Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:74799909..74801908-chr6:74804659..74806220,2	K562	blood:

rSNPs within LD-proxies of this variant (count:26)

rs_ID	r²[population]
rs12665051	0.86[ASN][1000 genomes]
rs1934013	0.93[AMR][1000 genomes];0.90[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1934021	0.88[ASN][1000 genomes]
rs2486229	0.86[ASN][1000 genomes]
rs28540037	0.87[ASN][1000 genomes]
rs4708121	0.91[ASN][1000 genomes]
rs4708122	0.90[ASN][1000 genomes]
rs4708124	0.90[ASN][1000 genomes]
rs4708125	0.91[ASN][1000 genomes]
rs6921555	0.91[ASN][1000 genomes]
rs9341446	0.92[AFR][1000 genomes];0.99[AMR][1000 genomes];0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9350522	0.91[ASN][1000 genomes]
rs9350523	0.91[ASN][1000 genomes]
rs9350524	0.90[ASN][1000 genomes]
rs9352063	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];0.98[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9352066	0.91[ASN][1000 genomes]
rs9352067	0.91[ASN][1000 genomes]
rs9359059	0.91[ASN][1000 genomes]
rs9359060	0.91[ASN][1000 genomes]
rs9359061	0.91[ASN][1000 genomes]
rs9359062	0.91[ASN][1000 genomes]
rs9360734	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9360735	0.91[ASN][1000 genomes]
rs9360736	0.91[ASN][1000 genomes]
rs9360737	0.91[ASN][1000 genomes]
rs9447153	0.91[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1030389	chr6:74606701-74811706	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Bivalent Enhancer Active TSS	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
2	esv3394316	chr6:74630005-74935625	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS Active TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
3	nsv603733	chr6:74666559-74944460	Enhancers Weak transcription Flanking Active TSS Active TSS ZNF genes & repeats Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	esv3327625	chr6:74716120-74971605	Enhancers Weak transcription ZNF genes & repeats Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
5	nsv1017333	chr6:74776830-74907758	Enhancers Flanking Active TSS Active TSS Weak transcription Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 gene(s)	inside rSNPs	diseases
6	nsv538307	chr6:74776830-74907758	Enhancers Weak transcription Flanking Active TSS Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	1 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	chr6:74798000-74800800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr6:74800200-74802000	Enhancers	Rectal Smooth Muscle	rectum
3	chr6:74800600-74800800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr6:74800600-74800800	Enhancers	Stomach Smooth Muscle	stomach
5	chr6:74800600-74802000	Enhancers	Colon Smooth Muscle	Colon

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