Variant report

(count:28 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	MYC	chr5:96424323-96425518	K562	blood:	n/a	n/a
2	TBL1XR1	chr5:96424320-96424977	K562	blood:	n/a	n/a
3	RCOR1	chr5:96424200-96425988	K562	blood:	n/a	n/a
4	MAX	chr5:96424675-96425512	K562	blood:	n/a	n/a
5	ARID3A	chr5:96424587-96424845	K562	blood:	n/a	n/a
6	IRF1	chr5:96424398-96425478	K562	blood:	n/a	n/a
7	POLR2A	chr5:96424468-96424804	K562	blood:	n/a	n/a
8	TEAD4	chr5:96424298-96424809	K562	blood:	n/a	n/a
9	IRF1	chr5:96424510-96424834	K562	blood:	n/a	n/a
10	PML	chr5:96424494-96425475	K562	blood:	n/a	n/a
11	MAFK	chr5:96424657-96424734	K562	blood:	n/a	n/a
12	ATF1	chr5:96424591-96425404	K562	blood:	n/a	n/a
13	UBTF	chr5:96424464-96424753	K562	blood:	n/a	n/a
14	ZMIZ1	chr5:96424602-96425275	K562	blood:	n/a	n/a
15	MAX	chr5:96424442-96425525	K562	blood:	n/a	n/a
16	EP300	chr5:96424511-96424850	K562	blood:	n/a	n/a
17	CBX3	chr5:96424434-96425591	K562	blood:	n/a	n/a
18	HEY1	chr5:96424629-96425211	K562	blood:	n/a	n/a
19	TAL1	chr5:96424583-96424801	K562	blood:	n/a	n/a
20	ZNF143	chr5:96424443-96425605	K562	blood:	n/a	n/a
21	CEBPD	chr5:96424449-96424938	K562	blood:	n/a	n/a
22	GATA1	chr5:96424422-96424905	PBDE	blood:	n/a	n/a
23	JUND	chr5:96424391-96425590	K562	blood:	n/a	n/a
24	POLR2A	chr5:96424501-96425121	K562	blood:	n/a	n/a
25	TEAD4	chr5:96424369-96425668	K562	blood:	n/a	n/a
26	POLR2A	chr5:96424645-96425475	K562	blood:	n/a	n/a
27	TBP	chr5:96424428-96425466	K562	blood:	n/a	n/a
28	MAZ	chr5:96424476-96425574	K562	blood:	n/a	n/a

No data

Variant related genes	Relation type
ENSG00000251606	TF binding region

rSNPs within LD-proxies of this variant (count:7)

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	nsv432755	chr5:95987984-96657483	Weak transcription Enhancers Strong transcription Flanking Active TSS Genic enhancers Transcr. at gene 5' and 3' Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	66 gene(s)	inside rSNPs	diseases
2	nsv598962	chr5:96057891-96893164	Weak transcription Strong transcription Enhancers Bivalent/Poised TSS Genic enhancers Flanking Active TSS Active TSS ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent Enhancer Flanking Bivalent TSS/Enh	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	49 gene(s)	inside rSNPs	diseases
3	nsv4924	chr5:96391451-96437233	Enhancers Active TSS Weak transcription Strong transcription Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer ZNF genes & repeats Genic enhancers	TF binding region CpG island Chromatin interactive region lncRNA	2 gene(s)	inside rSNPs	diseases
4	nsv969966	chr5:96418895-96427787	Strong transcription Enhancers Weak transcription Genic enhancers Flanking Active TSS ZNF genes & repeats Active TSS Bivalent Enhancer	TF binding region CpG island Chromatin interactive region	1 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	chr5:96421800-96424800	Enhancers	Primary neutrophils fromperipheralblood	blood
2	chr5:96421800-96425000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr5:96422600-96425400	Strong transcription	Primary B cells from cord blood	blood
4	chr5:96422600-96426400	Strong transcription	Primary B cells from peripheral blood	blood
5	chr5:96423200-96430200	Weak transcription	Fetal Muscle Leg	muscle
6	chr5:96424200-96425000	Enhancers	Monocytes-CD14+_RO01746	blood
7	chr5:96424200-96425800	Enhancers	Primary monocytes fromperipheralblood	blood
8	chr5:96424600-96424800	Enhancers	K562	blood

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