Variant report

Variant	rs57606521
Chromosome Location	chr16:81137042-81137043
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:81130019..81131773-chr16:81135530..81138449,2	K562	blood:

Extended variants
information (count: 75 )
Associated
traits (count: 4 )

rSNPs within LD-proxies of this variant (count:66)

rs_ID	r²[population]
rs1048194	1.00[ASN][1000 genomes]
rs1050364	0.80[EUR][1000 genomes]
rs10514512	0.80[EUR][1000 genomes]
rs10514513	0.80[EUR][1000 genomes]
rs10514514	0.80[EUR][1000 genomes]
rs10514515	0.80[EUR][1000 genomes]
rs12443549	0.82[EUR][1000 genomes]
rs12444137	0.82[EUR][1000 genomes]
rs12444747	1.00[ASN][1000 genomes]
rs12445303	0.80[EUR][1000 genomes]
rs12448806	0.92[AFR][1000 genomes];0.95[AMR][1000 genomes];0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12598621	0.80[EUR][1000 genomes]
rs1563072	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs1563075	0.83[EUR][1000 genomes]
rs1563077	0.80[EUR][1000 genomes]
rs16954513	1.00[ASN][1000 genomes]
rs16954572	0.80[EUR][1000 genomes]
rs16954582	0.80[EUR][1000 genomes]
rs1814543	0.81[EUR][1000 genomes]
rs2316730	0.93[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2316731	0.83[EUR][1000 genomes]
rs2317085	0.86[EUR][1000 genomes]
rs2317086	0.85[EUR][1000 genomes]
rs2317087	0.93[EUR][1000 genomes]
rs28391685	0.80[EUR][1000 genomes]
rs28613188	0.80[EUR][1000 genomes]
rs28672349	0.80[EUR][1000 genomes]
rs4306521	0.80[EUR][1000 genomes]
rs4324141	0.80[EUR][1000 genomes]
rs4324142	0.80[EUR][1000 genomes]
rs4324143	0.80[EUR][1000 genomes]
rs4454990	0.86[EUR][1000 genomes]
rs4889227	0.80[EUR][1000 genomes]
rs4889231	0.80[EUR][1000 genomes]
rs55939311	0.82[EUR][1000 genomes]
rs56032321	0.80[EUR][1000 genomes]
rs56119129	0.80[EUR][1000 genomes]
rs56166222	0.82[EUR][1000 genomes]
rs56198248	0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56286107	0.87[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56375210	0.84[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs56395947	0.80[EUR][1000 genomes]
rs59177227	0.80[EUR][1000 genomes]
rs59685942	0.80[EUR][1000 genomes]
rs61082942	0.80[EUR][1000 genomes]
rs7188508	0.80[EUR][1000 genomes]
rs7204040	0.80[EUR][1000 genomes]
rs73597252	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8052490	0.80[EUR][1000 genomes]
rs8056972	0.80[EUR][1000 genomes]
rs8059692	0.82[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8177851	0.86[AMR][1000 genomes];0.86[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8177876	0.85[AMR][1000 genomes];0.89[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs8177940	0.80[EUR][1000 genomes]
rs8177942	0.82[EUR][1000 genomes]
rs8177943	0.80[EUR][1000 genomes]
rs8177948	0.80[EUR][1000 genomes]
rs8177950	0.80[EUR][1000 genomes]
rs874437	0.89[EUR][1000 genomes]
rs9923732	0.80[EUR][1000 genomes]
rs9925940	0.80[EUR][1000 genomes]
rs9925943	0.80[EUR][1000 genomes]
rs9926174	0.80[EUR][1000 genomes]
rs9929586	0.80[EUR][1000 genomes]
rs9933184	0.80[EUR][1000 genomes]
rs9938965	0.80[EUR][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	nsv948534	chr16:80867635-81160492	Enhancers Weak transcription Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	55 gene(s)	inside rSNPs	diseases
2	nsv532569	chr16:80980356-81700149	Weak transcription Flanking Active TSS Genic enhancers Enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	71 gene(s)	inside rSNPs	diseases
3	nsv532597	chr16:81009718-81388348	Active TSS Weak transcription Strong transcription Flanking Active TSS Enhancers Genic enhancers ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	56 gene(s)	inside rSNPs	diseases
4	nsv427984	chr16:81026691-81320341	Enhancers Genic enhancers Flanking Active TSS Weak transcription Active TSS ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
5	esv2422360	chr16:81066033-81180727	Flanking Active TSS Weak transcription Strong transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	33 gene(s)	inside rSNPs	diseases
6	esv2751615	chr16:81093099-81307599	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	30 gene(s)	inside rSNPs	diseases
7	nsv530715	chr16:81117168-81252875	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Bivalent/Poised TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
8	nsv907005	chr16:81121353-81194912	Flanking Active TSS Active TSS Weak transcription Enhancers Bivalent/Poised TSS Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
9	nsv1067144	chr16:81129298-81181641	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases

mRNA abundance (count:4)

SNP	Gene	Cis/trans	Tissue	Source
rs57606521	C16orf46	Cis_1M	lymphoblastoid	RTeQTL
rs57606521	GCSH///LOC654085///LOC730107	Cis_1M	lymphoblastoid	RTeQTL
rs57606521	GCSH///LOC730107	Cis_1M	lymphoblastoid	RTeQTL
rs57606521	CENPN	Cis_1M	lymphoblastoid	RTeQTL

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:81130000-81141200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr16:81130000-81187600	Weak transcription	Right Atrium	heart
3	chr16:81131000-81140400	Weak transcription	Adipose Nuclei	Adipose
4	chr16:81136400-81137400	Enhancers	HepG2	liver

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