Variant report

Variant	rs7042977
Chromosome Location	chr9:108188856-108188857
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs10121953	0.82[YRI][hapmap];0.85[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs12348331	1.00[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs16924584	0.81[AMR][1000 genomes]
rs7018526	1.00[YRI][hapmap];0.98[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7025836	0.92[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7031606	0.80[YRI][hapmap];0.80[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7032034	0.80[YRI][hapmap];0.80[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs7036215	0.96[YRI][hapmap];0.92[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7857578	0.89[YRI][hapmap];0.94[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7859070	0.81[AMR][1000 genomes]

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	nsv1037750	chr9:108027692-108251733	Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	9 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr9:108177800-108194200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr9:108177800-108194200	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr9:108182600-108193800	Weak transcription	Brain Angular Gyrus	brain
4	chr9:108182600-108193800	Weak transcription	Brain Cingulate Gyrus	brain
5	chr9:108182800-108193600	Weak transcription	Brain Substantia Nigra	brain
6	chr9:108182800-108193800	Weak transcription	Brain Inferior Temporal Lobe	brain
7	chr9:108183000-108194000	Weak transcription	Brain Anterior Caudate	brain
8	chr9:108184400-108193600	Weak transcription	Brain Hippocampus Middle	brain
9	chr9:108188000-108189000	Enhancers	Liver	Liver
10	chr9:108188800-108193600	Weak transcription	Skeletal Muscle Male	skeletal muscle

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Input of quick search could be:

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

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