Variant report

Variant	rs73107053
Chromosome Location	chr1:217362174-217362175
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 13 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:11)

rs_ID	r²[population]
rs12070441	1.00[AMR][1000 genomes]
rs73103054	1.00[AMR][1000 genomes]
rs73103072	1.00[AMR][1000 genomes]
rs73103075	1.00[AMR][1000 genomes]
rs73103078	1.00[AMR][1000 genomes]
rs73103086	1.00[AMR][1000 genomes]
rs73103102	1.00[AMR][1000 genomes]
rs73104927	1.00[AMR][1000 genomes]
rs73104933	1.00[AMR][1000 genomes]
rs73104936	1.00[AMR][1000 genomes]
rs73107043	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv549207	chr1:217333272-217455903	Weak transcription Active TSS Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv1003559	chr1:217354095-217418732	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:217360600-217362200	Enhancers	Stomach Smooth Muscle	stomach
2	chr1:217360800-217362200	Enhancers	Colon Smooth Muscle	Colon
3	chr1:217360800-217362200	Enhancers	Fetal Stomach	stomach
4	chr1:217360800-217362400	Enhancers	Fetal Heart	heart
5	chr1:217361200-217362200	Enhancers	Cortex derived primary cultured neurospheres	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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