Variant report

Variant	rs36190401
Chromosome Location	chr4:81312161-81312162
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 16 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs12648594	0.86[ASN][1000 genomes]
rs12650756	0.80[EUR][1000 genomes]
rs13111397	0.82[EUR][1000 genomes]
rs13115510	0.82[EUR][1000 genomes]
rs13124220	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13129636	0.82[EUR][1000 genomes]
rs13146627	0.82[EUR][1000 genomes]
rs1495484	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs17004908	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs34636382	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs34890603	0.82[EUR][1000 genomes]
rs35565546	0.82[EUR][1000 genomes]
rs36027051	0.85[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs6820209	0.87[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7672761	0.85[EUR][1000 genomes]
rs7684929	0.85[AMR][1000 genomes];0.84[EUR][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:81308200-81314800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
2	chr4:81308600-81314600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr4:81311200-81314000	Weak transcription	Osteobl	bone

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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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