Variant report

Variant	rs7635303
Chromosome Location	chr3:143333969-143333970
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:10)

rs_ID	r²[population]
rs16854284	1.00[AMR][1000 genomes]
rs16854298	1.00[AMR][1000 genomes]
rs16854305	1.00[AMR][1000 genomes]
rs16854317	1.00[AMR][1000 genomes]
rs58486910	1.00[AMR][1000 genomes]
rs59581279	1.00[AMR][1000 genomes]
rs72997837	1.00[AMR][1000 genomes]
rs73009471	1.00[AMR][1000 genomes]
rs73009482	1.00[AMR][1000 genomes]
rs7650491	1.00[AFR][1000 genomes];1.00[AMR][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	nsv949288	chr3:142793323-143585882	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
2	nsv829745	chr3:143278512-143405626	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:143297600-143339000	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr3:143300400-143336800	Weak transcription	Primary T cells from cord blood	blood
3	chr3:143324200-143340000	Weak transcription	Primary B cells from cord blood	blood
4	chr3:143324400-143353800	Weak transcription	Sigmoid Colon	Sigmoid Colon
5	chr3:143324600-143336400	Weak transcription	Fetal Stomach	stomach
6	chr3:143328200-143376200	Weak transcription	Ovary	ovary
7	chr3:143328400-143346000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr3:143329600-143337200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr3:143329800-143334800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr3:143331200-143334400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr3:143332600-143337200	Weak transcription	Primary monocytes fromperipheralblood	blood
12	chr3:143332800-143334200	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chr3:143332800-143334400	Enhancers	HSMMtube	muscle
14	chr3:143333400-143334000	Enhancers	Placenta Amnion	Placenta Amnion

Quick Search:

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

what's new

Quick links