Variant report

Variant	rs10265373
Chromosome Location	chr7:17966552-17966553
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:17941921..17944497-chr7:17966021..17968110,2	K562	blood:
2	chr7:17963843..17966777-chr7:17969342..17971472,2	K562	blood:
3	chr7:17965161..17967568-chr7:17969266..17972579,3	K562	blood:

Extended variants
information (count: 103 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:93)

rs_ID	r²[population]
rs10216315	0.94[ASW][hapmap];1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.95[MEX][hapmap];0.94[MKK][hapmap];0.98[TSI][hapmap];0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10227224	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10227501	0.95[CEU][hapmap];0.94[CHB][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs10227582	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10231926	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs10233816	0.84[ASW][hapmap];0.96[CEU][hapmap];0.87[JPT][hapmap];0.84[LWK][hapmap];0.92[YRI][hapmap];0.86[AFR][1000 genomes]
rs10447542	0.96[CEU][hapmap]
rs11768866	0.86[CHB][hapmap];0.97[CHD][hapmap];0.84[GIH][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs11973277	0.96[CEU][hapmap];0.86[JPT][hapmap];0.92[YRI][hapmap];0.95[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs11983260	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.98[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12699918	0.82[CHB][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs12699919	0.96[CEU][hapmap];0.87[JPT][hapmap]
rs1357796	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs1404414	0.81[GIH][hapmap]
rs1404422	0.81[GIH][hapmap]
rs1404424	0.87[ASN][1000 genomes]
rs1464804	1.00[CHB][hapmap];0.88[ASN][1000 genomes]
rs1524775	0.81[CHB][hapmap];0.92[CHD][hapmap];0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs1524776	0.86[CHB][hapmap];0.81[CHD][hapmap];0.81[GIH][hapmap];0.86[JPT][hapmap]
rs1568815	1.00[CEU][hapmap];0.87[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1568817	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.80[AFR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1568818	0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2103144	0.88[ASN][1000 genomes]
rs2177652	0.86[CHB][hapmap];0.82[CHD][hapmap];0.86[JPT][hapmap]
rs2691555	0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs2691557	0.87[ASN][1000 genomes]
rs2691558	0.84[AFR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2691559	0.85[CHB][hapmap];0.90[JPT][hapmap];0.87[ASN][1000 genomes]
rs2691560	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691561	0.94[ASW][hapmap];0.96[CEU][hapmap];0.95[CHB][hapmap];0.97[CHD][hapmap];0.95[GIH][hapmap];1.00[JPT][hapmap];0.93[LWK][hapmap];0.96[MEX][hapmap];0.91[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691562	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691563	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691564	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691565	0.84[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2691566	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691567	0.83[AFR][1000 genomes];0.86[AMR][1000 genomes];0.91[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2691568	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691569	0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691570	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[JPT][hapmap];0.86[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691571	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2691572	0.92[CEU][hapmap];0.87[JPT][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes]
rs2691574	0.96[CEU][hapmap];0.85[JPT][hapmap];0.95[YRI][hapmap]
rs2691576	0.89[ASW][hapmap];0.96[CEU][hapmap];0.87[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes]
rs2691577	0.84[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2691578	0.93[ASN][1000 genomes]
rs2691579	0.85[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs2691580	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs2691583	0.81[GIH][hapmap]
rs2691600	0.86[CHB][hapmap];0.85[JPT][hapmap]
rs2691601	0.81[GIH][hapmap]
rs2691609	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs2691611	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs2691612	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs2691615	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2714853	0.84[AFR][1000 genomes]
rs2714854	0.89[ASW][hapmap];0.96[CEU][hapmap];0.87[JPT][hapmap];0.85[LWK][hapmap];0.91[MEX][hapmap];0.92[YRI][hapmap];0.84[AFR][1000 genomes]
rs2714855	0.96[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.83[AFR][1000 genomes];0.93[ASN][1000 genomes]
rs2714856	0.85[AFR][1000 genomes]
rs2714857	1.00[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2714858	0.96[CEU][hapmap];0.87[JPT][hapmap];0.85[LWK][hapmap];0.89[YRI][hapmap];0.84[AFR][1000 genomes]
rs2714859	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.92[YRI][hapmap];0.80[AFR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2714860	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2714861	0.82[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2714863	0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2714864	0.91[CHB][hapmap];0.97[CHD][hapmap];1.00[JPT][hapmap];0.81[LWK][hapmap];0.81[YRI][hapmap];0.98[ASN][1000 genomes]
rs2714865	0.86[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2714866	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.89[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2714867	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.87[AFR][1000 genomes];0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2714868	1.00[CEU][hapmap];0.94[CHB][hapmap];0.95[JPT][hapmap];0.91[YRI][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2714869	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2714870	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.96[YRI][hapmap];0.83[AFR][1000 genomes];0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2714871	0.95[CHB][hapmap];0.81[CHD][hapmap];0.84[ASN][1000 genomes]
rs2714872	0.95[CHB][hapmap];0.81[CHD][hapmap];0.87[ASN][1000 genomes]
rs2714878	1.00[CEU][hapmap];0.81[CHB][hapmap];0.92[YRI][hapmap];0.97[EUR][1000 genomes]
rs2723494	0.81[GIH][hapmap]
rs2723501	0.81[GIH][hapmap]
rs2723502	0.81[GIH][hapmap]
rs2723515	0.81[GIH][hapmap]
rs2723540	0.86[CHB][hapmap];0.86[JPT][hapmap];0.82[ASN][1000 genomes]
rs2723553	0.81[GIH][hapmap]
rs35819944	0.88[ASN][1000 genomes]
rs4532510	0.89[ASN][1000 genomes]
rs4543433	0.86[CHB][hapmap];0.97[CHD][hapmap];0.87[GIH][hapmap];0.91[JPT][hapmap];0.89[ASN][1000 genomes]
rs4719525	0.87[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4721670	0.81[AFR][1000 genomes]
rs4721671	0.95[CHB][hapmap];0.82[CHD][hapmap];1.00[JPT][hapmap];0.93[ASN][1000 genomes]
rs6952907	0.96[CEU][hapmap];0.86[JPT][hapmap];0.92[YRI][hapmap];0.93[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs6955984	0.83[ASN][1000 genomes]
rs6962380	0.96[CEU][hapmap];0.87[JPT][hapmap]
rs6973480	0.82[CHD][hapmap];0.81[GIH][hapmap];0.91[JPT][hapmap];0.81[ASN][1000 genomes]
rs7802343	0.96[CEU][hapmap];0.86[JPT][hapmap];0.93[LWK][hapmap];0.92[YRI][hapmap];0.92[AFR][1000 genomes]
rs949451	0.81[GIH][hapmap]
rs9942602	0.83[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv533938	chr7:17254118-18040301	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	32 gene(s)	inside rSNPs	diseases
2	nsv1024398	chr7:17630148-18545073	Strong transcription Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
3	nsv538764	chr7:17630148-18545073	Strong transcription Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
4	nsv830913	chr7:17848480-18034218	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
5	nsv1026629	chr7:17862477-18362404	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
6	nsv1025023	chr7:17865796-18357630	Enhancers Active TSS Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases
7	nsv1030201	chr7:17898410-18491985	Enhancers Strong transcription Active TSS Bivalent/Poised TSS Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	16 gene(s)	inside rSNPs	diseases
8	nsv887808	chr7:17920613-18150005	Enhancers Flanking Active TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1018517	chr7:17926468-18127372	Weak transcription Flanking Bivalent TSS/Enh Strong transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv606357	chr7:17938491-18375245	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs10265373	SNX13	cis	Adipose Subcutaneous	GTEx

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17911400-17977400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:17955000-17977400	Weak transcription	Fetal Intestine Small	intestine
3	chr7:17955400-17967000	Weak transcription	Lung	lung
4	chr7:17955400-17973000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr7:17959000-17971400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:17959600-17972800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr7:17960800-17967800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
8	chr7:17960800-17970200	Weak transcription	Primary T cells fromperipheralblood	blood
9	chr7:17961000-17971200	Weak transcription	Primary T cells from cord blood	blood
10	chr7:17961800-17977400	Weak transcription	Brain Angular Gyrus	brain
11	chr7:17961800-17978800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr7:17962000-17967600	Weak transcription	Small Intestine	intestine
13	chr7:17962000-17970200	Weak transcription	Primary B cells from peripheral blood	blood
14	chr7:17962000-17970200	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr7:17962000-17973400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
16	chr7:17962000-17975800	Weak transcription	Hela-S3	cervix
17	chr7:17962200-17973200	Weak transcription	Primary B cells from cord blood	blood
18	chr7:17962200-17977400	Weak transcription	Brain Cingulate Gyrus	brain
19	chr7:17962400-17978600	Weak transcription	Aorta	Aorta
20	chr7:17963400-17967200	Weak transcription	Primary T helper cells fromperipheralblood	blood
21	chr7:17963400-17969200	Weak transcription	Primary neutrophils fromperipheralblood	blood
22	chr7:17963400-17970200	Weak transcription	Ovary	ovary
23	chr7:17963400-17972400	Weak transcription	Right Ventricle	heart
24	chr7:17963400-17977000	Weak transcription	Fetal Lung	lung
25	chr7:17963400-17977400	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:17963800-17977800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr7:17964000-17967200	Weak transcription	Fetal Heart	heart
28	chr7:17964200-17970400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr7:17964200-17970800	Weak transcription	Colon Smooth Muscle	Colon
30	chr7:17964200-17971000	Weak transcription	Pancreatic Islets	Pancreatic Islet
31	chr7:17964400-17969600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
32	chr7:17964800-17970400	Weak transcription	Gastric	stomach
33	chr7:17965000-17967200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
34	chr7:17965000-17970200	Weak transcription	Psoas Muscle	Psoas
35	chr7:17965200-17970600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chr7:17965400-17970200	Weak transcription	H1 Cell Line	embryonic stem cell
37	chr7:17965400-17977200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
38	chr7:17965600-17970400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr7:17965800-17967600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
40	chr7:17966200-17966600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
41	chr7:17966200-17966600	Enhancers	Left Ventricle	heart
42	chr7:17966200-17966600	Enhancers	Pancreas	Pancrea
43	chr7:17966200-17966600	Enhancers	Right Atrium	heart
44	chr7:17966200-17966800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
45	chr7:17966400-17966600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr7:17966400-17966600	Enhancers	Primary T helper cells PMA-I stimulated	--
47	chr7:17966400-17966600	Enhancers	Duodenum Mucosa	Duodenum
48	chr7:17966400-17967600	Weak transcription	Primary T helper naive cells from peripheral blood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links