Variant report

Variant	rs6975632
Chromosome Location	chr7:120937228-120937229
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:120933404..120935085-chr7:120937028..120938793,2	K562	blood:

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:22)

rs_ID	r²[population]
rs10225647	0.85[YRI][hapmap];1.00[AMR][1000 genomes]
rs10232028	1.00[AMR][1000 genomes]
rs10237944	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs10248910	1.00[AMR][1000 genomes]
rs10270194	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10274424	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs12111905	0.87[YRI][hapmap];1.00[AMR][1000 genomes]
rs12534517	1.00[AMR][1000 genomes]
rs12535821	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs12536771	1.00[YRI][hapmap]
rs13438018	1.00[YRI][hapmap];1.00[AMR][1000 genomes]
rs17143353	0.85[YRI][hapmap];1.00[AMR][1000 genomes]
rs17143357	0.85[YRI][hapmap];1.00[AMR][1000 genomes]
rs28635533	1.00[AMR][1000 genomes]
rs2896303	1.00[AMR][1000 genomes]
rs56835233	1.00[AMR][1000 genomes]
rs57412322	1.00[AMR][1000 genomes]
rs59723881	1.00[AMR][1000 genomes]
rs6943177	1.00[AMR][1000 genomes]
rs6944198	1.00[AMR][1000 genomes]
rs6944409	1.00[YRI][hapmap];0.84[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6960006	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

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	nsv1025430	chr7:120638930-121179289	Weak transcription Enhancers Flanking Active TSS Strong transcription Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	25 gene(s)	inside rSNPs	diseases
2	nsv1034353	chr7:120818382-121040576	Enhancers Bivalent Enhancer Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
3	nsv1026322	chr7:120841937-121188037	Weak transcription Strong transcription Enhancers Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
4	nsv539102	chr7:120841937-121188037	Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
5	esv2755350	chr7:120848049-121119049	Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Bivalent/Poised TSS Active 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 miRNA target site	19 gene(s)	inside rSNPs	diseases
6	nsv1027619	chr7:120906437-120976630	Enhancers Bivalent Enhancer Strong transcription Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
7	esv2757237	chr7:120908459-120993326	Enhancers Weak transcription Strong transcription Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
8	esv2759558	chr7:120908459-120993326	Flanking Active TSS Strong transcription Enhancers Weak transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	4 gene(s)	inside rSNPs	diseases
9	nsv1032054	chr7:120926379-121432971	Enhancers Weak transcription Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases
10	nsv539103	chr7:120926379-121432971	Weak transcription Enhancers Bivalent Enhancer Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120888800-120937800	Weak transcription	Colon Smooth Muscle	Colon
2	chr7:120926200-120941000	Weak transcription	Sigmoid Colon	Sigmoid Colon
3	chr7:120926600-120937600	Weak transcription	Ovary	ovary
4	chr7:120929200-120941200	Weak transcription	NHDF-Ad	bronchial
5	chr7:120929400-120941400	Weak transcription	NHLF	lung
6	chr7:120929600-120938000	Weak transcription	Osteobl	bone
7	chr7:120929600-120944800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr7:120929800-120937600	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr7:120930200-120938200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chr7:120932000-120942400	Weak transcription	Lung	lung
11	chr7:120932800-120942400	Weak transcription	Esophagus	oesophagus
12	chr7:120933400-120941600	Weak transcription	Right Ventricle	heart
13	chr7:120933600-120942000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:120933800-120941400	Weak transcription	Fetal Stomach	stomach
15	chr7:120933800-120941800	Weak transcription	Left Ventricle	heart
16	chr7:120933800-120942200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
17	chr7:120934000-120939600	Weak transcription	Aorta	Aorta
18	chr7:120935200-120938400	Strong transcription	HSMM	muscle
19	chr7:120935800-120941400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
20	chr7:120936000-120938200	Weak transcription	Fetal Heart	heart
21	chr7:120936000-120939800	Weak transcription	Stomach Smooth Muscle	stomach
22	chr7:120936000-120944000	Weak transcription	HSMMtube	muscle
23	chr7:120936200-120938000	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr7:120936200-120938000	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr7:120936200-120940400	Weak transcription	Duodenum Smooth Muscle	Duodenum
26	chr7:120936600-120941200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr7:120936600-120945000	Weak transcription	Liver	Liver
28	chr7:120937000-120944000	Weak transcription	Adipose Nuclei	Adipose
29	chr7:120937200-120940600	Strong transcription	K562	blood

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