Variant report

Variant	rs7673408
Chromosome Location	chr4:127990303-127990304
allele	C/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]
rs13141365	0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs13142099	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1397431	1.00[ASN][1000 genomes]
rs28373335	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs340439	0.90[ASN][1000 genomes]
rs340440	0.84[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs340441	1.00[ASN][1000 genomes]
rs340446	1.00[ASN][1000 genomes]
rs340449	1.00[ASN][1000 genomes]
rs34660635	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62333854	0.84[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs6825686	1.00[JPT][hapmap]
rs6840035	0.85[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7662706	1.00[JPT][hapmap]
rs7670859	0.82[AMR][1000 genomes];0.83[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7700208	1.00[ASN][1000 genomes]
rs965298	1.00[JPT][hapmap];1.00[YRI][hapmap]

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	nsv830055	chr4:127794875-127993821	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:127989200-127991600	Enhancers	H1 Cell Line	embryonic stem cell
2	chr4:127989800-127991000	Enhancers	Cortex derived primary cultured neurospheres	brain
3	chr4:127990000-127991400	Enhancers	HUES64 Cell Line	embryonic stem cell

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