Variant report

Variant	rs2691611
Chromosome Location	chr7:17883427-17883428
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:17882358..17885096-chr7:17950396..17953115,2	K562	blood:

Extended variants
information (count: 155 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:143)

rs_ID	r²[population]
rs10216315	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs10227224	0.90[CHB][hapmap];0.88[JPT][hapmap]
rs10227501	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs10227582	0.89[CHB][hapmap];0.84[JPT][hapmap]
rs10249221	0.83[EUR][1000 genomes]
rs10264355	0.93[EUR][1000 genomes]
rs10264445	0.86[EUR][1000 genomes]
rs10264447	0.81[AFR][1000 genomes];0.85[EUR][1000 genomes]
rs10265373	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs1051603	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs11768866	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs11983260	0.90[CHB][hapmap];0.86[JPT][hapmap]
rs12699918	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1357796	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.85[YRI][hapmap];0.90[AFR][1000 genomes];0.85[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1404414	1.00[CEU][hapmap];0.86[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1404421	0.92[EUR][1000 genomes]
rs1404422	0.91[CEU][hapmap];0.93[EUR][1000 genomes]
rs1404424	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1404425	0.93[EUR][1000 genomes]
rs1464804	0.86[CHB][hapmap]
rs1524774	1.00[CEU][hapmap];0.87[YRI][hapmap];0.84[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1524775	1.00[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.95[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1524776	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1524777	1.00[CEU][hapmap];0.93[EUR][1000 genomes]
rs1568817	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs1830006	0.93[EUR][1000 genomes]
rs1852010	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs1852011	0.80[AFR][1000 genomes];0.91[EUR][1000 genomes]
rs1965534	0.93[EUR][1000 genomes]
rs1997019	0.93[EUR][1000 genomes]
rs2030725	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2103144	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2140710	0.96[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2177652	0.87[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.86[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2254176	0.82[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2389858	0.92[CEU][hapmap]
rs2462512	0.95[CEU][hapmap];0.82[CHB][hapmap];0.83[AFR][1000 genomes];0.82[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2691552	0.97[EUR][1000 genomes]
rs2691553	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2691555	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2691557	0.96[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2691559	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.93[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs2691561	0.81[CHB][hapmap];0.86[JPT][hapmap]
rs2691562	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2691564	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2691566	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2691570	0.81[CHB][hapmap];0.81[JPT][hapmap]
rs2691580	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2691581	0.93[EUR][1000 genomes]
rs2691582	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2691583	0.90[CEU][hapmap];0.81[YRI][hapmap];0.84[AFR][1000 genomes];0.92[EUR][1000 genomes]
rs2691585	0.93[EUR][1000 genomes]
rs2691586	0.93[EUR][1000 genomes]
rs2691589	0.92[EUR][1000 genomes]
rs2691592	0.92[EUR][1000 genomes]
rs2691593	0.92[EUR][1000 genomes]
rs2691594	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2691595	0.92[EUR][1000 genomes]
rs2691596	0.92[EUR][1000 genomes]
rs2691597	1.00[CEU][hapmap];0.96[EUR][1000 genomes]
rs2691600	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.81[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2691601	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2691602	1.00[CEU][hapmap];0.87[YRI][hapmap];0.91[AFR][1000 genomes];0.96[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2691604	0.93[EUR][1000 genomes]
rs2691605	1.00[CEU][hapmap];0.98[EUR][1000 genomes]
rs2691607	0.81[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2691609	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691610	0.93[EUR][1000 genomes]
rs2691612	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.91[YRI][hapmap];0.97[AFR][1000 genomes];0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691613	0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2691615	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2691616	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2691617	0.86[EUR][1000 genomes]
rs2691618	1.00[CEU][hapmap];0.86[YRI][hapmap];0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2691620	1.00[CEU][hapmap];0.87[YRI][hapmap];0.88[AFR][1000 genomes];0.96[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2691621	0.93[EUR][1000 genomes]
rs2691623	0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2691625	0.91[EUR][1000 genomes]
rs2691627	0.93[EUR][1000 genomes]
rs2691628	0.93[EUR][1000 genomes]
rs2691629	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2691630	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2714855	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2714857	0.86[CHB][hapmap];0.86[JPT][hapmap]
rs2714859	0.82[CHB][hapmap];0.90[JPT][hapmap]
rs2714864	0.86[JPT][hapmap]
rs2714866	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2714867	0.82[CHB][hapmap];0.85[JPT][hapmap]
rs2714868	0.80[JPT][hapmap]
rs2714869	0.85[CHB][hapmap];0.85[JPT][hapmap]
rs2714870	0.82[CHB][hapmap];0.86[JPT][hapmap]
rs2714871	0.81[CHB][hapmap]
rs2714872	0.81[CHB][hapmap]
rs2714875	0.90[EUR][1000 genomes]
rs2714876	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2714877	1.00[CEU][hapmap];0.86[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2723494	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2723496	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2723497	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2723498	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2723499	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2723500	0.80[AFR][1000 genomes];0.93[EUR][1000 genomes]
rs2723501	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2723502	1.00[CEU][hapmap];0.81[YRI][hapmap];0.80[AFR][1000 genomes];0.93[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs2723503	0.93[EUR][1000 genomes]
rs2723504	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2723505	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2723506	0.92[EUR][1000 genomes]
rs2723507	0.92[EUR][1000 genomes]
rs2723508	0.92[EUR][1000 genomes]
rs2723515	1.00[CEU][hapmap];0.94[EUR][1000 genomes]
rs2723540	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.83[YRI][hapmap];0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2723545	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs2723552	1.00[CEU][hapmap];0.95[EUR][1000 genomes]
rs2723553	1.00[CEU][hapmap];0.90[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs2723554	0.93[EUR][1000 genomes]
rs2723555	0.94[EUR][1000 genomes]
rs2723556	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs2723562	0.94[EUR][1000 genomes]
rs2723567	0.97[EUR][1000 genomes]
rs2723569	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2723570	0.91[AFR][1000 genomes];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2723571	1.00[CEU][hapmap];0.83[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2723572	1.00[CEU][hapmap];0.82[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs35819944	0.95[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4316058	0.95[CEU][hapmap];0.93[EUR][1000 genomes]
rs4532510	0.94[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4543433	1.00[CEU][hapmap];1.00[CHB][hapmap];0.95[JPT][hapmap];0.95[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs4721661	0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4721665	1.00[CEU][hapmap];0.87[YRI][hapmap];0.88[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs4721666	1.00[CEU][hapmap];0.82[YRI][hapmap]
rs4721671	0.90[CHB][hapmap];0.85[JPT][hapmap]
rs67452591	0.95[EUR][1000 genomes]
rs6953831	0.90[EUR][1000 genomes]
rs6955984	0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs6958131	0.83[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6958211	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6973480	0.95[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.86[YRI][hapmap];0.85[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs6978097	0.91[EUR][1000 genomes]
rs6978103	0.89[EUR][1000 genomes]
rs949451	0.95[CEU][hapmap];0.81[YRI][hapmap];0.82[AFR][1000 genomes];0.93[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs9942602	0.83[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs998342	0.81[AFR][1000 genomes];0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv869352	chr7:17237983-17932878	Weak transcription Enhancers ZNF genes & repeats Strong transcription Genic enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
2	nsv1021524	chr7:17251148-17963307	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
3	nsv534309	chr7:17254118-17932878	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
4	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
5	nsv887804	chr7:17571140-17885468	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
6	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
7	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
8	esv1802979	chr7:17816528-17908546	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
9	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
10	esv1792752	chr7:17853983-17908546	Strong transcription ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
11	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
12	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

No data

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:17812600-17887600	Weak transcription	Gastric	stomach
2	chr7:17817400-17887600	Weak transcription	Pancreas	Pancrea
3	chr7:17823600-17887600	Weak transcription	Brain Cingulate Gyrus	brain
4	chr7:17825800-17887600	Weak transcription	Colonic Mucosa	Colon
5	chr7:17834000-17887800	Weak transcription	Right Ventricle	heart
6	chr7:17834800-17888800	Weak transcription	Brain Substantia Nigra	brain
7	chr7:17838800-17887600	Weak transcription	Rectal Smooth Muscle	rectum
8	chr7:17839000-17932600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr7:17841200-17883800	Weak transcription	HMEC	breast
10	chr7:17841200-17902600	Weak transcription	Brain Anterior Caudate	brain
11	chr7:17846000-17900600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr7:17847400-17887600	Weak transcription	Ovary	ovary
13	chr7:17847400-17887600	Weak transcription	Spleen	Spleen
14	chr7:17847600-17887600	Weak transcription	Fetal Stomach	stomach
15	chr7:17852600-17887800	Weak transcription	Brain Hippocampus Middle	brain
16	chr7:17852600-17896000	Weak transcription	Fetal Kidney	kidney
17	chr7:17852600-17902800	Weak transcription	Colon Smooth Muscle	Colon
18	chr7:17852800-17887000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr7:17852800-17890200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr7:17852800-17895000	Weak transcription	Brain Germinal Matrix	brain
21	chr7:17853400-17884200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr7:17853400-17887600	Weak transcription	Aorta	Aorta
23	chr7:17853600-17887400	Weak transcription	Left Ventricle	heart
24	chr7:17853600-17888000	Weak transcription	Stomach Smooth Muscle	stomach
25	chr7:17853800-17914000	Weak transcription	Hela-S3	cervix
26	chr7:17854000-17884000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr7:17854000-17887800	Weak transcription	Fetal Muscle Trunk	muscle
28	chr7:17854000-17900800	Weak transcription	K562	blood
29	chr7:17855200-17887400	Weak transcription	Fetal Intestine Small	intestine
30	chr7:17855200-17887400	Weak transcription	Fetal Muscle Leg	muscle
31	chr7:17855400-17887600	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr7:17857200-17887400	Weak transcription	NHLF	lung
33	chr7:17859200-17887600	Weak transcription	Esophagus	oesophagus
34	chr7:17860800-17885000	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr7:17862800-17888000	Weak transcription	Skeletal Muscle Male	skeletal muscle
36	chr7:17862800-17894800	Weak transcription	Psoas Muscle	Psoas
37	chr7:17863800-17884400	Weak transcription	NHEK	skin
38	chr7:17870600-17887600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr7:17871800-17887600	Strong transcription	Primary monocytes fromperipheralblood	blood
40	chr7:17872600-17889400	Weak transcription	Fetal Brain Male	brain
41	chr7:17873200-17886200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr7:17873800-17883800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr7:17873800-17887600	Weak transcription	Fetal Brain Female	brain
44	chr7:17875200-17884000	Weak transcription	NHDF-Ad	bronchial
45	chr7:17875600-17884800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr7:17876000-17883600	Strong transcription	Primary B cells from cord blood	blood
47	chr7:17876200-17901000	Weak transcription	Brain Inferior Temporal Lobe	brain
48	chr7:17877600-17902600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
49	chr7:17877800-17917400	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr7:17878000-17896000	Weak transcription	Brain Angular Gyrus	brain

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links