Variant report

Variant	rs7783282
Chromosome Location	chr7:107850759-107850760
allele	C/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 53 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:47)

rs_ID	r²[population]
rs10487842	0.92[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs10487843	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs10953560	0.96[AMR][1000 genomes];0.81[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11980184	0.89[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11980771	0.84[AMR][1000 genomes]
rs11984362	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs12531607	0.84[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs12534073	0.84[AMR][1000 genomes];0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs12534706	0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs12538125	0.86[AMR][1000 genomes]
rs12705439	0.88[AMR][1000 genomes];0.82[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13228675	0.87[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs13231463	0.87[AMR][1000 genomes]
rs13237289	0.89[AMR][1000 genomes]
rs13242621	0.87[AMR][1000 genomes];0.89[ASN][1000 genomes]
rs13245910	0.94[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13247108	0.86[AMR][1000 genomes]
rs1548950	0.88[AMR][1000 genomes]
rs17155187	0.87[AMR][1000 genomes];0.93[ASN][1000 genomes]
rs17155196	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs17331230	0.84[AMR][1000 genomes]
rs2191046	0.84[AMR][1000 genomes]
rs2193252	0.86[AMR][1000 genomes]
rs2193253	0.91[AMR][1000 genomes]
rs2193254	0.85[AMR][1000 genomes]
rs2267876	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs2267877	0.88[AMR][1000 genomes]
rs2267878	0.86[AMR][1000 genomes]
rs2272617	0.86[AMR][1000 genomes]
rs2299992	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs2299996	0.89[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs2299999	0.85[AMR][1000 genomes]
rs2300000	0.91[AMR][1000 genomes]
rs2300002	0.88[AMR][1000 genomes]
rs34754517	0.84[AMR][1000 genomes]
rs55643449	0.87[AMR][1000 genomes]
rs67133820	0.87[AMR][1000 genomes];0.85[ASN][1000 genomes]
rs6958333	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs6977003	0.89[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs6980041	0.85[AMR][1000 genomes];0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs71568512	0.87[AMR][1000 genomes]
rs73199565	0.88[AMR][1000 genomes]
rs7784186	0.86[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs7789291	0.87[AMR][1000 genomes]
rs7795834	0.84[AMR][1000 genomes]
rs7796675	0.86[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs7809003	0.84[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1033979	chr7:107003734-107877761	Strong transcription Enhancers Weak transcription Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	62 gene(s)	inside rSNPs	diseases
2	esv3348839	chr7:107377311-108286538	Weak transcription Enhancers Flanking Active TSS Genic enhancers ZNF genes & repeats Strong transcription Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	91 gene(s)	inside rSNPs	diseases
3	nsv949344	chr7:107396502-107987085	Weak transcription Enhancers Strong transcription Active TSS Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh 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	25 gene(s)	inside rSNPs	diseases
4	nsv831089	chr7:107687618-107877240	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	inside rSNPs	diseases
5	nsv831090	chr7:107786650-108011196	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
6	nsv888941	chr7:107796150-107863395	ZNF genes & repeats Weak transcription Enhancers Strong transcription Genic enhancers Active TSS Flanking Active TSS Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:34 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:107786800-107857800	Weak transcription	Brain Cingulate Gyrus	brain
2	chr7:107818200-107851800	Weak transcription	HSMMtube	muscle
3	chr7:107820600-107867400	Weak transcription	Brain Angular Gyrus	brain
4	chr7:107820800-107851200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr7:107821000-107852200	Weak transcription	Fetal Muscle Leg	muscle
6	chr7:107828000-107852000	Weak transcription	Pancreas	Pancrea
7	chr7:107828800-107851400	Weak transcription	Fetal Intestine Small	intestine
8	chr7:107830400-107857200	Weak transcription	Fetal Brain Female	brain
9	chr7:107830400-107886400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr7:107835000-107851400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr7:107836800-107851200	Weak transcription	HMEC	breast
12	chr7:107836800-107852000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr7:107841200-107851800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr7:107841800-107851800	Weak transcription	Placenta	Placenta
15	chr7:107843600-107852000	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr7:107844400-107851000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr7:107844600-107853200	Weak transcription	Fetal Muscle Trunk	muscle
18	chr7:107846200-107851200	Weak transcription	Pancreatic Islets	Pancreatic Islet
19	chr7:107846400-107852200	Weak transcription	Thymus	Thymus
20	chr7:107846600-107851600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr7:107847400-107852000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr7:107847400-107854000	Weak transcription	Brain Germinal Matrix	brain
23	chr7:107847400-107854400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
24	chr7:107847600-107857400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr7:107847600-107863200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
26	chr7:107848000-107851400	Weak transcription	HUVEC	blood vessel
27	chr7:107848200-107851200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr7:107849200-107851200	Genic enhancers	A549	lung
29	chr7:107849400-107851200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr7:107849400-107863000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr7:107850000-107851800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr7:107850000-107851800	Weak transcription	HepG2	liver
33	chr7:107850200-107851000	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr7:107850400-107851800	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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