Variant report

Variant	rs1345901
Chromosome Location	chr16:79728049-79728050
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 55 )
Associated
traits (count: 1 )

rSNPs within LD-proxies of this variant (count:50)

rs_ID	r²[population]
rs11150187	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs11150188	0.88[EUR][1000 genomes]
rs11150189	0.88[EUR][1000 genomes]
rs11150190	0.83[EUR][1000 genomes]
rs11150191	0.81[AMR][1000 genomes];0.89[EUR][1000 genomes]
rs11644082	0.83[EUR][1000 genomes]
rs11644758	0.85[CEU][hapmap];0.82[EUR][1000 genomes]
rs11644799	0.83[EUR][1000 genomes]
rs11644836	0.88[EUR][1000 genomes]
rs11645076	0.83[EUR][1000 genomes]
rs11646791	0.88[EUR][1000 genomes]
rs11864901	0.88[EUR][1000 genomes]
rs12444166	0.86[CEU][hapmap];0.88[EUR][1000 genomes]
rs12449109	0.83[EUR][1000 genomes]
rs12449161	0.81[EUR][1000 genomes]
rs1424231	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs16950982	0.88[EUR][1000 genomes]
rs16950997	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs17689024	0.82[EUR][1000 genomes]
rs17689159	0.82[EUR][1000 genomes]
rs17689455	0.81[EUR][1000 genomes]
rs17689625	0.80[EUR][1000 genomes]
rs17767383	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs17767419	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs17767491	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs17767742	0.80[EUR][1000 genomes]
rs17767904	0.80[EUR][1000 genomes]
rs28773265	0.80[EUR][1000 genomes]
rs3813580	0.80[EUR][1000 genomes]
rs3813582	0.80[EUR][1000 genomes]
rs56738967	0.82[EUR][1000 genomes]
rs56892402	0.83[EUR][1000 genomes]
rs59617251	0.80[EUR][1000 genomes]
rs7187128	0.86[CEU][hapmap];0.83[EUR][1000 genomes]
rs7188445	0.88[EUR][1000 genomes]
rs7190187	0.88[EUR][1000 genomes]
rs7195321	0.88[EUR][1000 genomes]
rs7202240	0.81[EUR][1000 genomes]
rs7202770	0.86[CEU][hapmap];0.84[EUR][1000 genomes]
rs7203756	0.82[CEU][hapmap];0.81[EUR][1000 genomes]
rs73575076	0.81[EUR][1000 genomes]
rs73575079	0.81[EUR][1000 genomes]
rs73575085	0.80[EUR][1000 genomes]
rs73575086	0.80[EUR][1000 genomes]
rs73575095	0.80[EUR][1000 genomes]
rs74037508	0.83[EUR][1000 genomes]
rs74037509	0.82[EUR][1000 genomes]
rs8047723	0.85[CEU][hapmap];0.85[EUR][1000 genomes]
rs8048928	0.85[EUR][1000 genomes]
rs8053589	0.90[EUR][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	nsv573285	chr16:79158182-80127326	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	28 gene(s)	inside rSNPs	diseases
2	nsv906992	chr16:79649394-79769790	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Active TSS Bivalent/Poised TSS Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	12 gene(s)	inside rSNPs	diseases
3	nsv530714	chr16:79661581-79925435	Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
4	nsv833296	chr16:79692236-79889727	Enhancers Active TSS Bivalent Enhancer Weak transcription Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	16 gene(s)	inside rSNPs	diseases
5	nsv518748	chr16:79716333-79729031	Weak transcription Enhancers ZNF genes & repeats Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

mRNA abundance (count:1)

SNP	Gene	Cis/trans	Tissue	Source
rs1345901	RP11-345M22.2	cis	Thyroid	GTEx

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:79720400-79736800	Weak transcription	Aorta	Aorta
2	chr16:79722400-79728600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr16:79725200-79732200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr16:79725400-79731800	Weak transcription	NHLF	lung
5	chr16:79727800-79732400	Weak transcription	Fetal Heart	heart

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