Variant report

Variant	rs73437042
Chromosome Location	chr15:75484078-75484079
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:15)

rs_ID	r²[population]
rs28362067	1.00[AMR][1000 genomes]
rs57509570	1.00[AMR][1000 genomes]
rs57654778	1.00[AMR][1000 genomes]
rs58397909	1.00[AMR][1000 genomes]
rs59078717	1.00[AMR][1000 genomes]
rs73437018	1.00[AMR][1000 genomes]
rs73437030	1.00[AMR][1000 genomes]
rs73437031	1.00[AMR][1000 genomes]
rs73437049	0.83[AFR][1000 genomes]
rs73437054	1.00[AMR][1000 genomes]
rs73437055	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73437074	1.00[AMR][1000 genomes]
rs73438811	1.00[AMR][1000 genomes]
rs8023648	1.00[AMR][1000 genomes]
rs8039385	1.00[AMR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv904383	chr15:75382542-75520378	Weak transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer Strong transcription Flanking Active TSS Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv1796196	chr15:75389382-75531124	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
3	nsv1039713	chr15:75394213-75674389	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Active TSS Genic enhancers Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
4	nsv1037713	chr15:75401213-75665304	Weak transcription Enhancers Strong transcription Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	96 gene(s)	inside rSNPs	diseases
5	nsv1053212	chr15:75428467-75534408	Flanking Active TSS Bivalent Enhancer Active TSS Enhancers Strong transcription Weak transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	41 gene(s)	inside rSNPs	diseases
6	nsv833056	chr15:75452947-75614590	Enhancers Strong transcription Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:75473000-75487600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:75475400-75487800	Weak transcription	Right Atrium	heart
3	chr15:75475600-75487600	Weak transcription	Pancreas	Pancrea
4	chr15:75477200-75492600	Weak transcription	Spleen	Spleen
5	chr15:75478600-75486200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr15:75483200-75484200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr15:75483400-75484200	Enhancers	Fetal Heart	heart
8	chr15:75483400-75484400	Bivalent Enhancer	HepG2	liver
9	chr15:75483600-75484600	Enhancers	Ovary	ovary
10	chr15:75483800-75487600	Weak transcription	Fetal Intestine Small	intestine
11	chr15:75484000-75485600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
12	chr15:75484000-75487600	Weak transcription	Left Ventricle	heart

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dbSNP/dbVar ID: rs12345 /nsv7879
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chromosomal regions: chr1:12345-34567

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