Variant report

Variant	nsv537250
Chromosome Location	chr4:129778025-129905116
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1224)
CpG islands
(count:366)
Chromatin interactive
region (count:61)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:9)

(count:1224 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:129866424-129866624	K562	blood:	n/a	n/a
2	ARID3A	chr4:129879403-129879765	HepG2	liver:	n/a	n/a
3	ATF2	chr4:129834181-129834816	GM12878	blood:	n/a	n/a
4	ATF2	chr4:129838788-129839413	GM12878	blood:	n/a	n/a
5	ATF2	chr4:129792908-129793330	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:129838782-129839408	GM12878	blood:	n/a	n/a
7	ATF2	chr4:129784142-129785043	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:129784543-129785016	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr4:129834221-129834957	GM12878	blood:	n/a	n/a
10	ATF2	chr4:129787441-129787873	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr4:129786523-129786934	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr4:129788328-129788944	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF2	chr4:129780996-129781553	GM12878	blood:	n/a	n/a
14	ATF2	chr4:129837715-129838462	GM12878	blood:	n/a	n/a
15	ATF2	chr4:129837905-129838481	GM12878	blood:	n/a	n/a
16	ATF2	chr4:129780849-129781956	GM12878	blood:	n/a	n/a
17	ATF2	chr4:129783230-129784319	GM12878	blood:	n/a	n/a
18	BACH1	chr4:129902627-129902712	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr4:129787497-129787679	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr4:129901252-129901452	K562	blood:	n/a	n/a
21	BACH1	chr4:129797317-129797325	K562	blood:	n/a	n/a
22	BATF	chr4:129780951-129781563	GM12878	blood:	n/a	n/a
23	BATF	chr4:129837910-129838268	GM12878	blood:	n/a	n/a
24	BATF	chr4:129783709-129784080	GM12878	blood:	n/a	n/a
25	BATF	chr4:129827779-129828010	GM12878	blood:	n/a	chr4:129827877-129827888
26	BATF	chr4:129838922-129839343	GM12878	blood:	n/a	n/a
27	BATF	chr4:129838911-129839317	GM12878	blood:	n/a	n/a
28	BCL11A	chr4:129838977-129839324	GM12878	blood:	n/a	n/a
29	BCL11A	chr4:129839033-129839295	GM12878	blood:	n/a	n/a
30	BCL3	chr4:129783711-129784235	GM12878	blood:	n/a	n/a
31	BCL3	chr4:129781008-129781514	GM12878	blood:	n/a	chr4:129781133-129781142
32	BCL3	chr4:129779078-129779384	GM12878	blood:	n/a	n/a
33	BCL3	chr4:129780325-129780841	GM12878	blood:	n/a	n/a
34	BCL3	chr4:129838908-129839307	GM12878	blood:	n/a	n/a
35	BCL3	chr4:129834252-129834735	GM12878	blood:	n/a	n/a
36	BCL3	chr4:129780204-129780967	GM12878	blood:	n/a	chr4:129780293-129780302
37	BCL3	chr4:129834324-129834632	GM12878	blood:	n/a	n/a
38	BCLAF1	chr4:129838854-129839425	GM12878	blood:	n/a	n/a
39	BCLAF1	chr4:129838883-129839358	GM12878	blood:	n/a	n/a
40	BCLAF1	chr4:129837821-129838334	GM12878	blood:	n/a	n/a
41	BCLAF1	chr4:129781125-129781552	GM12878	blood:	n/a	chr4:129781133-129781142
42	BCLAF1	chr4:129837719-129838296	GM12878	blood:	n/a	n/a
43	BHLHE40	chr4:129838803-129839362	GM12878	blood:	n/a	n/a
44	BHLHE40	chr4:129838002-129838412	GM12878	blood:	n/a	n/a
45	BHLHE40	chr4:129784557-129784867	HepG2	liver:	n/a	n/a
46	BHLHE40	chr4:129783863-129784093	GM12878	blood:	n/a	n/a
47	BRCA1	chr4:129797349-129797464	H1-hESC	embryonic stem cell:	n/a	n/a
48	BRCA1	chr4:129784704-129784802	HepG2	liver:	n/a	n/a
49	BRCA1	chr4:129787527-129787528	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr4:129784634-129784936	H1-hESC	embryonic stem cell:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:129793434-129793484	BE2_C	brain:	n/a
2	chr4:129805520-129805570	GM12878	blood:	n/a
3	chr4:129805520-129805570	K562	blood:	n/a
4	chr4:129793434-129793484	PrEC	prostate:	n/a
5	chr4:129784819-129784869	BE2_C	brain:	n/a
6	chr4:129805520-129805570	NH-A	brain:	n/a
7	chr4:129805520-129805570	HepG2	liver:	n/a
8	chr4:129781682-129781732	SAEC	small airway:	n/a
9	chr4:129784819-129784869	HRCEpiC	kidney:	n/a
10	chr4:129783057-129783107	HCPEpiC	choroid plexus:	n/a
11	chr4:129785576-129785626	A549	lung:	n/a
12	chr4:129805520-129805570	T-47D	breast:	n/a
13	chr4:129781682-129781732	T-47D	breast:	n/a
14	chr4:129785576-129785626	HEEpiC	esophagus:	n/a
15	chr4:129781682-129781732	MCF10A-Er-Src	breast:	n/a
16	chr4:129785576-129785626	HRCEpiC	kidney:	n/a
17	chr4:129785576-129785626	AG04450	lung:	fetal
18	chr4:129805520-129805570	HCPEpiC	choroid plexus:	n/a
19	chr4:129784819-129784869	Hela-S3	cervix:	n/a
20	chr4:129784819-129784869	NHBE	bronchial:	n/a
21	chr4:129785576-129785626	ProgFib	skin:	n/a
22	chr4:129784819-129784869	H1-hESC	embryonic stem cell:	embryo
23	chr4:129783057-129783107	SK-N-SH	brain:	n/a
24	chr4:129784819-129784869	NH-A	brain:	n/a
25	chr4:129784819-129784869	ECC-1	luminal epithelium:	n/a
26	chr4:129784819-129784869	HAEpiC	amniotic membrane:	n/a
27	chr4:129784819-129784869	Caco-2	colon:	n/a
28	chr4:129785576-129785626	Jurkat	blood:	n/a
29	chr4:129784819-129784869	LNCaP	prostate:	n/a
30	chr4:129781682-129781732	SK-N-MC	brain:	n/a
31	chr4:129783057-129783107	HCF	heart:	n/a
32	chr4:129781682-129781732	BJ	skin:	n/a
33	chr4:129784819-129784869	MCF-7	breast:	n/a
34	chr4:129793434-129793484	HNPCEpiC	eye:	n/a
35	chr4:129805520-129805570	SAEC	small airway:	n/a
36	chr4:129805520-129805570	PrEC	prostate:	n/a
37	chr4:129783057-129783107	NB4	blood:	n/a
38	chr4:129793434-129793484	NHDF-neo	bronchial:	n/a
39	chr4:129793434-129793484	SK-N-SH	brain:	n/a
40	chr4:129785576-129785626	T-47D	breast:	n/a
41	chr4:129781682-129781732	HepG2	liver:	n/a
42	chr4:129781682-129781732	NH-A	brain:	n/a
43	chr4:129793434-129793484	SKMC	muscle:	n/a
44	chr4:129785576-129785626	Hela-S3	cervix:	n/a
45	chr4:129784819-129784869	Jurkat	blood:	n/a
46	chr4:129781682-129781732	U87	brain:	n/a
47	chr4:129793434-129793484	SAEC	small airway:	n/a
48	chr4:129781682-129781732	HIPEpiC	eye:	n/a
49	chr4:129784819-129784869	HCM	heart:	n/a
50	chr4:129784819-129784869	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:129883398..129885861-chr4:129887383..129889506,2	K562	blood:
2	chr4:129863629..129866387-chr4:129870052..129872955,2	K562	blood:
3	chr4:129796835..129799070-chr4:129823245..129825174,2	K562	blood:
4	chr4:129869703..129871375-chr4:129874757..129876510,2	K562	blood:
5	chr4:129486871..129489829-chr4:129782805..129785623,2	K562	blood:
6	chr4:129792576..129794412-chr4:129795148..129798091,2	MCF-7	breast:
7	chr4:129798920..129801366-chr4:129805840..129808673,2	K562	blood:
8	chr4:129731039..129733137-chr4:129832126..129834778,3	K562	blood:
9	chr4:129759776..129761947-chr4:129777321..129779431,2	K562	blood:
10	chr4:129798920..129801366-chr4:129805840..129808673,2	K562	blood:
11	chr4:129830344..129833253-chr4:129837741..129840090,2	K562	blood:
12	chr4:129810865..129812723-chr4:129812841..129815400,2	K562	blood:
13	chr4:129796835..129799070-chr4:129823245..129825174,2	K562	blood:
14	chr4:129896690..129899278-chr4:129899361..129901444,2	MCF-7	breast:
15	chr4:129772388..129774921-chr4:129778989..129781160,2	MCF-7	breast:
16	chr4:129730756..129732301-chr4:129776228..129778833,2	K562	blood:
17	chr4:129774305..129776412-chr4:129777976..129779919,2	K562	blood:
18	chr4:129881359..129883041-chr4:129899761..129902463,2	K562	blood:
19	chr4:129729755..129733795-chr4:129783264..129786218,5	MCF-7	breast:
20	chr4:129902026..129904676-chr4:129907660..129909341,2	K562	blood:
21	chr4:129731868..129734211-chr4:129779413..129782328,2	K562	blood:
22	chr4:129869703..129871375-chr4:129874757..129876510,2	K562	blood:
23	chr4:129885302..129888048-chr4:129911143..129913987,2	K562	blood:
24	chr4:129896690..129899278-chr4:129899361..129901444,2	MCF-7	breast:
25	chr4:129731707..129733254-chr4:129789500..129791100,2	MCF-7	breast:
26	chr4:129834048..129836614-chr4:129837936..129840499,3	K562	blood:
27	chr4:129863629..129866387-chr4:129870052..129872955,2	K562	blood:
28	chr4:129375124..129376026-chr4:129784426..129785119,2	MCF-7	breast:
29	chr4:129900386..129903021-chr4:129908411..129910284,2	MCF-7	breast:
30	chr4:129495559..129496404-chr4:129784372..129785130,3	MCF-7	breast:
31	chr4:129881359..129883041-chr4:129899761..129902463,2	K562	blood:
32	chr4:129830344..129833253-chr4:129837741..129840090,2	K562	blood:
33	chr4:129810865..129812723-chr4:129812841..129815400,2	K562	blood:
34	chr4:129834245..129836614-chr4:129838172..129840499,2	K562	blood:
35	chr4:129731505..129733452-chr4:129799174..129801929,2	MCF-7	breast:
36	chr4:129792576..129794412-chr4:129795148..129798091,2	MCF-7	breast:
37	chr4:129893731..129895681-chr4:129897472..129899242,2	K562	blood:
38	chr4:129784722..129788908-chr4:129789150..129792648,4	K562	blood:
39	chr4:129348761..129349614-chr4:129784409..129785296,3	MCF-7	breast:
40	chr4:129802100..129804907-chr4:129805391..129807043,2	K562	blood:
41	chr4:129883398..129885861-chr4:129887383..129889705,3	K562	blood:
42	chr4:129112511..129113107-chr4:129784791..129785303,2	K562	blood:
43	chr4:129732016..129733966-chr4:129800387..129802773,2	K562	blood:
44	chr4:129770197..129772164-chr4:129783210..129785874,2	K562	blood:
45	chr4:129834048..129836614-chr4:129837936..129840499,3	K562	blood:
46	chr4:129486483..129487185-chr4:129784609..129785425,2	MCF-7	breast:
47	chr4:129802100..129804907-chr4:129805391..129807043,2	K562	blood:
48	chr4:129886935..129889219-chr4:130012773..130015050,2	K562	blood:
49	chr4:129495601..129496471-chr4:129784448..129785345,3	K562	blood:
50	chr4:129787325..129790041-chr4:129799398..129801047,2	K562	blood:

No data

(count:9 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	PHF17	hsa-miR-124-3p	chr4:129796320-129796339
2	PHF17	hsa-miR-124-3p	chr4:129795562-129795568
3	PHF17	hsa-miR-21-5p	chr4:129794503-129794525
4	PHF17	hsa-miR-145-5p	chr4:129784899-129784923
5	PHF17	hsa-miR-124-3p	chr4:129796332-129796338
6	PHF17	hsa-miR-155-5p	chr4:129794659-129794681
7	PHF17	hsa-miR-155-5p	chr4:129794674-129794681
8	PHF17	hsa-miR-124-3p	chr4:129795549-129795568
9	PHF17	hsa-miR-145-5p	chr4:129784570-129784593

Variant related genes	Relation type
SCLT1	TF binding region
SCLT1	CpG island
ENSG00000251432	chromatin interactions
ENSG00000151470	chromatin interactions
ENSG00000151466	chromatin interactions
ENSG00000077684	chromatin interactions

Extended variants
information (count: 4477 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4477 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4975274	chr4:129778076-129778077	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs184992109	chr4:129778082-129778083	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs189117402	chr4:129778089-129778090	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs533373652	chr4:129778115-129778116	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs148240566	chr4:129778195-129778196	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs532603138	chr4:129778222-129778223	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs62317924	chr4:129778232-129778233	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs536272118	chr4:129778236-129778237	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs546257677	chr4:129778237-129778238	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs192800955	chr4:129778370-129778371	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs567087690	chr4:129778388-129778389	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs114387632	chr4:129778393-129778394	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs370607222	chr4:129778450-129778451	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs372979071	chr4:129778457-129778458	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs140331727	chr4:129778459-129778460	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs375950317	chr4:129778483-129778484	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201538651	chr4:129778484-129778485	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs17013835	chr4:129778510-129778511	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs200666132	chr4:129778552-129778553	Strong transcription Weak transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs373639332	chr4:129778620-129778621	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs553259649	chr4:129778650-129778651	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs201334089	chr4:129778651-129778652	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574351118	chr4:129778687-129778688	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs367951774	chr4:129778693-129778694	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs115531380	chr4:129778696-129778697	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs184765856	chr4:129778745-129778746	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs114570617	chr4:129778806-129778807	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs546123335	chr4:129778823-129778824	Strong transcription Weak transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs564231571	chr4:129778843-129778844	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs150373800	chr4:129778858-129778859	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs535384989	chr4:129778875-129778876	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs138238607	chr4:129778893-129778894	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs562871411	chr4:129778900-129778901	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs573878120	chr4:129778904-129778905	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530090553	chr4:129778954-129778955	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs548700939	chr4:129778963-129778964	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs548336536	chr4:129778989-129778990	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs114826776	chr4:129778996-129778997	Strong transcription Weak transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116033203	chr4:129779002-129779003	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs147459858	chr4:129779018-129779019	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138362077	chr4:129779023-129779024	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116330854	chr4:129779037-129779038	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs556206227	chr4:129779071-129779072	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370604444	chr4:129779072-129779073	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2162126	chr4:129779076-129779077	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs73850015	chr4:129779102-129779103	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs553441188	chr4:129779106-129779107	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571434024	chr4:129779107-129779108	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs368461365	chr4:129779134-129779135	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558113217	chr4:129779142-129779143	Strong transcription Weak transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Hepatocellular carcinoma	16750200	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
Gastric cancer	16891809	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:1827 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:129753600-129798600	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
2	chr4:129753800-129795000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:129760400-129783400	Strong transcription	HUES48 Cell Line	embryonic stem cell
4	chr4:129761600-129779400	Strong transcription	Fetal Stomach	stomach
5	chr4:129761600-129782000	Strong transcription	Fetal Intestine Small	intestine
6	chr4:129761600-129785000	Strong transcription	Thymus	Thymus
7	chr4:129762000-129782800	Strong transcription	Primary B cells from peripheral blood	blood
8	chr4:129762400-129784200	Strong transcription	H9 Cell Line	embryonic stem cell
9	chr4:129762800-129784200	Strong transcription	HUES64 Cell Line	embryonic stem cell
10	chr4:129763000-129783800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
11	chr4:129763000-129785800	Strong transcription	iPS-20b Cell Line	embryonic stem cell
12	chr4:129763000-129787200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr4:129763200-129784000	Strong transcription	ES-I3 Cell Line	embryonic stem cell
14	chr4:129763200-129784000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
15	chr4:129763400-129784200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr4:129763600-129780400	Strong transcription	H1 Cell Line	embryonic stem cell
17	chr4:129763600-129786600	Strong transcription	Fetal Intestine Large	intestine
18	chr4:129763800-129780400	Strong transcription	iPS DF 6.9 Cell Line	embryonic stem cell
19	chr4:129763800-129780400	Strong transcription	Duodenum Mucosa	Duodenum
20	chr4:129763800-129783400	Strong transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr4:129763800-129784000	Strong transcription	Rectal Mucosa Donor 29	rectum
22	chr4:129763800-129784200	Strong transcription	Brain Germinal Matrix	brain
23	chr4:129764000-129784000	Strong transcription	Fetal Brain Female	brain
24	chr4:129764800-129779600	Strong transcription	Duodenum Smooth Muscle	Duodenum
25	chr4:129766600-129780200	Strong transcription	Adipose Nuclei	Adipose
26	chr4:129766600-129780200	Strong transcription	Lung	lung
27	chr4:129766600-129783400	Strong transcription	HUES6 Cell Line	embryonic stem cell
28	chr4:129766600-129784200	Strong transcription	HepG2	liver
29	chr4:129766800-129779400	Strong transcription	Brain Inferior Temporal Lobe	brain
30	chr4:129767200-129784400	Strong transcription	Aorta	Aorta
31	chr4:129767400-129783800	Strong transcription	Brain Angular Gyrus	brain
32	chr4:129767400-129784000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
33	chr4:129767600-129779400	Strong transcription	Rectal Smooth Muscle	rectum
34	chr4:129767600-129780200	Strong transcription	Stomach Smooth Muscle	stomach
35	chr4:129767800-129784200	Strong transcription	Liver	Liver
36	chr4:129768000-129780400	Strong transcription	Gastric	stomach
37	chr4:129768000-129784000	Strong transcription	Brain Anterior Caudate	brain
38	chr4:129768600-129784000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr4:129768800-129778800	Weak transcription	Psoas Muscle	Psoas
40	chr4:129768800-129779200	Strong transcription	Left Ventricle	heart
41	chr4:129768800-129779400	Strong transcription	Skeletal Muscle Male	skeletal muscle
42	chr4:129768800-129780200	Strong transcription	Skeletal Muscle Female	skeletal muscle
43	chr4:129768800-129784400	Weak transcription	Stomach Mucosa	stomach
44	chr4:129769000-129778400	Weak transcription	Right Atrium	heart
45	chr4:129769200-129778800	Strong transcription	Pancreas	Pancrea
46	chr4:129769200-129779000	Strong transcription	Right Ventricle	heart
47	chr4:129769200-129783600	Strong transcription	A549	lung
48	chr4:129769800-129784200	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr4:129770600-129784000	Strong transcription	Cortex derived primary cultured neurospheres	brain
50	chr4:129772200-129778400	Weak transcription	Small Intestine	intestine

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