Variant report

Variant	rs7795709
Chromosome Location	chr7:111433419-111433420
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs3213631	1.00[JPT][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];1.00[ASN][1000 genomes]
rs3801780	1.00[MEX][hapmap]
rs57136946	0.86[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs58952011	0.84[AFR][1000 genomes]
rs6952833	0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs6964105	0.89[AFR][1000 genomes];0.83[ASN][1000 genomes]
rs73434205	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73434206	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73434207	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73434210	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73434211	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73434215	0.88[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73434223	0.99[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs73434233	0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs73434236	0.99[AFR][1000 genomes];0.87[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7793316	0.89[AFR][1000 genomes]
rs7801388	1.00[MEX][hapmap]

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	nsv608196	chr7:111073710-111794368	Enhancers Strong transcription Active TSS Weak transcription Bivalent Enhancer Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	27 gene(s)	inside rSNPs	diseases
2	nsv869375	chr7:111105151-111470811	Weak transcription Enhancers Active TSS ZNF genes & repeats Strong transcription Flanking Active TSS Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	20 gene(s)	inside rSNPs	diseases
3	nsv608215	chr7:111183610-111533520	Strong transcription Flanking Active TSS Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
4	nsv1021527	chr7:111194596-111851619	Weak transcription Enhancers Strong transcription Bivalent Enhancer Flanking Active TSS Genic enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
5	nsv539086	chr7:111194596-111851619	Enhancers Weak transcription Active TSS Strong transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
6	nsv1028740	chr7:111227747-111679401	Weak transcription Enhancers Active TSS ZNF genes & repeats Genic enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
7	nsv1015267	chr7:111303294-111714771	Weak transcription Strong transcription Enhancers Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv539087	chr7:111303294-111714771	Enhancers Active TSS Weak transcription Flanking Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
9	nsv539088	chr7:111333899-111722341	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
10	nsv531435	chr7:111333900-111926292	Weak transcription Enhancers Strong transcription Genic enhancers Active TSS ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
11	nsv491934	chr7:111333900-111975504	Active TSS Strong transcription Weak transcription Enhancers Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
12	nsv1034375	chr7:111337109-111459099	Enhancers Active TSS Weak transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
13	nsv532335	chr7:111411990-112054905	Enhancers Strong transcription Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
14	nsv5901	chr7:111428283-111472968	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers Flanking Active TSS Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:111379600-111433600	Weak transcription	Esophagus	oesophagus
2	chr7:111390400-111435600	Weak transcription	Psoas Muscle	Psoas
3	chr7:111398000-111435000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr7:111398200-111434000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr7:111400400-111435800	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chr7:111404600-111435400	Weak transcription	NHEK	skin
7	chr7:111406800-111435600	Weak transcription	Osteobl	bone
8	chr7:111409400-111434000	Weak transcription	Fetal Brain Female	brain
9	chr7:111412000-111435800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr7:111417200-111435200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr7:111418000-111434400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr7:111418400-111433800	Weak transcription	Brain Germinal Matrix	brain
13	chr7:111418400-111435600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr7:111419800-111435400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr7:111423600-111435600	Weak transcription	Right Ventricle	heart
16	chr7:111426000-111435200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr7:111426200-111434000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr7:111429000-111434800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr7:111429000-111435400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr7:111429000-111435600	Weak transcription	Brain Substantia Nigra	brain
21	chr7:111429000-111435800	Weak transcription	Brain Inferior Temporal Lobe	brain
22	chr7:111430000-111436000	Weak transcription	Fetal Brain Male	brain
23	chr7:111430200-111435600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr7:111430400-111435400	Weak transcription	Brain Anterior Caudate	brain
25	chr7:111430600-111433800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr7:111430600-111433800	Weak transcription	Left Ventricle	heart
27	chr7:111430600-111434000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:111430600-111434000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr7:111430600-111434000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
30	chr7:111430600-111434000	Weak transcription	Pancreas	Pancrea
31	chr7:111430600-111434400	Weak transcription	Skeletal Muscle Male	skeletal muscle
32	chr7:111430600-111435200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr7:111430600-111435400	Weak transcription	Brain Cingulate Gyrus	brain
34	chr7:111430600-111435400	Weak transcription	HUVEC	blood vessel
35	chr7:111430600-111435800	Weak transcription	Brain Angular Gyrus	brain
36	chr7:111430600-111436000	Weak transcription	HepG2	liver
37	chr7:111430800-111433800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
38	chr7:111430800-111433800	Weak transcription	Ovary	ovary
39	chr7:111431000-111433800	Weak transcription	Lung	lung
40	chr7:111432000-111434200	Strong transcription	Liver	Liver
41	chr7:111432800-111434600	Strong transcription	Fetal Lung	lung
42	chr7:111432800-111435800	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr7:111433000-111434000	Strong transcription	Stomach Smooth Muscle	stomach
44	chr7:111433000-111434200	Strong transcription	Duodenum Smooth Muscle	Duodenum
45	chr7:111433000-111435000	Strong transcription	Cortex derived primary cultured neurospheres	brain
46	chr7:111433400-111435000	Weak transcription	Brain Hippocampus Middle	brain
47	chr7:111433400-111439200	ZNF genes & repeats	Adipose Nuclei	Adipose

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