Variant report

Variant	nsv1023427
Chromosome Location	chr4:187392594-187454677
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	chr4:187394041-187394370	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:187393967-187394511	K562	blood:	n/a	n/a
3	ATF1	chr4:187420491-187420916	K562	blood:	n/a	n/a
4	ATF1	chr4:187421894-187422344	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	chr4:187421756-187422525	K562	blood:	n/a	n/a
9	BHLHE40	chr4:187442068-187442244	K562	blood:	n/a	n/a
10	BHLHE40	chr4:187422808-187423008	K562	blood:	n/a	n/a
11	CBX3	chr4:187411097-187411357	K562	blood:	n/a	n/a
12	CBX3	chr4:187421712-187422622	K562	blood:	n/a	n/a
13	CBX3	chr4:187421797-187422410	K562	blood:	n/a	n/a
14	CCNT2	chr4:187421964-187422263	K562	blood:	n/a	n/a
15	CEBPB	chr4:187421769-187422320	K562	blood:	n/a	n/a
16	CEBPB	chr4:187420609-187420949	K562	blood:	n/a	n/a
17	CEBPB	chr4:187394195-187394430	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr4:187432638-187432777	HepG2	liver:	n/a	chr4:187432667-187432678
19	CEBPB	chr4:187432537-187432726	K562	blood:	n/a	chr4:187432667-187432678
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	chr4:187394056-187394233	A549	lung:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
25	CTCF	chr4:187394180-187394330	GM12864	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
26	CTCF	chr4:187394120-187394270	HCT-116	colon:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
27	CTCF	chr4:187394120-187394270	GM12872	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
28	CTCF	chr4:187394311-187394318	ProgFib	skin:	n/a	n/a
29	CTCF	chr4:187394092-187394328	Pancreas_OC	pancreas:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
30	CTCF	chr4:187394120-187394270	HA-sp	spinal cord:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
31	CTCF	chr4:187394120-187394270	AG09319	gingival:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
32	CTCF	chr4:187406900-187407050	RPTEC	kidney:	n/a	chr4:187406975-187406984 chr4:187406974-187406987 chr4:187406971-187406984 chr4:187406969-187406987
33	CTCF	chr4:187394160-187394310	GM12869	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
34	CTCF	chr4:187394160-187394310	NHLF	lung:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
35	CTCF	chr4:187394100-187394250	GM12871	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
36	CTCF	chr4:187393940-187394090	GM12870	blood:	n/a	n/a
37	CTCF	chr4:187394160-187394310	HEK293	kidney:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
38	CTCF	chr4:187394001-187394501	IMR90	lung:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
39	CTCF	chr4:187406880-187407030	HRPEpiC	eye:	n/a	chr4:187406975-187406984 chr4:187406974-187406987 chr4:187406971-187406984 chr4:187406969-187406987
40	CTCF	chr4:187401760-187401910	HepG2	liver:	n/a	n/a
41	CTCF	chr4:187394008-187394473	K562	blood:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
42	CTCF	chr4:187421971-187422103	MCF-7	breast:	n/a	n/a
43	CTCF	chr4:187394056-187394484	H1-hESC	embryonic stem cell:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
44	CTCF	chr4:187406860-187407010	AG04450	lung:	n/a	chr4:187406975-187406984 chr4:187406974-187406987 chr4:187406971-187406984 chr4:187406969-187406987
45	CTCF	chr4:187406920-187407070	HBMEC	blood vessel:	n/a	chr4:187406975-187406984 chr4:187406974-187406987 chr4:187406971-187406984 chr4:187406969-187406987
46	CTCF	chr4:187394140-187394290	AG09319	gingival:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
47	CTCF	chr4:187421980-187422130	K562	blood:	n/a	n/a
48	CTCF	chr4:187394340-187394490	GM12869	blood:	n/a	n/a
49	CTCF	chr4:187394160-187394310	HRE	kidney:	n/a	chr4:187394193-187394209 chr4:187394194-187394215
50	CTCF	chr4:187394082-187394336	LNCaP	prostate:	n/a	chr4:187394193-187394209 chr4:187394194-187394215

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:187422341-187422391	HNPCEpiC	eye:	n/a
2	chr4:187422341-187422391	HNPCEpiC	eye:	n/a
3	chr4:187418419-187418469	GM19239	blood:	n/a
4	chr4:187422341-187422391	GM06990	blood:	n/a
5	chr4:187422005-187422055	BE2_C	brain:	n/a
6	chr4:187404958-187405008	AG09309	skin:	n/a
7	chr4:187422895-187422945	NHBE	bronchial:	n/a
8	chr4:187422895-187422945	ECC-1	luminal epithelium:	n/a
9	chr4:187422341-187422391	LNCaP	prostate:	n/a
10	chr4:187404923-187404973	HRPEpiC	eye:	n/a
11	chr4:187404958-187405008	SK-N-MC	brain:	n/a
12	chr4:187422119-187422169	MCF10A-Er-Src	breast:	n/a
13	chr4:187422114-187422164	AoSMC	blood vessel:	n/a
14	chr4:187422114-187422164	NT2-D1	testis:	n/a
15	chr4:187418419-187418469	HCPEpiC	choroid plexus:	n/a
16	chr4:187426127-187426177	HCF	heart:	n/a
17	chr4:187394380-187394430	ovcar-3	ovarian:	n/a
18	chr4:187407036-187407086	SAEC	small airway:	n/a
19	chr4:187426127-187426177	SK-N-SH_RA	brain:	n/a
20	chr4:187422895-187422945	Hela-S3	cervix:	n/a
21	chr4:187426127-187426177	HL-60	blood:	n/a
22	chr4:187422091-187422141	HCPEpiC	choroid plexus:	n/a
23	chr4:187418419-187418469	HUVEC	blood vessel:	n/a
24	chr4:187426127-187426177	Caco-2	colon:	n/a
25	chr4:187418419-187418469	NT2-D1	testis:	n/a
26	chr4:187422895-187422945	HRE	kidney:	n/a
27	chr4:187404988-187405038	GM12892	blood:	n/a
28	chr4:187422091-187422141	HepG2	liver:	n/a
29	chr4:187418419-187418469	GM12891	blood:	n/a
30	chr4:187404988-187405038	AG10803	skin:	n/a
31	chr4:187422119-187422169	HCT-116	colon:	n/a
32	chr4:187418419-187418469	AG04449	skin:	fetal
33	chr4:187404923-187404973	SK-N-SH_RA	brain:	n/a
34	chr4:187422114-187422164	GM12891	blood:	n/a
35	chr4:187422114-187422164	MCF-7	breast:	n/a
36	chr4:187418419-187418469	MCF10A-Er-Src	breast:	n/a
37	chr4:187422341-187422391	BJ	skin:	n/a
38	chr4:187422341-187422391	HCT-116	colon:	n/a
39	chr4:187422895-187422945	HL-60	blood:	n/a
40	chr4:187422895-187422945	HCF	heart:	n/a
41	chr4:187422895-187422945	U87	brain:	n/a
42	chr4:187426127-187426177	RPTEC	kidney:	n/a
43	chr4:187404923-187404973	AG04450	lung:	fetal
44	chr4:187422895-187422945	HEEpiC	esophagus:	n/a
45	chr4:187394380-187394430	AG10803	skin:	n/a
46	chr4:187418419-187418469	Hepatocyte	liver:	n/a
47	chr4:187422341-187422391	HEK293	kidney:	embryo
48	chr4:187426127-187426177	NT2-D1	testis:	n/a
49	chr4:187404988-187405038	HCF	heart:	n/a
50	chr4:187404958-187405008	HEK293	kidney:	embryo

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MTNR1A-1	chr4:187421999-187422151	ENSG00000251165.1
2	lnc-FAT1-5	chr4:187409184-187409778	predAs_chen_AV690772_1
3	lnc-MTNR1A-1	chr4:187421999-187422212	NONHSAT099658
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
ENSG00000168412	chromatin interactions
ENSG00000212387	chromatin interactions
ENSG00000251165	chromatin interactions
ENSG00000272297	chromatin interactions
ENSG00000188825	chromatin interactions

Extended variants
information (count: 2588 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:2588 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs533769575	chr4:187392610-187392611	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553615807	chr4:187392613-187392614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181984278	chr4:187392621-187392622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs147346016	chr4:187392636-187392637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138044751	chr4:187392666-187392667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs62348914	chr4:187392736-187392737	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs541207932	chr4:187392754-187392755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs552770000	chr4:187392768-187392769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6845924	chr4:187392799-187392800	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs143539407	chr4:187392844-187392845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs530301105	chr4:187392892-187392893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185174702	chr4:187392901-187392902	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs560741819	chr4:187392912-187392913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532845413	chr4:187392932-187392933	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs535257524	chr4:187392949-187392950	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs568830187	chr4:187392950-187392951	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs10016581	chr4:187392976-187392977	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537469187	chr4:187392985-187392986	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs189309275	chr4:187393044-187393045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs556743432	chr4:187393076-187393077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575171652	chr4:187393180-187393181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533709974	chr4:187393195-187393196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553552561	chr4:187393245-187393246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs4862702	chr4:187393265-187393266	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs4862703	chr4:187393313-187393314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140935705	chr4:187393335-187393336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577271933	chr4:187393336-187393337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574727131	chr4:187393339-187393340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs369593558	chr4:187393361-187393362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs58943128	chr4:187393362-187393363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201022038	chr4:187393363-187393364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556231814	chr4:187393389-187393390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs575573117	chr4:187393456-187393457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544652782	chr4:187393462-187393463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146959716	chr4:187393517-187393518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs370929681	chr4:187393633-187393634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs555069084	chr4:187393687-187393688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs575011791	chr4:187393704-187393705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs76149088	chr4:187393770-187393771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs147158470	chr4:187393788-187393789	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562030641	chr4:187393789-187393790	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs181217816	chr4:187393814-187393815	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs546453117	chr4:187393829-187393830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs74955798	chr4:187393912-187393913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs186529332	chr4:187393913-187393914	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs139359803	chr4:187393965-187393966	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs373398965	chr4:187394038-187394039	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs549536905	chr4:187394092-187394093	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs77491810	chr4:187394144-187394145	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs75209726	chr4:187394158-187394159	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	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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