Variant report

Variant	nsv1027771
Chromosome Location	chr4:187361404-187431973
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:187393967-187394511	K562	blood:	n/a	n/a
2	ARID3A	chr4:187394041-187394370	HepG2	liver:	n/a	n/a
3	ATF1	chr4:187421894-187422344	K562	blood:	n/a	n/a
4	ATF1	chr4:187420491-187420916	K562	blood:	n/a	n/a
5	ATF3	chr4:187394371-187394479	GM12878	blood:	n/a	n/a
6	ATF3	chr4:187421950-187422165	K562	blood:	n/a	n/a
7	BACH1	chr4:187392859-187392959	K562	blood:	n/a	n/a
8	BHLHE40	chr4:187362735-187362783	K562	blood:	n/a	n/a
9	BHLHE40	chr4:187422808-187423008	K562	blood:	n/a	n/a
10	BHLHE40	chr4:187421756-187422525	K562	blood:	n/a	n/a
11	CBX3	chr4:187373146-187373490	K562	blood:	n/a	n/a
12	CBX3	chr4:187373144-187373570	K562	blood:	n/a	n/a
13	CBX3	chr4:187421712-187422622	K562	blood:	n/a	n/a
14	CBX3	chr4:187373086-187373652	HCT-116	colon:	n/a	n/a
15	CBX3	chr4:187373072-187373601	HCT-116	colon:	n/a	n/a
16	CBX3	chr4:187411097-187411357	K562	blood:	n/a	n/a
17	CBX3	chr4:187421797-187422410	K562	blood:	n/a	n/a
18	CCNT2	chr4:187421964-187422263	K562	blood:	n/a	n/a
19	CCNT2	chr4:187362847-187363236	K562	blood:	n/a	n/a
20	CEBPB	chr4:187371102-187371494	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
21	CEBPB	chr4:187371090-187371490	ECC-1	luminal epithelium:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
22	CEBPB	chr4:187375483-187375595	HepG2	liver:	n/a	chr4:187375528-187375539
23	CEBPB	chr4:187371127-187371481	IMR90	lung:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
24	CEBPB	chr4:187371124-187371436	Hela-S3	cervix:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
25	CEBPB	chr4:187371144-187371490	HepG2	liver:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
26	CEBPB	chr4:187378231-187378496	HepG2	liver:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
27	CEBPB	chr4:187420609-187420949	K562	blood:	n/a	n/a
28	CEBPB	chr4:187371122-187371471	A549	lung:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
29	CEBPB	chr4:187371179-187371335	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
30	CEBPB	chr4:187379564-187379739	A549	lung:	n/a	n/a
31	CEBPB	chr4:187378227-187378457	IMR90	lung:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
32	CEBPB	chr4:187421769-187422320	K562	blood:	n/a	n/a
33	CEBPB	chr4:187375448-187375609	A549	lung:	n/a	chr4:187375528-187375539
34	CEBPB	chr4:187378200-187378477	A549	lung:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
35	CEBPB	chr4:187371108-187371409	K562	blood:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
36	CEBPB	chr4:187371106-187371462	ECC-1	luminal epithelium:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
37	CEBPB	chr4:187378219-187378507	K562	blood:	n/a	chr4:187378353-187378364 chr4:187378353-187378366
38	CEBPB	chr4:187371126-187371469	H1-hESC	embryonic stem cell:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
39	CEBPB	chr4:187371132-187371388	MCF-7	breast:	n/a	chr4:187371303-187371312 chr4:187371303-187371312 chr4:187371302-187371313 chr4:187371301-187371314 chr4:187371303-187371312
40	CEBPB	chr4:187394195-187394430	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPD	chr4:187362609-187362999	K562	blood:	n/a	n/a
42	CHD2	chr4:187420605-187420961	K562	blood:	n/a	n/a
43	CHD2	chr4:187421895-187422449	K562	blood:	n/a	n/a
44	CREB1	chr4:187421833-187422456	K562	blood:	n/a	n/a
45	CREB1	chr4:187421785-187422476	K562	blood:	n/a	n/a
46	CTCF	chr4:187394160-187394310	HCFaa	heart:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
47	CTCF	chr4:187394140-187394290	AG04450	lung:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
48	CTCF	chr4:187394147-187394322	MCF-7	breast:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
49	CTCF	chr4:187394051-187394382	K562	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
50	CTCF	chr4:187394160-187394310	BE2_C	brain:	n/a	chr4:187394193-187394209 chr4:187394194-187394215

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187407036-187407086	HCPEpiC	choroid plexus:	n/a
2	chr4:187422091-187422141	AG09309	skin:	n/a
3	chr4:187418419-187418469	HCF	heart:	n/a
4	chr4:187404923-187404973	U87	brain:	n/a
5	chr4:187422119-187422169	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:187422005-187422055	GM19239	blood:	n/a
7	chr4:187422091-187422141	NT2-D1	testis:	n/a
8	chr4:187394380-187394430	RPTEC	kidney:	n/a
9	chr4:187422895-187422945	Hepatocyte	liver:	n/a
10	chr4:187426127-187426177	A549	lung:	n/a
11	chr4:187422895-187422945	NT2-D1	testis:	n/a
12	chr4:187422114-187422164	T-47D	breast:	n/a
13	chr4:187426127-187426177	HPAEpiC	pulmonary alveolar:	n/a
14	chr4:187422091-187422141	HEK293	kidney:	embryo
15	chr4:187422341-187422391	CMK	blood:	n/a
16	chr4:187426127-187426177	HCM	heart:	n/a
17	chr4:187422005-187422055	Caco-2	colon:	n/a
18	chr4:187404958-187405008	RPTEC	kidney:	n/a
19	chr4:187422035-187422085	HCF	heart:	n/a
20	chr4:187422119-187422169	HRPEpiC	eye:	n/a
21	chr4:187422035-187422085	AG09319	gingival:	n/a
22	chr4:187422114-187422164	AoSMC	blood vessel:	n/a
23	chr4:187404988-187405038	MCF10A-Er-Src	breast:	n/a
24	chr4:187422341-187422391	Hela-S3	cervix:	n/a
25	chr4:187422341-187422391	SKMC	muscle:	n/a
26	chr4:187422119-187422169	PANC-1	pancreas:	n/a
27	chr4:187422091-187422141	AG09319	gingival:	n/a
28	chr4:187422341-187422391	HepG2	liver:	n/a
29	chr4:187422114-187422164	AG09309	skin:	n/a
30	chr4:187404923-187404973	HEK293	kidney:	embryo
31	chr4:187422895-187422945	HCPEpiC	choroid plexus:	n/a
32	chr4:187422091-187422141	SAEC	small airway:	n/a
33	chr4:187422119-187422169	HEEpiC	esophagus:	n/a
34	chr4:187422895-187422945	HMEC	breast:	n/a
35	chr4:187422119-187422169	NHDF-neo	bronchial:	n/a
36	chr4:187422114-187422164	NH-A	brain:	n/a
37	chr4:187422114-187422164	U87	brain:	n/a
38	chr4:187404923-187404973	AoSMC	blood vessel:	n/a
39	chr4:187404958-187405008	HCM	heart:	n/a
40	chr4:187404958-187405008	NH-A	brain:	n/a
41	chr4:187422005-187422055	U87	brain:	n/a
42	chr4:187394380-187394430	HEEpiC	esophagus:	n/a
43	chr4:187422119-187422169	SK-N-SH	brain:	n/a
44	chr4:187404923-187404973	HAEpiC	amniotic membrane:	n/a
45	chr4:187422114-187422164	HL-60	blood:	n/a
46	chr4:187422119-187422169	HCF	heart:	n/a
47	chr4:187407036-187407086	HUVEC	blood vessel:	n/a
48	chr4:187404923-187404973	BE2_C	brain:	n/a
49	chr4:187422895-187422945	ovcar-3	ovarian:	n/a
50	chr4:187422091-187422141	RPTEC	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:187402656..187405583-chr4:187422037..187423656,2	K562	blood:
2	chr4:187367777..187369317-chr4:187372463..187374481,2	MCF-7	breast:
3	chr4:187363385..187366676-chr4:187368218..187370374,3	K562	blood:
4	chr4:187393992..187394694-chr4:187476207..187476860,2	MCF-7	breast:
5	chr4:187365176..187367106-chr4:187368874..187370492,2	K562	blood:
6	chr4:187363385..187366676-chr4:187368218..187370374,3	K562	blood:
7	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
8	chr4:187363286..187364885-chr4:187368218..187369820,2	K562	blood:
9	chr4:187378015..187379794-chr4:187381538..187383252,2	K562	blood:
10	chr4:187371013..187372540-chr4:187375746..187378339,2	K562	blood:
11	chr4:187425444..187427113-chr4:187432314..187434673,2	K562	blood:
12	chr4:187394722..187395443-chr4:187508309..187509281,2	MCF-7	breast:
13	chr4:187418143..187425298-chr4:187427395..187434877,12	K562	blood:
14	chr4:187394348..187396815-chr4:187456742..187459587,2	K562	blood:
15	chr4:187393785..187394637-chr4:187475328..187475950,2	MCF-7	breast:
16	chr4:187371013..187372540-chr4:187375746..187378339,2	K562	blood:
17	chr4:187365176..187367106-chr4:187368874..187370492,2	K562	blood:
18	chr4:187424618..187426617-chr4:187440828..187442815,2	MCF-7	breast:
19	chr4:187421685..187424267-chr4:187426709..187429265,2	MCF-7	breast:
20	chr4:187414357..187416175-chr4:187420876..187423477,2	MCF-7	breast:
21	chr4:187363286..187364885-chr4:187368218..187369820,2	K562	blood:
22	chr4:187367777..187369317-chr4:187372463..187374481,2	MCF-7	breast:
23	chr4:187394154..187394722-chr4:187508267..187509221,2	K562	blood:
24	chr4:187400808..187402522-chr4:187420720..187422452,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTNR1A-1	chr4:187421999-187422212	NONHSAT099658
2	lnc-FAT1-5	chr4:187409184-187409778	predAs_chen_AV690772_1
3	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1
4	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1

Variant related genes	Relation type
F11-AS1	TF binding region
RNU6-1055P	TF binding region
F11-AS1	CpG island
RNU6-1055P	CpG island
ENSG00000212387	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000168412	chromatin interactions
ENSG00000272297	chromatin interactions

Extended variants
information (count: 3021 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:3021 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528420776	chr4:187362640-187362641	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs73020714	chr4:187362659-187362660	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114379361	chr4:187362681-187362682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs74991689	chr4:187362856-187362857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs564381687	chr4:187362873-187362874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528403888	chr4:187362894-187362895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs138674890	chr4:187362921-187362922	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs536040887	chr4:187362975-187362976	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs555733350	chr4:187362978-187362979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs371129650	chr4:187363063-187363064	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs35560747	chr4:187363074-187363075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs535043039	chr4:187363090-187363091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs74821604	chr4:187363106-187363107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs79214965	chr4:187363112-187363113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs536700363	chr4:187363116-187363117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs556647463	chr4:187363168-187363169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs535508753	chr4:187363213-187363214	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187802293	chr4:187363219-187363220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62348864	chr4:187363230-187363231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs559310760	chr4:187363260-187363261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs562337230	chr4:187363274-187363275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs573075245	chr4:187363294-187363295	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs34424049	chr4:187363305-187363306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs79786758	chr4:187363313-187363314	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs192431331	chr4:187363325-187363326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs533377172	chr4:187363337-187363338	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs183258043	chr4:187363392-187363393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs577044139	chr4:187365811-187365812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs572920457	chr4:187365819-187365820	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2084729	chr4:187365864-187365865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs145963581	chr4:187365896-187365897	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs11723706	chr4:187365904-187365905	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs575742189	chr4:187365925-187365926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190989796	chr4:187365929-187365930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs34103989	chr4:187365934-187365935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs561566087	chr4:187365941-187365942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs11132396	chr4:187365960-187365961	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
38	rs115025144	chr4:187365985-187365986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs560143434	chr4:187365989-187365990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs532155542	chr4:187365991-187365992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs373579734	chr4:187365993-187365994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs182383715	chr4:187365998-187365999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs186807678	chr4:187366087-187366088	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs142631221	chr4:187366093-187366094	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs113219201	chr4:187366157-187366158	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs72714133	chr4:187366158-187366159	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs533814811	chr4:187366163-187366164	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs6853097	chr4:187366173-187366174	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs190139325	chr4:187366182-187366183	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs147610455	chr4:187366198-187366199	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:306 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187362600-187363400	Enhancers	K562	blood
2	chr4:187365800-187366000	Enhancers	Rectal Mucosa Donor 31	rectum
3	chr4:187366000-187366800	Active TSS	Rectal Mucosa Donor 31	rectum
4	chr4:187366200-187366800	Active TSS	Rectal Mucosa Donor 29	rectum
5	chr4:187366800-187367000	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr4:187369800-187371000	Weak transcription	Pancreas	Pancrea
7	chr4:187372400-187375600	ZNF genes & repeats	Liver	Liver
8	chr4:187372800-187374400	ZNF genes & repeats	Adipose Nuclei	Adipose
9	chr4:187373200-187374400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr4:187374400-187382200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:187375200-187375400	ZNF genes & repeats	K562	blood
12	chr4:187375400-187392600	Weak transcription	K562	blood
13	chr4:187375800-187376400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
14	chr4:187378600-187381400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
15	chr4:187381400-187382600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr4:187381800-187383000	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:187382000-187382400	Enhancers	Fetal Lung	lung
18	chr4:187382200-187383000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:187388600-187388800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr4:187392600-187392800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:187392600-187392800	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr4:187392600-187393000	Enhancers	Fetal Intestine Small	intestine
23	chr4:187392600-187393000	Enhancers	K562	blood
24	chr4:187392800-187393000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:187392800-187394200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:187392800-187394200	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr4:187393000-187395200	Weak transcription	K562	blood
28	chr4:187393200-187394200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr4:187393800-187394800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr4:187393800-187394800	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr4:187394000-187394400	Enhancers	H9 Cell Line	embryonic stem cell
32	chr4:187394000-187394600	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:187394000-187394800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:187394200-187394400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr4:187394200-187394400	Enhancers	iPS-20b Cell Line	embryonic stem cell
36	chr4:187394200-187394400	Enhancers	Rectal Mucosa Donor 31	rectum
37	chr4:187394200-187394400	Bivalent Enhancer	HSMMtube	muscle
38	chr4:187394200-187394800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr4:187394200-187395800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
40	chr4:187394400-187394600	Enhancers	H1 Cell Line	embryonic stem cell
41	chr4:187394400-187394800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:187394800-187395000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr4:187395000-187395400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
44	chr4:187395200-187395400	Enhancers	H1 Cell Line	embryonic stem cell
45	chr4:187395200-187395400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr4:187395200-187395400	Enhancers	K562	blood
47	chr4:187395400-187403600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr4:187395400-187413600	Weak transcription	K562	blood
49	chr4:187395600-187395800	Enhancers	Rectal Mucosa Donor 31	rectum
50	chr4:187395600-187396000	Enhancers	Sigmoid Colon	Sigmoid Colon

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