Variant report

Variant	rs73026373
Chromosome Location	chr1:153530952-153530953
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 21 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:17)

rs_ID	r²[population]
rs11486186	1.00[AMR][1000 genomes]
rs11808118	1.00[AMR][1000 genomes]
rs28574283	1.00[AMR][1000 genomes]
rs34192791	1.00[AMR][1000 genomes]
rs59462422	0.86[AFR][1000 genomes]
rs61522372	0.86[AFR][1000 genomes]
rs61545193	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6682725	1.00[AMR][1000 genomes]
rs73009905	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73009929	1.00[AMR][1000 genomes]
rs73009949	1.00[AMR][1000 genomes]
rs73009950	1.00[AMR][1000 genomes]
rs73009952	1.00[AMR][1000 genomes]
rs73026324	0.81[AFR][1000 genomes]
rs73026360	0.86[AFR][1000 genomes]
rs73026363	0.86[AFR][1000 genomes]
rs73026369	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1010488	chr1:152901263-153670972	Genic enhancers Active TSS Strong transcription Bivalent/Poised TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
2	nsv535171	chr1:152901263-153670972	Enhancers Flanking Active TSS Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	236 gene(s)	inside rSNPs	diseases
3	nsv831603	chr1:153405842-153576143	Transcr. at gene 5' and 3' Bivalent Enhancer Weak transcription Enhancers Active TSS Flanking Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	148 gene(s)	inside rSNPs	diseases
4	nsv1007306	chr1:153413827-153541798	Weak transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Strong transcription ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	146 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:153522600-153538000	Weak transcription	Colonic Mucosa	Colon
2	chr1:153526600-153534000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
3	chr1:153527200-153536200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr1:153527200-153536400	Weak transcription	Spleen	Spleen
5	chr1:153527400-153531400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
6	chr1:153527400-153534400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr1:153527400-153535800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr1:153527400-153536200	Weak transcription	NHLF	lung
9	chr1:153527600-153532800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
10	chr1:153527600-153535200	Weak transcription	Esophagus	oesophagus
11	chr1:153527600-153536000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr1:153527600-153536200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chr1:153529400-153534600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr1:153530400-153531200	Genic enhancers	HMEC	breast
15	chr1:153530400-153531400	Genic enhancers	NHEK	skin
16	chr1:153530600-153532400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin

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dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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