Variant report

No.	Distal block	Cell Line	Cell type
1	chr1:59199775..59201323-chr1:59248930..59250619,2	MCF-7	breast:
2	chr1:59200101..59201638-chr1:59243115..59244926,2	K562	blood:
3	chr1:59200565..59206514-chr1:59243497..59250904,12	K562	blood:

Variant related genes	Relation type
ENSG00000177606	Chromatin interaction
ENSG00000234807	Chromatin interaction

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

rs_ID	r²[population]
rs11207299	0.83[EUR][1000 genomes]
rs12073211	0.84[EUR][1000 genomes]
rs1323281	0.99[AFR][1000 genomes];0.89[AMR][1000 genomes];0.89[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1323282	0.89[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs1323284	0.85[ASN][1000 genomes]
rs2760480	0.98[AFR][1000 genomes];0.88[AMR][1000 genomes];0.89[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs2760482	0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs2760483	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs2760485	0.86[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2811856	0.88[AMR][1000 genomes];0.96[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2811858	0.89[AMR][1000 genomes];0.95[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs2811865	0.99[AFR][1000 genomes];0.99[AMR][1000 genomes];0.99[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs2811866	0.98[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs2811867	0.98[AFR][1000 genomes];0.99[AMR][1000 genomes];1.00[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs4414067	0.83[EUR][1000 genomes]
rs4612650	0.83[EUR][1000 genomes]
rs4912375	0.83[EUR][1000 genomes]
rs55892958	0.83[EUR][1000 genomes]
rs61292499	0.83[EUR][1000 genomes]
rs999158	0.87[AMR][1000 genomes];0.95[EUR][1000 genomes];0.83[ASN][1000 genomes]

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	esv2754829	chr1:59197556-59215791	Weak transcription Enhancers ZNF genes & repeats Bivalent Enhancer Flanking Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:9 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:59192600-59204200	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr1:59198200-59201400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr1:59198200-59206200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr1:59198600-59205800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr1:59198800-59204000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr1:59198800-59207200	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr1:59200400-59205800	Weak transcription	NHDF-Ad	bronchial
8	chr1:59201000-59204000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr1:59201200-59201800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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