Variant report

Variant	rs7789887
Chromosome Location	chr7:3350051-3350052
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:3349072..3350762-chr7:3354639..3356462,2	K562	blood:
2	chr7:3349154..3351811-chr7:3384855..3387148,2	MCF-7	breast:

Extended variants
information (count: 125 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:113)

rs_ID	r²[population]
rs10224769	0.95[ASN][1000 genomes]
rs10228151	0.80[CEU][hapmap];0.90[CHB][hapmap]
rs10228723	0.99[ASN][1000 genomes]
rs10232431	0.85[CEU][hapmap]
rs10233166	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs10238520	0.92[ASN][1000 genomes]
rs10243467	0.96[CEU][hapmap]
rs10250421	0.95[CHB][hapmap]
rs10250444	0.81[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs10257982	0.82[AFR][1000 genomes];0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10258501	0.95[CHB][hapmap]
rs10260145	0.99[ASN][1000 genomes]
rs10261250	0.94[ASN][1000 genomes]
rs10261912	0.83[AFR][1000 genomes];0.94[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs10266047	0.85[CEU][hapmap];0.95[CHB][hapmap]
rs10268249	0.95[ASN][1000 genomes]
rs10268837	0.88[CEU][hapmap];0.95[CHB][hapmap]
rs10271803	1.00[CEU][hapmap];0.81[CHB][hapmap]
rs10276190	0.99[ASN][1000 genomes]
rs10276933	0.82[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs10807838	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10951155	0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs10951159	0.95[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1112428	0.82[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs11974620	0.96[ASN][1000 genomes]
rs12056172	0.90[CHB][hapmap]
rs12234397	0.82[CHB][hapmap]
rs12537113	0.95[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs12537528	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.89[YRI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs12537549	0.97[ASN][1000 genomes]
rs12540305	0.95[ASN][1000 genomes]
rs12673513	0.81[CHB][hapmap]
rs12700789	0.82[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs13221852	0.80[CEU][hapmap];0.82[CHB][hapmap]
rs13224926	0.83[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs13230698	0.97[ASN][1000 genomes]
rs1357311	1.00[CEU][hapmap]
rs1403158	0.84[CEU][hapmap];0.95[CHB][hapmap]
rs1525556	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs1525557	0.83[CHB][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17133334	0.86[CHB][hapmap]
rs2340848	1.00[CEU][hapmap]
rs34608458	0.99[ASN][1000 genomes]
rs34735349	0.99[ASN][1000 genomes]
rs4131987	0.80[CEU][hapmap];0.95[CHB][hapmap];0.82[ASN][1000 genomes]
rs4255031	0.91[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4295560	0.99[ASN][1000 genomes]
rs4298408	0.83[ASN][1000 genomes]
rs4316064	0.81[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs4320450	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4327753	1.00[CEU][hapmap];0.95[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.81[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4336505	0.98[ASN][1000 genomes]
rs4349886	0.97[ASN][1000 genomes]
rs4358698	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.93[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4385365	0.83[ASN][1000 genomes]
rs4443553	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4495320	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs4499989	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.81[AFR][1000 genomes];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4506106	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[AMR][1000 genomes];0.95[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4521670	1.00[CHB][hapmap];1.00[JPT][hapmap];0.96[ASN][1000 genomes]
rs4544975	0.80[CEU][hapmap];0.95[CHB][hapmap];0.81[ASN][1000 genomes]
rs4588749	0.98[ASN][1000 genomes]
rs4607498	0.84[CEU][hapmap];0.86[CHB][hapmap];0.84[ASN][1000 genomes]
rs4719883	1.00[CEU][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4719894	0.80[CEU][hapmap];0.95[CHB][hapmap];0.82[ASN][1000 genomes]
rs4719944	0.84[CEU][hapmap]
rs4722654	0.92[CEU][hapmap];0.90[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4722655	0.98[ASN][1000 genomes]
rs4722663	0.81[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs4722673	0.82[CEU][hapmap];0.99[ASN][1000 genomes]
rs4722674	0.99[ASN][1000 genomes]
rs4722693	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[ASN][1000 genomes]
rs4722696	0.96[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.90[YRI][hapmap];0.93[AMR][1000 genomes];0.97[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4722708	1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs4722709	0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4722710	0.82[ASN][1000 genomes]
rs4722712	0.80[ASN][1000 genomes]
rs4722853	0.85[CEU][hapmap]
rs6461983	0.98[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6461993	0.99[ASN][1000 genomes]
rs6461994	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs6462030	0.95[CHB][hapmap]
rs6462094	1.00[CEU][hapmap]
rs6651070	0.85[CEU][hapmap]
rs67586312	0.87[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs6949513	0.84[CEU][hapmap]
rs6958390	0.99[ASN][1000 genomes]
rs6959232	0.85[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.94[ASN][1000 genomes]
rs6959702	0.99[ASN][1000 genomes]
rs6962796	0.96[CEU][hapmap];0.82[CHB][hapmap]
rs6964838	0.84[CEU][hapmap]
rs6965684	0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs6966619	0.81[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs6974075	0.81[ASN][1000 genomes]
rs6980323	0.99[ASN][1000 genomes]
rs7780027	0.81[ASN][1000 genomes]
rs7785994	0.81[CEU][hapmap];0.91[CHB][hapmap];0.84[ASN][1000 genomes]
rs7791617	0.84[CEU][hapmap]
rs7791820	0.99[ASN][1000 genomes]
rs7794279	0.99[ASN][1000 genomes]
rs7797018	0.95[CEU][hapmap];0.95[CHB][hapmap];0.89[YRI][hapmap];0.82[AFR][1000 genomes];0.92[AMR][1000 genomes];0.89[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs7798418	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs7798672	0.98[ASN][1000 genomes]
rs7802250	0.85[CEU][hapmap];0.95[CHB][hapmap]
rs7803004	0.80[CEU][hapmap];0.90[CHB][hapmap]
rs7803993	0.82[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7811244	0.81[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.99[ASN][1000 genomes]
rs7811286	1.00[CEU][hapmap];0.91[CHB][hapmap];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs885011	0.81[CEU][hapmap];0.82[CHB][hapmap]
rs9648354	0.81[CEU][hapmap]
rs9969270	0.91[CHB][hapmap]
rs9986894	0.84[AFR][1000 genomes];0.97[AMR][1000 genomes];0.89[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9986896	0.95[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][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	nsv1023127	chr7:3216344-3466223	Flanking Active TSS Enhancers Weak transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
2	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
3	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
4	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
5	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
6	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
7	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
8	nsv1019515	chr7:3300048-3479972	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
9	nsv887324	chr7:3308195-3400105	Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
10	nsv605892	chr7:3341589-3424878	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
11	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
12	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

No data

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:3343800-3357000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr7:3344600-3366600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr7:3344800-3354600	Weak transcription	Pancreas	Pancrea
4	chr7:3346200-3362400	Weak transcription	Aorta	Aorta
5	chr7:3349600-3350200	Enhancers	Fetal Brain Male	brain
6	chr7:3350000-3350400	Weak transcription	Pancreatic Islets	Pancreatic Islet

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