Variant report

Variant	nsv604822
Chromosome Location	chr6:144968195-145001887
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:379)
CpG islands
(count:244)
Chromatin interactive
region (count:9)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:379 , 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	ARID3A	chr6:144982114-144982792	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:144974899-144975568	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:144969210-144970558	HepG2	liver:	n/a	n/a
4	ATF1	chr6:144968557-144968918	K562	blood:	n/a	n/a
5	BATF	chr6:144975329-144975766	GM12878	blood:	n/a	n/a
6	BATF	chr6:144996564-144996764	GM12878	blood:	n/a	n/a
7	BATF	chr6:144975030-144975313	GM12878	blood:	n/a	n/a
8	BATF	chr6:144975476-144975752	GM12878	blood:	n/a	n/a
9	BATF	chr6:144996565-144996787	GM12878	blood:	n/a	n/a
10	BATF	chr6:144975027-144975301	GM12878	blood:	n/a	n/a
11	BCL11A	chr6:144979031-144979298	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr6:144975387-144975699	GM12878	blood:	n/a	n/a
13	BCL3	chr6:144969306-144969888	A549	lung:	n/a	n/a
14	BCLAF1	chr6:144975068-144975808	GM12878	blood:	n/a	n/a
15	BHLHE40	chr6:144975028-144975698	GM12878	blood:	n/a	n/a
16	BRCA1	chr6:144975416-144975591	GM12878	blood:	n/a	n/a
17	CBX3	chr6:144994877-144995342	HCT-116	colon:	n/a	n/a
18	CBX3	chr6:144995045-144995319	K562	blood:	n/a	n/a
19	CEBPB	chr6:144969301-144969883	A549	lung:	n/a	n/a
20	CEBPB	chr6:144976577-144976809	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:144999878-145000247	IMR90	lung:	n/a	chr6:145000045-145000056
22	CEBPB	chr6:144999901-145000210	A549	lung:	n/a	chr6:145000045-145000056
23	CEBPB	chr6:144999866-145000220	HepG2	liver:	n/a	chr6:145000045-145000056
24	CEBPB	chr6:144968595-144968890	K562	blood:	n/a	n/a
25	CEBPB	chr6:144969109-144969794	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:144969381-144969791	A549	lung:	n/a	n/a
27	CEBPB	chr6:144982203-144982670	HepG2	liver:	n/a	chr6:144982623-144982635
28	CEBPB	chr6:144969359-144969689	HepG2	liver:	n/a	n/a
29	CHD2	chr6:144975073-144975589	GM12878	blood:	n/a	n/a
30	CREB1	chr6:144968536-144968960	K562	blood:	n/a	n/a
31	CTCF	chr6:144982460-144982610	AG04449	skin:	n/a	n/a
32	CTCF	chr6:144969506-144969724	K562	blood:	n/a	chr6:144969626-144969647
33	CTCF	chr6:144969611-144969636	GM10248	blood:	n/a	n/a
34	CTCF	chr6:144969520-144969670	HCPEpiC	choroid plexus:	n/a	chr6:144969626-144969647
35	CTCF	chr6:144969620-144969770	HRPEpiC	eye:	n/a	chr6:144969626-144969647
36	CTCF	chr6:144982380-144982530	AG04450	lung:	n/a	n/a
37	CTCF	chr6:144982400-144982550	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr6:144969580-144969730	AG09309	skin:	n/a	chr6:144969626-144969647
39	CTCF	chr6:144969420-144969690	HEEpiC	esophagus:	n/a	chr6:144969626-144969647
40	CTCF	chr6:144982440-144982590	NHEK	skin:	n/a	n/a
41	CTCF	chr6:144969564-144969681	LNCaP	prostate:	n/a	chr6:144969626-144969647
42	CTCF	chr6:144982440-144982590	Caco-2	colon:	n/a	n/a
43	CTCF	chr6:144969566-144969687	Pancreas_OC	pancreas:	n/a	chr6:144969626-144969647
44	CTCF	chr6:144969480-144969630	AG09319	gingival:	n/a	n/a
45	CTCF	chr6:144969560-144969710	HCFaa	heart:	n/a	chr6:144969626-144969647
46	CTCF	chr6:144969587-144969664	LNCaP	prostate:	n/a	chr6:144969626-144969647
47	CTCF	chr6:144969453-144969913	MCF-7	breast:	n/a	chr6:144969626-144969647
48	CTCF	chr6:144969680-144969830	HMEC	breast:	n/a	n/a
49	CTCF	chr6:144969500-144969650	HepG2	liver:	n/a	chr6:144969626-144969647
50	CTCF	chr6:144969460-144969610	HMEC	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:144968338-144968388	HAEpiC	amniotic membrane:	n/a
2	chr6:144980804-144980854	SKMC	muscle:	n/a
3	chr6:144980804-144980854	Caco-2	colon:	n/a
4	chr6:144982324-144982374	HepG2	liver:	n/a
5	chr6:144980804-144980854	HRE	kidney:	n/a
6	chr6:144980804-144980854	A549	lung:	n/a
7	chr6:144982324-144982374	PrEC	prostate:	n/a
8	chr6:144976500-144976550	Caco-2	colon:	n/a
9	chr6:144976500-144976550	ProgFib	skin:	n/a
10	chr6:144982324-144982374	HRPEpiC	eye:	n/a
11	chr6:144968338-144968388	Hepatocyte	liver:	n/a
12	chr6:144982324-144982374	AoSMC	blood vessel:	n/a
13	chr6:144982324-144982374	HIPEpiC	eye:	n/a
14	chr6:144968338-144968388	NH-A	brain:	n/a
15	chr6:144968338-144968388	AG09309	skin:	n/a
16	chr6:144982324-144982374	NH-A	brain:	n/a
17	chr6:144982324-144982374	MCF-7	breast:	n/a
18	chr6:144982324-144982374	ProgFib	skin:	n/a
19	chr6:144982324-144982374	ovcar-3	ovarian:	n/a
20	chr6:144976500-144976550	IMR90	lung:	fetal
21	chr6:144980804-144980854	AG10803	skin:	n/a
22	chr6:144976500-144976550	HIPEpiC	eye:	n/a
23	chr6:144980804-144980854	Hela-S3	cervix:	n/a
24	chr6:144976500-144976550	GM19239	blood:	n/a
25	chr6:144976500-144976550	SK-N-SH_RA	brain:	n/a
26	chr6:144982324-144982374	GM12892	blood:	n/a
27	chr6:144968338-144968388	LNCaP	prostate:	n/a
28	chr6:144980804-144980854	GM06990	blood:	n/a
29	chr6:144968338-144968388	NHBE	bronchial:	n/a
30	chr6:144980804-144980854	NHBE	bronchial:	n/a
31	chr6:144968338-144968388	GM12891	blood:	n/a
32	chr6:144968338-144968388	HRCEpiC	kidney:	n/a
33	chr6:144980804-144980854	LNCaP	prostate:	n/a
34	chr6:144982324-144982374	AG10803	skin:	n/a
35	chr6:144982324-144982374	H1-hESC	embryonic stem cell:	embryo
36	chr6:144976500-144976550	HNPCEpiC	eye:	n/a
37	chr6:144982324-144982374	GM12891	blood:	n/a
38	chr6:144976500-144976550	ovcar-3	ovarian:	n/a
39	chr6:144982324-144982374	NB4	blood:	n/a
40	chr6:144968338-144968388	PANC-1	pancreas:	n/a
41	chr6:144968338-144968388	ProgFib	skin:	n/a
42	chr6:144982324-144982374	Jurkat	blood:	n/a
43	chr6:144980804-144980854	HRCEpiC	kidney:	n/a
44	chr6:144980804-144980854	NH-A	brain:	n/a
45	chr6:144982324-144982374	ECC-1	luminal epithelium:	n/a
46	chr6:144976500-144976550	HCT-116	colon:	n/a
47	chr6:144980804-144980854	NB4	blood:	n/a
48	chr6:144982324-144982374	MCF10A-Er-Src	breast:	n/a
49	chr6:144980804-144980854	BJ	skin:	n/a
50	chr6:144976500-144976550	U87	brain:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:144983668..144985899-chr6:144987093..144989829,3	K562	blood:
2	chr6:144971392..144973828-chr6:144974911..144976890,2	MCF-7	breast:
3	chr6:144968706..144970963-chr6:144974805..144976323,2	MCF-7	breast:
4	chr6:144975553..144978023-chr6:144984205..144986983,2	K562	blood:
5	chr6:144971392..144973828-chr6:144974911..144976890,2	MCF-7	breast:
6	chr6:144975553..144978023-chr6:144984205..144986983,2	K562	blood:
7	chr6:144968706..144970963-chr6:144974805..144976323,2	MCF-7	breast:
8	chr6:144983668..144985899-chr6:144987093..144989829,3	K562	blood:
9	chr6:144966548..144968116-chr6:144970160..144972090,2	K562	blood:

No data

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

Extended variants
information (count: 1187 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:1187 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7753246	chr6:144968195-144968196	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs531892554	chr6:144968209-144968210	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs200281910	chr6:144968210-144968211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543662445	chr6:144968218-144968219	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs564985244	chr6:144968225-144968226	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs572693839	chr6:144968244-144968245	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs532363461	chr6:144968258-144968259	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs547906691	chr6:144968270-144968271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs559569595	chr6:144968332-144968333	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188931230	chr6:144968482-144968483	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs192597098	chr6:144968529-144968530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs116394498	chr6:144968570-144968571	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs553259288	chr6:144968611-144968612	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs79430932	chr6:144968619-144968620	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552494296	chr6:144968628-144968629	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs139038802	chr6:144968646-144968647	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566783109	chr6:144968687-144968688	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs534580889	chr6:144968745-144968746	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs73778363	chr6:144968781-144968782	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs184470637	chr6:144968866-144968867	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs535434008	chr6:144968928-144968929	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs189231178	chr6:144968934-144968935	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs149870466	chr6:144968964-144968965	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs576227346	chr6:144968974-144968975	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs543747539	chr6:144968993-144968994	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs545702187	chr6:144968996-144968997	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs576853483	chr6:144969020-144969021	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs73778364	chr6:144969125-144969126	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs372735023	chr6:144969172-144969173	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs559665302	chr6:144969173-144969174	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs114005436	chr6:144969248-144969249	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs535187947	chr6:144969297-144969298	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs542259284	chr6:144969354-144969355	Enhancers Weak transcription Strong transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs80164193	chr6:144969412-144969413	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs114446475	chr6:144969426-144969427	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs552532775	chr6:144969444-144969445	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs2204658	chr6:144969503-144969504	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs529354907	chr6:144969524-144969525	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs570783827	chr6:144969528-144969529	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs528355622	chr6:144969551-144969552	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs575278425	chr6:144969574-144969575	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs568005454	chr6:144969575-144969576	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs558284834	chr6:144969691-144969692	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs191766722	chr6:144969714-144969715	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs557854279	chr6:144969756-144969757	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs569952296	chr6:144969793-144969794	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs537228325	chr6:144969814-144969815	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs565096372	chr6:144969833-144969834	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs184690452	chr6:144969845-144969846	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs34380258	chr6:144969912-144969913	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:78)

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
Autism	22495311	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
Melanoma	18172304	CNVD
Cancer	21637783	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
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	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
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Breast cancer	17603634	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1105 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:144930600-144973000	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chr6:144947000-144969200	Weak transcription	Fetal Kidney	kidney
3	chr6:144948400-144973600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
4	chr6:144949200-144980200	Weak transcription	Fetal Thymus	thymus
5	chr6:144950200-144973600	Weak transcription	Primary T helper cells fromperipheralblood	blood
6	chr6:144951000-144974800	Weak transcription	Primary B cells from cord blood	blood
7	chr6:144951200-144974800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
8	chr6:144951600-144975000	Weak transcription	Primary T cells from cord blood	blood
9	chr6:144951800-144977600	Weak transcription	Dnd41	blood
10	chr6:144952600-144974600	Weak transcription	Primary B cells from peripheral blood	blood
11	chr6:144959600-144969200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr6:144959600-144974800	Weak transcription	Stomach Mucosa	stomach
13	chr6:144961200-144969000	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr6:144961200-144970600	Weak transcription	Psoas Muscle	Psoas
15	chr6:144961400-144969400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
16	chr6:144961400-144978600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr6:144962800-144973200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
18	chr6:144962800-144975000	Weak transcription	Fetal Lung	lung
19	chr6:144962800-144980200	Weak transcription	Ovary	ovary
20	chr6:144963000-144973200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
21	chr6:144964400-144970800	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr6:144964800-144970800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr6:144965000-144968800	Enhancers	HepG2	liver
24	chr6:144965000-144970600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr6:144965000-144970600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr6:144965000-144970600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
27	chr6:144965400-144974200	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
28	chr6:144965600-144982400	Weak transcription	HSMM	muscle
29	chr6:144965800-144970200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr6:144966000-144968200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr6:144966200-144969200	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr6:144966200-144970200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
33	chr6:144967000-144978600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
34	chr6:144967200-144968600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr6:144967200-144982000	Weak transcription	HSMMtube	muscle
36	chr6:144967400-144968200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
37	chr6:144967400-144968200	Enhancers	Cortex derived primary cultured neurospheres	brain
38	chr6:144967400-144968200	Enhancers	Brain Germinal Matrix	brain
39	chr6:144967400-144969600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
40	chr6:144967400-144970800	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr6:144967800-144968200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr6:144967800-144968200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr6:144967800-144980400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr6:144968000-144968600	Weak transcription	Pancreatic Islets	Pancreatic Islet
45	chr6:144968000-144969200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr6:144968000-144969200	Enhancers	Liver	Liver
47	chr6:144968200-144970200	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr6:144968200-144970400	Enhancers	H1 Cell Line	embryonic stem cell
49	chr6:144968200-144970600	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chr6:144968200-144970800	Enhancers	HUES48 Cell Line	embryonic stem cell

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