Variant report

Variant	rs7832144
Chromosome Location	chr8:63062581-63062582
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs10504344	0.93[EUR][1000 genomes]
rs12542544	0.86[ASN][1000 genomes]
rs12544805	0.93[EUR][1000 genomes]
rs1601056	0.90[ASN][1000 genomes]
rs34250977	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4256587	0.99[EUR][1000 genomes]
rs4268118	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4317559	0.99[EUR][1000 genomes]
rs4349974	0.80[AFR][1000 genomes];0.87[ASN][1000 genomes]
rs4383956	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4445217	0.99[EUR][1000 genomes]
rs4562310	0.84[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4610738	0.80[AFR][1000 genomes];0.95[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4738938	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4738939	1.00[EUR][1000 genomes]
rs6980515	0.99[EUR][1000 genomes]
rs7015635	0.86[ASN][1000 genomes]
rs7462666	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs7841863	1.00[EUR][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	nsv890955	chr8:62919691-63062581	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	2 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	chr8:63058800-63063600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:63060200-63064400	Enhancers	Hela-S3	cervix
3	chr8:63061200-63072200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr8:63062000-63063800	Enhancers	HMEC	breast
5	chr8:63062400-63063200	Enhancers	Muscle Satellite Cultured Cells	--

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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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