Variant report

Variant	rs4963814
Chromosome Location	chr12:25007495-25007496
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr12:25005197..25007956-chr12:25071824..25074312,2	K562	blood:
2	chr12:25003088..25005571-chr12:25006515..25009037,2	K562	blood:
3	chr12:25007357..25009487-chr12:25098229..25100452,2	K562	blood:
4	chr12:25007357..25008874-chr12:25098952..25100961,2	K562	blood:

Extended variants
information (count: 68 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10160847	0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10466757	0.89[ASN][1000 genomes]
rs10466800	0.88[ASN][1000 genomes]
rs1075061	0.92[CHB][hapmap];0.89[JPT][hapmap];0.84[ASN][1000 genomes]
rs1075063	0.84[ASN][1000 genomes]
rs10771134	0.95[ASN][1000 genomes]
rs10842417	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10842420	0.95[ASN][1000 genomes]
rs11613673	0.97[ASN][1000 genomes]
rs11613710	0.93[ASN][1000 genomes]
rs11615863	0.92[ASN][1000 genomes]
rs12227952	0.88[ASN][1000 genomes]
rs12228257	0.89[ASN][1000 genomes]
rs12229422	0.89[ASN][1000 genomes]
rs12301149	0.93[ASN][1000 genomes]
rs12424348	0.92[ASN][1000 genomes]
rs16928089	0.88[ASN][1000 genomes]
rs17372766	0.89[ASN][1000 genomes]
rs2133583	0.93[ASN][1000 genomes]
rs2133584	0.86[ASN][1000 genomes]
rs2220271	0.97[ASN][1000 genomes]
rs2353478	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs3736211	0.88[ASN][1000 genomes]
rs4963805	0.87[ASN][1000 genomes]
rs4963806	0.87[ASN][1000 genomes]
rs4963808	0.86[ASN][1000 genomes]
rs60104197	0.89[ASN][1000 genomes]
rs61914865	0.85[ASN][1000 genomes]
rs7138685	0.89[ASN][1000 genomes]
rs73061805	0.89[ASN][1000 genomes]
rs73061812	0.88[ASN][1000 genomes]
rs73061817	0.83[ASN][1000 genomes]
rs73079552	0.96[ASN][1000 genomes]
rs73079568	0.92[ASN][1000 genomes]
rs73079570	0.93[ASN][1000 genomes]
rs7308285	0.86[ASN][1000 genomes]
rs7961152	0.87[ASN][1000 genomes]
rs7961688	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7962203	1.00[YRI][hapmap];1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7973974	0.91[ASN][1000 genomes]
rs7976928	0.89[ASN][1000 genomes]
rs7977807	0.86[CHB][hapmap]
rs954199	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:25 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2422312	chr12:24519392-25221686	Weak transcription Enhancers Bivalent Enhancer Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	35 gene(s)	inside rSNPs	diseases
2	nsv898920	chr12:24648863-25147192	Enhancers Bivalent/Poised TSS Flanking Active TSS Weak transcription Strong transcription Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
3	nsv469169	chr12:24692383-25357680	Enhancers Active TSS Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
4	nsv557775	chr12:24692383-25357680	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	34 gene(s)	inside rSNPs	diseases
5	nsv932477	chr12:24705151-25346677	Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Strong transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
6	nsv1053309	chr12:24770995-25078227	Enhancers Weak transcription Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	11 gene(s)	inside rSNPs	diseases
7	nsv1067577	chr12:24791283-25346677	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
8	nsv529514	chr12:24791283-25346677	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
9	nsv1041221	chr12:24880443-25213168	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
10	nsv541425	chr12:24880443-25213168	Bivalent/Poised TSS Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
11	nsv469170	chr12:24891175-25204353	Weak transcription Strong transcription ZNF genes & repeats Enhancers Flanking Bivalent TSS/Enh Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
12	nsv557776	chr12:24891175-25204353	Enhancers Strong transcription ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
13	nsv557777	chr12:24891175-25205241	Flanking Active TSS Strong transcription Weak transcription Active TSS Enhancers ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
14	nsv469173	chr12:24891175-25207653	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
15	nsv557778	chr12:24891175-25207653	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
16	nsv1045302	chr12:24921100-25078227	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
17	nsv1049138	chr12:24921100-25164524	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
18	nsv1051319	chr12:24921100-25238936	Enhancers Weak transcription Flanking Active TSS Strong transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
19	nsv1054863	chr12:24941350-25078227	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Flanking Active TSS Genic enhancers Strong transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
20	nsv541426	chr12:24941350-25078227	Enhancers Strong transcription Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
21	nsv1051968	chr12:24941350-25138118	Weak transcription Active TSS Flanking Active TSS Enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
22	nsv541427	chr12:24941350-25138118	Active TSS Genic enhancers Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
23	nsv1037288	chr12:24941350-25238936	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
24	nsv541428	chr12:24941350-25238936	Flanking Active TSS Enhancers Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
25	nsv1041218	chr12:24972019-25304356	Weak transcription Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Active TSS Flanking Active TSS Genic enhancers 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:59 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:24964000-25013400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr12:24968000-25017600	Weak transcription	Fetal Thymus	thymus
3	chr12:24968400-25007800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
4	chr12:24971000-25054800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr12:24992000-25053000	Weak transcription	Fetal Stomach	stomach
6	chr12:24992400-25008800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr12:24992400-25033200	Weak transcription	Fetal Brain Male	brain
8	chr12:24992600-25053400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr12:24993400-25008400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr12:24993600-25010800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr12:24995200-25008800	Weak transcription	H9 Cell Line	embryonic stem cell
12	chr12:25000600-25008800	Weak transcription	HSMMtube	muscle
13	chr12:25002400-25008200	Weak transcription	Placenta	Placenta
14	chr12:25002400-25008800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr12:25002400-25008800	Weak transcription	HSMM	muscle
16	chr12:25002600-25009000	Weak transcription	Fetal Muscle Leg	muscle
17	chr12:25002600-25022200	Weak transcription	Lung	lung
18	chr12:25002800-25008800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr12:25002800-25015200	Weak transcription	HepG2	liver
20	chr12:25002800-25019200	Weak transcription	Fetal Muscle Trunk	muscle
21	chr12:25003000-25009000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr12:25003200-25009000	Enhancers	HUVEC	blood vessel
23	chr12:25003400-25010600	Weak transcription	Dnd41	blood
24	chr12:25003800-25007800	Weak transcription	Primary monocytes fromperipheralblood	blood
25	chr12:25004800-25008800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr12:25005000-25007800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr12:25005000-25008400	Weak transcription	H1 Cell Line	embryonic stem cell
28	chr12:25005000-25008800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr12:25005000-25019000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr12:25005200-25008800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr12:25005200-25008800	Weak transcription	Pancreas	Pancrea
32	chr12:25005200-25010800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr12:25005400-25008800	Weak transcription	K562	blood
34	chr12:25005600-25007800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr12:25005600-25009800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
36	chr12:25005600-25010600	Weak transcription	GM12878-XiMat	blood
37	chr12:25005800-25007600	Enhancers	NHEK	skin
38	chr12:25005800-25008800	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr12:25006000-25007600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
40	chr12:25006200-25009200	Enhancers	Osteobl	bone
41	chr12:25006400-25009400	Enhancers	Muscle Satellite Cultured Cells	--
42	chr12:25006600-25008200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr12:25006600-25009400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr12:25006800-25008200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr12:25006800-25008800	Enhancers	Primary hematopoietic stem cells short term culture	blood
46	chr12:25006800-25009200	Enhancers	NH-A	brain
47	chr12:25007000-25008000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr12:25007000-25008000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr12:25007000-25008200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr12:25007000-25008200	Enhancers	Primary hematopoietic stem cells	blood

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