Variant report

Variant	esv3392523
Chromosome Location	chr4:79859553-79862101
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:382)
CpG islands
(count:671)
Chromatin interactive
region (count:2)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:382 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79861092-79861293	K562	blood:	n/a	n/a
2	ATF1	chr4:79860428-79860778	K562	blood:	n/a	chr4:79860588-79860602
3	ATF3	chr4:79860298-79860756	K562	blood:	n/a	chr4:79860592-79860599 chr4:79860460-79860469 chr4:79860589-79860599 chr4:79860589-79860599
4	ATF3	chr4:79860353-79860754	H1-hESC	embryonic stem cell:	n/a	chr4:79860592-79860599 chr4:79860460-79860469 chr4:79860589-79860599 chr4:79860589-79860599
5	BACH1	chr4:79860390-79860553	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr4:79861939-79862235	GM12878	blood:	n/a	n/a
7	BCLAF1	chr4:79860302-79860806	GM12878	blood:	n/a	chr4:79860501-79860514 chr4:79860388-79860397 chr4:79860558-79860567 chr4:79860459-79860468 chr4:79860569-79860582 chr4:79860389-79860402 chr4:79860392-79860405 chr4:79860557-79860570 chr4:79860448-79860461
8	BHLHE40	chr4:79859982-79860084	HepG2	liver:	n/a	n/a
9	BHLHE40	chr4:79860381-79861177	GM12878	blood:	n/a	chr4:79860385-79860401 chr4:79860450-79860466 chr4:79860679-79860695
10	BHLHE40	chr4:79861371-79861378	K562	blood:	n/a	n/a
11	BHLHE40	chr4:79860453-79861141	K562	blood:	n/a	chr4:79860679-79860695
12	BHLHE40	chr4:79860373-79860797	HepG2	liver:	n/a	chr4:79860385-79860401 chr4:79860450-79860466 chr4:79860679-79860695
13	BRCA1	chr4:79860568-79860768	H1-hESC	embryonic stem cell:	n/a	n/a
14	BRCA1	chr4:79860429-79860674	HepG2	liver:	n/a	n/a
15	CBX3	chr4:79860441-79861108	K562	blood:	n/a	n/a
16	CCNT2	chr4:79860285-79860852	K562	blood:	n/a	n/a
17	CEBPB	chr4:79859197-79859718	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:79860436-79860635	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr4:79860397-79861306	Hela-S3	cervix:	n/a	n/a
20	CEBPD	chr4:79860268-79860740	HepG2	liver:	n/a	n/a
21	CHD1	chr4:79860540-79860996	GM12878	blood:	n/a	n/a
22	CHD2	chr4:79860431-79860831	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr4:79860440-79860640	GM12878	blood:	n/a	n/a
24	CHD2	chr4:79860498-79860731	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr4:79860324-79860837	H1-hESC	embryonic stem cell:	n/a	n/a
26	CREB1	chr4:79860388-79860826	ECC-1	luminal epithelium:	n/a	n/a
27	CREB1	chr4:79860452-79860737	A549	lung:	n/a	n/a
28	CREB1	chr4:79860085-79860893	K562	blood:	n/a	n/a
29	CREB1	chr4:79860319-79860807	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr4:79860300-79860808	GM12878	blood:	n/a	n/a
31	CREB1	chr4:79860307-79860822	HepG2	liver:	n/a	n/a
32	CREB1	chr4:79860239-79860758	A549	lung:	n/a	n/a
33	CREB1	chr4:79860236-79860997	K562	blood:	n/a	n/a
34	CREB1	chr4:79860041-79860893	HepG2	liver:	n/a	n/a
35	CTBP2	chr4:79860038-79860787	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr4:79860486-79860554	Kidney_OC	kidney:	n/a	n/a
37	CTCF	chr4:79860213-79860242	Fibrobl	skin:	n/a	n/a
38	CTCF	chr4:79860535-79860573	MCF-7	breast:	n/a	n/a
39	CTCF	chr4:79860464-79860594	Fibrobl	skin:	n/a	n/a
40	CTCF	chr4:79860556-79860867	K562	blood:	n/a	n/a
41	CTCF	chr4:79860640-79860790	HUVEC	blood vessel:	n/a	n/a
42	CTCF	chr4:79860397-79860916	GM12878	blood:	n/a	n/a
43	CTCF	chr4:79860736-79860786	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr4:79860188-79860260	GM19239	blood:	n/a	n/a
45	CTCF	chr4:79860580-79860730	GM12878	blood:	n/a	n/a
46	CTCF	chr4:79860508-79860564	GM19240	blood:	n/a	n/a
47	CTCF	chr4:79860256-79860359	MCF-7	breast:	n/a	n/a
48	CTCF	chr4:79860700-79860850	GM06990	blood:	n/a	n/a
49	CTCF	chr4:79860440-79860590	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr4:79860540-79860690	GM12866	blood:	n/a	n/a

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79860686-79860736	GM12891	blood:	n/a
2	chr4:79860379-79860429	MCF-7	breast:	n/a
3	chr4:79860507-79860557	SK-N-MC	brain:	n/a
4	chr4:79861272-79861322	SKMC	muscle:	n/a
5	chr4:79861284-79861334	MCF10A-Er-Src	breast:	n/a
6	chr4:79861064-79861114	PFSK-1	brain:	n/a
7	chr4:79861284-79861334	HEK293	kidney:	embryo
8	chr4:79860686-79860736	Hela-S3	cervix:	n/a
9	chr4:79860731-79860781	AG09309	skin:	n/a
10	chr4:79860764-79860814	AoSMC	blood vessel:	n/a
11	chr4:79861284-79861334	ECC-1	luminal epithelium:	n/a
12	chr4:79861398-79861448	MCF10A-Er-Src	breast:	n/a
13	chr4:79860379-79860429	HRCEpiC	kidney:	n/a
14	chr4:79861064-79861114	SK-N-SH_RA	brain:	n/a
15	chr4:79861398-79861448	GM19239	blood:	n/a
16	chr4:79861064-79861114	CMK	blood:	n/a
17	chr4:79860686-79860736	HEEpiC	esophagus:	n/a
18	chr4:79860731-79860781	BJ	skin:	n/a
19	chr4:79860507-79860557	HCT-116	colon:	n/a
20	chr4:79860764-79860814	HL-60	blood:	n/a
21	chr4:79860507-79860557	Caco-2	colon:	n/a
22	chr4:79861064-79861114	HCPEpiC	choroid plexus:	n/a
23	chr4:79860764-79860814	NB4	blood:	n/a
24	chr4:79861064-79861114	HRE	kidney:	n/a
25	chr4:79861398-79861448	ovcar-3	ovarian:	n/a
26	chr4:79861398-79861448	SKMC	muscle:	n/a
27	chr4:79861064-79861114	IMR90	lung:	fetal
28	chr4:79860706-79860756	PrEC	prostate:	n/a
29	chr4:79861272-79861322	HMEC	breast:	n/a
30	chr4:79860764-79860814	AG09309	skin:	n/a
31	chr4:79861064-79861114	Hepatocyte	liver:	n/a
32	chr4:79860507-79860557	SK-N-SH	brain:	n/a
33	chr4:79861398-79861448	Caco-2	colon:	n/a
34	chr4:79861064-79861114	ProgFib	skin:	n/a
35	chr4:79860507-79860557	BE2_C	brain:	n/a
36	chr4:79861284-79861334	K562	blood:	n/a
37	chr4:79860731-79860781	A549	lung:	n/a
38	chr4:79860227-79860277	U87	brain:	n/a
39	chr4:79861272-79861322	HL-60	blood:	n/a
40	chr4:79860227-79860277	HAEpiC	amniotic membrane:	n/a
41	chr4:79860379-79860429	Hela-S3	cervix:	n/a
42	chr4:79860686-79860736	Jurkat	blood:	n/a
43	chr4:79860706-79860756	AG09309	skin:	n/a
44	chr4:79860764-79860814	MCF-7	breast:	n/a
45	chr4:79860507-79860557	NB4	blood:	n/a
46	chr4:79860227-79860277	H1-hESC	embryonic stem cell:	embryo
47	chr4:79861064-79861114	HepG2	liver:	n/a
48	chr4:79860379-79860429	HPAEpiC	pulmonary alveolar:	n/a
49	chr4:79860507-79860557	GM12878	blood:	n/a
50	chr4:79860706-79860756	HUVEC	blood vessel:	n/a

(count:2 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:79471198..79473938-chr4:79857809..79860687,2	MCF-7	breast:
2	chr15:76603369..76604011-chr4:79859804..79860621,2	Hela-S3	cervix:

No data

Variant related genes	Relation type
PAQR3	TF binding region
PAQR3	CpG island
ENSG00000138772	chromatin interactions
ENSG00000140374	chromatin interactions

Extended variants
information (count: 100 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:100 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571612362	chr4:79859566-79859567	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs114882151	chr4:79859584-79859585	Active TSS Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs557174830	chr4:79859635-79859636	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs368852809	chr4:79859645-79859646	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs144489228	chr4:79859666-79859667	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs145366016	chr4:79859703-79859704	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs553316745	chr4:79859709-79859710	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs6534085	chr4:79859716-79859717	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs545422908	chr4:79859736-79859737	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs6534086	chr4:79859737-79859738	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs183559096	chr4:79859758-79859759	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs149183352	chr4:79859764-79859765	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563500520	chr4:79859806-79859807	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs6534087	chr4:79859824-79859825	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs542321138	chr4:79859846-79859847	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs374389748	chr4:79859879-79859880	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs186881768	chr4:79859948-79859949	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs528031491	chr4:79859984-79859985	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs556035835	chr4:79859985-79859986	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs545624667	chr4:79859988-79859989	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs541104186	chr4:79859991-79859992	Active TSS Weak transcription Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs550973769	chr4:79860086-79860087	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs34850162	chr4:79860087-79860088	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs142357688	chr4:79860100-79860101	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs531156474	chr4:79860132-79860133	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs368615363	chr4:79860140-79860141	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs373619943	chr4:79860153-79860154	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs373308554	chr4:79860169-79860170	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs536872778	chr4:79860173-79860174	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs200046650	chr4:79860208-79860209	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs376467729	chr4:79860213-79860214	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs376829588	chr4:79860215-79860216	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs141641594	chr4:79860268-79860269	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs373989676	chr4:79860286-79860287	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs150501146	chr4:79860289-79860290	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs201008818	chr4:79860297-79860298	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs376874926	chr4:79860298-79860299	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs370342425	chr4:79860307-79860308	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs199670616	chr4:79860337-79860338	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs372904339	chr4:79860352-79860353	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs139417001	chr4:79860361-79860362	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs559038377	chr4:79860374-79860375	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs577981157	chr4:79860379-79860380	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs373317980	chr4:79860404-79860405	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs377751585	chr4:79860405-79860406	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs537375187	chr4:79860508-79860509	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs376839231	chr4:79860517-79860518	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs573730119	chr4:79860534-79860535	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs542813764	chr4:79860536-79860537	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs559145910	chr4:79860551-79860552	Active TSS	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:76)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Glioblastoma multiforme	21922591	CNVD
Parkinson disease	21956041	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Multiple myeloma	17550852	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
primary effusion lymphomas	17116491	CNVD
Gastric cancer	16891809	CNVD
Prostate cancer	16573809	CNVD
Myelofibrosis	22110671	CNVD
Neuroblastoma	21899760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:450 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79794200-79859600	Weak transcription	Colonic Mucosa	Colon
2	chr4:79814600-79859600	Weak transcription	Fetal Kidney	kidney
3	chr4:79833000-79859800	Weak transcription	Esophagus	oesophagus
4	chr4:79833000-79859800	Weak transcription	Right Ventricle	heart
5	chr4:79833200-79859600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr4:79833600-79859800	Weak transcription	Placenta	Placenta
7	chr4:79845800-79860000	Weak transcription	Small Intestine	intestine
8	chr4:79849200-79859600	Weak transcription	Fetal Lung	lung
9	chr4:79850600-79859600	Weak transcription	HSMMtube	muscle
10	chr4:79850800-79859600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
11	chr4:79850800-79859600	Weak transcription	Ovary	ovary
12	chr4:79850800-79859800	Weak transcription	Left Ventricle	heart
13	chr4:79850800-79859800	Weak transcription	Pancreas	Pancrea
14	chr4:79850800-79860000	Weak transcription	Gastric	stomach
15	chr4:79850800-79860000	Weak transcription	Lung	lung
16	chr4:79850800-79860000	Weak transcription	Spleen	Spleen
17	chr4:79851400-79859600	Weak transcription	Monocytes-CD14+_RO01746	blood
18	chr4:79851800-79859600	Weak transcription	Fetal Muscle Trunk	muscle
19	chr4:79854000-79859800	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chr4:79855000-79859600	Weak transcription	Fetal Thymus	thymus
21	chr4:79857000-79859600	Weak transcription	Liver	Liver
22	chr4:79857800-79859600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr4:79858000-79859600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr4:79858000-79859600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr4:79858000-79859600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
26	chr4:79858000-79859600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:79858000-79859600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
28	chr4:79858000-79859600	Enhancers	Colon Smooth Muscle	Colon
29	chr4:79858000-79859600	Enhancers	HepG2	liver
30	chr4:79858000-79859800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
31	chr4:79858000-79859800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr4:79858400-79859600	Enhancers	Primary T helper cells fromperipheralblood	blood
33	chr4:79858400-79859600	Enhancers	Psoas Muscle	Psoas
34	chr4:79858600-79859600	Enhancers	Primary T killer memory cells from peripheral blood	blood
35	chr4:79858600-79859800	Weak transcription	Placenta Amnion	Placenta Amnion
36	chr4:79858600-79860000	Flanking Active TSS	Dnd41	blood
37	chr4:79858800-79859600	Enhancers	Primary T helper naive cells from peripheral blood	blood
38	chr4:79858800-79859600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
39	chr4:79858800-79859600	Enhancers	Fetal Intestine Small	intestine
40	chr4:79858800-79859800	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
41	chr4:79858800-79860200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr4:79859000-79859600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
43	chr4:79859000-79859600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:79859000-79859600	Enhancers	Primary B cells from peripheral blood	blood
45	chr4:79859000-79859600	Enhancers	Primary T cells fromperipheralblood	blood
46	chr4:79859000-79859600	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
47	chr4:79859000-79859600	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr4:79859000-79859600	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr4:79859000-79859600	Flanking Active TSS	Brain Hippocampus Middle	brain
50	chr4:79859000-79859600	Flanking Active TSS	Fetal Brain Male	brain

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