Variant report

Variant	rs35071663
Chromosome Location	chr3:70606311-70606312
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10511000	1.00[ASN][1000 genomes]
rs13066991	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13070884	1.00[ASN][1000 genomes]
rs13094712	1.00[ASN][1000 genomes]
rs1491602	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1565551	1.00[ASN][1000 genomes]
rs35751372	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35807064	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4491862	1.00[ASN][1000 genomes]
rs6549342	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs6786654	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs68093214	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs957343	0.84[AMR][1000 genomes];0.92[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs957344	0.84[AMR][1000 genomes];0.92[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	chr3:70600000-70607200	Weak transcription	Gastric	stomach
2	chr3:70603800-70607200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr3:70605200-70609400	Enhancers	Fetal Heart	heart

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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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