Variant report

Variant	rs12667561
Chromosome Location	chr7:69510532-69510533
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 99 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:78)

rs_ID	r²[population]
rs12112758	0.93[ASN][1000 genomes]
rs12113555	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12669794	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12673575	0.93[ASN][1000 genomes]
rs12698820	0.83[AMR][1000 genomes]
rs12698826	0.83[AMR][1000 genomes];0.92[ASN][1000 genomes]
rs12698835	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12698838	0.95[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12698841	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs12698843	0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs12698846	0.86[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs12698847	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12698850	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12698851	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12698853	0.83[AFR][1000 genomes];0.91[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs12698856	0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12698857	0.89[YRI][hapmap];0.83[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs12698861	0.81[AFR][1000 genomes];0.82[AMR][1000 genomes];0.91[ASN][1000 genomes]
rs12698862	0.80[AMR][1000 genomes]
rs12698864	0.89[ASN][1000 genomes]
rs12698865	0.93[ASN][1000 genomes]
rs12698867	0.93[ASN][1000 genomes]
rs12698873	0.91[ASN][1000 genomes]
rs12698882	0.86[ASN][1000 genomes]
rs12698883	0.86[ASN][1000 genomes]
rs13229395	0.93[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13229686	0.84[ASN][1000 genomes]
rs13231497	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13238017	0.86[ASN][1000 genomes]
rs13242485	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs13340492	0.84[ASN][1000 genomes]
rs1476104	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1476105	0.85[AFR][1000 genomes];0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17365011	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs17365333	0.87[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs17365375	0.87[AFR][1000 genomes];0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17462837	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17762460	0.86[ASN][1000 genomes]
rs2030705	0.85[ASN][1000 genomes]
rs2030706	0.86[ASN][1000 genomes]
rs2866275	0.86[ASN][1000 genomes]
rs34519726	0.89[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs35222730	0.80[EUR][1000 genomes]
rs35317642	0.80[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4318956	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs4623296	0.83[AFR][1000 genomes];0.91[ASN][1000 genomes]
rs58849135	0.86[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6415223	0.80[EUR][1000 genomes]
rs6460539	0.83[AFR][1000 genomes];0.89[ASN][1000 genomes]
rs67847242	0.93[ASN][1000 genomes]
rs6943610	0.86[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs6945241	0.83[ASN][1000 genomes]
rs6951909	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6953075	0.84[ASN][1000 genomes]
rs6970670	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6971237	0.86[ASN][1000 genomes]
rs6975814	0.84[ASN][1000 genomes]
rs735060	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs7779308	0.90[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs7780640	0.88[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7782771	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7783039	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7783592	0.82[AMR][1000 genomes]
rs7783748	0.82[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs7790084	0.85[AFR][1000 genomes];0.97[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs7791954	0.82[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs7796592	0.94[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs7799192	0.93[ASN][1000 genomes]
rs7800317	0.90[AFR][1000 genomes];0.97[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7800759	0.95[AFR][1000 genomes];0.97[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs7803814	0.83[AFR][1000 genomes];0.82[AMR][1000 genomes]
rs7806363	0.86[ASN][1000 genomes]
rs7807263	0.82[AFR][1000 genomes]
rs917717	0.91[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9638582	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9647931	0.83[ASN][1000 genomes]
rs9647932	0.82[ASN][1000 genomes]
rs9691023	0.87[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:21 , 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

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:69505800-69513200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr7:69506200-69512400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
3	chr7:69507200-69512800	Weak transcription	HUES64 Cell Line	embryonic stem cell
4	chr7:69508000-69513000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:69508400-69512400	Weak transcription	Fetal Lung	lung
6	chr7:69508400-69513000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr7:69509400-69512400	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr7:69509400-69512400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
9	chr7:69509400-69512600	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr7:69509400-69513000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
11	chr7:69509400-69513000	Weak transcription	Fetal Stomach	stomach
12	chr7:69509600-69512200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:69509600-69512600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr7:69509600-69512800	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr7:69510200-69510800	Weak transcription	Fetal Intestine Large	intestine
16	chr7:69510400-69511600	Enhancers	Fetal Intestine Small	intestine
17	chr7:69510400-69517400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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