Variant report

Variant	nsv1034848
Chromosome Location	chr6:23857972-23976276
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	ATF1	chr6:23872111-23872462	K562	blood:	n/a	n/a
2	CCNT2	chr6:23956182-23956382	K562	blood:	n/a	n/a
3	CCNT2	chr6:23873770-23873922	K562	blood:	n/a	n/a
4	CEBPB	chr6:23931161-23931449	H1-hESC	embryonic stem cell:	n/a	chr6:23931276-23931287 chr6:23931278-23931287 chr6:23931278-23931287 chr6:23931278-23931287 chr6:23931278-23931287
5	CEBPB	chr6:23965169-23965342	K562	blood:	n/a	chr6:23965289-23965300
6	CEBPB	chr6:23889235-23889561	HepG2	liver:	n/a	chr6:23889417-23889428
7	CEBPB	chr6:23954221-23954542	MCF-7	breast:	n/a	n/a
8	CEBPB	chr6:23965102-23965476	A549	lung:	n/a	chr6:23965289-23965300
9	CEBPB	chr6:23867481-23867697	IMR90	lung:	n/a	chr6:23867541-23867552 chr6:23867585-23867596
10	CEBPB	chr6:23879127-23879354	HepG2	liver:	n/a	chr6:23879241-23879252
11	CEBPB	chr6:23883401-23883634	A549	lung:	n/a	chr6:23883505-23883516
12	CEBPB	chr6:23889286-23889571	A549	lung:	n/a	chr6:23889417-23889428
13	CEBPB	chr6:23943467-23943680	HepG2	liver:	n/a	chr6:23943580-23943591
14	CEBPB	chr6:23965106-23965472	K562	blood:	n/a	chr6:23965289-23965300
15	CEBPB	chr6:23965237-23965374	HepG2	liver:	n/a	chr6:23965289-23965300
16	CEBPB	chr6:23965111-23965481	H1-hESC	embryonic stem cell:	n/a	chr6:23965289-23965300
17	CEBPB	chr6:23965067-23965484	MCF-7	breast:	n/a	chr6:23965289-23965300
18	CEBPB	chr6:23883336-23883679	HepG2	liver:	n/a	chr6:23883505-23883516
19	CEBPB	chr6:23965094-23965449	MCF-7	breast:	n/a	chr6:23965289-23965300
20	CEBPB	chr6:23889264-23889546	IMR90	lung:	n/a	chr6:23889417-23889428
21	CEBPB	chr6:23890796-23891174	Hela-S3	cervix:	n/a	chr6:23890971-23890982 chr6:23890956-23890967 chr6:23890969-23890980 chr6:23890971-23890982
22	CEBPB	chr6:23890803-23891143	HepG2	liver:	n/a	chr6:23890971-23890982 chr6:23890956-23890967 chr6:23890969-23890980 chr6:23890971-23890982
23	CEBPB	chr6:23931202-23931302	A549	lung:	n/a	chr6:23931276-23931287 chr6:23931278-23931287 chr6:23931278-23931287 chr6:23931278-23931287 chr6:23931278-23931287
24	CEBPB	chr6:23890765-23891159	MCF-7	breast:	n/a	chr6:23890971-23890982 chr6:23890956-23890967 chr6:23890969-23890980 chr6:23890971-23890982
25	CEBPB	chr6:23965108-23965481	HepG2	liver:	n/a	chr6:23965289-23965300
26	CEBPB	chr6:23931126-23931443	HepG2	liver:	n/a	chr6:23931276-23931287 chr6:23931278-23931287 chr6:23931278-23931287 chr6:23931278-23931287 chr6:23931278-23931287
27	CEBPB	chr6:23963411-23963772	MCF-7	breast:	n/a	n/a
28	CEBPB	chr6:23965097-23965486	Hela-S3	cervix:	n/a	chr6:23965289-23965300
29	CEBPB	chr6:23965108-23965478	IMR90	lung:	n/a	chr6:23965289-23965300
30	CEBPB	chr6:23867437-23867691	A549	lung:	n/a	chr6:23867541-23867552 chr6:23867585-23867596
31	CEBPB	chr6:23867406-23867756	HepG2	liver:	n/a	chr6:23867541-23867552 chr6:23867585-23867596
32	CHD2	chr6:23962169-23962193	GM12878	blood:	n/a	n/a
33	CTCF	chr6:23945780-23945930	BE2_C	brain:	n/a	n/a
34	CTCF	chr6:23887620-23887770	K562	blood:	n/a	n/a
35	CTCF	chr6:23966520-23966670	Hela-S3	cervix:	n/a	n/a
36	CTCF	chr6:23945780-23945930	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:23881416-23881436	A549	lung:	n/a	n/a
38	CTCF	chr6:23945780-23945930	WERI-Rb-1	eye:	n/a	n/a
39	CTCF	chr6:23945795-23945953	MCF-7	breast:	n/a	n/a
40	CTCF	chr6:23945740-23945890	MCF-7	breast:	n/a	n/a
41	CTCF	chr6:23945776-23945982	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:23861800-23861950	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr6:23963540-23963690	MCF-7	breast:	n/a	n/a
44	CTCF	chr6:23945625-23946117	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:23973932-23973992	GM13976	blood:	n/a	n/a
46	CTCF	chr6:23880980-23881130	WERI-Rb-1	eye:	n/a	n/a
47	CTCF	chr6:23945713-23945905	GM12878	blood:	n/a	n/a
48	CTCF	chr6:23943364-23943453	K562	blood:	n/a	n/a
49	CTCF	chr6:23923980-23924130	GM12869	blood:	n/a	n/a
50	E2F4	chr6:23928269-23928693	MCF10A-Er-Src	breast:	n/a	chr6:23928277-23928291

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:23955726-23955776	NHBE	bronchial:	n/a
2	chr6:23955726-23955776	GM12892	blood:	n/a
3	chr6:23955726-23955776	A549	lung:	n/a
4	chr6:23955726-23955776	ProgFib	skin:	n/a
5	chr6:23955726-23955776	CMK	blood:	n/a
6	chr6:23955726-23955776	HPAEpiC	pulmonary alveolar:	n/a
7	chr6:23955726-23955776	AG09309	skin:	n/a
8	chr6:23955726-23955776	HRPEpiC	eye:	n/a
9	chr6:23955726-23955776	NH-A	brain:	n/a
10	chr6:23955726-23955776	H1-hESC	embryonic stem cell:	embryo
11	chr6:23955726-23955776	GM12891	blood:	n/a
12	chr6:23955726-23955776	HEEpiC	esophagus:	n/a
13	chr6:23955726-23955776	ovcar-3	ovarian:	n/a
14	chr6:23955726-23955776	PrEC	prostate:	n/a
15	chr6:23955726-23955776	HNPCEpiC	eye:	n/a
16	chr6:23955726-23955776	MCF10A-Er-Src	breast:	n/a
17	chr6:23955726-23955776	NHDF-neo	bronchial:	n/a
18	chr6:23955726-23955776	GM06990	blood:	n/a
19	chr6:23955726-23955776	LNCaP	prostate:	n/a
20	chr6:23955726-23955776	AG04450	lung:	fetal
21	chr6:23955726-23955776	HAEpiC	amniotic membrane:	n/a
22	chr6:23955726-23955776	SK-N-SH	brain:	n/a
23	chr6:23955726-23955776	SAEC	small airway:	n/a
24	chr6:23955726-23955776	GM12878	blood:	n/a
25	chr6:23955726-23955776	U87	brain:	n/a
26	chr6:23955726-23955776	T-47D	breast:	n/a
27	chr6:23955726-23955776	PANC-1	pancreas:	n/a
28	chr6:23955726-23955776	AoSMC	blood vessel:	n/a
29	chr6:23955726-23955776	HCF	heart:	n/a
30	chr6:23955726-23955776	ECC-1	luminal epithelium:	n/a
31	chr6:23955726-23955776	PFSK-1	brain:	n/a
32	chr6:23955726-23955776	K562	blood:	n/a
33	chr6:23955726-23955776	HMEC	breast:	n/a
34	chr6:23955726-23955776	Jurkat	blood:	n/a
35	chr6:23955726-23955776	Caco-2	colon:	n/a
36	chr6:23955726-23955776	NT2-D1	testis:	n/a
37	chr6:23955726-23955776	SKMC	muscle:	n/a
38	chr6:23955726-23955776	BE2_C	brain:	n/a
39	chr6:23955726-23955776	HUVEC	blood vessel:	n/a
40	chr6:23955726-23955776	HRE	kidney:	n/a
41	chr6:23955726-23955776	NB4	blood:	n/a
42	chr6:23955726-23955776	HEK293	kidney:	embryo
43	chr6:23955726-23955776	SK-N-SH_RA	brain:	n/a
44	chr6:23955726-23955776	Hepatocyte	liver:	n/a
45	chr6:23955726-23955776	GM19239	blood:	n/a
46	chr6:23955726-23955776	AG04449	skin:	fetal
47	chr6:23955726-23955776	HRCEpiC	kidney:	n/a
48	chr6:23955726-23955776	HCM	heart:	n/a
49	chr6:23955726-23955776	RPTEC	kidney:	n/a
50	chr6:23955726-23955776	IMR90	lung:	fetal

No.	Distal block	Cell Line	Cell type
1	chr6:23879136..23881788-chr6:23889140..23891647,2	K562	blood:
2	chr6:23933203..23935134-chr6:23935922..23937472,2	K562	blood:
3	chr6:23883681..23885208-chr6:23886637..23889627,2	MCF-7	breast:
4	chr6:23976164..23979074-chr6:23981156..23983505,2	MCF-7	breast:
5	chr6:23918439..23920690-chr6:23924109..23926782,2	MCF-7	breast:
6	chr6:23923563..23926014-chr6:23927623..23930582,2	MCF-7	breast:
7	chr10:102117039..102117661-chr6:23910880..23911790,2	Hela-S3	cervix:
8	chr6:23952885..23955459-chr6:23957501..23960494,2	K562	blood:
9	chr6:23923563..23926014-chr6:23927623..23930582,2	MCF-7	breast:
10	chr6:23933203..23935134-chr6:23935922..23937472,2	K562	blood:
11	chr6:23918439..23920690-chr6:23924109..23926782,2	MCF-7	breast:
12	chr17:57920621..57922223-chr6:23884700..23886484,2	MCF-7	breast:
13	chr6:23951517..23954441-chr6:23956245..23958507,2	MCF-7	breast:
14	chr6:23951517..23954441-chr6:23956245..23958507,2	MCF-7	breast:
15	chr6:23952885..23955459-chr6:23957501..23960494,2	K562	blood:
16	chr6:23883681..23885208-chr6:23886637..23889627,2	MCF-7	breast:
17	chr6:23879136..23881788-chr6:23889140..23891647,2	K562	blood:

Variant related genes	Relation type
SPTLC1P2	TF binding region
ENSG00000220748	TF binding region
SPTLC1P2	CpG island
ENSG00000220748	CpG island

Extended variants
information (count: 2897 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:2897 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs146921113	chr6:23858731-23858732	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs376707403	chr6:23858749-23858750	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs544743131	chr6:23858751-23858752	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs115167434	chr6:23858752-23858753	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs554802554	chr6:23858757-23858758	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs558861083	chr6:23858764-23858765	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs137913490	chr6:23858778-23858779	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs75380382	chr6:23858795-23858796	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs143284236	chr6:23858796-23858797	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs150486374	chr6:23858799-23858800	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs543918245	chr6:23858819-23858820	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs541865864	chr6:23858829-23858830	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs138345236	chr6:23858830-23858831	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs533045145	chr6:23861071-23861072	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs377215309	chr6:23861084-23861085	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs551596566	chr6:23861095-23861096	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs569701556	chr6:23861114-23861115	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs148165878	chr6:23861116-23861117	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs555137598	chr6:23861121-23861122	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs73379944	chr6:23861139-23861140	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs77621697	chr6:23861142-23861143	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs187032771	chr6:23861158-23861159	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs111823512	chr6:23861178-23861179	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs572817703	chr6:23861182-23861183	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs141119192	chr6:23861183-23861184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs558335828	chr6:23861228-23861229	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs576525474	chr6:23861229-23861230	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs150234740	chr6:23861231-23861232	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs576650227	chr6:23861766-23861767	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs572302060	chr6:23861782-23861783	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs537277782	chr6:23861783-23861784	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs555531175	chr6:23861785-23861786	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs574842397	chr6:23861795-23861796	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs573842730	chr6:23861848-23861849	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs541079356	chr6:23861854-23861855	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs373650249	chr6:23861873-23861874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs559330319	chr6:23861916-23861917	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs577925635	chr6:23861925-23861926	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs10946644	chr6:23861947-23861948	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs563464073	chr6:23861972-23861973	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs530818503	chr6:23861978-23861979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs369497231	chr6:23861983-23861984	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs548949432	chr6:23862009-23862010	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs373533942	chr6:23862014-23862015	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs58278641	chr6:23869040-23869041	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs191216696	chr6:23869109-23869110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565750055	chr6:23869142-23869143	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs539100288	chr6:23869174-23869175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs11756885	chr6:23869417-23869418	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs58398055	chr6:23869420-23869421	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:105)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Myelodysplastic syndrome	21251322	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	17550852	CNVD
Ewing''s sarcoma	17952124	CNVD
Gastric cancer	16891809	CNVD
Ovarian cancer	21781307	CNVD
Autism	21448237	CNVD
Cancer	20164919	CNVD
Melanoma	18172304	CNVD
Breast cancer	22844521	CNVD
HIV/AIDS	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Breast cancer	22522925	CNVD
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ependymoma	19289631	CNVD
Gestational infection	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Osteosarcoma	16790693	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17133270	CNVD
Autism	22495311	CNVD
Burkitt''s lymphoma	19759907	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cancer	16790693	CNVD
Breast cancer	22032731	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	16790693	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Retinoblastoma	16790693	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
T-cell lymphomas	19863542	CNVD
Urothelial carcinoma	18382360	CNVD
Lung cancer	19153074	CNVD
Breast cancer	21364760	CNVD
Cancer	21183584	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Williams-beuren syndrome	16971481	CNVD
Uveal melanoma	20484589	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:124 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:23869000-23869200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr6:23869400-23870400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:23869800-23871200	Enhancers	Fetal Brain Male	brain
4	chr6:23870400-23877200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr6:23870600-23871000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr6:23870600-23871200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr6:23870600-23871200	Enhancers	Brain Germinal Matrix	brain
8	chr6:23870600-23871400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
9	chr6:23870600-23872200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:23870800-23871200	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr6:23871200-23872200	Weak transcription	Fetal Brain Male	brain
12	chr6:23871200-23873600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:23871200-23874600	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr6:23871200-23874800	Weak transcription	Brain Germinal Matrix	brain
15	chr6:23871400-23874400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr6:23872200-23872600	Enhancers	Fetal Brain Male	brain
17	chr6:23872200-23872600	Active TSS	Fetal Lung	lung
18	chr6:23872200-23872600	ZNF genes & repeats	Pancreas	Pancrea
19	chr6:23872200-23873200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr6:23873000-23874800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
21	chr6:23873000-23876400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr6:23873200-23873600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr6:23873600-23876200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr6:23873600-23881800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr6:23874000-23876000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr6:23874400-23876000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
27	chr6:23874600-23874800	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr6:23874800-23875200	Weak transcription	Cortex derived primary cultured neurospheres	brain
29	chr6:23874800-23875400	Enhancers	Brain Germinal Matrix	brain
30	chr6:23875200-23876200	Enhancers	Cortex derived primary cultured neurospheres	brain
31	chr6:23875400-23876000	Weak transcription	Brain Germinal Matrix	brain
32	chr6:23876000-23876200	Enhancers	Brain Germinal Matrix	brain
33	chr6:23876000-23877000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr6:23876200-23876600	Weak transcription	Cortex derived primary cultured neurospheres	brain
35	chr6:23876600-23877400	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr6:23877000-23877200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:23879800-23880000	Enhancers	Pancreatic Islets	Pancreatic Islet
38	chr6:23881800-23883000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr6:23887200-23887600	Enhancers	Brain Germinal Matrix	brain
40	chr6:23890200-23890400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:23890400-23890600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr6:23890400-23890600	Enhancers	Liver	Liver
43	chr6:23890400-23890800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
44	chr6:23890400-23890800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr6:23890400-23890800	Enhancers	NHDF-Ad	bronchial
46	chr6:23890600-23890800	Enhancers	Adipose Nuclei	Adipose
47	chr6:23890600-23890800	Flanking Active TSS	Liver	Liver
48	chr6:23890600-23891400	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
49	chr6:23890800-23891000	Active TSS	Liver	Liver
50	chr6:23890800-23891200	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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