Variant report

Variant	rs34301482
Chromosome Location	chr15:93107024-93107025
allele	-/A
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 18 )
Associated
traits (count: 0)

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

rs_ID	r²[population]
rs12915754	0.84[AFR][1000 genomes]
rs1390786	0.96[EUR][1000 genomes]
rs1472372	0.96[EUR][1000 genomes]
rs17647392	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.89[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs17647569	0.96[EUR][1000 genomes]
rs17647695	0.96[EUR][1000 genomes]
rs17704035	0.93[EUR][1000 genomes]
rs17704159	0.93[EUR][1000 genomes]
rs56839229	0.84[EUR][1000 genomes]
rs56910829	0.96[EUR][1000 genomes]
rs59944160	0.84[EUR][1000 genomes]
rs61557975	0.93[EUR][1000 genomes]
rs74029143	0.93[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv948621	chr15:92688981-93158095	Enhancers Bivalent/Poised TSS ZNF genes & repeats Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	28 gene(s)	inside rSNPs	diseases
2	nsv1037972	chr15:92804908-93270761	Flanking Bivalent TSS/Enh Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	39 gene(s)	inside rSNPs	diseases
3	nsv904499	chr15:92914795-93472582	Bivalent Enhancer Flanking Active TSS Genic enhancers Strong transcription Active TSS Transcr. at gene 5' and 3' Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA	163 gene(s)	inside rSNPs	diseases
4	nsv948738	chr15:93070742-93728147	Strong transcription Weak transcription Flanking Active TSS Enhancers Genic enhancers Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	169 gene(s)	inside rSNPs	diseases
5	esv1505742	chr15:93107024-93107025	Enhancers Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:93104000-93108200	Enhancers	Fetal Lung	lung
2	chr15:93106000-93125800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr15:93106200-93108200	Enhancers	HUVEC	blood vessel
4	chr15:93106400-93108200	Enhancers	Primary hematopoietic stem cells	blood
5	chr15:93106600-93107200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
6	chr15:93106600-93107200	Enhancers	Lung	lung
7	chr15:93106600-93108000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr15:93106600-93108000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr15:93106600-93108000	Enhancers	Fetal Stomach	stomach
10	chr15:93106600-93108200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:93106600-93113200	Weak transcription	Fetal Muscle Leg	muscle
12	chr15:93106800-93107200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr15:93107000-93113200	Weak transcription	Left Ventricle	heart

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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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