Variant report

Variant	nsv881147
Chromosome Location	chr4:188690307-188938468
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1017)
CpG islands
(count:2201)
Chromatin interactive
region (count:11)
LncRNA
region (count:24)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1017 , 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	chr4:188735920-188736251	K562	blood:	n/a	n/a
2	ATF2	chr4:188926433-188926974	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr4:188916749-188917170	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr4:188915055-188915396	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr4:188850148-188850549	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr4:188917657-188917951	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr4:188916764-188917071	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:188916526-188917174	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr4:188936288-188936488	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr4:188896133-188896354	GM12878	blood:	n/a	chr4:188896272-188896283
11	BHLHE40	chr4:188923505-188923772	K562	blood:	n/a	n/a
12	BHLHE40	chr4:188929455-188929456	HepG2	liver:	n/a	n/a
13	BRCA1	chr4:188909297-188909449	Hela-S3	cervix:	n/a	n/a
14	BRCA1	chr4:188923496-188923905	Hela-S3	cervix:	n/a	n/a
15	BRCA1	chr4:188917816-188917938	H1-hESC	embryonic stem cell:	n/a	n/a
16	BRCA1	chr4:188936021-188936859	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr4:188829199-188829608	IMR90	lung:	n/a	n/a
18	CEBPB	chr4:188839840-188839977	IMR90	lung:	n/a	n/a
19	CEBPB	chr4:188873512-188873759	A549	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
20	CEBPB	chr4:188735771-188736121	A549	lung:	n/a	n/a
21	CEBPB	chr4:188936287-188936507	ECC-1	luminal epithelium:	n/a	n/a
22	CEBPB	chr4:188735860-188736134	MCF-7	breast:	n/a	n/a
23	CEBPB	chr4:188728718-188728984	HepG2	liver:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
24	CEBPB	chr4:188936268-188936828	A549	lung:	n/a	n/a
25	CEBPB	chr4:188690662-188690861	H1-hESC	embryonic stem cell:	n/a	chr4:188690750-188690761
26	CEBPB	chr4:188916852-188917179	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr4:188735832-188736143	HepG2	liver:	n/a	n/a
28	CEBPB	chr4:188936262-188936771	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr4:188923470-188923960	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr4:188936139-188936670	A549	lung:	n/a	n/a
31	CEBPB	chr4:188929371-188929912	A549	lung:	n/a	n/a
32	CEBPB	chr4:188769070-188769319	IMR90	lung:	n/a	chr4:188769178-188769189
33	CEBPB	chr4:188690622-188690921	IMR90	lung:	n/a	chr4:188690750-188690761
34	CEBPB	chr4:188929383-188929936	A549	lung:	n/a	n/a
35	CEBPB	chr4:188929463-188929848	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:188936053-188937221	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr4:188873586-188873809	IMR90	lung:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
38	CEBPB	chr4:188898167-188898421	HepG2	liver:	n/a	chr4:188898278-188898291 chr4:188898279-188898290
39	CEBPB	chr4:188690722-188690811	A549	lung:	n/a	chr4:188690750-188690761
40	CEBPB	chr4:188752270-188752506	HepG2	liver:	n/a	chr4:188752367-188752378
41	CEBPB	chr4:188769054-188769316	HepG2	liver:	n/a	chr4:188769178-188769189
42	CEBPB	chr4:188728777-188728937	A549	lung:	n/a	chr4:188728839-188728852 chr4:188728839-188728850 chr4:188728841-188728852
43	CEBPB	chr4:188875669-188875935	HepG2	liver:	n/a	chr4:188875825-188875836
44	CEBPB	chr4:188690637-188690931	HepG2	liver:	n/a	chr4:188690750-188690761
45	CEBPB	chr4:188735766-188736151	K562	blood:	n/a	n/a
46	CEBPB	chr4:188929269-188929961	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr4:188735760-188736147	K562	blood:	n/a	n/a
48	CEBPB	chr4:188735851-188736097	H1-hESC	embryonic stem cell:	n/a	n/a
49	CEBPB	chr4:188873517-188873689	Hela-S3	cervix:	n/a	chr4:188873674-188873685 chr4:188873635-188873646
50	CEBPB	chr4:188875779-188875862	H1-hESC	embryonic stem cell:	n/a	chr4:188875825-188875836

(count:2201 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188843522-188843572	GM19239	blood:	n/a
2	chr4:188918072-188918122	HEEpiC	esophagus:	n/a
3	chr4:188916865-188916915	GM06990	blood:	n/a
4	chr4:188916814-188916864	Hepatocyte	liver:	n/a
5	chr4:188736336-188736386	ECC-1	luminal epithelium:	n/a
6	chr4:188843522-188843572	GM19239	blood:	n/a
7	chr4:188918072-188918122	HEEpiC	esophagus:	n/a
8	chr4:188916865-188916915	GM06990	blood:	n/a
9	chr4:188916814-188916864	Hepatocyte	liver:	n/a
10	chr4:188736336-188736386	ECC-1	luminal epithelium:	n/a
11	chr4:188916814-188916864	HEEpiC	esophagus:	n/a
12	chr4:188843522-188843572	MCF10A-Er-Src	breast:	n/a
13	chr4:188858709-188858759	U87	brain:	n/a
14	chr4:188917251-188917301	GM12892	blood:	n/a
15	chr4:188895421-188895471	AoSMC	blood vessel:	n/a
16	chr4:188916496-188916546	HL-60	blood:	n/a
17	chr4:188916726-188916776	HepG2	liver:	n/a
18	chr4:188858709-188858759	HepG2	liver:	n/a
19	chr4:188915407-188915457	IMR90	lung:	fetal
20	chr4:188916581-188916631	PFSK-1	brain:	n/a
21	chr4:188891490-188891540	H1-hESC	embryonic stem cell:	embryo
22	chr4:188736336-188736386	HRPEpiC	eye:	n/a
23	chr4:188924717-188924767	T-47D	breast:	n/a
24	chr4:188924612-188924662	K562	blood:	n/a
25	chr4:188916724-188916774	HNPCEpiC	eye:	n/a
26	chr4:188916726-188916776	HRE	kidney:	n/a
27	chr4:188917173-188917223	BE2_C	brain:	n/a
28	chr4:188891490-188891540	HRPEpiC	eye:	n/a
29	chr4:188918931-188918981	SK-N-SH_RA	brain:	n/a
30	chr4:188824073-188824123	NT2-D1	testis:	n/a
31	chr4:188895421-188895471	ProgFib	skin:	n/a
32	chr4:188895390-188895440	SK-N-SH_RA	brain:	n/a
33	chr4:188916581-188916631	HUVEC	blood vessel:	n/a
34	chr4:188895421-188895471	GM12891	blood:	n/a
35	chr4:188824073-188824123	HRPEpiC	eye:	n/a
36	chr4:188736112-188736162	NHBE	bronchial:	n/a
37	chr4:188913931-188913981	HL-60	blood:	n/a
38	chr4:188858971-188859021	HAEpiC	amniotic membrane:	n/a
39	chr4:188895407-188895457	BJ	skin:	n/a
40	chr4:188916867-188916917	A549	lung:	n/a
41	chr4:188916943-188916993	PFSK-1	brain:	n/a
42	chr4:188891490-188891540	HCPEpiC	choroid plexus:	n/a
43	chr4:188829287-188829337	AoSMC	blood vessel:	n/a
44	chr4:188916581-188916631	HMEC	breast:	n/a
45	chr4:188858709-188858759	GM19239	blood:	n/a
46	chr4:188918072-188918122	MCF-7	breast:	n/a
47	chr4:188736172-188736222	HUVEC	blood vessel:	n/a
48	chr4:188736172-188736222	PFSK-1	brain:	n/a
49	chr4:188916668-188916718	HCM	heart:	n/a
50	chr4:188916496-188916546	ProgFib	skin:	n/a

(count:11 , 50 per page) page: 1

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

(count:24 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099726
2	lnc-TRIML2-2	chr4:188866817-188867016	NONHSAT099725
3	lnc-ZFP42-8	chr4:188808721-188808809	l_2822_chr4:188790794-188818331_testes
4	lnc-ZFP42-1	chr4:188735823-188736246	XLOC_003831
5	lnc-ZFP42-8	chr4:188790795-188791294	l_2822_chr4:188790794-188818331_testes
6	lnc-TRIML2-2	chr4:188881466-188881649	NONHSAT099725
7	lnc-TRIML2-2	chr4:188913836-188914027	NONHSAT099725
8	lnc-TRIML2-9	chr4:188771634-188772347	l_2820_chr4:188691027-188804581_testes
9	lnc-ZFP42-8	chr4:188818285-188818331	l_2822_chr4:188790794-188818331_testes
10	lnc-TRIML2-2	chr4:188908697-188908733	NONHSAT099726
11	lnc-TRIML2-2	chr4:188881466-188881648	XLOC_004222
12	lnc-ZFP42-8	chr4:188863112-188863571	l_2822_chr4:188790794-188818331_testes
13	lnc-TRIML2-9	chr4:188771044-188771493	l_2820_chr4:188691027-188804581_testes
14	lnc-TRIML2-2	chr4:188881751-188881835	NONHSAT099725
15	lnc-ZFP42-1	chr4:188735822-188736272	NONHSAT099722
16	lnc-TRIML2-2	chr4:188866788-188867016	XLOC_004222
17	lnc-ZFP42-1	chr4:188789601-188789707	XLOC_003831
18	lnc-ZFP42-9	chr4:188771634-188772147	l_2821_chr4:188771633-188780051_testes
19	lnc-ZFP42-8	chr4:188869892-188870239	l_2822_chr4:188790794-188818331_testes
20	lnc-TRIML2-9	chr4:188804358-188804581	l_2820_chr4:188691027-188804581_testes
21	lnc-TRIML2-9	chr4:188691028-188691351	l_2820_chr4:188691027-188804581_testes
22	lnc-ZFP42-9	chr4:188779825-188780051	l_2821_chr4:188771633-188780051_testes
23	lnc-TRIML2-9	chr4:188716229-188716412	l_2820_chr4:188691027-188804581_testes
24	lnc-ZFP42-1	chr4:188789600-188789707	NONHSAT099722

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: 5261 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:5261 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs150344567	chr4:188691042-188691043	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs544499198	chr4:188691069-188691070	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs554528749	chr4:188691093-188691094	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs574616412	chr4:188691111-188691112	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs533621711	chr4:188691123-188691124	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs138059176	chr4:188691126-188691127	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs545249937	chr4:188691127-188691128	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs545065157	chr4:188691132-188691133	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs368693344	chr4:188691151-188691152	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs530763900	chr4:188691155-188691156	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs551264114	chr4:188691160-188691161	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs567851406	chr4:188691166-188691167	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs533169404	chr4:188691175-188691176	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs113844260	chr4:188691180-188691181	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs185783902	chr4:188691181-188691182	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs367687971	chr4:188691185-188691186	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs552256576	chr4:188691186-188691187	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs189729802	chr4:188691188-188691189	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs554895748	chr4:188691190-188691191	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs574622989	chr4:188691191-188691192	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs534026121	chr4:188691194-188691195	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs553564902	chr4:188691195-188691196	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs576598660	chr4:188691196-188691197	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs575742465	chr4:188691200-188691201	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs542634204	chr4:188691201-188691202	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs564995462	chr4:188691202-188691203	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs575632256	chr4:188691208-188691209	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs10003564	chr4:188691211-188691212	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs181288262	chr4:188691222-188691223	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs528593160	chr4:188691246-188691247	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs140912496	chr4:188691249-188691250	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs368621040	chr4:188691250-188691251	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs70938665	chr4:188691257-188691258	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs540678893	chr4:188691267-188691268	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs186970567	chr4:188691275-188691276	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs111964803	chr4:188691285-188691286	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs191646804	chr4:188691288-188691289	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs112703318	chr4:188691289-188691290	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs183280539	chr4:188691290-188691291	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs112603344	chr4:188691299-188691300	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs568013807	chr4:188691306-188691307	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs533855101	chr4:188691307-188691308	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs566779473	chr4:188691329-188691330	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs533787653	chr4:188691332-188691333	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs10014263	chr4:188691337-188691338	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs558669767	chr4:188691338-188691339	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs575625121	chr4:188691339-188691340	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs527388078	chr4:188691340-188691341	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs189809114	chr4:188691345-188691346	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs561149154	chr4:188691349-188691350	Inactive region	lncRNA	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:590 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188691400-188692200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr4:188691400-188692200	Enhancers	iPS-15b Cell Line	embryonic stem cell
3	chr4:188691600-188692200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chr4:188691800-188692400	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr4:188692200-188693400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr4:188693600-188693800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:188699000-188699400	Enhancers	H1 Cell Line	embryonic stem cell
8	chr4:188699000-188699800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr4:188699400-188699800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:188699400-188703600	Weak transcription	H1 Cell Line	embryonic stem cell
11	chr4:188699800-188710400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr4:188700400-188701400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:188700400-188701800	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr4:188701000-188701800	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr4:188701200-188701600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:188701200-188701600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr4:188703600-188703800	Enhancers	H1 Cell Line	embryonic stem cell
18	chr4:188703600-188704000	Enhancers	Fetal Brain Male	brain
19	chr4:188703800-188704400	Enhancers	A549	lung
20	chr4:188706000-188706200	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr4:188706000-188706400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr4:188706200-188707000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr4:188710400-188711400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:188711400-188714600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:188717600-188717800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:188718800-188719600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
27	chr4:188719200-188719600	Enhancers	iPS-20b Cell Line	embryonic stem cell
28	chr4:188719200-188720200	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:188719200-188720200	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr4:188719400-188719800	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr4:188719400-188719800	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr4:188719400-188719800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:188719400-188719800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr4:188719400-188720200	Enhancers	H1 Cell Line	embryonic stem cell
35	chr4:188719600-188719800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
36	chr4:188719600-188719800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr4:188719600-188720000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
38	chr4:188719600-188720600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr4:188719600-188721200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr4:188721000-188721200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr4:188730600-188730800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:188730800-188736000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr4:188732800-188733200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr4:188735000-188735800	Enhancers	Pancreas	Pancrea
45	chr4:188735800-188736200	Active TSS	Brain Substantia Nigra	brain
46	chr4:188735800-188736200	ZNF genes & repeats	Placenta	Placenta
47	chr4:188735800-188736400	Active TSS	Brain Germinal Matrix	brain
48	chr4:188735800-188736400	Active TSS	Brain Hippocampus Middle	brain
49	chr4:188735800-188736600	Active TSS	Fetal Muscle Trunk	muscle
50	chr4:188735800-188736600	Active TSS	Pancreas	Pancrea

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