Variant report

Variant	rs6978526
Chromosome Location	chr7:78057393-78057394
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:19)

rs_ID	r²[population]
rs10485886	0.97[AFR][1000 genomes]
rs12532329	0.99[AFR][1000 genomes];0.97[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12532363	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs12533284	0.94[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs17150719	0.92[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs17150722	0.81[EUR][1000 genomes]
rs28573255	0.87[EUR][1000 genomes]
rs62468772	0.86[EUR][1000 genomes]
rs62468774	0.87[EUR][1000 genomes]
rs62468775	1.00[EUR][1000 genomes]
rs6466211	0.89[AFR][1000 genomes]
rs6466212	0.93[AFR][1000 genomes]
rs6466213	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs6959336	0.90[AFR][1000 genomes]
rs6959624	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6972004	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs6975027	0.86[AMR][1000 genomes];0.99[EUR][1000 genomes]
rs6975990	0.90[EUR][1000 genomes]
rs6977890	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][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:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78049600-78066200	Weak transcription	Ovary	ovary
2	chr7:78051600-78064200	Weak transcription	Brain Substantia Nigra	brain
3	chr7:78052400-78064200	Weak transcription	Brain Anterior Caudate	brain
4	chr7:78054600-78058600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr7:78056800-78064600	Weak transcription	Brain Inferior Temporal Lobe	brain

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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