Variant report

Variant	nsv886465
Chromosome Location	chr6:102318339-102466397
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:217)
CpG islands
(count:61)
Chromatin interactive
region (count:20)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:217 , 50 per page) page: 1 2 3 4 5

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	chr6:102327588-102327954	GM12878	blood:	n/a	n/a
3	BATF	chr6:102434348-102434631	GM12878	blood:	n/a	n/a
4	BATF	chr6:102331364-102331593	GM12878	blood:	n/a	n/a
5	BATF	chr6:102434381-102434731	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:102434194-102434690	GM12878	blood:	n/a	n/a
7	CEBPB	chr6:102379717-102379919	ECC-1	luminal epithelium:	n/a	chr6:102379822-102379835
8	CEBPB	chr6:102359560-102359811	A549	lung:	n/a	chr6:102359688-102359699
9	CEBPB	chr6:102359504-102359870	IMR90	lung:	n/a	chr6:102359688-102359699
10	CEBPB	chr6:102331363-102331953	IMR90	lung:	n/a	n/a
11	CEBPB	chr6:102355347-102355775	HepG2	liver:	n/a	n/a
12	CEBPB	chr6:102335573-102335864	HepG2	liver:	n/a	chr6:102335715-102335726
13	CEBPB	chr6:102430470-102430482	K562	blood:	n/a	n/a
14	CEBPB	chr6:102379676-102379923	IMR90	lung:	n/a	chr6:102379822-102379835
15	CEBPB	chr6:102359527-102359859	HepG2	liver:	n/a	chr6:102359688-102359699
16	CEBPB	chr6:102335594-102335841	A549	lung:	n/a	chr6:102335715-102335726
17	CEBPB	chr6:102331435-102331696	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr6:102340481-102340681	HepG2	liver:	n/a	chr6:102340605-102340618 chr6:102340605-102340618 chr6:102340519-102340530 chr6:102340606-102340617
19	CEBPB	chr6:102340485-102340685	K562	blood:	n/a	chr6:102340605-102340618 chr6:102340605-102340618 chr6:102340519-102340530 chr6:102340606-102340617
20	CREB1	chr6:102327645-102328015	GM12878	blood:	n/a	n/a
21	CTCF	chr6:102409300-102409450	WERI-Rb-1	eye:	n/a	n/a
22	CTCF	chr6:102409385-102409477	GM12891	blood:	n/a	n/a
23	CTCF	chr6:102409380-102409530	HEK293	kidney:	n/a	n/a
24	CTCF	chr6:102409347-102409493	HepG2	liver:	n/a	n/a
25	CTCF	chr6:102409415-102409503	HepG2	liver:	n/a	n/a
26	CTCF	chr6:102409398-102409542	MCF-7	breast:	n/a	n/a
27	CTCF	chr6:102409434-102409464	A549	lung:	n/a	n/a
28	CTCF	chr6:102409386-102409480	Fibrobl	skin:	n/a	n/a
29	CTCF	chr6:102346499-102346520	GM13976	blood:	n/a	n/a
30	CTCF	chr6:102460620-102460688	GM20000	blood:	n/a	n/a
31	CTCF	chr6:102409369-102409493	GM12878	blood:	n/a	n/a
32	CTCF	chr6:102409361-102409478	MCF-7	breast:	n/a	n/a
33	CTCF	chr6:102409440-102409590	GM12865	blood:	n/a	n/a
34	CTCF	chr6:102409277-102409614	GM12878	blood:	n/a	n/a
35	CTCF	chr6:102452580-102452597	GM13976	blood:	n/a	n/a
36	CTCF	chr6:102409417-102409472	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr6:102409300-102409450	Caco-2	colon:	n/a	n/a
38	CTCF	chr6:102409395-102409522	MCF-7	breast:	n/a	n/a
39	CTCF	chr6:102409465-102409468	A549	lung:	n/a	n/a
40	CTCF	chr6:102448689-102448726	GM20000	blood:	n/a	n/a
41	CTCF	chr6:102409361-102409524	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr6:102409340-102409490	HepG2	liver:	n/a	n/a
43	CTCF	chr6:102409470-102409478	A549	lung:	n/a	n/a
44	CTCF	chr6:102409364-102409560	MCF-7	breast:	n/a	n/a
45	CTCF	chr6:102409365-102409527	MCF-7	breast:	n/a	n/a
46	CTCF	chr6:102409360-102409510	GM12865	blood:	n/a	n/a
47	CTCF	chr6:102326900-102327050	AG04449	skin:	n/a	n/a
48	E2F4	chr6:102333344-102333467	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr6:102325634-102325947	MCF10A-Er-Src	breast:	n/a	n/a
50	E2F4	chr6:102332181-102332519	MCF10A-Er-Src	breast:	n/a	chr6:102332365-102332374

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:102326919-102326969	H1-hESC	embryonic stem cell:	embryo
2	chr6:102326919-102326969	GM12891	blood:	n/a
3	chr6:102326919-102326969	HL-60	blood:	n/a
4	chr6:102326919-102326969	HepG2	liver:	n/a
5	chr6:102326919-102326969	HUVEC	blood vessel:	n/a
6	chr6:102326919-102326969	Caco-2	colon:	n/a
7	chr6:102326919-102326969	HNPCEpiC	eye:	n/a
8	chr6:102326919-102326969	NT2-D1	testis:	n/a
9	chr6:102326919-102326969	LNCaP	prostate:	n/a
10	chr6:102326919-102326969	PrEC	prostate:	n/a
11	chr6:102326919-102326969	AG09319	gingival:	n/a
12	chr6:102326919-102326969	GM19239	blood:	n/a
13	chr6:102326919-102326969	HCT-116	colon:	n/a
14	chr6:102326919-102326969	SKMC	muscle:	n/a
15	chr6:102326919-102326969	HRE	kidney:	n/a
16	chr6:102326919-102326969	IMR90	lung:	fetal
17	chr6:102326919-102326969	GM06990	blood:	n/a
18	chr6:102326919-102326969	HCM	heart:	n/a
19	chr6:102326919-102326969	MCF-7	breast:	n/a
20	chr6:102326919-102326969	Jurkat	blood:	n/a
21	chr6:102326919-102326969	BJ	skin:	n/a
22	chr6:102326919-102326969	AG09309	skin:	n/a
23	chr6:102326919-102326969	A549	lung:	n/a
24	chr6:102326919-102326969	HEK293	kidney:	embryo
25	chr6:102326919-102326969	HRPEpiC	eye:	n/a
26	chr6:102326919-102326969	HPAEpiC	pulmonary alveolar:	n/a
27	chr6:102326919-102326969	CMK	blood:	n/a
28	chr6:102326919-102326969	AoSMC	blood vessel:	n/a
29	chr6:102326919-102326969	AG04450	lung:	fetal
30	chr6:102326919-102326969	MCF10A-Er-Src	breast:	n/a
31	chr6:102326919-102326969	HRCEpiC	kidney:	n/a
32	chr6:102326919-102326969	HAEpiC	amniotic membrane:	n/a
33	chr6:102326919-102326969	ECC-1	luminal epithelium:	n/a
34	chr6:102326919-102326969	ovcar-3	ovarian:	n/a
35	chr6:102326919-102326969	GM12878	blood:	n/a
36	chr6:102326919-102326969	HMEC	breast:	n/a
37	chr6:102326919-102326969	AG04449	skin:	fetal
38	chr6:102326919-102326969	AG10803	skin:	n/a
39	chr6:102326919-102326969	NH-A	brain:	n/a
40	chr6:102326919-102326969	K562	blood:	n/a
41	chr6:102326919-102326969	HCPEpiC	choroid plexus:	n/a
42	chr6:102326919-102326969	PANC-1	pancreas:	n/a
43	chr6:102326919-102326969	BE2_C	brain:	n/a
44	chr6:102326919-102326969	ProgFib	skin:	n/a
45	chr6:102326919-102326969	SK-N-SH	brain:	n/a
46	chr6:102326919-102326969	SAEC	small airway:	n/a
47	chr6:102326919-102326969	GM12892	blood:	n/a
48	chr6:102326919-102326969	HCF	heart:	n/a
49	chr6:102326919-102326969	NHBE	bronchial:	n/a
50	chr6:102326919-102326969	NB4	blood:	n/a

(count:20 , 50 per page) page: 1

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

No data

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

Extended variants
information (count: 1320 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:1320 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372488359	chr6:102323823-102323824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs531136547	chr6:102323829-102323830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs78645512	chr6:102323853-102323854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567414324	chr6:102323854-102323855	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551998664	chr6:102323872-102323873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528062820	chr6:102323878-102323879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs545250019	chr6:102323882-102323883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs202203413	chr6:102323884-102323885	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs62419301	chr6:102323885-102323886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs184994256	chr6:102323887-102323888	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs386408076	chr6:102323894-102323895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs397729005	chr6:102323907-102323908	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs571427506	chr6:102323916-102323917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538894407	chr6:102323937-102323938	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs556849785	chr6:102323952-102323953	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs1610029	chr6:102323971-102323972	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs536091349	chr6:102324013-102324014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs555433720	chr6:102324025-102324026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs574113218	chr6:102324109-102324110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs541046072	chr6:102324130-102324131	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs553304393	chr6:102324135-102324136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1538792	chr6:102324137-102324138	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs189846932	chr6:102324138-102324139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs73761455	chr6:102324178-102324179	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs12660708	chr6:102324179-102324180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs73496632	chr6:102324211-102324212	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs543282109	chr6:102324314-102324315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs75200771	chr6:102324347-102324348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs368176541	chr6:102324359-102324360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138440119	chr6:102324360-102324361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs77802114	chr6:102324361-102324362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs76162817	chr6:102324362-102324363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs2791841	chr6:102324363-102324364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs139588011	chr6:102324365-102324366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs200359260	chr6:102324367-102324368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs34929195	chr6:102324391-102324392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs34389808	chr6:102324393-102324394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs34014105	chr6:102324396-102324397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs374783154	chr6:102324406-102324407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs546397311	chr6:102324418-102324419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571185533	chr6:102324487-102324488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs554895585	chr6:102324519-102324520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs532017673	chr6:102324568-102324569	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs371753369	chr6:102324639-102324640	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs550460707	chr6:102324641-102324642	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs553684641	chr6:102324724-102324725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs1610028	chr6:102324791-102324792	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs146619405	chr6:102324801-102324802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs73496635	chr6:102324809-102324810	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs550806382	chr6:102324862-102324863	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:110)

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
Cancer	20164919	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:102323800-102324800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
2	chr6:102323800-102325200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr6:102324200-102324800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:102324200-102324800	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr6:102324400-102324600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr6:102324400-102324800	Enhancers	Brain Germinal Matrix	brain
7	chr6:102326200-102327000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:102326600-102327000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr6:102326600-102327000	Enhancers	Fetal Heart	heart
10	chr6:102326600-102327200	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr6:102326600-102327200	Active TSS	Ovary	ovary
12	chr6:102327000-102327200	Enhancers	iPS-15b Cell Line	embryonic stem cell
13	chr6:102327000-102327400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:102327000-102331600	Weak transcription	Fetal Heart	heart
15	chr6:102327200-102327600	Enhancers	GM12878-XiMat	blood
16	chr6:102327200-102331400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr6:102327400-102327800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr6:102327400-102327800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
19	chr6:102327400-102328200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr6:102327800-102328000	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr6:102327800-102328600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr6:102331400-102332000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr6:102331400-102332000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr6:102331400-102332000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr6:102331400-102333200	Enhancers	Muscle Satellite Cultured Cells	--
26	chr6:102331600-102332000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr6:102331600-102332400	Enhancers	Fetal Heart	heart
28	chr6:102332000-102333000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
29	chr6:102333000-102333200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr6:102335400-102335800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr6:102340000-102340400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr6:102345600-102346800	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr6:102354600-102355600	Enhancers	Liver	Liver
34	chr6:102355200-102356000	Enhancers	HepG2	liver
35	chr6:102355600-102356000	Flanking Active TSS	Liver	Liver
36	chr6:102358600-102359000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
37	chr6:102358800-102360800	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr6:102359000-102360000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
39	chr6:102360000-102360600	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
40	chr6:102360200-102360600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr6:102360200-102360600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr6:102360200-102360600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr6:102360200-102360600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr6:102360600-102360800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr6:102370600-102370800	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:102371000-102372400	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr6:102372400-102372800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr6:102374600-102374800	Enhancers	Liver	Liver
49	chr6:102376600-102377200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr6:102377200-102379200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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