Variant report

Variant	rs1325169
Chromosome Location	chr10:45369209-45369210
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	chr10:45360538..45361172-chr10:45369033..45369961,2	K562	blood:

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

rSNPs within LD-proxies of this variant (count:31)

rs_ID	r²[population]
rs1002321	0.96[ASN][1000 genomes]
rs1018702	0.96[ASN][1000 genomes]
rs1034161	0.92[ASN][1000 genomes]
rs10508890	0.99[ASN][1000 genomes]
rs11813749	1.00[EUR][1000 genomes]
rs12569373	1.00[EUR][1000 genomes]
rs12570026	1.00[EUR][1000 genomes]
rs12570392	1.00[EUR][1000 genomes]
rs12570753	1.00[EUR][1000 genomes]
rs12571227	1.00[EUR][1000 genomes]
rs12571338	1.00[EUR][1000 genomes]
rs12571649	1.00[EUR][1000 genomes]
rs12572145	1.00[EUR][1000 genomes]
rs12572451	1.00[EUR][1000 genomes]
rs12572976	1.00[EUR][1000 genomes]
rs12573247	0.85[AMR][1000 genomes]
rs12573461	1.00[EUR][1000 genomes]
rs1325170	0.99[ASN][1000 genomes]
rs1573903	1.00[EUR][1000 genomes]
rs17157164	0.99[ASN][1000 genomes]
rs17157167	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17157326	1.00[CEU][hapmap]
rs2274885	1.00[CEU][hapmap]
rs3814569	1.00[CEU][hapmap]
rs4948650	1.00[CEU][hapmap]
rs55689732	1.00[EUR][1000 genomes]
rs57657317	1.00[EUR][1000 genomes]
rs59114620	1.00[EUR][1000 genomes]
rs60593524	1.00[EUR][1000 genomes]
rs73275080	1.00[EUR][1000 genomes]
rs7910103	0.98[ASN][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	esv2760155	chr10:45203117-45371777	Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1050711	chr10:45203117-45371777	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1052977	chr10:45203117-45373945	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1037692	chr10:45208025-45371777	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1052669	chr10:45208025-45373945	Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv1054383	chr10:45210690-45370067	Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	nsv1044334	chr10:45210690-45373945	Weak transcription Enhancers Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv517161	chr10:45210690-45416256	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
9	nsv1050496	chr10:45227530-45382154	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv831844	chr10:45228791-45407762	Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv1038316	chr10:45247684-45371316	Active TSS Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv540585	chr10:45247684-45371316	Weak transcription Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv831845	chr10:45300268-45460395	Enhancers Genic enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer 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	18 gene(s)	inside rSNPs	diseases
14	nsv831846	chr10:45322236-45556370	Bivalent Enhancer Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:21 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:45361000-45374000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr10:45365200-45374000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr10:45368000-45370400	Enhancers	Stomach Smooth Muscle	stomach
4	chr10:45368400-45370000	Enhancers	Fetal Lung	lung
5	chr10:45368400-45370200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr10:45368400-45370200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr10:45368400-45370200	Enhancers	Fetal Stomach	stomach
8	chr10:45368400-45370600	Enhancers	Fetal Heart	heart
9	chr10:45368600-45369400	Weak transcription	Adipose Nuclei	Adipose
10	chr10:45368600-45370200	Enhancers	Fetal Muscle Leg	muscle
11	chr10:45368600-45370600	Enhancers	Left Ventricle	heart
12	chr10:45368600-45370600	Enhancers	Pancreas	Pancrea
13	chr10:45368600-45370600	Enhancers	Psoas Muscle	Psoas
14	chr10:45368600-45370600	Enhancers	Right Ventricle	heart
15	chr10:45368600-45371600	Weak transcription	Gastric	stomach
16	chr10:45368800-45369800	Weak transcription	Aorta	Aorta
17	chr10:45369200-45369400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr10:45369200-45369400	Enhancers	Brain Angular Gyrus	brain
19	chr10:45369200-45370000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr10:45369200-45370200	Enhancers	Fetal Brain Female	brain
21	chr10:45369200-45370600	Enhancers	Right Atrium	heart

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