rs12090339	0.82[AFR][1000 genomes]
rs12090478	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59793111	1.00[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs6661599	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74157851	0.82[AFR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:209297000-209297400	Active TSS	Spleen	Spleen
2	chr1:209297000-209306200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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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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