Variant report

Variant	rs1794688
Chromosome Location	chr6:33465595-33465596
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:33463213..33467360-chr6:33468926..33472563,4	K562	blood:
2	chr6:33463213..33466886-chr6:33468926..33471484,3	K562	blood:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs1536042	1.00[ASN][1000 genomes]
rs16869178	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1705000	1.00[ASN][1000 genomes]
rs17221716	1.00[ASN][1000 genomes]
rs1755041	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1755042	1.00[ASN][1000 genomes]
rs1755054	1.00[ASN][1000 genomes]
rs1794686	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2068236	1.00[ASN][1000 genomes]
rs2147655	1.00[ASN][1000 genomes]
rs2395451	1.00[ASN][1000 genomes]
rs35433260	1.00[ASN][1000 genomes]
rs4711333	1.00[ASN][1000 genomes]
rs4711334	1.00[ASN][1000 genomes]
rs4713647	1.00[ASN][1000 genomes]
rs4713652	1.00[ASN][1000 genomes]
rs472990	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs480568	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs485623	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs535584	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs542056	1.00[ASN][1000 genomes]
rs542725	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs549719	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55700437	1.00[ASN][1000 genomes]
rs557559	1.00[ASN][1000 genomes]
rs560218	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs561276	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs572824	1.00[ASN][1000 genomes]
rs59473078	1.00[ASN][1000 genomes]
rs59572422	1.00[ASN][1000 genomes]
rs59841013	1.00[ASN][1000 genomes]
rs61687548	1.00[ASN][1000 genomes]
rs6900438	1.00[ASN][1000 genomes]
rs6900824	1.00[ASN][1000 genomes]
rs6906691	1.00[ASN][1000 genomes]
rs6906810	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6907034	1.00[ASN][1000 genomes]
rs6907978	1.00[ASN][1000 genomes]
rs6928341	1.00[ASN][1000 genomes]
rs6934454	1.00[ASN][1000 genomes]
rs71536195	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73741556	1.00[ASN][1000 genomes]
rs73741557	1.00[ASN][1000 genomes]
rs7742747	1.00[ASN][1000 genomes]
rs7743118	1.00[ASN][1000 genomes]
rs7752930	1.00[ASN][1000 genomes]
rs7757391	1.00[ASN][1000 genomes]
rs7757722	1.00[ASN][1000 genomes]
rs7759154	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7775313	1.00[ASN][1000 genomes]
rs806604	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9368770	1.00[ASN][1000 genomes]
rs9689326	0.87[EUR][1000 genomes];1.00[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	nsv830637	chr6:33329365-33510704	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	nsv602832	chr6:33382241-33520221	Weak transcription Active TSS Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	41 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:33453000-33474000	Weak transcription	Right Atrium	heart

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