Variant report

Variant	rs1937485
Chromosome Location	chr6:161284895-161284896
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:161282793..161285621-chr6:161332343..161335165,2	K562	blood:

Extended variants
information (count: 45 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs1247513	1.00[ASN][1000 genomes]
rs1247541	0.91[ASN][1000 genomes]
rs1247553	1.00[CHB][hapmap]
rs1247561	0.82[ASN][1000 genomes]
rs1247562	0.82[ASN][1000 genomes]
rs1247563	0.82[ASN][1000 genomes]
rs1247568	0.82[ASN][1000 genomes]
rs1247570	0.82[ASN][1000 genomes]
rs1406891	1.00[CHB][hapmap]
rs1614840	0.82[ASN][1000 genomes]
rs1620921	0.82[ASN][1000 genomes]
rs1621801	0.82[ASN][1000 genomes]
rs1652463	0.91[ASN][1000 genomes]
rs1652471	1.00[CHB][hapmap];0.91[ASN][1000 genomes]
rs1740442	0.82[ASN][1000 genomes]
rs1740443	0.82[ASN][1000 genomes]
rs1740444	0.82[ASN][1000 genomes]
rs1830524	1.00[CHB][hapmap]
rs1892347	0.84[ASN][1000 genomes]
rs1892348	0.92[ASN][1000 genomes]
rs1937486	0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1937487	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2255792	0.90[AFR][1000 genomes];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2465850	0.92[ASN][1000 genomes]
rs2465857	0.92[ASN][1000 genomes]
rs2465859	0.92[ASN][1000 genomes]
rs2489936	0.92[ASN][1000 genomes]
rs2489938	0.92[ASN][1000 genomes]
rs2565724	1.00[CHB][hapmap]
rs2802356	0.82[ASN][1000 genomes]
rs28711930	0.91[ASN][1000 genomes]
rs2953494	0.84[ASN][1000 genomes]
rs2953495	0.84[ASN][1000 genomes]
rs2997094	0.92[ASN][1000 genomes]
rs2997095	0.84[ASN][1000 genomes]
rs62435345	0.92[ASN][1000 genomes]
rs783156	0.82[ASN][1000 genomes]
rs9355844	0.91[ASN][1000 genomes]
rs9456598	0.91[ASN][1000 genomes]
rs9458048	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3352911	chr6:161140543-161324358	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Genic enhancers Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv830853	chr6:161180005-161376481	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2422347	chr6:161211171-161442377	Flanking Active TSS Enhancers Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
4	esv1837673	chr6:161216608-161318009	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv886816	chr6:161225303-161286450	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:161282000-161285400	Weak transcription	Right Atrium	heart
2	chr6:161284800-161285200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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