Variant report

Variant	rs6041837
Chromosome Location	chr20:13049147-13049148
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 78 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:63)

rs_ID	r²[population]
rs17190831	0.86[EUR][1000 genomes]
rs17190880	0.86[EUR][1000 genomes]
rs17263020	0.86[EUR][1000 genomes]
rs17263047	0.84[EUR][1000 genomes]
rs17263054	0.84[EUR][1000 genomes]
rs1835661	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2236127	0.86[EUR][1000 genomes]
rs2327689	0.86[EUR][1000 genomes]
rs3848769	0.86[EUR][1000 genomes]
rs3848771	0.86[EUR][1000 genomes]
rs3848772	0.86[EUR][1000 genomes]
rs3848774	0.86[EUR][1000 genomes]
rs3896153	0.86[EUR][1000 genomes]
rs3906632	0.86[EUR][1000 genomes]
rs3906633	0.86[EUR][1000 genomes]
rs3910132	0.86[EUR][1000 genomes]
rs3910133	0.86[EUR][1000 genomes]
rs4081898	0.86[EUR][1000 genomes]
rs4281972	0.86[EUR][1000 genomes]
rs4289254	0.86[EUR][1000 genomes]
rs4456765	0.86[EUR][1000 genomes]
rs55740854	0.83[EUR][1000 genomes]
rs55760041	0.86[EUR][1000 genomes]
rs55851607	0.86[EUR][1000 genomes]
rs56015929	0.86[EUR][1000 genomes]
rs56164839	0.86[EUR][1000 genomes]
rs58115914	0.83[EUR][1000 genomes]
rs6041836	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6041841	0.93[AFR][1000 genomes];0.89[EUR][1000 genomes]
rs6131425	0.89[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs6131426	0.86[EUR][1000 genomes]
rs6131427	0.86[EUR][1000 genomes]
rs6131428	0.86[EUR][1000 genomes]
rs6131429	0.86[EUR][1000 genomes]
rs6131432	0.86[EUR][1000 genomes]
rs6131437	0.83[EUR][1000 genomes]
rs6134754	0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs6134768	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6134769	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs6134770	0.86[EUR][1000 genomes]
rs6134771	0.85[EUR][1000 genomes]
rs6134772	0.86[EUR][1000 genomes]
rs6134773	0.86[EUR][1000 genomes]
rs6134774	0.86[EUR][1000 genomes]
rs6134775	0.86[EUR][1000 genomes]
rs6134776	0.86[EUR][1000 genomes]
rs6134777	0.86[EUR][1000 genomes]
rs6134778	0.86[EUR][1000 genomes]
rs6134779	0.86[EUR][1000 genomes]
rs6134783	0.83[EUR][1000 genomes]
rs62203585	0.86[EUR][1000 genomes]
rs7262974	0.81[EUR][1000 genomes]
rs7271775	0.86[EUR][1000 genomes]
rs735215	0.86[EUR][1000 genomes]
rs735216	0.86[EUR][1000 genomes]
rs8113891	0.86[EUR][1000 genomes]
rs8114046	0.91[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs8119762	0.86[EUR][1000 genomes]
rs8119848	0.86[EUR][1000 genomes]
rs8119959	0.86[EUR][1000 genomes]
rs8120012	0.86[EUR][1000 genomes]
rs8124052	0.86[EUR][1000 genomes]
rs8125180	0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:15 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1057219	chr20:12729479-13338337	Weak transcription Enhancers Active TSS Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
2	nsv912684	chr20:12734299-13311983	Active TSS Bivalent/Poised TSS Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
3	nsv1067036	chr20:12737436-13338337	Bivalent/Poised TSS Weak transcription Enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	esv3488304	chr20:12738054-13341279	Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	esv3488305	chr20:12738054-13341279	Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
6	nsv518184	chr20:12743808-13344672	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent/Poised TSS Strong transcription Genic enhancers Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
7	nsv1063587	chr20:12756524-13330103	Weak transcription Enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
8	nsv544185	chr20:12756524-13330103	Enhancers Strong transcription Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
9	nsv916296	chr20:12756605-13329940	Enhancers Bivalent Enhancer Strong transcription Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
10	nsv1067720	chr20:12756725-13329963	Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
11	nsv532513	chr20:12756725-13329963	Genic enhancers Weak transcription Strong transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
12	nsv1064901	chr20:12773504-13318421	Weak transcription Active TSS Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
13	nsv833923	chr20:12904689-13064426	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
14	nsv833924	chr20:12997093-13189239	Enhancers Strong transcription Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
15	esv3425983	chr20:13046768-13461834	Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:13003800-13049600	Weak transcription	Lung	lung
2	chr20:13026000-13049400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr20:13028400-13060200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr20:13030600-13074000	Weak transcription	Ovary	ovary
5	chr20:13039600-13065600	Weak transcription	Thymus	Thymus
6	chr20:13040600-13052400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr20:13042600-13076800	Weak transcription	Pancreas	Pancrea
8	chr20:13042800-13054200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr20:13043000-13049200	Weak transcription	Placenta	Placenta
10	chr20:13043800-13051000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr20:13046800-13054200	Weak transcription	Aorta	Aorta
12	chr20:13047200-13052400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr20:13047200-13054200	Weak transcription	Right Ventricle	heart
14	chr20:13048000-13050000	Enhancers	Rectal Mucosa Donor 31	rectum
15	chr20:13048400-13049400	Enhancers	HepG2	liver
16	chr20:13048400-13050000	Enhancers	Fetal Intestine Large	intestine
17	chr20:13048600-13050000	Enhancers	Stomach Mucosa	stomach
18	chr20:13048800-13049800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr20:13048800-13049800	Enhancers	NHEK	skin
20	chr20:13049000-13049400	Enhancers	Liver	Liver
21	chr20:13049000-13049400	Weak transcription	Fetal Intestine Small	intestine
22	chr20:13049000-13049400	Enhancers	HMEC	breast
23	chr20:13049000-13049800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr20:13049000-13049800	Enhancers	Hela-S3	cervix

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