Variant report

Variant	nsv876992
Chromosome Location	chr3:75867951-76029306
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	chr3:75913346-75913538	K562	blood:	n/a	n/a
4	ATF1	chr3:75998476-75998676	K562	blood:	n/a	n/a
5	ATF1	chr3:75986254-75986287	K562	blood:	n/a	n/a
6	ATF1	chr3:75985241-75985450	K562	blood:	n/a	n/a
7	ATF1	chr3:75986623-75986792	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	chr3:75874370-75874457	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr3:75868362-75868385	K562	blood:	n/a	n/a
12	BACH1	chr3:75878357-75878369	K562	blood:	n/a	n/a
13	BACH1	chr3:75914793-75914977	K562	blood:	n/a	n/a
14	BACH1	chr3:75936348-75936578	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr3:75955701-75956187	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chr3:75893348-75893483	GM12878	blood:	n/a	n/a
17	BATF	chr3:75877295-75877525	GM12878	blood:	n/a	n/a
18	BATF	chr3:75889332-75889534	GM12878	blood:	n/a	n/a
19	BATF	chr3:75891229-75891473	GM12878	blood:	n/a	n/a
20	BATF	chr3:75878535-75878822	GM12878	blood:	n/a	n/a
21	BCL11A	chr3:75869794-75870055	GM12878	blood:	n/a	n/a
22	BCL11A	chr3:75909079-75909236	GM12878	blood:	n/a	n/a
23	BCL11A	chr3:75887272-75887513	GM12878	blood:	n/a	n/a
24	BCL11A	chr3:75878675-75878839	GM12878	blood:	n/a	n/a
25	BCL11A	chr3:75890145-75890444	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:75996667-75996686	GM12878	blood:	n/a	n/a
27	BHLHE40	chr3:75991823-75991949	GM12878	blood:	n/a	n/a
28	BRCA1	chr3:75908182-75908326	GM12878	blood:	n/a	n/a
29	BRCA1	chr3:75908178-75908315	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr3:75991825-75991831	K562	blood:	n/a	n/a
31	CEBPB	chr3:75945762-75945954	HepG2	liver:	n/a	chr3:75945863-75945874
32	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
33	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
34	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
35	CEBPB	chr3:75878512-75878531	K562	blood:	n/a	n/a
36	CEBPB	chr3:76025393-76025671	HepG2	liver:	n/a	chr3:76025511-76025522
37	CEBPB	chr3:75913710-75913839	A549	lung:	n/a	chr3:75913757-75913770 chr3:75913757-75913768
38	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
39	CEBPZ	chr3:75991161-75991361	HepG2	liver:	n/a	n/a
40	CEBPZ	chr3:75983702-75983951	HepG2	liver:	n/a	n/a
41	CHD1	chr3:75878497-75878510	GM12878	blood:	n/a	n/a
42	CHD2	chr3:75955746-75956057	H1-hESC	embryonic stem cell:	n/a	chr3:75955999-75956009
43	CHD2	chr3:75988257-75988329	GM12878	blood:	n/a	n/a
44	CTBP2	chr3:75955733-75956447	H1-hESC	embryonic stem cell:	n/a	n/a
45	CTCF	chr3:75955720-75955870	HAc	cerebellar:	n/a	n/a
46	CTCF	chr3:75902880-75903030	AG04450	lung:	n/a	n/a
47	CTCF	chr3:75902940-75903090	WI-38	lung:	n/a	chr3:75903020-75903041 chr3:75903018-75903036
48	CTCF	chr3:75886100-75886250	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr3:75886160-75886310	MCF-7	breast:	n/a	n/a
50	CTCF	chr3:75989500-75989650	AG10803	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:75958299-75958349	HNPCEpiC	eye:	n/a
2	chr3:75959386-75959436	HAEpiC	amniotic membrane:	n/a
3	chr3:75956295-75956345	Jurkat	blood:	n/a
4	chr3:75958299-75958349	BE2_C	brain:	n/a
5	chr3:75956119-75956169	HUVEC	blood vessel:	n/a
6	chr3:75958299-75958349	MCF-7	breast:	n/a
7	chr3:75958299-75958349	Hela-S3	cervix:	n/a
8	chr3:75956295-75956345	HEK293	kidney:	embryo
9	chr3:75955844-75955894	AG09319	gingival:	n/a
10	chr3:75955844-75955894	SK-N-SH	brain:	n/a
11	chr3:75959386-75959436	PrEC	prostate:	n/a
12	chr3:75956119-75956169	NHDF-neo	bronchial:	n/a
13	chr3:75958299-75958349	HL-60	blood:	n/a
14	chr3:75958299-75958349	HAEpiC	amniotic membrane:	n/a
15	chr3:75956119-75956169	AG04449	skin:	fetal
16	chr3:75956295-75956345	LNCaP	prostate:	n/a
17	chr3:75956295-75956345	Hepatocyte	liver:	n/a
18	chr3:75959386-75959436	ProgFib	skin:	n/a
19	chr3:75956295-75956345	IMR90	lung:	fetal
20	chr3:75956119-75956169	GM12878	blood:	n/a
21	chr3:75959386-75959436	MCF-7	breast:	n/a
22	chr3:75956119-75956169	HPAEpiC	pulmonary alveolar:	n/a
23	chr3:75958299-75958349	A549	lung:	n/a
24	chr3:75956295-75956345	NH-A	brain:	n/a
25	chr3:75956119-75956169	HNPCEpiC	eye:	n/a
26	chr3:75956295-75956345	HPAEpiC	pulmonary alveolar:	n/a
27	chr3:75959386-75959436	Caco-2	colon:	n/a
28	chr3:75959386-75959436	NHBE	bronchial:	n/a
29	chr3:75956295-75956345	SKMC	muscle:	n/a
30	chr3:75955844-75955894	MCF-7	breast:	n/a
31	chr3:75956295-75956345	K562	blood:	n/a
32	chr3:75956295-75956345	AG04450	lung:	fetal
33	chr3:75956119-75956169	H1-hESC	embryonic stem cell:	embryo
34	chr3:75956119-75956169	SAEC	small airway:	n/a
35	chr3:75956119-75956169	SK-N-SH_RA	brain:	n/a
36	chr3:75955844-75955894	HEK293	kidney:	embryo
37	chr3:75956295-75956345	GM12878	blood:	n/a
38	chr3:75958299-75958349	HepG2	liver:	n/a
39	chr3:75959386-75959436	Hepatocyte	liver:	n/a
40	chr3:75956119-75956169	NT2-D1	testis:	n/a
41	chr3:75956295-75956345	SK-N-SH_RA	brain:	n/a
42	chr3:75956119-75956169	K562	blood:	n/a
43	chr3:75956295-75956345	HNPCEpiC	eye:	n/a
44	chr3:75959386-75959436	GM12878	blood:	n/a
45	chr3:75956295-75956345	HUVEC	blood vessel:	n/a
46	chr3:75958299-75958349	SKMC	muscle:	n/a
47	chr3:75959386-75959436	A549	lung:	n/a
48	chr3:75958299-75958349	PANC-1	pancreas:	n/a
49	chr3:75956119-75956169	NHBE	bronchial:	n/a
50	chr3:75958299-75958349	HRPEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:26208095..26209894-chr3:75988198..75990401,2	MCF-7	breast:
2	chr20:26206073..26206971-chr3:75991464..75992265,2	MCF-7	breast:
3	chr20:26201563..26203476-chr3:75993448..75995749,2	K562	blood:
4	chr20:26208071..26209607-chr3:75987301..75988916,2	K562	blood:
5	chr3:75867624..75868149-chr3:76093803..76094658,2	MCF-7	breast:
6	chr20:26201915..26204776-chr3:75992954..75996738,5	MCF-7	breast:
7	chr1:143540009..143542435-chr3:75911879..75914281,2	MCF-7	breast:
8	chr20:26199924..26201625-chr3:75995563..75997738,2	MCF-7	breast:

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

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

Extended variants
information (count: 2721 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:2721 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6775554	chr3:75867951-75867952	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373482692	chr3:75867962-75867963	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs574892327	chr3:75867970-75867971	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs376516878	chr3:75867983-75867984	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542422762	chr3:75868040-75868041	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114216400	chr3:75868058-75868059	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs113179843	chr3:75868095-75868096	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs185643910	chr3:75868101-75868102	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62266852	chr3:75868128-75868129	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs575930354	chr3:75868131-75868132	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs139237230	chr3:75868133-75868134	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs62266853	chr3:75868136-75868137	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113319488	chr3:75868152-75868153	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs11717095	chr3:75868154-75868155	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs62266854	chr3:75868161-75868162	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs145593569	chr3:75868171-75868172	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550890465	chr3:75868189-75868190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs139315634	chr3:75868235-75868236	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs562227409	chr3:75868254-75868255	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs561205942	chr3:75868258-75868259	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs72898799	chr3:75868285-75868286	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs550778344	chr3:75868300-75868301	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs552508283	chr3:75868305-75868306	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs139533357	chr3:75868322-75868323	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs143912316	chr3:75868323-75868324	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs144119424	chr3:75868345-75868346	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs112255417	chr3:75868347-75868348	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs377089322	chr3:75868354-75868355	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs370208165	chr3:75868373-75868374	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs374133992	chr3:75868376-75868377	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs368103663	chr3:75868386-75868387	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs371972229	chr3:75868391-75868392	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs113217302	chr3:75868394-75868395	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs151147275	chr3:75868430-75868431	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs33968227	chr3:75868447-75868448	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs180998871	chr3:75868459-75868460	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs566426089	chr3:75868472-75868473	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs533778203	chr3:75868482-75868483	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs570618862	chr3:75868502-75868503	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs112731142	chr3:75868532-75868533	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs368470484	chr3:75868551-75868552	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs372719690	chr3:75868552-75868553	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs140062488	chr3:75868555-75868556	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs112147227	chr3:75868563-75868564	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs35471945	chr3:75868571-75868572	Enhancers ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs535657482	chr3:75868597-75868598	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs184142236	chr3:75868623-75868624	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557576427	chr3:75868632-75868633	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575847030	chr3:75868643-75868644	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369952586	chr3:75868646-75868647	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:253 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:75866000-75868000	Weak transcription	HUES64 Cell Line	embryonic stem cell
2	chr3:75866000-75868000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr3:75866200-75868000	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr3:75866200-75868200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr3:75867600-75868400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr3:75867600-75868800	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr3:75867600-75868800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr3:75867600-75869000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr3:75867800-75868600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr3:75868000-75868400	Enhancers	H1 Cell Line	embryonic stem cell
11	chr3:75868000-75868400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
12	chr3:75868000-75868600	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr3:75868200-75868600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
14	chr3:75868400-75868600	Enhancers	H9 Cell Line	embryonic stem cell
15	chr3:75868600-75871800	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr3:75868600-75871800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chr3:75868800-75871800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr3:75869000-75871800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr3:75871800-75872000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chr3:75871800-75872000	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr3:75871800-75872200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr3:75871800-75872600	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr3:75872000-75872400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chr3:75872000-75872600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr3:75872400-75872800	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr3:75872600-75873400	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr3:75874200-75874400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr3:75874400-75878200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr3:75878200-75878400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
30	chr3:75880200-75880800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr3:75888800-75889600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr3:75889200-75889400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr3:75889400-75890000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr3:75890000-75890400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr3:75890400-75891800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr3:75891800-75892000	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr3:75899200-75899600	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
38	chr3:75899200-75899800	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chr3:75899400-75900000	Bivalent/Poised TSS	HUES6 Cell Line	embryonic stem cell
40	chr3:75899400-75900600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
41	chr3:75899600-75900000	Bivalent/Poised TSS	HUES64 Cell Line	embryonic stem cell
42	chr3:75899800-75900000	Active TSS	ES-I3 Cell Line	embryonic stem cell
43	chr3:75900000-75900200	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
44	chr3:75900000-75900200	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
45	chr3:75900000-75900400	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
46	chr3:75900000-75900400	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
47	chr3:75900000-75900400	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
48	chr3:75900000-75900400	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
49	chr3:75900000-75900400	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr3:75900200-75900600	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell

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