Variant report

Variant	nsv1011365
Chromosome Location	chr4:79714695-79779723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:271)
CpG islands
(count:61)
Chromatin interactive
region (count:56)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:271 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:79720703-79720910	K562	blood:	n/a	n/a
2	ARID3A	chr4:79728318-79728363	K562	blood:	n/a	n/a
3	ARID3A	chr4:79722369-79722589	K562	blood:	n/a	n/a
4	ARID3A	chr4:79718777-79719370	K562	blood:	n/a	n/a
5	ARID3A	chr4:79729012-79729045	K562	blood:	n/a	n/a
6	ATF2	chr4:79766511-79767010	GM12878	blood:	n/a	n/a
7	BACH1	chr4:79742405-79742478	K562	blood:	n/a	n/a
8	BACH1	chr4:79717903-79718073	K562	blood:	n/a	n/a
9	CBX3	chr4:79720878-79721306	K562	blood:	n/a	n/a
10	CBX3	chr4:79728176-79728603	K562	blood:	n/a	n/a
11	CBX3	chr4:79728142-79728647	K562	blood:	n/a	n/a
12	CCNT2	chr4:79727528-79727629	K562	blood:	n/a	n/a
13	CCNT2	chr4:79715343-79715537	K562	blood:	n/a	n/a
14	CEBPB	chr4:79767434-79767778	IMR90	lung:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
15	CEBPB	chr4:79766793-79767090	A549	lung:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
16	CEBPB	chr4:79766781-79767118	Hela-S3	cervix:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
17	CEBPB	chr4:79767431-79767721	HepG2	liver:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
18	CEBPB	chr4:79767468-79767708	A549	lung:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
19	CEBPB	chr4:79725668-79725765	HepG2	liver:	n/a	chr4:79725678-79725689
20	CEBPB	chr4:79767474-79767766	K562	blood:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
21	CEBPB	chr4:79741073-79741088	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:79757946-79758020	K562	blood:	n/a	n/a
23	CEBPB	chr4:79766793-79767104	HepG2	liver:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
24	CEBPB	chr4:79725553-79725808	K562	blood:	n/a	chr4:79725678-79725689
25	CEBPB	chr4:79766768-79767081	IMR90	lung:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
26	CEBPB	chr4:79766845-79767080	K562	blood:	n/a	chr4:79766977-79766990 chr4:79766978-79766989 chr4:79766936-79766949 chr4:79766936-79766947
27	CEBPB	chr4:79767439-79767774	Hela-S3	cervix:	n/a	chr4:79767601-79767612 chr4:79767600-79767611 chr4:79767587-79767598
28	CEBPB	chr4:79725657-79725765	A549	lung:	n/a	chr4:79725678-79725689
29	CEBPB	chr4:79740967-79741220	K562	blood:	n/a	chr4:79741199-79741208 chr4:79741071-79741082 chr4:79741071-79741082
30	CEBPB	chr4:79763289-79763593	K562	blood:	n/a	chr4:79763466-79763479
31	CHD2	chr4:79720633-79720811	K562	blood:	n/a	n/a
32	CHD2	chr4:79715073-79715401	K562	blood:	n/a	n/a
33	CREB1	chr4:79766427-79767200	GM12878	blood:	n/a	n/a
34	CREB1	chr4:79766603-79767098	GM12878	blood:	n/a	n/a
35	CTCF	chr4:79719200-79719350	HEEpiC	esophagus:	n/a	n/a
36	CTCF	chr4:79747534-79747563	Lung_OC	lung:	n/a	n/a
37	CTCF	chr4:79760460-79760610	GM12873	blood:	n/a	n/a
38	CTCF	chr4:79778420-79778570	AG04449	skin:	n/a	n/a
39	CTCF	chr4:79742384-79742414	K562	blood:	n/a	n/a
40	CUX1	chr4:79733528-79733585	K562	blood:	n/a	n/a
41	CUX1	chr4:79743634-79743828	K562	blood:	n/a	n/a
42	CUX1	chr4:79721435-79721635	K562	blood:	n/a	n/a
43	E2F4	chr4:79726171-79726361	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr4:79742281-79742496	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr4:79717723-79717823	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr4:79758054-79758391	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F6	chr4:79719144-79719282	K562	blood:	n/a	n/a
48	E2F6	chr4:79718958-79719556	H1-hESC	embryonic stem cell:	n/a	n/a
49	E2F6	chr4:79719028-79719464	H1-hESC	embryonic stem cell:	n/a	n/a
50	EBF1	chr4:79778465-79778589	GM12878	blood:	n/a	chr4:79778468-79778477 chr4:79778468-79778478 chr4:79778467-79778478

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:79732488-79732538	HepG2	liver:	n/a
2	chr4:79732488-79732538	AG09309	skin:	n/a
3	chr4:79732488-79732538	HEK293	kidney:	embryo
4	chr4:79732488-79732538	NH-A	brain:	n/a
5	chr4:79732488-79732538	LNCaP	prostate:	n/a
6	chr4:79732488-79732538	AG09319	gingival:	n/a
7	chr4:79732488-79732538	HCM	heart:	n/a
8	chr4:79732488-79732538	HPAEpiC	pulmonary alveolar:	n/a
9	chr4:79732488-79732538	T-47D	breast:	n/a
10	chr4:79732488-79732538	ECC-1	luminal epithelium:	n/a
11	chr4:79732488-79732538	ovcar-3	ovarian:	n/a
12	chr4:79732488-79732538	AG04449	skin:	fetal
13	chr4:79732488-79732538	HNPCEpiC	eye:	n/a
14	chr4:79732488-79732538	A549	lung:	n/a
15	chr4:79732488-79732538	HRE	kidney:	n/a
16	chr4:79732488-79732538	NHDF-neo	bronchial:	n/a
17	chr4:79732488-79732538	GM19239	blood:	n/a
18	chr4:79732488-79732538	SK-N-MC	brain:	n/a
19	chr4:79732488-79732538	Hela-S3	cervix:	n/a
20	chr4:79732488-79732538	PANC-1	pancreas:	n/a
21	chr4:79732488-79732538	HCT-116	colon:	n/a
22	chr4:79732488-79732538	BJ	skin:	n/a
23	chr4:79732488-79732538	ProgFib	skin:	n/a
24	chr4:79732488-79732538	HAEpiC	amniotic membrane:	n/a
25	chr4:79732488-79732538	GM12891	blood:	n/a
26	chr4:79732488-79732538	HL-60	blood:	n/a
27	chr4:79732488-79732538	RPTEC	kidney:	n/a
28	chr4:79732488-79732538	Hepatocyte	liver:	n/a
29	chr4:79732488-79732538	HRCEpiC	kidney:	n/a
30	chr4:79732488-79732538	PFSK-1	brain:	n/a
31	chr4:79732488-79732538	HRPEpiC	eye:	n/a
32	chr4:79732488-79732538	HIPEpiC	eye:	n/a
33	chr4:79732488-79732538	GM12878	blood:	n/a
34	chr4:79732488-79732538	Caco-2	colon:	n/a
35	chr4:79732488-79732538	MCF-7	breast:	n/a
36	chr4:79732488-79732538	BE2_C	brain:	n/a
37	chr4:79732488-79732538	NT2-D1	testis:	n/a
38	chr4:79732488-79732538	GM06990	blood:	n/a
39	chr4:79732488-79732538	MCF10A-Er-Src	breast:	n/a
40	chr4:79732488-79732538	U87	brain:	n/a
41	chr4:79732488-79732538	SKMC	muscle:	n/a
42	chr4:79732488-79732538	NHBE	bronchial:	n/a
43	chr4:79732488-79732538	AG04450	lung:	fetal
44	chr4:79732488-79732538	IMR90	lung:	fetal
45	chr4:79732488-79732538	HEEpiC	esophagus:	n/a
46	chr4:79732488-79732538	GM12892	blood:	n/a
47	chr4:79732488-79732538	SK-N-SH	brain:	n/a
48	chr4:79732488-79732538	H1-hESC	embryonic stem cell:	embryo
49	chr4:79732488-79732538	AoSMC	blood vessel:	n/a
50	chr4:79732488-79732538	AG10803	skin:	n/a

(count:56 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:79747042..79749439-chr4:79778018..79780903,2	K562	blood:
2	chr4:79695668..79697243-chr4:79725186..79727930,2	K562	blood:
3	chr4:79725596..79728159-chr4:79729927..79731920,2	K562	blood:
4	chr4:79720788..79722594-chr4:79731131..79733817,2	MCF-7	breast:
5	chr4:79715007..79717955-chr4:79723142..79725042,2	K562	blood:
6	chr4:79743529..79746797-chr4:79749528..79753927,4	K562	blood:
7	chr4:79769347..79772550-chr4:79776506..79778988,3	K562	blood:
8	chr4:79727891..79730446-chr4:79730868..79733426,2	K562	blood:
9	chr4:79718867..79721352-chr4:79723446..79725108,2	K562	blood:
10	chr4:79696515..79698358-chr4:79778442..79780983,2	K562	blood:
11	chr4:79571062..79573548-chr4:79735105..79737173,2	K562	blood:
12	chr4:79773476..79776467-chr4:79776731..79781526,5	K562	blood:
13	chr4:79720788..79722594-chr4:79731131..79733817,2	MCF-7	breast:
14	chr4:79695514..79698154-chr4:79721600..79724620,3	MCF-7	breast:
15	chr4:79731165..79732753-chr4:79743062..79744642,2	K562	blood:
16	chr4:79743779..79746797-chr4:79749010..79752930,4	K562	blood:
17	chr4:79760812..79762742-chr4:79764884..79766656,2	K562	blood:
18	chr4:79473307..79475885-chr4:79776923..79779312,2	K562	blood:
19	chr4:79550103..79553175-chr4:79717288..79720915,3	K562	blood:
20	chr4:79738518..79741060-chr4:79744387..79746561,2	MCF-7	breast:
21	chr4:79743529..79746797-chr4:79749528..79753927,4	K562	blood:
22	chr4:79715007..79717955-chr4:79723142..79725042,2	K562	blood:
23	chr4:79722414..79724525-chr4:79727218..79728941,2	K562	blood:
24	chr4:79727891..79730446-chr4:79730868..79733426,2	K562	blood:
25	chr4:79725596..79728159-chr4:79729927..79731920,2	K562	blood:
26	chr4:79738518..79741060-chr4:79744387..79746561,2	MCF-7	breast:
27	chr4:79696715..79699509-chr4:79734582..79736119,2	K562	blood:
28	chr4:79743779..79746797-chr4:79749010..79752930,4	K562	blood:
29	chr4:79719962..79721538-chr4:79737317..79739683,2	K562	blood:
30	chr4:79542792..79544409-chr4:79720591..79722991,2	K562	blood:
31	chr4:79761796..79764662-chr4:79771041..79772636,2	K562	blood:
32	chr4:79734454..79742756-chr4:79743096..79750218,11	K562	blood:
33	chr4:79749269..79751904-chr4:79770998..79773929,2	K562	blood:
34	chr4:79778433..79779969-chr4:79781094..79783460,2	MCF-7	breast:
35	chr4:79697257..79699576-chr4:79770892..79773352,2	MCF-7	breast:
36	chr4:79774563..79776854-chr4:79782145..79784064,2	K562	blood:
37	chr4:79696613..79699103-chr4:79739804..79741544,2	K562	blood:
38	chr4:79613754..79615926-chr4:79712733..79714899,2	K562	blood:
39	chr4:79655479..79657150-chr4:79715165..79717948,2	K562	blood:
40	chr4:79612882..79614522-chr4:79714996..79717232,2	K562	blood:
41	chr4:79498073..79500124-chr4:79717103..79719533,2	K562	blood:
42	chr4:79674995..79676989-chr4:79751851..79754832,2	K562	blood:
43	chr4:79761242..79763220-chr4:79764884..79767301,3	K562	blood:
44	chr4:79719962..79721538-chr4:79737317..79739683,2	K562	blood:
45	chr4:79770645..79772901-chr4:79776506..79779680,4	K562	blood:
46	chr4:79718867..79721352-chr4:79723446..79725108,2	K562	blood:
47	chr4:79696453..79698645-chr4:79751602..79753557,2	MCF-7	breast:
48	chr4:79760812..79762742-chr4:79764884..79766656,2	K562	blood:
49	chr4:79761242..79763220-chr4:79764884..79767301,3	K562	blood:
50	chr4:79762332..79763887-chr4:79767751..79769373,2	K562	blood:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5096	chr4:79741918-79741938	MIMAT0020603

No data

Variant related genes	Relation type
MIR5096	TF binding region
BMP2K	TF binding region
MIR5096	CpG island
BMP2K	CpG island
ENSG00000138772	chromatin interactions
ENSG00000138756	chromatin interactions
ENSG00000260278	chromatin interactions
ENSG00000266270	chromatin interactions

Extended variants
information (count: 2316 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2316 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs76799603	chr4:79714700-79714701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs552579672	chr4:79714702-79714703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs138704929	chr4:79714711-79714712	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs141719508	chr4:79714764-79714765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs184297505	chr4:79714826-79714827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs550898953	chr4:79714869-79714870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs556687507	chr4:79714893-79714894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs576646210	chr4:79714932-79714933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs542223687	chr4:79714949-79714950	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs552767908	chr4:79715067-79715068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146220272	chr4:79715075-79715076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189055487	chr4:79715125-79715126	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs35935401	chr4:79715133-79715134	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561961570	chr4:79715163-79715164	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114213841	chr4:79715345-79715346	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs114563984	chr4:79715364-79715365	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs115118633	chr4:79715365-79715366	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs34785491	chr4:79715387-79715388	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs561254261	chr4:79715394-79715395	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs137918034	chr4:79715398-79715399	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs574900616	chr4:79715416-79715417	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540843307	chr4:79715426-79715427	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149458622	chr4:79715469-79715470	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs532621376	chr4:79715531-79715532	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs541370635	chr4:79715565-79715566	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs552743839	chr4:79715582-79715583	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs115468840	chr4:79715607-79715608	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs148609640	chr4:79715634-79715635	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs375263463	chr4:79715649-79715650	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550862218	chr4:79715717-79715718	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369365020	chr4:79715726-79715727	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564575551	chr4:79715728-79715729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs533352744	chr4:79715738-79715739	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115487636	chr4:79715808-79715809	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536183550	chr4:79715819-79715820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532044413	chr4:79715856-79715857	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs563020919	chr4:79715864-79715865	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs181724271	chr4:79715906-79715907	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs116309664	chr4:79715907-79715908	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs528974606	chr4:79715974-79715975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2114203	chr4:79715976-79715977	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs558232261	chr4:79716014-79716015	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77583761	chr4:79716016-79716017	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537462754	chr4:79716067-79716068	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554935346	chr4:79716071-79716072	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs186128495	chr4:79716187-79716188	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs565546700	chr4:79716190-79716191	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540602091	chr4:79716227-79716228	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560726671	chr4:79716231-79716232	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs3775521	chr4:79716279-79716280	Weak transcription ZNF genes & repeats Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:79699000-79717200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
2	chr4:79699400-79722600	Weak transcription	Fetal Thymus	thymus
3	chr4:79700200-79732800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr4:79700400-79718200	Weak transcription	Duodenum Mucosa	Duodenum
5	chr4:79701600-79719200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
6	chr4:79702000-79731200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr4:79703000-79720800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr4:79703200-79720800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr4:79703400-79720800	Weak transcription	Sigmoid Colon	Sigmoid Colon
10	chr4:79705600-79731200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr4:79706000-79720000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
12	chr4:79706000-79720200	Weak transcription	Primary T cells from cord blood	blood
13	chr4:79706000-79720200	Weak transcription	NHEK	skin
14	chr4:79706000-79720800	Weak transcription	Skeletal Muscle Female	skeletal muscle
15	chr4:79706200-79718000	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr4:79706200-79718200	Weak transcription	Fetal Lung	lung
17	chr4:79706200-79722200	Weak transcription	HSMM	muscle
18	chr4:79706600-79722800	Weak transcription	Brain Substantia Nigra	brain
19	chr4:79707000-79721000	Weak transcription	HUES48 Cell Line	embryonic stem cell
20	chr4:79707400-79715800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:79707600-79715000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
22	chr4:79707600-79721800	Weak transcription	Fetal Muscle Leg	muscle
23	chr4:79707800-79715200	Weak transcription	Left Ventricle	heart
24	chr4:79707800-79715800	Weak transcription	Dnd41	blood
25	chr4:79707800-79716000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
26	chr4:79707800-79720800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr4:79707800-79720800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
28	chr4:79708200-79719000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:79708800-79719000	Weak transcription	Right Atrium	heart
30	chr4:79709000-79720800	Weak transcription	NHLF	lung
31	chr4:79709200-79717000	Weak transcription	Brain Cingulate Gyrus	brain
32	chr4:79709200-79723800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr4:79709200-79731200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr4:79709400-79718200	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr4:79709400-79724000	Weak transcription	Fetal Intestine Small	intestine
36	chr4:79709600-79716000	Weak transcription	NHDF-Ad	bronchial
37	chr4:79709600-79718400	Weak transcription	Fetal Heart	heart
38	chr4:79709600-79720600	Weak transcription	Osteobl	bone
39	chr4:79709600-79721400	Weak transcription	Brain Anterior Caudate	brain
40	chr4:79710000-79720200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
41	chr4:79710000-79720600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr4:79710400-79716000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:79710400-79725200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr4:79710800-79715800	Weak transcription	Fetal Intestine Large	intestine
45	chr4:79711000-79720800	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr4:79712600-79715200	Weak transcription	Primary B cells from peripheral blood	blood
47	chr4:79712800-79717800	Weak transcription	Primary hematopoietic stem cells	blood
48	chr4:79713000-79716000	Weak transcription	Primary B cells from cord blood	blood
49	chr4:79713400-79715000	Weak transcription	K562	blood
50	chr4:79713600-79716400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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