Variant report

Variant	nsv830743
Chromosome Location	chr6:102284082-102459192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:349)
CpG islands
(count:123)
Chromatin interactive
region (count:23)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:349 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr6:102327575-102327933	GM12878	blood:	n/a	n/a
2	BATF	chr6:102293655-102293876	GM12878	blood:	n/a	n/a
3	BATF	chr6:102331364-102331593	GM12878	blood:	n/a	n/a
4	BATF	chr6:102434381-102434731	GM12878	blood:	n/a	n/a
5	BATF	chr6:102293651-102293827	GM12878	blood:	n/a	n/a
6	BATF	chr6:102434348-102434631	GM12878	blood:	n/a	n/a
7	BATF	chr6:102327588-102327954	GM12878	blood:	n/a	n/a
8	BCL11A	chr6:102293606-102293891	GM12878	blood:	n/a	n/a
9	BHLHE40	chr6:102293508-102293918	GM12878	blood:	n/a	n/a
10	BHLHE40	chr6:102434194-102434690	GM12878	blood:	n/a	n/a
11	CEBPB	chr6:102359560-102359811	A549	lung:	n/a	chr6:102359688-102359699
12	CEBPB	chr6:102379676-102379923	IMR90	lung:	n/a	chr6:102379822-102379835
13	CEBPB	chr6:102340485-102340685	K562	blood:	n/a	chr6:102340605-102340618 chr6:102340605-102340618 chr6:102340519-102340530 chr6:102340606-102340617
14	CEBPB	chr6:102379717-102379919	ECC-1	luminal epithelium:	n/a	chr6:102379822-102379835
15	CEBPB	chr6:102340481-102340681	HepG2	liver:	n/a	chr6:102340605-102340618 chr6:102340605-102340618 chr6:102340519-102340530 chr6:102340606-102340617
16	CEBPB	chr6:102331363-102331953	IMR90	lung:	n/a	n/a
17	CEBPB	chr6:102335573-102335864	HepG2	liver:	n/a	chr6:102335715-102335726
18	CEBPB	chr6:102359504-102359870	IMR90	lung:	n/a	chr6:102359688-102359699
19	CEBPB	chr6:102430470-102430482	K562	blood:	n/a	n/a
20	CEBPB	chr6:102331435-102331696	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr6:102355347-102355775	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:102359527-102359859	HepG2	liver:	n/a	chr6:102359688-102359699
23	CEBPB	chr6:102335594-102335841	A549	lung:	n/a	chr6:102335715-102335726
24	CREB1	chr6:102327645-102328015	GM12878	blood:	n/a	n/a
25	CTCF	chr6:102290700-102290850	HepG2	liver:	n/a	n/a
26	CTCF	chr6:102290740-102290890	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr6:102290760-102290993	GM12878	blood:	n/a	n/a
28	CTCF	chr6:102409440-102409590	GM12865	blood:	n/a	n/a
29	CTCF	chr6:102290700-102290850	BE2_C	brain:	n/a	n/a
30	CTCF	chr6:102290680-102290830	BE2_C	brain:	n/a	n/a
31	CTCF	chr6:102326900-102327050	AG04449	skin:	n/a	n/a
32	CTCF	chr6:102295740-102295890	Caco-2	colon:	n/a	n/a
33	CTCF	chr6:102409365-102409527	MCF-7	breast:	n/a	n/a
34	CTCF	chr6:102409300-102409450	Caco-2	colon:	n/a	n/a
35	CTCF	chr6:102290780-102290930	HEK293	kidney:	n/a	n/a
36	CTCF	chr6:102290674-102290963	MCF-7	breast:	n/a	n/a
37	CTCF	chr6:102409398-102409542	MCF-7	breast:	n/a	n/a
38	CTCF	chr6:102290740-102290890	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:102290700-102290850	SAEC	small airway:	n/a	n/a
40	CTCF	chr6:102290740-102290890	WI-38	lung:	n/a	n/a
41	CTCF	chr6:102295720-102295870	NHEK	skin:	n/a	n/a
42	CTCF	chr6:102290780-102290930	NHDF-neo	bronchial:	n/a	n/a
43	CTCF	chr6:102290760-102290910	HBMEC	blood vessel:	n/a	n/a
44	CTCF	chr6:102346499-102346520	GM13976	blood:	n/a	n/a
45	CTCF	chr6:102409386-102409480	Fibrobl	skin:	n/a	n/a
46	CTCF	chr6:102290740-102290890	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr6:102290660-102290810	RPTEC	kidney:	n/a	n/a
48	CTCF	chr6:102290680-102290830	HCT-116	colon:	n/a	n/a
49	CTCF	chr6:102290700-102290850	HRPEpiC	eye:	n/a	n/a
50	CTCF	chr6:102290800-102290950	RPTEC	kidney:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:102295679-102295729	SAEC	small airway:	n/a
2	chr6:102295679-102295729	SAEC	small airway:	n/a
3	chr6:102295679-102295729	HCF	heart:	n/a
4	chr6:102326919-102326969	HCPEpiC	choroid plexus:	n/a
5	chr6:102295679-102295729	NHBE	bronchial:	n/a
6	chr6:102295679-102295729	NH-A	brain:	n/a
7	chr6:102326919-102326969	SAEC	small airway:	n/a
8	chr6:102326919-102326969	LNCaP	prostate:	n/a
9	chr6:102295679-102295729	NHDF-neo	bronchial:	n/a
10	chr6:102326919-102326969	IMR90	lung:	fetal
11	chr6:102295679-102295729	NT2-D1	testis:	n/a
12	chr6:102326919-102326969	A549	lung:	n/a
13	chr6:102295679-102295729	AoSMC	blood vessel:	n/a
14	chr6:102295679-102295729	HEK293	kidney:	embryo
15	chr6:102326919-102326969	AG10803	skin:	n/a
16	chr6:102326919-102326969	GM12878	blood:	n/a
17	chr6:102295679-102295729	HMEC	breast:	n/a
18	chr6:102326919-102326969	AG04449	skin:	fetal
19	chr6:102295679-102295729	AG09319	gingival:	n/a
20	chr6:102326919-102326969	HRCEpiC	kidney:	n/a
21	chr6:102295679-102295729	U87	brain:	n/a
22	chr6:102295679-102295729	MCF10A-Er-Src	breast:	n/a
23	chr6:102295679-102295729	MCF-7	breast:	n/a
24	chr6:102295679-102295729	BJ	skin:	n/a
25	chr6:102295679-102295729	IMR90	lung:	fetal
26	chr6:102295679-102295729	AG04450	lung:	fetal
27	chr6:102326919-102326969	HUVEC	blood vessel:	n/a
28	chr6:102295679-102295729	K562	blood:	n/a
29	chr6:102295679-102295729	SK-N-SH	brain:	n/a
30	chr6:102295679-102295729	SK-N-SH_RA	brain:	n/a
31	chr6:102326919-102326969	PANC-1	pancreas:	n/a
32	chr6:102326919-102326969	HPAEpiC	pulmonary alveolar:	n/a
33	chr6:102295679-102295729	Hepatocyte	liver:	n/a
34	chr6:102326919-102326969	AG04450	lung:	fetal
35	chr6:102295679-102295729	Jurkat	blood:	n/a
36	chr6:102326919-102326969	CMK	blood:	n/a
37	chr6:102326919-102326969	BJ	skin:	n/a
38	chr6:102295679-102295729	HCM	heart:	n/a
39	chr6:102326919-102326969	K562	blood:	n/a
40	chr6:102326919-102326969	HNPCEpiC	eye:	n/a
41	chr6:102295679-102295729	NB4	blood:	n/a
42	chr6:102295679-102295729	HepG2	liver:	n/a
43	chr6:102295679-102295729	GM19239	blood:	n/a
44	chr6:102326919-102326969	Hepatocyte	liver:	n/a
45	chr6:102326919-102326969	HAEpiC	amniotic membrane:	n/a
46	chr6:102295679-102295729	HPAEpiC	pulmonary alveolar:	n/a
47	chr6:102295679-102295729	AG09309	skin:	n/a
48	chr6:102295679-102295729	HCT-116	colon:	n/a
49	chr6:102326919-102326969	ProgFib	skin:	n/a
50	chr6:102326919-102326969	GM19239	blood:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:102423740..102426359-chr6:102431274..102433245,2	K562	blood:
2	chr6:102388911..102391649-chr6:102394397..102396742,2	MCF-7	breast:
3	chr6:102377981..102380751-chr6:102384114..102385937,2	K562	blood:
4	chr6:102332291..102334019-chr6:102343556..102346119,2	MCF-7	breast:
5	chr6:102427557..102429881-chr6:102433659..102436642,2	MCF-7	breast:
6	chr6:102304730..102306857-chr6:102309249..102312127,2	MCF-7	breast:
7	chr6:102332291..102334019-chr6:102343556..102346119,2	MCF-7	breast:
8	chr6:102423740..102426359-chr6:102431274..102433245,2	K562	blood:
9	chr6:102408799..102411775-chr6:102415336..102416958,2	MCF-7	breast:
10	chr6:102352732..102355186-chr6:102357901..102361862,3	K562	blood:
11	chr6:102312465..102314279-chr6:102350590..102352223,2	K562	blood:
12	chr6:102451733..102454626-chr6:102454747..102456750,2	MCF-7	breast:
13	chr6:102312465..102314279-chr6:102350590..102352223,2	K562	blood:
14	chr6:102353130..102355186-chr6:102359232..102361862,2	K562	blood:
15	chr6:102451733..102454626-chr6:102454747..102456750,2	MCF-7	breast:
16	chr6:102368803..102370851-chr6:102488591..102491392,2	K562	blood:
17	chr6:102388911..102391649-chr6:102394397..102396742,2	MCF-7	breast:
18	chr6:102352732..102355186-chr6:102357901..102361862,3	K562	blood:
19	chr6:102408799..102411775-chr6:102415336..102416958,2	MCF-7	breast:
20	chr6:102304730..102306857-chr6:102309249..102312127,2	MCF-7	breast:
21	chr6:102377981..102380751-chr6:102384114..102385937,2	K562	blood:
22	chr6:102353130..102355186-chr6:102359232..102361862,2	K562	blood:
23	chr6:102427557..102429881-chr6:102433659..102436642,2	MCF-7	breast:

No data

Variant related genes	Relation type
GRIK2	TF binding region
GRIK2	CpG island

Extended variants
information (count: 1405 )
Associated
traits (count: 111 )

Variant overlapped rSNPs/rCNVs (count:1405 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564617119	chr6:102292829-102292830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs576721776	chr6:102292831-102292832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs151069288	chr6:102292869-102292870	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141350986	chr6:102292877-102292878	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs533292891	chr6:102292878-102292879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374180218	chr6:102292891-102292892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs561957830	chr6:102292903-102292904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs397887149	chr6:102292905-102292906	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs141006426	chr6:102292930-102292931	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs553013356	chr6:102292949-102292950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs376908182	chr6:102292984-102292985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs547110127	chr6:102293007-102293008	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149794021	chr6:102293080-102293081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2791826	chr6:102293089-102293090	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs146737854	chr6:102293090-102293091	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs569847858	chr6:102293100-102293101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs544885734	chr6:102293134-102293135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2791827	chr6:102293189-102293190	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs543725006	chr6:102293605-102293606	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527858372	chr6:102293613-102293614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs145564528	chr6:102293616-102293617	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528647929	chr6:102293629-102293630	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs573871535	chr6:102293660-102293661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs9390788	chr6:102293671-102293672	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs566074730	chr6:102293693-102293694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs371294787	chr6:102293716-102293717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs533094491	chr6:102293718-102293719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs76695892	chr6:102293756-102293757	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs563304442	chr6:102293806-102293807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs370085172	chr6:102293833-102293834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs530798042	chr6:102293872-102293873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs537175433	chr6:102293878-102293879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs538517121	chr6:102293879-102293880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141274825	chr6:102293882-102293883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs116944636	chr6:102293890-102293891	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs567601759	chr6:102293893-102293894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550709228	chr6:102293917-102293918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs574655336	chr6:102293919-102293920	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567241238	chr6:102293924-102293925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs138085747	chr6:102293933-102293934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs565995353	chr6:102293944-102293945	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs185696951	chr6:102293970-102293971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs149036563	chr6:102294022-102294023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs112033609	chr6:102294042-102294043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs537077513	chr6:102294050-102294051	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555627104	chr6:102294052-102294053	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs574037042	chr6:102294104-102294105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs541223789	chr6:102294268-102294269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs553535645	chr6:102294331-102294332	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs143011054	chr6:102294371-102294372	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:111)

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
Endometrioid adenocarcinoma	16974079	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
lymphocytic leukemia	21291569	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	16272173	CNVD
Prostate cancer	18632612	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Lung adenocarcinoma	21935476	CNVD
Prostate cancer	17245344	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	20823134	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	17640729	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
small cell lung cancer	20016488	CNVD
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	17170743	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21785460	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Myelofibrosis	22110671	CNVD
Obesity	21045960	CNVD
Liver carcinoma	19366792	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Urothelial carcinoma	21177765	CNVD
Autism	22543975	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD

Chromatin state (count:98 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102292800-102293200	Enhancers	Primary T cells fromperipheralblood	blood
2	chr6:102292800-102293200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
3	chr6:102293600-102293800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr6:102293800-102297400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr6:102293800-102297600	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr6:102294200-102295400	Enhancers	iPS-20b Cell Line	embryonic stem cell
7	chr6:102294200-102297400	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr6:102294200-102297400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr6:102294400-102297400	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr6:102295200-102295600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
11	chr6:102295200-102296400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr6:102295400-102295800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
13	chr6:102295400-102295800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr6:102295400-102296000	Enhancers	H1 Cell Line	embryonic stem cell
15	chr6:102295400-102296000	Enhancers	H9 Cell Line	embryonic stem cell
16	chr6:102295400-102296200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr6:102295400-102296400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr6:102295600-102295800	Enhancers	Gastric	stomach
19	chr6:102295800-102296200	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr6:102296000-102297000	Weak transcription	H1 Cell Line	embryonic stem cell
21	chr6:102296200-102297200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr6:102296200-102297200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
23	chr6:102296400-102296800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr6:102296400-102296800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
25	chr6:102296800-102297200	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr6:102296800-102297400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:102297000-102297400	Enhancers	H1 Cell Line	embryonic stem cell
28	chr6:102297200-102297400	Enhancers	iPS-20b Cell Line	embryonic stem cell
29	chr6:102297200-102297400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr6:102299600-102300000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr6:102300000-102300400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:102300200-102301600	Enhancers	Muscle Satellite Cultured Cells	--
33	chr6:102323800-102324800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr6:102323800-102325200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr6:102324200-102324800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr6:102324200-102324800	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr6:102324400-102324600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr6:102324400-102324800	Enhancers	Brain Germinal Matrix	brain
39	chr6:102326200-102327000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr6:102326600-102327000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
41	chr6:102326600-102327000	Enhancers	Fetal Heart	heart
42	chr6:102326600-102327200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
43	chr6:102326600-102327200	Active TSS	Ovary	ovary
44	chr6:102327000-102327200	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr6:102327000-102327400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:102327000-102331600	Weak transcription	Fetal Heart	heart
47	chr6:102327200-102327600	Enhancers	GM12878-XiMat	blood
48	chr6:102327200-102331400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
49	chr6:102327400-102327800	Enhancers	HUES48 Cell Line	embryonic stem cell
50	chr6:102327400-102327800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell

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