Variant report

Variant	rs1283923
Chromosome Location	chr6:44652502-44652503
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 9 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs1283932	0.90[EUR][1000 genomes]
rs1680901	0.93[AFR][1000 genomes];1.00[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2817117	0.93[EUR][1000 genomes]
rs527082	0.90[EUR][1000 genomes]
rs633313	0.92[EUR][1000 genomes]
rs649700	0.89[EUR][1000 genomes]
rs660953	0.92[EUR][1000 genomes]
rs663933	0.96[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs679769	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes]

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:44644400-44652800	Weak transcription	HMEC	breast
2	chr6:44648200-44652600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr6:44648600-44652800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
4	chr6:44648800-44652600	Weak transcription	NHEK	skin
5	chr6:44652200-44654000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	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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