Variant report

Variant	rs56303477
Chromosome Location	chr1:180350046-180350047
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	chr1:180349414..180351217-chr1:180352650..180354645,2	K562	blood:

Extended variants
information (count: 91 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:83)

rs_ID	r²[population]
rs10494528	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10494529	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs10913988	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10913990	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10913991	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10913992	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10913995	0.82[AMR][1000 genomes];0.93[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10913996	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10914004	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs10914012	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11487431	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12058221	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12062561	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12065388	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12069389	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12070624	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12071353	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12076995	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12077656	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12077791	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12077839	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12081494	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12083900	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12084039	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12087060	0.91[EUR][1000 genomes]
rs12087325	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12089373	0.84[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12093073	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1339721	0.86[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs16856042	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4403592	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55660948	0.89[EUR][1000 genomes]
rs55962675	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs56333717	0.89[EUR][1000 genomes]
rs56747078	0.91[EUR][1000 genomes]
rs57070632	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs57424497	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57493263	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs58145394	0.93[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs58369506	0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59357483	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59371134	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs60528279	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61024380	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6425635	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6659477	0.94[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66619942	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6663823	0.95[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6667388	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6670242	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6673113	0.91[EUR][1000 genomes]
rs6676778	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs66913400	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6696075	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67071426	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67343454	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs67517246	0.91[EUR][1000 genomes]
rs67621570	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs67623108	0.91[EUR][1000 genomes]
rs67716213	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs67830766	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs68010689	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs68046305	0.89[EUR][1000 genomes]
rs72714816	0.84[EUR][1000 genomes]
rs72714819	0.84[EUR][1000 genomes]
rs72714820	0.84[EUR][1000 genomes]
rs72714824	0.84[EUR][1000 genomes]
rs72714859	0.84[EUR][1000 genomes]
rs72714872	0.89[EUR][1000 genomes]
rs72714883	0.89[EUR][1000 genomes]
rs72714890	0.89[EUR][1000 genomes]
rs72714891	0.89[EUR][1000 genomes]
rs72714892	0.89[EUR][1000 genomes]
rs72714894	0.89[EUR][1000 genomes]
rs72714896	0.89[EUR][1000 genomes]
rs72716605	0.89[EUR][1000 genomes]
rs72716619	0.84[EUR][1000 genomes]
rs72716624	0.84[EUR][1000 genomes]
rs73037411	0.82[AMR][1000 genomes];0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs73048237	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7542223	0.95[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7552701	0.84[EUR][1000 genomes]
rs9662762	0.83[AFR][1000 genomes];0.89[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1003739	chr1:180027760-180483292	Enhancers ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
2	nsv535217	chr1:180027760-180483292	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	67 gene(s)	inside rSNPs	diseases
3	nsv527918	chr1:180279710-180443808	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	6 gene(s)	inside rSNPs	diseases
4	nsv1013716	chr1:180287338-180477072	Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
5	nsv535221	chr1:180287338-180477072	Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	39 gene(s)	inside rSNPs	diseases
6	esv2762200	chr1:180300936-180493841	ZNF genes & repeats Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	40 gene(s)	inside rSNPs	diseases
7	nsv1003359	chr1:180300936-180727561	Enhancers Strong transcription Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
8	nsv1009742	chr1:180342203-180385459	Weak transcription Enhancers Strong transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:180333000-180356200	Weak transcription	Ovary	ovary
2	chr1:180341200-180401400	Weak transcription	Osteobl	bone
3	chr1:180343600-180356400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr1:180348200-180382600	Weak transcription	Pancreas	Pancrea
5	chr1:180348800-180350200	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr1:180348800-180350800	ZNF genes & repeats	Monocytes-CD14+_RO01746	blood
7	chr1:180349000-180350200	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr1:180349200-180350200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr1:180349400-180351400	Weak transcription	Primary hematopoietic stem cells	blood
10	chr1:180349400-180356600	Weak transcription	Aorta	Aorta
11	chr1:180349400-180364200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr1:180349400-180407000	Weak transcription	Esophagus	oesophagus
13	chr1:180349800-180351200	Weak transcription	HUVEC	blood vessel

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