Variant report

No.	Distal block	Cell Line	Cell type
1	chr7:127891784..127894770-chr7:127895759..127898036,2	K562	blood:
2	chr7:127887971..127892049-chr7:127893662..127896900,5	MCF-7	breast:
3	chr7:127879043..127881860-chr7:127893734..127896612,2	MCF-7	breast:

Variant related genes	Relation type
ENSG00000174697	Chromatin interaction

rSNPs within LD-proxies of this variant (count:24)

rs_ID	r²[population]
rs10243710	0.86[EUR][1000 genomes]
rs10264361	0.83[AFR][1000 genomes];0.96[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10276311	0.87[EUR][1000 genomes]
rs1376349	0.89[EUR][1000 genomes]
rs2021808	0.89[EUR][1000 genomes]
rs2060713	0.86[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2122627	0.81[ASW][hapmap];0.85[CEU][hapmap];0.93[LWK][hapmap];1.00[MEX][hapmap];0.87[MKK][hapmap];1.00[TSI][hapmap];1.00[YRI][hapmap];0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs2167271	0.85[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];1.00[EUR][1000 genomes]
rs28954080	1.00[EUR][1000 genomes]
rs28954101	1.00[EUR][1000 genomes]
rs4236625	0.85[CEU][hapmap];1.00[MEX][hapmap];1.00[TSI][hapmap];0.84[AMR][1000 genomes];0.98[EUR][1000 genomes]
rs4731424	0.85[CEU][hapmap];0.88[EUR][1000 genomes]
rs4731427	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes]
rs6976458	0.82[EUR][1000 genomes]
rs7795794	0.92[AFR][1000 genomes];0.92[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs791603	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs791604	0.84[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs791606	0.84[EUR][1000 genomes]
rs791607	0.86[EUR][1000 genomes]
rs791608	0.86[EUR][1000 genomes]
rs791609	0.86[EUR][1000 genomes]
rs791616	0.83[YRI][hapmap];0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs791617	0.88[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[EUR][1000 genomes]
rs791620	0.82[AFR][1000 genomes];0.84[AMR][1000 genomes];1.00[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	nsv1022385	chr7:127246656-127971194	Weak transcription Bivalent Enhancer Enhancers Active TSS Bivalent/Poised TSS Strong transcription Genic enhancers Flanking Bivalent TSS/Enh Flanking Active TSS ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
2	nsv539120	chr7:127246656-127971194	Enhancers Weak transcription Active TSS Genic enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	37 gene(s)	inside rSNPs	diseases
3	esv33413	chr7:127800064-127929303	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Flanking Active TSS Bivalent/Poised TSS Active TSS Strong transcription Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA	13 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:4 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:127887600-127894000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr7:127893400-127895000	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr7:127893400-127895000	Weak transcription	Monocytes-CD14+_RO01746	blood
4	chr7:127893600-127895200	Strong transcription	Adipose Nuclei	Adipose

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