Variant report

Variant	nsv879926
Chromosome Location	chr4:128652227-128766074
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1766)
CpG islands
(count:856)
Chromatin interactive
region (count:96)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:1766 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

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	chr4:128692810-128693068	K562	blood:	n/a	n/a
3	ARID3A	chr4:128704302-128704787	HepG2	liver:	n/a	n/a
4	ARID3A	chr4:128653832-128654129	K562	blood:	n/a	n/a
5	ARID3A	chr4:128703288-128703855	HepG2	liver:	n/a	n/a
6	ARID3A	chr4:128658272-128658704	K562	blood:	n/a	n/a
7	ARID3A	chr4:128705029-128705424	HepG2	liver:	n/a	n/a
8	ARID3A	chr4:128681078-128681272	HepG2	liver:	n/a	n/a
9	ARID3A	chr4:128697170-128697199	K562	blood:	n/a	n/a
10	ATF1	chr4:128704314-128704827	K562	blood:	n/a	n/a
11	ATF1	chr4:128692637-128692941	K562	blood:	n/a	n/a
12	ATF1	chr4:128653837-128654173	K562	blood:	n/a	n/a
13	ATF2	chr4:128703535-128703945	GM12878	blood:	n/a	n/a
14	ATF2	chr4:128703349-128703797	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr4:128750040-128750665	GM12878	blood:	n/a	n/a
16	ATF2	chr4:128704002-128704389	GM12878	blood:	n/a	n/a
17	ATF2	chr4:128703223-128704431	GM12878	blood:	n/a	n/a
18	ATF3	chr4:128670080-128670482	K562	blood:	n/a	n/a
19	BACH1	chr4:128703574-128704164	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr4:128750180-128750513	GM12878	blood:	n/a	n/a
21	BATF	chr4:128750187-128750520	GM12878	blood:	n/a	n/a
22	BATF	chr4:128731775-128732029	GM12878	blood:	n/a	n/a
23	BCL11A	chr4:128750197-128750480	GM12878	blood:	n/a	n/a
24	BCL11A	chr4:128703506-128704165	GM12878	blood:	n/a	chr4:128703900-128703909
25	BCL3	chr4:128703426-128703891	A549	lung:	n/a	chr4:128703493-128703506
26	BCLAF1	chr4:128703045-128704359	GM12878	blood:	n/a	chr4:128703900-128703909 chr4:128703493-128703506 chr4:128703393-128703402 chr4:128703415-128703428
27	BCLAF1	chr4:128703164-128704359	GM12878	blood:	n/a	chr4:128703900-128703909 chr4:128703493-128703506 chr4:128703393-128703402 chr4:128703415-128703428
28	BCLAF1	chr4:128750043-128750650	GM12878	blood:	n/a	n/a
29	BHLHE40	chr4:128702911-128704629	K562	blood:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
30	BHLHE40	chr4:128697106-128697324	GM12878	blood:	n/a	n/a
31	BHLHE40	chr4:128702794-128704390	GM12878	blood:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
32	BHLHE40	chr4:128703316-128704638	HepG2	liver:	n/a	chr4:128703366-128703382 chr4:128704206-128704222 chr4:128704209-128704225
33	BHLHE40	chr4:128765729-128766181	K562	blood:	n/a	n/a
34	BRCA1	chr4:128703327-128704113	H1-hESC	embryonic stem cell:	n/a	n/a
35	BRCA1	chr4:128704266-128704582	GM12878	blood:	n/a	n/a
36	BRCA1	chr4:128703576-128704518	HepG2	liver:	n/a	n/a
37	BRCA1	chr4:128703299-128705533	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr4:128703553-128704042	GM12878	blood:	n/a	n/a
39	CBX3	chr4:128670109-128670502	K562	blood:	n/a	n/a
40	CBX3	chr4:128709647-128710059	K562	blood:	n/a	n/a
41	CBX3	chr4:128670168-128670534	HCT-116	colon:	n/a	n/a
42	CBX3	chr4:128663246-128663643	K562	blood:	n/a	n/a
43	CBX3	chr4:128765591-128766257	K562	blood:	n/a	n/a
44	CBX3	chr4:128670087-128670514	K562	blood:	n/a	n/a
45	CBX3	chr4:128702501-128704742	K562	blood:	n/a	n/a
46	CCNT2	chr4:128704430-128704649	K562	blood:	n/a	n/a
47	CCNT2	chr4:128702731-128704211	K562	blood:	n/a	n/a
48	CEBPB	chr4:128709657-128710032	HepG2	liver:	n/a	n/a
49	CEBPB	chr4:128709681-128710055	K562	blood:	n/a	n/a
50	CEBPB	chr4:128683586-128683799	HepG2	liver:	n/a	chr4:128683659-128683670

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:128703599-128703649	CMK	blood:	n/a
2	chr4:128703180-128703230	U87	brain:	n/a
3	chr4:128703599-128703649	CMK	blood:	n/a
4	chr4:128703180-128703230	U87	brain:	n/a
5	chr4:128703088-128703138	HepG2	liver:	n/a
6	chr4:128704518-128704568	HRE	kidney:	n/a
7	chr4:128702014-128702064	HRCEpiC	kidney:	n/a
8	chr4:128704088-128704138	HRE	kidney:	n/a
9	chr4:128704651-128704701	HCF	heart:	n/a
10	chr4:128704651-128704701	HIPEpiC	eye:	n/a
11	chr4:128703335-128703385	CMK	blood:	n/a
12	chr4:128704651-128704701	SKMC	muscle:	n/a
13	chr4:128694731-128694781	IMR90	lung:	fetal
14	chr4:128703088-128703138	CMK	blood:	n/a
15	chr4:128702014-128702064	GM12878	blood:	n/a
16	chr4:128754061-128754111	Hela-S3	cervix:	n/a
17	chr4:128702014-128702064	BE2_C	brain:	n/a
18	chr4:128703180-128703230	HCM	heart:	n/a
19	chr4:128694731-128694781	HCM	heart:	n/a
20	chr4:128702014-128702064	Hela-S3	cervix:	n/a
21	chr4:128699484-128699534	HL-60	blood:	n/a
22	chr4:128703599-128703649	NH-A	brain:	n/a
23	chr4:128703180-128703230	HMEC	breast:	n/a
24	chr4:128703599-128703649	AG04450	lung:	fetal
25	chr4:128703335-128703385	AG04449	skin:	fetal
26	chr4:128702014-128702064	HCM	heart:	n/a
27	chr4:128702014-128702064	AoSMC	blood vessel:	n/a
28	chr4:128699484-128699534	ProgFib	skin:	n/a
29	chr4:128704088-128704138	RPTEC	kidney:	n/a
30	chr4:128704651-128704701	SK-N-MC	brain:	n/a
31	chr4:128703702-128703752	PrEC	prostate:	n/a
32	chr4:128703702-128703752	Jurkat	blood:	n/a
33	chr4:128654094-128654144	HUVEC	blood vessel:	n/a
34	chr4:128703088-128703138	Hepatocyte	liver:	n/a
35	chr4:128703702-128703752	IMR90	lung:	fetal
36	chr4:128704088-128704138	Hela-S3	cervix:	n/a
37	chr4:128703599-128703649	HepG2	liver:	n/a
38	chr4:128704518-128704568	CMK	blood:	n/a
39	chr4:128704651-128704701	BE2_C	brain:	n/a
40	chr4:128699484-128699534	HCT-116	colon:	n/a
41	chr4:128704518-128704568	MCF-7	breast:	n/a
42	chr4:128654094-128654144	AG04449	skin:	fetal
43	chr4:128699484-128699534	NHDF-neo	bronchial:	n/a
44	chr4:128703088-128703138	AG09319	gingival:	n/a
45	chr4:128654094-128654144	GM12891	blood:	n/a
46	chr4:128703702-128703752	SK-N-SH_RA	brain:	n/a
47	chr4:128703088-128703138	HRPEpiC	eye:	n/a
48	chr4:128707242-128707292	Caco-2	colon:	n/a
49	chr4:128704518-128704568	HIPEpiC	eye:	n/a
50	chr4:128703088-128703138	SAEC	small airway:	n/a

(count:96 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr4:128684085..128685592-chr4:128688518..128690302,2	K562	blood:
2	chr4:128740214..128742882-chr4:128752992..128755528,3	K562	blood:
3	chr4:128716381..128718336-chr4:128718377..128720060,2	K562	blood:
4	chr4:128666387..128668298-chr4:128668505..128671466,2	K562	blood:
5	chr4:128702686..128704491-chr4:128713459..128716230,3	MCF-7	breast:
6	chr4:128526261..128527082-chr4:128709454..128710321,2	MCF-7	breast:
7	chr4:128701212..128704782-chr4:128885853..128888301,4	MCF-7	breast:
8	chr4:128651856..128654321-chr4:128662379..128665043,2	K562	blood:
9	chr4:128728798..128731364-chr4:128739602..128743482,3	K562	blood:
10	chr4:128728488..128731790-chr4:128810171..128812661,3	K562	blood:
11	chr4:128728798..128731364-chr4:128739602..128743482,3	K562	blood:
12	chr4:128701837..128704817-chr4:128712358..128715283,2	MCF-7	breast:
13	chr4:128702203..128705505-chr4:128800773..128804170,4	MCF-7	breast:
14	chr4:128697244..128699961-chr4:128704246..128706827,2	MCF-7	breast:
15	chr4:128703531..128705249-chr4:130014655..130017577,2	K562	blood:
16	chr4:128744268..128745932-chr4:128800646..128802208,2	K562	blood:
17	chr4:128691903..128693530-chr4:128709934..128712766,2	K562	blood:
18	chr4:128657662..128659612-chr4:128665725..128667631,2	K562	blood:
19	chr4:128682228..128685843-chr4:128701255..128705452,5	MCF-7	breast:
20	chr4:128684085..128685592-chr4:128688518..128690302,2	K562	blood:
21	chr4:128686775..128688582-chr4:128798600..128801332,2	K562	blood:
22	chr4:128735114..128737929-chr4:128739500..128741438,2	K562	blood:
23	chr4:128702580..128705894-chr4:128810025..128813296,3	K562	blood:
24	chr11:76155451..76155958-chr4:128703322..128703844,2	Hela-S3	cervix:
25	chr4:128653835..128656903-chr4:128701461..128704105,3	K562	blood:
26	chr4:128708991..128711452-chr4:128712949..128715693,2	K562	blood:
27	chr4:128722353..128724955-chr4:128727148..128728727,2	K562	blood:
28	chr4:128666387..128668298-chr4:128668505..128671466,2	K562	blood:
29	chr4:128735443..128738310-chr4:128746786..128749882,3	K562	blood:
30	chr4:128751053..128753977-chr4:128762581..128764135,2	MCF-7	breast:
31	chr4:128703573..128706367-chr4:128719172..128720901,2	K562	blood:
32	chr4:128754147..128756975-chr4:128757959..128759964,2	MCF-7	breast:
33	chr4:128735614..128737197-chr4:128742449..128744815,2	K562	blood:
34	chr4:128714333..128715858-chr4:128734487..128736194,2	K562	blood:
35	chr4:128525866..128527137-chr4:128653218..128654151,10	K562	blood:
36	chr4:128722353..128724955-chr4:128727148..128728727,2	K562	blood:
37	chr4:128689601..128691361-chr4:128702000..128704848,2	K562	blood:
38	chr4:128754147..128756975-chr4:128757959..128759964,2	MCF-7	breast:
39	chr4:128748778..128750311-chr4:128751376..128753620,2	K562	blood:
40	chr4:128701694..128705366-chr4:128716916..128719720,4	MCF-7	breast:
41	chr11:47206754..47207663-chr4:128703485..128704269,2	Hela-S3	cervix:
42	chr4:128699357..128701844-chr4:128885755..128888672,2	K562	blood:
43	chr4:128702037..128703745-chr4:128710698..128712624,2	K562	blood:
44	chr4:128708991..128711452-chr4:128712949..128715693,2	K562	blood:
45	chr4:128702197..128705040-chr4:128708577..128711566,4	MCF-7	breast:
46	chr4:128702671..128704706-chr4:128715949..128719074,3	MCF-7	breast:
47	chr4:128748778..128750311-chr4:128751376..128753620,2	K562	blood:
48	chr4:128657662..128659612-chr4:128665725..128667631,2	K562	blood:
49	chr4:128735114..128737929-chr4:128739500..128741438,2	K562	blood:
50	chr4:128716381..128718336-chr4:128718377..128720060,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC25A31-2	chr4:128741583-128741676	NONHSAT098242
2	lnc-MFSD8-1	chr4:128761353-128765195	ENSG00000261668.1
3	lnc-HSPA4L-1	chr4:128758922-128760428	NONHSAT098243
4	lnc-HSPA4L-1	chr4:128758922-128761883	NONHSAT098244
5	lnc-SLC25A31-2	chr4:128734173-128734630	NONHSAT098242
6	lnc-HSPA4L-1	chr4:128760853-128761885	NONHSAT098243
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	SLC25A31	hsa-miR-335-5p	chr4:128695378-128695400
2	HSPA4L	hsa-miR-155-5p	chr4:128754359-128754381
3	HSPA4L	hsa-miR-16-5p	chr4:128754202-128754208
4	HSPA4L	hsa-miR-16-5p	chr4:128754187-128754209

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
ENSG00000151466	chromatin interactions
ENSG00000165912	chromatin interactions
ENSG00000255135	chromatin interactions
ENSG00000123815	chromatin interactions
ENSG00000164074	chromatin interactions
ENSG00000142731	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000138709	chromatin interactions
ENSG00000201778	chromatin interactions
ENSG00000164073	chromatin interactions
ENSG00000088298	chromatin interactions
ENSG00000126005	chromatin interactions
ENSG00000151470	chromatin interactions
ENSG00000164070	chromatin interactions
ENSG00000163660	chromatin interactions
ENSG00000086544	chromatin interactions
ENSG00000251821	chromatin interactions

Extended variants
information (count: 2996 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:2996 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4834214	chr4:128652227-128652228	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552408753	chr4:128652230-128652231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182933489	chr4:128652273-128652274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187635335	chr4:128652283-128652284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370180135	chr4:128652288-128652289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs537440345	chr4:128652347-128652348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555776970	chr4:128652370-128652371	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs569318885	chr4:128652396-128652397	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs541260063	chr4:128652420-128652421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs374856325	chr4:128652427-128652428	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs78696712	chr4:128652473-128652474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553845609	chr4:128652539-128652540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs143403825	chr4:128652551-128652552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs546021915	chr4:128652576-128652577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192412271	chr4:128652586-128652587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576444729	chr4:128652609-128652610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs544601684	chr4:128652612-128652613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146747194	chr4:128652624-128652625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs575528340	chr4:128652633-128652634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs554794580	chr4:128652661-128652662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs541918249	chr4:128652677-128652678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs560639185	chr4:128652720-128652721	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184821556	chr4:128652785-128652786	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552396590	chr4:128652789-128652790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs139426477	chr4:128652831-128652832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs374117519	chr4:128652869-128652870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs62335568	chr4:128652958-128652959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs187567826	chr4:128652970-128652971	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs60887431	chr4:128652971-128652972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192813403	chr4:128653025-128653026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs567926850	chr4:128653076-128653077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143542833	chr4:128653091-128653092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs184572629	chr4:128653104-128653105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35320228	chr4:128653105-128653106	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs545982963	chr4:128653120-128653121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs568265233	chr4:128653137-128653138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539632489	chr4:128653251-128653252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548036680	chr4:128653275-128653276	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs576383370	chr4:128653307-128653308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537307438	chr4:128653391-128653392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs111617365	chr4:128653399-128653400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs151249143	chr4:128653414-128653415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs542257266	chr4:128653519-128653520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189888586	chr4:128653530-128653531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181499785	chr4:128653594-128653595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs372094590	chr4:128653601-128653602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs140471448	chr4:128653617-128653618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528633489	chr4:128653657-128653658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs545967903	chr4:128653737-128653738	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs72616939	chr4:128653738-128653739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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:793 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:128644400-128658800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr4:128644600-128652600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr4:128645000-128654200	Weak transcription	Cortex derived primary cultured neurospheres	brain
4	chr4:128654000-128654200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:128654000-128654400	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr4:128654200-128654400	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr4:128658200-128658400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr4:128658200-128659000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr4:128658200-128659000	Enhancers	K562	blood
10	chr4:128658400-128658600	Enhancers	Fetal Intestine Large	intestine
11	chr4:128658600-128659000	Enhancers	Fetal Lung	lung
12	chr4:128658600-128659000	Enhancers	Fetal Muscle Trunk	muscle
13	chr4:128658800-128659000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:128659000-128661600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr4:128660000-128661600	Weak transcription	Aorta	Aorta
16	chr4:128661600-128662000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:128661600-128662000	ZNF genes & repeats	Aorta	Aorta
18	chr4:128677400-128681200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr4:128680800-128681600	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr4:128681200-128681800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:128681200-128681800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr4:128692600-128693200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:128692600-128693400	Enhancers	NHEK	skin
24	chr4:128692800-128693600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:128693000-128693400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
26	chr4:128693000-128693400	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr4:128693000-128693600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:128693600-128694600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:128693600-128702200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:128694600-128694800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:128694800-128695200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr4:128695200-128697200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr4:128695800-128696000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr4:128696200-128697400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chr4:128696800-128699400	Enhancers	GM12878-XiMat	blood
36	chr4:128697200-128697400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:128697200-128697400	Enhancers	K562	blood
38	chr4:128697200-128698600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:128697400-128698000	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr4:128697600-128698000	Enhancers	HMEC	breast
41	chr4:128697600-128698800	Weak transcription	K562	blood
42	chr4:128697600-128699400	Enhancers	HepG2	liver
43	chr4:128697600-128701800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr4:128697800-128698000	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr4:128698000-128698800	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr4:128698000-128702400	Weak transcription	HMEC	breast
47	chr4:128698200-128699000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr4:128698600-128699000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr4:128698600-128699800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr4:128698600-128700000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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