Variant report

Variant	rs17032618
Chromosome Location	chr2:67065700-67065701
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 5 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:3)

rs_ID	r²[population]
rs17032617	1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17032622	1.00[CHB][hapmap];1.00[JPT][hapmap];1.00[YRI][hapmap];0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs17032628	1.00[AMR][1000 genomes];1.00[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	nsv1009027	chr2:66947462-67114455	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
2	nsv874246	chr2:67001969-67147854	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:18 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:67055400-67066800	Weak transcription	Fetal Kidney	kidney
2	chr2:67055400-67066800	Weak transcription	Rectal Smooth Muscle	rectum
3	chr2:67056800-67066800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr2:67060800-67066200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:67061400-67066600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr2:67061400-67066600	Weak transcription	Colon Smooth Muscle	Colon
7	chr2:67061400-67072800	Weak transcription	Pancreas	Pancrea
8	chr2:67061600-67067000	Weak transcription	Fetal Lung	lung
9	chr2:67063600-67068200	Weak transcription	Placenta Amnion	Placenta Amnion
10	chr2:67065200-67066800	Enhancers	NHEK	skin
11	chr2:67065200-67068200	Enhancers	HMEC	breast
12	chr2:67065200-67069000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr2:67065400-67066000	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr2:67065600-67067400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
15	chr2:67065600-67067400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr2:67065600-67067800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr2:67065600-67068400	Enhancers	NH-A	brain
18	chr2:67065600-67068600	Enhancers	NHDF-Ad	bronchial

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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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