Variant report

Variant	rs926925
Chromosome Location	chr6:107156861-107156862
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 14 )
Associated
traits (count: 3 )

rSNPs within LD-proxies of this variant (count:14)

rs_ID	r²[population]
rs10499044	0.86[JPT][hapmap]
rs17067644	0.83[MEX][hapmap]
rs1852982	0.98[ASN][1000 genomes]
rs2642463	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2642465	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs2642466	0.91[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2748291	0.96[AFR][1000 genomes];0.94[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs2748293	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes]
rs2798362	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2798363	0.84[AFR][1000 genomes];0.81[AMR][1000 genomes];0.81[ASN][1000 genomes]
rs2798364	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs3127663	0.89[EUR][1000 genomes]
rs6940205	0.80[GIH][hapmap];0.86[TSI][hapmap]
rs9398105	0.82[AFR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]

mRNA abundance (count:3)

SNP	Gene	Cis/trans	Tissue	Source
rs926925	PREP	cis	parietal	SCAN
rs926925	RTN4IP1	cis	parietal	SCAN
rs926925	AIM1	cis	cerebellum	SCAN

Chromatin state (count:6 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:107142600-107157400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:107151000-107162200	Weak transcription	Fetal Kidney	kidney
3	chr6:107152400-107161400	Weak transcription	Pancreas	Pancrea
4	chr6:107154200-107160400	Weak transcription	Primary B cells from cord blood	blood
5	chr6:107154400-107158200	Weak transcription	Primary B cells from peripheral blood	blood
6	chr6:107155000-107157800	Weak transcription	Primary neutrophils fromperipheralblood	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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