Variant report

Variant	rs35120085
Chromosome Location	chr19:44540102-44540103
allele	-/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:44537819..44540662-chr19:44542616..44544259,2	K562	blood:
2	chr19:44535729..44539292-chr19:44539752..44542558,4	K562	blood:

Extended variants
information (count: 39 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:37)

rs_ID	r²[population]
rs11083735	0.81[ASN][1000 genomes]
rs11083736	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs11083737	0.83[ASN][1000 genomes]
rs11666432	0.81[ASN][1000 genomes]
rs12610472	0.83[ASN][1000 genomes]
rs1474061	0.81[ASN][1000 genomes]
rs1996409	0.81[ASN][1000 genomes]
rs2138823	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2138824	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2176431	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs3826941	0.83[ASN][1000 genomes]
rs4239528	0.83[ASN][1000 genomes]
rs4299256	0.81[ASN][1000 genomes]
rs4371266	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4375771	0.83[ASN][1000 genomes]
rs4444434	0.83[ASN][1000 genomes]
rs4550576	0.81[ASN][1000 genomes]
rs4555257	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4580302	0.81[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs4803668	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs4803672	0.84[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs55798868	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs56003307	0.85[ASN][1000 genomes]
rs56230322	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs56250154	0.80[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs57895932	0.81[ASN][1000 genomes]
rs62119177	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs6509135	0.84[ASN][1000 genomes]
rs6509137	0.83[ASN][1000 genomes]
rs7251015	0.81[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs7252213	0.81[ASN][1000 genomes]
rs7255192	0.84[ASN][1000 genomes]
rs8105003	0.81[ASN][1000 genomes]
rs8109313	0.83[ASN][1000 genomes]
rs8109615	0.84[ASN][1000 genomes]
rs8110348	0.81[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs9646633	0.81[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	nsv469650	chr19:44405994-44555426	Active TSS Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
2	nsv833840	chr19:44520620-44715760	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 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	chr19:44530800-44542600	ZNF genes & repeats	Liver	Liver
2	chr19:44536800-44540400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr19:44537000-44540200	Weak transcription	Placenta Amnion	Placenta Amnion

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