Variant report

Variant	rs9285664
Chromosome Location	chr5:145053794-145053795
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10036664	1.00[AMR][1000 genomes]
rs10040204	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10043538	1.00[AMR][1000 genomes]
rs10043961	1.00[AMR][1000 genomes]
rs10052024	1.00[AMR][1000 genomes]
rs10052169	1.00[AMR][1000 genomes]
rs10054314	1.00[AMR][1000 genomes]
rs10073313	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs10077242	1.00[AMR][1000 genomes]
rs10476875	1.00[AMR][1000 genomes]
rs13354398	1.00[AMR][1000 genomes]
rs13356403	1.00[AMR][1000 genomes]
rs13436791	1.00[AMR][1000 genomes]
rs13436850	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs2217647	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs28507009	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs4345360	1.00[AMR][1000 genomes]
rs73302023	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs868778	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv883004	chr5:144945649-145068001	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
2	nsv883005	chr5:144945649-145107586	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Strong transcription Active TSS	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:145028400-145060400	Weak transcription	Pancreas	Pancrea
2	chr5:145053200-145054000	Enhancers	Fetal Lung	lung
3	chr5:145053200-145060400	Weak transcription	Left Ventricle	heart

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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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