Variant report

Variant	nsv1015939
Chromosome Location	chr4:187388958-187454620
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:468)
CpG islands
(count:854)
Chromatin interactive
region (count:26)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:468 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

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	chr4:187421950-187422165	K562	blood:	n/a	n/a
6	ATF3	chr4:187394371-187394479	GM12878	blood:	n/a	n/a
7	BACH1	chr4:187392859-187392959	K562	blood:	n/a	n/a
8	BHLHE40	chr4:187442068-187442244	K562	blood:	n/a	n/a
9	BHLHE40	chr4:187421756-187422525	K562	blood:	n/a	n/a
10	BHLHE40	chr4:187422808-187423008	K562	blood:	n/a	n/a
11	CBX3	chr4:187421797-187422410	K562	blood:	n/a	n/a
12	CBX3	chr4:187411097-187411357	K562	blood:	n/a	n/a
13	CBX3	chr4:187421712-187422622	K562	blood:	n/a	n/a
14	CCNT2	chr4:187421964-187422263	K562	blood:	n/a	n/a
15	CEBPB	chr4:187420609-187420949	K562	blood:	n/a	n/a
16	CEBPB	chr4:187432537-187432726	K562	blood:	n/a	chr4:187432667-187432678
17	CEBPB	chr4:187421769-187422320	K562	blood:	n/a	n/a
18	CEBPB	chr4:187432638-187432777	HepG2	liver:	n/a	chr4:187432667-187432678
19	CEBPB	chr4:187394195-187394430	H1-hESC	embryonic stem cell:	n/a	n/a
20	CHD2	chr4:187421895-187422449	K562	blood:	n/a	n/a
21	CHD2	chr4:187420605-187420961	K562	blood:	n/a	n/a
22	CREB1	chr4:187421833-187422456	K562	blood:	n/a	n/a
23	CREB1	chr4:187421785-187422476	K562	blood:	n/a	n/a
24	CTCF	chr4:187394140-187394290	HMF	breast:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
25	CTCF	chr4:187394120-187394270	AG10803	skin:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
26	CTCF	chr4:187394140-187394290	HVMF	connective:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
27	CTCF	chr4:187394055-187394544	K562	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
28	CTCF	chr4:187409005-187409051	Kidney_OC	kidney:	n/a	n/a
29	CTCF	chr4:187394140-187394290	HPAF	blood vessel:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
30	CTCF	chr4:187394280-187394430	A549	lung:	n/a	n/a
31	CTCF	chr4:187394120-187394270	GM12872	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
32	CTCF	chr4:187394120-187394270	MCF-7	breast:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
33	CTCF	chr4:187394096-187394289	Lung_OC	lung:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
34	CTCF	chr4:187394420-187394570	NHEK	skin:	n/a	n/a
35	CTCF	chr4:187394180-187394330	GM12864	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
36	CTCF	chr4:187394260-187394410	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:187393720-187393870	HEEpiC	esophagus:	n/a	n/a
38	CTCF	chr4:187406860-187407010	AG04450	lung:	n/a	chr4:187406975-187406984 chr4:187406974-187406987 chr4:187406971-187406984 chr4:187406969-187406987
39	CTCF	chr4:187394080-187394230	GM06990	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
40	CTCF	chr4:187394140-187394290	HMEC	breast:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
41	CTCF	chr4:187394160-187394310	HVMF	connective:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
42	CTCF	chr4:187394141-187394458	Gliobla	brain:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
43	CTCF	chr4:187394100-187394250	HCPEpiC	choroid plexus:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
44	CTCF	chr4:187430660-187430698	GM20000	blood:	n/a	n/a
45	CTCF	chr4:187394126-187394306	GM12878	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
46	CTCF	chr4:187394160-187394310	NHLF	lung:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
47	CTCF	chr4:187394147-187394322	MCF-7	breast:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
48	CTCF	chr4:187394160-187394310	HRE	kidney:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
49	CTCF	chr4:187394084-187394317	Hela-S3	cervix:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
50	CTCF	chr4:187393878-187393897	LNCaP	prostate:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187422895-187422945	SK-N-SH	brain:	n/a
2	chr4:187422114-187422164	AG09309	skin:	n/a
3	chr4:187422091-187422141	NHBE	bronchial:	n/a
4	chr4:187422119-187422169	IMR90	lung:	fetal
5	chr4:187407036-187407086	AoSMC	blood vessel:	n/a
6	chr4:187422119-187422169	SK-N-SH_RA	brain:	n/a
7	chr4:187394380-187394430	HepG2	liver:	n/a
8	chr4:187404958-187405008	GM19239	blood:	n/a
9	chr4:187404988-187405038	PFSK-1	brain:	n/a
10	chr4:187394380-187394430	HCM	heart:	n/a
11	chr4:187404958-187405008	NT2-D1	testis:	n/a
12	chr4:187404958-187405008	U87	brain:	n/a
13	chr4:187407036-187407086	AG04450	lung:	fetal
14	chr4:187422035-187422085	GM12878	blood:	n/a
15	chr4:187422114-187422164	HCT-116	colon:	n/a
16	chr4:187404988-187405038	HCM	heart:	n/a
17	chr4:187394380-187394430	ovcar-3	ovarian:	n/a
18	chr4:187394380-187394430	HNPCEpiC	eye:	n/a
19	chr4:187407036-187407086	PANC-1	pancreas:	n/a
20	chr4:187422091-187422141	CMK	blood:	n/a
21	chr4:187404958-187405008	HCPEpiC	choroid plexus:	n/a
22	chr4:187394380-187394430	HMEC	breast:	n/a
23	chr4:187404923-187404973	LNCaP	prostate:	n/a
24	chr4:187422341-187422391	HRPEpiC	eye:	n/a
25	chr4:187394380-187394430	BJ	skin:	n/a
26	chr4:187422341-187422391	SKMC	muscle:	n/a
27	chr4:187418419-187418469	HMEC	breast:	n/a
28	chr4:187422119-187422169	Hepatocyte	liver:	n/a
29	chr4:187422119-187422169	CMK	blood:	n/a
30	chr4:187404958-187405008	CMK	blood:	n/a
31	chr4:187422091-187422141	AG04449	skin:	fetal
32	chr4:187422005-187422055	NT2-D1	testis:	n/a
33	chr4:187404958-187405008	SK-N-SH	brain:	n/a
34	chr4:187418419-187418469	Caco-2	colon:	n/a
35	chr4:187422035-187422085	SKMC	muscle:	n/a
36	chr4:187422035-187422085	HAEpiC	amniotic membrane:	n/a
37	chr4:187407036-187407086	GM12878	blood:	n/a
38	chr4:187407036-187407086	GM06990	blood:	n/a
39	chr4:187404958-187405008	HRCEpiC	kidney:	n/a
40	chr4:187422005-187422055	PrEC	prostate:	n/a
41	chr4:187422035-187422085	BE2_C	brain:	n/a
42	chr4:187404988-187405038	ECC-1	luminal epithelium:	n/a
43	chr4:187422895-187422945	Caco-2	colon:	n/a
44	chr4:187422341-187422391	HAEpiC	amniotic membrane:	n/a
45	chr4:187404958-187405008	BJ	skin:	n/a
46	chr4:187422091-187422141	HL-60	blood:	n/a
47	chr4:187407036-187407086	HMEC	breast:	n/a
48	chr4:187404958-187405008	PrEC	prostate:	n/a
49	chr4:187422895-187422945	HRPEpiC	eye:	n/a
50	chr4:187407036-187407086	SK-N-SH_RA	brain:	n/a

(count:26 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:187394154..187394722-chr4:187508267..187509221,2	K562	blood:
2	chr4:187393992..187394694-chr4:187476207..187476860,2	MCF-7	breast:
3	chr4:187447764..187449411-chr4:187453319..187455061,2	K562	blood:
4	chr4:187425444..187427113-chr4:187432314..187434673,2	K562	blood:
5	chr4:187424618..187426617-chr4:187440828..187442815,2	MCF-7	breast:
6	chr4:187424618..187426617-chr4:187440828..187442815,2	MCF-7	breast:
7	chr4:187400808..187402522-chr4:187420720..187422452,2	MCF-7	breast:
8	chr4:187425444..187427113-chr4:187432314..187434673,2	K562	blood:
9	chr4:187449413..187452478-chr4:187454571..187457368,4	K562	blood:
10	chr4:187454593..187456201-chr4:187457410..187459187,2	K562	blood:
11	chr4:187418143..187425298-chr4:187427395..187434877,12	K562	blood:
12	chr4:187448150..187450256-chr4:187458216..187460408,2	K562	blood:
13	chr11:62608697..62609221-chr4:187449246..187449766,2	Hela-S3	cervix:
14	chr4:187422105..187424397-chr4:187432409..187434171,2	K562	blood:
15	chr4:187394722..187395443-chr4:187508309..187509281,2	MCF-7	breast:
16	chr4:187414357..187416175-chr4:187420876..187423477,2	MCF-7	breast:
17	chr4:187450978..187452522-chr4:187454014..187456071,2	K562	blood:
18	chr4:187393785..187394637-chr4:187475328..187475950,2	MCF-7	breast:
19	chr4:187447764..187449411-chr4:187453319..187455061,2	K562	blood:
20	chr4:187394348..187396815-chr4:187456742..187459587,2	K562	blood:
21	chr4:187450978..187452522-chr4:187454014..187456071,2	K562	blood:
22	chr4:187449413..187452478-chr4:187454571..187457368,4	K562	blood:
23	chr4:187421685..187424267-chr4:187426709..187429265,2	MCF-7	breast:
24	chr4:187419835..187422222-chr4:187436024..187437802,2	K562	blood:
25	chr17:41464198..41466205-chr4:187449246..187450766,2	MCF-7	breast:
26	chr4:187402656..187405583-chr4:187422037..187423656,2	K562	blood:

(count:4 , 50 per page) page: 1

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

No data

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
ENSG00000168412	chromatin interactions
ENSG00000272297	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2774 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2774 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10003777	chr4:187388958-187388959	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs566035361	chr4:187388963-187388964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs116548936	chr4:187388979-187388980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577436491	chr4:187389063-187389064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs546033781	chr4:187389074-187389075	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114850663	chr4:187389093-187389094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531849177	chr4:187389111-187389112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542504594	chr4:187389142-187389143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77225045	chr4:187389161-187389162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs76405336	chr4:187389165-187389166	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562071611	chr4:187389219-187389220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs375184628	chr4:187389243-187389244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533516651	chr4:187389247-187389248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565008539	chr4:187389254-187389255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62348894	chr4:187389269-187389270	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs547320448	chr4:187389306-187389307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs139886831	chr4:187389309-187389310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547007066	chr4:187389327-187389328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372360904	chr4:187389345-187389346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570187828	chr4:187389441-187389442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs35979119	chr4:187389456-187389457	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs142986060	chr4:187389478-187389479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs569824575	chr4:187389498-187389499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193218909	chr4:187389510-187389511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555615727	chr4:187389524-187389525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34018982	chr4:187389530-187389531	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs185691101	chr4:187389594-187389595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs80043648	chr4:187389636-187389637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186582617	chr4:187389642-187389643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577371483	chr4:187389645-187389646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs28485091	chr4:187389648-187389649	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs7692535	chr4:187389655-187389656	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs191470368	chr4:187389677-187389678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs542089899	chr4:187389684-187389685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs183960419	chr4:187389698-187389699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs528002041	chr4:187389740-187389741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs116887731	chr4:187389770-187389771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs540712446	chr4:187389825-187389826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs563750739	chr4:187389830-187389831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs532829942	chr4:187389856-187389857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs73022709	chr4:187389903-187389904	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs28435998	chr4:187389925-187389926	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs529049450	chr4:187389980-187389981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535796063	chr4:187389989-187389990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554515626	chr4:187390006-187390007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs62348895	chr4:187390023-187390024	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs565933934	chr4:187390028-187390029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543471478	chr4:187390064-187390065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs28557416	chr4:187390122-187390123	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs139651023	chr4:187390140-187390141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Ependymoma	20639864	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:302 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:187375400-187392600	Weak transcription	K562	blood
2	chr4:187392600-187392800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr4:187392600-187392800	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr4:187392600-187393000	Enhancers	Fetal Intestine Small	intestine
5	chr4:187392600-187393000	Enhancers	K562	blood
6	chr4:187392800-187393000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:187392800-187394200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:187392800-187394200	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr4:187393000-187395200	Weak transcription	K562	blood
10	chr4:187393200-187394200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr4:187393800-187394800	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:187393800-187394800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chr4:187394000-187394400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr4:187394000-187394600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr4:187394000-187394800	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr4:187394200-187394400	Enhancers	HUES6 Cell Line	embryonic stem cell
17	chr4:187394200-187394400	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr4:187394200-187394400	Enhancers	Rectal Mucosa Donor 31	rectum
19	chr4:187394200-187394400	Bivalent Enhancer	HSMMtube	muscle
20	chr4:187394200-187394800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr4:187394200-187395800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:187394400-187394600	Enhancers	H1 Cell Line	embryonic stem cell
23	chr4:187394400-187394800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
24	chr4:187394800-187395000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:187395000-187395400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr4:187395200-187395400	Enhancers	H1 Cell Line	embryonic stem cell
27	chr4:187395200-187395400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr4:187395200-187395400	Enhancers	K562	blood
29	chr4:187395400-187403600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr4:187395400-187413600	Weak transcription	K562	blood
31	chr4:187395600-187395800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr4:187395600-187396000	Enhancers	Sigmoid Colon	Sigmoid Colon
33	chr4:187403200-187403400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:187403200-187403400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr4:187403200-187403400	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr4:187403200-187404000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr4:187403200-187404000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr4:187403200-187404200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr4:187403400-187403600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
40	chr4:187403400-187403600	Enhancers	Brain Hippocampus Middle	brain
41	chr4:187403400-187403800	Enhancers	H9 Cell Line	embryonic stem cell
42	chr4:187403400-187404000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr4:187403400-187404200	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr4:187403400-187406200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr4:187403400-187407800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr4:187403600-187403800	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:187403600-187403800	Enhancers	Brain Germinal Matrix	brain
48	chr4:187403600-187404200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr4:187403800-187404000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr4:187403800-187404000	Bivalent Enhancer	Brain Angular Gyrus	brain

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