Variant report

Variant	rs59101778
Chromosome Location	chr21:41088699-41088700
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	chr21:41082155..41084385-chr21:41086359..41088868,2	K562	blood:
2	chr21:41078662..41082504-chr21:41085801..41089448,3	MCF-7	breast:

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10483058	0.81[ASN][1000 genomes]
rs11909296	0.86[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs12233297	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12233347	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12233349	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12626178	0.87[ASN][1000 genomes]
rs12626186	0.92[ASN][1000 genomes]
rs12626201	0.92[ASN][1000 genomes]
rs12626282	0.92[ASN][1000 genomes]
rs12627345	0.92[ASN][1000 genomes]
rs12627452	0.92[ASN][1000 genomes]
rs16998157	0.82[ASN][1000 genomes]
rs16998163	1.00[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs16998166	0.86[ASN][1000 genomes]
rs2410177	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2410178	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2837128	0.91[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55707904	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs55901439	0.82[ASN][1000 genomes]
rs56112847	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs57092838	0.95[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs57845654	0.93[ASN][1000 genomes]
rs57952155	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58037814	0.86[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs58098823	0.92[ASN][1000 genomes]
rs58955754	1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs59600504	0.92[ASN][1000 genomes]
rs59639087	0.84[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs59710242	0.86[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs59990779	0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs60661700	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60728916	0.84[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs62235479	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs62235484	0.87[ASN][1000 genomes]
rs62235485	0.81[ASN][1000 genomes]
rs62235486	0.81[ASN][1000 genomes]
rs62235487	0.81[ASN][1000 genomes]
rs62235490	0.87[ASN][1000 genomes]
rs62235491	0.87[ASN][1000 genomes]
rs62235496	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62235497	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs62235511	0.87[ASN][1000 genomes]
rs7282484	0.82[ASN][1000 genomes]
rs73363758	1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73904403	0.92[ASN][1000 genomes]
rs73904404	0.87[ASN][1000 genomes]
rs8127272	0.84[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1061454	chr21:40757973-41265404	Strong transcription Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
2	nsv1057956	chr21:40907707-41393396	Enhancers Strong transcription ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
3	nsv544444	chr21:40907707-41393396	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
4	nsv1065086	chr21:41034806-41429078	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
5	nsv544445	chr21:41034806-41429078	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
6	nsv834099	chr21:41076873-41206030	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:7 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:41069000-41095000	Weak transcription	Pancreas	Pancrea
2	chr21:41075800-41101800	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr21:41079400-41109600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr21:41083200-41103000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr21:41087000-41091800	Weak transcription	Fetal Heart	heart
6	chr21:41088200-41093600	Weak transcription	Rectal Mucosa Donor 31	rectum
7	chr21:41088200-41105000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links