Variant report

(count:23 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr16:65160900-65161050	HVMF	connective:	n/a	n/a
2	CTCF	chr16:65160920-65161070	K562	blood:	n/a	n/a
3	CTCF	chr16:65160900-65161050	GM12864	blood:	n/a	n/a
4	CTCF	chr16:65160980-65161130	BJ	skin:	n/a	n/a
5	CTCF	chr16:65160754-65161051	IMR90	lung:	n/a	n/a
6	CTCF	chr16:65160900-65161050	NHLF	lung:	n/a	n/a
7	CTCF	chr16:65160920-65161070	GM12867	blood:	n/a	n/a
8	CTCF	chr16:65160920-65161070	HEEpiC	esophagus:	n/a	n/a
9	CTCF	chr16:65160900-65161050	HFF	foreskin:	n/a	n/a
10	CTCF	chr16:65160900-65161050	AG04450	lung:	n/a	n/a
11	CTCF	chr16:65160960-65161110	HAc	cerebellar:	n/a	n/a
12	CTCF	chr16:65160900-65161050	RPTEC	kidney:	n/a	n/a
13	RAD21	chr16:65160694-65161105	H1-hESC	embryonic stem cell:	n/a	n/a
14	RAD21	chr16:65160748-65161086	H1-hESC	embryonic stem cell:	n/a	n/a
15	ZNF143	chr16:65160765-65161100	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr16:65160900-65161050	HEEpiC	esophagus:	n/a	n/a
17	CTCF	chr16:65160920-65161070	HEK293	kidney:	n/a	n/a
18	RAD21	chr16:65160813-65161055	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr16:65160900-65161050	GM06990	blood:	n/a	n/a
20	CTCF	chr16:65160844-65161045	GM12878	blood:	n/a	n/a
21	CTCF	chr16:65160790-65161083	K562	blood:	n/a	n/a
22	CTCF	chr16:65160900-65161050	HCM	heart:	n/a	n/a
23	CTCF	chr16:65160821-65161077	GM12878	blood:	n/a	n/a

No data

Variant related genes	Relation type
CDH11	TF binding region

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	nsv833260	chr16:65050647-65218759	Enhancers Strong transcription Flanking Active TSS Weak transcription Flanking Bivalent TSS/Enh Genic enhancers Bivalent/Poised TSS Transcr. at gene 5' and 3' Active TSS Bivalent Enhancer ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA	10 gene(s)	inside rSNPs	diseases
2	esv34131	chr16:65137094-65379496	Flanking Active TSS Weak transcription Active TSS Enhancers Bivalent/Poised TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3' Strong transcription Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	15 gene(s)	inside rSNPs	diseases
3	esv3328210	chr16:65160551-65164549	Active TSS Enhancers	TF binding region	1 gene(s)	inside rSNPs	diseases
4	esv3372719	chr16:65160876-65163424	Enhancers	TF binding region	1 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	chr16:65161000-65161200	Enhancers	HUES6 Cell Line	embryonic stem cell

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