Variant report

Variant	rs73589728
Chromosome Location	chr16:82429497-82429498
allele	A/C
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr16:82407069..82409171-chr16:82427658..82429625,2	K562	blood:
2	chr16:82415353..82417549-chr16:82428298..82430992,2	MCF-7	breast:

Extended variants
information (count: 55 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:45)

rs_ID	r²[population]
rs11861006	1.00[EUR][1000 genomes]
rs12103242	1.00[EUR][1000 genomes]
rs13330301	1.00[EUR][1000 genomes]
rs13334879	1.00[EUR][1000 genomes]
rs16956989	1.00[EUR][1000 genomes]
rs16957207	1.00[EUR][1000 genomes]
rs16957221	1.00[AMR][1000 genomes]
rs16957222	1.00[AMR][1000 genomes]
rs16957226	1.00[AMR][1000 genomes]
rs16957342	1.00[EUR][1000 genomes]
rs16957354	1.00[EUR][1000 genomes]
rs3843713	1.00[EUR][1000 genomes]
rs3901526	1.00[EUR][1000 genomes]
rs4405544	1.00[EUR][1000 genomes]
rs55838821	1.00[EUR][1000 genomes]
rs56872498	1.00[EUR][1000 genomes]
rs57628849	1.00[EUR][1000 genomes]
rs57746771	1.00[EUR][1000 genomes]
rs58650213	1.00[EUR][1000 genomes]
rs59073682	1.00[EUR][1000 genomes]
rs59169797	1.00[EUR][1000 genomes]
rs60548806	1.00[EUR][1000 genomes]
rs7189184	1.00[EUR][1000 genomes]
rs7201792	1.00[EUR][1000 genomes]
rs7201997	1.00[EUR][1000 genomes]
rs7203485	1.00[EUR][1000 genomes]
rs7204522	1.00[EUR][1000 genomes]
rs73589708	1.00[EUR][1000 genomes]
rs73589710	1.00[EUR][1000 genomes]
rs73589711	1.00[AMR][1000 genomes]
rs73589713	1.00[AMR][1000 genomes]
rs73591673	1.00[EUR][1000 genomes]
rs74030314	1.00[EUR][1000 genomes]
rs74030315	1.00[EUR][1000 genomes]
rs74032627	1.00[EUR][1000 genomes]
rs74032640	1.00[EUR][1000 genomes]
rs74032644	1.00[EUR][1000 genomes]
rs74032656	1.00[EUR][1000 genomes]
rs8049135	1.00[EUR][1000 genomes]
rs8056958	1.00[EUR][1000 genomes]
rs8057752	1.00[EUR][1000 genomes]
rs8063417	1.00[EUR][1000 genomes]
rs8063751	1.00[EUR][1000 genomes]
rs9928499	1.00[EUR][1000 genomes]
rs9936348	1.00[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	nsv532598	chr16:82034475-82738733	Active TSS Enhancers Weak transcription Strong transcription Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA	28 gene(s)	inside rSNPs	diseases
2	nsv532599	chr16:82074439-82926863	Weak transcription Flanking Active TSS Enhancers Active TSS Bivalent/Poised TSS Strong transcription Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
3	nsv573367	chr16:82140561-83040846	Active TSS Weak transcription Flanking Active TSS ZNF genes & repeats Enhancers Transcr. at gene 5' and 3' Bivalent/Poised TSS Genic enhancers Bivalent Enhancer Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	27 gene(s)	inside rSNPs	diseases
4	esv1844598	chr16:82195234-82429790	Enhancers Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Transcr. at gene 5' and 3' Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
5	esv1847414	chr16:82195234-82429790	Enhancers Active TSS Weak transcription Strong transcription Genic enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	14 gene(s)	inside rSNPs	diseases
6	nsv1065896	chr16:82213517-82731994	Flanking Active TSS Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Strong transcription Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	11 gene(s)	inside rSNPs	diseases
7	nsv1057341	chr16:82363800-83198907	Enhancers Weak transcription Flanking Active TSS Genic enhancers Strong transcription Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
8	nsv542997	chr16:82363800-83198907	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Genic enhancers Bivalent Enhancer Strong transcription Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	12 gene(s)	inside rSNPs	diseases
9	nsv1063681	chr16:82370611-82449440	Enhancers Flanking Active TSS ZNF genes & repeats Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	inside rSNPs	diseases
10	nsv1901	chr16:82416516-82461174	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:2 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr16:82428400-82430800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr16:82429200-82429600	Enhancers	Fetal Brain Male	brain

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