Variant report

Variant	nsv830836
Chromosome Location	chr6:146423405-146598983
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:351)
CpG islands
(count:61)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:351 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:146569448-146569677	K562	blood:	n/a	n/a
2	BACH1	chr6:146583467-146583520	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr6:146474172-146474518	GM12878	blood:	n/a	n/a
4	BATF	chr6:146474251-146474520	GM12878	blood:	n/a	n/a
5	BCLAF1	chr6:146474282-146474515	GM12878	blood:	n/a	n/a
6	CBX3	chr6:146564813-146565096	K562	blood:	n/a	n/a
7	CEBPB	chr6:146515446-146516003	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr6:146569360-146569604	A549	lung:	n/a	chr6:146569527-146569538
9	CEBPB	chr6:146598395-146598497	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr6:146585699-146585750	IMR90	lung:	n/a	chr6:146585726-146585737
11	CEBPB	chr6:146537471-146537478	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr6:146513199-146513501	HepG2	liver:	n/a	chr6:146513203-146513216 chr6:146513203-146513216 chr6:146513384-146513395 chr6:146513346-146513357 chr6:146513203-146513216
13	CEBPB	chr6:146513262-146513426	A549	lung:	n/a	chr6:146513384-146513395 chr6:146513346-146513357
14	CEBPB	chr6:146459189-146459389	IMR90	lung:	n/a	n/a
15	CEBPB	chr6:146439066-146439125	K562	blood:	n/a	chr6:146439086-146439097 chr6:146439084-146439097 chr6:146439084-146439097
16	CEBPB	chr6:146480449-146480716	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr6:146458036-146458074	HepG2	liver:	n/a	chr6:146458043-146458054
18	CEBPB	chr6:146592796-146593147	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr6:146480453-146480659	IMR90	lung:	n/a	n/a
20	CEBPB	chr6:146576815-146576962	K562	blood:	n/a	chr6:146576871-146576882
21	CEBPB	chr6:146545619-146545909	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr6:146424836-146425193	HepG2	liver:	n/a	chr6:146425007-146425018
23	CEBPB	chr6:146522904-146523123	HepG2	liver:	n/a	chr6:146522980-146522991
24	CEBPB	chr6:146480431-146480773	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:146582342-146582524	HepG2	liver:	n/a	chr6:146582402-146582415 chr6:146582403-146582414
26	CEBPB	chr6:146477852-146478138	A549	lung:	n/a	chr6:146477999-146478010
27	CEBPB	chr6:146448908-146449088	IMR90	lung:	n/a	n/a
28	CEBPB	chr6:146578795-146579123	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr6:146480476-146480771	A549	lung:	n/a	n/a
30	CEBPB	chr6:146459211-146459238	K562	blood:	n/a	n/a
31	CEBPB	chr6:146576790-146576929	A549	lung:	n/a	chr6:146576871-146576882
32	CEBPB	chr6:146437100-146437241	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr6:146424841-146425172	A549	lung:	n/a	chr6:146425007-146425018
34	CEBPB	chr6:146424890-146425163	IMR90	lung:	n/a	chr6:146425007-146425018
35	CEBPB	chr6:146585580-146585891	HepG2	liver:	n/a	chr6:146585726-146585737
36	CEBPB	chr6:146477884-146478169	K562	blood:	n/a	chr6:146477999-146478010
37	CEBPB	chr6:146424812-146425194	H1-hESC	embryonic stem cell:	n/a	chr6:146425007-146425018
38	CEBPB	chr6:146477862-146478178	IMR90	lung:	n/a	chr6:146477999-146478010
39	CEBPB	chr6:146576708-146577037	HepG2	liver:	n/a	chr6:146576871-146576882
40	CEBPB	chr6:146547414-146547542	HepG2	liver:	n/a	n/a
41	CEBPB	chr6:146477840-146478185	HepG2	liver:	n/a	chr6:146477999-146478010
42	CEBPB	chr6:146569410-146569631	HepG2	liver:	n/a	chr6:146569527-146569538
43	CTCF	chr6:146433080-146433230	GM12873	blood:	n/a	n/a
44	CTCF	chr6:146490940-146491090	AG10803	skin:	n/a	n/a
45	CTCF	chr6:146433120-146433270	SAEC	small airway:	n/a	n/a
46	CTCF	chr6:146537880-146538030	MCF-7	breast:	n/a	chr6:146537971-146537979 chr6:146537966-146537979 chr6:146537964-146537982 chr6:146537965-146537981
47	CTCF	chr6:146506760-146506910	GM12872	blood:	n/a	n/a
48	CTCF	chr6:146537940-146538090	MCF-7	breast:	n/a	chr6:146537971-146537979 chr6:146537966-146537979 chr6:146537964-146537982 chr6:146537965-146537981
49	CTCF	chr6:146466940-146467090	HEK293	kidney:	n/a	n/a
50	CTCF	chr6:146570899-146570931	GM13976	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:146531540-146531590	AG10803	skin:	n/a
2	chr6:146531540-146531590	HNPCEpiC	eye:	n/a
3	chr6:146531540-146531590	HRE	kidney:	n/a
4	chr6:146531540-146531590	GM19239	blood:	n/a
5	chr6:146531540-146531590	T-47D	breast:	n/a
6	chr6:146531540-146531590	NT2-D1	testis:	n/a
7	chr6:146531540-146531590	HRPEpiC	eye:	n/a
8	chr6:146531540-146531590	Jurkat	blood:	n/a
9	chr6:146531540-146531590	NH-A	brain:	n/a
10	chr6:146531540-146531590	A549	lung:	n/a
11	chr6:146531540-146531590	HMEC	breast:	n/a
12	chr6:146531540-146531590	HUVEC	blood vessel:	n/a
13	chr6:146531540-146531590	BJ	skin:	n/a
14	chr6:146531540-146531590	HEK293	kidney:	embryo
15	chr6:146531540-146531590	SK-N-SH_RA	brain:	n/a
16	chr6:146531540-146531590	HCF	heart:	n/a
17	chr6:146531540-146531590	PrEC	prostate:	n/a
18	chr6:146531540-146531590	H1-hESC	embryonic stem cell:	embryo
19	chr6:146531540-146531590	LNCaP	prostate:	n/a
20	chr6:146531540-146531590	AG09309	skin:	n/a
21	chr6:146531540-146531590	ECC-1	luminal epithelium:	n/a
22	chr6:146531540-146531590	HEEpiC	esophagus:	n/a
23	chr6:146531540-146531590	AG04450	lung:	fetal
24	chr6:146531540-146531590	AG09319	gingival:	n/a
25	chr6:146531540-146531590	NHDF-neo	bronchial:	n/a
26	chr6:146531540-146531590	ovcar-3	ovarian:	n/a
27	chr6:146531540-146531590	IMR90	lung:	fetal
28	chr6:146531540-146531590	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:146531540-146531590	NHBE	bronchial:	n/a
30	chr6:146531540-146531590	BE2_C	brain:	n/a
31	chr6:146531540-146531590	HL-60	blood:	n/a
32	chr6:146531540-146531590	GM12878	blood:	n/a
33	chr6:146531540-146531590	GM12892	blood:	n/a
34	chr6:146531540-146531590	RPTEC	kidney:	n/a
35	chr6:146531540-146531590	HCPEpiC	choroid plexus:	n/a
36	chr6:146531540-146531590	MCF10A-Er-Src	breast:	n/a
37	chr6:146531540-146531590	HCT-116	colon:	n/a
38	chr6:146531540-146531590	CMK	blood:	n/a
39	chr6:146531540-146531590	SK-N-MC	brain:	n/a
40	chr6:146531540-146531590	Hepatocyte	liver:	n/a
41	chr6:146531540-146531590	HRCEpiC	kidney:	n/a
42	chr6:146531540-146531590	SK-N-SH	brain:	n/a
43	chr6:146531540-146531590	Caco-2	colon:	n/a
44	chr6:146531540-146531590	HCM	heart:	n/a
45	chr6:146531540-146531590	SKMC	muscle:	n/a
46	chr6:146531540-146531590	HepG2	liver:	n/a
47	chr6:146531540-146531590	NB4	blood:	n/a
48	chr6:146531540-146531590	HAEpiC	amniotic membrane:	n/a
49	chr6:146531540-146531590	PFSK-1	brain:	n/a
50	chr6:146531540-146531590	GM06990	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:146526878..146529023-chr6:146553094..146554769,2	K562	blood:
2	chr6:146536618..146538923-chr6:146542956..146544904,2	MCF-7	breast:
3	chr6:146536618..146538923-chr6:146542956..146544904,2	MCF-7	breast:
4	chr6:146547469..146550285-chr6:146550363..146553095,2	K562	blood:
5	chr6:146541745..146544017-chr6:146545703..146548132,3	K562	blood:
6	chr6:146541745..146543405-chr6:146546212..146548132,2	K562	blood:
7	chr1:121484765..121486916-chr6:146556880..146559469,2	MCF-7	breast:
8	chr6:146523131..146524644-chr6:146526185..146529054,2	K562	blood:
9	chr6:146547469..146550285-chr6:146550363..146553095,2	K562	blood:
10	chr6:146541745..146544017-chr6:146545703..146548132,3	K562	blood:
11	chr6:146526878..146529023-chr6:146553094..146554769,2	K562	blood:
12	chr10:67683432..67684136-chr6:146499237..146499803,2	MCF-7	breast:
13	chr6:146541745..146543405-chr6:146546212..146548132,2	K562	blood:
14	chr20:26188443..26190652-chr6:146588836..146590356,3	K562	blood:
15	chr6:146523131..146524644-chr6:146526185..146529054,2	K562	blood:

No data

Variant related genes	Relation type
FUNDC2P3	TF binding region
FUNDC2P3	CpG island
ENSG00000227195	chromatin interactions

Extended variants
information (count: 2981 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2981 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376176190	chr6:146424465-146424466	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs565974645	chr6:146424498-146424499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs184881181	chr6:146424505-146424506	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs189924433	chr6:146424553-146424554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs11155452	chr6:146424631-146424632	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs181140549	chr6:146424701-146424702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs570286035	chr6:146424707-146424708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs184502188	chr6:146424708-146424709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs575584941	chr6:146424759-146424760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs554511303	chr6:146424767-146424768	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73784783	chr6:146424768-146424769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs374562428	chr6:146424864-146424865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs142131601	chr6:146424911-146424912	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs188154130	chr6:146424952-146424953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs182019334	chr6:146424968-146424969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377008059	chr6:146424989-146424990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs561178808	chr6:146425061-146425062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs574643396	chr6:146425100-146425101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543697569	chr6:146425115-146425116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs563587330	chr6:146425116-146425117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs151142617	chr6:146425162-146425163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560818135	chr6:146427408-146427409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs560834347	chr6:146427417-146427418	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs372457791	chr6:146427466-146427467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529594313	chr6:146427495-146427496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs548159984	chr6:146427521-146427522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377032289	chr6:146427526-146427527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs561714971	chr6:146427552-146427553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370949188	chr6:146427589-146427590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530522542	chr6:146427595-146427596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs550654471	chr6:146427598-146427599	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs529825504	chr6:146427607-146427608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541370703	chr6:146427620-146427621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570577248	chr6:146427652-146427653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs578013919	chr6:146427661-146427662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs539590644	chr6:146427696-146427697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs77290522	chr6:146427765-146427766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs566741676	chr6:146427794-146427795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs549898162	chr6:146427812-146427813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs555336081	chr6:146427827-146427828	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs575196090	chr6:146427842-146427843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs563912978	chr6:146427869-146427870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs537866853	chr6:146427901-146427902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs139584154	chr6:146427925-146427926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188050422	chr6:146427954-146427955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs540806500	chr6:146428021-146428022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs189807433	chr6:146428046-146428047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs17824144	chr6:146428071-146428072	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
49	rs183518489	chr6:146428116-146428117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs368297700	chr6:146428119-146428120	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Autism	22495311	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Cerebellar ataxia	22138850	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:218 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:146424400-146424600	Enhancers	Aorta	Aorta
2	chr6:146424400-146425000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr6:146424400-146425200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr6:146424400-146425200	Enhancers	H9 Cell Line	embryonic stem cell
5	chr6:146427400-146428200	Enhancers	Fetal Heart	heart
6	chr6:146427600-146428600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr6:146428200-146433000	Weak transcription	Fetal Heart	heart
8	chr6:146430400-146430600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr6:146432600-146433000	Enhancers	Fetal Brain Male	brain
10	chr6:146432800-146434800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr6:146433000-146433400	Enhancers	Fetal Brain Female	brain
12	chr6:146433000-146434000	Weak transcription	Fetal Brain Male	brain
13	chr6:146433000-146435400	Enhancers	Fetal Heart	heart
14	chr6:146433400-146433800	Weak transcription	Fetal Brain Female	brain
15	chr6:146433600-146434000	Enhancers	Brain Anterior Caudate	brain
16	chr6:146433800-146434400	Enhancers	Fetal Brain Female	brain
17	chr6:146434000-146434200	Enhancers	Fetal Brain Male	brain
18	chr6:146434200-146434600	Weak transcription	Fetal Brain Male	brain
19	chr6:146434600-146435200	Enhancers	Fetal Brain Male	brain
20	chr6:146456800-146457600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr6:146470600-146471000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr6:146470800-146471200	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr6:146470800-146471200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr6:146470800-146471200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:146470800-146471200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr6:146471000-146475200	Weak transcription	HUES64 Cell Line	embryonic stem cell
27	chr6:146471200-146474600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
28	chr6:146471200-146475000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
29	chr6:146471200-146475400	Weak transcription	HUES48 Cell Line	embryonic stem cell
30	chr6:146474000-146475000	Enhancers	GM12878-XiMat	blood
31	chr6:146474600-146475800	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr6:146474800-146475600	Enhancers	H1 Cell Line	embryonic stem cell
33	chr6:146475000-146475600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr6:146475000-146475600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr6:146475000-146475800	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr6:146475200-146475800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:146475200-146475800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:146475200-146475800	Enhancers	HUES64 Cell Line	embryonic stem cell
39	chr6:146475200-146476000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:146475400-146475800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr6:146475800-146477000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:146477000-146477200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:146477200-146477600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:146477600-146478000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr6:146487400-146488800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr6:146496000-146496200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:146496000-146496200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:146496200-146499200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:146498000-146498600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:146498000-146498800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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