Variant report

Variant	rs72706786
Chromosome Location	chr1:179671703-179671704
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10798697	0.83[ASN][1000 genomes]
rs10913830	0.83[ASN][1000 genomes]
rs11805051	0.83[ASN][1000 genomes]
rs12032339	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12047528	0.87[ASN][1000 genomes]
rs12565489	0.88[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs4133262	0.87[ASN][1000 genomes]
rs72706715	0.83[ASN][1000 genomes]
rs72706717	0.83[ASN][1000 genomes]
rs72706762	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72706766	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8179491	1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:179669800-179672200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr1:179670000-179674200	Enhancers	Stomach Mucosa	stomach
3	chr1:179671200-179672200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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