Variant report

Variant	rs72739147
Chromosome Location	chr15:58571401-58571402
allele	A/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:10)

rs_ID	r²[population]
rs11071371	0.85[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs12148399	0.83[AMR][1000 genomes]
rs12148780	0.83[AMR][1000 genomes]
rs16940011	0.83[AMR][1000 genomes]
rs16940017	0.85[AMR][1000 genomes]
rs28690720	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes]
rs2899623	0.83[AMR][1000 genomes]
rs2899624	0.83[AMR][1000 genomes]
rs56142310	1.00[AMR][1000 genomes];0.97[EUR][1000 genomes]
rs58038553	0.98[AMR][1000 genomes];0.97[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:10 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1047246	chr15:58375607-58707158	Enhancers Weak transcription Flanking Active TSS Active TSS Genic enhancers Bivalent Enhancer ZNF genes & repeats Strong transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
2	nsv833024	chr15:58447459-58621963	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Strong transcription Bivalent Enhancer Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv904264	chr15:58505122-58588510	Enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv904265	chr15:58517528-58588510	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	6 gene(s)	inside rSNPs	diseases
5	nsv1051058	chr15:58519922-59092530	Strong transcription Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
6	nsv542401	chr15:58519922-59092530	Strong transcription Weak transcription Active TSS Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	50 gene(s)	inside rSNPs	diseases
7	nsv529717	chr15:58519923-58756814	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
8	nsv1042201	chr15:58520746-58780710	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv569598	chr15:58552606-58852463	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
10	nsv569599	chr15:58563209-58579956	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:58554200-58574400	Weak transcription	Left Ventricle	heart
2	chr15:58564400-58582000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr15:58564800-58574400	Weak transcription	A549	lung
4	chr15:58568800-58572400	Enhancers	Liver	Liver
5	chr15:58569800-58574200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
6	chr15:58570200-58572000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:58570600-58571600	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr15:58570600-58572000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr15:58570600-58572200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr15:58570600-58572200	Enhancers	Fetal Thymus	thymus
11	chr15:58570800-58582200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
12	chr15:58571200-58571600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr15:58571200-58572000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr15:58571200-58572400	Enhancers	K562	blood
15	chr15:58571400-58571600	Enhancers	H9 Cell Line	embryonic stem cell
16	chr15:58571400-58571800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr15:58571400-58572000	Enhancers	HepG2	liver
18	chr15:58571400-58572200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin

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

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