Variant report

Variant	nsv596456
Chromosome Location	chr4:188786838-189016936
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1038)
CpG islands
(count:2810)
Chromatin interactive
region (count:16)
LncRNA
region (count:16)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1038 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr4:189002649-189002842	K562	blood:	n/a	n/a
2	ATF2	chr4:188916764-188917071	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:188915055-188915396	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:188953244-188953886	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:188916749-188917170	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:188850148-188850549	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:188917657-188917951	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr4:188926433-188926974	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:188964645-188964695	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr4:188936288-188936488	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:188916526-188917174	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr4:188952989-188953975	H1-hESC	embryonic stem cell:	n/a	n/a
13	BATF	chr4:188896133-188896354	GM12878	blood:	n/a	chr4:188896272-188896283
14	BATF	chr4:188989551-188989709	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:188953306-188953649	H1-hESC	embryonic stem cell:	n/a	n/a
16	BHLHE40	chr4:188923505-188923772	K562	blood:	n/a	n/a
17	BHLHE40	chr4:188929455-188929456	HepG2	liver:	n/a	n/a
18	BRCA1	chr4:188936021-188936859	Hela-S3	cervix:	n/a	n/a
19	BRCA1	chr4:188923496-188923905	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr4:188909297-188909449	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr4:188917816-188917938	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:188898167-188898421	HepG2	liver:	n/a	chr4:188898278-188898291 chr4:188898279-188898290
23	CEBPB	chr4:188936268-188936828	A549	lung:	n/a	n/a
24	CEBPB	chr4:188972434-188972808	A549	lung:	n/a	chr4:188972610-188972621
25	CEBPB	chr4:188873544-188873823	HepG2	liver:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
26	CEBPB	chr4:188839840-188839977	IMR90	lung:	n/a	n/a
27	CEBPB	chr4:188873512-188873759	A549	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
28	CEBPB	chr4:188875669-188875935	HepG2	liver:	n/a	chr4:188875825-188875836
29	CEBPB	chr4:188875779-188875862	H1-hESC	embryonic stem cell:	n/a	chr4:188875825-188875836
30	CEBPB	chr4:188916852-188917179	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chr4:188972503-188972708	K562	blood:	n/a	chr4:188972610-188972621
32	CEBPB	chr4:188873586-188873809	IMR90	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
33	CEBPB	chr4:188972436-188972883	HepG2	liver:	n/a	chr4:188972610-188972621
34	CEBPB	chr4:188873517-188873689	Hela-S3	cervix:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
35	CEBPB	chr4:188829199-188829608	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:188936053-188937221	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:188929269-188929961	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr4:189006896-189007140	IMR90	lung:	n/a	chr4:189007012-189007023
39	CEBPB	chr4:189002633-189002799	K562	blood:	n/a	n/a
40	CEBPB	chr4:188936262-188936771	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr4:188972564-188972701	H1-hESC	embryonic stem cell:	n/a	chr4:188972610-188972621
42	CEBPB	chr4:188929463-188929848	IMR90	lung:	n/a	n/a
43	CEBPB	chr4:188923470-188923960	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr4:189006901-189007158	HepG2	liver:	n/a	chr4:189007012-189007023
45	CEBPB	chr4:188936287-188936507	ECC-1	luminal epithelium:	n/a	n/a
46	CEBPB	chr4:188929383-188929936	A549	lung:	n/a	n/a
47	CEBPB	chr4:188936139-188936670	A549	lung:	n/a	n/a
48	CEBPB	chr4:188972446-188972753	IMR90	lung:	n/a	chr4:188972610-188972621
49	CEBPB	chr4:188929371-188929912	A549	lung:	n/a	n/a
50	CHD1	chr4:188919719-188919955	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188917856-188917906	HCT-116	colon:	n/a
2	chr4:188916496-188916546	GM19239	blood:	n/a
3	chr4:188953677-188953727	HRCEpiC	kidney:	n/a
4	chr4:188916865-188916915	NHDF-neo	bronchial:	n/a
5	chr4:188917856-188917906	HCT-116	colon:	n/a
6	chr4:188916496-188916546	GM19239	blood:	n/a
7	chr4:188953677-188953727	HRCEpiC	kidney:	n/a
8	chr4:188916865-188916915	NHDF-neo	bronchial:	n/a
9	chr4:188843522-188843572	AG04450	lung:	fetal
10	chr4:188952355-188952405	PANC-1	pancreas:	n/a
11	chr4:188952355-188952405	AoSMC	blood vessel:	n/a
12	chr4:188916496-188916546	SAEC	small airway:	n/a
13	chr4:188891490-188891540	NH-A	brain:	n/a
14	chr4:188891490-188891540	Jurkat	blood:	n/a
15	chr4:188858971-188859021	T-47D	breast:	n/a
16	chr4:188916865-188916915	NHBE	bronchial:	n/a
17	chr4:188953092-188953142	BJ	skin:	n/a
18	chr4:188953092-188953142	NH-A	brain:	n/a
19	chr4:188917856-188917906	SKMC	muscle:	n/a
20	chr4:188953527-188953577	Hela-S3	cervix:	n/a
21	chr4:188963430-188963480	H1-hESC	embryonic stem cell:	embryo
22	chr4:188924612-188924662	ProgFib	skin:	n/a
23	chr4:188824073-188824123	NB4	blood:	n/a
24	chr4:188916724-188916774	NT2-D1	testis:	n/a
25	chr4:188916724-188916774	MCF10A-Er-Src	breast:	n/a
26	chr4:188953178-188953228	AG09319	gingival:	n/a
27	chr4:188916724-188916774	CMK	blood:	n/a
28	chr4:188917251-188917301	PrEC	prostate:	n/a
29	chr4:189012434-189012484	HL-60	blood:	n/a
30	chr4:188963260-188963310	HL-60	blood:	n/a
31	chr4:188843522-188843572	SK-N-SH_RA	brain:	n/a
32	chr4:188924717-188924767	GM12892	blood:	n/a
33	chr4:188858709-188858759	SKMC	muscle:	n/a
34	chr4:188916668-188916718	AG09309	skin:	n/a
35	chr4:188916668-188916718	Hepatocyte	liver:	n/a
36	chr4:188916724-188916774	Caco-2	colon:	n/a
37	chr4:188953586-188953636	SK-N-MC	brain:	n/a
38	chr4:188953969-188954019	NHBE	bronchial:	n/a
39	chr4:188895421-188895471	HEEpiC	esophagus:	n/a
40	chr4:188963260-188963310	HCPEpiC	choroid plexus:	n/a
41	chr4:188953126-188953176	NB4	blood:	n/a
42	chr4:188915407-188915457	SK-N-SH_RA	brain:	n/a
43	chr4:188953178-188953228	LNCaP	prostate:	n/a
44	chr4:188924752-188924802	T-47D	breast:	n/a
45	chr4:188916581-188916631	IMR90	lung:	fetal
46	chr4:188963260-188963310	GM12878	blood:	n/a
47	chr4:188916867-188916917	Caco-2	colon:	n/a
48	chr4:189012434-189012484	HIPEpiC	eye:	n/a
49	chr4:188916724-188916774	HRPEpiC	eye:	n/a
50	chr4:188916709-188916759	GM12891	blood:	n/a

(count:16 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
2	chr4:188936272..188938284-chr4:188943091..188945323,2	MCF-7	breast:
3	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
4	chr4:188914670..188915671-chr4:189167438..189168869,4	MCF-7	breast:
5	chr4:188959730..188961356-chr4:188968354..188971076,2	MCF-7	breast:
6	chr4:188807826..188808346-chr6:74078319..74078839,2	MCF-7	breast:
7	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
8	chr4:188914704..188915349-chr4:188923417..188923946,2	MCF-7	breast:
9	chr4:188955745..188958212-chr4:188967134..188969834,2	K562	blood:
10	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
11	chr4:188955745..188958212-chr4:188967134..188969834,2	K562	blood:
12	chr4:188867496..188869174-chr4:188872429..188875179,2	MCF-7	breast:
13	chr4:188908545..188911160-chr4:188914079..188916849,2	K562	blood:
14	chr4:188959730..188961356-chr4:188968354..188971076,2	MCF-7	breast:
15	chr4:188914697..188915636-chr4:189293778..189294511,3	MCF-7	breast:
16	chr4:188914709..188915626-chr4:189293756..189294718,5	MCF-7	breast:

(count:16 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
2	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
3	lnc-TRIML2-2	chr4:188881466-188881648	XLOC_004222
4	lnc-ZFP42-8	chr4:188818285-188818331	l_2822_chr4:188790794-188818331_testes
5	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722
6	lnc-TRIML2-2	chr4:188881466-188881649	NONHSAT099725
7	lnc-TRIML2-2	chr4:188866817-188867016	NONHSAT099725
8	lnc-TRIML2-9	chr4:188804358-188804581	l_2820_chr4:188691027-188804581_testes
9	lnc-ZFP42-8	chr4:188808721-188808809	l_2822_chr4:188790794-188818331_testes
10	lnc-TRIML2-2	chr4:188908697-188908733	NONHSAT099726
11	lnc-TRIML2-2	chr4:188881751-188881835	NONHSAT099725
12	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099726
13	lnc-ZFP42-8	chr4:188863112-188863571	l_2822_chr4:188790794-188818331_testes
14	lnc-TRIML2-2	chr4:188866788-188867016	XLOC_004222
15	lnc-ZFP42-8	chr4:188869892-188870239	l_2822_chr4:188790794-188818331_testes
16	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099725

No data

Variant related genes	Relation type
ZFP42	TF binding region
ENSG00000213331	TF binding region
ZFP42	CpG island
ENSG00000213331	CpG island

Extended variants
information (count: 6096 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:6096 , 50 per page) page: 1 2 3 4 5 6 7 ... 122

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554905420	chr4:188787615-188787616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs575221495	chr4:188787631-188787632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534461829	chr4:188787660-188787661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs554428519	chr4:188787725-188787726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs577491890	chr4:188787759-188787760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs78119122	chr4:188787784-188787785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs573340924	chr4:188787792-188787793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs59899586	chr4:188787818-188787819	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs541462657	chr4:188787822-188787823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6839253	chr4:188787854-188787855	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs184051540	chr4:188787859-188787860	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs574495506	chr4:188787861-188787862	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189477659	chr4:188787893-188787894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140232899	chr4:188787931-188787932	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs6839450	chr4:188787949-188787950	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs72714670	chr4:188787986-188787987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs552689208	chr4:188788010-188788011	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569257173	chr4:188788047-188788048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs538298980	chr4:188788114-188788115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74511300	chr4:188788127-188788128	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182116044	chr4:188788150-188788151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs548309150	chr4:188788226-188788227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs73026068	chr4:188788329-188788330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534526279	chr4:188788376-188788377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs554489818	chr4:188788408-188788409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577553236	chr4:188788448-188788449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs539641837	chr4:188788471-188788472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs12643825	chr4:188788485-188788486	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs576063668	chr4:188788492-188788493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs573349010	chr4:188788528-188788529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs79867737	chr4:188788681-188788682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs561365750	chr4:188788688-188788689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571683548	chr4:188788707-188788708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs540971051	chr4:188788729-188788730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs75897083	chr4:188788732-188788733	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs564039159	chr4:188788742-188788743	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs76180764	chr4:188788764-188788765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369334838	chr4:188788841-188788842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs140712571	chr4:188788890-188788891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs28630493	chr4:188788896-188788897	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs145900931	chr4:188788906-188788907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs568501401	chr4:188788927-188788928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527676586	chr4:188788992-188788993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs548155417	chr4:188789018-188789019	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186720044	chr4:188789084-188789085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs369067962	chr4:188789086-188789087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs540084338	chr4:188789126-188789127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs138374412	chr4:188789150-188789151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs546527328	chr4:188789181-188789182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs141358334	chr4:188789218-188789219	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
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
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
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Cognitive impairment	21505072	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Tetralogy of Fallot	22912587	CNVD

Chromatin state (count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188787600-188787800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:188787800-188788400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:188788400-188789400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr4:188801600-188803200	Enhancers	Fetal Lung	lung
5	chr4:188802000-188802800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr4:188802800-188804600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:188803000-188803200	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr4:188803400-188804400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
9	chr4:188804200-188804400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:188804200-188804600	Enhancers	H1 Cell Line	embryonic stem cell
11	chr4:188804200-188805000	Enhancers	H9 Cell Line	embryonic stem cell
12	chr4:188804200-188805200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:188804200-188805200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr4:188804200-188805600	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr4:188804400-188805000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:188804400-188805400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr4:188804400-188805800	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr4:188804400-188805800	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr4:188804400-188805800	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr4:188804600-188805200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:188804600-188805200	Enhancers	iPS-15b Cell Line	embryonic stem cell
22	chr4:188804600-188805800	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr4:188804800-188805400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr4:188804800-188805400	Enhancers	Placenta Amnion	Placenta Amnion
25	chr4:188804800-188805800	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr4:188805000-188805400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:188805400-188805800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr4:188805800-188806200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr4:188810400-188810600	Bivalent Enhancer	Fetal Brain Male	brain
30	chr4:188811400-188812200	Enhancers	Fetal Muscle Trunk	muscle
31	chr4:188822600-188823200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr4:188823800-188824600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
33	chr4:188824600-188825000	Enhancers	NH-A	brain
34	chr4:188824600-188825200	Enhancers	Rectal Smooth Muscle	rectum
35	chr4:188824600-188828800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:188825000-188829600	Weak transcription	NH-A	brain
37	chr4:188828200-188830200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr4:188828800-188829000	Enhancers	Osteobl	bone
39	chr4:188828800-188829400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
40	chr4:188828800-188830000	Enhancers	Fetal Muscle Leg	muscle
41	chr4:188828800-188830000	Enhancers	Fetal Stomach	stomach
42	chr4:188829000-188829400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr4:188829000-188829400	Flanking Active TSS	Osteobl	bone
44	chr4:188829000-188829600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr4:188829000-188829600	Enhancers	Aorta	Aorta
46	chr4:188829000-188829600	Enhancers	Fetal Lung	lung
47	chr4:188829000-188829800	Enhancers	Ovary	ovary
48	chr4:188829000-188830000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr4:188829000-188830000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr4:188829000-188830000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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