Variant report

Variant	rs16886644
Chromosome Location	chr8:115933317-115933318
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	chr8:115932881..115936964-chr8:115939898..115942520,3	MCF-7	breast:

Extended variants
information (count: 51 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:40)

rs_ID	r²[population]
rs10089298	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10091415	0.85[ASN][1000 genomes]
rs10091791	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10092153	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10097028	0.81[ASN][1000 genomes]
rs10100619	0.97[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs10102001	0.93[ASN][1000 genomes]
rs10102095	0.93[ASN][1000 genomes]
rs10104655	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs10104735	0.93[ASN][1000 genomes]
rs10283035	0.85[ASN][1000 genomes]
rs11774300	0.89[ASN][1000 genomes]
rs11989097	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11992164	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12114421	0.87[ASN][1000 genomes]
rs13252248	0.93[ASN][1000 genomes]
rs13438839	0.81[ASN][1000 genomes]
rs1436711	0.88[EUR][1000 genomes]
rs1436712	0.85[EUR][1000 genomes]
rs1436718	0.88[EUR][1000 genomes]
rs1436719	0.88[EUR][1000 genomes]
rs1684978	0.90[EUR][1000 genomes]
rs16886740	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs1865875	0.88[EUR][1000 genomes]
rs1872782	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2575941	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2631808	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs28407161	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2884259	0.83[ASN][1000 genomes]
rs2884260	0.86[ASN][1000 genomes]
rs58169521	0.93[ASN][1000 genomes]
rs589833	0.97[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs62511966	0.84[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs62514699	0.84[AMR][1000 genomes];0.95[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs650317	0.88[EUR][1000 genomes]
rs6984638	0.93[ASN][1000 genomes]
rs6986541	0.87[ASN][1000 genomes]
rs73702660	0.84[ASN][1000 genomes]
rs756404	0.88[EUR][1000 genomes]
rs7846590	0.93[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:11 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv611976	chr8:115261134-116223865	Weak transcription Enhancers Active TSS Strong transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
2	nsv1018280	chr8:115307838-116189192	Enhancers Weak transcription Active TSS ZNF genes & repeats Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
3	nsv539726	chr8:115307838-116189192	Enhancers Flanking Active TSS Weak transcription Active TSS Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
4	nsv891372	chr8:115351857-116037119	Enhancers Active TSS ZNF genes & repeats Weak transcription Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
5	nsv891373	chr8:115351857-116295809	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer Strong transcription Genic enhancers Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
6	nsv891377	chr8:115395451-116110725	Enhancers Flanking Active TSS Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
7	nsv891395	chr8:115642536-116222842	Enhancers Flanking Active TSS Genic enhancers Weak transcription ZNF genes & repeats Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' Strong transcription Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
8	esv2754852	chr8:115803396-115958801	Active TSS Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
9	nsv891397	chr8:115810385-116129344	Enhancers Weak transcription Active TSS Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	n/a	inside rSNPs	diseases
10	esv2752194	chr8:115836494-115945911	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Flanking Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases
11	esv3349000	chr8:115899825-115937205	Enhancers Weak transcription Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Active TSS Active TSS	Chromatin interactive region	n/a	inside rSNPs	diseases

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:115932400-115933400	Transcr. at gene 5' and 3'	Dnd41	blood
2	chr8:115933000-115934000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr8:115933200-115934200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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