Variant report

Variant	rs7332631
Chromosome Location	chr13:49142069-49142070
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr13:49141688..49143234-chr13:49148647..49150198,2	MCF-7	breast:
2	chr13:49115025..49117372-chr13:49140241..49143183,2	MCF-7	breast:
3	chr13:49106056..49107969-chr13:49140390..49142172,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000136161	Chromatin interaction

Extended variants
information (count: 54 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:42)

rs_ID	r²[population]
rs10076	1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs10467381	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11840819	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11842402	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11842662	1.00[EUR][1000 genomes]
rs13378245	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17071695	1.00[CHD][hapmap]
rs17071917	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17071960	1.00[EUR][1000 genomes]
rs174858	1.00[CHD][hapmap]
rs2804085	1.00[CHD][hapmap];1.00[MEX][hapmap]
rs2804088	0.82[MEX][hapmap]
rs3020646	1.00[CHD][hapmap];1.00[MEX][hapmap]
rs411862	1.00[CHD][hapmap];1.00[MEX][hapmap]
rs4151590	1.00[CHD][hapmap];1.00[MEX][hapmap];0.94[AMR][1000 genomes]
rs449268	1.00[CHD][hapmap]
rs7322110	0.83[AMR][1000 genomes]
rs7984270	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7990103	0.94[AMR][1000 genomes]
rs9316386	1.00[CHD][hapmap]
rs9316390	0.80[YRI][hapmap];1.00[AMR][1000 genomes]
rs9316391	1.00[AMR][1000 genomes]
rs9316392	1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs9316396	1.00[CHD][hapmap]
rs9316403	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9316404	0.93[AMR][1000 genomes]
rs9332025	1.00[ASW][hapmap];1.00[CHD][hapmap];1.00[MEX][hapmap];0.88[MKK][hapmap];1.00[TSI][hapmap];1.00[AMR][1000 genomes]
rs9332036	0.83[AMR][1000 genomes]
rs9332053	1.00[MEX][hapmap];1.00[TSI][hapmap];0.83[AMR][1000 genomes]
rs9332066	1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap]
rs9591163	0.82[AMR][1000 genomes]
rs9591167	0.83[AMR][1000 genomes]
rs9591170	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9591171	1.00[CHD][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.89[EUR][1000 genomes]
rs9591174	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9591175	0.83[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs9595894	0.87[AMR][1000 genomes]
rs9595909	0.94[AMR][1000 genomes]
rs9595910	0.94[AMR][1000 genomes]
rs9595917	0.83[AMR][1000 genomes]
rs9595930	1.00[EUR][1000 genomes]
rs9595936	1.00[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv832602	chr13:49003159-49167781	Active TSS Enhancers Flanking Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	15 gene(s)	inside rSNPs	diseases
2	nsv1041275	chr13:49045566-49242357	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers 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	14 gene(s)	inside rSNPs	diseases
3	nsv541769	chr13:49045566-49242357	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Genic enhancers Active TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
4	nsv832604	chr13:49061081-49281807	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	14 gene(s)	inside rSNPs	diseases
5	nsv1049117	chr13:49089476-49928945	Enhancers Strong transcription Weak transcription Genic enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
6	nsv455881	chr13:49134412-49169570	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
7	nsv561591	chr13:49134412-49169570	Weak transcription Active TSS Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
8	esv3510341	chr13:49141769-49142303	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	esv3510352	chr13:49141804-49142278	Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
10	esv3510363	chr13:49141835-49142237	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	esv3398572	chr13:49141926-49142179	Enhancers Active TSS Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
12	esv3510374	chr13:49141940-49142178	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:49135000-49155000	Enhancers	Primary monocytes fromperipheralblood	blood
2	chr13:49137200-49153000	Weak transcription	Duodenum Mucosa	Duodenum
3	chr13:49137400-49145200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr13:49138800-49145600	Weak transcription	HUVEC	blood vessel
5	chr13:49139000-49144800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
6	chr13:49139600-49144400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
7	chr13:49140000-49144200	Weak transcription	K562	blood
8	chr13:49140800-49146400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr13:49141000-49145000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr13:49141200-49142200	Enhancers	Rectal Smooth Muscle	rectum
11	chr13:49141200-49147000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr13:49141400-49142800	Enhancers	Duodenum Smooth Muscle	Duodenum
13	chr13:49141400-49143400	Enhancers	Stomach Mucosa	stomach
14	chr13:49141400-49144800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
15	chr13:49141400-49145800	Enhancers	Fetal Stomach	stomach
16	chr13:49141400-49146200	Enhancers	HepG2	liver
17	chr13:49141400-49146400	Enhancers	Fetal Lung	lung
18	chr13:49141400-49146600	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr13:49141600-49142400	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr13:49141600-49142600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr13:49141600-49142600	Enhancers	Primary hematopoietic stem cells	blood
22	chr13:49141600-49142600	Flanking Active TSS	Colon Smooth Muscle	Colon
23	chr13:49141600-49142600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
24	chr13:49141600-49142600	Flanking Active TSS	HSMMtube	muscle
25	chr13:49141800-49142200	Enhancers	Ovary	ovary
26	chr13:49141800-49142400	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chr13:49141800-49142400	Active TSS	Psoas Muscle	Psoas
28	chr13:49141800-49142400	Active TSS	NHDF-Ad	bronchial
29	chr13:49141800-49142600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr13:49141800-49142600	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr13:49141800-49142600	Flanking Active TSS	Skeletal Muscle Male	skeletal muscle
32	chr13:49141800-49144000	Weak transcription	Fetal Kidney	kidney
33	chr13:49141800-49144200	Bivalent Enhancer	Primary B cells from cord blood	blood
34	chr13:49141800-49145600	Enhancers	Dnd41	blood
35	chr13:49141800-49145800	Enhancers	Placenta	Placenta
36	chr13:49141800-49146000	Enhancers	Fetal Muscle Leg	muscle
37	chr13:49141800-49150200	Weak transcription	Aorta	Aorta
38	chr13:49142000-49142200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:49142000-49142200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chr13:49142000-49142200	Active TSS	Stomach Smooth Muscle	stomach
41	chr13:49142000-49142200	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr13:49142000-49142400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr13:49142000-49142400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr13:49142000-49142400	Flanking Active TSS	HSMM	muscle
45	chr13:49142000-49142400	Flanking Active TSS	Osteobl	bone
46	chr13:49142000-49142600	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr13:49142000-49142600	Flanking Active TSS	Adipose Nuclei	Adipose
48	chr13:49142000-49142600	Enhancers	HMEC	breast
49	chr13:49142000-49142800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr13:49142000-49143000	Weak transcription	Brain Anterior Caudate	brain

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