Variant report

Variant	nsv5511
Chromosome Location	chr6:142550032-142594960
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:407)
CpG islands
(count:61)
Chromatin interactive
region (count:19)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:407 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:142580710-142581132	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:142553588-142554010	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:142586129-142587104	HepG2	liver:	n/a	n/a
4	ATF2	chr6:142567969-142568499	GM12878	blood:	n/a	n/a
5	BATF	chr6:142568055-142568444	GM12878	blood:	n/a	chr6:142568413-142568422
6	BATF	chr6:142568079-142568394	GM12878	blood:	n/a	n/a
7	BCL11A	chr6:142568120-142568402	GM12878	blood:	n/a	n/a
8	BHLHE40	chr6:142580727-142581056	HepG2	liver:	n/a	n/a
9	BHLHE40	chr6:142553614-142553906	HepG2	liver:	n/a	n/a
10	BHLHE40	chr6:142568081-142568503	GM12878	blood:	n/a	chr6:142568304-142568325
11	BRCA1	chr6:142553765-142553803	HepG2	liver:	n/a	n/a
12	BRCA1	chr6:142580655-142580981	HepG2	liver:	n/a	n/a
13	CEBPB	chr6:142555105-142555450	HepG2	liver:	n/a	chr6:142555289-142555300
14	CEBPB	chr6:142555232-142555314	H1-hESC	embryonic stem cell:	n/a	chr6:142555289-142555300
15	CEBPB	chr6:142563396-142563844	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr6:142578560-142578793	IMR90	lung:	n/a	chr6:142578633-142578644 chr6:142578752-142578763
17	CEBPB	chr6:142580397-142581083	HepG2	liver:	n/a	n/a
18	CEBPB	chr6:142555127-142555468	IMR90	lung:	n/a	chr6:142555289-142555300
19	CEBPB	chr6:142555151-142555396	K562	blood:	n/a	chr6:142555289-142555300
20	CEBPB	chr6:142592667-142592963	IMR90	lung:	n/a	n/a
21	CEBPB	chr6:142555154-142555434	A549	lung:	n/a	chr6:142555289-142555300
22	CEBPB	chr6:142580911-142580958	K562	blood:	n/a	n/a
23	CEBPB	chr6:142570503-142570788	HepG2	liver:	n/a	chr6:142570659-142570670
24	CEBPB	chr6:142578486-142578746	K562	blood:	n/a	chr6:142578633-142578644
25	CEBPB	chr6:142580016-142581136	HepG2	liver:	n/a	n/a
26	CEBPB	chr6:142580809-142581035	HepG2	liver:	n/a	n/a
27	CEBPB	chr6:142570491-142570814	H1-hESC	embryonic stem cell:	n/a	chr6:142570659-142570670
28	CEBPB	chr6:142578498-142578934	HepG2	liver:	n/a	chr6:142578633-142578644 chr6:142578752-142578763
29	CEBPB	chr6:142594938-142595049	A549	lung:	n/a	n/a
30	CEBPB	chr6:142592662-142592894	HepG2	liver:	n/a	n/a
31	CEBPB	chr6:142580482-142581048	A549	lung:	n/a	n/a
32	CHD2	chr6:142580553-142581074	HepG2	liver:	n/a	n/a
33	CHD2	chr6:142553705-142553737	HepG2	liver:	n/a	n/a
34	CTCF	chr6:142553685-142553813	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr6:142553653-142553730	GM19239	blood:	n/a	n/a
36	CTCF	chr6:142553820-142553970	GM12866	blood:	n/a	n/a
37	CTCF	chr6:142553780-142553930	HEK293	kidney:	n/a	n/a
38	CTCF	chr6:142553632-142553793	GM12891	blood:	n/a	n/a
39	CTCF	chr6:142553780-142553930	GM12866	blood:	n/a	n/a
40	CTCF	chr6:142553560-142553710	GM12867	blood:	n/a	n/a
41	CTCF	chr6:142553760-142553910	MCF-7	breast:	n/a	n/a
42	CTCF	chr6:142553700-142553850	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr6:142553580-142553730	HAc	cerebellar:	n/a	n/a
44	CTCF	chr6:142553620-142553770	SAEC	small airway:	n/a	n/a
45	CTCF	chr6:142553554-142553994	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chr6:142553248-142554194	SK-N-SH	brain:	n/a	n/a
47	CTCF	chr6:142553635-142553935	ProgFib	skin:	n/a	n/a
48	CTCF	chr6:142553720-142553870	HMEC	breast:	n/a	n/a
49	CTCF	chr6:142553700-142553850	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr6:142553720-142553870	GM06990	blood:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:142564220-142564270	NH-A	brain:	n/a
2	chr6:142564220-142564270	AG04449	skin:	fetal
3	chr6:142564220-142564270	MCF10A-Er-Src	breast:	n/a
4	chr6:142564220-142564270	GM12891	blood:	n/a
5	chr6:142564220-142564270	NHDF-neo	bronchial:	n/a
6	chr6:142564220-142564270	ProgFib	skin:	n/a
7	chr6:142564220-142564270	HPAEpiC	pulmonary alveolar:	n/a
8	chr6:142564220-142564270	PANC-1	pancreas:	n/a
9	chr6:142564220-142564270	PrEC	prostate:	n/a
10	chr6:142564220-142564270	HMEC	breast:	n/a
11	chr6:142564220-142564270	A549	lung:	n/a
12	chr6:142564220-142564270	HRPEpiC	eye:	n/a
13	chr6:142564220-142564270	SK-N-SH_RA	brain:	n/a
14	chr6:142564220-142564270	SKMC	muscle:	n/a
15	chr6:142564220-142564270	HCF	heart:	n/a
16	chr6:142564220-142564270	BJ	skin:	n/a
17	chr6:142564220-142564270	GM12878	blood:	n/a
18	chr6:142564220-142564270	HAEpiC	amniotic membrane:	n/a
19	chr6:142564220-142564270	PFSK-1	brain:	n/a
20	chr6:142564220-142564270	HNPCEpiC	eye:	n/a
21	chr6:142564220-142564270	U87	brain:	n/a
22	chr6:142564220-142564270	CMK	blood:	n/a
23	chr6:142564220-142564270	HUVEC	blood vessel:	n/a
24	chr6:142564220-142564270	AG04450	lung:	fetal
25	chr6:142564220-142564270	GM12892	blood:	n/a
26	chr6:142564220-142564270	HRE	kidney:	n/a
27	chr6:142564220-142564270	AG09309	skin:	n/a
28	chr6:142564220-142564270	HEK293	kidney:	embryo
29	chr6:142564220-142564270	K562	blood:	n/a
30	chr6:142564220-142564270	HIPEpiC	eye:	n/a
31	chr6:142564220-142564270	Caco-2	colon:	n/a
32	chr6:142564220-142564270	AG10803	skin:	n/a
33	chr6:142564220-142564270	ovcar-3	ovarian:	n/a
34	chr6:142564220-142564270	NT2-D1	testis:	n/a
35	chr6:142564220-142564270	ECC-1	luminal epithelium:	n/a
36	chr6:142564220-142564270	LNCaP	prostate:	n/a
37	chr6:142564220-142564270	HL-60	blood:	n/a
38	chr6:142564220-142564270	AoSMC	blood vessel:	n/a
39	chr6:142564220-142564270	SK-N-SH	brain:	n/a
40	chr6:142564220-142564270	GM06990	blood:	n/a
41	chr6:142564220-142564270	T-47D	breast:	n/a
42	chr6:142564220-142564270	HCT-116	colon:	n/a
43	chr6:142564220-142564270	AG09319	gingival:	n/a
44	chr6:142564220-142564270	SK-N-MC	brain:	n/a
45	chr6:142564220-142564270	HCPEpiC	choroid plexus:	n/a
46	chr6:142564220-142564270	Hela-S3	cervix:	n/a
47	chr6:142564220-142564270	NB4	blood:	n/a
48	chr6:142564220-142564270	GM19239	blood:	n/a
49	chr6:142564220-142564270	H1-hESC	embryonic stem cell:	embryo
50	chr6:142564220-142564270	IMR90	lung:	fetal

(count:19 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:142563411..142566462-chr6:142568328..142570215,3	MCF-7	breast:
2	chr6:142563411..142566462-chr6:142568328..142570215,3	MCF-7	breast:
3	chr6:142557760..142559826-chr6:142622267..142624414,2	MCF-7	breast:
4	chr6:142561290..142563575-chr6:142573357..142576182,2	MCF-7	breast:
5	chr6:142561318..142563576-chr6:142567229..142569702,2	MCF-7	breast:
6	chr6:142556063..142558298-chr6:142562723..142565350,3	K562	blood:
7	chr6:142562845..142565583-chr6:142567403..142569792,2	K562	blood:
8	chr6:142587554..142589196-chr6:142590216..142591755,2	MCF-7	breast:
9	chr6:142556063..142558298-chr6:142562723..142565350,3	K562	blood:
10	chr20:52209145..52211139-chr6:142575953..142578356,2	MCF-7	breast:
11	chr6:142587554..142589196-chr6:142590216..142591755,2	MCF-7	breast:
12	chr6:142588662..142590596-chr6:142592333..142594565,2	K562	blood:
13	chr6:142588662..142590596-chr6:142592333..142594565,2	K562	blood:
14	chr6:142587570..142589234-chr6:142593481..142595662,2	MCF-7	breast:
15	chr6:142587570..142589234-chr6:142593481..142595662,2	MCF-7	breast:
16	chr6:142561290..142563575-chr6:142573357..142576182,2	MCF-7	breast:
17	chr6:142571556..142574295-chr6:142622597..142624940,2	MCF-7	breast:
18	chr6:142562845..142565583-chr6:142567403..142569792,2	K562	blood:
19	chr6:142561318..142563576-chr6:142567229..142569702,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NMBR-1	chr6:142580541-142580769	XLOC_005861
2	lnc-NMBR-1	chr6:142580541-142580872	NONHSAT115306
3	lnc-NMBR-1	chr6:142572984-142573103	XLOC_005861
4	lnc-NMBR-1	chr6:142567956-142567985	NONHSAT115306

No data

Variant related genes	Relation type
ENSG00000237494	TF binding region
ENSG00000266843	TF binding region
ENSG00000237494	CpG island
ENSG00000266843	CpG island
ENSG00000171940	chromatin interactions
ENSG00000112414	chromatin interactions

Extended variants
information (count: 1747 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1747 , 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	rs571440382	chr6:142550039-142550040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs538737538	chr6:142550044-142550045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs545297829	chr6:142550049-142550050	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs554184606	chr6:142550051-142550052	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs572358507	chr6:142550069-142550070	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs142707599	chr6:142550106-142550107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555396910	chr6:142550120-142550121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs573962733	chr6:142550133-142550134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372650302	chr6:142550134-142550135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569698840	chr6:142550135-142550136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146951160	chr6:142550138-142550139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562665086	chr6:142550141-142550142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs577861903	chr6:142550142-142550143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544778081	chr6:142550147-142550148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs180939420	chr6:142550191-142550192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs138058737	chr6:142550201-142550202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548934328	chr6:142550265-142550266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs561450162	chr6:142550314-142550315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs565296172	chr6:142550316-142550317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs531866759	chr6:142550323-142550324	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs143200221	chr6:142550337-142550338	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs186136498	chr6:142550401-142550402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs116892321	chr6:142550408-142550409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs538251575	chr6:142550419-142550420	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547591047	chr6:142550423-142550424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs566138128	chr6:142550441-142550442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs112321413	chr6:142550445-142550446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554935693	chr6:142550446-142550447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574026669	chr6:142550457-142550458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs538137291	chr6:142550485-142550486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs556452904	chr6:142550492-142550493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs139358766	chr6:142550530-142550531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs545151892	chr6:142550534-142550535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560010943	chr6:142550556-142550557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs572083343	chr6:142550568-142550569	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190938008	chr6:142550592-142550593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560535481	chr6:142550618-142550619	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372600499	chr6:142550620-142550621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs225720	chr6:142550630-142550631	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs115940008	chr6:142550650-142550651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs181405765	chr6:142550658-142550659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs144398549	chr6:142550659-142550660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs148713595	chr6:142550671-142550672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs185889395	chr6:142550672-142550673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs60805031	chr6:142550686-142550687	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs225721	chr6:142550703-142550704	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs548342628	chr6:142550707-142550708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs225722	chr6:142550709-142550710	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs537399291	chr6:142550715-142550716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556510083	chr6:142550733-142550734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
Gastric cancer	17908304	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
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
Breast cancer	21364760	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
Acute monocytic leukemia	16498392	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
craniofacial dysmorphism	21918468	CNVD
Burkitt''s lymphoma	19759907	CNVD
Breast cancer	22522925	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:142535200-142552800	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:142535800-142553400	Weak transcription	Thymus	Thymus
3	chr6:142536000-142552800	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
4	chr6:142541200-142552800	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr6:142541200-142553200	Weak transcription	Primary T cells fromperipheralblood	blood
6	chr6:142541200-142553400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
7	chr6:142541400-142552800	Weak transcription	HUES64 Cell Line	embryonic stem cell
8	chr6:142541800-142550600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr6:142541800-142553200	Weak transcription	HepG2	liver
10	chr6:142542400-142550400	Weak transcription	Primary B cells from cord blood	blood
11	chr6:142542800-142553600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr6:142548000-142553400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:142552800-142553400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
14	chr6:142552800-142553600	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr6:142552800-142553600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr6:142552800-142553600	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr6:142552800-142554000	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr6:142552800-142554200	Enhancers	H1 Cell Line	embryonic stem cell
19	chr6:142553200-142553400	Enhancers	Primary T cells fromperipheralblood	blood
20	chr6:142553200-142553400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr6:142553200-142553400	Enhancers	Fetal Thymus	thymus
22	chr6:142553200-142553400	Enhancers	HepG2	liver
23	chr6:142553200-142553600	Enhancers	Pancreas	Pancrea
24	chr6:142553200-142554800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
25	chr6:142553400-142553600	Enhancers	Primary B cells from cord blood	blood
26	chr6:142553400-142553600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
27	chr6:142553400-142553600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr6:142553400-142553600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr6:142553400-142553600	Flanking Active TSS	HepG2	liver
30	chr6:142553400-142553800	Active TSS	ES-I3 Cell Line	embryonic stem cell
31	chr6:142553400-142553800	Active TSS	Primary T cells from cord blood	blood
32	chr6:142553400-142553800	Enhancers	Fetal Intestine Small	intestine
33	chr6:142553400-142553800	Flanking Active TSS	Fetal Thymus	thymus
34	chr6:142553400-142554000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr6:142553400-142554000	Active TSS	Primary T helper naive cells fromperipheralblood	blood
36	chr6:142553400-142554000	Enhancers	Primary T helper cells fromperipheralblood	blood
37	chr6:142553400-142554000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
38	chr6:142553400-142554000	Enhancers	Fetal Intestine Large	intestine
39	chr6:142553400-142554200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
40	chr6:142553400-142554200	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr6:142553400-142554200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
42	chr6:142553600-142553800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr6:142553600-142553800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr6:142553600-142553800	Flanking Bivalent TSS/Enh	Primary T cells fromperipheralblood	blood
45	chr6:142553600-142553800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr6:142553600-142554000	Enhancers	Primary B cells from peripheral blood	blood
47	chr6:142553600-142554000	Active TSS	Primary T helper naive cells from peripheral blood	blood
48	chr6:142553600-142554000	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
49	chr6:142553600-142554000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr6:142553600-142554000	Enhancers	Fetal Muscle Trunk	muscle

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