Variant report

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CBX3	chr19:39470318-39470873	K562	blood:	n/a	n/a
2	TEAD4	chr19:39470420-39470858	K562	blood:	n/a	n/a
3	RCOR1	chr19:39470520-39470724	K562	blood:	n/a	n/a
4	GATA2	chr19:39470498-39470908	K562	blood:	n/a	n/a
5	E2F6	chr19:39470446-39470618	K562	blood:	n/a	n/a
6	CEBPD	chr19:39470364-39470908	K562	blood:	n/a	n/a
7	TBL1XR1	chr19:39470556-39470735	K562	blood:	n/a	n/a
8	TAL1	chr19:39470448-39470890	K562	blood:	n/a	n/a
9	MAX	chr19:39470332-39470755	K562	blood:	n/a	chr19:39470507-39470520 chr19:39470508-39470519 chr19:39470511-39470518 chr19:39470508-39470519 chr19:39470509-39470518
10	CCNT2	chr19:39470572-39470767	K562	blood:	n/a	n/a
11	MAX	chr19:39470398-39470637	K562	blood:	n/a	chr19:39470507-39470520 chr19:39470508-39470519 chr19:39470511-39470518 chr19:39470508-39470519 chr19:39470509-39470518
12	EP300	chr19:39470569-39470854	K562	blood:	n/a	n/a
13	MYC	chr19:39470523-39470653	K562	blood:	n/a	n/a
14	USF1	chr19:39470357-39470744	K562	blood:	n/a	n/a
15	CTCF	chr19:39470500-39470650	GM12872	blood:	n/a	n/a
16	POLR2A	chr19:39470483-39470811	K562	blood:	n/a	n/a
17	TEAD4	chr19:39470392-39470816	K562	blood:	n/a	n/a
18	RCOR1	chr19:39470511-39470809	K562	blood:	n/a	n/a
19	GABPA	chr19:39470482-39470797	K562	blood:	n/a	n/a
20	ELF1	chr19:39470531-39470853	K562	blood:	n/a	n/a

No.	Distal block	Cell Line	Cell type
1	chr19:39420391..39423581-chr19:39468736..39471563,3	K562	blood:
2	chr19:39469273..39472050-chr19:39495885..39497816,2	MCF-7	breast:
3	chr19:39470454..39473191-chr19:39473840..39476726,2	MCF-7	breast:
4	chr19:39466590..39468490-chr19:39469783..39471749,2	MCF-7	breast:
5	chr19:39470241..39471919-chr19:39522742..39524502,2	MCF-7	breast:

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	nsv1057899	chr19:39088319-39475493	Flanking Active TSS Flanking Bivalent TSS/Enh Genic enhancers Weak transcription Transcr. at gene 5' and 3' Enhancers Bivalent Enhancer Active TSS Strong transcription Bivalent/Poised TSS ZNF genes & repeats	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	82 gene(s)	inside rSNPs	diseases
2	esv3318111	chr19:39470551-39471952	ZNF genes & repeats Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	inside rSNPs	diseases

No data

Chromatin state (count:8 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:39467400-39471200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr19:39467600-39471400	Weak transcription	Brain Hippocampus Middle	brain
3	chr19:39467600-39471400	Weak transcription	Fetal Muscle Trunk	muscle
4	chr19:39469400-39471400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr19:39470200-39471800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr19:39470400-39470800	ZNF genes & repeats	Liver	Liver
7	chr19:39470400-39470800	Enhancers	K562	blood
8	chr19:39470400-39472000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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