Variant report

No.	Distal block	Cell Line	Cell type
1	chr3:150479297..150481963-chr3:150584720..150587723,3	MCF-7	breast:
2	chr3:150478755..150482911-chr3:150581723..150585653,5	MCF-7	breast:
3	chr3:150584605..150586151-chr3:150588439..150591426,2	K562	blood:
4	chr3:150583250..150586861-chr3:150588416..150592183,4	K562	blood:

Variant related genes	Relation type
ENSG00000244265	Chromatin interaction
ENSG00000181788	Chromatin interaction

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

rs_ID	r²[population]
rs10513379	0.82[EUR][1000 genomes]
rs12629256	0.87[EUR][1000 genomes]
rs1444198	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1444199	0.89[AMR][1000 genomes];0.99[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs1444200	0.83[ASN][1000 genomes]
rs16862877	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs16862928	0.96[EUR][1000 genomes]
rs17283761	0.92[ASN][1000 genomes]
rs2034158	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs2037408	0.95[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2037409	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs4679986	0.88[ASN][1000 genomes]
rs4680004	0.92[ASN][1000 genomes]
rs4680006	0.95[ASN][1000 genomes]
rs4680007	0.94[ASN][1000 genomes]
rs56285716	0.93[ASN][1000 genomes]
rs56659353	0.89[AMR][1000 genomes];0.96[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs58091102	0.86[ASN][1000 genomes]
rs60979559	0.81[EUR][1000 genomes]
rs61132047	0.85[EUR][1000 genomes]
rs62282691	0.89[ASN][1000 genomes]
rs67193230	0.96[EUR][1000 genomes]
rs6768276	0.91[ASN][1000 genomes]
rs6775087	0.92[ASN][1000 genomes]
rs6781091	0.88[ASN][1000 genomes]
rs6783058	0.88[ASN][1000 genomes]
rs73152585	0.82[AFR][1000 genomes];1.00[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv532662	chr3:150180747-150633414	Weak transcription Flanking Active TSS Strong transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3' Bivalent Enhancer ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	101 gene(s)	inside rSNPs	diseases
2	nsv877646	chr3:150582992-150641304	Weak transcription Enhancers Active TSS Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:12 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:150583400-150588200	Weak transcription	Osteobl	bone
2	chr3:150583600-150586000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr3:150583600-150586200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr3:150583600-150588400	Weak transcription	Primary neutrophils fromperipheralblood	blood
5	chr3:150583800-150591200	Enhancers	Placenta	Placenta
6	chr3:150584400-150585800	Enhancers	Primary hematopoietic stem cells	blood
7	chr3:150584600-150585800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr3:150584600-150586000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr3:150584800-150587400	Weak transcription	Fetal Heart	heart
10	chr3:150584800-150587800	Weak transcription	Fetal Muscle Leg	muscle
11	chr3:150585000-150585200	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
12	chr3:150585000-150586000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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