Variant report

Variant	nsv603439
Chromosome Location	chr6:66115654-66232692
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:208)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:208 , 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	chr6:66120388-66120433	HepG2	liver:	n/a	n/a
2	ATF1	chr6:66160376-66160599	K562	blood:	n/a	n/a
3	ATF1	chr6:66171007-66171493	K562	blood:	n/a	n/a
4	CBX3	chr6:66193565-66193851	K562	blood:	n/a	n/a
5	CCNT2	chr6:66171045-66171349	K562	blood:	n/a	n/a
6	CCNT2	chr6:66139022-66139218	K562	blood:	n/a	n/a
7	CEBPB	chr6:66156810-66157084	K562	blood:	n/a	n/a
8	CEBPB	chr6:66230294-66230581	IMR90	lung:	n/a	n/a
9	CEBPB	chr6:66192989-66193263	HepG2	liver:	n/a	chr6:66193166-66193179 chr6:66193107-66193120 chr6:66193107-66193118
10	CEBPB	chr6:66143961-66144277	HepG2	liver:	n/a	n/a
11	CEBPB	chr6:66195051-66195251	IMR90	lung:	n/a	n/a
12	CEBPB	chr6:66156754-66157125	HepG2	liver:	n/a	chr6:66157101-66157114
13	CEBPB	chr6:66230260-66230571	HepG2	liver:	n/a	n/a
14	CEBPB	chr6:66138219-66138426	HepG2	liver:	n/a	chr6:66138267-66138278
15	CEBPB	chr6:66127902-66128153	HepG2	liver:	n/a	chr6:66128011-66128022 chr6:66128012-66128021
16	CEBPB	chr6:66120214-66120512	HepG2	liver:	n/a	n/a
17	CEBPD	chr6:66171023-66171458	K562	blood:	n/a	n/a
18	CTCF	chr6:66218761-66218798	GM20000	blood:	n/a	n/a
19	CTCF	chr6:66157717-66157767	LNCaP	prostate:	n/a	n/a
20	CTCF	chr6:66157600-66157750	BE2_C	brain:	n/a	n/a
21	CTCF	chr6:66157644-66157761	MCF-7	breast:	n/a	n/a
22	CTCF	chr6:66117250-66117306	GM20000	blood:	n/a	n/a
23	CTCF	chr6:66157720-66157870	MCF-7	breast:	n/a	n/a
24	CTCF	chr6:66157685-66157759	LNCaP	prostate:	n/a	n/a
25	CTCF	chr6:66119174-66119372	GM12878	blood:	n/a	n/a
26	CTCF	chr6:66157620-66157770	Caco-2	colon:	n/a	n/a
27	CTCF	chr6:66128422-66128491	Lung_OC	lung:	n/a	n/a
28	CTCF	chr6:66157620-66157770	HRPEpiC	eye:	n/a	n/a
29	CTCF	chr6:66157626-66157803	MCF-7	breast:	n/a	n/a
30	CTCF	chr6:66157560-66157710	BE2_C	brain:	n/a	n/a
31	CTCF	chr6:66157500-66157650	MCF-7	breast:	n/a	n/a
32	CTCF	chr6:66157771-66157802	LNCaP	prostate:	n/a	n/a
33	CTCF	chr6:66157563-66157836	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:66157678-66157758	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr6:66157640-66157790	WERI-Rb-1	eye:	n/a	n/a
36	CTCF	chr6:66201727-66201746	GM13977	blood:	n/a	n/a
37	CUX1	chr6:66170915-66171409	K562	blood:	n/a	n/a
38	CUX1	chr6:66138046-66138073	GM12878	blood:	n/a	n/a
39	E2F4	chr6:66229242-66229246	MCF10A-Er-Src	breast:	n/a	n/a
40	E2F4	chr6:66196398-66196435	MCF10A-Er-Src	breast:	n/a	n/a
41	E2F4	chr6:66136356-66136509	MCF10A-Er-Src	breast:	n/a	n/a
42	EP300	chr6:66204811-66205276	SK-N-SH_RA	brain:	n/a	n/a
43	EP300	chr6:66205017-66205334	SK-N-SH_RA	brain:	n/a	n/a
44	EP300	chr6:66171008-66171473	K562	blood:	n/a	n/a
45	EP300	chr6:66151712-66151970	K562	blood:	n/a	chr6:66151772-66151779
46	EP300	chr6:66205564-66205867	SK-N-SH_RA	brain:	n/a	n/a
47	FOS	chr6:66171113-66171444	HUVEC	blood vessel:	n/a	chr6:66171237-66171248
48	FOS	chr6:66157529-66157688	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr6:66170472-66170571	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr6:66157443-66157925	HUVEC	blood vessel:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66207286-66207336	GM12878	blood:	n/a
2	chr6:66207286-66207336	AG09319	gingival:	n/a
3	chr6:66207286-66207336	AG04449	skin:	fetal
4	chr6:66207286-66207336	HCM	heart:	n/a
5	chr6:66205227-66205277	NH-A	brain:	n/a
6	chr6:66205227-66205277	Hela-S3	cervix:	n/a
7	chr6:66205227-66205277	HMEC	breast:	n/a
8	chr6:66207286-66207336	GM19239	blood:	n/a
9	chr6:66207286-66207336	HUVEC	blood vessel:	n/a
10	chr6:66207286-66207336	BJ	skin:	n/a
11	chr6:66205227-66205277	AG09309	skin:	n/a
12	chr6:66207286-66207336	PANC-1	pancreas:	n/a
13	chr6:66207286-66207336	NHBE	bronchial:	n/a
14	chr6:66205227-66205277	PrEC	prostate:	n/a
15	chr6:66205227-66205277	SK-N-SH	brain:	n/a
16	chr6:66207286-66207336	HRE	kidney:	n/a
17	chr6:66205227-66205277	AG04450	lung:	fetal
18	chr6:66207286-66207336	BE2_C	brain:	n/a
19	chr6:66207286-66207336	SAEC	small airway:	n/a
20	chr6:66207286-66207336	ProgFib	skin:	n/a
21	chr6:66207286-66207336	MCF10A-Er-Src	breast:	n/a
22	chr6:66205227-66205277	BJ	skin:	n/a
23	chr6:66207286-66207336	RPTEC	kidney:	n/a
24	chr6:66207286-66207336	HRCEpiC	kidney:	n/a
25	chr6:66207286-66207336	ovcar-3	ovarian:	n/a
26	chr6:66205227-66205277	Hepatocyte	liver:	n/a
27	chr6:66207286-66207336	HepG2	liver:	n/a
28	chr6:66207286-66207336	HPAEpiC	pulmonary alveolar:	n/a
29	chr6:66207286-66207336	HL-60	blood:	n/a
30	chr6:66207286-66207336	GM06990	blood:	n/a
31	chr6:66207286-66207336	NB4	blood:	n/a
32	chr6:66205227-66205277	LNCaP	prostate:	n/a
33	chr6:66207286-66207336	Caco-2	colon:	n/a
34	chr6:66205227-66205277	MCF-7	breast:	n/a
35	chr6:66205227-66205277	PANC-1	pancreas:	n/a
36	chr6:66205227-66205277	SAEC	small airway:	n/a
37	chr6:66205227-66205277	HCPEpiC	choroid plexus:	n/a
38	chr6:66207286-66207336	Hela-S3	cervix:	n/a
39	chr6:66207286-66207336	K562	blood:	n/a
40	chr6:66207286-66207336	NH-A	brain:	n/a
41	chr6:66207286-66207336	Hepatocyte	liver:	n/a
42	chr6:66205227-66205277	K562	blood:	n/a
43	chr6:66205227-66205277	NT2-D1	testis:	n/a
44	chr6:66205227-66205277	HRE	kidney:	n/a
45	chr6:66207286-66207336	HCF	heart:	n/a
46	chr6:66205227-66205277	HEK293	kidney:	embryo
47	chr6:66207286-66207336	NT2-D1	testis:	n/a
48	chr6:66205227-66205277	HRPEpiC	eye:	n/a
49	chr6:66207286-66207336	GM12891	blood:	n/a
50	chr6:66207286-66207336	H1-hESC	embryonic stem cell:	embryo

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
2	chr6:66205424..66207848-chr6:66208785..66211406,2	K562	blood:
3	chr6:66158867..66160946-chr6:66172650..66174788,2	K562	blood:
4	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
5	chr6:66158867..66160946-chr6:66172650..66174788,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LGSN-7	chr6:66199254-66200600	NONHSAT113373
2	lnc-PHF3-3	chr6:66191784-66191981	ENSG00000230672.1
3	lnc-LGSN-7	chr6:66204556-66205500	NONHSAT113373
4	lnc-LGSN-7	chr6:66205752-66205886	NONHSAT113373
5	lnc-PHF3-3	chr6:66191208-66191429	ENSG00000230672.1

No data

Variant related genes	Relation type
ENSG00000265187	TF binding region
EYS	TF binding region
ENSG00000265187	CpG island
EYS	CpG island
ENSG00000188107	chromatin interactions

Extended variants
information (count: 1004 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1004 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543813251	chr6:66120220-66120221	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs563801782	chr6:66120238-66120239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs181332886	chr6:66120250-66120251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs546462434	chr6:66120261-66120262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs559685601	chr6:66120265-66120266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528635746	chr6:66120282-66120283	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs548608148	chr6:66120286-66120287	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568700239	chr6:66120328-66120329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs541730101	chr6:66120358-66120359	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs185623264	chr6:66120385-66120386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569446532	chr6:66120393-66120394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs538336902	chr6:66120414-66120415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs562030005	chr6:66120423-66120424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs557644499	chr6:66120434-66120435	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576025852	chr6:66120439-66120440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs147941572	chr6:66120440-66120441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190323547	chr6:66120451-66120452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs534783736	chr6:66120458-66120459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs527453251	chr6:66120475-66120476	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182966687	chr6:66120481-66120482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs140497895	chr6:66120486-66120487	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs375882636	chr6:66120491-66120492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551626482	chr6:66120492-66120493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs543873704	chr6:66120510-66120511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs74403490	chr6:66120526-66120527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs577462896	chr6:66120570-66120571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs531621202	chr6:66124232-66124233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568941316	chr6:66124299-66124300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs182767640	chr6:66124346-66124347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs371586062	chr6:66124372-66124373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs34373105	chr6:66124380-66124381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs559145635	chr6:66124473-66124474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs548455682	chr6:66124474-66124475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188635539	chr6:66124483-66124484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192980028	chr6:66124485-66124486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538262492	chr6:66124486-66124487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs548567391	chr6:66124497-66124498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536802879	chr6:66124554-66124555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs376664170	chr6:66124604-66124605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550511090	chr6:66124647-66124648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs576819604	chr6:66124676-66124677	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77407066	chr6:66124724-66124725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs537874038	chr6:66124747-66124748	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs557458067	chr6:66124803-66124804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571366327	chr6:66124834-66124835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs533651262	chr6:66124914-66124915	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs553788328	chr6:66124946-66124947	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs185517840	chr6:66124994-66124995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs542381740	chr6:66125011-66125012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs556070428	chr6:66125012-66125013	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

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
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Lung cancer	18438408	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	21364760	CNVD
Prostate cancer	16573809	CNVD
Ovarian cancer	19835627	CNVD
Myelofibrosis	22110671	CNVD
Cancer	21183584	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Developmental delay	21147756	CNVD
small cell lung cancer	20016488	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Dyslexia	22102821	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
Retinitis pigmentosa	21519034	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:44 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66120200-66120600	Enhancers	HepG2	liver
2	chr6:66124200-66124400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:66124400-66125000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr6:66125000-66127800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:66125200-66127800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr6:66126000-66126200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:66126000-66127000	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr6:66126200-66133200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr6:66126400-66127400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr6:66133200-66135000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr6:66155800-66156400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:66156400-66158600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:66157000-66160800	Enhancers	HUES64 Cell Line	embryonic stem cell
14	chr6:66157400-66158200	Enhancers	Brain Cingulate Gyrus	brain
15	chr6:66157400-66160600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr6:66157600-66158200	Enhancers	H9 Cell Line	embryonic stem cell
17	chr6:66157600-66158400	Enhancers	Brain Substantia Nigra	brain
18	chr6:66157600-66160600	Enhancers	HUES6 Cell Line	embryonic stem cell
19	chr6:66157600-66160600	Enhancers	Brain Hippocampus Middle	brain
20	chr6:66157800-66160400	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr6:66157800-66160600	Enhancers	iPS-18 Cell Line	embryonic stem cell
22	chr6:66158000-66160800	Enhancers	Fetal Brain Male	brain
23	chr6:66158200-66158400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
24	chr6:66158200-66160400	Weak transcription	H9 Cell Line	embryonic stem cell
25	chr6:66158400-66158600	Weak transcription	Brain Substantia Nigra	brain
26	chr6:66158600-66159000	Active TSS	Brain Substantia Nigra	brain
27	chr6:66158600-66160000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr6:66158800-66159200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr6:66158800-66159200	Enhancers	iPS-20b Cell Line	embryonic stem cell
30	chr6:66158800-66159200	Enhancers	Brain Germinal Matrix	brain
31	chr6:66159200-66160200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr6:66159200-66160200	Weak transcription	Brain Germinal Matrix	brain
33	chr6:66159600-66159800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chr6:66160200-66160400	Enhancers	Brain Germinal Matrix	brain
35	chr6:66160200-66160600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
36	chr6:66160200-66160800	Enhancers	H1 Cell Line	embryonic stem cell
37	chr6:66160400-66160800	Enhancers	H9 Cell Line	embryonic stem cell
38	chr6:66160600-66160800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
39	chr6:66170400-66171400	Enhancers	K562	blood
40	chr6:66171000-66171400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr6:66171000-66171600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr6:66171000-66171600	Enhancers	Fetal Heart	heart
43	chr6:66175000-66175400	Active TSS	Sigmoid Colon	Sigmoid Colon
44	chr6:66210400-66211000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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