Variant report

Variant	rs7778097
Chromosome Location	chr7:78158412-78158413
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs10271370	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1030013	0.95[ASN][1000 genomes]
rs11773635	0.87[EUR][1000 genomes]
rs13244963	0.91[EUR][1000 genomes]
rs17150934	0.95[ASN][1000 genomes]
rs17150961	0.85[AFR][1000 genomes];0.98[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs17371672	0.90[EUR][1000 genomes]
rs28626666	0.82[AMR][1000 genomes];0.91[EUR][1000 genomes]
rs58289607	0.95[ASN][1000 genomes]
rs60845180	0.97[ASN][1000 genomes]
rs6466259	0.94[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs6466265	0.90[EUR][1000 genomes]
rs67367279	0.86[EUR][1000 genomes]
rs725555	0.86[EUR][1000 genomes]
rs9692191	0.95[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1022764	chr7:77911072-78316607	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1022199	chr7:78054639-78469370	Enhancers Weak transcription Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
3	nsv538986	chr7:78054639-78469370	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:24 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78138400-78161800	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr7:78144200-78160000	Weak transcription	Brain Hippocampus Middle	brain
3	chr7:78144400-78158600	Weak transcription	Brain Inferior Temporal Lobe	brain
4	chr7:78153400-78159600	Weak transcription	Brain Angular Gyrus	brain
5	chr7:78155800-78159400	Weak transcription	Brain Cingulate Gyrus	brain
6	chr7:78156400-78160000	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr7:78156800-78160400	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr7:78157000-78172000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr7:78157400-78159000	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr7:78157400-78159800	Weak transcription	H9 Cell Line	embryonic stem cell
11	chr7:78157600-78159000	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr7:78157600-78160400	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr7:78158000-78160400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr7:78158000-78160400	Enhancers	NH-A	brain
15	chr7:78158200-78158800	Enhancers	H1 Cell Line	embryonic stem cell
16	chr7:78158200-78158800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
17	chr7:78158400-78158800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr7:78158400-78158800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr7:78158400-78158800	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr7:78158400-78158800	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr7:78158400-78158800	Flanking Active TSS	Osteobl	bone
22	chr7:78158400-78159000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr7:78158400-78159000	Enhancers	HUVEC	blood vessel
24	chr7:78158400-78159200	Enhancers	Brain Substantia Nigra	brain

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