Variant report

Variant	rs7786867
Chromosome Location	chr7:120707742-120707743
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 42 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:28)

rs_ID	r²[population]
rs10251692	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10255706	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10261386	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10271436	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10275526	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10953924	0.83[ASN][1000 genomes]
rs10953925	0.83[ASN][1000 genomes]
rs11766764	0.83[ASN][1000 genomes]
rs11977285	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12176609	0.84[AMR][1000 genomes];0.94[ASN][1000 genomes]
rs12666340	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12666345	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12670604	0.96[ASN][1000 genomes]
rs12670664	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12672958	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13246689	0.83[ASN][1000 genomes]
rs17143147	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.86[ASN][1000 genomes]
rs17536644	0.84[AFR][1000 genomes]
rs2192290	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2192291	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2402555	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2896300	0.80[ASN][1000 genomes]
rs55748177	0.81[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs55910643	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs56351875	0.82[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs60050503	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs6466766	0.84[ASN][1000 genomes]
rs6962509	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:14 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv831114	chr7:120595624-120804510	Weak transcription Enhancers Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv608327	chr7:120633006-120873078	Weak transcription Enhancers Genic enhancers Strong transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
3	esv2753621	chr7:120635049-120800049	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv1023611	chr7:120638930-120881658	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	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
6	nsv1030792	chr7:120662815-120917533	Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
7	nsv1031282	chr7:120667937-120887301	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
8	nsv539099	chr7:120667937-120887301	Flanking Active TSS Enhancers Genic enhancers Active TSS Weak transcription Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
9	nsv1019025	chr7:120667937-120918696	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
10	nsv539100	chr7:120667937-120918696	Genic enhancers Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
11	nsv534342	chr7:120667938-120887300	Weak transcription Flanking Active TSS Enhancers Active TSS Transcr. at gene 5' and 3' Genic enhancers Strong transcription ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
12	nsv889118	chr7:120683751-120800837	Enhancers Weak transcription Flanking Active TSS Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
13	nsv889119	chr7:120688463-120800837	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv889120	chr7:120691417-120800837	Enhancers Weak transcription Strong transcription Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:25 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:120682400-120719600	Weak transcription	Fetal Lung	lung
2	chr7:120689600-120709400	Weak transcription	HSMMtube	muscle
3	chr7:120690200-120709000	Weak transcription	Right Ventricle	heart
4	chr7:120690200-120709400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr7:120690400-120709000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
6	chr7:120690600-120709200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr7:120691200-120709000	Weak transcription	Adipose Nuclei	Adipose
8	chr7:120692800-120719000	Weak transcription	Left Ventricle	heart
9	chr7:120696600-120709400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr7:120696600-120709400	Weak transcription	NHLF	lung
11	chr7:120696800-120709200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr7:120703400-120709000	Weak transcription	Osteobl	bone
13	chr7:120704200-120716200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr7:120704600-120709000	Weak transcription	Colon Smooth Muscle	Colon
15	chr7:120704600-120709000	Weak transcription	Stomach Smooth Muscle	stomach
16	chr7:120704600-120709200	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr7:120704600-120709200	Weak transcription	Skeletal Muscle Female	skeletal muscle
18	chr7:120704600-120709400	Weak transcription	Ovary	ovary
19	chr7:120705200-120709200	Weak transcription	Aorta	Aorta
20	chr7:120706400-120709400	Weak transcription	NHDF-Ad	bronchial
21	chr7:120706800-120718200	Weak transcription	Psoas Muscle	Psoas
22	chr7:120707200-120708800	Weak transcription	K562	blood
23	chr7:120707200-120709200	Weak transcription	Liver	Liver
24	chr7:120707200-120709400	Weak transcription	HSMM	muscle
25	chr7:120707200-120716600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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