Variant report

Variant	rs12573451
Chromosome Location	chr10:28537830-28537831
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	chr10:28537244..28539673-chr10:28551271..28553158,2	MCF-7	breast:

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:8)

rs_ID	r²[population]
rs11006896	0.84[JPT][hapmap]
rs11006897	0.84[JPT][hapmap]
rs11006920	0.83[JPT][hapmap]
rs1148174	0.92[CHD][hapmap]
rs12268470	0.94[JPT][hapmap]
rs1413905	0.85[CHB][hapmap];0.80[JPT][hapmap];0.89[ASN][1000 genomes]
rs7908075	1.00[CEU][hapmap];1.00[TSI][hapmap]
rs9663446	0.81[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv917149	chr10:28018919-28688694	Enhancers Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	16 gene(s)	inside rSNPs	diseases
2	nsv525448	chr10:28337570-28563732	Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
3	nsv831817	chr10:28369836-28539930	Enhancers ZNF genes & repeats Active TSS Flanking Active TSS Weak transcription Strong transcription Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	nsv1041555	chr10:28419399-29304934	Flanking Bivalent TSS/Enh Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases
5	nsv1037863	chr10:28419399-29378871	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Bivalent Enhancer 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 miRNA target site	46 gene(s)	inside rSNPs	diseases
6	nsv540521	chr10:28419399-29378871	Flanking Active TSS Enhancers Weak transcription Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:36 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr10:28519000-28552000	Weak transcription	Fetal Stomach	stomach
2	chr10:28521200-28538600	Weak transcription	Left Ventricle	heart
3	chr10:28521800-28544400	Weak transcription	Pancreas	Pancrea
4	chr10:28527600-28539600	Weak transcription	Duodenum Smooth Muscle	Duodenum
5	chr10:28532400-28541200	Weak transcription	Stomach Smooth Muscle	stomach
6	chr10:28535600-28538200	Enhancers	Primary neutrophils fromperipheralblood	blood
7	chr10:28535800-28541200	Weak transcription	Psoas Muscle	Psoas
8	chr10:28535800-28551600	Weak transcription	Fetal Intestine Small	intestine
9	chr10:28536600-28538000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr10:28536600-28538000	Enhancers	HMEC	breast
11	chr10:28536800-28538000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr10:28536800-28538800	Enhancers	Primary monocytes fromperipheralblood	blood
13	chr10:28537400-28538400	Weak transcription	Right Atrium	heart
14	chr10:28537400-28538400	Weak transcription	Right Ventricle	heart
15	chr10:28537400-28552600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr10:28537600-28538000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
17	chr10:28537600-28538000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
18	chr10:28537600-28538000	Enhancers	NHEK	skin
19	chr10:28537600-28539400	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr10:28537600-28539600	Weak transcription	Colon Smooth Muscle	Colon
21	chr10:28537600-28539600	Weak transcription	HSMM	muscle
22	chr10:28537600-28540600	Weak transcription	Aorta	Aorta
23	chr10:28537600-28540600	Weak transcription	HSMMtube	muscle
24	chr10:28537600-28543000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr10:28537600-28549400	Weak transcription	Primary T helper cells fromperipheralblood	blood
26	chr10:28537600-28552600	Weak transcription	Primary T cells from cord blood	blood
27	chr10:28537800-28538200	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr10:28537800-28538800	Enhancers	Monocytes-CD14+_RO01746	blood
29	chr10:28537800-28541800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr10:28537800-28541800	Weak transcription	Esophagus	oesophagus
31	chr10:28537800-28542800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr10:28537800-28543000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
33	chr10:28537800-28543000	Weak transcription	Primary B cells from cord blood	blood
34	chr10:28537800-28543200	Weak transcription	Primary hematopoietic stem cells	blood
35	chr10:28537800-28543600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr10:28537800-28550200	Weak transcription	Primary T helper cells PMA-I stimulated	--

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