Variant report

Variant	rs1433911
Chromosome Location	chr11:4813884-4813885
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	11:4801044-4820112..11:5700314-5707362	H1-hESC	embryonic stem cell:	embryo
2	chr11:4789671..4792092-chr11:4812812..4815235,2	K562	blood:

Variant related genes	Relation type
ENSG00000132256	Chromatin interaction
ENSG00000188069	Chromatin interaction

Extended variants
information (count: 107 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:85)

rs_ID	r²[population]
rs10768241	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10768242	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10768244	0.90[ASN][1000 genomes]
rs10836651	1.00[JPT][hapmap]
rs10836652	0.90[ASN][1000 genomes]
rs10836653	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10836654	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10836672	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs10836677	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11033914	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11033918	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs11600780	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11601153	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11607628	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs11822216	0.91[CEU][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs12284164	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12785245	0.83[CEU][hapmap]
rs12787156	0.90[ASN][1000 genomes]
rs12787163	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs12788159	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12805337	1.00[CEU][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1347271	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1347272	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1368816	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1368830	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433901	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1433902	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1433903	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433907	1.00[CHB][hapmap];0.90[ASN][1000 genomes]
rs1433908	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433912	1.00[JPT][hapmap]
rs1433919	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433920	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433921	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1433922	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433923	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433924	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1433926	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1469751	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs1541946	0.83[CEU][hapmap]
rs16906303	1.00[ASN][1000 genomes]
rs17228176	0.83[CEU][hapmap]
rs17228183	0.83[CEU][hapmap]
rs17228218	0.84[CEU][hapmap]
rs17228295	1.00[ASN][1000 genomes]
rs1865282	0.83[CEU][hapmap];0.82[AMR][1000 genomes]
rs1865284	0.84[CEU][hapmap]
rs1865285	0.82[ASN][1000 genomes]
rs1991887	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1991888	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs1991889	1.00[JPT][hapmap];0.82[ASN][1000 genomes]
rs2053116	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2053117	1.00[CHB][hapmap];1.00[ASN][1000 genomes]
rs2117211	1.00[ASN][1000 genomes]
rs2412430	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs2412435	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs36098183	0.90[ASN][1000 genomes]
rs41520952	1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[ASN][1000 genomes]
rs4382897	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4910527	0.90[ASN][1000 genomes]
rs4910528	0.89[ASN][1000 genomes]
rs4910681	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4910682	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs4910683	0.90[ASN][1000 genomes]
rs4910684	0.91[CEU][hapmap]
rs5005347	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs5005348	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs5005349	0.90[ASN][1000 genomes]
rs6578528	0.90[ASN][1000 genomes]
rs6578529	0.90[ASN][1000 genomes]
rs6578530	0.90[ASN][1000 genomes]
rs6578531	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs6578532	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6578533	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs72868750	0.90[ASN][1000 genomes]
rs7930228	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7933099	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7933109	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7933423	0.82[ASN][1000 genomes]
rs7938153	0.90[ASN][1000 genomes]
rs7940131	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7941731	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7950667	0.90[ASN][1000 genomes]
rs7951201	1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs7952317	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1043803	chr11:4388448-4837042	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
2	nsv540916	chr11:4388448-4837042	Flanking Active TSS Weak transcription Strong transcription Active TSS Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	46 gene(s)	inside rSNPs	diseases
3	nsv1048224	chr11:4390227-4920324	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
4	nsv540917	chr11:4390227-4920324	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	53 gene(s)	inside rSNPs	diseases
5	esv3424302	chr11:4585155-4880050	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	36 gene(s)	inside rSNPs	diseases
6	nsv1054847	chr11:4642875-5200656	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	72 gene(s)	inside rSNPs	diseases
7	nsv896915	chr11:4659419-4844393	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
8	nsv832056	chr11:4673001-4824890	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	25 gene(s)	inside rSNPs	diseases
9	esv1806557	chr11:4778433-4820481	Weak transcription Enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
10	esv1809118	chr11:4782207-4843426	Enhancers Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	esv2760633	chr11:4803980-4910384	Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
12	nsv1035355	chr11:4805922-4907672	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv1039703	chr11:4806669-4910372	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
14	nsv553176	chr11:4806706-4909000	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
15	nsv553177	chr11:4806872-4871506	Enhancers Bivalent/Poised TSS Active TSS Weak transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
16	nsv553178	chr11:4806872-4909000	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
17	nsv553179	chr11:4806872-4910224	Enhancers Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
18	nsv1045537	chr11:4807304-4904064	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
19	nsv467665	chr11:4808227-4871481	ZNF genes & repeats Weak transcription Bivalent/Poised TSS Enhancers Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
20	nsv553180	chr11:4808227-4871481	Enhancers Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
21	nsv553181	chr11:4811933-4910224	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
22	esv19187	chr11:4813583-4820635	Enhancers ZNF genes & repeats Weak transcription	TF binding region Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:0 , 50 per page) page:

No data

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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