Variant report

Variant	rs10183198
Chromosome Location	chr2:21470987-21470988
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]
rs10166144	0.94[EUR][1000 genomes]
rs10170323	0.94[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10177017	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10177492	0.85[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13387827	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs13398007	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1848922	0.96[ASN][1000 genomes]
rs312029	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs67144154	0.81[EUR][1000 genomes]
rs7571647	0.86[ASN][1000 genomes]
rs9808284	0.89[ASN][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	chr2:21469000-21471000	Weak transcription	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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