Variant report

Variant	rs12955529
Chromosome Location	chr18:44935775-44935776
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:16)

rs_ID	r²[population]
rs10083906	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10853551	0.89[ASN][1000 genomes]
rs10853552	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11082578	0.88[ASN][1000 genomes]
rs11082579	0.88[ASN][1000 genomes]
rs11082583	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11875780	0.96[ASN][1000 genomes]
rs12956050	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1865370	0.89[AFR][1000 genomes];0.98[ASN][1000 genomes]
rs34885067	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4407146	0.88[ASN][1000 genomes]
rs7230517	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7230554	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]
rs7231544	0.81[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs7231597	0.99[ASN][1000 genomes]
rs8088348	0.81[AMR][1000 genomes];0.99[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv833641	chr18:44815063-45020202	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region lncRNA miRNA	2 gene(s)	inside rSNPs	diseases
2	esv1801141	chr18:44908270-44955409	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44932000-44935800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr18:44935200-44936200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr18:44935400-44936000	Enhancers	H9 Cell Line	embryonic stem cell
4	chr18:44935400-44936000	Weak transcription	ES-UCSF4 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