Variant report

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr19:39736545..39739451-chr19:39741300..39743196,2	K562	blood:

Variant related genes	Relation type
ENSG00000272395	Chromatin interaction

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

rs_ID	r²[population]
rs11881222	0.98[AMR][1000 genomes];0.96[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs11882871	0.88[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs12971396	0.97[ASN][1000 genomes]
rs12979860	0.83[AMR][1000 genomes];0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12980275	0.81[AMR][1000 genomes];0.83[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs12982533	0.86[AMR][1000 genomes];0.88[EUR][1000 genomes];0.83[ASN][1000 genomes]
rs12983038	0.97[ASN][1000 genomes]
rs28416813	0.83[AMR][1000 genomes];0.81[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs35790907	0.83[EUR][1000 genomes]
rs4803217	0.97[ASN][1000 genomes]
rs4803221	0.97[ASN][1000 genomes]
rs4803222	0.96[AFR][1000 genomes];0.98[AMR][1000 genomes];0.99[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs66531907	0.97[ASN][1000 genomes]
rs7248668	0.94[ASN][1000 genomes]
rs8099917	0.94[ASN][1000 genomes]
rs8105086	0.82[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs8105790	0.94[ASN][1000 genomes]
rs8107030	0.97[ASN][1000 genomes]
rs8109886	0.90[ASN][1000 genomes]
rs8109889	0.94[ASN][1000 genomes]
rs8113007	0.96[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:4 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv432048	chr19:39572060-39850060	Bivalent/Poised TSS Bivalent Enhancer Weak transcription Genic enhancers Flanking Bivalent TSS/Enh ZNF genes & repeats Active TSS Strong transcription Enhancers Flanking Active TSS Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	42 gene(s)	inside rSNPs	diseases
2	nsv833830	chr19:39709538-39837846	Enhancers Bivalent Enhancer Genic enhancers Strong transcription Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	32 gene(s)	inside rSNPs	diseases
3	nsv911678	chr19:39710903-39763765	Bivalent Enhancer Enhancers Flanking Active TSS Weak transcription Bivalent/Poised TSS Flanking Bivalent TSS/Enh Active TSS ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
4	nsv911679	chr19:39735106-39924129	Active TSS Flanking Active TSS Weak transcription Enhancers Strong transcription Bivalent Enhancer Transcr. at gene 5' and 3' Genic enhancers ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA miRNA target site	198 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39740200-39741800	Weak transcription	Primary hematopoietic stem cells	blood
2	chr19:39740400-39741600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
3	chr19:39741200-39743800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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