Variant report

Variant	rs7712427
Chromosome Location	chr5:147483640-147483641
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 134 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:130)

rs_ID	r²[population]
rs10041981	0.92[ASN][1000 genomes]
rs10052211	0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs10213873	0.83[AMR][1000 genomes];0.84[EUR][1000 genomes]
rs10515602	0.92[ASN][1000 genomes]
rs10515603	0.92[ASN][1000 genomes]
rs10875630	0.92[ASN][1000 genomes]
rs11168019	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs11168020	0.93[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11168021	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11168022	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11168023	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11168025	1.00[AFR][1000 genomes];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11168026	0.95[ASN][1000 genomes]
rs11168027	0.95[ASN][1000 genomes]
rs11168028	0.94[ASN][1000 genomes]
rs11168029	0.92[ASN][1000 genomes]
rs11168030	0.92[ASN][1000 genomes]
rs11168031	0.92[ASN][1000 genomes]
rs11168032	0.92[ASN][1000 genomes]
rs11168033	0.92[ASN][1000 genomes]
rs1155636	0.92[ASN][1000 genomes]
rs1155637	0.92[ASN][1000 genomes]
rs11741387	0.94[ASN][1000 genomes]
rs11741417	0.94[ASN][1000 genomes]
rs11743440	0.95[ASN][1000 genomes]
rs11745592	0.95[ASN][1000 genomes]
rs11948406	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11948461	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11955201	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11958432	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs11959273	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12187820	0.92[ASN][1000 genomes]
rs12188819	0.92[ASN][1000 genomes]
rs12514503	0.92[EUR][1000 genomes]
rs12518996	0.94[ASN][1000 genomes]
rs12519519	0.95[ASN][1000 genomes]
rs12654179	0.92[ASN][1000 genomes]
rs12657443	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12657460	0.92[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13160193	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs13160662	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13172395	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13181329	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1363722	0.95[ASN][1000 genomes]
rs1363723	0.95[ASN][1000 genomes]
rs1422991	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1422994	0.94[ASN][1000 genomes]
rs17704908	0.95[ASN][1000 genomes]
rs1978446	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1978447	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1978448	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2052531	0.95[ASN][1000 genomes]
rs2052532	0.95[ASN][1000 genomes]
rs2052534	0.92[ASN][1000 genomes]
rs2052535	0.92[ASN][1000 genomes]
rs2052536	0.90[ASN][1000 genomes]
rs2112765	0.92[ASN][1000 genomes]
rs2112766	0.92[ASN][1000 genomes]
rs2112767	0.92[ASN][1000 genomes]
rs2161434	0.92[ASN][1000 genomes]
rs2303061	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303062	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303063	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303065	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303066	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303067	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303068	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303071	0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2303072	0.92[ASN][1000 genomes]
rs2303073	0.92[ASN][1000 genomes]
rs2400477	0.92[ASN][1000 genomes]
rs2400478	0.92[ASN][1000 genomes]
rs2400479	0.95[ASN][1000 genomes]
rs28627452	0.92[ASN][1000 genomes]
rs3088193	0.91[ASN][1000 genomes]
rs33920397	0.95[ASN][1000 genomes]
rs34427102	0.91[ASN][1000 genomes]
rs34482796	0.92[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs34673384	0.87[ASN][1000 genomes]
rs35803917	0.90[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs3756689	0.92[ASN][1000 genomes]
rs3756690	0.92[ASN][1000 genomes]
rs3764926	0.94[ASN][1000 genomes]
rs3764927	0.95[ASN][1000 genomes]
rs3764928	0.95[ASN][1000 genomes]
rs3764930	0.92[ASN][1000 genomes]
rs3777129	0.87[ASN][1000 genomes]
rs3777134	0.95[ASN][1000 genomes]
rs3777135	0.95[ASN][1000 genomes]
rs3777136	0.93[ASN][1000 genomes]
rs3777137	0.93[ASN][1000 genomes]
rs3815736	0.87[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3822745	0.94[ASN][1000 genomes]
rs4235737	0.84[ASN][1000 genomes]
rs4235738	0.84[ASN][1000 genomes]
rs4315912	0.86[ASN][1000 genomes]
rs4334874	0.91[ASN][1000 genomes]
rs4349706	0.91[ASN][1000 genomes]
rs4354024	0.86[ASN][1000 genomes]
rs4362935	0.89[ASN][1000 genomes]
rs4368717	0.86[ASN][1000 genomes]
rs4371740	0.86[ASN][1000 genomes]
rs4385198	0.85[ASN][1000 genomes]
rs4440347	0.89[ASN][1000 genomes]
rs4502810	0.90[ASN][1000 genomes]
rs4519913	0.81[AMR][1000 genomes];0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs4588586	0.87[ASN][1000 genomes]
rs4642357	0.86[ASN][1000 genomes]
rs62388363	0.89[AMR][1000 genomes];0.97[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6580521	0.81[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6580522	0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6580524	0.94[ASN][1000 genomes]
rs6868182	0.90[ASN][1000 genomes]
rs6870820	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6872265	0.80[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6873836	0.92[ASN][1000 genomes]
rs6875266	0.95[ASN][1000 genomes]
rs6877585	0.91[ASN][1000 genomes]
rs6883868	0.95[ASN][1000 genomes]
rs6892205	0.83[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6894572	0.95[ASN][1000 genomes]
rs6895434	0.92[ASN][1000 genomes]
rs6896303	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7445392	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7700488	0.82[AMR][1000 genomes];0.96[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7711927	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7711953	0.95[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs7724165	0.81[AMR][1000 genomes];0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs880687	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs9325065	0.92[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033838	chr5:147360521-147484014	Flanking Active TSS Enhancers ZNF genes & repeats Weak transcription Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	nsv933225	chr5:147395849-147486560	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Strong transcription Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
3	nsv883015	chr5:147404281-147751035	Enhancers Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
4	nsv830515	chr5:147460852-147602247	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:20 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:147464200-147491200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr5:147464400-147488800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr5:147470400-147518400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
4	chr5:147470600-147508400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
5	chr5:147470600-147509000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr5:147471600-147514800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr5:147472000-147505000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr5:147472600-147497200	Weak transcription	H1 Cell Line	embryonic stem cell
9	chr5:147474200-147513400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr5:147474800-147490600	Weak transcription	NHEK	skin
11	chr5:147476800-147489800	Strong transcription	Hela-S3	cervix
12	chr5:147478200-147484000	Strong transcription	HUES6 Cell Line	embryonic stem cell
13	chr5:147479000-147500600	Strong transcription	HUES64 Cell Line	embryonic stem cell
14	chr5:147479200-147485800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr5:147479200-147494200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
16	chr5:147480800-147498200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr5:147481400-147513200	Weak transcription	Sigmoid Colon	Sigmoid Colon
18	chr5:147481600-147505000	Weak transcription	Esophagus	oesophagus
19	chr5:147482200-147509000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
20	chr5:147483600-147486400	Weak transcription	HUES48 Cell Line	embryonic stem cell

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links