Variant report

Variant	nsv879927
Chromosome Location	chr4:128668850-128766074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1521)
CpG islands
(count:793)
Chromatin interactive
region (count:85)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1521 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:128699250-128699431	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:128703288-128703855	HepG2	liver:	n/a	n/a
3	ARID3A	chr4:128692810-128693068	K562	blood:	n/a	n/a
4	ARID3A	chr4:128705029-128705424	HepG2	liver:	n/a	n/a
5	ARID3A	chr4:128697170-128697199	K562	blood:	n/a	n/a
6	ARID3A	chr4:128681078-128681272	HepG2	liver:	n/a	n/a
7	ARID3A	chr4:128704302-128704787	HepG2	liver:	n/a	n/a
8	ATF1	chr4:128692637-128692941	K562	blood:	n/a	n/a
9	ATF1	chr4:128704314-128704827	K562	blood:	n/a	n/a
10	ATF2	chr4:128703349-128703797	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:128704002-128704389	GM12878	blood:	n/a	n/a
12	ATF2	chr4:128750040-128750665	GM12878	blood:	n/a	n/a
13	ATF2	chr4:128703535-128703945	GM12878	blood:	n/a	n/a
14	ATF2	chr4:128703223-128704431	GM12878	blood:	n/a	n/a
15	ATF3	chr4:128670080-128670482	K562	blood:	n/a	n/a
16	BACH1	chr4:128703574-128704164	H1-hESC	embryonic stem cell:	n/a	n/a
17	BATF	chr4:128731775-128732029	GM12878	blood:	n/a	n/a
18	BATF	chr4:128750180-128750513	GM12878	blood:	n/a	n/a
19	BATF	chr4:128750187-128750520	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:128750197-128750480	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:128703506-128704165	GM12878	blood:	n/a	chr4:128703900-128703909
22	BCL3	chr4:128703426-128703891	A549	lung:	n/a	chr4:128703493-128703506
23	BCLAF1	chr4:128750043-128750650	GM12878	blood:	n/a	n/a
24	BCLAF1	chr4:128703164-128704359	GM12878	blood:	n/a	chr4:128703900-128703909 chr4:128703493-128703506 chr4:128703393-128703402 chr4:128703415-128703428
25	BCLAF1	chr4:128703045-128704359	GM12878	blood:	n/a	chr4:128703900-128703909 chr4:128703493-128703506 chr4:128703393-128703402 chr4:128703415-128703428
26	BHLHE40	chr4:128702911-128704629	K562	blood:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
27	BHLHE40	chr4:128765729-128766181	K562	blood:	n/a	n/a
28	BHLHE40	chr4:128703316-128704638	HepG2	liver:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
29	BHLHE40	chr4:128702794-128704390	GM12878	blood:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
30	BHLHE40	chr4:128697106-128697324	GM12878	blood:	n/a	n/a
31	BRCA1	chr4:128704266-128704582	GM12878	blood:	n/a	n/a
32	BRCA1	chr4:128703327-128704113	H1-hESC	embryonic stem cell:	n/a	n/a
33	BRCA1	chr4:128703553-128704042	GM12878	blood:	n/a	n/a
34	BRCA1	chr4:128703576-128704518	HepG2	liver:	n/a	n/a
35	BRCA1	chr4:128703299-128705533	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr4:128702501-128704742	K562	blood:	n/a	n/a
37	CBX3	chr4:128765591-128766257	K562	blood:	n/a	n/a
38	CBX3	chr4:128670109-128670502	K562	blood:	n/a	n/a
39	CBX3	chr4:128670168-128670534	HCT-116	colon:	n/a	n/a
40	CBX3	chr4:128670087-128670514	K562	blood:	n/a	n/a
41	CBX3	chr4:128709647-128710059	K562	blood:	n/a	n/a
42	CCNT2	chr4:128702731-128704211	K562	blood:	n/a	n/a
43	CCNT2	chr4:128704430-128704649	K562	blood:	n/a	n/a
44	CEBPB	chr4:128707018-128707128	A549	lung:	n/a	n/a
45	CEBPB	chr4:128709773-128709978	K562	blood:	n/a	n/a
46	CEBPB	chr4:128714222-128714349	A549	lung:	n/a	n/a
47	CEBPB	chr4:128686132-128686276	HepG2	liver:	n/a	chr4:128686203-128686214
48	CEBPB	chr4:128703489-128704096	GM12878	blood:	n/a	n/a
49	CEBPB	chr4:128700302-128700540	K562	blood:	n/a	n/a
50	CEBPB	chr4:128703570-128704298	K562	blood:	n/a	chr4:128704156-128704169

(count:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128703599-128703649	HAEpiC	amniotic membrane:	n/a
2	chr4:128703335-128703385	AoSMC	blood vessel:	n/a
3	chr4:128707242-128707292	MCF-7	breast:	n/a
4	chr4:128704651-128704701	HRCEpiC	kidney:	n/a
5	chr4:128707242-128707292	NHDF-neo	bronchial:	n/a
6	chr4:128703599-128703649	Hela-S3	cervix:	n/a
7	chr4:128704088-128704138	HRE	kidney:	n/a
8	chr4:128703702-128703752	HEEpiC	esophagus:	n/a
9	chr4:128703088-128703138	HRPEpiC	eye:	n/a
10	chr4:128754061-128754111	LNCaP	prostate:	n/a
11	chr4:128703702-128703752	HIPEpiC	eye:	n/a
12	chr4:128702014-128702064	ProgFib	skin:	n/a
13	chr4:128702014-128702064	PFSK-1	brain:	n/a
14	chr4:128702014-128702064	HPAEpiC	pulmonary alveolar:	n/a
15	chr4:128703180-128703230	U87	brain:	n/a
16	chr4:128703335-128703385	T-47D	breast:	n/a
17	chr4:128707242-128707292	ECC-1	luminal epithelium:	n/a
18	chr4:128704518-128704568	AoSMC	blood vessel:	n/a
19	chr4:128703335-128703385	HUVEC	blood vessel:	n/a
20	chr4:128704651-128704701	LNCaP	prostate:	n/a
21	chr4:128703702-128703752	GM06990	blood:	n/a
22	chr4:128703180-128703230	NHBE	bronchial:	n/a
23	chr4:128703088-128703138	AG10803	skin:	n/a
24	chr4:128704088-128704138	ECC-1	luminal epithelium:	n/a
25	chr4:128754061-128754111	HCF	heart:	n/a
26	chr4:128704088-128704138	HEK293	kidney:	embryo
27	chr4:128702014-128702064	A549	lung:	n/a
28	chr4:128704088-128704138	A549	lung:	n/a
29	chr4:128694731-128694781	HRPEpiC	eye:	n/a
30	chr4:128703180-128703230	SKMC	muscle:	n/a
31	chr4:128699484-128699534	NHDF-neo	bronchial:	n/a
32	chr4:128699484-128699534	AG10803	skin:	n/a
33	chr4:128704518-128704568	GM06990	blood:	n/a
34	chr4:128703088-128703138	HEK293	kidney:	embryo
35	chr4:128703088-128703138	MCF10A-Er-Src	breast:	n/a
36	chr4:128703702-128703752	PrEC	prostate:	n/a
37	chr4:128703599-128703649	GM12891	blood:	n/a
38	chr4:128754061-128754111	HRE	kidney:	n/a
39	chr4:128703599-128703649	HPAEpiC	pulmonary alveolar:	n/a
40	chr4:128754061-128754111	T-47D	breast:	n/a
41	chr4:128694731-128694781	BJ	skin:	n/a
42	chr4:128704088-128704138	LNCaP	prostate:	n/a
43	chr4:128703180-128703230	PrEC	prostate:	n/a
44	chr4:128703599-128703649	SKMC	muscle:	n/a
45	chr4:128699484-128699534	ECC-1	luminal epithelium:	n/a
46	chr4:128707242-128707292	HEK293	kidney:	embryo
47	chr4:128702014-128702064	SAEC	small airway:	n/a
48	chr4:128703180-128703230	H1-hESC	embryonic stem cell:	embryo
49	chr4:128754061-128754111	SK-N-SH_RA	brain:	n/a
50	chr4:128704651-128704701	NT2-D1	testis:	n/a

(count:85 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:128666387..128668298-chr4:128668505..128671466,2	K562	blood:
2	chr4:128716381..128718336-chr4:128718377..128720060,2	K562	blood:
3	chr4:128702580..128705894-chr4:128810025..128813296,3	K562	blood:
4	chr19:41222374..41223187-chr4:128703821..128704556,2	Hela-S3	cervix:
5	chr4:128748778..128750311-chr4:128751376..128753620,2	K562	blood:
6	chr4:128695663..128697275-chr4:128706487..128708747,2	K562	blood:
7	chr4:128727274..128729272-chr4:128736582..128738197,2	K562	blood:
8	chr4:128716381..128718336-chr4:128718377..128720060,2	K562	blood:
9	chr4:128684085..128685592-chr4:128688518..128690302,2	K562	blood:
10	chr4:128722353..128724955-chr4:128727148..128728727,2	K562	blood:
11	chr4:128735664..128737568-chr4:128800882..128803731,2	K562	blood:
12	chr4:128704579..128707662-chr4:128728712..128732375,3	K562	blood:
13	chr4:128702203..128705505-chr4:128800773..128804170,4	MCF-7	breast:
14	chr4:128684085..128685592-chr4:128688518..128690302,2	K562	blood:
15	chr4:128714333..128715858-chr4:128734487..128736194,2	K562	blood:
16	chr4:128714333..128715858-chr4:128734487..128736194,2	K562	blood:
17	chr4:128740214..128742882-chr4:128752992..128755528,3	K562	blood:
18	chr4:128686775..128688582-chr4:128798600..128801332,2	K562	blood:
19	chr4:128695663..128697275-chr4:128706487..128708747,2	K562	blood:
20	chr4:128702686..128704491-chr4:128713459..128716230,3	MCF-7	breast:
21	chr4:128699357..128701844-chr4:128885755..128888672,2	K562	blood:
22	chr11:47206754..47207663-chr4:128703485..128704269,2	Hela-S3	cervix:
23	chr4:128702265..128705282-chr4:128884841..128889213,7	K562	blood:
24	chr4:128708991..128711452-chr4:128712949..128715693,2	K562	blood:
25	chr4:128728488..128731790-chr4:128810171..128812661,3	K562	blood:
26	chr4:128728798..128731364-chr4:128739602..128743482,3	K562	blood:
27	chr4:128738564..128740889-chr4:128741678..128744567,2	K562	blood:
28	chr4:128728798..128731364-chr4:128739602..128743482,3	K562	blood:
29	chr4:128706259..128710771-chr4:128716445..128721111,5	MCF-7	breast:
30	chr12:120729413..120730207-chr4:128703177..128703844,2	Hela-S3	cervix:
31	chr4:128701663..128704492-chr4:128800560..128804784,7	MCF-7	breast:
32	chr11:76155451..76155958-chr4:128703322..128703844,2	Hela-S3	cervix:
33	chr4:128689601..128691361-chr4:128702000..128704848,2	K562	blood:
34	chr4:128695077..128697905-chr4:128698575..128703396,7	K562	blood:
35	chr4:128738564..128740889-chr4:128741678..128744567,2	K562	blood:
36	chr4:128701934..128705815-chr4:128979420..128984468,5	K562	blood:
37	chr4:128722353..128724955-chr4:128727148..128728727,2	K562	blood:
38	chr4:128697244..128699961-chr4:128704246..128706827,2	MCF-7	breast:
39	chr4:128697060..128698600-chr4:128725159..128726803,2	K562	blood:
40	chr4:128701934..128705815-chr4:128979420..128985014,7	K562	blood:
41	chr4:128702147..128704685-chr4:128980177..128982661,2	MCF-7	breast:
42	chr4:128755344..128757841-chr4:128802049..128804837,3	K562	blood:
43	chr4:128727274..128729272-chr4:128736582..128738197,2	K562	blood:
44	chr4:128754147..128756975-chr4:128757959..128759964,2	MCF-7	breast:
45	chr4:128697060..128698600-chr4:128725159..128726803,2	K562	blood:
46	chr4:128748778..128750311-chr4:128751376..128753620,2	K562	blood:
47	chr3:156871327..156871960-chr4:128702865..128703820,2	Hela-S3	cervix:
48	chr4:128735114..128737929-chr4:128739500..128741438,2	K562	blood:
49	chr4:128701837..128704817-chr4:128712358..128715283,2	MCF-7	breast:
50	chr4:128725012..128727924-chr4:128981101..128982953,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HSPA4L-1	chr4:128758922-128761883	NONHSAT098244
2	lnc-HSPA4L-1	chr4:128760853-128761885	NONHSAT098243
3	lnc-SLC25A31-2	chr4:128734173-128734630	NONHSAT098242
4	lnc-SLC25A31-2	chr4:128741583-128741676	NONHSAT098242
5	lnc-HSPA4L-1	chr4:128758922-128760428	NONHSAT098243
6	lnc-MFSD8-1	chr4:128761353-128765195	ENSG00000261668.1
7	lnc-SLC25A31-2	chr4:128739480-128739575	NONHSAT098242

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HSPA4L	hsa-miR-16-5p	chr4:128754202-128754208
2	HSPA4L	hsa-miR-16-5p	chr4:128754187-128754209
3	SLC25A31	hsa-miR-335-5p	chr4:128695378-128695400
4	HSPA4L	hsa-miR-155-5p	chr4:128754359-128754381

Variant related genes	Relation type
ENSG00000244021	TF binding region
HSPA4L	TF binding region
ENSG00000261668	TF binding region
ENSG00000244021	CpG island
HSPA4L	CpG island
ENSG00000261668	CpG island
ENSG00000164070	chromatin interactions
ENSG00000123815	chromatin interactions
ENSG00000088298	chromatin interactions
ENSG00000126005	chromatin interactions
ENSG00000151470	chromatin interactions
ENSG00000164073	chromatin interactions
ENSG00000251821	chromatin interactions
ENSG00000164074	chromatin interactions
ENSG00000086544	chromatin interactions
ENSG00000165912	chromatin interactions
ENSG00000142731	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000201778	chromatin interactions
ENSG00000138709	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000151466	chromatin interactions
ENSG00000202538	chromatin interactions

Extended variants
information (count: 2666 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2666 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191724239	chr4:128677563-128677564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs72616947	chr4:128677589-128677590	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs184315442	chr4:128677593-128677594	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs551924632	chr4:128677665-128677666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572622375	chr4:128677682-128677683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs546491918	chr4:128677708-128677709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143965532	chr4:128677745-128677746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs113297509	chr4:128677766-128677767	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs115264786	chr4:128677780-128677781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs146424755	chr4:128677815-128677816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529085266	chr4:128677825-128677826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs189061700	chr4:128677833-128677834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192167827	chr4:128677908-128677909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs149046020	chr4:128678079-128678080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs114322514	chr4:128678087-128678088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs570506950	chr4:128678088-128678089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs368120289	chr4:128678097-128678098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs531633057	chr4:128678113-128678114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs549845748	chr4:128678129-128678130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs568241611	chr4:128678162-128678163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs573646526	chr4:128678241-128678242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs554037740	chr4:128678292-128678293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566271409	chr4:128678461-128678462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs539696927	chr4:128678467-128678468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs542854801	chr4:128678483-128678484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs142111070	chr4:128678488-128678489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs185529504	chr4:128678498-128678499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112494475	chr4:128678522-128678523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs576097486	chr4:128678523-128678524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190454673	chr4:128678595-128678596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555481772	chr4:128678609-128678610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs114975074	chr4:128678611-128678612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs541137838	chr4:128678613-128678614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs559244698	chr4:128678626-128678627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533157809	chr4:128678658-128678659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs544890219	chr4:128678659-128678660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs112041252	chr4:128678701-128678702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs112769207	chr4:128678717-128678718	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549734647	chr4:128678751-128678752	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs146987335	chr4:128678792-128678793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs529328539	chr4:128678824-128678825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs116802736	chr4:128678848-128678849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs566139493	chr4:128678902-128678903	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531645447	chr4:128678913-128678914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532981049	chr4:128678939-128678940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs377568901	chr4:128678940-128678941	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs180778795	chr4:128679023-128679024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs551670778	chr4:128679024-128679025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs77445552	chr4:128679025-128679026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552089016	chr4:128679073-128679074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:72)

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
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	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
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Developmental delay	21147756	CNVD
Renal cell carcinoma	18765545	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myelofibrosis	22110671	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:776 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128677400-128681200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr4:128680800-128681600	Enhancers	Pancreatic Islets	Pancreatic Islet
3	chr4:128681200-128681800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
4	chr4:128681200-128681800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
5	chr4:128692600-128693200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:128692600-128693400	Enhancers	NHEK	skin
7	chr4:128692800-128693600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr4:128693000-128693400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
9	chr4:128693000-128693400	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr4:128693000-128693600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr4:128693600-128694600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr4:128693600-128702200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:128694600-128694800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr4:128694800-128695200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:128695200-128697200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:128695800-128696000	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr4:128696200-128697400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr4:128696800-128699400	Enhancers	GM12878-XiMat	blood
19	chr4:128697200-128697400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:128697200-128697400	Enhancers	K562	blood
21	chr4:128697200-128698600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:128697400-128698000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr4:128697600-128698000	Enhancers	HMEC	breast
24	chr4:128697600-128698800	Weak transcription	K562	blood
25	chr4:128697600-128699400	Enhancers	HepG2	liver
26	chr4:128697600-128701800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
27	chr4:128697800-128698000	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr4:128698000-128698800	Weak transcription	HUES64 Cell Line	embryonic stem cell
29	chr4:128698000-128702400	Weak transcription	HMEC	breast
30	chr4:128698200-128699000	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr4:128698600-128699000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr4:128698600-128699800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chr4:128698600-128700000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr4:128698800-128699000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr4:128698800-128699000	Enhancers	Gastric	stomach
36	chr4:128698800-128699800	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:128698800-128699800	Enhancers	K562	blood
38	chr4:128699000-128699800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
39	chr4:128699000-128702800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr4:128699000-128702800	Weak transcription	Gastric	stomach
41	chr4:128699400-128699600	Flanking Active TSS	GM12878-XiMat	blood
42	chr4:128699400-128699800	Flanking Active TSS	HepG2	liver
43	chr4:128699600-128699800	Enhancers	GM12878-XiMat	blood
44	chr4:128699800-128700000	Flanking Active TSS	GM12878-XiMat	blood
45	chr4:128699800-128700000	Enhancers	HepG2	liver
46	chr4:128699800-128701000	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
47	chr4:128699800-128702600	Weak transcription	K562	blood
48	chr4:128699800-128703000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr4:128700000-128700200	Enhancers	GM12878-XiMat	blood
50	chr4:128700000-128700600	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood

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