Variant report

Variant	rs62215786
Chromosome Location	chr20:24788084-24788085
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr20:24786455..24788540-chr20:24788618..24791423,2	MCF-7	breast:

Extended variants
information (count: 147 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:139)

rs_ID	r²[population]
rs1045772	1.00[ASN][1000 genomes]
rs11087490	1.00[ASN][1000 genomes]
rs1113871	1.00[ASN][1000 genomes]
rs11696281	1.00[ASN][1000 genomes]
rs11697953	1.00[ASN][1000 genomes]
rs11697965	1.00[ASN][1000 genomes]
rs11698426	1.00[ASN][1000 genomes]
rs11698613	1.00[ASN][1000 genomes]
rs12329446	1.00[ASN][1000 genomes]
rs12329447	1.00[ASN][1000 genomes]
rs12480836	1.00[ASN][1000 genomes]
rs1467769	1.00[ASN][1000 genomes]
rs1576649	1.00[ASN][1000 genomes]
rs28758726	1.00[ASN][1000 genomes]
rs2892278	1.00[ASN][1000 genomes]
rs34799975	1.00[ASN][1000 genomes]
rs4356723	1.00[ASN][1000 genomes]
rs55821861	1.00[ASN][1000 genomes]
rs55849863	1.00[ASN][1000 genomes]
rs56258611	1.00[ASN][1000 genomes]
rs56311685	1.00[ASN][1000 genomes]
rs56313512	1.00[ASN][1000 genomes]
rs58751902	1.00[ASN][1000 genomes]
rs6036921	1.00[ASN][1000 genomes]
rs6036927	1.00[ASN][1000 genomes]
rs6036928	1.00[ASN][1000 genomes]
rs6036932	1.00[ASN][1000 genomes]
rs6036938	1.00[ASN][1000 genomes]
rs6036944	1.00[ASN][1000 genomes]
rs6036949	1.00[ASN][1000 genomes]
rs6036980	1.00[ASN][1000 genomes]
rs6036985	1.00[ASN][1000 genomes]
rs6036986	1.00[ASN][1000 genomes]
rs6036988	1.00[ASN][1000 genomes]
rs6036989	1.00[ASN][1000 genomes]
rs6036990	1.00[ASN][1000 genomes]
rs6036991	1.00[ASN][1000 genomes]
rs6036992	1.00[ASN][1000 genomes]
rs6036993	1.00[ASN][1000 genomes]
rs6036994	1.00[ASN][1000 genomes]
rs6036997	1.00[ASN][1000 genomes]
rs6050001	1.00[ASN][1000 genomes]
rs6050003	1.00[ASN][1000 genomes]
rs6050005	1.00[ASN][1000 genomes]
rs6050006	1.00[ASN][1000 genomes]
rs6050013	1.00[ASN][1000 genomes]
rs6050014	1.00[ASN][1000 genomes]
rs6050016	1.00[ASN][1000 genomes]
rs6050017	1.00[ASN][1000 genomes]
rs6050019	1.00[ASN][1000 genomes]
rs6050023	1.00[ASN][1000 genomes]
rs6050041	1.00[ASN][1000 genomes]
rs6050042	1.00[ASN][1000 genomes]
rs6050045	1.00[ASN][1000 genomes]
rs6050047	1.00[ASN][1000 genomes]
rs6050049	1.00[ASN][1000 genomes]
rs6050061	1.00[ASN][1000 genomes]
rs6050075	1.00[ASN][1000 genomes]
rs6050107	1.00[ASN][1000 genomes]
rs6050126	1.00[ASN][1000 genomes]
rs6050130	1.00[ASN][1000 genomes]
rs6050143	1.00[ASN][1000 genomes]
rs6050151	1.00[ASN][1000 genomes]
rs6050152	1.00[ASN][1000 genomes]
rs6050160	1.00[ASN][1000 genomes]
rs6050161	1.00[ASN][1000 genomes]
rs6050162	1.00[ASN][1000 genomes]
rs6050163	1.00[ASN][1000 genomes]
rs6050164	1.00[ASN][1000 genomes]
rs6050166	1.00[ASN][1000 genomes]
rs6050167	1.00[ASN][1000 genomes]
rs6050168	1.00[ASN][1000 genomes]
rs6050169	1.00[ASN][1000 genomes]
rs6050171	1.00[ASN][1000 genomes]
rs6050176	1.00[ASN][1000 genomes]
rs6050180	1.00[ASN][1000 genomes]
rs6050183	1.00[ASN][1000 genomes]
rs6050184	1.00[ASN][1000 genomes]
rs6050185	1.00[ASN][1000 genomes]
rs6050186	1.00[ASN][1000 genomes]
rs6050187	1.00[ASN][1000 genomes]
rs6050189	1.00[ASN][1000 genomes]
rs6050191	1.00[ASN][1000 genomes]
rs6050193	1.00[ASN][1000 genomes]
rs6050197	1.00[ASN][1000 genomes]
rs6050202	1.00[ASN][1000 genomes]
rs6050203	1.00[ASN][1000 genomes]
rs6050204	1.00[ASN][1000 genomes]
rs6050205	1.00[ASN][1000 genomes]
rs6050208	1.00[ASN][1000 genomes]
rs6050209	1.00[ASN][1000 genomes]
rs6050216	1.00[ASN][1000 genomes]
rs6050217	1.00[ASN][1000 genomes]
rs6106964	1.00[ASN][1000 genomes]
rs6106974	1.00[ASN][1000 genomes]
rs6106976	1.00[ASN][1000 genomes]
rs6106977	1.00[ASN][1000 genomes]
rs6106979	1.00[ASN][1000 genomes]
rs6106980	1.00[ASN][1000 genomes]
rs6114886	1.00[ASN][1000 genomes]
rs6114888	1.00[ASN][1000 genomes]
rs6114931	1.00[ASN][1000 genomes]
rs6114939	1.00[ASN][1000 genomes]
rs6114942	1.00[ASN][1000 genomes]
rs6114943	1.00[ASN][1000 genomes]
rs6114944	1.00[ASN][1000 genomes]
rs6114945	1.00[ASN][1000 genomes]
rs6114946	1.00[ASN][1000 genomes]
rs6114949	1.00[ASN][1000 genomes]
rs6114950	1.00[ASN][1000 genomes]
rs6114951	1.00[ASN][1000 genomes]
rs6114953	1.00[ASN][1000 genomes]
rs6114954	1.00[ASN][1000 genomes]
rs6114956	1.00[ASN][1000 genomes]
rs6114959	1.00[ASN][1000 genomes]
rs6114960	1.00[ASN][1000 genomes]
rs61662783	1.00[ASN][1000 genomes]
rs62215084	1.00[ASN][1000 genomes]
rs62215085	1.00[ASN][1000 genomes]
rs62215112	1.00[ASN][1000 genomes]
rs62216695	1.00[AFR][1000 genomes]
rs62216716	1.00[ASN][1000 genomes]
rs62216719	1.00[ASN][1000 genomes]
rs6515557	1.00[ASN][1000 genomes]
rs7261161	1.00[ASN][1000 genomes]
rs7264679	1.00[ASN][1000 genomes]
rs7271963	1.00[ASN][1000 genomes]
rs73337274	1.00[ASN][1000 genomes]
rs73339206	1.00[ASN][1000 genomes]
rs73344911	1.00[ASN][1000 genomes]
rs74173658	1.00[AFR][1000 genomes];0.80[AMR][1000 genomes]
rs8114913	1.00[ASN][1000 genomes]
rs8119131	1.00[ASN][1000 genomes]
rs8121643	1.00[ASN][1000 genomes]
rs8121732	1.00[ASN][1000 genomes]
rs910132	1.00[ASN][1000 genomes]
rs910133	1.00[ASN][1000 genomes]
rs914306	1.00[ASN][1000 genomes]
rs9753729	1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:8 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv3332519	chr20:24535099-24815615	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS ZNF genes & repeats Genic enhancers Active TSS Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	4 gene(s)	inside rSNPs	diseases
2	nsv1061412	chr20:24629468-24887869	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer ZNF genes & repeats Active TSS Genic enhancers Strong transcription Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
3	nsv544216	chr20:24629468-24887869	Weak transcription Bivalent Enhancer Enhancers Flanking Active TSS Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent/Poised TSS Active TSS Strong transcription	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases
4	nsv1061281	chr20:24711635-24815107	Enhancers Weak transcription Active TSS Bivalent Enhancer Flanking Active TSS Strong transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Genic enhancers Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
5	nsv544217	chr20:24711635-24815107	Weak transcription Enhancers Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats Genic enhancers Strong transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
6	nsv912825	chr20:24715544-24813345	Weak transcription Enhancers Flanking Active TSS Bivalent Enhancer Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases
7	nsv1061455	chr20:24733120-24861801	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Genic enhancers Bivalent/Poised TSS	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases
8	nsv544218	chr20:24733120-24861801	Flanking Active TSS Enhancers Weak transcription Bivalent Enhancer Active TSS Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA	3 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24777200-24791400	Weak transcription	Spleen	Spleen
2	chr20:24783200-24790400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:24786800-24788200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr20:24787400-24788200	Enhancers	Fetal Lung	lung
5	chr20:24787400-24788200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
6	chr20:24787600-24788200	Enhancers	Fetal Muscle Leg	muscle
7	chr20:24787800-24788600	Enhancers	Placenta	Placenta
8	chr20:24788000-24788400	Bivalent Enhancer	Fetal Stomach	stomach

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