Variant report

Variant	nsv1027904
Chromosome Location	chr6:119709488-120001986
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:239)
LncRNA
region (count:40)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:239 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr6:119984260..119986895-chr6:119991023..119994308,3	MCF-7	breast:
2	chr6:119958747..119960423-chr6:119965333..119967748,2	K562	blood:
3	chr6:119929475..119932013-chr6:119937447..119940201,2	K562	blood:
4	chr6:119730170..119732878-chr6:119745962..119749242,4	K562	blood:
5	chr6:119975769..119978608-chr6:119981121..119983313,2	MCF-7	breast:
6	chr6:119865503..119867117-chr6:119868492..119870588,2	K562	blood:
7	chr6:119932862..119934948-chr6:119935688..119940006,3	K562	blood:
8	chr6:119959397..119961696-chr6:119965621..119967266,2	MCF-7	breast:
9	chr6:119938254..119941760-chr6:119945161..119948947,3	K562	blood:
10	chr6:119666964..119669354-chr6:119827597..119829582,2	K562	blood:
11	chr6:119949922..119952911-chr6:119994617..119997136,2	MCF-7	breast:
12	chr6:119748860..119751626-chr6:119758382..119761495,3	MCF-7	breast:
13	chr6:119913316..119915387-chr6:119941334..119943937,2	MCF-7	breast:
14	chr6:119826693..119828704-chr6:119831138..119833641,2	K562	blood:
15	chr6:119710272..119711806-chr6:119713612..119715669,2	K562	blood:
16	chr6:119770080..119773062-chr6:119774639..119776880,2	K562	blood:
17	chr6:119901984..119904533-chr6:119906505..119908924,3	K562	blood:
18	chr1:885039..887449-chr6:119865762..119867280,2	K562	blood:
19	chr6:119769489..119771005-chr6:119951026..119953518,2	MCF-7	breast:
20	chr6:119819182..119822549-chr6:119824303..119826707,4	K562	blood:
21	chr6:119911222..119913281-chr6:119914244..119916111,2	K562	blood:
22	chr6:119926625..119928908-chr6:119933015..119935117,2	K562	blood:
23	chr6:119787516..119789829-chr6:119805762..119807377,2	MCF-7	breast:
24	chr6:119857573..119859199-chr6:119859391..119862222,2	MCF-7	breast:
25	chr6:119873467..119875883-chr6:119877494..119879434,2	K562	blood:
26	chr6:119847994..119850529-chr6:119852799..119855892,3	K562	blood:
27	chr6:119941042..119943563-chr6:119947616..119949679,2	MCF-7	breast:
28	chr6:119972613..119974357-chr6:119975659..119977197,2	K562	blood:
29	chr6:119789332..119793434-chr6:119796076..119800106,5	K562	blood:
30	chr6:119887985..119889812-chr6:119892703..119894315,2	K562	blood:
31	chr6:119911222..119913281-chr6:119914244..119916111,2	K562	blood:
32	chr6:119772222..119774379-chr6:119780050..119782058,2	K562	blood:
33	chr6:119877630..119879253-chr6:119896427..119898133,2	MCF-7	breast:
34	chr6:119959081..119962140-chr6:119964515..119967197,3	K562	blood:
35	chr6:119748860..119751626-chr6:119758382..119761495,3	MCF-7	breast:
36	chr6:119877710..119881825-chr6:119881980..119886083,5	K562	blood:
37	chr6:119865503..119867117-chr6:119868492..119870588,2	K562	blood:
38	chr6:119847994..119850425-chr6:119853510..119855892,2	K562	blood:
39	chr6:119784285..119787164-chr6:119791659..119794640,2	K562	blood:
40	chr6:119669730..119672145-chr6:119907178..119910018,3	MCF-7	breast:
41	chr6:119730819..119732878-chr6:119745962..119748059,2	K562	blood:
42	chr6:119669576..119672211-chr6:119949412..119952003,2	MCF-7	breast:
43	chr6:119845567..119847113-chr6:119965948..119967870,2	K562	blood:
44	chr6:119849420..119852024-chr6:119886180..119888675,2	K562	blood:
45	chr6:119886809..119890000-chr6:119899522..119901622,3	K562	blood:
46	chr6:119861440..119863163-chr6:119863418..119865512,2	K562	blood:
47	chr6:119944693..119946342-chr6:119947208..119949593,2	K562	blood:
48	chr6:119772222..119774379-chr6:119780050..119782058,2	K562	blood:
49	chr6:119834976..119836723-chr6:119847440..119850148,2	K562	blood:
50	chr6:119873252..119875568-chr6:119875892..119878574,2	MCF-7	breast:

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

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

No data

Variant related genes	Relation type
ENSG00000104883	chromatin interactions
ENSG00000111885	chromatin interactions
ENSG00000111877	chromatin interactions
ENSG00000253194	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000265565	chromatin interactions
SNRPC	miRNA target sites
STAT5B	miRNA target sites
E2F3	miRNA target sites
CYB561D1	miRNA target sites
FAM168B	miRNA target sites

Extended variants
information (count: 8594 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:8594 , 50 per page) page: 1 2 3 4 5 6 7 ... 172

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs560968090	chr6:119709577-119709578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs140330806	chr6:119709578-119709579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs538756605	chr6:119709728-119709729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs558525532	chr6:119709830-119709831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs185875927	chr6:119709838-119709839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs190442520	chr6:119709918-119709919	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182519458	chr6:119709958-119709959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs575099987	chr6:119709979-119709980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs543995463	chr6:119709994-119709995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs557595392	chr6:119710004-119710005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187517642	chr6:119710036-119710037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545173671	chr6:119710075-119710076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs386705219	chr6:119710166-119710167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs145480353	chr6:119710185-119710186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs370197685	chr6:119710198-119710199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527333413	chr6:119710229-119710230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs6569076	chr6:119710290-119710291	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs118172868	chr6:119710346-119710347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs574468152	chr6:119710377-119710378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs114601944	chr6:119710421-119710422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549524400	chr6:119710437-119710438	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs115270761	chr6:119710453-119710454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200430366	chr6:119710465-119710466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs151167579	chr6:119710466-119710467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs5879502	chr6:119710470-119710471	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs200235527	chr6:119710471-119710472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs532459980	chr6:119710481-119710482	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs552286267	chr6:119710574-119710575	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs372359865	chr6:119710583-119710584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138064306	chr6:119710584-119710585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149536912	chr6:119710609-119710610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548578213	chr6:119710636-119710637	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs369826682	chr6:119710663-119710664	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs568617267	chr6:119710671-119710672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs537740303	chr6:119710684-119710685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143208774	chr6:119710691-119710692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs192035038	chr6:119710710-119710711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs386705220	chr6:119710754-119710755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs538723776	chr6:119710755-119710756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112786184	chr6:119710756-119710757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs183937147	chr6:119710771-119710772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201515444	chr6:119710806-119710807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs75520693	chr6:119710807-119710808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs35334117	chr6:119710822-119710823	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs4945636	chr6:119710844-119710845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs540636372	chr6:119710911-119710912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs1342311	chr6:119710923-119710924	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs74431665	chr6:119710932-119710933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375573936	chr6:119710945-119710946	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs543352486	chr6:119710976-119710977	Weak transcription	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:1438 , 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	chr6:119711400-119711800	Enhancers	K562	blood
4	chr6:119711600-119712000	ZNF genes & repeats	Pancreas	Pancrea
5	chr6:119712000-119717800	Weak transcription	Pancreas	Pancrea
6	chr6:119713600-119714400	Enhancers	Dnd41	blood
7	chr6:119715200-119717000	Enhancers	Primary B cells from peripheral blood	blood
8	chr6:119715400-119716200	Enhancers	Duodenum Mucosa	Duodenum
9	chr6:119715600-119716000	Enhancers	Primary B cells from cord blood	blood
10	chr6:119716200-119716800	Weak transcription	Duodenum Mucosa	Duodenum
11	chr6:119716200-119717200	ZNF genes & repeats	Primary hematopoietic stem cells	blood
12	chr6:119716800-119717000	Enhancers	Duodenum Mucosa	Duodenum
13	chr6:119717000-119717400	Bivalent Enhancer	Primary B cells from peripheral blood	blood
14	chr6:119720600-119720800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr6:119729800-119730600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr6:119729800-119730600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
17	chr6:119739000-119739400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
18	chr6:119746600-119747800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr6:119747000-119747200	Enhancers	Adipose Nuclei	Adipose
20	chr6:119747200-119747600	Flanking Active TSS	Adipose Nuclei	Adipose
21	chr6:119747200-119748400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr6:119747400-119748400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
23	chr6:119747600-119747800	Enhancers	Adipose Nuclei	Adipose
24	chr6:119747600-119748200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
25	chr6:119747800-119748000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr6:119747800-119748000	Flanking Active TSS	Adipose Nuclei	Adipose
27	chr6:119747800-119748000	Enhancers	Aorta	Aorta
28	chr6:119747800-119748200	Enhancers	Colon Smooth Muscle	Colon
29	chr6:119747800-119748200	Enhancers	Pancreas	Pancrea
30	chr6:119747800-119748200	Enhancers	HSMMtube	muscle
31	chr6:119747800-119748400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
32	chr6:119748000-119748200	Enhancers	Adipose Nuclei	Adipose
33	chr6:119748000-119750600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
34	chr6:119748200-119749800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:119748200-119750000	Weak transcription	HSMMtube	muscle
36	chr6:119748200-119767000	Weak transcription	Colon Smooth Muscle	Colon
37	chr6:119748400-119749800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr6:119749600-119750400	Enhancers	Fetal Intestine Small	intestine
39	chr6:119749600-119751000	Enhancers	K562	blood
40	chr6:119749800-119750400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr6:119749800-119750400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
42	chr6:119749800-119755000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr6:119750000-119750200	Enhancers	Pancreatic Islets	Pancreatic Islet
44	chr6:119750000-119750600	Enhancers	HSMMtube	muscle
45	chr6:119750000-119750800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr6:119750600-119751000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr6:119750600-119751000	Enhancers	Placenta Amnion	Placenta Amnion
48	chr6:119750800-119752000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
49	chr6:119751000-119752000	Weak transcription	Placenta Amnion	Placenta Amnion
50	chr6:119751000-119752200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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