Variant report

Variant	rs1798265
Chromosome Location	chr12:32280872-32280873
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr12:32257278..32259683-chr12:32278967..32281640,2	MCF-7	breast:
2	chr12:32258248..32259913-chr12:32280000..32281853,2	K562	blood:

Variant related genes	Relation type
ENSG00000151746	Chromatin interaction

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs10743783	0.84[ASN][1000 genomes]
rs10771917	0.85[ASN][1000 genomes]
rs10771921	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs10844137	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs10844139	0.83[AMR][1000 genomes]
rs1151009	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1151010	0.81[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs1151011	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1151012	0.83[AMR][1000 genomes];0.84[ASN][1000 genomes]
rs1151016	0.85[EUR][1000 genomes]
rs1151020	0.84[ASN][1000 genomes]
rs1260708	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1261166	0.84[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs1618256	0.83[EUR][1000 genomes]
rs1631036	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1673857	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1673858	0.87[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1684146	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs1684149	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1716937	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1716941	0.81[EUR][1000 genomes]
rs1798260	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2458120	0.83[AFR][1000 genomes];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs2594013	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2594014	0.85[ASN][1000 genomes]
rs2630566	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2630578	0.80[ASN][1000 genomes]
rs2630579	0.85[ASN][1000 genomes]
rs2652014	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs2652018	0.83[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs2668293	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2668299	0.84[ASN][1000 genomes]
rs2668301	0.85[ASN][1000 genomes]
rs2668302	0.85[ASN][1000 genomes]
rs2668303	0.85[ASN][1000 genomes]
rs2668306	0.85[ASN][1000 genomes]
rs2683491	0.80[EUR][1000 genomes]
rs4931612	0.80[ASN][1000 genomes]
rs4931613	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4931614	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs4931615	0.80[ASN][1000 genomes]
rs4931616	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]
rs6488034	0.83[AMR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3363806	chr12:31872264-32410283	Strong transcription Flanking Active TSS Enhancers Weak transcription Active TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
2	esv3508621	chr12:31872654-32410593	Weak transcription ZNF genes & repeats Active TSS Enhancers Strong transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
3	esv3508622	chr12:31872654-32410593	Weak transcription Genic enhancers Flanking Active TSS Enhancers Active TSS Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
4	nsv976030	chr12:32153446-32307541	Enhancers Active TSS Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv983498	chr12:32153446-32388092	Genic enhancers Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	nsv898969	chr12:32224948-32375677	Enhancers Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
7	nsv1042317	chr12:32228872-32316774	Weak transcription Enhancers Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	nsv1041733	chr12:32247427-32312547	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
9	nsv531960	chr12:32257285-32775277	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	19 gene(s)	inside rSNPs	diseases
10	esv2751096	chr12:32280340-32702784	Strong transcription Enhancers Weak transcription Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:58 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:32262400-32287400	Weak transcription	Primary T cells from cord blood	blood
2	chr12:32262400-32290200	Weak transcription	Primary B cells from cord blood	blood
3	chr12:32263200-32287000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
4	chr12:32268800-32287200	Weak transcription	Lung	lung
5	chr12:32269000-32285400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr12:32269000-32286400	Weak transcription	Primary B cells from peripheral blood	blood
7	chr12:32269000-32286400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
8	chr12:32269000-32287400	Weak transcription	Aorta	Aorta
9	chr12:32269000-32287400	Weak transcription	Spleen	Spleen
10	chr12:32269000-32340200	Weak transcription	Dnd41	blood
11	chr12:32269200-32287000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr12:32269200-32287200	Weak transcription	Primary hematopoietic stem cells	blood
13	chr12:32269400-32286800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:32269800-32286400	Weak transcription	Brain Hippocampus Middle	brain
15	chr12:32270600-32285800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr12:32270600-32287000	Weak transcription	HSMMtube	muscle
17	chr12:32270600-32287000	Weak transcription	HUVEC	blood vessel
18	chr12:32270600-32287200	Weak transcription	NHEK	skin
19	chr12:32272000-32288600	Weak transcription	Fetal Intestine Small	intestine
20	chr12:32272200-32287000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr12:32272200-32287200	Weak transcription	Left Ventricle	heart
22	chr12:32273600-32292200	Weak transcription	Small Intestine	intestine
23	chr12:32273800-32285400	Weak transcription	GM12878-XiMat	blood
24	chr12:32273800-32286200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr12:32273800-32286200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr12:32273800-32287000	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr12:32278000-32292200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr12:32278000-32292400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr12:32278200-32283400	Weak transcription	Ovary	ovary
30	chr12:32278200-32286200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
31	chr12:32278200-32287200	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr12:32278400-32283400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr12:32278400-32286200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr12:32278400-32286400	Weak transcription	NHLF	lung
35	chr12:32278400-32287000	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr12:32278400-32287200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr12:32278400-32292000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr12:32278600-32281200	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:32278600-32283000	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr12:32278600-32283400	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr12:32278600-32287000	Weak transcription	Brain Cingulate Gyrus	brain
42	chr12:32278600-32287000	Weak transcription	Osteobl	bone
43	chr12:32278600-32287200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr12:32278800-32286400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr12:32278800-32287000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr12:32278800-32291800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr12:32278800-32291800	Weak transcription	HSMM	muscle
48	chr12:32279800-32284800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr12:32280000-32286400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr12:32280200-32287000	Weak transcription	NH-A	brain

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