Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:210913946..210916328-chr1:210919386..210921041,2	MCF-7	breast:

rSNPs within LD-proxies of this variant (count:27)

rs_ID	r²[population]
rs10863854	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs11119583	0.88[ASN][1000 genomes]
rs11119588	0.96[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs11119589	0.96[AMR][1000 genomes];0.99[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1114880	0.87[ASN][1000 genomes]
rs12022273	0.91[ASN][1000 genomes]
rs12022312	0.91[ASN][1000 genomes]
rs12040025	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1317255	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1340128	0.88[ASN][1000 genomes]
rs1770212	0.83[ASN][1000 genomes]
rs1770214	0.86[ASN][1000 genomes]
rs1770215	0.85[ASN][1000 genomes]
rs1777244	0.87[ASN][1000 genomes]
rs1777252	0.87[ASN][1000 genomes]
rs1777254	0.85[ASN][1000 genomes]
rs1777255	0.86[ASN][1000 genomes]
rs1777256	0.84[ASN][1000 genomes]
rs1777257	0.83[ASN][1000 genomes]
rs1777263	0.88[ASN][1000 genomes]
rs1890844	0.86[EUR][1000 genomes]
rs1890846	0.88[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1934625	0.87[AMR][1000 genomes];0.94[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1934626	0.93[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs1934632	0.96[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs1934633	1.00[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs9429845	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];0.98[EUR][1000 genomes];0.98[ASN][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	nsv873148	chr1:210665583-210994339	Enhancers Weak transcription ZNF genes & repeats Flanking Active TSS Strong transcription Genic enhancers Bivalent Enhancer Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region lncRNA miRNA target site	3 gene(s)	inside rSNPs	diseases
2	nsv873153	chr1:210900481-210994339	Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases
3	nsv999018	chr1:210907239-210999306	Genic enhancers Enhancers Weak transcription Bivalent Enhancer Strong transcription Flanking Active TSS ZNF genes & repeats	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:210871200-210932000	Weak transcription	HSMM	muscle
2	chr1:210905600-210921200	Weak transcription	Brain Inferior Temporal Lobe	brain
3	chr1:210910600-210921200	Weak transcription	Brain Angular Gyrus	brain
4	chr1:210917400-210930800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr1:210919200-210920200	Enhancers	HSMMtube	muscle
6	chr1:210919400-210919800	Enhancers	A549	lung
7	chr1:210919600-210919800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr1:210919600-210921000	Weak transcription	Brain Hippocampus Middle	brain

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