Variant report

Variant	rs55826381
Chromosome Location	chr1:45572123-45572124
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:45569785..45572164-chr1:45588128..45590653,3	K562	blood:

Extended variants
information (count: 49 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:43)

rs_ID	r²[population]
rs1152028	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1226732	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1226750	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1612575	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs173208	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1969084	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs1995403	0.96[ASN][1000 genomes]
rs2105460	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs346685	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346686	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs346688	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346689	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346692	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346703	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346704	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346709	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346710	0.98[ASN][1000 genomes]
rs346711	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346718	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346720	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346725	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346726	0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs346730	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs409082	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs412055	0.87[AMR][1000 genomes];0.84[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4415614	0.87[AMR][1000 genomes];0.96[ASN][1000 genomes]
rs4660835	0.92[ASN][1000 genomes]
rs55842174	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs55884892	0.81[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs57805650	0.88[ASN][1000 genomes]
rs61574129	0.81[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs6429556	0.85[ASN][1000 genomes]
rs6693885	0.85[ASN][1000 genomes]
rs72684447	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72684454	0.87[AMR][1000 genomes];0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72684481	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72684482	0.96[ASN][1000 genomes]
rs72684485	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72684487	0.96[ASN][1000 genomes]
rs72684488	0.96[ASN][1000 genomes]
rs72684496	0.81[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs72684499	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs72686404	0.81[EUR][1000 genomes];0.96[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv529677	chr1:45179509-45748571	Weak transcription Enhancers ZNF genes & repeats Strong transcription Flanking Active TSS Active TSS Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	424 gene(s)	inside rSNPs	diseases
2	nsv1002026	chr1:45187594-45758048	Flanking Active TSS Enhancers Genic enhancers Strong transcription Weak transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	386 gene(s)	inside rSNPs	diseases
3	nsv915644	chr1:45282802-45696079	Enhancers Genic enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	98 gene(s)	inside rSNPs	diseases
4	nsv498036	chr1:45428030-46050934	Active TSS Enhancers Flanking Active TSS Genic enhancers Weak transcription Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	191 gene(s)	inside rSNPs	diseases
5	nsv546148	chr1:45500294-45627663	Weak transcription Enhancers Strong transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
6	esv3374969	chr1:45570890-45573738	Weak transcription ZNF genes & repeats Enhancers	Chromatin interactive region	1 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45568200-45594600	Weak transcription	Right Atrium	heart
2	chr1:45569000-45578000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr1:45570600-45572400	Weak transcription	HepG2	liver
4	chr1:45571400-45572400	ZNF genes & repeats	Fetal Stomach	stomach

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