Variant report

Variant	rs4767629
Chromosome Location	chr12:118255077-118255078
allele	G/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]
rs10850902	0.83[AMR][1000 genomes];0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs10850904	0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11615079	0.82[AMR][1000 genomes];0.92[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2062906	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs4766876	0.88[EUR][1000 genomes]
rs4766881	0.95[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4767627	0.85[EUR][1000 genomes]
rs4767628	0.83[EUR][1000 genomes]
rs895472	0.94[AMR][1000 genomes];0.98[EUR][1000 genomes];0.92[ASN][1000 genomes]

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:118253800-118266400	Weak transcription	Pancreatic Islets	Pancreatic Islet
2	chr12:118254200-118264000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr12:118254800-118257400	Enhancers	Dnd41	blood

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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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