Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:149628297..149630405-chr6:149634848..149636468,2	K562	blood:
2	chr6:149629573..149635646-chr6:149637142..149639783,10	MCF-7	breast:

Variant related genes	Relation type
ENSG00000055208	Chromatin interaction

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

rs_ID	r²[population]
rs479676	0.88[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs482388	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs485360	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs527010	0.84[AMR][1000 genomes];0.85[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs530516	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs532563	0.84[AMR][1000 genomes];0.91[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs541155	0.89[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs542194	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs543910	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs543973	0.90[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs545750	0.80[AMR][1000 genomes];0.89[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs560917	0.90[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs562677	0.90[EUR][1000 genomes];0.85[ASN][1000 genomes]
rs573148	0.88[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs574446	0.91[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs576227	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs643491	0.84[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs643921	0.81[AMR][1000 genomes];0.85[EUR][1000 genomes]
rs652070	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs702359	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs799389	0.81[AMR][1000 genomes];0.92[EUR][1000 genomes];0.89[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:5 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1024776	chr6:149398652-149654593	Weak transcription Active TSS Bivalent Enhancer Enhancers Flanking Active TSS Transcr. at gene 5' and 3' Strong transcription ZNF genes & repeats Genic enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	17 gene(s)	inside rSNPs	diseases
2	nsv1015360	chr6:149609804-149649982	Weak transcription Enhancers Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Genic enhancers Bivalent Enhancer Flanking Bivalent TSS/Enh Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
3	nsv1024106	chr6:149622349-149745053	Weak transcription Enhancers Flanking Active TSS Strong transcription Genic enhancers Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	10 gene(s)	inside rSNPs	diseases
4	esv18913	chr6:149629115-149633318	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	inside rSNPs	n/a
5	esv3402662	chr6:149630314-149630416	Weak transcription	Chromatin interactive region	1 gene(s)	inside rSNPs	n/a

No data

Chromatin state (count:3 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:149628000-149637800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr6:149628600-149631800	Weak transcription	HUES64 Cell Line	embryonic stem cell
3	chr6:149628600-149637200	Weak transcription	ES-I3 Cell Line	embryonic stem cell

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