Variant report

Variant	nsv462992
Chromosome Location	chr6:66628679-66821492
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:363)
CpG islands
(count:610)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:363 , 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	ATF2	chr6:66758631-66759010	GM12878	blood:	n/a	n/a
2	ATF2	chr6:66759094-66759332	GM12878	blood:	n/a	n/a
3	BACH1	chr6:66648198-66648208	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr6:66758953-66759296	GM12878	blood:	n/a	n/a
5	BATF	chr6:66631918-66632340	GM12878	blood:	n/a	n/a
6	BATF	chr6:66631968-66632296	GM12878	blood:	n/a	n/a
7	BATF	chr6:66760290-66760499	GM12878	blood:	n/a	chr6:66760390-66760401
8	BCL11A	chr6:66631888-66632357	GM12878	blood:	n/a	n/a
9	BCL11A	chr6:66631997-66632283	GM12878	blood:	n/a	n/a
10	BCL11A	chr6:66758646-66758963	GM12878	blood:	n/a	n/a
11	BCL3	chr6:66631951-66632190	GM12878	blood:	n/a	n/a
12	BCLAF1	chr6:66631985-66632241	GM12878	blood:	n/a	n/a
13	BHLHE40	chr6:66719831-66719935	GM12878	blood:	n/a	n/a
14	BHLHE40	chr6:66632014-66632283	GM12878	blood:	n/a	n/a
15	CEBPB	chr6:66758630-66759135	GM12878	blood:	n/a	n/a
16	CEBPB	chr6:66701567-66701886	Hela-S3	cervix:	n/a	chr6:66701690-66701701
17	CEBPB	chr6:66795134-66795326	HepG2	liver:	n/a	chr6:66795236-66795247
18	CEBPB	chr6:66701556-66701859	HepG2	liver:	n/a	chr6:66701690-66701701
19	CEBPB	chr6:66711140-66711453	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr6:66701577-66701831	A549	lung:	n/a	chr6:66701690-66701701
21	CEBPB	chr6:66792824-66793157	HepG2	liver:	n/a	chr6:66792993-66793004
22	CEBPB	chr6:66792842-66793125	K562	blood:	n/a	chr6:66792993-66793004
23	CEBPB	chr6:66799687-66799916	HepG2	liver:	n/a	n/a
24	CEBPB	chr6:66792838-66793183	H1-hESC	embryonic stem cell:	n/a	chr6:66792993-66793004
25	CEBPB	chr6:66701560-66701858	IMR90	lung:	n/a	chr6:66701690-66701701
26	CEBPB	chr6:66799727-66799937	A549	lung:	n/a	n/a
27	CEBPB	chr6:66813960-66814254	Hela-S3	cervix:	n/a	n/a
28	CEBPB	chr6:66759445-66759693	HepG2	liver:	n/a	chr6:66759563-66759574 chr6:66759600-66759611 chr6:66759562-66759575 chr6:66759600-66759613
29	CEBPB	chr6:66711119-66711450	HepG2	liver:	n/a	n/a
30	CEBPB	chr6:66792843-66793170	Hela-S3	cervix:	n/a	chr6:66792993-66793004
31	CEBPB	chr6:66792839-66793182	IMR90	lung:	n/a	chr6:66792993-66793004
32	CEBPB	chr6:66765930-66766246	HepG2	liver:	n/a	chr6:66766074-66766085
33	CEBPB	chr6:66792807-66793167	A549	lung:	n/a	chr6:66792993-66793004
34	CHD2	chr6:66631999-66632317	GM12878	blood:	n/a	n/a
35	CHD2	chr6:66758753-66759230	GM12878	blood:	n/a	n/a
36	CTCF	chr6:66757060-66757210	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:66757021-66757129	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:66804682-66804733	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:66757026-66757103	GM12878	blood:	n/a	n/a
40	CTCF	chr6:66708540-66708690	GM12873	blood:	n/a	n/a
41	CTCF	chr6:66756977-66757154	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:66750384-66750428	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr6:66759763-66759815	K562	blood:	n/a	n/a
44	CTCF	chr6:66756893-66757236	GM12878	blood:	n/a	n/a
45	CTCF	chr6:66804735-66804737	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:66804475-66804515	ProgFib	skin:	n/a	n/a
47	CTCF	chr6:66804456-66804502	MCF-7	breast:	n/a	n/a
48	CTCF	chr6:66684865-66684946	GM20000	blood:	n/a	n/a
49	CTCF	chr6:66804449-66804501	Pancreas_OC	pancreas:	n/a	n/a
50	CTCF	chr6:66757041-66757097	Hela-S3	cervix:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:66709543-66709593	HUVEC	blood vessel:	n/a
2	chr6:66708570-66708620	ovcar-3	ovarian:	n/a
3	chr6:66804704-66804754	HepG2	liver:	n/a
4	chr6:66804704-66804754	HAEpiC	amniotic membrane:	n/a
5	chr6:66708570-66708620	K562	blood:	n/a
6	chr6:66804261-66804311	AG04449	skin:	fetal
7	chr6:66819090-66819140	T-47D	breast:	n/a
8	chr6:66804631-66804681	Hela-S3	cervix:	n/a
9	chr6:66709459-66709509	HRCEpiC	kidney:	n/a
10	chr6:66804261-66804311	NB4	blood:	n/a
11	chr6:66800878-66800928	NT2-D1	testis:	n/a
12	chr6:66804830-66804880	HPAEpiC	pulmonary alveolar:	n/a
13	chr6:66709543-66709593	SK-N-SH_RA	brain:	n/a
14	chr6:66708681-66708731	BE2_C	brain:	n/a
15	chr6:66709543-66709593	T-47D	breast:	n/a
16	chr6:66804631-66804681	GM12878	blood:	n/a
17	chr6:66708570-66708620	HRCEpiC	kidney:	n/a
18	chr6:66804631-66804681	AG09309	skin:	n/a
19	chr6:66708570-66708620	HEK293	kidney:	embryo
20	chr6:66819090-66819140	ECC-1	luminal epithelium:	n/a
21	chr6:66709459-66709509	Jurkat	blood:	n/a
22	chr6:66804631-66804681	RPTEC	kidney:	n/a
23	chr6:66709543-66709593	SK-N-SH	brain:	n/a
24	chr6:66708570-66708620	A549	lung:	n/a
25	chr6:66804830-66804880	AoSMC	blood vessel:	n/a
26	chr6:66708681-66708731	NHBE	bronchial:	n/a
27	chr6:66800878-66800928	Caco-2	colon:	n/a
28	chr6:66800878-66800928	U87	brain:	n/a
29	chr6:66708570-66708620	PrEC	prostate:	n/a
30	chr6:66804261-66804311	AG04450	lung:	fetal
31	chr6:66819090-66819140	CMK	blood:	n/a
32	chr6:66804261-66804311	HRCEpiC	kidney:	n/a
33	chr6:66804261-66804311	NHDF-neo	bronchial:	n/a
34	chr6:66800878-66800928	HCM	heart:	n/a
35	chr6:66819090-66819140	GM06990	blood:	n/a
36	chr6:66708570-66708620	HUVEC	blood vessel:	n/a
37	chr6:66804704-66804754	MCF-7	breast:	n/a
38	chr6:66709459-66709509	Hepatocyte	liver:	n/a
39	chr6:66708570-66708620	NT2-D1	testis:	n/a
40	chr6:66804261-66804311	SK-N-MC	brain:	n/a
41	chr6:66800878-66800928	PFSK-1	brain:	n/a
42	chr6:66708570-66708620	Hela-S3	cervix:	n/a
43	chr6:66804704-66804754	Hela-S3	cervix:	n/a
44	chr6:66804261-66804311	AG09309	skin:	n/a
45	chr6:66708681-66708731	AG09319	gingival:	n/a
46	chr6:66709543-66709593	CMK	blood:	n/a
47	chr6:66819090-66819140	HPAEpiC	pulmonary alveolar:	n/a
48	chr6:66819090-66819140	HUVEC	blood vessel:	n/a
49	chr6:66709543-66709593	NT2-D1	testis:	n/a
50	chr6:66804261-66804311	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr6:66774856..66776961-chr6:66781125..66783110,2	MCF-7	breast:
2	chr6:66774856..66776961-chr6:66781125..66783110,2	MCF-7	breast:
3	chr6:66677113..66680051-chr6:66725985..66728195,2	K562	blood:
4	chr6:66697645..66699348-chr6:66753143..66756102,2	K562	blood:
5	chr6:66666961..66669216-chr6:66669694..66671348,2	MCF-7	breast:
6	chr3:149614783..149615556-chr6:66750597..66751356,2	MCF-7	breast:
7	chr6:66666961..66669216-chr6:66669694..66671348,2	MCF-7	breast:
8	chr6:66753689..66755338-chr6:66756434..66758951,2	K562	blood:
9	chr6:66677113..66678881-chr6:66726026..66728195,2	K562	blood:
10	chr6:66677113..66680051-chr6:66725985..66728195,2	K562	blood:
11	chr6:66697645..66699348-chr6:66753143..66756102,2	K562	blood:
12	chr6:66677113..66678881-chr6:66726026..66728195,2	K562	blood:
13	chr6:66753689..66755338-chr6:66756434..66758951,2	K562	blood:

No data

Variant related genes	Relation type
NUFIP1P	TF binding region
NUFIP1P	CpG island

Extended variants
information (count: 2714 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2714 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12214948	chr6:66633603-66633604	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552651970	chr6:66633618-66633619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs186363092	chr6:66633668-66633669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528791504	chr6:66633671-66633672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs80188754	chr6:66633675-66633676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs568661935	chr6:66633687-66633688	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373637757	chr6:66633723-66633724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs188788639	chr6:66633759-66633760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs6939062	chr6:66633781-66633782	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs569438406	chr6:66633804-66633805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs371562586	chr6:66633910-66633911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs6927036	chr6:66633911-66633912	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs558000742	chr6:66633916-66633917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs558561205	chr6:66633917-66633918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs544160563	chr6:66633918-66633919	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs571903520	chr6:66633933-66633934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs541320681	chr6:66633956-66633957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554539232	chr6:66633989-66633990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs181594614	chr6:66634072-66634073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543672068	chr6:66634084-66634085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs147803738	chr6:66634096-66634097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186156904	chr6:66634102-66634103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545937544	chr6:66634104-66634105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs190815306	chr6:66634137-66634138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs536228935	chr6:66634158-66634159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574203345	chr6:66634159-66634160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564646427	chr6:66634167-66634168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs35287893	chr6:66634224-66634225	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs559781744	chr6:66634228-66634229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531086247	chr6:66634233-66634234	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs184050385	chr6:66634240-66634241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs570699039	chr6:66634289-66634290	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538353385	chr6:66634306-66634307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs78722860	chr6:66634307-66634308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs565691390	chr6:66634330-66634331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs13207584	chr6:66634338-66634339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59322418	chr6:66634392-66634393	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs77896790	chr6:66634395-66634396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs200354713	chr6:66634398-66634399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs201153774	chr6:66634399-66634400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9345732	chr6:66634404-66634405	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs147992540	chr6:66634459-66634460	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs186059777	chr6:66634481-66634482	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190786616	chr6:66634486-66634487	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs140706121	chr6:66634493-66634494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs577066943	chr6:66634494-66634495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535336743	chr6:66634552-66634553	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116730335	chr6:66634557-66634558	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs559556752	chr6:66634558-66634559	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs573273183	chr6:66634564-66634565	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:108 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:66633600-66634000	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr6:66633600-66634000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr6:66634000-66634400	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:66634000-66634800	Weak transcription	HUES64 Cell Line	embryonic stem cell
5	chr6:66634400-66636000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr6:66634800-66635000	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr6:66635000-66635400	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr6:66635400-66635800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr6:66635600-66636000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr6:66635600-66636000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
11	chr6:66635600-66636200	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:66640000-66640200	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:66640200-66641400	Active TSS	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr6:66640200-66641600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
15	chr6:66641600-66641800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr6:66641800-66645200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
17	chr6:66645200-66645600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:66647400-66647800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
19	chr6:66647400-66647800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr6:66647400-66648400	Enhancers	Ovary	ovary
21	chr6:66647800-66648200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr6:66647800-66648200	Enhancers	Fetal Muscle Leg	muscle
23	chr6:66648200-66648400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr6:66648400-66653400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr6:66648400-66653600	Weak transcription	Ovary	ovary
26	chr6:66649000-66649200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:66649200-66650400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr6:66650400-66650800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:66650800-66653000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:66652600-66653800	Enhancers	Fetal Lung	lung
31	chr6:66653000-66653600	Enhancers	Duodenum Smooth Muscle	Duodenum
32	chr6:66653000-66654000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr6:66653400-66653800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr6:66653400-66653800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr6:66653400-66653800	Enhancers	Adipose Nuclei	Adipose
36	chr6:66653400-66653800	Enhancers	Fetal Stomach	stomach
37	chr6:66653400-66654000	Enhancers	Fetal Brain Male	brain
38	chr6:66653600-66654000	Enhancers	Ovary	ovary
39	chr6:66655400-66655800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr6:66655400-66656200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr6:66656200-66663600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr6:66663600-66664000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:66672800-66673600	Enhancers	Cortex derived primary cultured neurospheres	brain
44	chr6:66672800-66674200	Enhancers	Fetal Stomach	stomach
45	chr6:66688200-66690400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr6:66689800-66690200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr6:66699000-66699400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr6:66699200-66699400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:66699800-66701000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr6:66701000-66702200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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