Variant report

Variant	rs60846227
Chromosome Location	chr10:20006984-20006985
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

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

rSNPs within LD-proxies of this variant (count:32)

rs_ID	r²[population]
rs12248868	1.00[AMR][1000 genomes]
rs12249095	1.00[AMR][1000 genomes]
rs12261318	1.00[AMR][1000 genomes]
rs4265505	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56859308	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs57178679	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs58072866	1.00[EUR][1000 genomes]
rs58334588	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59209444	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59279697	1.00[EUR][1000 genomes]
rs59367240	1.00[EUR][1000 genomes]
rs59367543	0.81[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59849389	1.00[EUR][1000 genomes]
rs59958232	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60029230	1.00[EUR][1000 genomes]
rs60440775	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60885771	1.00[EUR][1000 genomes]
rs61340971	1.00[EUR][1000 genomes]
rs61657628	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7067789	1.00[EUR][1000 genomes]
rs7068752	1.00[EUR][1000 genomes]
rs7071134	1.00[EUR][1000 genomes]
rs7073446	1.00[EUR][1000 genomes]
rs7083316	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7083958	1.00[EUR][1000 genomes]
rs7086296	1.00[EUR][1000 genomes]
rs7087012	1.00[EUR][1000 genomes]
rs7090257	1.00[EUR][1000 genomes]
rs7091096	1.00[EUR][1000 genomes]
rs7099053	1.00[EUR][1000 genomes]
rs73597608	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs74122006	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:13 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2759737	chr10:19694144-20024994	Active TSS Flanking Active TSS Enhancers Weak transcription Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer 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
2	esv2758211	chr10:19714637-20024994	Weak transcription Active TSS ZNF genes & repeats Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv1049295	chr10:19740296-20509036	Weak transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
4	nsv1042877	chr10:19749314-20067572	Enhancers Weak transcription ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
5	esv34306	chr10:19777069-20117944	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3518965	chr10:19786251-20061305	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	esv3518966	chr10:19786310-20061256	Enhancers Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv825266	chr10:19807019-20037182	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
9	nsv831804	chr10:19859400-20035593	Active TSS Enhancers Flanking Active TSS Strong transcription Weak transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
10	nsv894933	chr10:19865757-20036080	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
11	nsv1039685	chr10:19935095-20039621	ZNF genes & repeats Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	nsv1046998	chr10:19973096-20031468	Weak transcription ZNF genes & repeats Enhancers Flanking Active TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
13	nsv523490	chr10:19974930-20041146	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	3 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	chr10:20003200-20008400	Weak transcription	Adipose Nuclei	Adipose
2	chr10:20003400-20051400	Weak transcription	Fetal Intestine Large	intestine
3	chr10:20003600-20008200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr10:20003600-20008400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr10:20003800-20007800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr10:20005000-20007200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr10:20006600-20007400	ZNF genes & repeats	Fetal Intestine Small	intestine

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