Variant report

Variant	rs1326986
Chromosome Location	chr10:19929513-19929514
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	chr10:19928272..19930845-chr10:19944987..19947653,2	K562	blood:

Extended variants
information (count: 67 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:53)

rs_ID	r²[population]
rs10508588	0.88[EUR][1000 genomes]
rs10508589	0.88[EUR][1000 genomes]
rs10508590	1.00[CEU][hapmap];1.00[GIH][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs10827679	0.98[EUR][1000 genomes]
rs10827696	0.88[EUR][1000 genomes]
rs10827723	1.00[EUR][1000 genomes]
rs10827724	1.00[EUR][1000 genomes]
rs10827726	1.00[EUR][1000 genomes]
rs10827728	0.85[EUR][1000 genomes]
rs10827732	0.83[EUR][1000 genomes]
rs10827733	0.83[EUR][1000 genomes]
rs10827734	0.83[EUR][1000 genomes]
rs10827735	0.83[EUR][1000 genomes]
rs10827736	0.83[EUR][1000 genomes]
rs10827738	0.83[EUR][1000 genomes]
rs10827743	0.83[EUR][1000 genomes]
rs11010357	0.84[AMR][1000 genomes]
rs11010652	0.91[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11010662	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs11010792	1.00[EUR][1000 genomes]
rs11010794	0.88[EUR][1000 genomes]
rs11010795	0.88[EUR][1000 genomes]
rs11010796	0.88[EUR][1000 genomes]
rs11010817	0.88[EUR][1000 genomes]
rs11010877	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11010881	0.88[EUR][1000 genomes]
rs11010886	0.88[EUR][1000 genomes]
rs11010896	0.83[EUR][1000 genomes]
rs11010903	0.83[EUR][1000 genomes]
rs11010972	0.83[EUR][1000 genomes]
rs11011078	0.81[EUR][1000 genomes]
rs12249987	0.83[EUR][1000 genomes]
rs12259525	0.83[EUR][1000 genomes]
rs12259745	0.83[EUR][1000 genomes]
rs12261044	1.00[EUR][1000 genomes]
rs12261359	0.88[EUR][1000 genomes]
rs12262868	0.83[EUR][1000 genomes]
rs12263598	0.83[EUR][1000 genomes]
rs12268966	0.88[EUR][1000 genomes]
rs12358323	0.88[EUR][1000 genomes]
rs12774709	0.91[AMR][1000 genomes]
rs12776678	1.00[CEU][hapmap]
rs12777618	0.83[EUR][1000 genomes]
rs1326966	0.81[EUR][1000 genomes]
rs1326972	0.83[EUR][1000 genomes]
rs1326988	0.88[EUR][1000 genomes]
rs1326990	0.88[EUR][1000 genomes]
rs1326991	1.00[EUR][1000 genomes]
rs1854075	0.83[EUR][1000 genomes]
rs2225082	0.83[EUR][1000 genomes]
rs34773396	0.91[AMR][1000 genomes]
rs35749706	0.86[EUR][1000 genomes]
rs7474617	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv466764	chr10:19400845-19979434	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	nsv550128	chr10:19400845-19979434	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	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
4	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
5	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
6	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
7	esv2757373	chr10:19776910-20004996	Weak transcription Enhancers Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
8	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
9	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
10	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
11	nsv894931	chr10:19796958-19987644	Enhancers Weak transcription ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
12	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
13	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
14	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

Variant related diseases (count:1)

Disease	PMID	Source
Ankylosing spondylitis	20062062	GWAS catalog

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:19928000-19929800	Enhancers	Primary hematopoietic stem cells short term culture	blood
2	chr10:19928000-19930400	Enhancers	Primary hematopoietic stem cells	blood
3	chr10:19928200-19930200	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr10:19928200-19934000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
5	chr10:19928200-19936400	Weak transcription	Duodenum Mucosa	Duodenum
6	chr10:19928400-19931400	Weak transcription	HSMMtube	muscle
7	chr10:19928400-19945600	Weak transcription	Fetal Intestine Small	intestine
8	chr10:19928600-19929600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
9	chr10:19928600-19930200	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr10:19928600-19932800	Weak transcription	Fetal Lung	lung
11	chr10:19928600-19933000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr10:19928600-19936800	Weak transcription	Fetal Intestine Large	intestine
13	chr10:19929400-19929800	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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