Variant report

Variant	rs12000720
Chromosome Location	chr9:104044194-104044195
allele	G/T
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]
rs10115417	1.00[ASN][1000 genomes]
rs10116399	1.00[YRI][hapmap];0.95[AFR][1000 genomes]
rs10122456	1.00[YRI][hapmap];0.90[AFR][1000 genomes]
rs10122687	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10124833	0.91[AFR][1000 genomes]
rs12000705	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12343249	0.83[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12347679	1.00[ASN][1000 genomes]
rs1329072	1.00[ASN][1000 genomes]
rs28490420	0.83[EUR][1000 genomes]
rs7037136	1.00[ASN][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:104038200-104054000	Weak transcription	Fetal Brain Male	brain
2	chr9:104039200-104050000	Weak transcription	HepG2	liver
3	chr9:104041400-104053000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr9:104043400-104053400	Weak transcription	Brain Cingulate Gyrus	brain

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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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