Variant report

(count:22 , 50 per page) page: 1

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	EP300	chr9:104116444-104117639	HepG2	liver:	n/a	n/a
2	NFIC	chr9:104115878-104117587	HepG2	liver:	n/a	n/a
3	HNF4A	chr9:104116600-104117549	HepG2	liver:	n/a	chr9:104117446-104117461
4	MAX	chr9:104115888-104117882	HepG2	liver:	n/a	n/a
5	TEAD4	chr9:104115896-104117654	HepG2	liver:	n/a	n/a
6	MAFF	chr9:104116610-104117618	HepG2	liver:	n/a	n/a
7	MAX	chr9:104116468-104117777	HepG2	liver:	n/a	n/a
8	NFIC	chr9:104116429-104117646	HepG2	liver:	n/a	n/a
9	USF1	chr9:104116644-104117457	A549	lung:	n/a	chr9:104117221-104117232
10	TCF12	chr9:104116065-104117598	A549	lung:	n/a	n/a
11	MAX	chr9:104116335-104117499	A549	lung:	n/a	n/a
12	BHLHE40	chr9:104116122-104117622	HepG2	liver:	n/a	n/a
13	EP300	chr9:104116707-104117502	HepG2	liver:	n/a	n/a
14	MBD4	chr9:104115931-104117779	HepG2	liver:	n/a	n/a
15	HDAC2	chr9:104116628-104117600	HepG2	liver:	n/a	n/a
16	POLR2A	chr9:104116192-104117569	HepG2	liver:	n/a	n/a
17	RCOR1	chr9:104116479-104117631	HepG2	liver:	n/a	n/a
18	MYBL2	chr9:104115963-104117702	HepG2	liver:	n/a	n/a
19	SP1	chr9:104115971-104117447	HepG2	liver:	n/a	n/a
20	MAX	chr9:104116592-104117786	HepG2	liver:	n/a	n/a
21	ARID3A	chr9:104115594-104117917	HepG2	liver:	n/a	n/a
22	USF2	chr9:104116597-104117627	HepG2	liver:	n/a	n/a

No data

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

No.	Distal block	Cell Line	Cell type
1	chr9:104114762..104117661-chr9:104119094..104121364,2	K562	blood:
2	chr9:104103557..104105942-chr9:104115837..104118700,2	K562	blood:
3	chr9:104115563..104118166-chr9:104124476..104126827,2	K562	blood:

No data

rSNPs within LD-proxies of this variant (count:11)

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

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv1037157	chr9:104045761-104149233	Enhancers Active TSS Strong transcription Weak transcription Flanking Active TSS ZNF genes & repeats Genic enhancers Bivalent Enhancer Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region lncRNA	8 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	chr9:104115000-104118400	Enhancers	Fetal Intestine Small	intestine
2	chr9:104115000-104119000	Enhancers	Stomach Mucosa	stomach
3	chr9:104115000-104119200	Enhancers	Fetal Intestine Large	intestine
4	chr9:104115400-104119200	Enhancers	Liver	Liver
5	chr9:104115600-104118200	Enhancers	Small Intestine	intestine
6	chr9:104116400-104118200	Enhancers	Rectal Mucosa Donor 31	rectum
7	chr9:104116600-104117600	Enhancers	Rectal Mucosa Donor 29	rectum
8	chr9:104116600-104117800	Enhancers	Pancreas	Pancrea
9	chr9:104117200-104117600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr9:104117200-104117600	Bivalent Enhancer	Sigmoid Colon	Sigmoid Colon
11	chr9:104117200-104117600	Flanking Active TSS	A549	lung
12	chr9:104117200-104117800	Enhancers	Colonic Mucosa	Colon
13	chr9:104117200-104118400	Enhancers	K562	blood
14	chr9:104117400-104117600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr9:104117400-104117800	Flanking Active TSS	Duodenum Mucosa	Duodenum
16	chr9:104117400-104119200	Enhancers	HepG2	liver

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