Variant report

Variant	nsv830154
Chromosome Location	chr4:174781983-174940640
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:722)
CpG islands
(count:366)
Chromatin interactive
region (count:29)
LncRNA
region (count:34)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:722 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:174799973-174800234	K562	blood:	n/a	n/a
2	BCL3	chr4:174838292-174838609	GM12878	blood:	n/a	n/a
3	BHLHE40	chr4:174825762-174825772	K562	blood:	n/a	n/a
4	BHLHE40	chr4:174799922-174800199	K562	blood:	n/a	n/a
5	BHLHE40	chr4:174861367-174861570	K562	blood:	n/a	n/a
6	BHLHE40	chr4:174912135-174912333	K562	blood:	n/a	n/a
7	BRCA1	chr4:174851422-174851491	GM12878	blood:	n/a	n/a
8	CCNT2	chr4:174854015-174854176	K562	blood:	n/a	n/a
9	CEBPB	chr4:174864660-174865020	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr4:174901482-174901702	A549	lung:	n/a	chr4:174901627-174901638
11	CEBPB	chr4:174812280-174812558	K562	blood:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
12	CEBPB	chr4:174830425-174830482	HepG2	liver:	n/a	chr4:174830471-174830482
13	CEBPB	chr4:174864681-174864902	K562	blood:	n/a	n/a
14	CEBPB	chr4:174783884-174784274	HepG2	liver:	n/a	chr4:174784114-174784125
15	CEBPB	chr4:174783874-174784258	IMR90	lung:	n/a	chr4:174784114-174784125
16	CEBPB	chr4:174939423-174939632	K562	blood:	n/a	n/a
17	CEBPB	chr4:174857010-174857360	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:174857142-174857342	A549	lung:	n/a	n/a
19	CEBPB	chr4:174838322-174838686	IMR90	lung:	n/a	chr4:174838416-174838424
20	CEBPB	chr4:174901482-174901774	IMR90	lung:	n/a	chr4:174901627-174901638 chr4:174901712-174901725
21	CEBPB	chr4:174864742-174864995	IMR90	lung:	n/a	n/a
22	CEBPB	chr4:174799939-174800243	IMR90	lung:	n/a	n/a
23	CEBPB	chr4:174939401-174939719	K562	blood:	n/a	n/a
24	CEBPB	chr4:174939499-174939606	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr4:174784029-174784160	H1-hESC	embryonic stem cell:	n/a	chr4:174784114-174784125
26	CEBPB	chr4:174783893-174784291	A549	lung:	n/a	chr4:174784114-174784125
27	CEBPB	chr4:174783876-174784272	K562	blood:	n/a	chr4:174784114-174784125
28	CEBPB	chr4:174812256-174812582	IMR90	lung:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
29	CEBPB	chr4:174814702-174814963	HepG2	liver:	n/a	chr4:174814834-174814845
30	CEBPB	chr4:174783928-174784265	Hela-S3	cervix:	n/a	chr4:174784114-174784125
31	CEBPB	chr4:174864666-174865010	K562	blood:	n/a	n/a
32	CEBPB	chr4:174800035-174800200	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr4:174901462-174901768	HepG2	liver:	n/a	chr4:174901627-174901638 chr4:174901712-174901725
34	CEBPB	chr4:174812281-174812585	A549	lung:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
35	CEBPB	chr4:174929384-174929699	HepG2	liver:	n/a	chr4:174929577-174929588
36	CEBPB	chr4:174812282-174812586	HepG2	liver:	n/a	chr4:174812451-174812460 chr4:174812449-174812460
37	CEBPD	chr4:174799832-174800224	K562	blood:	n/a	n/a
38	CREB1	chr4:174799920-174800122	A549	lung:	n/a	n/a
39	CTCF	chr4:174911191-174911873	A549	lung:	n/a	chr4:174911457-174911475 chr4:174911452-174911473 chr4:174911458-174911474
40	CTCF	chr4:174893540-174893690	MCF-7	breast:	n/a	n/a
41	CTCF	chr4:174911371-174911584	ProgFib	skin:	n/a	chr4:174911457-174911475 chr4:174911452-174911473 chr4:174911458-174911474
42	CTCF	chr4:174930066-174930320	K562	blood:	n/a	n/a
43	CTCF	chr4:174911380-174911530	AG10803	skin:	n/a	chr4:174911457-174911475 chr4:174911452-174911473 chr4:174911458-174911474
44	CTCF	chr4:174911380-174911530	GM12865	blood:	n/a	chr4:174911457-174911475 chr4:174911452-174911473 chr4:174911458-174911474
45	CTCF	chr4:174912100-174912250	SK-N-SH_RA	brain:	n/a	n/a
46	CTCF	chr4:174911320-174911470	K562	blood:	n/a	n/a
47	CTCF	chr4:174911380-174911530	K562	blood:	n/a	chr4:174911457-174911475 chr4:174911452-174911473 chr4:174911458-174911474
48	CTCF	chr4:174911380-174911530	AG04449	skin:	n/a	chr4:174911457-174911475 chr4:174911452-174911473 chr4:174911458-174911474
49	CTCF	chr4:174911300-174911450	HAc	cerebellar:	n/a	n/a
50	CTCF	chr4:174912040-174912190	BE2_C	brain:	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	chr4:174912178-174912228	SKMC	muscle:	n/a
2	chr4:174912114-174912164	SK-N-SH	brain:	n/a
3	chr4:174912278-174912328	Jurkat	blood:	n/a
4	chr4:174912210-174912260	BJ	skin:	n/a
5	chr4:174912278-174912328	NH-A	brain:	n/a
6	chr4:174912210-174912260	NHDF-neo	bronchial:	n/a
7	chr4:174912210-174912260	HRCEpiC	kidney:	n/a
8	chr4:174912071-174912121	ECC-1	luminal epithelium:	n/a
9	chr4:174912278-174912328	GM12892	blood:	n/a
10	chr4:174912114-174912164	RPTEC	kidney:	n/a
11	chr4:174912114-174912164	HPAEpiC	pulmonary alveolar:	n/a
12	chr4:174912071-174912121	HCPEpiC	choroid plexus:	n/a
13	chr4:174912278-174912328	HRCEpiC	kidney:	n/a
14	chr4:174912178-174912228	HAEpiC	amniotic membrane:	n/a
15	chr4:174895229-174895279	HEEpiC	esophagus:	n/a
16	chr4:174912071-174912121	HL-60	blood:	n/a
17	chr4:174912278-174912328	AG09309	skin:	n/a
18	chr4:174912114-174912164	AG04450	lung:	fetal
19	chr4:174912071-174912121	HNPCEpiC	eye:	n/a
20	chr4:174912114-174912164	GM12892	blood:	n/a
21	chr4:174912114-174912164	U87	brain:	n/a
22	chr4:174895229-174895279	U87	brain:	n/a
23	chr4:174912114-174912164	ProgFib	skin:	n/a
24	chr4:174912114-174912164	PFSK-1	brain:	n/a
25	chr4:174912210-174912260	AG04449	skin:	fetal
26	chr4:174912071-174912121	GM12891	blood:	n/a
27	chr4:174912178-174912228	GM19239	blood:	n/a
28	chr4:174895229-174895279	PrEC	prostate:	n/a
29	chr4:174912071-174912121	SK-N-SH_RA	brain:	n/a
30	chr4:174912278-174912328	MCF-7	breast:	n/a
31	chr4:174912071-174912121	MCF-7	breast:	n/a
32	chr4:174912210-174912260	AG10803	skin:	n/a
33	chr4:174912278-174912328	AG09319	gingival:	n/a
34	chr4:174912178-174912228	SK-N-MC	brain:	n/a
35	chr4:174895229-174895279	SK-N-SH	brain:	n/a
36	chr4:174912210-174912260	K562	blood:	n/a
37	chr4:174912071-174912121	HRCEpiC	kidney:	n/a
38	chr4:174895229-174895279	H1-hESC	embryonic stem cell:	embryo
39	chr4:174912114-174912164	AG09319	gingival:	n/a
40	chr4:174912071-174912121	ovcar-3	ovarian:	n/a
41	chr4:174912114-174912164	HCF	heart:	n/a
42	chr4:174912278-174912328	SK-N-SH	brain:	n/a
43	chr4:174912114-174912164	SAEC	small airway:	n/a
44	chr4:174912071-174912121	GM12878	blood:	n/a
45	chr4:174895229-174895279	AG04450	lung:	fetal
46	chr4:174912071-174912121	HEEpiC	esophagus:	n/a
47	chr4:174912114-174912164	HCT-116	colon:	n/a
48	chr4:174912114-174912164	Hela-S3	cervix:	n/a
49	chr4:174895229-174895279	Jurkat	blood:	n/a
50	chr4:174912114-174912164	NHDF-neo	bronchial:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:174853099..174855885-chr4:174859341..174861783,2	K562	blood:
2	chr4:174850174..174852634-chr4:174855213..174858058,2	K562	blood:
3	chr4:174850174..174852634-chr4:174855213..174858058,2	K562	blood:
4	chr4:174864605..174866141-chr4:174866793..174868362,2	K562	blood:
5	chr4:174789438..174791902-chr4:174794071..174796664,2	K562	blood:
6	chr4:174859507..174861754-chr4:174865873..174868149,2	K562	blood:
7	chr4:174814123..174816648-chr4:174817513..174819556,2	K562	blood:
8	chr4:174918419..174920333-chr4:174922806..174925607,2	K562	blood:
9	chr4:174915384..174916959-chr4:174921941..174923572,2	K562	blood:
10	chr4:174867285..174870306-chr4:174877689..174880210,3	K562	blood:
11	chr4:174867285..174870306-chr4:174877689..174880210,3	K562	blood:
12	chr4:174853099..174855885-chr4:174859341..174861783,2	K562	blood:
13	chr4:174898330..174900881-chr4:174901609..174904271,2	K562	blood:
14	chr4:174929400..174930958-chr4:174936098..174939019,2	MCF-7	breast:
15	chr4:174864605..174866141-chr4:174866793..174868362,2	K562	blood:
16	chr4:174873733..174876256-chr4:174880533..174882266,2	K562	blood:
17	chr4:174633329..174636278-chr4:174857380..174860257,2	K562	blood:
18	chr4:174909100..174911086-chr4:174911358..174913139,2	K562	blood:
19	chr4:174929400..174930958-chr4:174936098..174939019,2	MCF-7	breast:
20	chr4:174427083..174427720-chr4:174911085..174911952,3	MCF-7	breast:
21	chr4:174859507..174861754-chr4:174865873..174868149,2	K562	blood:
22	chr4:174873733..174876256-chr4:174880533..174882266,2	K562	blood:
23	chr4:174898330..174900881-chr4:174901609..174904271,2	K562	blood:
24	chr4:174918419..174920333-chr4:174922806..174925607,2	K562	blood:
25	chr4:174926262..174928381-chr4:174941011..174943411,2	MCF-7	breast:
26	chr4:174755123..174755970-chr4:174910868..174911899,5	MCF-7	breast:
27	chr4:174789438..174791902-chr4:174794071..174796664,2	K562	blood:
28	chr4:174665360..174668316-chr4:174784755..174786655,2	K562	blood:
29	chr4:174915384..174916959-chr4:174921941..174923572,2	K562	blood:

(count:34 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FBXO8-6	chr4:174824568-174824642	XLOC_004168
2	lnc-FBXO8-5	chr4:174911858-174912002	XLOC_004169
3	lnc-FBXO8-6	chr4:174832952-174833046	XLOC_004168
4	lnc-FBXO8-6	chr4:174832952-174833093	XLOC_004168
5	lnc-FBXO8-6	chr4:174821588-174821862	XLOC_004168
6	lnc-FBXO8-6	chr4:174817545-174817876	XLOC_004168
7	lnc-CEP44-4	chr4:174800521-174800556	l_2783_chr4:174800520-174818643_heart
8	lnc-FBXO8-8	chr4:174856441-174856707	l_2784_chr4:174852012-174855858_heart
9	lnc-FBXO8-5	chr4:174907844-174907950	XLOC_004169
10	lnc-FBXO8-6	chr4:174798622-174798846	XLOC_004168
11	lnc-FBXO8-6	chr4:174834223-174834403	XLOC_004168
12	lnc-CEP44-8	chr4:174849007-174849094	NONHSAT099307
13	lnc-CEP44-4	chr4:174818424-174818471	ENSG00000250708
14	lnc-CEP44-4	chr4:174850376-174850610	NONHSAT099305
15	lnc-CEP44-4	chr4:174818415-174818471	NONHSAT099305
16	lnc-FBXO8-8	chr4:174852013-174855240	l_2784_chr4:174852012-174855858_heart
17	lnc-CEP44-8	chr4:174852894-174852971	NONHSAT099307
18	lnc-FBXO8-8	chr4:174855643-174855858	l_2784_chr4:174852012-174855858_heart
19	lnc-CEP44-7	chr4:174893096-174893269	l_2785_chr4:174856882-174860902_heart
20	lnc-FBXO8-5	chr4:174845358-174846912	ENSG00000251216
21	lnc-CEP44-4	chr4:174849646-174849795	NONHSAT099305
22	lnc-CEP44-4	chr4:174844263-174844432	NONHSAT099305
23	lnc-CEP44-8	chr4:174834518-174834597	NONHSAT099307
24	lnc-FBXO8-5	chr4:174845360-174846912	XLOC_004169
25	lnc-CEP44-7	chr4:174859517-174860902	l_2785_chr4:174856882-174860902_heart
26	lnc-FBXO8-5	chr4:174903770-174903821	XLOC_004169
27	lnc-CEP44-4	chr4:174849646-174849795	ENSG00000250708
28	lnc-CEP44-4	chr4:174850376-174850676	ENSG00000250708
29	lnc-FBXO8-5	chr4:174849018-174849141	ENSG00000251216
30	lnc-CEP44-7	chr4:174856883-174856923	l_2785_chr4:174856882-174860902_heart
31	lnc-FBXO8-5	chr4:174849018-174849141	XLOC_004169
32	lnc-FBXO8-5	chr4:174911858-174912012	XLOC_004169
33	lnc-FBXO8-5	chr4:174911858-174912002	ENSG00000251216
34	lnc-CEP44-4	chr4:174816445-174818643	l_2783_chr4:174800520-174818643_heart

No data

Variant related genes	Relation type
ENSG00000251216	TF binding region
ENSG00000250708	TF binding region
ENSG00000250043	TF binding region
ENSG00000251216	CpG island
ENSG00000250708	CpG island
ENSG00000250043	CpG island
ENSG00000250708	chromatin interactions
ENSG00000251216	chromatin interactions

Extended variants
information (count: 3824 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:3824 , 50 per page) page: 1 2 3 4 5 6 7 ... 77

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs111772779	chr4:174793337-174793338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs564420447	chr4:174793413-174793414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540208833	chr4:174793432-174793433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs182640699	chr4:174793433-174793434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs540498123	chr4:174793531-174793532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs62337955	chr4:174793536-174793537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs552033382	chr4:174793568-174793569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76591509	chr4:174793654-174793655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs374682297	chr4:174793682-174793683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs141513256	chr4:174793707-174793708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs562519633	chr4:174793719-174793720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs78645115	chr4:174793753-174793754	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs147851848	chr4:174793772-174793773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571209413	chr4:174793827-174793828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534255977	chr4:174793844-174793845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187760499	chr4:174793862-174793863	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs191195205	chr4:174793883-174793884	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs546373988	chr4:174793916-174793917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs142322823	chr4:174793933-174793934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs6553733	chr4:174794014-174794015	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs576092349	chr4:174794042-174794043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs568954219	chr4:174794079-174794080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs76053130	chr4:174794088-174794089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs144660818	chr4:174794100-174794101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs377248463	chr4:174794152-174794153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs554556473	chr4:174794155-174794156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs574046881	chr4:174794222-174794223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs540196318	chr4:174794267-174794268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs553990471	chr4:174794297-174794298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573881956	chr4:174794316-174794317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542814652	chr4:174794321-174794322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs184825346	chr4:174794335-174794336	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531470317	chr4:174794355-174794356	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs140515808	chr4:174794365-174794366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs189641536	chr4:174795420-174795421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141525693	chr4:174795433-174795434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs558393511	chr4:174795463-174795464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs572074640	chr4:174795499-174795500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540700970	chr4:174795556-174795557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375956705	chr4:174795557-174795558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192856925	chr4:174795604-174795605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs574082043	chr4:174795616-174795617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs543716539	chr4:174795704-174795705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs374777542	chr4:174795777-174795778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115012422	chr4:174795778-174795779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs532617425	chr4:174795779-174795780	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs11133018	chr4:174795794-174795795	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs559677355	chr4:174795836-174795837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372774842	chr4:174795854-174795855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77342355	chr4:174795871-174795872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:73)

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
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
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
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Neuroblastoma	16790693	CNVD
Lung cancer	16773561	CNVD
Colorectal cancer	16774939	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	22127048	CNVD
Glioblastoma multiforme	22286061	CNVD
Neuroblastoma	21899760	CNVD
Gastric adenocarcinoma	19115996	CNVD
Burkitt''s lymphoma	19759907	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:388 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:174793200-174794400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:174793400-174794200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr4:174795400-174811000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:174796800-174797200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr4:174796800-174797200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
6	chr4:174797000-174797200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
7	chr4:174797200-174800000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr4:174799200-174800600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:174799600-174800600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
10	chr4:174799800-174800600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr4:174799800-174802000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:174800000-174800600	Enhancers	Fetal Lung	lung
13	chr4:174800000-174800600	Enhancers	Placenta Amnion	Placenta Amnion
14	chr4:174800000-174801800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr4:174800200-174801600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr4:174800600-174801600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr4:174800600-174801600	Weak transcription	Fetal Lung	lung
18	chr4:174800600-174804800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr4:174800600-174804800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:174801400-174802000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:174801600-174801800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:174801600-174813400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
23	chr4:174802000-174802200	Enhancers	Fetal Lung	lung
24	chr4:174802600-174803000	Weak transcription	Pancreas	Pancrea
25	chr4:174803000-174803200	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr4:174803200-174803400	Flanking Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:174804800-174805000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:174804800-174805200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr4:174804800-174806000	Enhancers	Ovary	ovary
30	chr4:174804800-174806200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:174810800-174811400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr4:174811000-174811200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:174811400-174811600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:174813400-174813800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr4:174822800-174823000	Enhancers	Rectal Smooth Muscle	rectum
36	chr4:174823200-174824400	Weak transcription	Rectal Smooth Muscle	rectum
37	chr4:174823800-174825400	Enhancers	Fetal Heart	heart
38	chr4:174824200-174824400	Enhancers	Stomach Smooth Muscle	stomach
39	chr4:174824400-174825600	Enhancers	Rectal Smooth Muscle	rectum
40	chr4:174825000-174825200	Enhancers	Stomach Smooth Muscle	stomach
41	chr4:174825400-174828200	Weak transcription	Fetal Heart	heart
42	chr4:174828200-174829000	Enhancers	Fetal Heart	heart
43	chr4:174828800-174829200	Enhancers	Gastric	stomach
44	chr4:174829000-174829200	Enhancers	Spleen	Spleen
45	chr4:174829000-174831200	Enhancers	Monocytes-CD14+_RO01746	blood
46	chr4:174829200-174830200	Weak transcription	Gastric	stomach
47	chr4:174829200-174830200	Weak transcription	Spleen	Spleen
48	chr4:174829200-174832400	Enhancers	Primary monocytes fromperipheralblood	blood
49	chr4:174829600-174830400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:174829800-174831800	Enhancers	Primary hematopoietic stem cells short term culture	blood

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