Variant report

Variant	nsv876993
Chromosome Location	chr3:75904105-76077143
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:75913424-75913483	K562	blood:	n/a	n/a
2	ARID3A	chr3:75991836-75991901	K562	blood:	n/a	n/a
3	ATF1	chr3:75986623-75986792	K562	blood:	n/a	n/a
4	ATF1	chr3:75986254-75986287	K562	blood:	n/a	n/a
5	ATF1	chr3:75913346-75913538	K562	blood:	n/a	n/a
6	ATF1	chr3:75998476-75998676	K562	blood:	n/a	n/a
7	ATF1	chr3:75985241-75985450	K562	blood:	n/a	n/a
8	ATF1	chr3:75991766-75991934	K562	blood:	n/a	n/a
9	ATF2	chr3:75955912-75956209	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr3:75955701-75956187	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:75936348-75936578	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:75914793-75914977	K562	blood:	n/a	n/a
13	BCL11A	chr3:75909079-75909236	GM12878	blood:	n/a	n/a
14	BHLHE40	chr3:75996667-75996686	GM12878	blood:	n/a	n/a
15	BHLHE40	chr3:75991823-75991949	GM12878	blood:	n/a	n/a
16	BRCA1	chr3:75908182-75908326	GM12878	blood:	n/a	n/a
17	BRCA1	chr3:75908178-75908315	Hela-S3	cervix:	n/a	n/a
18	CEBPB	chr3:76034701-76034915	H1-hESC	embryonic stem cell:	n/a	chr3:76034793-76034804
19	CEBPB	chr3:76025393-76025671	HepG2	liver:	n/a	chr3:76025511-76025522
20	CEBPB	chr3:76023890-76023921	H1-hESC	embryonic stem cell:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
21	CEBPB	chr3:76034636-76034981	K562	blood:	n/a	chr3:76034793-76034804
22	CEBPB	chr3:75945762-75945954	HepG2	liver:	n/a	chr3:75945863-75945874
23	CEBPB	chr3:76034609-76034974	HepG2	liver:	n/a	chr3:76034793-76034804
24	CEBPB	chr3:76034619-76034978	A549	lung:	n/a	chr3:76034793-76034804
25	CEBPB	chr3:76023773-76024060	A549	lung:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
26	CEBPB	chr3:75991825-75991831	K562	blood:	n/a	n/a
27	CEBPB	chr3:76023734-76024093	IMR90	lung:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
28	CEBPB	chr3:75913710-75913839	A549	lung:	n/a	chr3:75913757-75913770 chr3:75913757-75913768
29	CEBPB	chr3:76023733-76024088	HepG2	liver:	n/a	chr3:76023907-76023918 chr3:76023905-76023918 chr3:76023905-76023918 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023916 chr3:76023907-76023916 chr3:76023907-76023916 chr3:76023905-76023918
30	CEBPB	chr3:76034632-76034971	IMR90	lung:	n/a	chr3:76034793-76034804
31	CEBPZ	chr3:75983702-75983951	HepG2	liver:	n/a	n/a
32	CEBPZ	chr3:75991161-75991361	HepG2	liver:	n/a	n/a
33	CHD2	chr3:75988257-75988329	GM12878	blood:	n/a	n/a
34	CHD2	chr3:75955746-75956057	H1-hESC	embryonic stem cell:	n/a	chr3:75955999-75956009
35	CTBP2	chr3:75955733-75956447	H1-hESC	embryonic stem cell:	n/a	n/a
36	CTCF	chr3:76073920-76074070	AG04449	skin:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
37	CTCF	chr3:75955820-75955970	RPTEC	kidney:	n/a	chr3:75955887-75955900
38	CTCF	chr3:75908296-75908321	MCF-7	breast:	n/a	n/a
39	CTCF	chr3:76073866-76074124	K562	blood:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
40	CTCF	chr3:75994500-75994650	BE2_C	brain:	n/a	n/a
41	CTCF	chr3:76073760-76074106	MCF-7	breast:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
42	CTCF	chr3:76073880-76074030	GM12872	blood:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
43	CTCF	chr3:76073920-76074070	Caco-2	colon:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
44	CTCF	chr3:75959676-75959745	GM20000	blood:	n/a	n/a
45	CTCF	chr3:76073920-76074070	HPAF	blood vessel:	n/a	chr3:76073986-76074007 chr3:76073984-76074002
46	CTCF	chr3:75992420-75992570	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr3:75996600-75996750	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr3:75986660-75986810	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr3:76042224-76042309	GM10266	blood:	n/a	n/a
50	CTCF	chr3:75955800-75955950	NHEK	skin:	n/a	chr3:75955887-75955900

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:76063500-76063550	MCF10A-Er-Src	breast:	n/a
2	chr3:75958299-75958349	HAEpiC	amniotic membrane:	n/a
3	chr3:76062791-76062841	GM12892	blood:	n/a
4	chr3:75958299-75958349	SK-N-SH	brain:	n/a
5	chr3:75956295-75956345	AG04449	skin:	fetal
6	chr3:76062791-76062841	IMR90	lung:	fetal
7	chr3:76062325-76062375	NB4	blood:	n/a
8	chr3:75955844-75955894	HPAEpiC	pulmonary alveolar:	n/a
9	chr3:75959386-75959436	A549	lung:	n/a
10	chr3:76062791-76062841	HepG2	liver:	n/a
11	chr3:76063500-76063550	HIPEpiC	eye:	n/a
12	chr3:75958299-75958349	GM12892	blood:	n/a
13	chr3:76063343-76063393	HMEC	breast:	n/a
14	chr3:75955844-75955894	H1-hESC	embryonic stem cell:	embryo
15	chr3:76063343-76063393	Caco-2	colon:	n/a
16	chr3:75955844-75955894	ProgFib	skin:	n/a
17	chr3:75956295-75956345	HCF	heart:	n/a
18	chr3:75956295-75956345	HepG2	liver:	n/a
19	chr3:75958299-75958349	LNCaP	prostate:	n/a
20	chr3:76062791-76062841	GM12878	blood:	n/a
21	chr3:75959386-75959436	PFSK-1	brain:	n/a
22	chr3:75956119-75956169	HUVEC	blood vessel:	n/a
23	chr3:75956295-75956345	NHBE	bronchial:	n/a
24	chr3:76063500-76063550	GM12878	blood:	n/a
25	chr3:75958299-75958349	SK-N-MC	brain:	n/a
26	chr3:75956295-75956345	PANC-1	pancreas:	n/a
27	chr3:76062325-76062375	HRCEpiC	kidney:	n/a
28	chr3:75956119-75956169	AoSMC	blood vessel:	n/a
29	chr3:75956295-75956345	HCPEpiC	choroid plexus:	n/a
30	chr3:76062325-76062375	GM12878	blood:	n/a
31	chr3:76062325-76062375	BE2_C	brain:	n/a
32	chr3:75959386-75959436	U87	brain:	n/a
33	chr3:76062791-76062841	LNCaP	prostate:	n/a
34	chr3:75955844-75955894	CMK	blood:	n/a
35	chr3:75956119-75956169	CMK	blood:	n/a
36	chr3:75955844-75955894	HIPEpiC	eye:	n/a
37	chr3:75956295-75956345	GM06990	blood:	n/a
38	chr3:75958299-75958349	H1-hESC	embryonic stem cell:	embryo
39	chr3:76063500-76063550	HPAEpiC	pulmonary alveolar:	n/a
40	chr3:76063343-76063393	GM12891	blood:	n/a
41	chr3:76063500-76063550	HCF	heart:	n/a
42	chr3:76062791-76062841	T-47D	breast:	n/a
43	chr3:75959386-75959436	HRE	kidney:	n/a
44	chr3:76076212-76076262	HRPEpiC	eye:	n/a
45	chr3:75956119-75956169	HNPCEpiC	eye:	n/a
46	chr3:76063500-76063550	GM19239	blood:	n/a
47	chr3:75956119-75956169	NHDF-neo	bronchial:	n/a
48	chr3:76076212-76076262	HCM	heart:	n/a
49	chr3:76076212-76076262	HRE	kidney:	n/a
50	chr3:76063500-76063550	LNCaP	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
2	chr20:26208071..26209607-chr3:75987301..75988916,2	K562	blood:
3	chr1:143540009..143542435-chr3:75911879..75914281,2	MCF-7	breast:
4	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:
5	chr3:76073881..76074768-chr3:76093884..76094767,3	MCF-7	breast:
6	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:
7	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
8	chr20:26201915..26204776-chr3:75992954..75996738,5	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FRG2C-12	chr3:75955945-75956111	NONHSAT090553
2	lnc-FRG2C-12	chr3:75986632-75986776	NONHSAT090553

Variant related genes	Relation type
ENSG00000222883	TF binding region
ROBO2	TF binding region
ENSG00000222883	CpG island
ROBO2	CpG island

Extended variants
information (count: 2301 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:2301 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs77408041	chr3:75908006-75908007	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs368206529	chr3:75908010-75908011	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs112870948	chr3:75908013-75908014	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs185820142	chr3:75908023-75908024	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs79570669	chr3:75908026-75908027	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs201864210	chr3:75908041-75908042	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs375061656	chr3:75908047-75908048	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs79657503	chr3:75908096-75908097	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs62267827	chr3:75908100-75908101	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs531895242	chr3:75908102-75908103	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs201632588	chr3:75908103-75908104	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs112581885	chr3:75908119-75908120	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs550176812	chr3:75908167-75908168	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs75456130	chr3:75908170-75908171	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs80071730	chr3:75908182-75908183	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs571278086	chr3:75908196-75908197	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs538762558	chr3:75908201-75908202	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs77253124	chr3:75908202-75908203	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs201851821	chr3:75908248-75908249	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs200127876	chr3:75908249-75908250	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs74729423	chr3:75908258-75908259	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs75183910	chr3:75908270-75908271	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs565539625	chr3:75908275-75908276	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs375459072	chr3:75908276-75908277	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs369397909	chr3:75908297-75908298	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs373133160	chr3:75908304-75908305	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs377407767	chr3:75908313-75908314	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs369253042	chr3:75908333-75908334	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs139400581	chr3:75908385-75908386	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs373434665	chr3:75908386-75908387	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs376081958	chr3:75908391-75908392	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs370458604	chr3:75908395-75908396	ZNF genes & repeats Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs557584958	chr3:75912003-75912004	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs373965995	chr3:75912009-75912010	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs77985425	chr3:75912035-75912036	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs74347608	chr3:75912043-75912044	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs370263503	chr3:75912055-75912056	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs576005624	chr3:75912063-75912064	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs78267766	chr3:75912072-75912073	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs546257842	chr3:75912084-75912085	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs200089830	chr3:75912118-75912119	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs72900758	chr3:75912159-75912160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs75163668	chr3:75912175-75912176	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs573401127	chr3:75912180-75912181	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs201236533	chr3:75912210-75912211	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs376047735	chr3:75912226-75912227	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs540691307	chr3:75912230-75912231	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs569875001	chr3:75912231-75912232	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs369587381	chr3:75912236-75912237	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs375418826	chr3:75912250-75912251	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:84)

Disease	PMID	Source
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
Melanoma	18172304	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Hirschsprung''s Disease	21712996	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Cervical cancer	21062161	CNVD
Squamous cell cancer	20885788	CNVD
Autism	22102821	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Prostate cancer	18632612	CNVD
Metanephric adenoma	20802469	CNVD
Bipolar disorder	18458673	CNVD
Breast cancer	22032731	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21509527	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Colorectal cancer	16272173	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Soft tissue tumor	16732325	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Ovarian cancer	21720365	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21858162	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Melanoma	20877625	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:238 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75908000-75908400	ZNF genes & repeats	Fetal Brain Male	brain
2	chr3:75908000-75908400	Active TSS	Fetal Heart	heart
3	chr3:75912000-75913400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
4	chr3:75912200-75912800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr3:75912800-75914600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
6	chr3:75914600-75914800	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr3:75932600-75933800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr3:75932800-75933400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:75933400-75936200	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr3:75933800-75940400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
11	chr3:75936200-75936400	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr3:75939600-75940200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr3:75940200-75940800	Weak transcription	HUES48 Cell Line	embryonic stem cell
14	chr3:75940400-75940600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr3:75940800-75941000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr3:75941200-75941600	Enhancers	H1 Cell Line	embryonic stem cell
17	chr3:75954800-75955000	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
18	chr3:75954800-75955000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr3:75954800-75955400	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
20	chr3:75954800-75955400	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
21	chr3:75954800-75955600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
22	chr3:75955000-75955600	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:75955200-75955400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr3:75955200-75955600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr3:75955400-75955600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr3:75955400-75955600	Bivalent/Poised TSS	HUES48 Cell Line	embryonic stem cell
27	chr3:75955400-75955600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
28	chr3:75955400-75955600	Flanking Bivalent TSS/Enh	iPS-20b Cell Line	embryonic stem cell
29	chr3:75955400-75955600	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr3:75955400-75955600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr3:75955400-75955600	Active TSS	Brain Anterior Caudate	brain
32	chr3:75955400-75955600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
33	chr3:75955400-75955800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
34	chr3:75955400-75955800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr3:75955400-75955800	Active TSS	Brain Germinal Matrix	brain
36	chr3:75955400-75956400	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
37	chr3:75955400-75956400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
38	chr3:75955400-75956800	Active TSS	Fetal Brain Male	brain
39	chr3:75955400-75958400	Active TSS	Fetal Brain Female	brain
40	chr3:75955600-75955800	Flanking Bivalent TSS/Enh	H1 Cell Line	embryonic stem cell
41	chr3:75955600-75955800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr3:75955600-75955800	Bivalent Enhancer	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr3:75955600-75955800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr3:75955600-75955800	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
45	chr3:75955600-75955800	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr3:75955600-75955800	Active TSS	Adipose Nuclei	Adipose
47	chr3:75955600-75955800	Active TSS	Brain Cingulate Gyrus	brain
48	chr3:75955600-75955800	Flanking Bivalent TSS/Enh	Brain Inferior Temporal Lobe	brain
49	chr3:75955600-75955800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
50	chr3:75955600-75955800	Flanking Active TSS	Fetal Muscle Trunk	muscle

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