Variant report

Variant	rs7264053
Chromosome Location	chr20:53063262-53063263
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type
1	chr20:53062391..53065674-chr20:53071896..53077511,6	MCF-7	breast:
2	chr20:53061996..53063880-chr20:53065895..53070016,4	MCF-7	breast:
3	chr1:11968180..11970676-chr20:53062831..53064629,2	MCF-7	breast:
4	chr20:53046706..53049615-chr20:53062995..53067004,4	MCF-7	breast:
5	chr20:53056007..53058176-chr20:53061924..53063685,2	K562	blood:
6	chr20:53062423..53064765-chr20:53078870..53080771,2	MCF-7	breast:
7	chr20:53054401..53056125-chr20:53062337..53064075,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000201801	Chromatin interaction
ENSG00000199347	Chromatin interaction

Extended variants
information (count: 32 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs12329481	0.82[AMR][1000 genomes]
rs16999643	1.00[AFR][1000 genomes];0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs55665963	0.85[EUR][1000 genomes]
rs58143732	0.83[EUR][1000 genomes]
rs6014019	0.98[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6014020	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6023244	0.81[EUR][1000 genomes]
rs6023245	0.82[AMR][1000 genomes]
rs6023247	0.86[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6023248	0.80[EUR][1000 genomes]
rs6023251	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6023253	0.91[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6023254	0.85[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6023258	0.83[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6023262	0.82[AMR][1000 genomes]
rs6023263	0.83[AMR][1000 genomes]
rs60780716	0.83[EUR][1000 genomes]
rs6091886	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6097986	0.96[AFR][1000 genomes];0.95[AMR][1000 genomes];0.82[EUR][1000 genomes]
rs6097987	0.86[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6097988	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs6097998	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6097999	0.91[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs6098002	0.82[AMR][1000 genomes]
rs7264143	0.88[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs7271481	0.90[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs7271579	0.93[AMR][1000 genomes];0.87[EUR][1000 genomes]
rs73141254	0.98[EUR][1000 genomes]
rs73141258	0.85[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:3 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv586224	chr20:52474850-53279490	Flanking Active TSS Weak transcription Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Genic enhancers Active TSS Bivalent/Poised TSS Strong transcription ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	338 gene(s)	inside rSNPs	diseases
2	nsv834011	chr20:52858341-53086042	Enhancers ZNF genes & repeats Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS	Chromatin interactive region lncRNA	55 gene(s)	inside rSNPs	diseases
3	nsv834012	chr20:52921007-53097177	Flanking Active TSS Weak transcription Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	43 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:5 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:53062200-53066200	Weak transcription	Right Atrium	heart
2	chr20:53063200-53063600	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr20:53063200-53063600	Enhancers	iPS-20b Cell Line	embryonic stem cell
4	chr20:53063200-53064600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr20:53063200-53064800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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