Variant report

Variant	rs9359122
Chromosome Location	chr6:76127504-76127505
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr6:76125211..76128174-chr6:76133205..76135918,3	MCF-7	breast:
2	chr6:76127375..76129483-chr6:76137829..76140336,2	MCF-7	breast:
3	chr6:76126140..76128632-chr6:76129375..76131400,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000263533	Chromatin interaction

Extended variants
information (count: 66 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:56)

rs_ID	r²[population]
rs1018471	0.81[CHB][hapmap];0.81[TSI][hapmap]
rs10806035	0.80[CEU][hapmap];0.86[CHB][hapmap];0.82[CHD][hapmap];0.82[GIH][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap]
rs10943241	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs2250989	0.80[CEU][hapmap];0.80[GIH][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap]
rs240375	0.87[MEX][hapmap]
rs240379	0.80[CEU][hapmap]
rs240380	0.80[CEU][hapmap];0.87[MEX][hapmap];0.83[TSI][hapmap]
rs2703715	0.90[GIH][hapmap]
rs2748252	0.80[CEU][hapmap];0.82[CHB][hapmap];0.80[GIH][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap]
rs2808188	0.90[GIH][hapmap]
rs2808201	1.00[CEU][hapmap];0.97[GIH][hapmap];0.87[MEX][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs2808203	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap]
rs2808204	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2842446	0.84[CEU][hapmap]
rs2842459	0.81[CHB][hapmap]
rs2842462	0.82[CHB][hapmap];0.83[MEX][hapmap];0.81[TSI][hapmap]
rs2842463	0.82[CHB][hapmap];0.83[MEX][hapmap]
rs2951937	0.90[GIH][hapmap]
rs2951952	0.84[GIH][hapmap]
rs3935857	0.95[CHB][hapmap];0.90[JPT][hapmap];0.88[ASN][1000 genomes]
rs4131550	0.95[CHB][hapmap];0.90[JPT][hapmap];0.86[ASN][1000 genomes]
rs4273651	0.83[ASN][1000 genomes]
rs4275021	0.87[CEU][hapmap];1.00[CHB][hapmap];0.90[JPT][hapmap];0.81[AMR][1000 genomes];0.84[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4295446	0.84[ASN][1000 genomes]
rs4374801	0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4412169	0.93[AMR][1000 genomes];0.91[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs4535511	0.86[ASN][1000 genomes]
rs4541712	1.00[CHB][hapmap];0.90[JPT][hapmap];0.88[ASN][1000 genomes]
rs4568415	1.00[CHB][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs4588651	1.00[ASN][1000 genomes]
rs4708179	0.80[CEU][hapmap];0.86[CHB][hapmap];0.82[CHD][hapmap];0.82[GIH][hapmap];0.87[MEX][hapmap];0.86[TSI][hapmap]
rs4708181	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs6903526	1.00[CEU][hapmap];1.00[CHB][hapmap];0.98[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs6904580	1.00[ASW][hapmap];1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.89[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];1.00[TSI][hapmap];0.96[YRI][hapmap];0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6913979	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.90[ASN][1000 genomes]
rs6929270	0.83[ASW][hapmap];0.92[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.86[LWK][hapmap];0.96[MEX][hapmap];0.83[MKK][hapmap];0.98[TSI][hapmap];0.89[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6937768	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7451911	1.00[CHB][hapmap];0.98[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.92[ASN][1000 genomes]
rs7740648	0.86[ASN][1000 genomes]
rs7743227	0.84[CEU][hapmap];0.86[CHB][hapmap]
rs7766441	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.86[ASN][1000 genomes]
rs7771904	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];1.00[GIH][hapmap];1.00[JPT][hapmap];0.96[MEX][hapmap];0.98[TSI][hapmap];0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7772989	0.91[CHB][hapmap];0.85[GIH][hapmap]
rs9341514	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];0.88[ASN][1000 genomes]
rs9341515	0.89[AMR][1000 genomes];0.91[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9341516	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs9343283	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs9352202	0.80[CEU][hapmap];0.82[CHB][hapmap];0.82[CHD][hapmap];0.82[GIH][hapmap];0.87[MEX][hapmap];0.88[TSI][hapmap]
rs9352203	0.86[ASN][1000 genomes]
rs9352207	0.88[ASN][1000 genomes]
rs9443168	0.90[ASN][1000 genomes]
rs9443169	0.92[AMR][1000 genomes];0.90[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9443170	0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs9443171	1.00[CHB][hapmap];1.00[CHD][hapmap];0.92[GIH][hapmap];1.00[JPT][hapmap];1.00[ASN][1000 genomes]
rs9447475	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9689477	0.87[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1016804	chr6:75775846-76188585	Enhancers Weak transcription Strong transcription ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
2	nsv538310	chr6:75775846-76188585	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	38 gene(s)	inside rSNPs	diseases
3	nsv1024079	chr6:75848556-76238519	Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv1027915	chr6:75893542-76510113	Active TSS Enhancers Strong transcription Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
5	nsv538311	chr6:75893542-76510113	Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	70 gene(s)	inside rSNPs	diseases
6	nsv1022428	chr6:76023118-76575620	Weak transcription Strong transcription Enhancers Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
7	nsv538312	chr6:76023118-76575620	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	48 gene(s)	inside rSNPs	diseases
8	nsv1032245	chr6:76045537-76545703	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
9	nsv538313	chr6:76045537-76545703	Strong transcription Weak transcription Enhancers Active TSS Bivalent/Poised TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	47 gene(s)	inside rSNPs	diseases
10	nsv886182	chr6:76096230-76194007	Active TSS Weak transcription Enhancers Genic enhancers Flanking Active TSS Bivalent Enhancer Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:32 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:76112400-76133200	Weak transcription	Fetal Muscle Leg	muscle
2	chr6:76113200-76127600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr6:76119800-76132200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr6:76120000-76127600	Weak transcription	Right Atrium	heart
5	chr6:76122200-76127600	Enhancers	Fetal Heart	heart
6	chr6:76123200-76138800	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr6:76123400-76127800	Weak transcription	NH-A	brain
8	chr6:76123400-76128000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr6:76123400-76131400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:76123400-76131400	Weak transcription	Osteobl	bone
11	chr6:76123600-76127600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
12	chr6:76123600-76127800	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr6:76123600-76128600	Weak transcription	Fetal Brain Male	brain
14	chr6:76123800-76127600	Weak transcription	Right Ventricle	heart
15	chr6:76123800-76128800	Weak transcription	Adipose Nuclei	Adipose
16	chr6:76124600-76128000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr6:76124600-76131000	Weak transcription	Aorta	Aorta
18	chr6:76124800-76127600	Weak transcription	Psoas Muscle	Psoas
19	chr6:76124800-76128000	Weak transcription	NHDF-Ad	bronchial
20	chr6:76124800-76128000	Weak transcription	NHLF	lung
21	chr6:76124800-76131200	Weak transcription	Rectal Smooth Muscle	rectum
22	chr6:76125400-76127600	Weak transcription	Left Ventricle	heart
23	chr6:76125400-76128000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:76125400-76129800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:76126200-76128000	Weak transcription	Colon Smooth Muscle	Colon
26	chr6:76126200-76128200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chr6:76126400-76129600	Enhancers	HUVEC	blood vessel
28	chr6:76126600-76131000	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chr6:76127200-76127800	Flanking Active TSS	A549	lung
30	chr6:76127200-76129000	Enhancers	Hela-S3	cervix
31	chr6:76127400-76129000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr6:76127400-76129000	Enhancers	Fetal Lung	lung

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