Variant report

Variant	esv3447152
Chromosome Location	chr6:66027938-66253181
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:360)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:360 , 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	ARID3A	chr6:66049641-66049730	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:66120388-66120433	HepG2	liver:	n/a	n/a
3	ATF1	chr6:66171007-66171493	K562	blood:	n/a	n/a
4	ATF1	chr6:66160376-66160599	K562	blood:	n/a	n/a
5	BACH1	chr6:66066175-66066268	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr6:66193565-66193851	K562	blood:	n/a	n/a
7	CCNT2	chr6:66100608-66100682	K562	blood:	n/a	n/a
8	CCNT2	chr6:66171045-66171349	K562	blood:	n/a	n/a
9	CCNT2	chr6:66139022-66139218	K562	blood:	n/a	n/a
10	CEBPB	chr6:66037840-66038160	IMR90	lung:	n/a	chr6:66037990-66038001
11	CEBPB	chr6:66064226-66064435	H1-hESC	embryonic stem cell:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
12	CEBPB	chr6:66192989-66193263	HepG2	liver:	n/a	chr6:66193166-66193179 chr6:66193107-66193120 chr6:66193107-66193118
13	CEBPB	chr6:66109620-66109995	HepG2	liver:	n/a	chr6:66109790-66109801 chr6:66109810-66109821
14	CEBPB	chr6:66064211-66064491	A549	lung:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
15	CEBPB	chr6:66064192-66064538	HepG2	liver:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
16	CEBPB	chr6:66156754-66157125	HepG2	liver:	n/a	chr6:66157101-66157114
17	CEBPB	chr6:66037851-66038095	A549	lung:	n/a	chr6:66037990-66038001
18	CEBPB	chr6:66127902-66128153	HepG2	liver:	n/a	chr6:66128011-66128022 chr6:66128012-66128021
19	CEBPB	chr6:66064245-66064517	Hela-S3	cervix:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
20	CEBPB	chr6:66064262-66064425	K562	blood:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
21	CEBPB	chr6:66195051-66195251	IMR90	lung:	n/a	n/a
22	CEBPB	chr6:66248614-66248879	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr6:66230294-66230581	IMR90	lung:	n/a	n/a
24	CEBPB	chr6:66230260-66230571	HepG2	liver:	n/a	n/a
25	CEBPB	chr6:66037858-66038164	HepG2	liver:	n/a	chr6:66037990-66038001
26	CEBPB	chr6:66143961-66144277	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:66064204-66064473	IMR90	lung:	n/a	chr6:66064368-66064379 chr6:66064370-66064381 chr6:66064370-66064379
28	CEBPB	chr6:66156810-66157084	K562	blood:	n/a	n/a
29	CEBPB	chr6:66120214-66120512	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:66138219-66138426	HepG2	liver:	n/a	chr6:66138267-66138278
31	CEBPB	chr6:66066493-66066779	HepG2	liver:	n/a	chr6:66066621-66066632
32	CEBPD	chr6:66076790-66077115	K562	blood:	n/a	n/a
33	CEBPD	chr6:66171023-66171458	K562	blood:	n/a	n/a
34	CTCF	chr6:66157720-66157870	MCF-7	breast:	n/a	n/a
35	CTCF	chr6:66037034-66037060	GM13976	blood:	n/a	n/a
36	CTCF	chr6:66157644-66157761	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:66157600-66157750	BE2_C	brain:	n/a	n/a
38	CTCF	chr6:66245328-66245391	Fibrobl	skin:	n/a	n/a
39	CTCF	chr6:66157717-66157767	LNCaP	prostate:	n/a	n/a
40	CTCF	chr6:66245342-66245403	Medullo	brain:	n/a	n/a
41	CTCF	chr6:66028325-66028381	GM13976	blood:	n/a	n/a
42	CTCF	chr6:66128422-66128491	Lung_OC	lung:	n/a	n/a
43	CTCF	chr6:66119174-66119372	GM12878	blood:	n/a	n/a
44	CTCF	chr6:66218761-66218798	GM20000	blood:	n/a	n/a
45	CTCF	chr6:66117250-66117306	GM20000	blood:	n/a	n/a
46	CTCF	chr6:66157685-66157759	LNCaP	prostate:	n/a	n/a
47	CTCF	chr6:66157563-66157836	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:66157771-66157802	LNCaP	prostate:	n/a	n/a
49	CTCF	chr6:66157620-66157770	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr6:66060640-66060910	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66205227-66205277	GM12891	blood:	n/a
2	chr6:66205227-66205277	H1-hESC	embryonic stem cell:	embryo
3	chr6:66207286-66207336	HCF	heart:	n/a
4	chr6:66205227-66205277	AoSMC	blood vessel:	n/a
5	chr6:66207286-66207336	Hela-S3	cervix:	n/a
6	chr6:66207286-66207336	GM12891	blood:	n/a
7	chr6:66207286-66207336	HMEC	breast:	n/a
8	chr6:66205227-66205277	IMR90	lung:	fetal
9	chr6:66205227-66205277	HRCEpiC	kidney:	n/a
10	chr6:66205227-66205277	HCF	heart:	n/a
11	chr6:66205227-66205277	HUVEC	blood vessel:	n/a
12	chr6:66207286-66207336	BE2_C	brain:	n/a
13	chr6:66207286-66207336	SK-N-SH_RA	brain:	n/a
14	chr6:66207286-66207336	GM06990	blood:	n/a
15	chr6:66205227-66205277	NHDF-neo	bronchial:	n/a
16	chr6:66205227-66205277	ovcar-3	ovarian:	n/a
17	chr6:66205227-66205277	HMEC	breast:	n/a
18	chr6:66205227-66205277	HCT-116	colon:	n/a
19	chr6:66207286-66207336	HRCEpiC	kidney:	n/a
20	chr6:66207286-66207336	T-47D	breast:	n/a
21	chr6:66205227-66205277	SK-N-MC	brain:	n/a
22	chr6:66205227-66205277	AG09309	skin:	n/a
23	chr6:66205227-66205277	HCPEpiC	choroid plexus:	n/a
24	chr6:66207286-66207336	HepG2	liver:	n/a
25	chr6:66207286-66207336	A549	lung:	n/a
26	chr6:66207286-66207336	SKMC	muscle:	n/a
27	chr6:66207286-66207336	HPAEpiC	pulmonary alveolar:	n/a
28	chr6:66207286-66207336	Jurkat	blood:	n/a
29	chr6:66207286-66207336	HAEpiC	amniotic membrane:	n/a
30	chr6:66205227-66205277	RPTEC	kidney:	n/a
31	chr6:66205227-66205277	ECC-1	luminal epithelium:	n/a
32	chr6:66205227-66205277	SK-N-SH_RA	brain:	n/a
33	chr6:66205227-66205277	SAEC	small airway:	n/a
34	chr6:66207286-66207336	MCF-7	breast:	n/a
35	chr6:66207286-66207336	GM12892	blood:	n/a
36	chr6:66205227-66205277	Hepatocyte	liver:	n/a
37	chr6:66205227-66205277	NH-A	brain:	n/a
38	chr6:66207286-66207336	HL-60	blood:	n/a
39	chr6:66205227-66205277	Hela-S3	cervix:	n/a
40	chr6:66207286-66207336	SK-N-SH	brain:	n/a
41	chr6:66205227-66205277	NT2-D1	testis:	n/a
42	chr6:66207286-66207336	NHDF-neo	bronchial:	n/a
43	chr6:66207286-66207336	HCT-116	colon:	n/a
44	chr6:66205227-66205277	AG09319	gingival:	n/a
45	chr6:66205227-66205277	K562	blood:	n/a
46	chr6:66205227-66205277	PFSK-1	brain:	n/a
47	chr6:66207286-66207336	AoSMC	blood vessel:	n/a
48	chr6:66207286-66207336	PrEC	prostate:	n/a
49	chr6:66207286-66207336	H1-hESC	embryonic stem cell:	embryo
50	chr6:66207286-66207336	HCPEpiC	choroid plexus:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:66205424..66207848-chr6:66208785..66211406,2	K562	blood:
2	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
3	chr6:66060579..66062154-chr6:66063684..66065572,2	MCF-7	breast:
4	chr6:66078369..66080351-chr6:66082016..66084974,2	K562	blood:
5	chr6:66078369..66080351-chr6:66082016..66084974,2	K562	blood:
6	chr6:66051771..66054306-chr6:66063446..66065850,2	K562	blood:
7	chr6:66249610..66251834-chr6:66299808..66302442,2	K562	blood:
8	chr6:66097248..66097748-chr7:48217360..48217884,2	MCF-7	breast:
9	chr6:66060579..66062154-chr6:66063684..66065572,2	MCF-7	breast:
10	chr6:66228230..66230523-chr6:66231359..66233821,2	MCF-7	breast:
11	chr6:66158867..66160946-chr6:66172650..66174788,2	K562	blood:
12	chr6:66051771..66054306-chr6:66063446..66065850,2	K562	blood:
13	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	chr6:66205752-66205886	NONHSAT113373
2	lnc-LGSN-7	chr6:66204556-66205500	NONHSAT113373
3	lnc-PHF3-3	chr6:66191208-66191429	ENSG00000230672.1
4	lnc-LGSN-7	chr6:66199254-66200600	NONHSAT113373
5	lnc-PHF3-3	chr6:66191784-66191981	ENSG00000230672.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	EYS	hsa-miR-124-3p	chr6:66040931-66040951

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: 1653 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1653 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs28602178	chr6:66028604-66028605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs28578179	chr6:66028605-66028606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs557155193	chr6:66028650-66028651	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs28845468	chr6:66028653-66028654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs193254018	chr6:66028723-66028724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs549955768	chr6:66028728-66028729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs182111542	chr6:66028745-66028746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568285903	chr6:66028751-66028752	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577253219	chr6:66028760-66028761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546119278	chr6:66028777-66028778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs373584729	chr6:66045001-66045002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs530200433	chr6:66045026-66045027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs111746102	chr6:66045049-66045050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200079430	chr6:66045064-66045065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs369587617	chr6:66045070-66045071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1502965	chr6:66045077-66045078	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs370023427	chr6:66045085-66045086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs537886538	chr6:66045096-66045097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs547387002	chr6:66045100-66045101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs145435440	chr6:66045101-66045102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1502964	chr6:66045118-66045119	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs77096978	chr6:66045121-66045122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs368170644	chr6:66045126-66045127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs553417420	chr6:66045145-66045146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs190462222	chr6:66045165-66045166	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371782585	chr6:66045200-66045201	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs73741294	chr6:66045215-66045216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs182051647	chr6:66045264-66045265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs375185440	chr6:66045291-66045292	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs73741295	chr6:66045314-66045315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs545466240	chr6:66045323-66045324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs565258389	chr6:66045332-66045333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs12663402	chr6:66045334-66045335	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs184855473	chr6:66045367-66045368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs574914257	chr6:66045384-66045385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577337414	chr6:66045424-66045425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs78034260	chr6:66045426-66045427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs369988120	chr6:66045433-66045434	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs371690532	chr6:66045481-66045482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs542143308	chr6:66045531-66045532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111533653	chr6:66045534-66045535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs188055511	chr6:66045541-66045542	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs111904837	chr6:66045547-66045548	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs372365421	chr6:66045554-66045555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550994314	chr6:66045556-66045557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376799054	chr6:66045564-66045565	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs572543707	chr6:66045568-66045569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs569102650	chr6:66045589-66045590	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs180966896	chr6:66045597-66045598	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547091969	chr6:66045610-66045611	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Epilepsy	20502679	CNVD
Dyslexia	22102821	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Bipolar disorder	19114987	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19212409	CNVD
Retinitis pigmentosa	21519034	CNVD
Pancreatic cancer	17952125	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:66 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66028600-66028800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:66045000-66045800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
3	chr6:66061400-66062200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr6:66061600-66061800	Enhancers	Fetal Lung	lung
5	chr6:66076000-66077200	Enhancers	Fetal Stomach	stomach
6	chr6:66095800-66097200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
7	chr6:66096600-66097000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:66099200-66099600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr6:66108200-66109200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr6:66109200-66110000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr6:66110000-66110200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:66120200-66120600	Enhancers	HepG2	liver
13	chr6:66124200-66124400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr6:66124400-66125000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr6:66125000-66127800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr6:66125200-66127800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr6:66126000-66126200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:66126000-66127000	Enhancers	Cortex derived primary cultured neurospheres	brain
19	chr6:66126200-66133200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr6:66126400-66127400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
21	chr6:66133200-66135000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:66155800-66156400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:66156400-66158600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr6:66157000-66160800	Enhancers	HUES64 Cell Line	embryonic stem cell
25	chr6:66157400-66158200	Enhancers	Brain Cingulate Gyrus	brain
26	chr6:66157400-66160600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr6:66157600-66158200	Enhancers	H9 Cell Line	embryonic stem cell
28	chr6:66157600-66158400	Enhancers	Brain Substantia Nigra	brain
29	chr6:66157600-66160600	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr6:66157600-66160600	Enhancers	Brain Hippocampus Middle	brain
31	chr6:66157800-66160400	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chr6:66157800-66160600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr6:66158000-66160800	Enhancers	Fetal Brain Male	brain
34	chr6:66158200-66158400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
35	chr6:66158200-66160400	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr6:66158400-66158600	Weak transcription	Brain Substantia Nigra	brain
37	chr6:66158600-66159000	Active TSS	Brain Substantia Nigra	brain
38	chr6:66158600-66160000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:66158800-66159200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:66158800-66159200	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr6:66158800-66159200	Enhancers	Brain Germinal Matrix	brain
42	chr6:66159200-66160200	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chr6:66159200-66160200	Weak transcription	Brain Germinal Matrix	brain
44	chr6:66159600-66159800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
45	chr6:66160200-66160400	Enhancers	Brain Germinal Matrix	brain
46	chr6:66160200-66160600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:66160200-66160800	Enhancers	H1 Cell Line	embryonic stem cell
48	chr6:66160400-66160800	Enhancers	H9 Cell Line	embryonic stem cell
49	chr6:66160600-66160800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
50	chr6:66170400-66171400	Enhancers	K562	blood

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