Variant report

Variant	rs8037082
Chromosome Location	chr15:51734596-51734597
allele	A/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 22 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:13)

rs_ID	r²[population]
rs10220907	0.94[ASN][1000 genomes]
rs12101851	0.90[ASN][1000 genomes]
rs2271677	0.81[ASN][1000 genomes]
rs28886978	0.87[ASN][1000 genomes]
rs60490752	0.84[ASN][1000 genomes]
rs7167954	0.94[ASN][1000 genomes]
rs7172287	1.00[ASN][1000 genomes]
rs7172619	0.97[ASN][1000 genomes]
rs72729245	0.94[ASN][1000 genomes]
rs74013295	0.90[ASN][1000 genomes]
rs74013297	0.90[ASN][1000 genomes]
rs8025629	0.94[ASN][1000 genomes]
rs8028658	0.88[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:9 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv569400	chr15:50874964-51767265	ZNF genes & repeats Weak transcription Strong transcription Active TSS Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
2	esv34532	chr15:51276128-51752856	Flanking Active TSS Weak transcription Strong transcription Enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	21 gene(s)	inside rSNPs	diseases
3	esv2758382	chr15:51282257-51830339	Enhancers Bivalent/Poised TSS Weak transcription Bivalent Enhancer Strong transcription Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
4	esv2760031	chr15:51282257-51830339	Weak transcription Enhancers Strong transcription Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS Active TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	22 gene(s)	inside rSNPs	diseases
5	nsv471243	chr15:51345485-52018096	Weak transcription Enhancers Active TSS Flanking Active TSS Genic enhancers Strong transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
6	esv2757600	chr15:51352249-51783981	Weak transcription Bivalent Enhancer Enhancers Strong transcription Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Genic enhancers 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	21 gene(s)	inside rSNPs	diseases
7	nsv904216	chr15:51631479-51739808	Bivalent Enhancer Enhancers Strong transcription Active TSS Weak transcription Genic enhancers Flanking Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
8	nsv904217	chr15:51695653-51881980	Strong transcription Weak transcription Enhancers ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	6 gene(s)	inside rSNPs	diseases
9	esv13368	chr15:51705468-51735025	Weak transcription Strong transcription Enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:15 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51707200-51738800	Weak transcription	Placenta	Placenta
2	chr15:51707400-51740200	Weak transcription	Brain Hippocampus Middle	brain
3	chr15:51731000-51740600	Weak transcription	Brain Substantia Nigra	brain
4	chr15:51731200-51737200	Weak transcription	A549	lung
5	chr15:51731200-51738600	Weak transcription	Brain Inferior Temporal Lobe	brain
6	chr15:51731400-51735000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr15:51732000-51740600	Weak transcription	Stomach Smooth Muscle	stomach
8	chr15:51732800-51738600	Weak transcription	Brain Angular Gyrus	brain
9	chr15:51732800-51740200	Weak transcription	K562	blood
10	chr15:51733000-51740600	Weak transcription	Brain Anterior Caudate	brain
11	chr15:51733200-51735000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr15:51733800-51735400	Weak transcription	Aorta	Aorta
13	chr15:51733800-51740000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
14	chr15:51734000-51740600	Weak transcription	Sigmoid Colon	Sigmoid Colon
15	chr15:51734400-51737000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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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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