Variant report

Variant	rs13233776
Chromosome Location	chr7:80361222-80361223
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 17 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11768155	0.98[ASN][1000 genomes]
rs12530485	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs12539736	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1527467	0.81[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs1527468	0.89[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs17154368	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1852538	0.88[AMR][1000 genomes];0.98[ASN][1000 genomes]
rs1852539	1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1949972	1.00[JPT][hapmap];0.98[ASN][1000 genomes]
rs2272351	0.98[ASN][1000 genomes]
rs2886792	0.89[JPT][hapmap];0.98[ASN][1000 genomes]
rs3778672	1.00[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs3807092	1.00[JPT][hapmap]
rs6979109	1.00[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs73370806	0.98[ASN][1000 genomes]
rs7456998	0.87[AFR][1000 genomes];0.94[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:1 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv888524	chr7:80107798-80723062	Active TSS Strong transcription Enhancers Genic enhancers Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	20 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs13233776	CD36	cis	Whole Blood	GTEx

Chromatin state (count:14 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:80355400-80365800	Weak transcription	HSMM	muscle
2	chr7:80359200-80369000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr7:80359400-80365800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr7:80359400-80369600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr7:80359400-80370200	Weak transcription	NHLF	lung
6	chr7:80359400-80378000	Weak transcription	Psoas Muscle	Psoas
7	chr7:80359600-80362400	Weak transcription	Fetal Stomach	stomach
8	chr7:80359600-80362600	Weak transcription	Fetal Lung	lung
9	chr7:80359600-80373800	Weak transcription	Fetal Muscle Leg	muscle
10	chr7:80359800-80363000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr7:80360400-80361400	Enhancers	Primary monocytes fromperipheralblood	blood
12	chr7:80360600-80377800	Weak transcription	Left Ventricle	heart
13	chr7:80361000-80361600	Enhancers	Fetal Heart	heart
14	chr7:80361200-80361400	Enhancers	Rectal Smooth Muscle	rectum

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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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