Variant report

Variant	nsv595731
Chromosome Location	chr4:152790580-152831309
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:240)
CpG islands
(count:122)
Chromatin interactive
region (count:11)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:240 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr4:152809343-152810130	GM12878	blood:	n/a	n/a
2	ATF2	chr4:152803022-152804149	GM12878	blood:	n/a	n/a
3	ATF2	chr4:152809281-152810219	GM12878	blood:	n/a	n/a
4	ATF2	chr4:152803112-152804069	GM12878	blood:	n/a	n/a
5	ATF2	chr4:152808205-152809175	GM12878	blood:	n/a	n/a
6	ATF2	chr4:152808277-152809195	GM12878	blood:	n/a	n/a
7	BATF	chr4:152803669-152804037	GM12878	blood:	n/a	chr4:152803880-152803890
8	BATF	chr4:152808574-152808994	GM12878	blood:	n/a	n/a
9	BATF	chr4:152803353-152804151	GM12878	blood:	n/a	chr4:152803510-152803523 chr4:152803880-152803890
10	BATF	chr4:152830103-152830473	GM12878	blood:	n/a	n/a
11	BATF	chr4:152809440-152809995	GM12878	blood:	n/a	n/a
12	BATF	chr4:152808319-152808968	GM12878	blood:	n/a	n/a
13	BCL11A	chr4:152808349-152808937	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:152795348-152795763	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL11A	chr4:152803271-152803628	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:152803677-152804055	GM12878	blood:	n/a	chr4:152803878-152803887
17	BCL11A	chr4:152808382-152808996	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:152809611-152810010	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:152795463-152795749	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr4:152809516-152810105	GM12878	blood:	n/a	n/a
21	BCL3	chr4:152809392-152810015	GM12878	blood:	n/a	n/a
22	BCLAF1	chr4:152808362-152809124	GM12878	blood:	n/a	n/a
23	BCLAF1	chr4:152803493-152804073	GM12878	blood:	n/a	chr4:152803878-152803887
24	BCLAF1	chr4:152808369-152808991	GM12878	blood:	n/a	n/a
25	BCLAF1	chr4:152809441-152810002	GM12878	blood:	n/a	n/a
26	BHLHE40	chr4:152803276-152804021	GM12878	blood:	n/a	n/a
27	BHLHE40	chr4:152808376-152809146	GM12878	blood:	n/a	n/a
28	BHLHE40	chr4:152806046-152806143	K562	blood:	n/a	chr4:152806107-152806120 chr4:152806109-152806118 chr4:152806109-152806118 chr4:152806108-152806117
29	BHLHE40	chr4:152809448-152810269	GM12878	blood:	n/a	n/a
30	CEBPB	chr4:152809313-152810190	GM12878	blood:	n/a	n/a
31	CHD1	chr4:152803862-152804116	GM12878	blood:	n/a	n/a
32	CHD2	chr4:152809457-152810107	GM12878	blood:	n/a	n/a
33	CHD2	chr4:152803533-152804150	GM12878	blood:	n/a	n/a
34	CHD2	chr4:152795494-152795803	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr4:152808440-152809021	GM12878	blood:	n/a	n/a
36	CTCF	chr4:152815899-152815956	GM20000	blood:	n/a	n/a
37	CTCF	chr4:152809800-152809950	GM12865	blood:	n/a	n/a
38	CTCF	chr4:152809660-152809810	GM12872	blood:	n/a	n/a
39	CTCF	chr4:152815213-152815276	Medullo	brain:	n/a	n/a
40	CTCF	chr4:152812500-152812650	GM12873	blood:	n/a	n/a
41	CTCF	chr4:152809840-152809990	GM12872	blood:	n/a	n/a
42	CTCF	chr4:152808720-152808870	AoAF	blood vessel:	n/a	n/a
43	CTCF	chr4:152830929-152830999	Lung_OC	lung:	n/a	n/a
44	CTCF	chr4:152804016-152804059	GM12891	blood:	n/a	n/a
45	CTCF	chr4:152809740-152809890	GM12878	blood:	n/a	n/a
46	CTCF	chr4:152809560-152809710	GM12873	blood:	n/a	n/a
47	CTCF	chr4:152809560-152809710	GM12872	blood:	n/a	n/a
48	CTCF	chr4:152809800-152809950	GM12875	blood:	n/a	n/a
49	CTCF	chr4:152809712-152809940	GM12878	blood:	n/a	n/a
50	CTCF	chr4:152826835-152826876	Lung_OC	lung:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:152801238-152801288	BJ	skin:	n/a
2	chr4:152801238-152801288	T-47D	breast:	n/a
3	chr4:152801238-152801288	MCF-7	breast:	n/a
4	chr4:152801238-152801288	GM12891	blood:	n/a
5	chr4:152801238-152801288	GM19239	blood:	n/a
6	chr4:152808142-152808192	Jurkat	blood:	n/a
7	chr4:152808142-152808192	HNPCEpiC	eye:	n/a
8	chr4:152808142-152808192	SK-N-MC	brain:	n/a
9	chr4:152808142-152808192	NHBE	bronchial:	n/a
10	chr4:152808142-152808192	HEK293	kidney:	embryo
11	chr4:152801238-152801288	PFSK-1	brain:	n/a
12	chr4:152801238-152801288	H1-hESC	embryonic stem cell:	embryo
13	chr4:152808142-152808192	NH-A	brain:	n/a
14	chr4:152801238-152801288	GM06990	blood:	n/a
15	chr4:152801238-152801288	HMEC	breast:	n/a
16	chr4:152801238-152801288	GM12878	blood:	n/a
17	chr4:152808142-152808192	Caco-2	colon:	n/a
18	chr4:152808142-152808192	Hela-S3	cervix:	n/a
19	chr4:152801238-152801288	HCM	heart:	n/a
20	chr4:152801238-152801288	PANC-1	pancreas:	n/a
21	chr4:152801238-152801288	HCF	heart:	n/a
22	chr4:152808142-152808192	Hepatocyte	liver:	n/a
23	chr4:152801238-152801288	AG09319	gingival:	n/a
24	chr4:152808142-152808192	ECC-1	luminal epithelium:	n/a
25	chr4:152801238-152801288	HepG2	liver:	n/a
26	chr4:152801238-152801288	NHDF-neo	bronchial:	n/a
27	chr4:152801238-152801288	LNCaP	prostate:	n/a
28	chr4:152808142-152808192	T-47D	breast:	n/a
29	chr4:152808142-152808192	HCPEpiC	choroid plexus:	n/a
30	chr4:152801238-152801288	HRPEpiC	eye:	n/a
31	chr4:152801238-152801288	SAEC	small airway:	n/a
32	chr4:152808142-152808192	NT2-D1	testis:	n/a
33	chr4:152801238-152801288	HNPCEpiC	eye:	n/a
34	chr4:152808142-152808192	ProgFib	skin:	n/a
35	chr4:152808142-152808192	HCM	heart:	n/a
36	chr4:152801238-152801288	SK-N-SH	brain:	n/a
37	chr4:152801238-152801288	CMK	blood:	n/a
38	chr4:152808142-152808192	IMR90	lung:	fetal
39	chr4:152808142-152808192	K562	blood:	n/a
40	chr4:152808142-152808192	HL-60	blood:	n/a
41	chr4:152801238-152801288	ovcar-3	ovarian:	n/a
42	chr4:152808142-152808192	AG04449	skin:	fetal
43	chr4:152801238-152801288	PrEC	prostate:	n/a
44	chr4:152808142-152808192	HRE	kidney:	n/a
45	chr4:152808142-152808192	HRCEpiC	kidney:	n/a
46	chr4:152808142-152808192	GM06990	blood:	n/a
47	chr4:152808142-152808192	A549	lung:	n/a
48	chr4:152808142-152808192	HAEpiC	amniotic membrane:	n/a
49	chr4:152801238-152801288	HUVEC	blood vessel:	n/a
50	chr4:152808142-152808192	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:152803724..152805338-chr4:152808624..152810923,2	K562	blood:
2	chr4:152805506..152807725-chr4:152813069..152815634,2	K562	blood:
3	chr4:152803737..152805745-chr4:152816897..152818541,2	MCF-7	breast:
4	chr4:152803737..152805745-chr4:152816897..152818541,2	MCF-7	breast:
5	chr4:152791629..152793817-chr4:152795687..152797994,2	K562	blood:
6	chr4:152804097..152806378-chr4:152817285..152819187,2	K562	blood:
7	chr4:152804097..152806378-chr4:152817285..152819187,2	K562	blood:
8	chr4:152791629..152793817-chr4:152795687..152797994,2	K562	blood:
9	chr4:152804253..152807006-chr4:152811957..152814569,2	K562	blood:
10	chr4:152805506..152807725-chr4:152813069..152815634,2	K562	blood:
11	chr4:152803724..152805338-chr4:152808624..152810923,2	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PET112-2	chr4:152826097-152826465	XLOC_004124
2	lnc-PET112-2	chr4:152812455-152812481	XLOC_004124
3	lnc-PET112-2	chr4:152812382-152812481	NONHSAT098772
4	lnc-PET112-1	chr4:152809643-152809730	XLOC_004123
5	lnc-PET112-2	chr4:152831150-152831312	XLOC_004124
6	lnc-PET112-2	chr4:152831150-152831322	XLOC_004124
7	lnc-FAM160A1-10	chr4:152808057-152810405	l_2755_chr4:152807157-152811090_testes
8	lnc-PET112-2	chr4:152827184-152827273	XLOC_004124
9	lnc-PET112-2	chr4:152827184-152827273	NONHSAT098772
10	lnc-PET112-2	chr4:152831150-152831322	XLOC_004124
11	lnc-PET112-2	chr4:152826084-152826465	XLOC_004124
12	lnc-PET112-2	chr4:152831150-152831316	NONHSAT098772
13	lnc-PET112-2	chr4:152826089-152826465	XLOC_004124
14	lnc-PET112-2	chr4:152827184-152827273	XLOC_004124
15	lnc-PET112-2	chr4:152827184-152827273	XLOC_004124
16	lnc-FAM160A1-10	chr4:152810553-152811090	l_2755_chr4:152807157-152811090_testes
17	lnc-PET112-1	chr4:152812319-152812415	XLOC_004123
18	lnc-FAM160A1-10	chr4:152807158-152808055	l_2755_chr4:152807157-152811090_testes
19	lnc-PET112-1	chr4:152808695-152808915	XLOC_004123

No data

Variant related genes	Relation type
ENSG00000249708	TF binding region
ENSG00000249708	CpG island
ENSG00000249708	chromatin interactions
ZIC3	miRNA target sites
ZFYVE26	miRNA target sites
ZNF148	miRNA target sites
ZHX3	miRNA target sites
GSN	miRNA target sites
SFRS2IP	miRNA target sites

Extended variants
information (count: 1500 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1500 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17027997	chr4:152790580-152790581	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs361167	chr4:152790628-152790629	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs534136865	chr4:152790632-152790633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs71618383	chr4:152790636-152790637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs559065391	chr4:152790662-152790663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs577636045	chr4:152790692-152790693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs538507176	chr4:152790728-152790729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs144249201	chr4:152790740-152790741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs557032254	chr4:152790767-152790768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs367744848	chr4:152790777-152790778	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs542754696	chr4:152790793-152790794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs560811743	chr4:152790804-152790805	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs142316958	chr4:152790842-152790843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs151278989	chr4:152790894-152790895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs564703012	chr4:152790897-152790898	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs192189480	chr4:152790915-152790916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550437801	chr4:152790929-152790930	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs60850965	chr4:152790936-152790937	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs530029846	chr4:152790964-152790965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548521583	chr4:152790971-152790972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182267863	chr4:152790985-152790986	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186937309	chr4:152791006-152791007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs526984	chr4:152791109-152791110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552821927	chr4:152791134-152791135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs11445977	chr4:152791135-152791136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs526868	chr4:152791158-152791159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571043218	chr4:152791159-152791160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574506010	chr4:152791195-152791196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542376	chr4:152791201-152791202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs541647071	chr4:152791250-152791251	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs556893999	chr4:152791286-152791287	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2628087	chr4:152791312-152791313	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191786097	chr4:152791336-152791337	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs75019728	chr4:152791348-152791349	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147418488	chr4:152791361-152791362	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs146114964	chr4:152791362-152791363	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs199691336	chr4:152791363-152791364	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs139197406	chr4:152791376-152791377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs70943607	chr4:152791386-152791387	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2666983	chr4:152791403-152791404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs554503326	chr4:152791413-152791414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183085526	chr4:152791428-152791429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs555509006	chr4:152791430-152791431	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs47132	chr4:152791435-152791436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs544196236	chr4:152791436-152791437	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs558357081	chr4:152791441-152791442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs576624394	chr4:152791460-152791461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs73862589	chr4:152791464-152791465	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs562449898	chr4:152791517-152791518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs78354074	chr4:152791532-152791533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	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
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	16272173	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	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
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:152781200-152794800	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr4:152789000-152791200	Weak transcription	Fetal Brain Male	brain
3	chr4:152789000-152796200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr4:152789400-152793800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:152791200-152791400	Enhancers	Fetal Brain Male	brain
6	chr4:152791400-152800200	Weak transcription	Fetal Brain Male	brain
7	chr4:152793800-152794000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr4:152793800-152794000	Enhancers	Thymus	Thymus
9	chr4:152794000-152794400	Weak transcription	Aorta	Aorta
10	chr4:152794000-152795000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr4:152794600-152796800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr4:152794800-152795600	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr4:152794800-152796400	Enhancers	H9 Cell Line	embryonic stem cell
14	chr4:152794800-152796400	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr4:152794800-152796600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr4:152794800-152796600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:152794800-152796600	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr4:152794800-152797400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr4:152795000-152796600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr4:152795000-152796600	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr4:152795000-152798000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
22	chr4:152795400-152796400	Enhancers	Cortex derived primary cultured neurospheres	brain
23	chr4:152795600-152796000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr4:152795600-152796000	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
25	chr4:152795600-152796000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr4:152795800-152796400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr4:152795800-152798000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
28	chr4:152796000-152796600	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr4:152796000-152799800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr4:152796000-152801000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr4:152796200-152796600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
32	chr4:152796200-152796800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr4:152796400-152799600	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr4:152796400-152800200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr4:152796400-152808200	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr4:152796600-152799600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr4:152796600-152800400	Weak transcription	HUES48 Cell Line	embryonic stem cell
38	chr4:152796600-152800600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
39	chr4:152796600-152806800	Weak transcription	HUES64 Cell Line	embryonic stem cell
40	chr4:152796600-152807200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr4:152796800-152797000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr4:152796800-152800200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
43	chr4:152797000-152798000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr4:152797400-152800200	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr4:152798000-152800000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
46	chr4:152798000-152801600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr4:152799200-152799800	Enhancers	Brain Germinal Matrix	brain
48	chr4:152799600-152801600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:152799600-152802200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr4:152799800-152800800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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