Variant report

No.	Distal block	Cell Line	Cell type
1	chr3:43674060..43677264-chr3:43731030..43734285,4	K562	blood:
2	chr3:43677109..43678918-chr3:43689320..43690947,2	K562	blood:
3	chr3:43661892..43664956-chr3:43673949..43677419,4	K562	blood:
4	chr3:43669714..43671935-chr3:43674866..43677671,2	K562	blood:
5	chr3:43672724..43677719-chr3:43679824..43684004,5	K562	blood:
6	chr3:43676123..43678238-chr3:43731263..43733024,2	MCF-7	breast:
7	chr3:43594419..43596904-chr3:43675477..43678114,2	K562	blood:

Variant related genes	Relation type
ENSG00000160746	Chromatin interaction
ENSG00000011198	Chromatin interaction

rSNPs within LD-proxies of this variant (count:29)

rs_ID	r²[population]
rs1013758	0.88[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs10461013	0.81[AFR][1000 genomes];0.82[EUR][1000 genomes]
rs10461015	0.92[AFR][1000 genomes];0.97[AMR][1000 genomes];0.94[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs11130004	0.84[EUR][1000 genomes]
rs11130005	0.96[AFR][1000 genomes];0.86[EUR][1000 genomes];0.82[ASN][1000 genomes]
rs12486736	0.85[EUR][1000 genomes]
rs12638282	0.85[EUR][1000 genomes]
rs13319147	0.82[AFR][1000 genomes];0.90[AMR][1000 genomes];0.94[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs1351631	0.81[EUR][1000 genomes]
rs1384435	0.85[EUR][1000 genomes]
rs1564434	0.81[EUR][1000 genomes]
rs17030517	0.81[EUR][1000 genomes]
rs1842807	0.82[AFR][1000 genomes]
rs1975997	0.81[EUR][1000 genomes]
rs2101064	0.85[EUR][1000 genomes]
rs3772160	0.82[AFR][1000 genomes];0.89[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs4264704	0.81[EUR][1000 genomes]
rs61102363	0.83[AFR][1000 genomes];0.81[EUR][1000 genomes]
rs737516	0.85[EUR][1000 genomes]
rs9311340	0.81[EUR][1000 genomes]
rs9809643	0.96[AFR][1000 genomes];0.87[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs9814737	0.84[EUR][1000 genomes]
rs9815196	0.81[EUR][1000 genomes]
rs9829067	0.85[EUR][1000 genomes]
rs9830697	0.81[EUR][1000 genomes]
rs9834786	0.80[AMR][1000 genomes];0.82[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs9835793	0.81[EUR][1000 genomes]
rs9852783	0.96[AFR][1000 genomes];0.93[AMR][1000 genomes];0.85[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs9873316	0.84[EUR][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	nsv834673	chr3:43622985-43799876	Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats Weak transcription Active TSS Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:13 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:43664200-43688400	Weak transcription	Aorta	Aorta
2	chr3:43671200-43680200	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr3:43672200-43680000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr3:43674200-43677600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr3:43674400-43680200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr3:43674400-43682800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr3:43675000-43679000	Weak transcription	HUVEC	blood vessel
8	chr3:43675000-43679200	Weak transcription	Muscle Satellite Cultured Cells	--
9	chr3:43675000-43679400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr3:43675000-43680000	Weak transcription	A549	lung
11	chr3:43675400-43677600	Weak transcription	K562	blood
12	chr3:43676400-43680400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr3:43676600-43680200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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