Variant report

Variant	rs4146961
Chromosome Location	chr9:85627554-85627555
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr9:85624001..85625732-chr9:85627362..85629069,2	MCF-7	breast:
2	chr9:85626061..85627670-chr9:85628324..85631017,2	MCF-7	breast:
3	chr9:85619463..85621402-chr9:85626088..85628025,2	MCF-7	breast:
4	chr9:85624665..85627555-chr9:85675813..85678218,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000165105	Chromatin interaction

Extended variants
information (count: 74 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:72)

rs_ID	r²[population]
rs1008171	0.89[CEU][hapmap];0.85[CHB][hapmap];1.00[JPT][hapmap];0.83[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1010480	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs10115768	0.91[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10116216	0.81[CEU][hapmap]
rs10116254	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10121156	0.81[EUR][1000 genomes]
rs10121204	1.00[CEU][hapmap];0.96[YRI][hapmap];0.93[AFR][1000 genomes];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs10121376	0.86[EUR][1000 genomes]
rs10121395	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10126033	0.96[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs10735559	0.89[CEU][hapmap];0.81[EUR][1000 genomes]
rs10746694	0.95[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10780561	0.92[CEU][hapmap];0.82[EUR][1000 genomes]
rs10780562	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs10780563	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10780564	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10780565	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10780567	1.00[CEU][hapmap];0.85[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs10867924	0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.94[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs10867925	0.94[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs10867926	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs10867927	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10867928	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10867929	1.00[CEU][hapmap];0.83[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs10867930	0.81[JPT][hapmap]
rs1125915	0.82[CEU][hapmap]
rs13302349	0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1393562	1.00[CEU][hapmap];0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs1393563	0.89[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1393564	0.93[CEU][hapmap];0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1393565	1.00[CEU][hapmap];0.89[EUR][1000 genomes]
rs1502682	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1502683	0.89[CEU][hapmap]
rs1502684	0.89[CEU][hapmap];0.83[EUR][1000 genomes]
rs1502685	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs1546315	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.91[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1546316	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1546317	1.00[CEU][hapmap];0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs1580881	1.00[CEU][hapmap];0.91[YRI][hapmap];0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs1976455	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs1995423	0.90[JPT][hapmap]
rs2062761	0.81[CEU][hapmap];0.95[JPT][hapmap];0.90[ASN][1000 genomes]
rs2279814	1.00[CEU][hapmap];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs29001503	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs4146960	1.00[CEU][hapmap];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4301515	1.00[CEU][hapmap];0.87[CHB][hapmap];1.00[JPT][hapmap];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs4348583	0.96[CEU][hapmap];0.96[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs4355855	0.89[CEU][hapmap];0.82[EUR][1000 genomes]
rs4385545	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs4391505	0.89[CEU][hapmap]
rs4460464	0.81[CEU][hapmap]
rs4623517	1.00[CEU][hapmap];0.87[EUR][1000 genomes]
rs4628323	0.91[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs4877244	1.00[CEU][hapmap];0.94[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs4877725	0.89[CEU][hapmap]
rs4877726	0.85[JPT][hapmap]
rs6559693	0.83[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6559694	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6559695	0.96[CEU][hapmap];0.81[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs7019227	1.00[CEU][hapmap];0.95[YRI][hapmap];0.93[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7024864	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7029133	0.85[AMR][1000 genomes]
rs7045914	0.89[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7847666	1.00[CEU][hapmap];0.86[CHB][hapmap];1.00[JPT][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs7854101	1.00[CEU][hapmap];0.93[CHB][hapmap];1.00[JPT][hapmap];0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7864688	0.81[EUR][1000 genomes]
rs7866666	1.00[CEU][hapmap];0.95[YRI][hapmap];0.88[AFR][1000 genomes];0.97[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs7867614	0.89[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7872982	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs871512	0.90[JPT][hapmap]
rs952450	1.00[CEU][hapmap];0.96[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs998119	0.96[AMR][1000 genomes];0.92[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	nsv1050771	chr9:85416931-85643417	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv893511	chr9:85495968-85833127	Weak transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:35 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:85594800-85628200	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr9:85603000-85628200	Weak transcription	Fetal Stomach	stomach
3	chr9:85603200-85643800	Weak transcription	Duodenum Mucosa	Duodenum
4	chr9:85608800-85628000	Weak transcription	Fetal Kidney	kidney
5	chr9:85610800-85642000	Weak transcription	Fetal Intestine Large	intestine
6	chr9:85613600-85643400	Weak transcription	Colonic Mucosa	Colon
7	chr9:85617200-85628000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr9:85617200-85628200	Weak transcription	HMEC	breast
9	chr9:85617200-85645800	Weak transcription	Stomach Mucosa	stomach
10	chr9:85621000-85645400	Weak transcription	Gastric	stomach
11	chr9:85623000-85628400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr9:85623200-85630600	Weak transcription	Cortex derived primary cultured neurospheres	brain
13	chr9:85623600-85634800	Weak transcription	Pancreas	Pancrea
14	chr9:85623600-85643200	Weak transcription	Fetal Intestine Small	intestine
15	chr9:85625800-85628000	Weak transcription	Rectal Mucosa Donor 31	rectum
16	chr9:85626000-85629800	Enhancers	Osteobl	bone
17	chr9:85626200-85629800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr9:85626400-85628200	Weak transcription	Aorta	Aorta
19	chr9:85626600-85629600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr9:85626600-85629800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr9:85626600-85629800	Enhancers	Muscle Satellite Cultured Cells	--
22	chr9:85626800-85628200	Enhancers	Fetal Lung	lung
23	chr9:85626800-85628600	Enhancers	Primary T cells from cord blood	blood
24	chr9:85627000-85628000	Enhancers	NHDF-Ad	bronchial
25	chr9:85627000-85628200	Enhancers	A549	lung
26	chr9:85627000-85630200	Enhancers	NHLF	lung
27	chr9:85627200-85628000	Enhancers	Adipose Nuclei	Adipose
28	chr9:85627200-85628000	Weak transcription	Rectal Smooth Muscle	rectum
29	chr9:85627200-85628200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr9:85627200-85628200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
31	chr9:85627200-85628200	Weak transcription	Colon Smooth Muscle	Colon
32	chr9:85627200-85629000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr9:85627200-85630000	Enhancers	NH-A	brain
34	chr9:85627400-85627800	Weak transcription	Rectal Mucosa Donor 29	rectum
35	chr9:85627400-85629000	Enhancers	ES-I3 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links