Variant report

Variant	rs7128469
Chromosome Location	chr11:9142797-9142798
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr11:9131737..9134967-chr11:9139541..9142848,3	MCF-7	breast:
2	chr11:9142265..9143151-chr11:9527999..9528931,2	K562	blood:
3	chr11:9114649..9115533-chr11:9142208..9142895,3	MCF-7	breast:
4	chr11:9113356..9115182-chr11:9141033..9143763,3	MCF-7	breast:
5	chr11:9142149..9143121-chr19:58289599..58290538,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DENND5A-1	chr11:9142717-9142948	XLOC_009370

Extended variants
information (count: 53 )
Associated
traits (count: 4 )

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

rs_ID	r²[population]
rs10047438	0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs1039210	0.80[CEU][hapmap];0.92[JPT][hapmap];0.94[YRI][hapmap];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10769991	0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs10769992	0.88[CEU][hapmap]
rs10769994	0.81[AFR][1000 genomes];0.92[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs10769995	0.92[JPT][hapmap];0.89[YRI][hapmap]
rs10769996	0.92[JPT][hapmap]
rs10769997	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10769998	0.81[AMR][1000 genomes]
rs10770006	0.89[YRI][hapmap]
rs10770008	0.89[YRI][hapmap]
rs10770010	0.89[YRI][hapmap]
rs10840175	0.94[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10840176	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10840178	0.83[ASN][1000 genomes]
rs10840179	0.84[ASN][1000 genomes]
rs10840183	0.85[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs10840185	0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs11042188	0.89[ASN][1000 genomes]
rs11042189	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs11042195	0.92[JPT][hapmap];0.82[ASN][1000 genomes]
rs11042200	0.83[CEU][hapmap];0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs11604616	0.92[JPT][hapmap];0.83[ASN][1000 genomes]
rs12291375	0.86[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs17256375	0.92[JPT][hapmap]
rs1827011	0.92[CEU][hapmap];0.86[CHB][hapmap];0.93[GIH][hapmap];0.91[MEX][hapmap];0.82[TSI][hapmap];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs1874822	0.96[CEU][hapmap];0.91[JPT][hapmap];0.94[AMR][1000 genomes];0.94[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1997628	0.82[ASN][1000 genomes]
rs2133217	0.80[CEU][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs2291839	0.82[JPT][hapmap]
rs2316087	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2647533	0.88[CEU][hapmap]
rs2647537	0.92[CEU][hapmap];0.93[GIH][hapmap];0.84[JPT][hapmap];0.83[MEX][hapmap];0.84[EUR][1000 genomes]
rs2742556	0.87[ASW][hapmap];0.96[CEU][hapmap];0.93[GIH][hapmap];0.92[JPT][hapmap];0.91[MEX][hapmap];0.82[MKK][hapmap];0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs2742557	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs4910035	0.92[AMR][1000 genomes];0.91[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs5011703	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs7109745	0.93[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs7121013	0.83[YRI][hapmap]
rs7123970	0.92[JPT][hapmap];0.89[YRI][hapmap]
rs7394878	0.82[JPT][hapmap];0.87[MEX][hapmap]
rs7395151	0.84[CEU][hapmap];0.89[YRI][hapmap];0.91[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs7395347	0.92[JPT][hapmap];0.84[ASN][1000 genomes]
rs7395846	0.95[CEU][hapmap];0.91[JPT][hapmap];0.94[YRI][hapmap];0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs7396705	0.81[AFR][1000 genomes];0.93[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs7925308	0.82[JPT][hapmap]
rs7930507	0.82[JPT][hapmap];0.91[MEX][hapmap]
rs7931872	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7947251	0.96[CEU][hapmap];0.92[JPT][hapmap];0.94[AMR][1000 genomes];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9888257	0.82[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3413845	chr11:8887279-9285127	Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	47 gene(s)	inside rSNPs	diseases
2	esv33264	chr11:9007612-9311131	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
3	nsv896985	chr11:9013002-9152463	Weak transcription Enhancers Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs7128469	TRIM5	cis	cerebellum	SCAN
rs7128469	OR56A1	cis	cerebellum	SCAN
rs7128469	TMEM41B	cis	multi-tissue	Pritchard
rs7128469	EIF4G2	cis	cerebellum	SCAN

Chromatin state (count:55 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr11:9113600-9159800	Weak transcription	Right Ventricle	heart
2	chr11:9121800-9154800	Weak transcription	Brain Substantia Nigra	brain
3	chr11:9125000-9142800	Weak transcription	Left Ventricle	heart
4	chr11:9130800-9153600	Weak transcription	Brain Angular Gyrus	brain
5	chr11:9131200-9143000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
6	chr11:9132000-9153200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr11:9134000-9153000	Weak transcription	Brain Germinal Matrix	brain
8	chr11:9134000-9154000	Weak transcription	Osteobl	bone
9	chr11:9134200-9154000	Weak transcription	NHDF-Ad	bronchial
10	chr11:9134800-9159000	Weak transcription	Brain Hippocampus Middle	brain
11	chr11:9134800-9161200	Weak transcription	Fetal Brain Male	brain
12	chr11:9135200-9152600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr11:9135400-9143000	Weak transcription	Fetal Muscle Trunk	muscle
14	chr11:9135600-9153000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr11:9136400-9159200	Weak transcription	Brain Anterior Caudate	brain
16	chr11:9136800-9143000	Weak transcription	Fetal Brain Female	brain
17	chr11:9137200-9145400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr11:9137200-9159000	Weak transcription	Fetal Heart	heart
19	chr11:9137800-9146200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr11:9141200-9144000	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
21	chr11:9141200-9153000	Weak transcription	Stomach Smooth Muscle	stomach
22	chr11:9141400-9151800	Weak transcription	Psoas Muscle	Psoas
23	chr11:9141400-9153600	Weak transcription	Primary T cells from cord blood	blood
24	chr11:9141400-9153800	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr11:9141600-9151800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr11:9141600-9158400	Weak transcription	Pancreas	Pancrea
27	chr11:9141800-9143600	Enhancers	iPS-15b Cell Line	embryonic stem cell
28	chr11:9141800-9143600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr11:9141800-9143800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr11:9142000-9142800	Genic enhancers	HSMM	muscle
31	chr11:9142000-9143600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr11:9142000-9143600	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
33	chr11:9142000-9148400	Weak transcription	Right Atrium	heart
34	chr11:9142000-9157200	Weak transcription	NHLF	lung
35	chr11:9142200-9142800	Enhancers	K562	blood
36	chr11:9142200-9143400	Enhancers	H9 Cell Line	embryonic stem cell
37	chr11:9142200-9143400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
38	chr11:9142200-9143600	Enhancers	H1 Cell Line	embryonic stem cell
39	chr11:9142400-9142800	Enhancers	Fetal Muscle Leg	muscle
40	chr11:9142400-9143000	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr11:9142400-9143400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr11:9142400-9143400	Strong transcription	Aorta	Aorta
43	chr11:9142400-9143800	Strong transcription	Fetal Stomach	stomach
44	chr11:9142400-9163000	Weak transcription	Placenta Amnion	Placenta Amnion
45	chr11:9142600-9142800	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr11:9142600-9142800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr11:9142600-9142800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr11:9142600-9142800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr11:9142600-9143000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr11:9142600-9143600	Enhancers	HUES6 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links