Variant report

Variant	rs12065974
Chromosome Location	chr1:217130042-217130043
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]
rs12079985	1.00[YRI][hapmap];0.85[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12094687	1.00[TSI][hapmap];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58515283	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs58711391	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs59057619	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6604650	1.00[YRI][hapmap];0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73099410	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73099418	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73099452	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73099455	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs73099466	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217122400-217146200	Weak transcription	Pancreas	Pancrea
2	chr1:217125200-217135400	Weak transcription	Fetal Heart	heart
3	chr1:217127000-217130200	Weak transcription	HUES64 Cell Line	embryonic stem cell

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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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