Variant report

Variant	nsv1030539
Chromosome Location	chr6:153849956-154044445
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:713)
CpG islands
(count:62)
Chromatin interactive
region (count:15)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:713 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr6:153905881-153906041	K562	blood:	n/a	n/a
2	ATF1	chr6:153957237-153957391	K562	blood:	n/a	n/a
3	BACH1	chr6:153879499-153879587	K562	blood:	n/a	n/a
4	BACH1	chr6:153976662-153976923	H1-hESC	embryonic stem cell:	n/a	chr6:153976823-153976837
5	BATF	chr6:153930775-153930928	GM12878	blood:	n/a	n/a
6	BHLHE40	chr6:153990255-153990488	HepG2	liver:	n/a	n/a
7	CBX3	chr6:154026621-154026824	K562	blood:	n/a	n/a
8	CBX3	chr6:153930777-153930967	K562	blood:	n/a	n/a
9	CBX3	chr6:153930763-153930942	K562	blood:	n/a	n/a
10	CCNT2	chr6:153928717-153928846	K562	blood:	n/a	n/a
11	CCNT2	chr6:153916244-153916502	K562	blood:	n/a	n/a
12	CCNT2	chr6:153910179-153910456	K562	blood:	n/a	n/a
13	CEBPB	chr6:153993548-153993887	HepG2	liver:	n/a	chr6:153993697-153993708
14	CEBPB	chr6:153994368-153994699	A549	lung:	n/a	chr6:153994510-153994521
15	CEBPB	chr6:153955715-153955909	A549	lung:	n/a	n/a
16	CEBPB	chr6:153966477-153966828	H1-hESC	embryonic stem cell:	n/a	chr6:153966658-153966669
17	CEBPB	chr6:153994358-153994666	K562	blood:	n/a	chr6:153994510-153994521
18	CEBPB	chr6:153966570-153966812	K562	blood:	n/a	chr6:153966658-153966669
19	CEBPB	chr6:153994370-153994639	H1-hESC	embryonic stem cell:	n/a	chr6:153994510-153994521
20	CEBPB	chr6:153965246-153965589	HepG2	liver:	n/a	chr6:153965408-153965419
21	CEBPB	chr6:153905348-153905588	HepG2	liver:	n/a	n/a
22	CEBPB	chr6:153965332-153965486	A549	lung:	n/a	chr6:153965408-153965419
23	CEBPB	chr6:153994343-153994697	HepG2	liver:	n/a	chr6:153994510-153994521
24	CEBPB	chr6:153977509-153977801	HepG2	liver:	n/a	chr6:153977784-153977795
25	CEBPB	chr6:154032998-154033287	HepG2	liver:	n/a	chr6:154033160-154033171
26	CEBPB	chr6:153965243-153965559	IMR90	lung:	n/a	chr6:153965408-153965419
27	CEBPB	chr6:153917192-153917392	A549	lung:	n/a	n/a
28	CEBPB	chr6:153977557-153977760	A549	lung:	n/a	n/a
29	CEBPB	chr6:153954472-153954733	HepG2	liver:	n/a	chr6:153954629-153954640 chr6:153954675-153954687
30	CEBPB	chr6:153877071-153877217	A549	lung:	n/a	chr6:153877136-153877147 chr6:153877136-153877145
31	CEBPB	chr6:153966477-153966817	A549	lung:	n/a	chr6:153966658-153966669
32	CEBPB	chr6:153966497-153966840	IMR90	lung:	n/a	chr6:153966658-153966669
33	CEBPB	chr6:153901156-153901336	HepG2	liver:	n/a	n/a
34	CEBPB	chr6:153917146-153917387	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr6:154033048-154033292	IMR90	lung:	n/a	chr6:154033160-154033171
36	CEBPB	chr6:153966471-153966836	HepG2	liver:	n/a	chr6:153966658-153966669
37	CEBPB	chr6:153994366-153994679	IMR90	lung:	n/a	chr6:153994510-153994521
38	CEBPB	chr6:154033079-154033236	H1-hESC	embryonic stem cell:	n/a	chr6:154033160-154033171
39	CEBPB	chr6:153965249-153965510	K562	blood:	n/a	chr6:153965408-153965419
40	CEBPB	chr6:153876984-153877376	HepG2	liver:	n/a	chr6:153877136-153877147 chr6:153877136-153877145
41	CHD1	chr6:153915650-153915664	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr6:153884152-153884438	HepG2	liver:	n/a	n/a
43	CHD2	chr6:153884131-153884474	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr6:153874900-153875050	GM12869	blood:	n/a	n/a
45	CTCF	chr6:153984200-153984350	HCPEpiC	choroid plexus:	n/a	chr6:153984288-153984306 chr6:153984283-153984304
46	CTCF	chr6:153874902-153875104	ProgFib	skin:	n/a	n/a
47	CTCF	chr6:153884260-153884410	HCT-116	colon:	n/a	n/a
48	CTCF	chr6:153884240-153884390	HepG2	liver:	n/a	n/a
49	CTCF	chr6:153874880-153875030	K562	blood:	n/a	n/a
50	CTCF	chr6:153874920-153875070	HAc	cerebellar:	n/a	n/a

(count:62 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:153938192-153938242	U87	brain:	n/a
2	chr6:153938192-153938242	U87	brain:	n/a
3	chr6:153938192-153938242	PFSK-1	brain:	n/a
4	chr6:153938192-153938242	MCF10A-Er-Src	breast:	n/a
5	chr6:153938192-153938242	HEK293	kidney:	embryo
6	chr6:153938192-153938242	Hela-S3	cervix:	n/a
7	chr6:153938192-153938242	Hepatocyte	liver:	n/a
8	chr6:153938192-153938242	CMK	blood:	n/a
9	chr6:153938192-153938242	SK-N-MC	brain:	n/a
10	chr6:153938192-153938242	HL-60	blood:	n/a
11	chr6:153938192-153938242	PrEC	prostate:	n/a
12	chr6:153938192-153938242	ECC-1	luminal epithelium:	n/a
13	chr6:153938192-153938242	GM19239	blood:	n/a
14	chr6:153938192-153938242	BE2_C	brain:	n/a
15	chr6:153938192-153938242	HPAEpiC	pulmonary alveolar:	n/a
16	chr6:153938192-153938242	A549	lung:	n/a
17	chr6:153938192-153938242	HCPEpiC	choroid plexus:	n/a
18	chr6:153938192-153938242	HRE	kidney:	n/a
19	chr6:153938192-153938242	BJ	skin:	n/a
20	chr6:153938192-153938242	MCF-7	breast:	n/a
21	chr6:153938192-153938242	HUVEC	blood vessel:	n/a
22	chr6:153938192-153938242	SAEC	small airway:	n/a
23	chr6:153938192-153938242	AG09309	skin:	n/a
24	chr6:153938192-153938242	HAEpiC	amniotic membrane:	n/a
25	chr6:153938192-153938242	HepG2	liver:	n/a
26	chr6:153938192-153938242	AG10803	skin:	n/a
27	chr6:153938192-153938242	NT2-D1	testis:	n/a
28	chr6:153938192-153938242	HCT-116	colon:	n/a
29	chr6:153938192-153938242	LNCaP	prostate:	n/a
30	chr6:153938192-153938242	NHDF-neo	bronchial:	n/a
31	chr6:153938192-153938242	NH-A	brain:	n/a
32	chr6:153938192-153938242	GM12892	blood:	n/a
33	chr6:153938192-153938242	SK-N-SH	brain:	n/a
34	chr6:153938192-153938242	GM06990	blood:	n/a
35	chr6:153938192-153938242	HRPEpiC	eye:	n/a
36	chr6:153938192-153938242	AoSMC	blood vessel:	n/a
37	chr6:153938192-153938242	Caco-2	colon:	n/a
38	chr6:153938192-153938242	PANC-1	pancreas:	n/a
39	chr6:153938192-153938242	HRCEpiC	kidney:	n/a
40	chr6:153938192-153938242	HMEC	breast:	n/a
41	chr6:153938192-153938242	NB4	blood:	n/a
42	chr6:153938192-153938242	AG09319	gingival:	n/a
43	chr6:153938192-153938242	Jurkat	blood:	n/a
44	chr6:153938192-153938242	HCF	heart:	n/a
45	chr6:153938192-153938242	HEEpiC	esophagus:	n/a
46	chr6:153938192-153938242	HNPCEpiC	eye:	n/a
47	chr6:153938192-153938242	ovcar-3	ovarian:	n/a
48	chr6:153938192-153938242	SKMC	muscle:	n/a
49	chr6:153938192-153938242	NHBE	bronchial:	n/a
50	chr6:153938192-153938242	RPTEC	kidney:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:153877632..153879379-chr6:153880129..153881781,2	K562	blood:
2	chr6:153803007..153804639-chr6:153864655..153867623,2	K562	blood:
3	chr6:153974470..153975994-chr6:153980413..153982287,2	K562	blood:
4	chr6:153957358..153959044-chr6:153959696..153961775,2	MCF-7	breast:
5	chr16:30564268..30564883-chr6:153979585..153980484,2	MCF-7	breast:
6	chr6:153957358..153959044-chr6:153959696..153961775,2	MCF-7	breast:
7	chr6:153974470..153975994-chr6:153980413..153982287,2	K562	blood:
8	chr6:153551779..153552872-chr6:153874689..153875516,4	MCF-7	breast:
9	chr6:153858319..153861041-chr6:153861487..153863317,2	K562	blood:
10	chr6:153858319..153861041-chr6:153861487..153863317,2	K562	blood:
11	chr6:153955865..153957510-chr6:153961881..153963802,2	K562	blood:
12	chr6:153916840..153919030-chr6:153923609..153925708,2	K562	blood:
13	chr6:153916840..153919030-chr6:153923609..153925708,2	K562	blood:
14	chr6:153955865..153957510-chr6:153961881..153963802,2	K562	blood:
15	chr6:153877632..153879379-chr6:153880129..153881781,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL590867.1-2	chr6:153860947-153861008	XLOC_005508
2	lnc-AL590867.1-6	chr6:153987601-153987801	NONHSAT115624
3	lnc-AL590867.1-2	chr6:153861937-153862090	XLOC_005508

No data

Variant related genes	Relation type
ENSG00000220514	TF binding region
ENSG00000217160	TF binding region
ENSG00000242246	TF binding region
MTND4P13	TF binding region
ENSG00000217044	TF binding region
RNU6-896P	TF binding region
ENSG00000218776	TF binding region
ENSG00000220733	TF binding region
ENSG00000220514	CpG island
ENSG00000217160	CpG island
ENSG00000242246	CpG island
MTND4P13	CpG island
ENSG00000217044	CpG island
RNU6-896P	CpG island
ENSG00000218776	CpG island
ENSG00000220733	CpG island
ENSG00000213121	chromatin interactions

Extended variants
information (count: 2768 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:2768 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs529484898	chr6:153858233-153858234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs144231728	chr6:153858244-153858245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs180866482	chr6:153858251-153858252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556110818	chr6:153858256-153858257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573361422	chr6:153858263-153858264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs727754	chr6:153858284-153858285	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs565471878	chr6:153858306-153858307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs148753797	chr6:153858318-153858319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs545106080	chr6:153858326-153858327	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs1674726	chr6:153858614-153858615	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs142303358	chr6:153858624-153858625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs374441403	chr6:153858637-153858638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189151812	chr6:153858693-153858694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs554665176	chr6:153858712-153858713	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1781924	chr6:153858738-153858739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs12208691	chr6:153858863-153858864	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs572459050	chr6:153858922-153858923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559225189	chr6:153858968-153858969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs181946880	chr6:153858995-153858996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185721941	chr6:153859008-153859009	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188867916	chr6:153859018-153859019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs563329535	chr6:153859019-153859020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs1321301	chr6:153859024-153859025	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs542652443	chr6:153859041-153859042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35397960	chr6:153859063-153859064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs557268389	chr6:153859085-153859086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs57617449	chr6:153859092-153859093	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs546556717	chr6:153859198-153859199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs76290871	chr6:153859224-153859225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs532135779	chr6:153859228-153859229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs200554514	chr6:153859241-153859242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs201833702	chr6:153859244-153859245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564131284	chr6:153859260-153859261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569057784	chr6:153859263-153859264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs536341299	chr6:153859304-153859305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs1321302	chr6:153859316-153859317	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs186534483	chr6:153859321-153859322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs534532885	chr6:153859352-153859353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs559257623	chr6:153859373-153859374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs1321303	chr6:153859374-153859375	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs191342313	chr6:153859388-153859389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs618396	chr6:153859410-153859411	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs114493936	chr6:153859447-153859448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs542341588	chr6:153859463-153859464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560967336	chr6:153859511-153859512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs182641329	chr6:153859552-153859553	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs543187712	chr6:153859603-153859604	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564792237	chr6:153859623-153859624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370262560	chr6:153859629-153859630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532269841	chr6:153859642-153859643	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
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
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	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
Lung cancer	18438408	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17850661	CNVD
Renal cell carcinoma	18765545	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Breast cancer	20556506	CNVD
Hirschsprung''s Disease	21712996	CNVD
Testicular germ cell tumor	18059402	CNVD
Developmental delay	21147756	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Developmental delay	19459884	CNVD
Hearing loss	19459884	CNVD
Microcephaly	19459884	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:189 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:153858200-153858400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr6:153858600-153859400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
3	chr6:153859400-153859600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr6:153859400-153861800	Enhancers	Dnd41	blood
5	chr6:153859600-153860000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
6	chr6:153859600-153860200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr6:153860400-153860600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr6:153860600-153861400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr6:153860600-153861600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr6:153882800-153883600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr6:153883600-153885000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr6:153884200-153884400	Enhancers	Aorta	Aorta
13	chr6:153884400-153885200	Weak transcription	Aorta	Aorta
14	chr6:153885000-153886400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr6:153885200-153886200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:153885200-153886200	Enhancers	Aorta	Aorta
17	chr6:153885200-153886800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr6:153885800-153886200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
19	chr6:153885800-153886200	Enhancers	Adipose Nuclei	Adipose
20	chr6:153885800-153886200	Enhancers	Lung	lung
21	chr6:153885800-153886200	Enhancers	Right Atrium	heart
22	chr6:153886200-153889000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:153886800-153889800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:153889000-153890000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:153889200-153890000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr6:153889800-153890400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr6:153890000-153890400	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr6:153890000-153890600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr6:153890400-153891000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr6:153892400-153894800	Enhancers	Fetal Lung	lung
31	chr6:153894800-153895200	Weak transcription	Fetal Lung	lung
32	chr6:153895200-153897200	Enhancers	Fetal Lung	lung
33	chr6:153897200-153900600	Weak transcription	Fetal Lung	lung
34	chr6:153900600-153901000	ZNF genes & repeats	Fetal Lung	lung
35	chr6:153901000-153904400	Weak transcription	Fetal Lung	lung
36	chr6:153903200-153903400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr6:153904400-153904600	Enhancers	Fetal Lung	lung
38	chr6:153904600-153911600	Weak transcription	Fetal Lung	lung
39	chr6:153909600-153909800	Enhancers	Brain Germinal Matrix	brain
40	chr6:153910400-153910600	Enhancers	Fetal Brain Male	brain
41	chr6:153911200-153912000	Enhancers	Dnd41	blood
42	chr6:153911600-153911800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:153911600-153911800	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr6:153911600-153912200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr6:153911600-153912400	Enhancers	Pancreatic Islets	Pancreatic Islet
46	chr6:153911600-153912800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chr6:153911600-153913400	Enhancers	Fetal Lung	lung
48	chr6:153911800-153912000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr6:153912000-153912200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr6:153912000-153912400	Flanking Active TSS	Dnd41	blood

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