Variant report

Variant	rs1794892
Chromosome Location	chr12:121533973-121533974
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:12)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:121498251..121499029-chr12:121533532..121534500,2	MCF-7	breast:
2	chr12:121533631..121534218-chr12:121667773..121668734,2	K562	blood:
3	chr12:121447247..121448275-chr12:121533293..121534356,3	MCF-7	breast:
4	chr12:121498108..121499039-chr12:121533443..121534521,4	MCF-7	breast:
5	chr12:121499386..121500506-chr12:121533456..121534392,4	K562	blood:
6	chr12:121531941..121534103-chr12:121555507..121557731,2	K562	blood:
7	chr12:121442771..121443720-chr12:121533793..121534340,2	K562	blood:
8	chr12:121533067..121535799-chr12:121628437..121630049,2	K562	blood:
9	chr12:121532324..121533988-chr12:121647782..121650405,2	MCF-7	breast:
10	chr12:121498058..121498974-chr12:121533466..121534380,2	K562	blood:
11	chr12:121528483..121531655-chr12:121531657..121534218,3	MCF-7	breast:
12	chr12:121525079..121528154-chr12:121532572..121535295,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000135124	Chromatin interaction

Extended variants
information (count: 92 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs11065444	0.95[ASN][1000 genomes]
rs1180000	1.00[ASN][1000 genomes]
rs1180001	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1180002	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1180003	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1180004	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1180005	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs1180006	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1180007	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs1180010	0.93[AMR][1000 genomes];0.95[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1180011	0.81[EUR][1000 genomes]
rs1180012	0.81[EUR][1000 genomes]
rs1182936	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1185890	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1186228	0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12297280	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12310654	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12310981	0.98[ASN][1000 genomes]
rs12312648	0.95[ASN][1000 genomes]
rs12312695	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12312758	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs12314721	1.00[CHB][hapmap];0.92[JPT][hapmap];0.95[ASN][1000 genomes]
rs12821512	0.95[ASN][1000 genomes]
rs12830607	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1618331	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1626124	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1653598	0.88[CHB][hapmap]
rs1718119	0.88[CHB][hapmap]
rs1718133	0.88[CHB][hapmap]
rs1718136	0.88[CHB][hapmap]
rs1794895	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1794896	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1794897	0.80[EUR][1000 genomes]
rs1794899	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1794900	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1794902	1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs1796412	0.94[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1796413	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1796416	1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs1796417	0.98[ASN][1000 genomes]
rs1796421	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1796422	0.80[EUR][1000 genomes]
rs1796423	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs208278	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs208279	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs208282	0.95[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.90[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs208283	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs208298	0.88[CHB][hapmap]
rs208305	0.88[CHB][hapmap]
rs208307	0.88[CHB][hapmap]
rs208311	0.86[CHB][hapmap]
rs2263270	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2263271	0.81[EUR][1000 genomes]
rs2461473	0.97[ASN][1000 genomes]
rs2464842	0.87[ASN][1000 genomes]
rs2516210	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2567991	0.88[CHB][hapmap]
rs2708091	0.82[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs35694882	0.95[ASN][1000 genomes]
rs504677	0.88[CHB][hapmap]
rs523581	0.97[ASN][1000 genomes]
rs552299	0.97[ASN][1000 genomes]
rs589384	0.98[ASN][1000 genomes]
rs621255	0.98[ASN][1000 genomes]
rs637649	0.97[ASN][1000 genomes]
rs648316	0.97[ASN][1000 genomes]
rs651221	0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs651606	0.95[ASN][1000 genomes]
rs651673	0.97[ASN][1000 genomes]
rs652121	0.97[ASN][1000 genomes]
rs71454678	0.95[ASN][1000 genomes]
rs891781	0.88[CHB][hapmap]
rs9805004	1.00[CHB][hapmap];1.00[JPT][hapmap];0.95[ASN][1000 genomes]
rs9971689	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9971789	1.00[ASN][1000 genomes]
rs9971861	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9971870	0.98[ASN][1000 genomes]
rs9971935	0.98[ASN][1000 genomes]
rs9971953	1.00[ASN][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	nsv521928	chr12:121041728-121761800	Genic enhancers Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Enhancers Strong transcription ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	68 gene(s)	inside rSNPs	diseases
2	nsv899559	chr12:121324727-121592689	Active TSS Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
3	nsv899560	chr12:121371233-121560581	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer 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	23 gene(s)	inside rSNPs	diseases
4	nsv899562	chr12:121376416-121565870	Weak transcription Flanking Active TSS Active TSS Strong transcription Enhancers Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
5	esv2758318	chr12:121415845-121584813	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
6	esv2759917	chr12:121415845-121584813	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
7	nsv1039216	chr12:121421701-121538491	Active TSS Flanking Active TSS Enhancers Strong transcription Flanking Bivalent TSS/Enh Weak transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
8	nsv832531	chr12:121440495-121604232	Flanking Active TSS Enhancers Active TSS Strong transcription Weak transcription Genic enhancers 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	15 gene(s)	inside rSNPs	diseases
9	nsv560454	chr12:121457073-121745742	Strong transcription Enhancers Active TSS Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats 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	29 gene(s)	inside rSNPs	diseases
10	nsv430537	chr12:121487632-121579955	Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
11	nsv1054878	chr12:121519880-121761800	Flanking Active TSS Genic enhancers Strong transcription Weak transcription Enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	26 gene(s)	inside rSNPs	diseases
12	nsv455729	chr12:121525591-121761800	Enhancers Strong transcription Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
13	nsv560455	chr12:121525591-121761800	Weak transcription Strong transcription Enhancers Genic enhancers Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh 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	25 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:121531000-121534400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
2	chr12:121533000-121534600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr12:121533200-121534000	Bivalent/Poised TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr12:121533200-121534000	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
5	chr12:121533200-121534000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
6	chr12:121533200-121534000	Enhancers	Left Ventricle	heart
7	chr12:121533200-121534000	Enhancers	Stomach Mucosa	stomach
8	chr12:121533200-121534200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
9	chr12:121533200-121534200	Flanking Active TSS	Primary T helper naive cells fromperipheralblood	blood
10	chr12:121533200-121534200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
11	chr12:121533200-121534400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
12	chr12:121533200-121534400	Enhancers	Fetal Thymus	thymus
13	chr12:121533200-121534600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
14	chr12:121533200-121534600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
15	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
16	chr12:121533400-121534000	Active TSS	H9 Cell Line	embryonic stem cell
17	chr12:121533400-121534000	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
18	chr12:121533400-121534000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
19	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr12:121533400-121534000	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
21	chr12:121533400-121534000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
22	chr12:121533400-121534000	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
23	chr12:121533400-121534000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
24	chr12:121533400-121534000	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
25	chr12:121533400-121534000	Bivalent/Poised TSS	Muscle Satellite Cultured Cells	--
26	chr12:121533400-121534000	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
27	chr12:121533400-121534000	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr12:121533400-121534000	Flanking Active TSS	Brain Substantia Nigra	brain
30	chr12:121533400-121534000	Flanking Active TSS	Colonic Mucosa	Colon
31	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	Fetal Adrenal Gland	Adrenal Gland
32	chr12:121533400-121534000	Bivalent/Poised TSS	Fetal Brain Female	brain
33	chr12:121533400-121534000	Active TSS	Fetal Kidney	kidney
34	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	Fetal Muscle Trunk	muscle
35	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	Skeletal Muscle Male	skeletal muscle
36	chr12:121533400-121534000	Enhancers	Spleen	Spleen
37	chr12:121533400-121534000	Flanking Active TSS	Dnd41	blood
38	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	HepG2	liver
39	chr12:121533400-121534000	Bivalent/Poised TSS	NHDF-Ad	bronchial
40	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	NHEK	skin
41	chr12:121533400-121534000	Flanking Bivalent TSS/Enh	Osteobl	bone
42	chr12:121533400-121534200	Flanking Active TSS	Primary T cells from cord blood	blood
43	chr12:121533400-121534200	Flanking Active TSS	Primary hematopoietic stem cells	blood
44	chr12:121533400-121534200	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
45	chr12:121533400-121534200	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr12:121533400-121534200	Flanking Active TSS	Liver	Liver
47	chr12:121533400-121534200	Enhancers	Lung	lung
48	chr12:121533400-121534400	Enhancers	Breast Myoepithelial Primary Cells	Breast
49	chr12:121533400-121534400	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
50	chr12:121533400-121534400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood

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