Variant report

Variant	rs73353059
Chromosome Location	chr6:5053916-5053917
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 23 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:15)

rs_ID	r²[population]
rs12332997	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs34008599	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs55796617	1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs56193336	0.91[AMR][1000 genomes]
rs56346886	0.86[EUR][1000 genomes]
rs57093437	0.91[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs58769332	0.97[EUR][1000 genomes]
rs59365793	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73349204	1.00[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73353056	1.00[EUR][1000 genomes]
rs73353070	0.84[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73359952	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73365168	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]
rs73365181	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs9504306	1.00[AMR][1000 genomes];0.86[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1023527	chr6:4729592-5387176	Strong transcription Weak transcription Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	29 gene(s)	inside rSNPs	diseases
2	esv2422499	chr6:4745428-5073222	Enhancers Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
3	nsv462622	chr6:4904380-5172009	Active TSS Enhancers Strong transcription Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
4	nsv600871	chr6:4904380-5172009	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Strong transcription Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	19 gene(s)	inside rSNPs	diseases
5	nsv1033905	chr6:4955826-5080904	Weak transcription Flanking Active TSS Active TSS Enhancers Strong transcription ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	13 gene(s)	inside rSNPs	diseases
6	nsv600872	chr6:4975313-5342190	Weak transcription Active TSS Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	24 gene(s)	inside rSNPs	diseases
7	nsv1031837	chr6:4996667-5418726	Enhancers Weak transcription ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	23 gene(s)	inside rSNPs	diseases
8	nsv1017380	chr6:5007870-5152551	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS Genic enhancers ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	15 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:5051400-5054000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr6:5052600-5054800	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr6:5052600-5054800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr6:5052600-5054800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr6:5052800-5054200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr6:5053000-5055600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
7	chr6:5053400-5054800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr6:5053400-5055000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr6:5053400-5055400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
10	chr6:5053600-5054800	Enhancers	Fetal Muscle Leg	muscle
11	chr6:5053600-5055400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr6:5053800-5054200	Enhancers	HUVEC	blood vessel
13	chr6:5053800-5054800	Enhancers	Primary hematopoietic stem cells	blood

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