Variant report

Variant	nsv533518
Chromosome Location	chr6:119712186-119998618
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:237)
LncRNA
region (count:40)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:237 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:119941629..119944103-chr6:119947152..119949648,3	MCF-7	breast:
2	chr6:119671918..119674788-chr6:119887253..119890815,3	K562	blood:
3	chr6:119767806..119768327-chr6:120289096..120289698,2	MCF-7	breast:
4	chr6:119877630..119879253-chr6:119896427..119898133,2	MCF-7	breast:
5	chr6:119847994..119850425-chr6:119853510..119855892,2	K562	blood:
6	chr6:119859295..119861022-chr6:119888141..119890185,2	K562	blood:
7	chr19:7548018..7548521-chr6:119989005..119989505,2	NB4	blood:
8	chr6:119929475..119932013-chr6:119937447..119940201,2	K562	blood:
9	chr6:119754671..119756379-chr6:119758564..119760913,2	K562	blood:
10	chr6:119942931..119945440-chr6:119949735..119951548,2	K562	blood:
11	chr6:119834976..119836723-chr6:119847440..119850148,2	K562	blood:
12	chr6:119949922..119952911-chr6:119994617..119997136,2	MCF-7	breast:
13	chr6:119887985..119889812-chr6:119892703..119894315,2	K562	blood:
14	chr6:119670586..119672922-chr6:119876709..119878662,2	MCF-7	breast:
15	chr6:119826693..119828704-chr6:119831138..119833641,2	K562	blood:
16	chr6:119888384..119890000-chr6:119898868..119901022,2	K562	blood:
17	chr6:119254596..119256652-chr6:119886468..119889040,2	K562	blood:
18	chr6:119930273..119931958-chr6:119933352..119935627,2	MCF-7	breast:
19	chr6:119936573..119939342-chr6:119940727..119942239,2	K562	blood:
20	chr6:58777220..58778210-chr6:119855510..119856349,2	MCF-7	breast:
21	chr6:119710272..119711806-chr6:119713612..119715669,2	K562	blood:
22	chr6:119871284..119874195-chr6:119885805..119888764,2	K562	blood:
23	chr6:119840170..119840723-chr8:442816..443696,2	MCF-7	breast:
24	chr6:119843554..119845445-chr6:119857020..119859893,3	K562	blood:
25	chr6:119772222..119774379-chr6:119780050..119782058,2	K562	blood:
26	chr6:119822678..119825294-chr6:119837894..119839723,2	MCF-7	breast:
27	chr6:119798609..119800243-chr6:119802774..119804740,2	K562	blood:
28	chr6:119819182..119822549-chr6:119824303..119826707,4	K562	blood:
29	chr6:119901984..119904533-chr6:119906505..119908924,3	K562	blood:
30	chr6:119893616..119895863-chr6:119897291..119899011,2	K562	blood:
31	chr6:119769489..119771005-chr6:119951026..119953518,2	MCF-7	breast:
32	chr6:119772222..119775042-chr6:119777092..119781550,4	K562	blood:
33	chr6:119904409..119907006-chr6:119913661..119916610,3	K562	blood:
34	chr6:119787516..119789829-chr6:119805762..119807377,2	MCF-7	breast:
35	chr6:119959081..119962140-chr6:119964515..119967197,3	K562	blood:
36	chr6:119976021..119977588-chr6:120002539..120005250,2	MCF-7	breast:
37	chr6:119949922..119952911-chr6:119994617..119997136,2	MCF-7	breast:
38	chr6:119959397..119961696-chr6:119965621..119967266,2	MCF-7	breast:
39	chr6:119847994..119850529-chr6:119852799..119855892,3	K562	blood:
40	chr6:119670600..119672144-chr6:119753052..119754839,2	MCF-7	breast:
41	chr6:119886557..119888360-chr6:119890485..119892590,2	K562	blood:
42	chr6:119857573..119859199-chr6:119859391..119862222,2	MCF-7	breast:
43	chr6:119845567..119847113-chr6:119965948..119967870,2	K562	blood:
44	chr6:119947059..119949590-chr6:119958918..119960859,2	K562	blood:
45	chr6:119886809..119890000-chr6:119899522..119901622,3	K562	blood:
46	chr6:119849420..119852024-chr6:119886180..119888675,2	K562	blood:
47	chr6:119800351..119802770-chr6:119806330..119807871,2	K562	blood:
48	chr6:119871284..119874195-chr6:119885805..119888764,2	K562	blood:
49	chr6:119932862..119934948-chr6:119935688..119940006,3	K562	blood:
50	chr6:119959751..119961414-chr6:119961596..119964388,2	K562	blood:

(count:40 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAN1A1-2	chr6:119835287-119835320	ucscGeneNc_uc003pyn_1
2	lnc-ASF1A-3	chr6:119870973-119871058	XLOC_005449
3	lnc-MAN1A1-1	chr6:119793588-119793621	NONHSAT114715
4	lnc-MAN1A1-1	chr6:119773712-119776358	NONHSAT114717
5	lnc-MAN1A1-1	chr6:119774358-119776358	XLOC_005819
6	lnc-MAN1A1-1	chr6:119790762-119790879	NONHSAT114717
7	lnc-MAN1A1-1	chr6:119790762-119790879	ENSG00000249211
8	lnc-MAN1A1-1	chr6:119800983-119801472	NONHSAT114715
9	lnc-MAN1A1-1	chr6:119713836-119713874	NONHSAT114715
10	lnc-MAN1A1-1	chr6:119776221-119776299	NONHSAT114715
11	lnc-ASF1A-2	chr6:119738759-119738843	XLOC_005448
12	lnc-MAN1A1-1	chr6:119793588-119793621	NONHSAT114717
13	lnc-ASF1A-3	chr6:119855070-119855105	XLOC_005449
14	lnc-MAN1A1-1	chr6:119777275-119777540	NONHSAT114717
15	lnc-ASF1A-7	chr6:119807968-119807976	NONHSAT114718
16	lnc-MAN1A1-1	chr6:119778083-119778349	ENSG00000249211
17	lnc-MAN1A1-1	chr6:119777275-119777540	XLOC_005819
18	lnc-MAN1A1-2	chr6:119819782-119820048	ucscGeneNc_uc003pyn_1
19	lnc-ASF1A-3	chr6:119871395-119871560	XLOC_005449
20	lnc-MAN1A1-1	chr6:119777275-119777540	ENSG00000249211
21	lnc-MAN1A1-1	chr6:119812331-119812467	NONHSAT114717
22	lnc-MAN1A1-1	chr6:119812331-119812467	XLOC_005819
23	lnc-MAN1A1-2	chr6:119816057-119818057	ucscGeneNc_uc003pyn_1
24	lnc-ASF1A-3	chr6:119855041-119855105	XLOC_005449
25	lnc-MAN1A1-1	chr6:119853468-119853925	NONHSAT114715
26	lnc-MAN1A1-1	chr6:119940963-119941477	NONHSAT114715
27	lnc-MAN1A1-1	chr6:119778083-119778349	NONHSAT114717
28	lnc-MAN1A1-2	chr6:119818974-119819239	ucscGeneNc_uc003pyn_1
29	lnc-ASF1A-3	chr6:119916051-119916089	XLOC_005449
30	lnc-MAN1A1-2	chr6:119832461-119832578	ucscGeneNc_uc003pyn_1
31	lnc-ASF1A-7	chr6:119801006-119804785	NONHSAT114718
32	lnc-ASF1A-3	chr6:119870973-119871058	XLOC_005449
33	lnc-MAN1A1-1	chr6:119773712-119776358	ENSG00000249211
34	lnc-ASF1A-3	chr6:119871395-119871560	XLOC_005449
35	lnc-MAN1A1-1	chr6:119778083-119778349	XLOC_005819
36	lnc-MAN1A1-1	chr6:119790762-119790879	XLOC_005819
37	lnc-MAN1A1-1	chr6:119712329-119712425	NONHSAT114715
38	lnc-MAN1A1-1	chr6:119812331-119812467	NONHSAT114715
39	lnc-MAN1A1-2	chr6:119854030-119854166	ucscGeneNc_uc003pyn_1
40	lnc-MAN1A1-1	chr6:119793588-119793621	XLOC_005819

No data

Variant related genes	Relation type
ENSG00000111885	chromatin interactions
ENSG00000253194	chromatin interactions
ENSG00000265565	chromatin interactions
ENSG00000104883	chromatin interactions
ENSG00000111877	chromatin interactions
STAT5B	miRNA target sites
E2F3	miRNA target sites
SNRPC	miRNA target sites
FAM168B	miRNA target sites
CYB561D1	miRNA target sites

Extended variants
information (count: 8398 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:8398 , 50 per page) page: 1 2 3 4 5 6 7 ... 168

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528571153	chr6:119712237-119712238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs77285861	chr6:119712268-119712269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs577665143	chr6:119712363-119712364	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
4	rs562050887	chr6:119712428-119712429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs530958632	chr6:119712472-119712473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs145888158	chr6:119712514-119712515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs545044453	chr6:119712550-119712551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs184213868	chr6:119712573-119712574	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs183814628	chr6:119712599-119712600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs114371529	chr6:119712624-119712625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs555977481	chr6:119712670-119712671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546832745	chr6:119712700-119712701	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs567100720	chr6:119712702-119712703	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9398510	chr6:119712750-119712751	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs148504443	chr6:119712760-119712761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs572276249	chr6:119712769-119712770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs80030735	chr6:119712784-119712785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536613453	chr6:119712814-119712815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs189027922	chr6:119712871-119712872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576677403	chr6:119712885-119712886	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs181665966	chr6:119712927-119712928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs35186481	chr6:119712974-119712975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs558680491	chr6:119712980-119712981	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552880330	chr6:119712993-119712994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs78315348	chr6:119713041-119713042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs541938503	chr6:119713055-119713056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs562138123	chr6:119713058-119713059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs185114225	chr6:119713117-119713118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs117740291	chr6:119713137-119713138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531880650	chr6:119713139-119713140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs564476403	chr6:119713154-119713155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs533454821	chr6:119713155-119713156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs547305912	chr6:119713170-119713171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs549911608	chr6:119713171-119713172	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs190757590	chr6:119713232-119713233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529460411	chr6:119713235-119713236	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs146569651	chr6:119713258-119713259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs567774441	chr6:119713347-119713348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540617394	chr6:119713447-119713448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs182121725	chr6:119713477-119713478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs185337379	chr6:119713554-119713555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570464614	chr6:119713556-119713557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539339621	chr6:119713595-119713596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs117424297	chr6:119713601-119713602	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs573079603	chr6:119713623-119713624	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs141302147	chr6:119713671-119713672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs372593956	chr6:119713721-119713722	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs742962	chr6:119713746-119713747	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs575762578	chr6:119713768-119713769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs113868464	chr6:119713777-119713778	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
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
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	20067559	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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	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
Burkitt''s lymphoma	18698080	CNVD
Ovarian cancer	21720365	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	16461572	CNVD
Neurocytoma	17123091	CNVD
Cancer	20164920	CNVD
Breast cancer	21364760	CNVD
Chordoma	21602918	CNVD
Kartagener syndrome	16639409	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Follicular lymphoma	18703704	CNVD
Mental retardation	17621639	CNVD
Hypoplastic	20877625	CNVD
Hypotonia	20877625	CNVD
Mental retardation	20877625	CNVD
Microcephaly	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	CNVD
micrognathia	20877625	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Metastatic melanoma	18483359	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Breast cancer	18698023	CNVD
Mental retardation	18854857	CNVD
Leukemia	18688285	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Liver carcinoma	19366792	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:119689600-119720600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr6:119708400-119716200	Weak transcription	Primary hematopoietic stem cells	blood
3	chr6:119712000-119717800	Weak transcription	Pancreas	Pancrea
4	chr6:119713600-119714400	Enhancers	Dnd41	blood
5	chr6:119715200-119717000	Enhancers	Primary B cells from peripheral blood	blood
6	chr6:119715400-119716200	Enhancers	Duodenum Mucosa	Duodenum
7	chr6:119715600-119716000	Enhancers	Primary B cells from cord blood	blood
8	chr6:119716200-119716800	Weak transcription	Duodenum Mucosa	Duodenum
9	chr6:119716200-119717200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
10	chr6:119716800-119717000	Enhancers	Duodenum Mucosa	Duodenum
11	chr6:119717000-119717400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
12	chr6:119720600-119720800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr6:119729800-119730600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr6:119729800-119730600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr6:119739000-119739400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr6:119746600-119747800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
17	chr6:119747000-119747200	Enhancers	Adipose Nuclei	Adipose
18	chr6:119747200-119747600	Flanking Active TSS	Adipose Nuclei	Adipose
19	chr6:119747200-119748400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:119747400-119748400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
21	chr6:119747600-119747800	Enhancers	Adipose Nuclei	Adipose
22	chr6:119747600-119748200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr6:119747800-119748000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
24	chr6:119747800-119748000	Flanking Active TSS	Adipose Nuclei	Adipose
25	chr6:119747800-119748000	Enhancers	Aorta	Aorta
26	chr6:119747800-119748200	Enhancers	Colon Smooth Muscle	Colon
27	chr6:119747800-119748200	Enhancers	Pancreas	Pancrea
28	chr6:119747800-119748200	Enhancers	HSMMtube	muscle
29	chr6:119747800-119748400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr6:119748000-119748200	Enhancers	Adipose Nuclei	Adipose
31	chr6:119748000-119750600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chr6:119748200-119749800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr6:119748200-119750000	Weak transcription	HSMMtube	muscle
34	chr6:119748200-119767000	Weak transcription	Colon Smooth Muscle	Colon
35	chr6:119748400-119749800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr6:119749600-119750400	Enhancers	Fetal Intestine Small	intestine
37	chr6:119749600-119751000	Enhancers	K562	blood
38	chr6:119749800-119750400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
39	chr6:119749800-119750400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
40	chr6:119749800-119755000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr6:119750000-119750200	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr6:119750000-119750600	Enhancers	HSMMtube	muscle
43	chr6:119750000-119750800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr6:119750600-119751000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
45	chr6:119750600-119751000	Enhancers	Placenta Amnion	Placenta Amnion
46	chr6:119750800-119752000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr6:119751000-119752000	Weak transcription	Placenta Amnion	Placenta Amnion
48	chr6:119751000-119752200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
49	chr6:119751800-119753000	Enhancers	Placenta	Placenta
50	chr6:119752000-119752200	Enhancers	Placenta Amnion	Placenta Amnion

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