Variant report

Variant	rs1770756
Chromosome Location	chr18:14866355-14866356
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 31 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12457328	0.82[AMR][1000 genomes];0.86[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1622544	0.91[ASN][1000 genomes]
rs1713886	0.86[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1713892	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1713893	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1713895	0.86[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1713897	0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs1770754	0.84[ASN][1000 genomes]
rs1970446	0.81[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs28454867	0.80[EUR][1000 genomes]
rs2945650	0.82[ASN][1000 genomes]
rs3126404	0.83[ASN][1000 genomes]
rs4113248	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs4890750	0.81[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs55721158	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs55929438	0.81[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs61670085	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes]
rs66720816	0.81[AMR][1000 genomes];0.81[EUR][1000 genomes]
rs786050	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs786051	0.84[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs786052	0.81[AMR][1000 genomes]
rs9284405	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs9303869	0.80[EUR][1000 genomes]
rs9675641	0.83[ASN][1000 genomes]
rs9748546	0.83[EUR][1000 genomes]
rs9797358	0.83[ASN][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	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	nsv961033	chr18:14838212-14874870	Weak transcription Flanking Active TSS Enhancers ZNF genes & repeats Active TSS	TF binding region	1 gene(s)	inside rSNPs	diseases
5	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

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:14865200-14866400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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