Variant report

Variant	rs72972233
Chromosome Location	chr3:133396205-133396206
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]
rs55736717	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs55935735	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56047244	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs58689485	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs59755236	0.87[AFR][1000 genomes]
rs59787433	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7629360	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7639533	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:133393800-133406800	Weak transcription	Brain Substantia Nigra	brain
2	chr3:133394000-133399600	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr3:133395400-133396400	Enhancers	Liver	Liver
4	chr3:133396200-133398800	Weak transcription	HepG2	liver

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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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