Variant report

Variant	rs1441004
Chromosome Location	chr8:49845783-49845784
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10097264	0.87[EUR][1000 genomes]
rs10100077	0.87[EUR][1000 genomes]
rs10808734	0.80[EUR][1000 genomes]
rs11515036	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs12682003	0.83[AMR][1000 genomes]
rs13265564	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1441005	0.85[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs17641604	0.85[AMR][1000 genomes]
rs1837690	0.81[AMR][1000 genomes]
rs1992375	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2385117	0.83[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs2385120	0.87[AMR][1000 genomes];0.92[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs2582778	0.84[EUR][1000 genomes]
rs870397	0.83[AMR][1000 genomes]

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:49837800-49846200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
2	chr8:49842000-49846400	Weak transcription	HMEC	breast
3	chr8:49842200-49846400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr8:49844200-49846400	Weak transcription	Esophagus	oesophagus
5	chr8:49845400-49848400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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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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