Variant report

Variant	rs2462664
Chromosome Location	chr7:112745043-112745044
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr7:112737881..112740697-chr7:112741857..112745616,3	K562	blood:
2	chr7:112744968..112747353-chr7:112748372..112751369,2	K562	blood:
3	chr7:112744397..112746764-chr7:112748583..112750338,2	MCF-7	breast:

Extended variants
information (count: 86 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:75)

rs_ID	r²[population]
rs1008056	0.92[ASN][1000 genomes]
rs1013638	0.96[ASN][1000 genomes]
rs10225200	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10228219	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10228566	0.96[ASN][1000 genomes]
rs10232392	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10232914	0.98[ASN][1000 genomes]
rs10241250	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10241676	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10241909	0.98[ASN][1000 genomes]
rs10245805	0.98[ASN][1000 genomes]
rs10246011	0.96[ASN][1000 genomes]
rs10246012	0.98[ASN][1000 genomes]
rs10249359	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10252483	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10257270	0.94[ASN][1000 genomes]
rs10258099	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10261482	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10261563	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10261938	1.00[CHB][hapmap]
rs10267369	0.98[ASN][1000 genomes]
rs10267575	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10267803	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10269536	0.96[ASN][1000 genomes]
rs10270797	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs10278104	1.00[CHB][hapmap];1.00[JPT][hapmap];0.82[AFR][1000 genomes]
rs10278248	1.00[JPT][hapmap]
rs10278935	0.96[ASN][1000 genomes]
rs10500019	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1051878	0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1051997	0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12670138	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12672405	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs12672763	1.00[JPT][hapmap]
rs1575013	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs1590155	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs1599792	1.00[JPT][hapmap]
rs17160251	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs17160260	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs1807909	0.96[ASN][1000 genomes]
rs2037657	0.87[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2140913	1.00[JPT][hapmap]
rs2177800	0.86[YRI][hapmap];0.83[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2245985	0.96[ASN][1000 genomes]
rs2246723	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2246724	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];0.82[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2246845	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2249253	0.96[ASN][1000 genomes]
rs2249501	0.98[ASN][1000 genomes]
rs2249511	0.98[ASN][1000 genomes]
rs2249612	0.98[ASN][1000 genomes]
rs2250343	0.84[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2253640	0.92[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2253773	0.84[YRI][hapmap];0.81[AFR][1000 genomes];0.88[AMR][1000 genomes];0.93[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2254842	0.84[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2264731	0.96[ASN][1000 genomes]
rs2264732	0.84[YRI][hapmap];0.81[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2272261	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs2462665	0.84[YRI][hapmap];0.82[AFR][1000 genomes];0.88[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs2692601	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs2699400	0.81[AFR][1000 genomes];0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28658090	0.98[ASN][1000 genomes]
rs55822923	0.94[ASN][1000 genomes]
rs55836916	0.98[ASN][1000 genomes]
rs56182321	0.96[ASN][1000 genomes]
rs56202345	0.96[ASN][1000 genomes]
rs56311133	0.98[ASN][1000 genomes]
rs56408134	0.98[ASN][1000 genomes]
rs73198873	0.98[ASN][1000 genomes]
rs73198882	0.98[ASN][1000 genomes]
rs7787425	1.00[JPT][hapmap]
rs7803528	0.86[ASN][1000 genomes]
rs872944	1.00[CHB][hapmap];1.00[JPT][hapmap]
rs9656199	0.96[ASN][1000 genomes]
rs9656200	0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2758131	chr7:112492127-112768628	ZNF genes & repeats Enhancers Flanking Active TSS Weak transcription Strong transcription Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv2759556	chr7:112492127-112768628	Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	esv3355135	chr7:112616979-113134651	Active TSS Weak transcription Enhancers Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv435847	chr7:112618576-113134022	Active TSS Enhancers Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
5	esv3430638	chr7:112620663-113134403	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3442221	chr7:112620665-113134971	Enhancers Weak transcription Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv993501	chr7:112625029-113125338	Enhancers Bivalent/Poised TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv1022066	chr7:112630168-113122748	Active TSS Flanking Bivalent TSS/Enh Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv539090	chr7:112630168-113122748	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Strong transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	esv3406708	chr7:112744141-112746689	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a
11	esv3381421	chr7:112744366-112746489	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:112740400-112756000	Weak transcription	Muscle Satellite Cultured Cells	--
2	chr7:112740600-112753200	Weak transcription	K562	blood
3	chr7:112740600-112757600	Weak transcription	Right Atrium	heart
4	chr7:112740600-112758000	Weak transcription	Aorta	Aorta
5	chr7:112741000-112757600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr7:112743000-112757800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr7:112743400-112748200	Weak transcription	Placenta Amnion	Placenta Amnion
8	chr7:112743400-112749600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr7:112743400-112754200	Weak transcription	Fetal Heart	heart

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