Variant report

Variant	rs7802689
Chromosome Location	chr7:78044981-78044982
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 10 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10262046	0.93[CHB][hapmap];0.81[JPT][hapmap]
rs10953556	1.00[CHB][hapmap];0.92[JPT][hapmap];0.94[ASN][1000 genomes]
rs17150696	1.00[YRI][hapmap];0.91[AFR][1000 genomes]
rs17417090	0.94[CEU][hapmap];1.00[CHB][hapmap];0.92[JPT][hapmap];1.00[YRI][hapmap];0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs1860537	1.00[YRI][hapmap];0.81[AFR][1000 genomes]
rs2191330	0.92[CHB][hapmap]
rs6944339	0.86[YRI][hapmap]
rs6947316	0.93[CHB][hapmap];0.81[JPT][hapmap];0.84[YRI][hapmap]
rs6947591	0.92[CHB][hapmap]

Variant overlapped rSNPs/rCNVs (count:1 , 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

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:78023000-78047200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr7:78029000-78045000	Weak transcription	Brain Anterior Caudate	brain
3	chr7:78029000-78045200	Weak transcription	Brain Substantia Nigra	brain
4	chr7:78036200-78047200	Weak transcription	Brain Angular Gyrus	brain
5	chr7:78041200-78047200	Weak transcription	Pancreatic Islets	Pancreatic Islet
6	chr7:78041800-78045200	Weak transcription	Brain Hippocampus Middle	brain
7	chr7:78044400-78045600	Enhancers	Brain Cingulate Gyrus	brain
8	chr7:78044800-78045600	Enhancers	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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