Variant report

Variant	rs1713886
Chromosome Location	chr18:14860231-14860232
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 44 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:34)

rs_ID	r²[population]
rs10468701	0.81[EUR][1000 genomes]
rs10468702	0.80[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs10775422	0.81[EUR][1000 genomes]
rs12457328	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs12607816	0.80[EUR][1000 genomes]
rs12966403	0.80[EUR][1000 genomes]
rs12970537	0.81[EUR][1000 genomes]
rs1622544	0.90[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1713892	0.83[AMR][1000 genomes];0.86[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1713893	0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs1713895	0.83[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs1713897	0.81[ASN][1000 genomes]
rs1770754	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1770756	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1970446	0.93[AFR][1000 genomes];0.91[AMR][1000 genomes];0.91[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs28454867	0.84[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs2945650	0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs3126404	0.93[AMR][1000 genomes];0.89[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs3878726	0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs4113248	0.83[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs4890750	0.82[AMR][1000 genomes];0.90[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs55721158	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs55774912	0.82[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55929438	0.96[AMR][1000 genomes];0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs9284405	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs9303862	0.81[EUR][1000 genomes]
rs9303863	0.81[EUR][1000 genomes]
rs9303869	0.85[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9675641	0.86[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9676173	0.80[EUR][1000 genomes]
rs9709715	0.81[EUR][1000 genomes]
rs9748546	0.85[EUR][1000 genomes]
rs9797358	0.81[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs9989501	0.80[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	nsv428006	chr18:14087067-14874733	Weak transcription Flanking Bivalent TSS/Enh Enhancers Flanking Active TSS Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	36 gene(s)	inside rSNPs	diseases
2	nsv916419	chr18:14418522-15165372	Enhancers Active TSS Weak transcription Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	esv2751771	chr18:14704694-15106727	Flanking Bivalent TSS/Enh Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA miRNA	18 gene(s)	inside rSNPs	diseases
4	esv2756821	chr18:14741611-14865985	Weak transcription Enhancers Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island lncRNA miRNA	8 gene(s)	inside rSNPs	diseases
5	nsv961033	chr18:14838212-14874870	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
6	nsv909434	chr18:14841828-15149366	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	9 gene(s)	inside rSNPs	diseases
7	esv3418863	chr18:14852952-14862050	Enhancers ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
8	esv3421096	chr18:14854802-14862150	Weak transcription ZNF genes & repeats	n/a	n/a	inside rSNPs	diseases
9	esv3444314	chr18:14855302-14861000	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases
10	nsv512518	chr18:14855492-14860951	ZNF genes & repeats Weak transcription	n/a	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14860200-14860400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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