Variant report

Variant	rs392686
Chromosome Location	chr21:46023668-46023669
allele	G/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr21:46023322..46027722-chr21:46030622..46034722,4	MCF-7	breast:
2	chr21:46023116..46026036-chr21:46032352..46034707,2	K562	blood:

Variant related genes	Relation type
ENSG00000187766	Chromatin interaction

Extended variants
information (count: 114 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:98)

rs_ID	r²[population]
rs1211061	0.82[CHB][hapmap]
rs1211088	0.94[CHB][hapmap];0.88[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.85[EUR][1000 genomes]
rs1211089	0.93[CHB][hapmap];0.85[EUR][1000 genomes]
rs1211103	0.81[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.86[YRI][hapmap];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1211118	0.90[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs1211121	1.00[CEU][hapmap];0.91[CHB][hapmap];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1211122	0.94[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs1211123	1.00[CEU][hapmap];0.86[CHB][hapmap];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs1211129	0.93[EUR][1000 genomes]
rs1211130	0.93[EUR][1000 genomes]
rs12627104	0.81[ASN][1000 genomes]
rs12627414	0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[MEX][hapmap];0.82[ASN][1000 genomes]
rs170849	0.87[CEU][hapmap];0.90[CHD][hapmap];0.82[MEX][hapmap]
rs2226687	0.95[CHD][hapmap];0.82[MEX][hapmap]
rs233262	0.82[CEU][hapmap]
rs233264	0.86[CEU][hapmap]
rs233265	0.86[CEU][hapmap]
rs233267	0.81[EUR][1000 genomes]
rs233268	0.87[CEU][hapmap];0.82[CHB][hapmap];0.95[CHD][hapmap];0.88[GIH][hapmap];0.85[EUR][1000 genomes]
rs233269	0.85[EUR][1000 genomes]
rs233270	0.87[CEU][hapmap];0.82[GIH][hapmap];0.81[EUR][1000 genomes]
rs233271	0.85[EUR][1000 genomes]
rs233272	0.87[CEU][hapmap];0.88[GIH][hapmap];0.83[EUR][1000 genomes]
rs2838598	1.00[ASW][hapmap];1.00[CHB][hapmap];0.95[CHD][hapmap];1.00[JPT][hapmap];0.98[LWK][hapmap];1.00[MEX][hapmap];0.97[MKK][hapmap];1.00[YRI][hapmap];1.00[AFR][1000 genomes];0.86[AMR][1000 genomes];1.00[ASN][1000 genomes]
rs367771	0.86[CEU][hapmap];0.85[EUR][1000 genomes]
rs370092	0.94[ASW][hapmap];0.88[CHB][hapmap];0.86[CHD][hapmap];0.89[GIH][hapmap];0.85[LWK][hapmap];0.88[MKK][hapmap];0.84[TSI][hapmap];0.89[YRI][hapmap];0.85[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs371248	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap]
rs377234	1.00[CEU][hapmap];0.94[CHB][hapmap];0.85[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.98[EUR][1000 genomes]
rs377263	1.00[CEU][hapmap];0.93[GIH][hapmap];0.91[TSI][hapmap];0.88[EUR][1000 genomes]
rs377573	0.93[EUR][1000 genomes]
rs379858	0.82[CHB][hapmap]
rs382935	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.81[LWK][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.86[YRI][hapmap];0.80[AFR][1000 genomes];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs384645	1.00[CEU][hapmap];0.94[CHB][hapmap];1.00[YRI][hapmap];0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs385033	0.87[AFR][1000 genomes];0.90[AMR][1000 genomes];0.85[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs389936	0.85[EUR][1000 genomes]
rs390630	0.81[EUR][1000 genomes]
rs392451	1.00[CEU][hapmap];0.94[CHB][hapmap];0.98[EUR][1000 genomes]
rs395781	0.93[EUR][1000 genomes]
rs398680	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.91[LWK][hapmap];1.00[MEX][hapmap];0.95[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.90[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs400170	0.85[EUR][1000 genomes]
rs400368	0.82[CHB][hapmap]
rs400406	0.81[EUR][1000 genomes]
rs403981	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.93[EUR][1000 genomes]
rs404341	1.00[CEU][hapmap];0.94[CHB][hapmap];0.81[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.98[EUR][1000 genomes]
rs408183	0.90[EUR][1000 genomes]
rs408516	0.85[EUR][1000 genomes]
rs408958	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[JPT][hapmap];0.97[AFR][1000 genomes];0.93[AMR][1000 genomes];0.93[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs409239	0.93[EUR][1000 genomes]
rs409893	0.94[CHB][hapmap];0.85[EUR][1000 genomes]
rs411254	1.00[CEU][hapmap];0.95[CHD][hapmap];0.82[MEX][hapmap];0.81[EUR][1000 genomes]
rs415753	1.00[CEU][hapmap];1.00[CHB][hapmap];1.00[CHD][hapmap];0.96[GIH][hapmap];1.00[JPT][hapmap];0.91[TSI][hapmap];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs416056	1.00[CEU][hapmap];0.92[CHB][hapmap];0.98[EUR][1000 genomes]
rs417538	1.00[CEU][hapmap];0.93[CHB][hapmap];0.98[EUR][1000 genomes]
rs418260	0.94[CHB][hapmap];0.80[GIH][hapmap];0.82[MEX][hapmap]
rs423954	0.81[EUR][1000 genomes]
rs425276	0.93[EUR][1000 genomes]
rs425823	1.00[CEU][hapmap];0.83[JPT][hapmap];0.81[EUR][1000 genomes]
rs430609	0.82[CHB][hapmap]
rs434716	0.82[CHB][hapmap]
rs437149	0.86[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs438444	0.81[EUR][1000 genomes]
rs442110	0.88[EUR][1000 genomes]
rs442226	1.00[CEU][hapmap];0.94[CHB][hapmap];0.91[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs442849	0.85[EUR][1000 genomes]
rs443484	0.81[EUR][1000 genomes]
rs445214	0.87[CEU][hapmap];0.90[CHD][hapmap]
rs446817	1.00[CEU][hapmap];0.84[AFR][1000 genomes];0.90[AMR][1000 genomes];0.95[EUR][1000 genomes]
rs451948	0.81[EUR][1000 genomes]
rs452002	1.00[ASW][hapmap];1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];0.96[LWK][hapmap];1.00[MEX][hapmap];1.00[MKK][hapmap];0.91[TSI][hapmap];1.00[YRI][hapmap];0.92[AFR][1000 genomes];0.93[AMR][1000 genomes];0.98[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs452547	0.98[EUR][1000 genomes]
rs455413	0.82[CHB][hapmap]
rs455562	0.82[CHB][hapmap]
rs455714	0.82[CHB][hapmap]
rs455777	0.82[CHB][hapmap]
rs455906	0.93[CHB][hapmap];0.83[EUR][1000 genomes]
rs456019	1.00[CEU][hapmap];0.82[CHB][hapmap];1.00[CHD][hapmap];0.85[GIH][hapmap];0.92[JPT][hapmap];0.83[EUR][1000 genomes]
rs456444	0.82[CHB][hapmap]
rs457322	0.82[CHB][hapmap]
rs459644	0.88[GIH][hapmap];0.91[TSI][hapmap];0.81[EUR][1000 genomes]
rs459845	0.82[CHB][hapmap]
rs459915	0.82[CHB][hapmap]
rs460064	0.82[CHB][hapmap]
rs460085	0.82[CHB][hapmap]
rs460122	0.82[CHB][hapmap]
rs462254	0.82[CHB][hapmap]
rs463239	0.82[CHB][hapmap]
rs463267	0.82[CHB][hapmap]
rs463668	0.82[CHB][hapmap]
rs464281	0.82[CHB][hapmap]
rs464504	0.82[CHB][hapmap]
rs464684	0.82[CHB][hapmap]
rs465930	0.82[CHB][hapmap]
rs466094	0.82[CHB][hapmap]
rs466628	0.83[EUR][1000 genomes]
rs487102	1.00[CEU][hapmap];1.00[CHD][hapmap];0.83[JPT][hapmap];0.82[MEX][hapmap];0.81[EUR][1000 genomes]
rs56274513	0.83[ASN][1000 genomes]
rs659638	1.00[CEU][hapmap];0.94[CHB][hapmap];0.90[CHD][hapmap];1.00[GIH][hapmap];1.00[MEX][hapmap];0.91[TSI][hapmap];0.83[AMR][1000 genomes];0.98[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs8132500	0.82[CHB][hapmap];1.00[CHD][hapmap];0.92[JPT][hapmap]

Variant overlapped rSNPs/rCNVs (count:16 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv33817	chr21:45169412-46031810	Weak transcription Bivalent/Poised TSS Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	121 gene(s)	inside rSNPs	diseases
2	nsv913943	chr21:45740823-46031810	Enhancers Bivalent Enhancer Active TSS Flanking Active TSS Strong transcription Weak transcription Genic enhancers 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	52 gene(s)	inside rSNPs	diseases
3	nsv913946	chr21:45838632-46031810	Bivalent Enhancer ZNF genes & repeats Active TSS Enhancers Weak transcription Strong transcription Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	34 gene(s)	inside rSNPs	diseases
4	nsv913948	chr21:45860912-46031810	Flanking Active TSS Enhancers Bivalent Enhancer Weak transcription Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	29 gene(s)	inside rSNPs	diseases
5	nsv1056424	chr21:45894901-46031810	Weak transcription Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Active TSS Flanking Bivalent TSS/Enh Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv544475	chr21:45894901-46031810	Enhancers Flanking Active TSS Bivalent Enhancer Bivalent/Poised TSS ZNF genes & repeats Weak transcription Active TSS Genic enhancers Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
7	nsv1055163	chr21:45895663-46031810	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
8	nsv1065798	chr21:45941000-46097463	Flanking Active TSS Bivalent Enhancer Enhancers Weak transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
9	nsv869108	chr21:45941000-46097463	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS ZNF genes & repeats Active TSS Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
10	nsv544476	chr21:45941000-46097463	Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Genic enhancers Active TSS Flanking Bivalent TSS/Enh Bivalent/Poised TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases
11	nsv913950	chr21:45985068-46097463	Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Weak transcription ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	18 gene(s)	inside rSNPs	diseases
12	nsv913952	chr21:45988426-46031810	Enhancers Bivalent Enhancer Weak transcription Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	8 gene(s)	inside rSNPs	diseases
13	esv2751931	chr21:45990446-46031810	Enhancers Weak transcription Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS Genic enhancers ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
14	nsv587810	chr21:45992131-46031810	Enhancers Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS ZNF genes & repeats Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	7 gene(s)	inside rSNPs	diseases
15	nsv916258	chr21:45995986-46624705	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Bivalent/Poised TSS Active TSS Transcr. at gene 5' and 3' ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	102 gene(s)	inside rSNPs	diseases
16	nsv913953	chr21:46012524-46031810	ZNF genes & repeats Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr21:46018400-46048400	Weak transcription	Right Atrium	heart
2	chr21:46020400-46024600	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr21:46023200-46024200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell

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