Variant report

Variant	rs7007348
Chromosome Location	chr8:63063638-63063639
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:11)

rs_ID	r²[population]
rs16928580	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs16928599	1.00[ASN][1000 genomes]
rs17237587	1.00[ASN][1000 genomes]
rs17810421	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs59158455	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs60099345	0.86[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs61214522	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72649311	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72649343	1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs72666340	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs7821022	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:63060200-63064400	Enhancers	Hela-S3	cervix
2	chr8:63061200-63072200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
3	chr8:63062000-63063800	Enhancers	HMEC	breast

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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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