Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr5:37803620-37803910	NHDF-neo	bronchial:	n/a	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr5:37802721..37804855-chr5:37805974..37808582,2	K562	blood:

Variant related genes	Relation type
ENSG00000238335	TF binding region

rSNPs within LD-proxies of this variant (count:25)

rs_ID	r²[population]
rs10054159	0.99[AMR][1000 genomes];0.96[EUR][1000 genomes]
rs10069455	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10070843	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs10071586	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs10076344	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.97[ASN][1000 genomes]
rs10076391	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.99[ASN][1000 genomes]
rs10473069	0.90[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs10941365	0.99[AMR][1000 genomes];0.94[EUR][1000 genomes]
rs11111	0.96[ASN][1000 genomes]
rs12055296	0.98[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];0.98[ASN][1000 genomes]
rs13361833	0.90[ASN][1000 genomes]
rs2910701	0.88[ASN][1000 genomes]
rs2910705	0.89[ASN][1000 genomes]
rs2910706	0.89[ASN][1000 genomes]
rs2910707	0.90[ASN][1000 genomes]
rs2910797	0.90[ASN][1000 genomes]
rs2973045	0.88[ASN][1000 genomes]
rs2973046	0.89[ASN][1000 genomes]
rs2973047	0.90[ASN][1000 genomes]
rs60262907	0.85[AMR][1000 genomes];0.92[EUR][1000 genomes]
rs67720228	0.89[ASN][1000 genomes]
rs7730024	0.89[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs884344	0.90[ASN][1000 genomes]
rs9283747	0.99[AMR][1000 genomes];0.93[EUR][1000 genomes]
rs9292674	0.88[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[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	nsv949716	chr5:37179341-37967352	Weak transcription Strong transcription Flanking Active TSS Enhancers Bivalent Enhancer Active TSS ZNF genes & repeats Bivalent/Poised TSS Flanking Bivalent TSS/Enh Genic enhancers Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	58 gene(s)	inside rSNPs	diseases
2	nsv1023871	chr5:37330018-37804744	Enhancers Strong transcription Weak transcription Active TSS ZNF genes & repeats Genic enhancers Flanking Active TSS Transcr. at gene 5' and 3' Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
3	nsv537729	chr5:37330018-37804744	Weak transcription Flanking Active TSS Strong transcription Genic enhancers Enhancers Active TSS ZNF genes & repeats Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer	TF binding region CpG island Chromatin interactive region lncRNA	23 gene(s)	inside rSNPs	diseases
4	nsv597846	chr5:37430215-37813591	Weak transcription Strong transcription Enhancers ZNF genes & repeats Genic enhancers Flanking Active TSS Active TSS Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA	5 gene(s)	inside rSNPs	diseases

No data

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:37803600-37804000	Enhancers	NHDF-Ad	bronchial

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