Variant report

Variant	rs352153
Chromosome Location	chr3:52211184-52211185
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr3:52209175..52211275-chr3:52220260..52222070,2	K562	blood:
2	chr3:52206232..52208818-chr3:52209949..52213336,4	K562	blood:
3	chr3:52208921..52211752-chr3:52239089..52241335,2	MCF-7	breast:
4	chr3:52209128..52211243-chr3:52227235..52228874,2	MCF-7	breast:
5	chr3:52205965..52208673-chr3:52209831..52213095,4	K562	blood:

Variant related genes	Relation type
ENSG00000023330	Chromatin interaction

Extended variants
information (count: 59 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs123681	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12386365	0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13314125	0.94[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13319566	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs164638	0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs164639	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17051957	0.91[EUR][1000 genomes]
rs17051977	0.87[AFR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs171294	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs183029	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2304505	0.87[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28452586	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs28659792	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs352146	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs352147	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs352148	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs352149	0.81[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs352150	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs352151	0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs55664415	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs55834589	0.88[EUR][1000 genomes]
rs56281986	0.98[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs56322622	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs57335685	0.91[EUR][1000 genomes]
rs57466127	0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs59890038	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6781635	0.94[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs72964042	0.85[EUR][1000 genomes]
rs72964044	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs7638246	0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs808787	0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs876782	0.91[EUR][1000 genomes]
rs893056	0.94[EUR][1000 genomes]
rs9809254	0.88[EUR][1000 genomes]
rs9809977	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9811707	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9815010	0.93[AMR][1000 genomes];1.00[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9816434	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9817653	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9830293	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9841469	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9843299	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9843852	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9846049	0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs9847073	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9847092	0.94[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9857878	0.94[EUR][1000 genomes]
rs9860982	0.91[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9868101	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9882775	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv519445	chr3:52004317-52367932	Bivalent/Poised TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	134 gene(s)	inside rSNPs	diseases
2	nsv876786	chr3:52041566-52236762	Enhancers Strong transcription Flanking Active TSS Weak transcription Transcr. at gene 5' and 3' Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
3	nsv984541	chr3:52055970-52285682	Genic enhancers Active TSS Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	45 gene(s)	inside rSNPs	diseases
4	nsv470572	chr3:52123313-52350212	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	103 gene(s)	inside rSNPs	diseases
5	nsv460537	chr3:52148233-52290550	Active TSS Weak transcription Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
6	nsv590301	chr3:52148233-52290550	Enhancers Flanking Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
7	nsv508218	chr3:52155869-52290410	Active TSS Flanking Active TSS Weak transcription Enhancers Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	41 gene(s)	inside rSNPs	diseases
8	nsv834694	chr3:52178983-52335821	Flanking Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	102 gene(s)	inside rSNPs	diseases
9	nsv834695	chr3:52199701-52400577	Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	98 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:30 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:52204800-52215600	Weak transcription	Right Ventricle	heart
2	chr3:52208400-52212800	Enhancers	Primary monocytes fromperipheralblood	blood
3	chr3:52209200-52212000	Enhancers	Spleen	Spleen
4	chr3:52209400-52211200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
5	chr3:52209800-52211600	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr3:52210000-52212200	Enhancers	Esophagus	oesophagus
7	chr3:52210000-52218200	Enhancers	Liver	Liver
8	chr3:52210200-52213200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr3:52210400-52211600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr3:52210400-52212000	Enhancers	Gastric	stomach
11	chr3:52210400-52212200	Enhancers	Adipose Nuclei	Adipose
12	chr3:52210400-52212200	Flanking Active TSS	HepG2	liver
13	chr3:52210400-52213200	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr3:52210600-52211400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
15	chr3:52210600-52211600	Enhancers	Lung	lung
16	chr3:52210600-52211600	Enhancers	NHEK	skin
17	chr3:52210600-52212000	Enhancers	Stomach Mucosa	stomach
18	chr3:52210600-52212600	Enhancers	Fetal Lung	lung
19	chr3:52210800-52211200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
20	chr3:52211000-52211200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr3:52211000-52211200	Flanking Active TSS	Hela-S3	cervix
22	chr3:52211000-52211400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr3:52211000-52211600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr3:52211000-52211600	Enhancers	HMEC	breast
25	chr3:52211000-52211800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr3:52211000-52212000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr3:52211000-52212000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
28	chr3:52211000-52212000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr3:52211000-52212600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
30	chr3:52211000-52212800	Enhancers	Placenta	Placenta

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links