Variant report

Variant	rs8131111
Chromosome Location	chr21:45126767-45126768
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr21:45121738..45123738-chr21:45125330..45128089,2	K562	blood:
2	chr21:45123530..45125041-chr21:45125684..45127237,2	MCF-7	breast:
3	chr21:45126696..45129955-chr21:45130404..45132264,4	MCF-7	breast:
4	chr21:45120451..45123154-chr21:45126649..45128378,2	MCF-7	breast:

Extended variants
information (count: 71 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:61)

rs_ID	r²[population]
rs10211901	0.86[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs10854486	0.80[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs11089093	0.86[AMR][1000 genomes];0.89[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11700909	0.87[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11700913	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs11702544	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs11909064	0.87[EUR][1000 genomes]
rs13051953	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2006113	0.91[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2051407	0.81[EUR][1000 genomes]
rs2070533	0.92[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2155722	0.80[AMR][1000 genomes];0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2186924	0.94[ASN][1000 genomes]
rs2236665	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2236666	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2236667	0.94[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2250773	0.94[EUR][1000 genomes]
rs2251253	0.88[EUR][1000 genomes]
rs2298562	0.93[EUR][1000 genomes]
rs2329593	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs2838344	0.87[EUR][1000 genomes]
rs2838345	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2838348	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs2838350	0.90[EUR][1000 genomes]
rs2838351	0.85[EUR][1000 genomes]
rs2838353	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2838354	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs3819161	0.91[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs4818858	0.93[EUR][1000 genomes]
rs4818859	0.83[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4818860	0.80[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4818861	0.94[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4819283	0.93[EUR][1000 genomes]
rs4819285	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4819286	0.90[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4819287	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4819288	0.95[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs4819289	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4819290	0.87[AMR][1000 genomes];0.88[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4819291	0.91[AMR][1000 genomes];0.96[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4819292	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs4819293	0.86[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4819294	0.86[AMR][1000 genomes];0.98[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs4819295	0.88[ASN][1000 genomes]
rs4819296	0.89[ASN][1000 genomes]
rs6417730	0.90[ASN][1000 genomes]
rs6518315	0.92[ASN][1000 genomes]
rs7282122	0.91[EUR][1000 genomes]
rs7282405	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs7283428	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs762400	0.93[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs8129601	0.83[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs8133276	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs914197	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs914198	0.85[AMR][1000 genomes];0.95[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9306160	0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9941787	0.95[EUR][1000 genomes]
rs9977076	0.86[EUR][1000 genomes]
rs9978858	0.90[EUR][1000 genomes]
rs9982727	0.94[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs9983670	0.92[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	nsv913873	chr21:44879869-45142427	Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Bivalent Enhancer Active TSS Transcr. at gene 5' and 3' Strong transcription Bivalent/Poised TSS Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	64 gene(s)	inside rSNPs	diseases
2	nsv913874	chr21:45041790-45191005	Enhancers Strong transcription Weak transcription ZNF genes & repeats Flanking Active TSS Genic enhancers Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	36 gene(s)	inside rSNPs	diseases
3	nsv531544	chr21:45071371-45202912	Enhancers Flanking Active TSS Weak transcription Strong transcription Genic enhancers Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	39 gene(s)	inside rSNPs	diseases
4	nsv1066728	chr21:45089877-45131723	Enhancers Genic enhancers Strong transcription Active TSS Weak transcription Bivalent/Poised TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	7 gene(s)	inside rSNPs	diseases
5	nsv531545	chr21:45095397-45395904	Enhancers Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Strong transcription Active TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
6	nsv1066613	chr21:45108233-45148136	Genic enhancers Enhancers Weak transcription Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh Active TSS Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
7	esv3424986	chr21:45118675-45158421	Flanking Active TSS Enhancers Weak transcription Active TSS Genic enhancers Strong transcription Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
8	esv3329872	chr21:45118725-45158757	Active TSS Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription Genic enhancers Strong transcription Transcr. at gene 5' and 3' Flanking Bivalent TSS/Enh Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	23 gene(s)	inside rSNPs	diseases
9	nsv913875	chr21:45119629-45191005	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Flanking Active TSS Strong transcription Active TSS Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	31 gene(s)	inside rSNPs	diseases
10	nsv913876	chr21:45119629-45267193	Enhancers Weak transcription Active TSS Flanking Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	46 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:45111000-45130600	Weak transcription	HSMM	muscle
2	chr21:45115000-45130800	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr21:45115800-45131800	Weak transcription	Muscle Satellite Cultured Cells	--
4	chr21:45116600-45132200	Weak transcription	NHLF	lung
5	chr21:45117000-45127400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr21:45123200-45138200	Weak transcription	Ovary	ovary
7	chr21:45123400-45131600	Weak transcription	NHEK	skin
8	chr21:45123600-45130400	Weak transcription	Primary monocytes fromperipheralblood	blood
9	chr21:45123600-45131200	Weak transcription	Stomach Mucosa	stomach
10	chr21:45123600-45132200	Weak transcription	Brain Cingulate Gyrus	brain
11	chr21:45123600-45138400	Weak transcription	Right Atrium	heart
12	chr21:45123800-45130800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr21:45123800-45131000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
14	chr21:45123800-45131600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr21:45123800-45132000	Weak transcription	HSMMtube	muscle
16	chr21:45126400-45126800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr21:45126400-45126800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr21:45126400-45126800	Flanking Active TSS	HepG2	liver
19	chr21:45126400-45126800	Enhancers	Monocytes-CD14+_RO01746	blood
20	chr21:45126400-45127200	Enhancers	Primary T cells fromperipheralblood	blood
21	chr21:45126600-45126800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr21:45126600-45126800	Enhancers	GM12878-XiMat	blood
23	chr21:45126600-45126800	Enhancers	NHDF-Ad	bronchial
24	chr21:45126600-45126800	Enhancers	Osteobl	bone
25	chr21:45126600-45127800	Enhancers	Hela-S3	cervix
26	chr21:45126600-45128600	Enhancers	A549	lung

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