Variant report

Variant	rs35507685
Chromosome Location	chr1:159193128-159193129
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 15 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs11265145	0.86[AFR][1000 genomes]
rs11265146	0.80[AFR][1000 genomes]
rs11265147	0.90[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11265148	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11265151	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs11265153	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12067678	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs12068651	0.85[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs16841937	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs3027047	0.83[AFR][1000 genomes]
rs3027050	0.83[AFR][1000 genomes]
rs3027057	0.86[AFR][1000 genomes]
rs34152791	1.00[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs56113018	0.86[AFR][1000 genomes];0.85[AMR][1000 genomes]
rs59437380	0.81[AFR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:159190400-159193400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr1:159193000-159199200	Weak transcription	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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