Variant report

Variant	rs36048782
Chromosome Location	chr15:73319789-73319790
allele	A/G
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:17)

rs_ID	r²[population]
rs12903656	0.88[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs12908090	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12909626	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs12913381	1.00[ASN][1000 genomes]
rs12917161	1.00[AFR][1000 genomes];0.94[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2415214	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]
rs34691393	1.00[ASN][1000 genomes]
rs34770199	1.00[ASN][1000 genomes]
rs34846029	1.00[ASN][1000 genomes]
rs35206920	1.00[ASN][1000 genomes]
rs35686353	1.00[ASN][1000 genomes]
rs35988290	1.00[ASN][1000 genomes]
rs36019616	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4636887	1.00[ASN][1000 genomes]
rs7176144	0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs7179577	1.00[ASN][1000 genomes]
rs72739406	1.00[AFR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3352103	chr15:73191535-73454001	Bivalent/Poised TSS Active TSS Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv482421	chr15:73279141-73426897	Enhancers Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Weak transcription Strong transcription Transcr. at gene 5' and 3' Bivalent Enhancer Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region	7 gene(s)	inside rSNPs	diseases
3	nsv904338	chr15:73313691-73483718	Enhancers Active TSS Strong transcription ZNF genes & repeats Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:73315000-73321200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr15:73315400-73320600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr15:73316400-73321800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr15:73317000-73320400	Weak transcription	Fetal Lung	lung
5	chr15:73318600-73321800	Enhancers	Fetal Brain Female	brain
6	chr15:73318600-73327600	Enhancers	Fetal Intestine Small	intestine
7	chr15:73318800-73328000	Enhancers	Fetal Intestine Large	intestine
8	chr15:73319000-73322000	Enhancers	Fetal Brain Male	brain
9	chr15:73319400-73320600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chr15:73319400-73321600	Weak transcription	H9 Cell Line	embryonic stem cell

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

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