Variant report

Variant	rs6694126
Chromosome Location	chr1:220693001-220693002
allele	C/T
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]
rs12065752	0.87[AMR][1000 genomes]
rs17007868	1.00[ASW][hapmap];1.00[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs17007991	1.00[MEX][hapmap]
rs17041786	1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs56911985	1.00[AMR][1000 genomes]
rs73101823	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7514351	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7537531	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:220691000-220695000	Weak transcription	NHEK	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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