Variant report

Variant	nsv1013341
Chromosome Location	chr4:93588723-93693087
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:258)
CpG islands
(count:61)
Chromatin interactive
region (count:8)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:93668507-93668738	GM12878	blood:	n/a	n/a
2	CEBPB	chr4:93655856-93656165	IMR90	lung:	n/a	chr4:93655985-93655996
3	CEBPB	chr4:93592781-93592941	H1-hESC	embryonic stem cell:	n/a	n/a
4	CEBPB	chr4:93684631-93684724	HepG2	liver:	n/a	chr4:93684658-93684669
5	CEBPB	chr4:93655972-93656033	K562	blood:	n/a	chr4:93655985-93655996
6	CEBPB	chr4:93638386-93638647	HepG2	liver:	n/a	chr4:93638520-93638531
7	CEBPB	chr4:93646297-93646482	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:93689167-93689298	H1-hESC	embryonic stem cell:	n/a	chr4:93689218-93689229
9	CEBPB	chr4:93681954-93682242	HepG2	liver:	n/a	chr4:93682086-93682097
10	CEBPB	chr4:93655882-93656153	HepG2	liver:	n/a	chr4:93655985-93655996
11	CEBPB	chr4:93638461-93638652	A549	lung:	n/a	chr4:93638520-93638531
12	CEBPB	chr4:93594437-93594615	K562	blood:	n/a	chr4:93594475-93594486
13	CEBPB	chr4:93644439-93644669	HepG2	liver:	n/a	chr4:93644563-93644574 chr4:93644563-93644576
14	CEBPB	chr4:93684639-93684709	A549	lung:	n/a	chr4:93684658-93684669
15	CEBPB	chr4:93681975-93682265	A549	lung:	n/a	chr4:93682086-93682097
16	CEBPB	chr4:93591113-93591283	K562	blood:	n/a	chr4:93591137-93591150
17	CEBPB	chr4:93655912-93656149	MCF-7	breast:	n/a	chr4:93655985-93655996
18	CEBPB	chr4:93689119-93689335	K562	blood:	n/a	chr4:93689218-93689229
19	CEBPB	chr4:93655859-93656159	H1-hESC	embryonic stem cell:	n/a	chr4:93655985-93655996
20	CEBPB	chr4:93646285-93646553	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr4:93594339-93594550	HepG2	liver:	n/a	chr4:93594475-93594486
22	CTCF	chr4:93656339-93656437	LNCaP	prostate:	n/a	n/a
23	CTCF	chr4:93656310-93656609	MCF-7	breast:	n/a	n/a
24	CTCF	chr4:93656280-93656430	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr4:93656260-93656410	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr4:93632908-93632972	LNCaP	prostate:	n/a	n/a
27	CTCF	chr4:93656380-93656530	HL-60	blood:	n/a	n/a
28	CTCF	chr4:93619206-93619306	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:93656366-93656436	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr4:93656360-93656510	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:93656352-93656544	GM12878	blood:	n/a	n/a
32	CTCF	chr4:93656360-93656510	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr4:93656360-93656510	BE2_C	brain:	n/a	n/a
34	CTCF	chr4:93656300-93656450	HA-sp	spinal cord:	n/a	n/a
35	CTCF	chr4:93656340-93656490	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr4:93656297-93656484	MCF-7	breast:	n/a	n/a
37	CTCF	chr4:93646301-93646350	GM13977	blood:	n/a	n/a
38	CTCF	chr4:93664207-93664263	GM10248	blood:	n/a	n/a
39	CTCF	chr4:93682740-93682890	GM12872	blood:	n/a	n/a
40	CTCF	chr4:93656340-93656490	HCT-116	colon:	n/a	n/a
41	CTCF	chr4:93656360-93656510	HRPEpiC	eye:	n/a	n/a
42	CTCF	chr4:93656320-93656470	BE2_C	brain:	n/a	n/a
43	CTCF	chr4:93656320-93656470	HPF	lung:	n/a	n/a
44	CTCF	chr4:93656280-93656430	NHEK	skin:	n/a	n/a
45	CTCF	chr4:93656340-93656490	HPAF	blood vessel:	n/a	n/a
46	CTCF	chr4:93656320-93656470	HBMEC	blood vessel:	n/a	n/a
47	CTCF	chr4:93656320-93656470	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:93619226-93619317	Gliobla	brain:	n/a	n/a
49	CTCF	chr4:93656331-93656470	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr4:93656371-93656425	MCF-7	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:93646144-93646194	NH-A	brain:	n/a
2	chr4:93646144-93646194	HNPCEpiC	eye:	n/a
3	chr4:93646144-93646194	BE2_C	brain:	n/a
4	chr4:93646144-93646194	SKMC	muscle:	n/a
5	chr4:93646144-93646194	SK-N-SH_RA	brain:	n/a
6	chr4:93646144-93646194	HRCEpiC	kidney:	n/a
7	chr4:93646144-93646194	CMK	blood:	n/a
8	chr4:93646144-93646194	ProgFib	skin:	n/a
9	chr4:93646144-93646194	HMEC	breast:	n/a
10	chr4:93646144-93646194	Jurkat	blood:	n/a
11	chr4:93646144-93646194	BJ	skin:	n/a
12	chr4:93646144-93646194	RPTEC	kidney:	n/a
13	chr4:93646144-93646194	GM12878	blood:	n/a
14	chr4:93646144-93646194	AG04450	lung:	fetal
15	chr4:93646144-93646194	IMR90	lung:	fetal
16	chr4:93646144-93646194	NHDF-neo	bronchial:	n/a
17	chr4:93646144-93646194	NT2-D1	testis:	n/a
18	chr4:93646144-93646194	AoSMC	blood vessel:	n/a
19	chr4:93646144-93646194	HCPEpiC	choroid plexus:	n/a
20	chr4:93646144-93646194	HRE	kidney:	n/a
21	chr4:93646144-93646194	HRPEpiC	eye:	n/a
22	chr4:93646144-93646194	AG09319	gingival:	n/a
23	chr4:93646144-93646194	GM12892	blood:	n/a
24	chr4:93646144-93646194	GM06990	blood:	n/a
25	chr4:93646144-93646194	AG04449	skin:	fetal
26	chr4:93646144-93646194	NHBE	bronchial:	n/a
27	chr4:93646144-93646194	HCT-116	colon:	n/a
28	chr4:93646144-93646194	PrEC	prostate:	n/a
29	chr4:93646144-93646194	HUVEC	blood vessel:	n/a
30	chr4:93646144-93646194	Hepatocyte	liver:	n/a
31	chr4:93646144-93646194	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:93646144-93646194	H1-hESC	embryonic stem cell:	embryo
33	chr4:93646144-93646194	SK-N-MC	brain:	n/a
34	chr4:93646144-93646194	HIPEpiC	eye:	n/a
35	chr4:93646144-93646194	HEK293	kidney:	embryo
36	chr4:93646144-93646194	AG09309	skin:	n/a
37	chr4:93646144-93646194	MCF-7	breast:	n/a
38	chr4:93646144-93646194	A549	lung:	n/a
39	chr4:93646144-93646194	T-47D	breast:	n/a
40	chr4:93646144-93646194	K562	blood:	n/a
41	chr4:93646144-93646194	MCF10A-Er-Src	breast:	n/a
42	chr4:93646144-93646194	LNCaP	prostate:	n/a
43	chr4:93646144-93646194	ECC-1	luminal epithelium:	n/a
44	chr4:93646144-93646194	PFSK-1	brain:	n/a
45	chr4:93646144-93646194	HepG2	liver:	n/a
46	chr4:93646144-93646194	Hela-S3	cervix:	n/a
47	chr4:93646144-93646194	ovcar-3	ovarian:	n/a
48	chr4:93646144-93646194	GM19239	blood:	n/a
49	chr4:93646144-93646194	GM12891	blood:	n/a
50	chr4:93646144-93646194	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:93640334..93641891-chr4:93646345..93648572,2	MCF-7	breast:
2	chr4:93640334..93641891-chr4:93646345..93648572,2	MCF-7	breast:
3	chr4:93679131..93681725-chr4:93686462..93688437,2	K562	blood:
4	chr4:93679723..93682037-chr4:93683419..93685148,2	K562	blood:
5	chr4:93679723..93682037-chr4:93683419..93685148,2	K562	blood:
6	chr4:93679131..93681725-chr4:93686462..93688437,2	K562	blood:
7	chr4:93667707..93669873-chr4:93672761..93675696,2	K562	blood:
8	chr4:93667707..93669873-chr4:93672761..93675696,2	K562	blood:

No data

Variant related genes	Relation type
MTND1P19	TF binding region
MTND1P19	CpG island

Extended variants
information (count: 4096 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4096 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577016329	chr4:93588734-93588735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77442819	chr4:93588736-93588737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs62309230	chr4:93588808-93588809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs553596856	chr4:93588842-93588843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs529873357	chr4:93588854-93588855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs78058070	chr4:93588855-93588856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536025890	chr4:93588865-93588866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs544053075	chr4:93588888-93588889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs114425675	chr4:93588915-93588916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs544677245	chr4:93588926-93588927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs564574205	chr4:93588928-93588929	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs558501670	chr4:93588937-93588938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs578048249	chr4:93588989-93588990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540282094	chr4:93588992-93588993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs559580805	chr4:93588999-93589000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs77853606	chr4:93589015-93589016	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542000748	chr4:93589059-93589060	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs201639573	chr4:93589062-93589063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs561506334	chr4:93589135-93589136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs75050397	chr4:93589137-93589138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs550235588	chr4:93589144-93589145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs142491839	chr4:93589147-93589148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs562834132	chr4:93589148-93589149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs193298881	chr4:93589156-93589157	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567151663	chr4:93589195-93589196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs62309231	chr4:93589223-93589224	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs59589253	chr4:93589235-93589236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs569427206	chr4:93589278-93589279	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542361582	chr4:93589344-93589345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs62309232	chr4:93589379-93589380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs185126316	chr4:93589392-93589393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs190276421	chr4:93589393-93589394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs540597330	chr4:93589428-93589429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs531398613	chr4:93589453-93589454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62309233	chr4:93589511-93589512	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs191622797	chr4:93589513-93589514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541713615	chr4:93589580-93589581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs561671799	chr4:93589589-93589590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs571239457	chr4:93589612-93589613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs184259893	chr4:93589619-93589620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs530584764	chr4:93589639-93589640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs115230294	chr4:93589645-93589646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188153376	chr4:93589649-93589650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559419684	chr4:93589665-93589666	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180811691	chr4:93589671-93589672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374727269	chr4:93589716-93589717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566302477	chr4:93589724-93589725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs528884551	chr4:93589736-93589737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186201391	chr4:93589740-93589741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs569583752	chr4:93589748-93589749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
lymphocytic leukemia	21291569	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
Parkinson disease	18923514	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	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
Chronic lymphocytic leukemia	20421269	CNVD
Myelodysplastic syndrome	21251322	CNVD
Lung cancer	18438408	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Autism	18414403	CNVD
primary effusion lymphomas	17116491	CNVD
Mental retardation	20522426	CNVD
delayed speech	20522426	CNVD
growth disorder	20522426	CNVD
Olfactory neuroblastoma	18408657	CNVD
small cell lung cancer	20016488	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
Colorectal cancer	20459617	CNVD
Acute monocytic leukemia	16498392	CNVD
Multiple myeloma	16616336	CNVD
Esophageal adenocarcinoma	18820669	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Parkinson disease	20877625	CNVD
Hirschsprung''s Disease	21712996	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
Cancer	19907438	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Bipolar disorder	19114987	CNVD
Autism	20841430	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:93579800-93590600	Weak transcription	HUES48 Cell Line	embryonic stem cell
2	chr4:93587800-93591800	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr4:93590400-93590800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr4:93590600-93591400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr4:93590600-93592000	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr4:93590600-93592000	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr4:93591400-93592000	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr4:93591400-93592400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr4:93591400-93592400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:93591800-93592600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr4:93592000-93595200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr4:93592400-93592600	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr4:93595200-93595600	Strong transcription	HUES48 Cell Line	embryonic stem cell
14	chr4:93595600-93598600	Weak transcription	HUES48 Cell Line	embryonic stem cell
15	chr4:93598200-93599200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr4:93598600-93599200	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr4:93599200-93624000	Weak transcription	HUES48 Cell Line	embryonic stem cell
18	chr4:93601600-93602000	Enhancers	Brain Angular Gyrus	brain
19	chr4:93606400-93612600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr4:93606400-93617200	Weak transcription	HUES64 Cell Line	embryonic stem cell
21	chr4:93607600-93612200	Weak transcription	H1 Cell Line	embryonic stem cell
22	chr4:93618200-93618800	Enhancers	Fetal Intestine Large	intestine
23	chr4:93622800-93623200	Enhancers	Liver	Liver
24	chr4:93623000-93623800	Enhancers	Fetal Intestine Small	intestine
25	chr4:93629200-93631600	Weak transcription	H1 Cell Line	embryonic stem cell
26	chr4:93630200-93635000	Weak transcription	HUES6 Cell Line	embryonic stem cell
27	chr4:93630200-93655400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
28	chr4:93630600-93635800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr4:93631600-93633000	Strong transcription	H1 Cell Line	embryonic stem cell
30	chr4:93633000-93646000	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr4:93635000-93636000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chr4:93635800-93636000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr4:93635800-93636000	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr4:93635800-93636400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:93636000-93653600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr4:93636000-93687200	Weak transcription	HUES48 Cell Line	embryonic stem cell
37	chr4:93649400-93649800	Enhancers	NHEK	skin
38	chr4:93649600-93650000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr4:93649600-93653600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr4:93650000-93654000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr4:93651200-93652000	Enhancers	Cortex derived primary cultured neurospheres	brain
42	chr4:93653600-93654000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr4:93653600-93654000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr4:93653600-93654800	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr4:93654000-93654200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr4:93654000-93655200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr4:93654000-93655200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr4:93654000-93658200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chr4:93654200-93654400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:93654400-93654600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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