Variant report

Variant	rs11767997
Chromosome Location	chr7:69517668-69517669
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 111 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:89)

rs_ID	r²[population]
rs1014417	0.81[ASN][1000 genomes]
rs10234205	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs10235487	0.87[AFR][1000 genomes];0.85[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs10235781	0.92[ASN][1000 genomes]
rs10235860	0.85[AFR][1000 genomes];0.92[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10245786	0.81[ASN][1000 genomes]
rs10251306	0.82[AFR][1000 genomes]
rs10257549	0.82[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs10258962	0.85[ASN][1000 genomes]
rs10268235	0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10268924	0.93[ASN][1000 genomes]
rs10270616	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs10273270	0.94[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs10279392	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs1035010	0.87[AFR][1000 genomes];0.82[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs1035013	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10452738	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11508453	0.82[ASN][1000 genomes]
rs11761141	0.81[AFR][1000 genomes];0.86[AMR][1000 genomes]
rs11978431	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12112638	0.82[ASN][1000 genomes]
rs12698816	0.80[AMR][1000 genomes];0.83[ASN][1000 genomes]
rs12698822	0.86[AMR][1000 genomes]
rs12698825	0.80[AFR][1000 genomes];0.87[AMR][1000 genomes];0.90[ASN][1000 genomes]
rs12698830	0.85[AFR][1000 genomes];0.94[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs12698841	0.80[EUR][1000 genomes]
rs12698842	0.94[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12698849	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12698855	0.96[ASN][1000 genomes]
rs12698871	0.93[ASN][1000 genomes]
rs13226538	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13228123	0.96[ASN][1000 genomes]
rs13237811	0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs13242485	0.80[EUR][1000 genomes]
rs1474368	0.88[ASN][1000 genomes]
rs1558413	0.96[AFR][1000 genomes];0.99[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17140933	0.83[ASN][1000 genomes]
rs2159678	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs2865805	0.81[ASN][1000 genomes]
rs2866075	0.86[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs28770244	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs34221396	0.81[ASN][1000 genomes]
rs34617709	0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs35222730	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs35696945	0.84[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6415223	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6460536	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6460537	0.93[ASN][1000 genomes]
rs6651055	0.93[ASN][1000 genomes]
rs6944725	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6949651	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6950485	1.00[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6950647	0.93[ASN][1000 genomes]
rs6951921	0.84[AFR][1000 genomes];0.94[AMR][1000 genomes];0.84[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6953170	0.87[AFR][1000 genomes];0.92[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6957126	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6958981	0.84[AFR][1000 genomes];0.87[AMR][1000 genomes]
rs6961164	0.86[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs6961345	0.93[ASN][1000 genomes]
rs6962999	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6963882	0.84[ASN][1000 genomes]
rs6963904	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6966036	0.80[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs6974687	0.94[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs6975279	0.93[ASN][1000 genomes]
rs6978134	0.81[ASN][1000 genomes]
rs6979355	0.80[AMR][1000 genomes];0.82[ASN][1000 genomes]
rs726372	0.81[ASN][1000 genomes]
rs73442405	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs7779010	0.81[ASN][1000 genomes]
rs7779308	0.80[EUR][1000 genomes]
rs7784584	0.91[ASN][1000 genomes]
rs7786073	0.81[ASN][1000 genomes]
rs7790729	0.93[ASN][1000 genomes]
rs7791101	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7794623	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7795152	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7796080	0.93[ASN][1000 genomes]
rs7796973	0.83[ASN][1000 genomes]
rs7797340	0.85[AFR][1000 genomes];0.91[AMR][1000 genomes];0.83[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7801117	0.81[ASN][1000 genomes]
rs7805470	0.91[ASN][1000 genomes]
rs7809303	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs7809934	0.87[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs870920	0.91[ASN][1000 genomes]
rs873835	0.91[ASN][1000 genomes]
rs877687	0.82[ASN][1000 genomes]
rs917717	0.80[EUR][1000 genomes]
rs9638268	0.85[AMR][1000 genomes];0.99[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:22 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1021538	chr7:69130236-69575753	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
2	nsv538917	chr7:69130236-69575753	Enhancers Weak transcription Genic enhancers Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv817276	chr7:69130237-69736834	Enhancers Weak transcription Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
4	nsv1018749	chr7:69149029-69995112	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv492242	chr7:69330737-69520566	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv1018289	chr7:69383450-69650885	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Active TSS Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
7	nsv538922	chr7:69383450-69650885	Weak transcription Enhancers Flanking Active TSS Active TSS Strong transcription ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
8	nsv532782	chr7:69383651-70189959	Weak transcription Genic enhancers Enhancers Active TSS Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
9	nsv1034281	chr7:69403828-69548378	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
10	nsv538923	chr7:69403828-69548378	Weak transcription Active TSS Enhancers Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
11	nsv1034182	chr7:69406172-69529294	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
12	nsv538924	chr7:69406172-69529294	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
13	esv2758119	chr7:69412504-69594161	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
14	esv2759536	chr7:69412504-69594161	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
15	nsv607429	chr7:69430748-69553093	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
16	nsv1028705	chr7:69453983-69524628	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
17	nsv1020488	chr7:69465268-69671126	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
18	nsv1022932	chr7:69496659-69564369	ZNF genes & repeats Weak transcription Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
19	nsv538925	chr7:69496659-69564369	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
20	nsv1034817	chr7:69507871-69578892	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
21	nsv538926	chr7:69507871-69578892	Enhancers Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases
22	nsv1028975	chr7:69513266-69578892	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69512600-69525600	Weak transcription	Left Ventricle	heart
2	chr7:69513600-69521600	Weak transcription	Fetal Intestine Small	intestine
3	chr7:69513800-69525800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr7:69516200-69520800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr7:69516600-69518600	Enhancers	HSMM	muscle
6	chr7:69516800-69518000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:69516800-69518000	Enhancers	Fetal Stomach	stomach
8	chr7:69516800-69518200	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr7:69516800-69519000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr7:69517000-69518600	Enhancers	HSMMtube	muscle
11	chr7:69517200-69518000	Enhancers	Adipose Nuclei	Adipose
12	chr7:69517200-69518000	Enhancers	Colon Smooth Muscle	Colon
13	chr7:69517200-69518400	Enhancers	Osteobl	bone
14	chr7:69517200-69519200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
15	chr7:69517400-69517800	Enhancers	iPS-20b Cell Line	embryonic stem cell
16	chr7:69517400-69517800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr7:69517400-69517800	Enhancers	Brain Anterior Caudate	brain
18	chr7:69517400-69517800	Enhancers	Fetal Muscle Leg	muscle
19	chr7:69517400-69517800	Enhancers	Psoas Muscle	Psoas
20	chr7:69517400-69517800	Enhancers	NHDF-Ad	bronchial
21	chr7:69517400-69518000	Enhancers	Brain Cingulate Gyrus	brain
22	chr7:69517400-69518000	Enhancers	Fetal Intestine Large	intestine
23	chr7:69517400-69518000	Enhancers	Pancreatic Islets	Pancreatic Islet
24	chr7:69517400-69518600	Enhancers	Brain Hippocampus Middle	brain
25	chr7:69517400-69518600	Enhancers	Fetal Heart	heart
26	chr7:69517400-69519800	Enhancers	Fetal Lung	lung
27	chr7:69517600-69518000	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr7:69517600-69518000	Enhancers	Duodenum Smooth Muscle	Duodenum
29	chr7:69517600-69518000	Enhancers	Fetal Kidney	kidney
30	chr7:69517600-69518000	Enhancers	Rectal Smooth Muscle	rectum
31	chr7:69517600-69519000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr7:69517600-69521600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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