Variant report

Variant	nsv821637
Chromosome Location	chr4:104134839-104246167
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:234)
CpG islands
(count:183)
Chromatin interactive
region (count:8)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:234 , 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	ARID3A	chr4:104227844-104228137	HepG2	liver:	n/a	n/a
2	ARID3A	chr4:104178714-104179009	K562	blood:	n/a	n/a
3	ARID3A	chr4:104177441-104177991	K562	blood:	n/a	n/a
4	BACH1	chr4:104178412-104179029	K562	blood:	n/a	n/a
5	BACH1	chr4:104178638-104178985	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:104185099-104185243	GM12878	blood:	n/a	n/a
7	BHLHE40	chr4:104228861-104229061	HepG2	liver:	n/a	n/a
8	CEBPB	chr4:104170895-104171246	IMR90	lung:	n/a	chr4:104171066-104171079
9	CEBPB	chr4:104170928-104171215	Hela-S3	cervix:	n/a	chr4:104171066-104171079
10	CEBPB	chr4:104219128-104219366	HepG2	liver:	n/a	chr4:104219276-104219287
11	CEBPB	chr4:104219154-104219355	A549	lung:	n/a	chr4:104219276-104219287
12	CEBPB	chr4:104170943-104171177	HepG2	liver:	n/a	chr4:104171066-104171079
13	CEBPB	chr4:104219134-104219376	K562	blood:	n/a	chr4:104219276-104219287
14	CEBPB	chr4:104170953-104171183	A549	lung:	n/a	chr4:104171066-104171079
15	CEBPB	chr4:104219117-104219359	K562	blood:	n/a	chr4:104219276-104219287
16	CEBPB	chr4:104219116-104219412	IMR90	lung:	n/a	chr4:104219276-104219287
17	CHD2	chr4:104228023-104228347	HepG2	liver:	n/a	n/a
18	CTCF	chr4:104186477-104186531	GM20000	blood:	n/a	n/a
19	CTCF	chr4:104239820-104239970	GM12869	blood:	n/a	n/a
20	CTCF	chr4:104200336-104200388	GM13977	blood:	n/a	n/a
21	CTCF	chr4:104207064-104207141	LNCaP	prostate:	n/a	n/a
22	CTCF	chr4:104138360-104138510	GM12869	blood:	n/a	n/a
23	CTCF	chr4:104139900-104140050	GM12866	blood:	n/a	n/a
24	CTCF	chr4:104161243-104161322	GM20000	blood:	n/a	n/a
25	CTCF	chr4:104201333-104201384	Medullo	brain:	n/a	n/a
26	CTCF	chr4:104146323-104146362	Pancreas_OC	pancreas:	n/a	n/a
27	CTCF	chr4:104242900-104243050	NHLF	lung:	n/a	n/a
28	CTCF	chr4:104152246-104152269	Kidney_OC	kidney:	n/a	n/a
29	CUX1	chr4:104178783-104179307	K562	blood:	n/a	n/a
30	CUX1	chr4:104168797-104168804	GM12878	blood:	n/a	n/a
31	E2F4	chr4:104165498-104165666	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr4:104224691-104224891	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr4:104225705-104225876	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr4:104147079-104147101	MCF10A-Er-Src	breast:	n/a	n/a
35	EBF1	chr4:104148017-104148303	GM12878	blood:	n/a	n/a
36	EGR1	chr4:104177295-104177506	K562	blood:	n/a	n/a
37	EGR1	chr4:104177308-104177546	K562	blood:	n/a	n/a
38	ELF1	chr4:104177284-104177594	K562	blood:	n/a	n/a
39	ELK1	chr4:104182139-104182181	GM12878	blood:	n/a	n/a
40	EP300	chr4:104152343-104152402	K562	blood:	n/a	n/a
41	EP300	chr4:104227795-104228311	MCF-7	breast:	n/a	n/a
42	EP300	chr4:104179122-104179334	K562	blood:	n/a	n/a
43	FAM48A	chr4:104198770-104198861	GM12878	blood:	n/a	n/a
44	FOS	chr4:104135838-104135903	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr4:104135769-104135937	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr4:104224311-104224493	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr4:104224322-104224577	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr4:104165465-104165812	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr4:104197849-104198018	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr4:104165465-104165763	MCF10A-Er-Src	breast:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:104227316-104227366	MCF-7	breast:	n/a
2	chr4:104239655-104239705	AG09319	gingival:	n/a
3	chr4:104177163-104177213	SAEC	small airway:	n/a
4	chr4:104239655-104239705	SK-N-SH_RA	brain:	n/a
5	chr4:104227316-104227366	NT2-D1	testis:	n/a
6	chr4:104227316-104227366	HCF	heart:	n/a
7	chr4:104239655-104239705	HEEpiC	esophagus:	n/a
8	chr4:104177163-104177213	HRCEpiC	kidney:	n/a
9	chr4:104177163-104177213	HAEpiC	amniotic membrane:	n/a
10	chr4:104239655-104239705	PANC-1	pancreas:	n/a
11	chr4:104177163-104177213	HCPEpiC	choroid plexus:	n/a
12	chr4:104177163-104177213	AG10803	skin:	n/a
13	chr4:104177163-104177213	HIPEpiC	eye:	n/a
14	chr4:104177163-104177213	PANC-1	pancreas:	n/a
15	chr4:104177163-104177213	HRE	kidney:	n/a
16	chr4:104177163-104177213	LNCaP	prostate:	n/a
17	chr4:104177163-104177213	HRPEpiC	eye:	n/a
18	chr4:104227316-104227366	HCPEpiC	choroid plexus:	n/a
19	chr4:104177163-104177213	HepG2	liver:	n/a
20	chr4:104227316-104227366	PrEC	prostate:	n/a
21	chr4:104227316-104227366	ECC-1	luminal epithelium:	n/a
22	chr4:104227316-104227366	Caco-2	colon:	n/a
23	chr4:104177163-104177213	MCF10A-Er-Src	breast:	n/a
24	chr4:104227316-104227366	HEEpiC	esophagus:	n/a
25	chr4:104177163-104177213	Hepatocyte	liver:	n/a
26	chr4:104239655-104239705	HCT-116	colon:	n/a
27	chr4:104177163-104177213	NH-A	brain:	n/a
28	chr4:104177163-104177213	HUVEC	blood vessel:	n/a
29	chr4:104227316-104227366	CMK	blood:	n/a
30	chr4:104239655-104239705	U87	brain:	n/a
31	chr4:104239655-104239705	AG04449	skin:	fetal
32	chr4:104227316-104227366	A549	lung:	n/a
33	chr4:104239655-104239705	HCF	heart:	n/a
34	chr4:104239655-104239705	MCF10A-Er-Src	breast:	n/a
35	chr4:104227316-104227366	PANC-1	pancreas:	n/a
36	chr4:104177163-104177213	K562	blood:	n/a
37	chr4:104239655-104239705	K562	blood:	n/a
38	chr4:104227316-104227366	HNPCEpiC	eye:	n/a
39	chr4:104177163-104177213	NB4	blood:	n/a
40	chr4:104227316-104227366	T-47D	breast:	n/a
41	chr4:104239655-104239705	SK-N-MC	brain:	n/a
42	chr4:104177163-104177213	ovcar-3	ovarian:	n/a
43	chr4:104239655-104239705	GM12891	blood:	n/a
44	chr4:104227316-104227366	SKMC	muscle:	n/a
45	chr4:104239655-104239705	AoSMC	blood vessel:	n/a
46	chr4:104227316-104227366	SK-N-SH_RA	brain:	n/a
47	chr4:104239655-104239705	A549	lung:	n/a
48	chr4:104177163-104177213	GM19239	blood:	n/a
49	chr4:104177163-104177213	NHBE	bronchial:	n/a
50	chr4:104227316-104227366	AG09319	gingival:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:104213569..104215673-chr4:104223134..104225892,2	MCF-7	breast:
2	chr4:104213569..104215673-chr4:104223134..104225892,2	MCF-7	breast:
3	chr4:104117492..104119427-chr4:104178040..104180048,2	K562	blood:
4	chr4:104181685..104183408-chr4:104209717..104212156,2	K562	blood:
5	chr4:104181685..104183408-chr4:104209717..104212156,2	K562	blood:
6	chr4:104243719..104245643-chr4:104247001..104248713,2	K562	blood:
7	chr4:104180046..104181574-chr4:104181582..104183273,2	K562	blood:
8	chr4:104180046..104181574-chr4:104181582..104183273,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CISD2-3	chr4:104177316-104177451	ENSG00000248740

No data

Variant related genes	Relation type
ENSG00000248740	TF binding region
ENSG00000248740	CpG island

Extended variants
information (count: 2388 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2388 , 50 per page) page: 1 2 3 4 5 6 7 ... 48

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190110905	chr4:104144406-104144407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573327887	chr4:104144452-104144453	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs540607833	chr4:104144485-104144486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs560451498	chr4:104144549-104144550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs138934416	chr4:104144575-104144576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs79017201	chr4:104144621-104144622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs572400379	chr4:104144637-104144638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs78234022	chr4:104144652-104144653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs181672211	chr4:104144662-104144663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs111787037	chr4:104144688-104144689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs141474882	chr4:104144692-104144693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77596659	chr4:104144693-104144694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs150839066	chr4:104144714-104144715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138180123	chr4:104144722-104144723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185520973	chr4:104144723-104144724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs566027852	chr4:104144772-104144773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs376341162	chr4:104144799-104144800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs370771338	chr4:104144825-104144826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs533207791	chr4:104144890-104144891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2169512	chr4:104144891-104144892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113018714	chr4:104144908-104144909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs569804208	chr4:104144951-104144952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374712423	chr4:104144963-104144964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377435700	chr4:104144974-104144975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs370403931	chr4:104144978-104144979	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs149560249	chr4:104144993-104144994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72666828	chr4:104144995-104144996	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs140631962	chr4:104145019-104145020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs552501524	chr4:104145022-104145023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142857105	chr4:104145027-104145028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs546444974	chr4:104145038-104145039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs190282285	chr4:104145039-104145040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12509895	chr4:104145066-104145067	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
34	rs543641144	chr4:104145086-104145087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs370975964	chr4:104145096-104145097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs562205657	chr4:104145112-104145113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs543486436	chr4:104145126-104145127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180856613	chr4:104145156-104145157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs186288237	chr4:104145169-104145170	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536484814	chr4:104145172-104145173	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555150471	chr4:104145182-104145183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559744725	chr4:104145201-104145202	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs533097295	chr4:104145228-104145229	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs191901397	chr4:104145294-104145295	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569833928	chr4:104145296-104145297	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530773147	chr4:104145372-104145373	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs537766215	chr4:104145510-104145511	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs72948126	chr4:104145515-104145516	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs56138287	chr4:104145530-104145531	ZNF genes & repeats Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs534372472	chr4:104145555-104145556	ZNF genes & repeats Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	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
Melanoma	18172304	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Hepatocellular carcinoma	16750200	CNVD
Myxofibrosarcoma	16751306	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	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
Adenoid cystic carcinoma	18698036	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	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
Ovarian cancer	21720365	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	16573809	CNVD
Multiple myeloma	16616336	CNVD
Melanoma	20688739	CNVD
Breast cancer	16397240	CNVD
Acute myeloid leukemia	18000384	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Myelofibrosis	22110671	CNVD
myeloid cancer	21057493	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21215367	CNVD

Chromatin state (count:201 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:104144400-104146800	Enhancers	Fetal Intestine Small	intestine
2	chr4:104144600-104145400	Enhancers	HepG2	liver
3	chr4:104145000-104145200	Enhancers	Rectal Mucosa Donor 31	rectum
4	chr4:104145000-104145400	Enhancers	Stomach Mucosa	stomach
5	chr4:104145000-104146600	Enhancers	Fetal Intestine Large	intestine
6	chr4:104145200-104146200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr4:104145800-104149000	Weak transcription	H1 Cell Line	embryonic stem cell
8	chr4:104165400-104166000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:104176600-104177600	Active TSS	iPS-15b Cell Line	embryonic stem cell
10	chr4:104176600-104179800	Active TSS	HUES6 Cell Line	embryonic stem cell
11	chr4:104177000-104177800	Active TSS	HUES64 Cell Line	embryonic stem cell
12	chr4:104177000-104177800	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr4:104177000-104178000	Active TSS	H9 Cell Line	embryonic stem cell
14	chr4:104177000-104178800	Active TSS	H1 Cell Line	embryonic stem cell
15	chr4:104177000-104178800	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr4:104177000-104179200	Active TSS	ES-I3 Cell Line	embryonic stem cell
17	chr4:104177200-104178800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
18	chr4:104177200-104178800	Active TSS	iPS-18 Cell Line	embryonic stem cell
19	chr4:104177200-104179400	Active TSS	HepG2	liver
20	chr4:104177200-104180000	Active TSS	K562	blood
21	chr4:104177400-104178200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr4:104177600-104178000	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
23	chr4:104177600-104179400	Active TSS	iPS-20b Cell Line	embryonic stem cell
24	chr4:104177800-104178200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr4:104177800-104179400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
26	chr4:104178000-104178800	Active TSS	iPS-15b Cell Line	embryonic stem cell
27	chr4:104178800-104179000	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr4:104178800-104179800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr4:104178800-104180400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr4:104179000-104183000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chr4:104179200-104180200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
32	chr4:104179400-104181000	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr4:104179600-104180000	Enhancers	HepG2	liver
34	chr4:104179800-104180200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr4:104179800-104180600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr4:104180200-104180400	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr4:104180400-104180800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr4:104180600-104181000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr4:104180800-104183000	Weak transcription	HUES48 Cell Line	embryonic stem cell
40	chr4:104181000-104183200	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr4:104183000-104183400	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr4:104183000-104183600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr4:104183200-104183600	Enhancers	HUES64 Cell Line	embryonic stem cell
44	chr4:104189600-104193800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chr4:104192600-104192800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
46	chr4:104192600-104193000	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chr4:104192800-104193000	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr4:104192800-104200800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:104193000-104193400	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chr4:104193000-104194400	Weak transcription	iPS-15b Cell Line	embryonic stem cell

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