Variant report

Variant	nsv1020545
Chromosome Location	chr6:69119445-69310136
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:758)
CpG islands
(count:0)
Chromatin interactive
region (count:43)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:758 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:69285930-69286092	K562	blood:	n/a	n/a
2	ARID3A	chr6:69178389-69178711	K562	blood:	n/a	n/a
3	ARID3A	chr6:69268977-69269258	K562	blood:	n/a	n/a
4	ARID3A	chr6:69286347-69286554	K562	blood:	n/a	n/a
5	ATF1	chr6:69269660-69269929	K562	blood:	n/a	n/a
6	ATF1	chr6:69178169-69178665	K562	blood:	n/a	n/a
7	ATF1	chr6:69269025-69269265	K562	blood:	n/a	n/a
8	ATF3	chr6:69269027-69269319	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr6:69269014-69269315	K562	blood:	n/a	n/a
10	ATF3	chr6:69269051-69269336	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr6:69239233-69239251	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr6:69204892-69204954	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr6:69196503-69196515	H1-hESC	embryonic stem cell:	n/a	n/a
14	BHLHE40	chr6:69285801-69286173	K562	blood:	n/a	n/a
15	CBX3	chr6:69285895-69286129	K562	blood:	n/a	n/a
16	CBX3	chr6:69285828-69286210	K562	blood:	n/a	n/a
17	CCNT2	chr6:69178467-69178669	K562	blood:	n/a	n/a
18	CEBPB	chr6:69268791-69269405	K562	blood:	n/a	chr6:69269192-69269203
19	CEBPB	chr6:69178503-69178771	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr6:69189397-69189527	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr6:69268981-69269385	ECC-1	luminal epithelium:	n/a	chr6:69269192-69269203
22	CEBPB	chr6:69178223-69178778	Hela-S3	cervix:	n/a	n/a
23	CEBPB	chr6:69269014-69269223	K562	blood:	n/a	chr6:69269192-69269203
24	CEBPB	chr6:69151992-69152254	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr6:69268826-69269374	Hela-S3	cervix:	n/a	chr6:69269192-69269203
26	CEBPB	chr6:69285848-69286246	ECC-1	luminal epithelium:	n/a	n/a
27	CEBPB	chr6:69269006-69269410	MCF-7	breast:	n/a	chr6:69269192-69269203
28	CEBPB	chr6:69268990-69269396	ECC-1	luminal epithelium:	n/a	chr6:69269192-69269203
29	CEBPB	chr6:69268998-69269598	H1-hESC	embryonic stem cell:	n/a	chr6:69269192-69269203
30	CEBPB	chr6:69269105-69269267	A549	lung:	n/a	chr6:69269192-69269203
31	CEBPB	chr6:69178485-69178781	MCF-7	breast:	n/a	n/a
32	CEBPB	chr6:69178501-69178787	K562	blood:	n/a	n/a
33	CEBPB	chr6:69268925-69269424	K562	blood:	n/a	chr6:69269192-69269203
34	CEBPB	chr6:69269019-69269346	HepG2	liver:	n/a	chr6:69269192-69269203
35	CEBPD	chr6:69178296-69178761	K562	blood:	n/a	n/a
36	CEBPD	chr6:69178276-69178811	K562	blood:	n/a	n/a
37	CTCF	chr6:69282550-69282702	GM12891	blood:	n/a	n/a
38	CTCF	chr6:69153760-69153910	HPAF	blood vessel:	n/a	n/a
39	CTCF	chr6:69178572-69178672	GM19240	blood:	n/a	n/a
40	CTCF	chr6:69282468-69282728	Gliobla	brain:	n/a	n/a
41	CTCF	chr6:69178500-69178650	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr6:69282475-69282768	T-47D	breast:	n/a	n/a
43	CTCF	chr6:69269060-69269210	BE2_C	brain:	n/a	chr6:69269108-69269126 chr6:69269113-69269121
44	CTCF	chr6:69282540-69282690	RPTEC	kidney:	n/a	n/a
45	CTCF	chr6:69282321-69282790	K562	blood:	n/a	n/a
46	CTCF	chr6:69282220-69282370	GM12873	blood:	n/a	n/a
47	CTCF	chr6:69282520-69282670	GM12875	blood:	n/a	n/a
48	CTCF	chr6:69153720-69153870	HVMF	connective:	n/a	n/a
49	CTCF	chr6:69286000-69286150	RPTEC	kidney:	n/a	n/a
50	CTCF	chr6:69268914-69269373	SK-N-SH	brain:	n/a	chr6:69269108-69269126 chr6:69269113-69269121

No data

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:69053885..69054455-chr6:69178429..69178979,2	MCF-7	breast:
2	chr6:69191363..69194136-chr6:69196139..69198220,2	K562	blood:
3	chr6:69266569..69269694-chr6:69271036..69273043,3	K562	blood:
4	chr6:69282204..69283004-chr6:69488215..69489132,4	MCF-7	breast:
5	chr17:41400752..41402306-chr6:69141039..69142539,2	MCF-7	breast:
6	chr6:69282574..69283109-chr6:69488255..69488898,2	K562	blood:
7	chr6:69286611..69288197-chr6:69290507..69292702,2	K562	blood:
8	chr6:69174891..69177006-chr6:69177848..69180556,2	K562	blood:
9	chr6:69283640..69286439-chr6:69288403..69290275,2	K562	blood:
10	chr6:69187451..69191074-chr6:69191437..69194576,4	K562	blood:
11	chr6:69301094..69303705-chr6:69318926..69320788,2	K562	blood:
12	chr6:69188166..69190733-chr6:69192752..69194576,2	K562	blood:
13	chr6:69263146..69264657-chr6:69267088..69269602,2	MCF-7	breast:
14	chr22:20918726..20919648-chr6:69136151..69136812,2	MCF-7	breast:
15	chr6:69286611..69288197-chr6:69290507..69292702,2	K562	blood:
16	chr6:69131492..69134265-chr6:69138928..69141362,2	MCF-7	breast:
17	chr6:69174891..69177006-chr6:69177848..69180556,2	K562	blood:
18	chr6:69252350..69255145-chr6:69257038..69258708,2	K562	blood:
19	chr6:69285861..69288826-chr6:69344334..69346177,2	K562	blood:
20	chr6:69187451..69191074-chr6:69191437..69194576,4	K562	blood:
21	chr6:69053595..69054445-chr6:69282510..69283038,2	K562	blood:
22	chr6:69266569..69269694-chr6:69271036..69273043,3	K562	blood:
23	chr6:69281088..69283265-chr6:69488145..69489862,2	K562	blood:
24	chr17:41463798..41466662-chr6:69229976..69232995,3	K562	blood:
25	chr6:69283640..69286439-chr6:69288403..69290275,2	K562	blood:
26	chr6:69148448..69150705-chr6:69177431..69180205,2	K562	blood:
27	chr6:69182580..69184340-chr6:69184575..69186290,2	K562	blood:
28	chr6:69252350..69255145-chr6:69257038..69258708,2	K562	blood:
29	chr6:69191363..69194136-chr6:69196139..69198220,2	K562	blood:
30	chr6:69131492..69134265-chr6:69138928..69141362,2	MCF-7	breast:
31	chr6:69053724..69054431-chr6:69178564..69179099,2	K562	blood:
32	chr6:69263146..69264657-chr6:69267088..69269602,2	MCF-7	breast:
33	chr6:69053703..69054300-chr6:69207678..69208508,2	MCF-7	breast:
34	chr6:69287462..69289135-chr6:69323588..69325496,2	K562	blood:
35	chr17:41382033..41383660-chr6:69231475..69232975,2	K562	blood:
36	chr6:69182580..69184340-chr6:69184575..69186290,2	K562	blood:
37	chr15:65868328..65869022-chr6:69293826..69294756,2	Hela-S3	cervix:
38	chr3:73158464..73161460-chr6:69141039..69142539,2	K562	blood:
39	chr17:41380252..41382150-chr6:69231475..69232995,3	MCF-7	breast:
40	chr6:69188166..69190733-chr6:69192752..69194576,2	K562	blood:
41	chr17:41380326..41381992-chr6:69231475..69232995,3	MCF-7	breast:
42	chr6:69148448..69150705-chr6:69177431..69180205,2	K562	blood:
43	chr6:69053946..69055088-chr6:69178263..69178883,3	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000218834	TF binding region
ENSG00000266675	TF binding region
ENSG00000230910	chromatin interactions
ENSG00000135298	chromatin interactions
ENSG00000236383	chromatin interactions
ENSG00000188825	chromatin interactions
ENSG00000223247	chromatin interactions

Extended variants
information (count: 1701 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1701 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs546653458	chr6:69119446-69119447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs183135134	chr6:69119494-69119495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs566482593	chr6:69119498-69119499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs186189272	chr6:69119522-69119523	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs545998225	chr6:69119534-69119535	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535395836	chr6:69119538-69119539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190509662	chr6:69119546-69119547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9454509	chr6:69119557-69119558	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs201601122	chr6:69119582-69119583	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs149402662	chr6:69119584-69119585	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34370401	chr6:69119585-69119586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35880594	chr6:69119586-69119587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs564307480	chr6:69119588-69119589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs386407453	chr6:69119594-69119595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs398001895	chr6:69119607-69119608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs36007613	chr6:69119614-69119615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs531933698	chr6:69119621-69119622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs577250275	chr6:69119635-69119636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs577763442	chr6:69119672-69119673	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs74676982	chr6:69119718-69119719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs544124426	chr6:69119743-69119744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553414962	chr6:69119747-69119748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs138292672	chr6:69119763-69119764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs562228752	chr6:69119808-69119809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs529328969	chr6:69119813-69119814	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs547808330	chr6:69119831-69119832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs566181124	chr6:69119859-69119860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs542162312	chr6:69119941-69119942	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs183410673	chr6:69119985-69119986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs575752275	chr6:69120000-69120001	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544921074	chr6:69120012-69120013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533423417	chr6:69120035-69120036	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs189035406	chr6:69120084-69120085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs115777821	chr6:69120092-69120093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs540488053	chr6:69120111-69120112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs560165841	chr6:69120161-69120162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs141895062	chr6:69120189-69120190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs548527944	chr6:69120242-69120243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs568504106	chr6:69120245-69120246	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192476201	chr6:69120246-69120247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs551238005	chr6:69120290-69120291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs571482867	chr6:69120320-69120321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs573666791	chr6:69120344-69120345	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs114427480	chr6:69120361-69120362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs553689612	chr6:69120367-69120368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs182758991	chr6:69120368-69120369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs566918598	chr6:69120432-69120433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116475758	chr6:69120446-69120447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs555946892	chr6:69120467-69120468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs115894787	chr6:69120518-69120519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
Prostate cancer	16573809	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
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
Wilms tumour	21544195	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:177 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:69119200-69120000	Enhancers	Fetal Brain Male	brain
2	chr6:69120000-69120600	Weak transcription	Fetal Brain Male	brain
3	chr6:69120600-69120800	Enhancers	Fetal Brain Male	brain
4	chr6:69126200-69126400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
5	chr6:69137600-69138400	Enhancers	NH-A	brain
6	chr6:69139800-69142400	Weak transcription	Stomach Mucosa	stomach
7	chr6:69147600-69148000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr6:69154800-69155000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr6:69155200-69155800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:69155800-69156000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr6:69156000-69156600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr6:69156800-69157000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr6:69157000-69157400	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr6:69161800-69167400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
15	chr6:69165600-69166200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr6:69175400-69175800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr6:69175400-69176000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
18	chr6:69181800-69182400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr6:69181800-69182400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:69182000-69182200	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr6:69182400-69183400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr6:69182400-69183400	Weak transcription	Cortex derived primary cultured neurospheres	brain
23	chr6:69182400-69185600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:69183400-69183800	Enhancers	Cortex derived primary cultured neurospheres	brain
25	chr6:69183400-69184200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr6:69184200-69185800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
27	chr6:69185600-69187400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chr6:69185800-69186400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:69185800-69186800	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr6:69185800-69187600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:69186000-69187600	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr6:69186200-69187600	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr6:69186200-69187800	Enhancers	HUES48 Cell Line	embryonic stem cell
34	chr6:69186400-69187600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr6:69186800-69187600	Enhancers	H9 Cell Line	embryonic stem cell
36	chr6:69187400-69188800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:69187600-69188800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chr6:69188800-69189200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr6:69188800-69189600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:69192600-69193200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr6:69193200-69194200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr6:69194200-69194400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr6:69208000-69208400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:69235800-69236200	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr6:69236000-69236600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:69259000-69259400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr6:69266200-69266600	Enhancers	Cortex derived primary cultured neurospheres	brain
48	chr6:69266600-69268800	Weak transcription	Cortex derived primary cultured neurospheres	brain
49	chr6:69268600-69269200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr6:69268800-69269200	Enhancers	Cortex derived primary cultured neurospheres	brain

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