Variant report

Variant	rs17009642
Chromosome Location	chr1:221389865-221389866
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10489957	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11802047	0.85[EUR][1000 genomes]
rs12408324	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1592083	0.80[EUR][1000 genomes]
rs17009643	0.89[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17009664	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35316503	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs35768495	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4846689	0.90[ASN][1000 genomes]
rs4846693	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4846695	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4846696	0.84[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs4846697	0.86[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs4846699	0.80[EUR][1000 genomes]
rs4846700	0.85[EUR][1000 genomes]
rs56704721	0.85[EUR][1000 genomes]
rs59293137	0.87[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs59638807	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6700159	0.80[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv997685	chr1:220993527-221863416	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv535299	chr1:220993527-221863416	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
3	nsv873199	chr1:221136672-221451217	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:221379800-221390200	Weak transcription	Psoas Muscle	Psoas
2	chr1:221389400-221390400	Enhancers	Primary B cells from cord blood	blood
3	chr1:221389800-221390600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:221389800-221391200	Enhancers	Primary B cells from peripheral blood	blood

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