Variant report

Variant	nsv886677
Chromosome Location	chr6:133454738-133515602
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	chr6:133506110-133506140	K562	blood:	n/a	n/a
2	BACH1	chr6:133510199-133510234	H1-hESC	embryonic stem cell:	n/a	n/a
3	CEBPB	chr6:133491090-133491336	H1-hESC	embryonic stem cell:	n/a	chr6:133491144-133491155 chr6:133491144-133491155
4	CEBPB	chr6:133481822-133481901	IMR90	lung:	n/a	n/a
5	CEBPB	chr6:133457963-133458163	HepG2	liver:	n/a	chr6:133458059-133458070
6	CEBPB	chr6:133512450-133512823	ECC-1	luminal epithelium:	n/a	n/a
7	CEBPB	chr6:133477881-133478176	IMR90	lung:	n/a	n/a
8	CEBPB	chr6:133491808-133492179	IMR90	lung:	n/a	chr6:133491984-133491995
9	CEBPB	chr6:133491832-133492158	HepG2	liver:	n/a	chr6:133491984-133491995
10	CEBPB	chr6:133491827-133492159	A549	lung:	n/a	chr6:133491984-133491995
11	CEBPB	chr6:133512463-133512947	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr6:133491733-133492216	MCF-7	breast:	n/a	chr6:133491984-133491995
13	CEBPB	chr6:133491818-133492148	H1-hESC	embryonic stem cell:	n/a	chr6:133491984-133491995
14	CEBPB	chr6:133491790-133492175	Hela-S3	cervix:	n/a	chr6:133491984-133491995
15	CEBPB	chr6:133477911-133478150	A549	lung:	n/a	n/a
16	CEBPB	chr6:133491762-133492187	MCF-7	breast:	n/a	chr6:133491984-133491995
17	CTCF	chr6:133506020-133506170	HUVEC	blood vessel:	n/a	chr6:133506131-133506152
18	CTCF	chr6:133505680-133505830	AG10803	skin:	n/a	n/a
19	CTCF	chr6:133506060-133506210	HPF	lung:	n/a	chr6:133506131-133506152
20	CTCF	chr6:133506040-133506190	GM12801	blood:	n/a	chr6:133506131-133506152
21	CTCF	chr6:133506100-133506250	WERI-Rb-1	eye:	n/a	chr6:133506131-133506152
22	CTCF	chr6:133506072-133506192	Spleen_OC	spleen:	n/a	chr6:133506131-133506152
23	CTCF	chr6:133505913-133506403	HCT-116	colon:	n/a	chr6:133506131-133506152
24	CTCF	chr6:133505983-133506257	Medullo	brain:	n/a	chr6:133506131-133506152
25	CTCF	chr6:133513060-133513210	HBMEC	blood vessel:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
26	CTCF	chr6:133505910-133506436	IMR90	lung:	n/a	chr6:133506131-133506152
27	CTCF	chr6:133512980-133513130	NHLF	lung:	n/a	n/a
28	CTCF	chr6:133506440-133506590	HMF	breast:	n/a	n/a
29	CTCF	chr6:133482440-133482590	HEK293	kidney:	n/a	n/a
30	CTCF	chr6:133513040-133513190	HPAF	blood vessel:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
31	CTCF	chr6:133513080-133513230	A549	lung:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
32	CTCF	chr6:133506080-133506230	K562	blood:	n/a	chr6:133506131-133506152
33	CTCF	chr6:133506020-133506170	RPTEC	kidney:	n/a	chr6:133506131-133506152
34	CTCF	chr6:133506020-133506170	HCT-116	colon:	n/a	chr6:133506131-133506152
35	CTCF	chr6:133506040-133506190	HPF	lung:	n/a	chr6:133506131-133506152
36	CTCF	chr6:133505800-133505950	GM12864	blood:	n/a	n/a
37	CTCF	chr6:133473391-133473432	GM20000	blood:	n/a	n/a
38	CTCF	chr6:133513080-133513230	HCM	heart:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
39	CTCF	chr6:133513040-133513190	HRPEpiC	eye:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
40	CTCF	chr6:133506060-133506210	HepG2	liver:	n/a	chr6:133506131-133506152
41	CTCF	chr6:133506380-133506530	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr6:133513100-133513250	AG04449	skin:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
43	CTCF	chr6:133513100-133513250	MCF-7	breast:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
44	CTCF	chr6:133506080-133506230	HEK293	kidney:	n/a	chr6:133506131-133506152
45	CTCF	chr6:133513027-133513285	GM12878	blood:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
46	CTCF	chr6:133505720-133505870	Caco-2	colon:	n/a	n/a
47	CTCF	chr6:133513060-133513210	SAEC	small airway:	n/a	chr6:133513154-133513175 chr6:133513152-133513170 chr6:133513155-133513168
48	CTCF	chr6:133506060-133506210	Hela-S3	cervix:	n/a	chr6:133506131-133506152
49	CTCF	chr6:133506140-133506290	GM12873	blood:	n/a	n/a
50	CTCF	chr6:133505919-133506354	A549	lung:	n/a	chr6:133506131-133506152

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:133468924-133468974	U87	brain:	n/a
2	chr6:133480830-133480880	HAEpiC	amniotic membrane:	n/a
3	chr6:133468924-133468974	HCPEpiC	choroid plexus:	n/a
4	chr6:133486947-133486997	PrEC	prostate:	n/a
5	chr6:133486947-133486997	Hela-S3	cervix:	n/a
6	chr6:133480830-133480880	HepG2	liver:	n/a
7	chr6:133486947-133486997	BE2_C	brain:	n/a
8	chr6:133486947-133486997	RPTEC	kidney:	n/a
9	chr6:133480830-133480880	Jurkat	blood:	n/a
10	chr6:133468924-133468974	LNCaP	prostate:	n/a
11	chr6:133486947-133486997	ECC-1	luminal epithelium:	n/a
12	chr6:133486947-133486997	K562	blood:	n/a
13	chr6:133486947-133486997	NHBE	bronchial:	n/a
14	chr6:133480830-133480880	BE2_C	brain:	n/a
15	chr6:133480830-133480880	H1-hESC	embryonic stem cell:	embryo
16	chr6:133486947-133486997	PANC-1	pancreas:	n/a
17	chr6:133468924-133468974	ECC-1	luminal epithelium:	n/a
18	chr6:133486947-133486997	NT2-D1	testis:	n/a
19	chr6:133468924-133468974	RPTEC	kidney:	n/a
20	chr6:133468924-133468974	AG09309	skin:	n/a
21	chr6:133486947-133486997	HCM	heart:	n/a
22	chr6:133480830-133480880	ovcar-3	ovarian:	n/a
23	chr6:133486947-133486997	IMR90	lung:	fetal
24	chr6:133480830-133480880	HIPEpiC	eye:	n/a
25	chr6:133468924-133468974	AG04449	skin:	fetal
26	chr6:133468924-133468974	HRCEpiC	kidney:	n/a
27	chr6:133468924-133468974	T-47D	breast:	n/a
28	chr6:133468924-133468974	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:133480830-133480880	RPTEC	kidney:	n/a
30	chr6:133486947-133486997	SKMC	muscle:	n/a
31	chr6:133486947-133486997	T-47D	breast:	n/a
32	chr6:133468924-133468974	PANC-1	pancreas:	n/a
33	chr6:133480830-133480880	HCF	heart:	n/a
34	chr6:133486947-133486997	HEEpiC	esophagus:	n/a
35	chr6:133480830-133480880	NH-A	brain:	n/a
36	chr6:133486947-133486997	HL-60	blood:	n/a
37	chr6:133468924-133468974	K562	blood:	n/a
38	chr6:133480830-133480880	LNCaP	prostate:	n/a
39	chr6:133486947-133486997	ovcar-3	ovarian:	n/a
40	chr6:133486947-133486997	GM06990	blood:	n/a
41	chr6:133486947-133486997	SK-N-MC	brain:	n/a
42	chr6:133486947-133486997	AG04449	skin:	fetal
43	chr6:133480830-133480880	GM06990	blood:	n/a
44	chr6:133486947-133486997	HAEpiC	amniotic membrane:	n/a
45	chr6:133480830-133480880	HL-60	blood:	n/a
46	chr6:133468924-133468974	ProgFib	skin:	n/a
47	chr6:133468924-133468974	AG04450	lung:	fetal
48	chr6:133480830-133480880	PFSK-1	brain:	n/a
49	chr6:133486947-133486997	AG10803	skin:	n/a
50	chr6:133480830-133480880	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr6:133484970..133486703-chr6:133490391..133493056,2	MCF-7	breast:
2	chr6:133505838..133506428-chr6:133832666..133833298,2	MCF-7	breast:
3	chr6:133432444..133434710-chr6:133454320..133456376,2	K562	blood:
4	chr6:133133722..133135487-chr6:133500551..133504315,3	K562	blood:
5	chr6:133451353..133453711-chr6:133454744..133456553,2	MCF-7	breast:
6	chr6:133423980..133426292-chr6:133454398..133456094,2	K562	blood:
7	chr6:133151552..133152231-chr6:133505787..133506589,2	MCF-7	breast:
8	chr6:133512728..133513279-chr6:133689484..133690000,2	MCF-7	breast:
9	chr6:133484970..133486703-chr6:133490391..133493056,2	MCF-7	breast:
10	chr6:133283739..133284591-chr6:133505537..133506147,2	MCF-7	breast:
11	chr6:133139428..133141767-chr6:133455373..133456926,2	K562	blood:
12	chr6:133505840..133506389-chr6:133833295..133833930,2	MCF-7	breast:
13	chr6:133505707..133506822-chr6:133833315..133834160,3	MCF-7	breast:

Variant related genes	Relation type
MTCYBP4	TF binding region
MTCYBP4	CpG island
ENSG00000227954	chromatin interactions

Extended variants
information (count: 1310 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1310 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6913444	chr6:133454738-133454739	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531725228	chr6:133454755-133454756	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545694414	chr6:133454804-133454805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs562612841	chr6:133454806-133454807	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs199563540	chr6:133454821-133454822	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs370221521	chr6:133454885-133454886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs574864077	chr6:133454909-133454910	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs531692369	chr6:133454931-133454932	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541779436	chr6:133454987-133454988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs561784391	chr6:133455028-133455029	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527959837	chr6:133455029-133455030	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs60602170	chr6:133455053-133455054	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs567410916	chr6:133455103-133455104	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs368428209	chr6:133455153-133455154	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs17062132	chr6:133455254-133455255	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs374120561	chr6:133455352-133455353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550401382	chr6:133455373-133455374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs60247951	chr6:133455375-133455376	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs77655558	chr6:133455402-133455403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs548203532	chr6:133455431-133455432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs139386548	chr6:133455440-133455441	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533830210	chr6:133455456-133455457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553998685	chr6:133455499-133455500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182197824	chr6:133455533-133455534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539570473	chr6:133455550-133455551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs555948352	chr6:133455600-133455601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs576116696	chr6:133455609-133455610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs79142198	chr6:133455738-133455739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs368744681	chr6:133455769-133455770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs572373637	chr6:133455801-133455802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs541091249	chr6:133455807-133455808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564755196	chr6:133455852-133455853	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377380139	chr6:133455885-133455886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs533467012	chr6:133455908-133455909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs185209519	chr6:133455946-133455947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs563919344	chr6:133455967-133455968	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200588602	chr6:133456008-133456009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531412634	chr6:133456009-133456010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565504131	chr6:133456067-133456068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs548338181	chr6:133456116-133456117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs58777641	chr6:133456208-133456209	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs533754059	chr6:133456220-133456221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs112637568	chr6:133456230-133456231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146413175	chr6:133456274-133456275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73773545	chr6:133456307-133456308	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs139800904	chr6:133456343-133456344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs143317835	chr6:133456362-133456363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs575868974	chr6:133456401-133456402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs183255804	chr6:133456418-133456419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145507382	chr6:133456440-133456441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

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
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	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
Ependymoma	16718352	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
Prostate cancer	18632612	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Invasive pancreatic ductal carcinoma	16982739	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
Non-muscle invasive bladder neoplasm	19445696	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21785460	CNVD
Kartagener syndrome	16639409	CNVD
Breast cancer	17133270	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:160 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:133448600-133455200	Enhancers	Fetal Muscle Leg	muscle
2	chr6:133453800-133457600	Weak transcription	Brain Germinal Matrix	brain
3	chr6:133454000-133457400	Weak transcription	Brain Substantia Nigra	brain
4	chr6:133454200-133455400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr6:133454200-133457000	Weak transcription	Fetal Muscle Trunk	muscle
6	chr6:133454200-133457200	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr6:133454200-133457200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr6:133454600-133457200	Weak transcription	Fetal Kidney	kidney
9	chr6:133454600-133457400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
10	chr6:133455200-133456400	Weak transcription	Fetal Muscle Leg	muscle
11	chr6:133456400-133456600	Enhancers	Fetal Muscle Leg	muscle
12	chr6:133456600-133457000	Weak transcription	Fetal Muscle Leg	muscle
13	chr6:133457000-133457400	Enhancers	Fetal Muscle Trunk	muscle
14	chr6:133457000-133457600	Enhancers	Fetal Muscle Leg	muscle
15	chr6:133457200-133458000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:133457200-133459200	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chr6:133457400-133457800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr6:133457400-133458200	Enhancers	Brain Substantia Nigra	brain
19	chr6:133457600-133457800	Enhancers	Fetal Kidney	kidney
20	chr6:133457600-133458000	Enhancers	Brain Angular Gyrus	brain
21	chr6:133457600-133458000	Enhancers	Brain Cingulate Gyrus	brain
22	chr6:133457600-133458000	Enhancers	Brain Germinal Matrix	brain
23	chr6:133457600-133458000	Enhancers	Fetal Brain Male	brain
24	chr6:133457600-133458800	Weak transcription	Fetal Muscle Leg	muscle
25	chr6:133459000-133459200	Enhancers	Fetal Muscle Leg	muscle
26	chr6:133468800-133469000	Active TSS	HUES64 Cell Line	embryonic stem cell
27	chr6:133468800-133469200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
28	chr6:133468800-133469200	Active TSS	H9 Cell Line	embryonic stem cell
29	chr6:133468800-133469200	Active TSS	HUES6 Cell Line	embryonic stem cell
30	chr6:133468800-133469600	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr6:133469000-133469200	Enhancers	H1 Cell Line	embryonic stem cell
32	chr6:133469000-133469200	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
33	chr6:133478600-133478800	Enhancers	Fetal Kidney	kidney
34	chr6:133479400-133479600	Enhancers	Fetal Kidney	kidney
35	chr6:133480000-133480800	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr6:133480200-133480600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr6:133480200-133481000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:133480200-133481000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
39	chr6:133480200-133482000	Enhancers	Brain Cingulate Gyrus	brain
40	chr6:133480200-133482400	Enhancers	Brain Hippocampus Middle	brain
41	chr6:133480400-133481000	Enhancers	Brain Anterior Caudate	brain
42	chr6:133480400-133481800	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr6:133480600-133481200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
44	chr6:133480600-133481200	Enhancers	Brain Substantia Nigra	brain
45	chr6:133480600-133482000	Enhancers	Brain Angular Gyrus	brain
46	chr6:133480600-133485600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
47	chr6:133481200-133481600	Weak transcription	Brain Substantia Nigra	brain
48	chr6:133481600-133482200	Enhancers	Brain Substantia Nigra	brain
49	chr6:133481800-133482200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr6:133481800-133482400	Weak transcription	Brain Inferior Temporal Lobe	brain

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