Variant report

Variant	rs10271803
Chromosome Location	chr7:3496243-3496244
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 108 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:79)

rs_ID	r²[population]
rs10215256	0.95[JPT][hapmap];0.87[ASN][1000 genomes]
rs10228151	0.81[CEU][hapmap];0.91[CHB][hapmap];0.87[JPT][hapmap];0.80[ASN][1000 genomes]
rs10232431	0.85[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.83[ASN][1000 genomes]
rs10233166	0.82[CHB][hapmap]
rs10243467	0.96[CEU][hapmap];0.95[JPT][hapmap];0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10250421	0.86[CHB][hapmap]
rs10250444	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs10254665	0.91[JPT][hapmap];0.87[ASN][1000 genomes]
rs10256740	0.87[ASN][1000 genomes]
rs10258501	0.85[CHB][hapmap];0.82[JPT][hapmap]
rs10266047	0.85[CEU][hapmap];0.86[CHB][hapmap];0.87[JPT][hapmap];0.83[ASN][1000 genomes]
rs10268837	0.87[CEU][hapmap];0.83[CHB][hapmap]
rs10276933	0.81[CHB][hapmap];0.83[JPT][hapmap]
rs10807838	1.00[CEU][hapmap];0.82[CHB][hapmap];0.85[MEX][hapmap];0.88[TSI][hapmap]
rs10951155	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs1112428	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs12056172	0.82[CHB][hapmap]
rs12537528	0.96[CEU][hapmap];0.82[CHB][hapmap];0.91[MEX][hapmap];0.84[TSI][hapmap];0.81[AMR][1000 genomes]
rs12673513	0.83[CHB][hapmap]
rs12700789	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs13221852	0.81[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];0.94[ASN][1000 genomes]
rs13224926	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs13237637	0.93[ASN][1000 genomes]
rs1357311	1.00[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.82[AMR][1000 genomes];0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1403158	0.85[CEU][hapmap];0.86[CHB][hapmap]
rs1403162	0.83[ASN][1000 genomes]
rs1525556	0.82[CHB][hapmap]
rs1996824	0.85[AMR][1000 genomes];0.88[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2178630	0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2340848	0.80[ASW][hapmap];1.00[CEU][hapmap];0.87[CHB][hapmap];0.95[JPT][hapmap];0.80[LWK][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4131987	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs4255031	0.90[CEU][hapmap];0.80[CHB][hapmap]
rs4316064	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs4320450	0.82[CEU][hapmap];0.86[CHB][hapmap]
rs4327753	1.00[CEU][hapmap];0.81[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs4358698	0.92[CEU][hapmap];0.82[CHB][hapmap];0.81[AMR][1000 genomes]
rs4443553	0.82[CHB][hapmap]
rs4495320	0.82[CEU][hapmap];0.82[CHB][hapmap]
rs4499989	0.96[CEU][hapmap];0.82[CHB][hapmap]
rs4506106	0.96[CEU][hapmap];0.82[CHB][hapmap];0.84[TSI][hapmap]
rs4521670	0.82[CHB][hapmap]
rs4544975	0.86[CHB][hapmap]
rs4607498	0.82[CEU][hapmap];0.83[JPT][hapmap]
rs4719883	1.00[CEU][hapmap]
rs4719894	0.86[CHB][hapmap];0.83[JPT][hapmap]
rs4719944	0.85[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4722654	0.92[CEU][hapmap]
rs4722663	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs4722693	0.82[CHB][hapmap]
rs4722696	0.96[CEU][hapmap];0.82[CHB][hapmap];0.81[AMR][1000 genomes]
rs4722708	0.82[CHB][hapmap]
rs4722709	0.80[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs4722827	0.94[ASN][1000 genomes]
rs4722853	0.81[CEU][hapmap];0.80[ASN][1000 genomes]
rs6461994	0.82[CHB][hapmap]
rs6462030	0.86[CHB][hapmap];0.82[JPT][hapmap]
rs6462094	1.00[CEU][hapmap];0.86[CHB][hapmap];0.80[JPT][hapmap];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6462105	0.83[ASN][1000 genomes]
rs6651070	0.85[CEU][hapmap];0.83[JPT][hapmap]
rs6949513	0.85[CEU][hapmap];0.95[CHB][hapmap];0.95[JPT][hapmap];0.98[ASN][1000 genomes]
rs6959232	0.82[CEU][hapmap];0.81[CHB][hapmap]
rs6962796	0.96[CEU][hapmap];0.91[CHB][hapmap];0.95[JPT][hapmap];1.00[MEX][hapmap];0.81[MKK][hapmap];0.93[TSI][hapmap];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs6964838	0.85[CEU][hapmap];0.82[CHB][hapmap];0.87[JPT][hapmap];0.81[ASN][1000 genomes]
rs6966619	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs6974577	0.83[ASN][1000 genomes]
rs7785994	0.82[CHB][hapmap];0.83[JPT][hapmap]
rs7789887	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs7790869	0.82[EUR][1000 genomes]
rs7791617	0.85[CEU][hapmap];0.87[CHB][hapmap];0.91[JPT][hapmap];0.85[ASN][1000 genomes]
rs7797018	0.95[CEU][hapmap];0.84[CHB][hapmap];0.84[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7798418	0.82[AMR][1000 genomes];0.80[EUR][1000 genomes]
rs7802250	0.85[CEU][hapmap];0.86[CHB][hapmap];0.82[JPT][hapmap];0.83[ASN][1000 genomes]
rs7803004	0.81[CEU][hapmap];0.91[CHB][hapmap];0.83[JPT][hapmap];0.80[ASN][1000 genomes]
rs7803993	0.82[CHB][hapmap]
rs7811244	0.82[CHB][hapmap]
rs7811286	1.00[CEU][hapmap];0.82[CHB][hapmap];0.83[JPT][hapmap];0.91[MEX][hapmap];0.86[TSI][hapmap]
rs885011	0.81[CEU][hapmap];0.95[JPT][hapmap];0.85[ASN][1000 genomes]
rs9648354	0.81[CEU][hapmap];0.87[CHB][hapmap];0.86[JPT][hapmap]
rs9969270	0.82[CHB][hapmap];0.83[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:29 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1018173	chr7:3258989-3879848	Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
2	nsv538660	chr7:3258989-3879848	Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
3	esv2758100	chr7:3286625-3560229	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
4	esv2759500	chr7:3286625-3560229	Genic enhancers Flanking Bivalent TSS/Enh Weak transcription Enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
5	nsv1016555	chr7:3298478-3872512	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
6	nsv538661	chr7:3298478-3872512	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
7	nsv1020764	chr7:3348458-3554820	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
8	nsv538662	chr7:3348458-3554820	Weak transcription Enhancers ZNF genes & repeats Active TSS Strong transcription Flanking Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv1030484	chr7:3364990-3506102	Enhancers ZNF genes & repeats Flanking Active TSS Active TSS Weak transcription Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	esv2764026	chr7:3365002-3618361	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	nsv1018105	chr7:3365441-3506102	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
12	nsv1026361	chr7:3366960-3502600	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
13	nsv538664	chr7:3366960-3502600	Active TSS Weak transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
14	nsv605893	chr7:3368197-3505231	Enhancers Weak transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
15	nsv1015296	chr7:3381813-3560401	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
16	nsv1029937	chr7:3408050-3506316	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
17	nsv538668	chr7:3408050-3506316	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
18	nsv916071	chr7:3423207-3697428	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Strong transcription Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
19	nsv887330	chr7:3424878-3515437	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
20	nsv528715	chr7:3451251-3598581	Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Active TSS Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
21	nsv887332	chr7:3455249-3521000	Active TSS Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
22	nsv605902	chr7:3464896-3598581	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
23	nsv605903	chr7:3472721-3527925	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Strong transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
24	nsv887333	chr7:3475716-3542488	Flanking Active TSS Enhancers Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
25	nsv869723	chr7:3482682-3566293	Weak transcription ZNF genes & repeats Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS Strong transcription Genic enhancers Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases
26	nsv1026295	chr7:3485871-3505092	Weak transcription Enhancers Flanking Active TSS Strong transcription ZNF genes & repeats Genic enhancers Active TSS	n/a	n/a	inside rSNPs	diseases
27	esv2761095	chr7:3487114-3496243	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases
28	nsv464270	chr7:3490865-3581357	Weak transcription Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	Chromatin interactive region	n/a	inside rSNPs	diseases
29	nsv605904	chr7:3490865-3581357	Enhancers Genic enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3480000-3508600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr7:3489000-3496400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr7:3489000-3496400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr7:3491000-3496400	Weak transcription	Aorta	Aorta
5	chr7:3491200-3526600	Weak transcription	Pancreas	Pancrea
6	chr7:3493400-3496400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr7:3493600-3506000	Weak transcription	HSMM	muscle
8	chr7:3494400-3497400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr7:3495000-3497000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr7:3495600-3496800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr7:3496000-3507000	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr7:3496200-3497000	Enhancers	iPS-20b Cell Line	embryonic stem cell

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