Variant report

Variant	rs6943727
Chromosome Location	chr7:136396111-136396112
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs10237943	0.90[ASN][1000 genomes]
rs10254377	1.00[ASN][1000 genomes]
rs10257944	1.00[ASN][1000 genomes]
rs10258085	1.00[ASN][1000 genomes]
rs10266414	1.00[ASN][1000 genomes]
rs10279562	0.90[ASN][1000 genomes]
rs1364489	1.00[ASN][1000 genomes]
rs2350451	1.00[ASN][1000 genomes]
rs28736424	1.00[ASN][1000 genomes]
rs62485204	1.00[ASN][1000 genomes]
rs6467684	1.00[ASN][1000 genomes]
rs6950239	1.00[ASN][1000 genomes]
rs6970010	1.00[ASN][1000 genomes]
rs6974097	1.00[ASN][1000 genomes]
rs73727424	0.90[ASN][1000 genomes]
rs7810141	1.00[ASN][1000 genomes]
rs9642057	1.00[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv518439	chr7:136134265-136452082	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:136394000-136396200	Enhancers	Fetal Heart	heart

Quick Search:

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

what's new

Quick links