Variant report

Variant	rs73369025
Chromosome Location	chr7:80109567-80109568
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11973868	0.97[ASN][1000 genomes]
rs11983825	1.00[ASN][1000 genomes]
rs17154004	0.97[ASN][1000 genomes]
rs17154059	0.93[ASN][1000 genomes]
rs6960247	0.97[ASN][1000 genomes]
rs6966209	0.93[ASN][1000 genomes]
rs73369091	1.00[AMR][1000 genomes]
rs73369095	1.00[AMR][1000 genomes]
rs73371009	1.00[AMR][1000 genomes]
rs73386756	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73386759	0.97[ASN][1000 genomes]
rs7796785	0.90[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv429785	chr7:79589749-80177049	Bivalent/Poised TSS Weak transcription Active TSS Enhancers Strong transcription Flanking Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases
2	nsv831042	chr7:79984079-80122312	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
3	nsv1030961	chr7:80032525-80197468	Weak transcription Enhancers Active TSS Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
4	nsv538991	chr7:80032525-80197468	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
5	nsv949205	chr7:80039695-80211200	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
6	nsv888523	chr7:80088592-80142217	Weak transcription Enhancers Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
7	nsv607680	chr7:80097576-80142217	Weak transcription Flanking Active TSS Enhancers Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
8	nsv888524	chr7:80107798-80723062	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 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	chr7:80096800-80113000	Enhancers	Hela-S3	cervix
2	chr7:80099600-80109600	Weak transcription	NH-A	brain
3	chr7:80102400-80110000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr7:80102400-80110000	Weak transcription	Left Ventricle	heart
5	chr7:80103200-80110000	Weak transcription	Duodenum Mucosa	Duodenum
6	chr7:80104600-80110200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr7:80106000-80110000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
8	chr7:80106000-80110200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr7:80106200-80110000	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr7:80107400-80109600	Weak transcription	Adipose Nuclei	Adipose
11	chr7:80107400-80109800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr7:80107400-80110200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr7:80107400-80112200	Weak transcription	Right Atrium	heart
14	chr7:80107600-80111600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr7:80108400-80109600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr7:80108400-80109800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
17	chr7:80108400-80109800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr7:80108400-80109800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr7:80108400-80109800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr7:80108400-80109800	Weak transcription	A549	lung
21	chr7:80108400-80110000	Weak transcription	Muscle Satellite Cultured Cells	--
22	chr7:80108400-80110000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
23	chr7:80108400-80110200	Weak transcription	Osteobl	bone
24	chr7:80108400-80116200	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr7:80108600-80109600	Weak transcription	NHEK	skin
26	chr7:80108600-80110200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr7:80108600-80110200	Enhancers	Placenta	Placenta
28	chr7:80108600-80110400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr7:80109000-80110000	Weak transcription	Skeletal Muscle Male	skeletal muscle
30	chr7:80109400-80110400	Enhancers	Placenta Amnion	Placenta Amnion
31	chr7:80109400-80111600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
32	chr7:80109400-80113000	Enhancers	HMEC	breast

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