Variant report

Variant	rs71565149
Chromosome Location	chr7:67419074-67419075
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]
rs12698647	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs12698648	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs13225889	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs13231555	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17144995	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs17144997	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34295996	0.86[EUR][1000 genomes]
rs34427036	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs34970171	0.88[EUR][1000 genomes]
rs35101002	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs35149002	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs66882065	1.00[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs67668110	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs73144043	0.95[AMR][1000 genomes];1.00[EUR][1000 genomes]

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:67416000-67419200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr7:67418800-67422000	Enhancers	Cortex derived primary cultured neurospheres	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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