Variant report

Variant	rs73413321
Chromosome Location	chr7:106671173-106671174
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]
rs12113322	0.87[ASN][1000 genomes]
rs17153745	0.87[ASN][1000 genomes]
rs56132452	0.99[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56266717	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60714435	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73413319	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73413323	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73413330	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73413336	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73413342	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7798500	0.87[ASN][1000 genomes]

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:106669800-106672400	Weak transcription	Adipose Nuclei	Adipose
2	chr7:106670200-106671400	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr7:106670200-106671400	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr7:106670200-106676800	Weak transcription	Fetal Brain Male	brain
5	chr7:106670400-106672200	Enhancers	K562	blood
6	chr7:106670800-106674000	Weak transcription	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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