Variant report

Variant	rs73026018
Chromosome Location	chr3:160359903-160359904
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 24 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs11706421	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11710775	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs11713410	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs16831329	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73026022	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73026025	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73026035	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73026039	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73026053	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73026057	1.00[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs73877929	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs7622468	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:12 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532666	chr3:159777847-160703202	Enhancers Weak transcription ZNF genes & repeats Strong transcription Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' Flanking Active TSS Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	271 gene(s)	inside rSNPs	diseases
2	nsv1000453	chr3:159853305-160366357	Active TSS Flanking Active TSS Enhancers Weak transcription Genic enhancers Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
3	nsv536779	chr3:159853305-160366357	Strong transcription Enhancers Transcr. at gene 5' and 3' Weak transcription Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	259 gene(s)	inside rSNPs	diseases
4	nsv877703	chr3:160325458-160398885	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	5 gene(s)	inside rSNPs	diseases
5	esv2757019	chr3:160351021-160380161	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
6	esv2759194	chr3:160351021-160380161	Enhancers Flanking Active TSS Bivalent Enhancer Weak transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
7	nsv10343	chr3:160355620-160366624	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
8	esv3463584	chr3:160355760-160366323	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
9	esv3463585	chr3:160355760-160366323	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
10	nsv822307	chr3:160355841-160366230	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	inside rSNPs	diseases
11	esv2421521	chr3:160356940-160362285	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
12	esv2763313	chr3:160356940-160362285	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:17 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:160358200-160361000	Enhancers	Hela-S3	cervix
2	chr3:160358800-160360400	Enhancers	HUVEC	blood vessel
3	chr3:160359000-160360400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:160359400-160360000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr3:160359400-160360000	Enhancers	Skeletal Muscle Male	skeletal muscle
6	chr3:160359400-160360200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr3:160359400-160360200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr3:160359400-160360200	Enhancers	Osteobl	bone
9	chr3:160359600-160360200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr3:160359600-160360200	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr3:160359600-160360200	Enhancers	NH-A	brain
12	chr3:160359600-160360400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr3:160359800-160360200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr3:160359800-160360200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr3:160359800-160360200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr3:160359800-160360200	Enhancers	Psoas Muscle	Psoas
17	chr3:160359800-160360200	Enhancers	Stomach Smooth Muscle	stomach

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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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