Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr7:135932004-135932526	K562	blood:	n/a	n/a
2	RCOR1	chr7:135931930-135932420	K562	blood:	n/a	n/a
3	ATF1	chr7:135931923-135932438	K562	blood:	n/a	n/a
4	IRF1	chr7:135932028-135932289	K562	blood:	n/a	n/a
5	CUX1	chr7:135932102-135932440	K562	blood:	n/a	n/a
6	ARID3A	chr7:135931947-135932309	K562	blood:	n/a	n/a
7	EP300	chr7:135931865-135932342	K562	blood:	n/a	chr7:135931883-135931893 chr7:135932328-135932342 chr7:135931952-135931962
8	CTCF	chr7:135932180-135932330	GM06990	blood:	n/a	n/a
9	TBL1XR1	chr7:135931976-135932265	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr7:135925867..135928083-chr7:135931669..135933724,2	K562	blood:

Variant related genes	Relation type
ENSG00000220982	TF binding region

rSNPs within LD-proxies of this variant (count:20)

rs_ID	r²[population]
rs11763331	0.87[AFR][1000 genomes]
rs11765861	0.91[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs11767724	0.82[AFR][1000 genomes]
rs11767797	0.82[AFR][1000 genomes]
rs11767854	0.82[AFR][1000 genomes]
rs12707290	0.82[AFR][1000 genomes]
rs13234186	0.95[AFR][1000 genomes]
rs1426474	0.90[AFR][1000 genomes]
rs34023094	0.90[AFR][1000 genomes]
rs34307610	0.85[AFR][1000 genomes]
rs34444115	0.88[AFR][1000 genomes]
rs34602243	0.85[AFR][1000 genomes]
rs34920483	0.90[AFR][1000 genomes]
rs60742194	0.92[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs67205433	0.82[AFR][1000 genomes]
rs67970409	0.82[AFR][1000 genomes]
rs6974175	0.90[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs6974879	0.84[AFR][1000 genomes];0.91[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs730693	0.90[AFR][1000 genomes]
rs73460870	0.90[AFR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv889236	chr7:135884571-135943264	ZNF genes & repeats Weak transcription Enhancers Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
2	nsv1034145	chr7:135893502-135986088	Flanking Active TSS Enhancers Weak transcription ZNF genes & repeats Flanking Bivalent TSS/Enh Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv1033206	chr7:135899512-135978595	Enhancers Weak transcription Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv1018084	chr7:135901545-135983684	Weak transcription Enhancers Active TSS ZNF genes & repeats Flanking Active TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1025030	chr7:135901545-135986088	Weak transcription Enhancers Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Flanking Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:135930800-135933800	Enhancers	K562	blood

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