Variant report

Variant	rs3732790
Chromosome Location	chr3:113847283-113847284
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 11 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs10934254	0.82[EUR][1000 genomes]
rs10934255	0.82[EUR][1000 genomes]
rs11715906	0.82[EUR][1000 genomes]
rs12636133	0.82[EUR][1000 genomes]
rs1385884	0.82[EUR][1000 genomes]
rs1486012	0.82[EUR][1000 genomes]
rs2087017	0.82[EUR][1000 genomes]
rs3773679	0.96[CEU][hapmap];0.95[CHB][hapmap];0.85[JPT][hapmap];0.88[AMR][1000 genomes];0.90[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs963468	1.00[ASW][hapmap];0.96[CEU][hapmap];0.90[JPT][hapmap];0.92[TSI][hapmap];1.00[YRI][hapmap];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv877352	chr3:113744010-113870078	Strong transcription Weak transcription Enhancers Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
2	nsv877353	chr3:113789029-113879562	Strong transcription Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region miRNA target site	4 gene(s)	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs3732790	CD200R1L	cis	cerebellum	SCAN

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:113841800-113847400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr3:113841800-113847400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
3	chr3:113846600-113848600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr3:113846800-113847800	Enhancers	HUVEC	blood vessel
5	chr3:113847000-113847600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
6	chr3:113847000-113847600	Enhancers	NHLF	lung
7	chr3:113847000-113847800	Enhancers	NH-A	brain
8	chr3:113847000-113847800	Enhancers	Osteobl	bone
9	chr3:113847200-113847800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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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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