Variant report

(count:26 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr19:45074645-45075031	HepG2	liver:	n/a	n/a
2	TBP	chr19:45074682-45074921	HepG2	liver:	n/a	n/a
3	HNF4G	chr19:45074620-45074995	HepG2	liver:	n/a	n/a
4	POLR2A	chr19:45074436-45075476	HepG2	liver:	n/a	n/a
5	RAD21	chr19:45074075-45075025	HepG2	liver:	n/a	n/a
6	HEY1	chr19:45074553-45075065	HepG2	liver:	n/a	n/a
7	CEBPD	chr19:45074660-45074974	HepG2	liver:	n/a	n/a
8	MAFF	chr19:45074626-45074962	HepG2	liver:	n/a	n/a
9	RCOR1	chr19:45074821-45075036	HepG2	liver:	n/a	n/a
10	POLR2A	chr19:45074529-45075016	HepG2	liver:	n/a	n/a
11	EP300	chr19:45074635-45074910	HepG2	liver:	n/a	n/a
12	MYBL2	chr19:45074587-45075197	HepG2	liver:	n/a	n/a
13	EP300	chr19:45074591-45075068	HepG2	liver:	n/a	n/a
14	CEBPB	chr19:45074580-45074973	HepG2	liver:	n/a	n/a
15	CEBPB	chr19:45074691-45074929	HepG2	liver:	n/a	n/a
16	HNF4A	chr19:45074633-45074937	HepG2	liver:	n/a	n/a
17	POLR2A	chr19:45074696-45074952	HepG2	liver:	n/a	n/a
18	SP1	chr19:45074491-45075033	HepG2	liver:	n/a	n/a
19	POLR2A	chr19:45074763-45074891	HepG2	liver:	n/a	n/a
20	HDAC2	chr19:45074594-45074996	HepG2	liver:	n/a	n/a
21	CTCF	chr19:45073694-45075713	A549	lung:	n/a	chr19:45075149-45075162
22	EP300	chr19:45074732-45074987	HepG2	liver:	n/a	n/a
23	TEAD4	chr19:45074580-45075218	HepG2	liver:	n/a	n/a
24	POLR2A	chr19:45074643-45074920	HepG2	liver:	n/a	n/a
25	ARID3A	chr19:45074625-45074997	HepG2	liver:	n/a	n/a
26	CEBPB	chr19:45074641-45075024	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr19:45074225..45075084-chr19:45160196..45161185,6	K562	blood:
2	chr19:45074025..45075864-chr19:45246101..45248322,2	MCF-7	breast:
3	chr19:45074128..45076823-chr19:45084175..45086201,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000224366	TF binding region

Variant overlapped rSNPs/rCNVs (count:2 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1062812	chr19:45042262-45214796	Enhancers Flanking Active TSS Weak transcription Genic enhancers Active TSS ZNF genes & repeats Strong transcription Bivalent/Poised TSS Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA	20 gene(s)	inside rSNPs	diseases
2	nsv960931	chr19:45073821-45102725	Weak transcription Enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	5 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:16 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:45070400-45080400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr19:45070600-45075200	Weak transcription	Primary monocytes fromperipheralblood	blood
3	chr19:45073800-45076400	Enhancers	K562	blood
4	chr19:45074200-45075600	Enhancers	A549	lung
5	chr19:45074200-45076000	Flanking Active TSS	HepG2	liver
6	chr19:45074400-45075000	Bivalent Enhancer	Stomach Mucosa	stomach
7	chr19:45074400-45075200	Flanking Active TSS	Duodenum Mucosa	Duodenum
8	chr19:45074400-45075600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr19:45074400-45075600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr19:45074400-45077800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
11	chr19:45074400-45078200	Enhancers	Fetal Intestine Large	intestine
12	chr19:45074600-45075000	Enhancers	Fetal Kidney	kidney
13	chr19:45074800-45075000	Enhancers	Rectal Mucosa Donor 29	rectum
14	chr19:45074800-45076200	Enhancers	Liver	Liver
15	chr19:45074800-45076200	Enhancers	Monocytes-CD14+_RO01746	blood
16	chr19:45074800-45077800	Enhancers	Fetal Intestine Small	intestine

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