Variant report

Variant	rs35777541
Chromosome Location	chr2:21471028-21471029
allele	C/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]
rs12472945	0.86[AMR][1000 genomes]
rs12478996	0.93[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs12623269	0.92[EUR][1000 genomes]
rs1397400	0.86[AMR][1000 genomes]
rs1877061	0.92[EUR][1000 genomes]
rs312027	0.97[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs34340041	0.89[EUR][1000 genomes]
rs67758164	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs71437405	0.93[EUR][1000 genomes]
rs71437406	0.87[AFR][1000 genomes];0.81[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs925864	0.89[EUR][1000 genomes]

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:21462200-21480800	Weak transcription	Aorta	Aorta
2	chr2:21468000-21473400	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr2:21468600-21473400	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr2:21471000-21471200	Enhancers	Brain Substantia Nigra	brain

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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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