Variant report

Variant	rs56930105
Chromosome Location	chr2:10982487-10982488
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 4 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:4)

rs_ID	r²[population]
rs55719303	0.81[ASN][1000 genomes]
rs59164865	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs62120278	0.80[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73174567	0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:10979400-11000400	Weak transcription	Fetal Brain Male	brain
2	chr2:10981400-10982800	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
3	chr2:10981600-10982800	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:10981800-10983600	Enhancers	Skeletal Muscle Male	skeletal muscle
5	chr2:10982000-10983600	Enhancers	Skeletal Muscle Female	skeletal muscle
6	chr2:10982200-10982800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin

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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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