Variant report

Variant	rs60777884
Chromosome Location	chr15:78132693-78132694
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 25 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:16)

rs_ID	r²[population]
rs11072672	0.81[AFR][1000 genomes]
rs11852882	1.00[AMR][1000 genomes]
rs11853677	1.00[AMR][1000 genomes]
rs11854277	1.00[AMR][1000 genomes]
rs11858739	1.00[AMR][1000 genomes]
rs4886913	0.81[AFR][1000 genomes]
rs56875053	1.00[AMR][1000 genomes]
rs57128446	1.00[AMR][1000 genomes]
rs57309564	1.00[AMR][1000 genomes]
rs57442101	1.00[AMR][1000 genomes]
rs58400094	1.00[AMR][1000 genomes]
rs58710415	1.00[AMR][1000 genomes]
rs60880256	1.00[AMR][1000 genomes]
rs61085022	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes]
rs7164311	0.88[AFR][1000 genomes]
rs72730744	0.82[AFR][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	nsv1040852	chr15:77160237-78137541	Enhancers Flanking Active TSS Active TSS Strong transcription Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	esv1806097	chr15:77817889-78301377	Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Active TSS Genic enhancers Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	30 gene(s)	inside rSNPs	diseases
3	nsv529491	chr15:77932659-78751516	Genic enhancers Bivalent Enhancer Enhancers Weak transcription Strong transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	80 gene(s)	inside rSNPs	diseases
4	nsv833062	chr15:78035206-78220358	Enhancers Bivalent Enhancer Weak transcription Flanking Active TSS Active TSS Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
5	nsv904424	chr15:78059488-78158893	Enhancers Active TSS Weak transcription Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv904425	chr15:78064664-78153850	Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Active TSS Flanking Active TSS ZNF genes & repeats Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
7	esv1833316	chr15:78081307-78328108	Enhancers Weak transcription Strong transcription Bivalent/Poised TSS Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	18 gene(s)	inside rSNPs	diseases
8	nsv904426	chr15:78090630-78264164	Active TSS Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Weak transcription Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	11 gene(s)	inside rSNPs	diseases
9	nsv904427	chr15:78129964-78251431	Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers ZNF genes & repeats Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:78124800-78132800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:78128800-78133200	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr15:78131800-78134200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:78132400-78132800	Bivalent Enhancer	Fetal Intestine Large	intestine
5	chr15:78132400-78133400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr15:78132400-78134200	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr15:78132400-78134800	Enhancers	Fetal Intestine Small	intestine
8	chr15:78132600-78133000	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr15:78132600-78133200	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr15:78132600-78133600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr15:78132600-78134000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr15:78132600-78134000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr15:78132600-78134200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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

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