Variant report

Variant	rs73752326
Chromosome Location	chr5:15838437-15838438
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 20 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:9)

rs_ID	r²[population]
rs16867720	1.00[AMR][1000 genomes]
rs60563254	1.00[AMR][1000 genomes]
rs60782876	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs6897069	0.83[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73752327	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs73752328	0.81[AFR][1000 genomes]
rs73752329	0.81[AFR][1000 genomes]
rs73752334	0.81[AFR][1000 genomes]
rs73752337	0.81[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv516929	chr5:15087791-15870300	Enhancers Active TSS Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
2	nsv1023068	chr5:15095221-15863583	Enhancers Weak transcription Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
3	nsv869040	chr5:15097602-15866117	Active TSS Weak transcription Enhancers Strong transcription Genic enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv530222	chr5:15151662-15851485	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
5	nsv1028089	chr5:15636285-15883910	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
6	nsv537676	chr5:15636285-15883910	Weak transcription Enhancers ZNF genes & repeats Active TSS Genic enhancers Flanking Active TSS Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv1024248	chr5:15638067-15863583	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv537677	chr5:15638067-15863583	Weak transcription Enhancers Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Bivalent Enhancer	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
9	nsv880755	chr5:15670377-15938553	Weak transcription Flanking Active TSS Enhancers Active TSS Strong transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	4 gene(s)	inside rSNPs	diseases
10	esv2763894	chr5:15714022-15863332	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers ZNF genes & repeats Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
11	nsv1031483	chr5:15738485-15926083	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Strong transcription Genic enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:15833800-15840800	Weak transcription	Psoas Muscle	Psoas
2	chr5:15834000-15839000	Enhancers	Fetal Lung	lung
3	chr5:15835000-15838600	Enhancers	HSMMtube	muscle
4	chr5:15836600-15838600	Enhancers	Right Atrium	heart
5	chr5:15837000-15838600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr5:15837000-15838600	Enhancers	NHLF	lung
7	chr5:15837000-15841800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr5:15837400-15838600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr5:15837800-15839000	Enhancers	Ovary	ovary
10	chr5:15837800-15841800	Weak transcription	Fetal Stomach	stomach
11	chr5:15838000-15838600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr5:15838000-15838600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
13	chr5:15838000-15838600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr5:15838000-15838600	Enhancers	Left Ventricle	heart
15	chr5:15838200-15838600	Enhancers	Right Ventricle	heart
16	chr5:15838200-15838800	Flanking Active TSS	Fetal Heart	heart
17	chr5:15838200-15842200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
18	chr5:15838400-15840000	Weak transcription	Colon Smooth Muscle	Colon

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dbSNP/dbVar ID: rs12345 /nsv7879
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