Variant report

Variant	rs2157581
Chromosome Location	chr1:169499190-169499191
allele	A/G
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:11)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:169447411..169449419-chr1:169497697..169499792,2	MCF-7	breast:
2	chr1:169478952..169480932-chr1:169498032..169500995,2	MCF-7	breast:
3	chr1:169449894..169459462-chr1:169475885..169501963,75	MCF-7	breast:
4	chr1:169490192..169493609-chr1:169495804..169500257,7	MCF-7	breast:
5	chr1:169485353..169488291-chr1:169497708..169499497,2	K562	blood:
6	chr1:169475721..169488506-chr1:169493331..169501885,21	MCF-7	breast:
7	chr1:169464842..169466756-chr1:169497919..169499478,2	MCF-7	breast:
8	chr1:169452411..169456753-chr1:169494976..169501006,10	MCF-7	breast:
9	chr1:169480009..169482936-chr1:169495810..169499823,3	K562	blood:
10	chr1:169454264..169456422-chr1:169495447..169500944,4	K562	blood:
11	chr1:169461099..169462759-chr1:169496804..169499532,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000213062	Chromatin interaction
ENSG00000117479	Chromatin interaction
ENSG00000198734	Chromatin interaction

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs1046712	0.93[ASN][1000 genomes]
rs10800454	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10800456	0.90[ASN][1000 genomes]
rs1557570	0.87[EUR][1000 genomes]
rs1557572	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1894694	0.90[ASN][1000 genomes]
rs2239852	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2301515	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs3820060	0.85[EUR][1000 genomes]
rs4656185	0.84[EUR][1000 genomes]
rs4656687	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs6030	0.89[EUR][1000 genomes]
rs61805767	1.00[ASN][1000 genomes]
rs6686805	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs6701330	0.88[EUR][1000 genomes]
rs7535409	0.85[EUR][1000 genomes]
rs916438	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9332599	0.81[EUR][1000 genomes]
rs9332665	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv10418	chr1:169059628-169621268	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats 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	56 gene(s)	inside rSNPs	diseases
2	nsv872533	chr1:169490401-169508576	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:45 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:169484800-169501000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
2	chr1:169485400-169510600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
3	chr1:169487400-169501000	Weak transcription	Right Ventricle	heart
4	chr1:169491600-169500800	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
5	chr1:169492000-169499800	Weak transcription	Left Ventricle	heart
6	chr1:169494000-169502800	Strong transcription	HepG2	liver
7	chr1:169494800-169499200	Enhancers	Stomach Mucosa	stomach
8	chr1:169496000-169499200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr1:169496000-169515200	Strong transcription	Liver	Liver
10	chr1:169496800-169500000	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chr1:169497200-169499200	Enhancers	H1 Cell Line	embryonic stem cell
12	chr1:169497200-169499400	Enhancers	Fetal Intestine Large	intestine
13	chr1:169497200-169499600	Enhancers	Dnd41	blood
14	chr1:169497200-169500000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr1:169497600-169499800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr1:169498200-169499200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr1:169498200-169499200	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr1:169498200-169499200	Enhancers	Hela-S3	cervix
19	chr1:169498200-169500000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr1:169498400-169499200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
21	chr1:169498400-169499600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:169498400-169499600	Enhancers	Fetal Intestine Small	intestine
23	chr1:169498400-169499800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr1:169498400-169524000	Weak transcription	Placenta	Placenta
25	chr1:169498600-169499400	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr1:169498600-169500200	Enhancers	HSMMtube	muscle
27	chr1:169498600-169506200	Strong transcription	Monocytes-CD14+_RO01746	blood
28	chr1:169498600-169507600	Weak transcription	Pancreatic Islets	Pancreatic Islet
29	chr1:169498800-169499200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
30	chr1:169498800-169499200	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
31	chr1:169498800-169499400	Weak transcription	K562	blood
32	chr1:169498800-169501600	Strong transcription	Primary monocytes fromperipheralblood	blood
33	chr1:169499000-169499200	Enhancers	Rectal Mucosa Donor 29	rectum
34	chr1:169499000-169499600	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr1:169499000-169500000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chr1:169499000-169500000	Weak transcription	Placenta Amnion	Placenta Amnion
37	chr1:169499000-169500000	Weak transcription	HSMM	muscle
38	chr1:169499000-169500200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr1:169499000-169500200	Enhancers	HMEC	breast
40	chr1:169499000-169500200	Enhancers	NHEK	skin
41	chr1:169499000-169500600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr1:169499000-169501800	Strong transcription	Primary neutrophils fromperipheralblood	blood
43	chr1:169499000-169504200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr1:169499000-169508400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
45	chr1:169499000-169519000	Weak transcription	Primary T helper cells fromperipheralblood	blood

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