Variant report

No.	Distal block	Cell Line	Cell type
1	chr6:147221999..147224137-chr6:147543696..147547016,3	MCF-7	breast:
2	chr6:147221492..147224047-chr6:147523320..147525428,2	K562	blood:
3	chr6:147221960..147224216-chr6:147538711..147540256,2	MCF-7	breast:
4	chr6:147222212..147229913-chr6:147522379..147526472,14	MCF-7	breast:
5	chr6:147221788..147226460-chr6:147542201..147549451,7	K562	blood:
6	chr6:147221766..147223377-chr6:147555409..147557127,2	K562	blood:
7	chr6:147220668..147222971-chr6:147322912..147325249,2	K562	blood:

Variant related genes	Relation type
ENSG00000164506	Chromatin interaction
ENSG00000233452	Chromatin interaction

rSNPs within LD-proxies of this variant (count:21)

rs_ID	r²[population]
rs1119876	0.89[ASN][1000 genomes]
rs13195494	0.81[AFR][1000 genomes]
rs1324683	0.89[ASN][1000 genomes]
rs1324685	0.84[ASN][1000 genomes]
rs1408575	0.99[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs1924691	0.82[AMR][1000 genomes];0.85[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs1924693	0.93[ASN][1000 genomes]
rs2224906	0.83[ASN][1000 genomes]
rs2328769	0.92[ASN][1000 genomes]
rs6926192	0.87[ASN][1000 genomes]
rs7740261	0.87[ASN][1000 genomes]
rs7751561	0.92[AMR][1000 genomes];0.93[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs7755795	0.83[AFR][1000 genomes];0.92[ASN][1000 genomes]
rs7766908	0.92[AMR][1000 genomes];0.94[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs927672	0.83[AMR][1000 genomes];0.85[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs9377033	0.92[ASN][1000 genomes]
rs9377034	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9386175	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs9390437	0.92[ASN][1000 genomes]
rs9403826	0.94[AFR][1000 genomes];0.95[AMR][1000 genomes];0.92[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs9403827	0.94[AFR][1000 genomes];0.91[AMR][1000 genomes];0.85[EUR][1000 genomes];0.88[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	nsv830838	chr6:147090745-147274669	Enhancers Flanking Active TSS Weak transcription Bivalent Enhancer Transcr. at gene 5' and 3' Active TSS Bivalent/Poised TSS ZNF genes & repeats Strong transcription Genic enhancers Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	21 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147215200-147224200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:147216000-147224600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:147218000-147225800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr6:147218200-147226600	Weak transcription	NHLF	lung
5	chr6:147219800-147223800	Weak transcription	Primary hematopoietic stem cells	blood
6	chr6:147220000-147223200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
7	chr6:147220400-147223800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
8	chr6:147220600-147223200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr6:147221400-147224800	Enhancers	K562	blood
10	chr6:147222000-147226000	Weak transcription	Stomach Smooth Muscle	stomach

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