Variant report

Variant	esv1818503
Chromosome Location	chr2:76777279-76882935
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:445)
CpG islands
(count:183)
Chromatin interactive
region (count:6)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:445 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:76826892-76827267	HepG2	liver:	n/a	n/a
2	ATF2	chr2:76868112-76868533	GM12878	blood:	n/a	n/a
3	BACH1	chr2:76826863-76827150	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr2:76826886-76827145	GM12878	blood:	n/a	n/a
5	BATF	chr2:76868153-76868459	GM12878	blood:	n/a	chr2:76868323-76868334 chr2:76868324-76868334 chr2:76868320-76868330
6	BCL11A	chr2:76868123-76868435	GM12878	blood:	n/a	chr2:76868323-76868332 chr2:76868322-76868331
7	BHLHE40	chr2:76826921-76827181	K562	blood:	n/a	n/a
8	BHLHE40	chr2:76826935-76827215	GM12878	blood:	n/a	n/a
9	BRCA1	chr2:76826858-76827249	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr2:76797632-76797940	IMR90	lung:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
11	CEBPB	chr2:76797064-76797289	MCF-7	breast:	n/a	n/a
12	CEBPB	chr2:76826891-76827167	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr2:76796956-76797326	HepG2	liver:	n/a	n/a
14	CEBPB	chr2:76797598-76797957	HepG2	liver:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
15	CEBPB	chr2:76797051-76797266	A549	lung:	n/a	n/a
16	CEBPB	chr2:76796996-76797228	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr2:76797619-76797897	K562	blood:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
18	CEBPB	chr2:76797009-76797286	IMR90	lung:	n/a	n/a
19	CEBPB	chr2:76797647-76797927	A549	lung:	n/a	chr2:76797773-76797790 chr2:76797774-76797787 chr2:76797774-76797785 chr2:76797775-76797786
20	CHD1	chr2:76808522-76808533	GM12878	blood:	n/a	n/a
21	CHD2	chr2:76826886-76827202	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr2:76791146-76791215	HepG2	liver:	n/a	n/a
23	CREB1	chr2:76856448-76856731	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr2:76826892-76827198	HepG2	liver:	n/a	n/a
25	CTCF	chr2:76827040-76827190	AG04450	lung:	n/a	n/a
26	CTCF	chr2:76826940-76827090	GM12875	blood:	n/a	n/a
27	CTCF	chr2:76826980-76827130	Hela-S3	cervix:	n/a	n/a
28	CTCF	chr2:76826920-76827070	BE2_C	brain:	n/a	n/a
29	CTCF	chr2:76826622-76827481	A549	lung:	n/a	n/a
30	CTCF	chr2:76827000-76827150	HMF	breast:	n/a	n/a
31	CTCF	chr2:76827040-76827190	AG09319	gingival:	n/a	n/a
32	CTCF	chr2:76827000-76827150	HEEpiC	esophagus:	n/a	n/a
33	CTCF	chr2:76826954-76827169	A549	lung:	n/a	n/a
34	CTCF	chr2:76826960-76827110	Caco-2	colon:	n/a	n/a
35	CTCF	chr2:76826917-76827237	HUVEC	blood vessel:	n/a	n/a
36	CTCF	chr2:76826920-76827070	HCT-116	colon:	n/a	n/a
37	CTCF	chr2:76826885-76827162	ECC-1	luminal epithelium:	n/a	n/a
38	CTCF	chr2:76826960-76827110	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr2:76826960-76827110	GM12864	blood:	n/a	n/a
40	CTCF	chr2:76851646-76851678	Hela-S3	cervix:	n/a	n/a
41	CTCF	chr2:76827020-76827170	HVMF	connective:	n/a	n/a
42	CTCF	chr2:76826960-76827110	GM12865	blood:	n/a	n/a
43	CTCF	chr2:76827000-76827150	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr2:76826980-76827130	AG04449	skin:	n/a	n/a
45	CTCF	chr2:76826980-76827130	GM12873	blood:	n/a	n/a
46	CTCF	chr2:76826677-76827355	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:76827000-76827150	AoAF	blood vessel:	n/a	n/a
48	CTCF	chr2:76827400-76827550	GM12868	blood:	n/a	n/a
49	CTCF	chr2:76827000-76827150	HUVEC	blood vessel:	n/a	n/a
50	CTCF	chr2:76835020-76835170	HA-sp	spinal cord:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:76806361-76806411	A549	lung:	n/a
2	chr2:76880863-76880913	HIPEpiC	eye:	n/a
3	chr2:76806361-76806411	HMEC	breast:	n/a
4	chr2:76880863-76880913	NH-A	brain:	n/a
5	chr2:76839078-76839128	K562	blood:	n/a
6	chr2:76839078-76839128	MCF-7	breast:	n/a
7	chr2:76880863-76880913	HCT-116	colon:	n/a
8	chr2:76880863-76880913	ECC-1	luminal epithelium:	n/a
9	chr2:76806361-76806411	BJ	skin:	n/a
10	chr2:76806361-76806411	GM12892	blood:	n/a
11	chr2:76806361-76806411	AoSMC	blood vessel:	n/a
12	chr2:76839078-76839128	Hepatocyte	liver:	n/a
13	chr2:76806361-76806411	NHBE	bronchial:	n/a
14	chr2:76806361-76806411	ovcar-3	ovarian:	n/a
15	chr2:76806361-76806411	HIPEpiC	eye:	n/a
16	chr2:76880863-76880913	AG09309	skin:	n/a
17	chr2:76839078-76839128	IMR90	lung:	fetal
18	chr2:76880863-76880913	HNPCEpiC	eye:	n/a
19	chr2:76839078-76839128	MCF10A-Er-Src	breast:	n/a
20	chr2:76880863-76880913	PFSK-1	brain:	n/a
21	chr2:76839078-76839128	GM12891	blood:	n/a
22	chr2:76839078-76839128	SAEC	small airway:	n/a
23	chr2:76880863-76880913	HRE	kidney:	n/a
24	chr2:76806361-76806411	AG10803	skin:	n/a
25	chr2:76806361-76806411	NH-A	brain:	n/a
26	chr2:76880863-76880913	ProgFib	skin:	n/a
27	chr2:76806361-76806411	PFSK-1	brain:	n/a
28	chr2:76880863-76880913	AoSMC	blood vessel:	n/a
29	chr2:76839078-76839128	Caco-2	colon:	n/a
30	chr2:76839078-76839128	AG10803	skin:	n/a
31	chr2:76806361-76806411	NT2-D1	testis:	n/a
32	chr2:76880863-76880913	HRCEpiC	kidney:	n/a
33	chr2:76806361-76806411	NHDF-neo	bronchial:	n/a
34	chr2:76806361-76806411	ECC-1	luminal epithelium:	n/a
35	chr2:76806361-76806411	U87	brain:	n/a
36	chr2:76839078-76839128	BE2_C	brain:	n/a
37	chr2:76839078-76839128	AG09309	skin:	n/a
38	chr2:76839078-76839128	NH-A	brain:	n/a
39	chr2:76806361-76806411	PANC-1	pancreas:	n/a
40	chr2:76806361-76806411	PrEC	prostate:	n/a
41	chr2:76806361-76806411	HNPCEpiC	eye:	n/a
42	chr2:76839078-76839128	CMK	blood:	n/a
43	chr2:76839078-76839128	ovcar-3	ovarian:	n/a
44	chr2:76806361-76806411	AG04450	lung:	fetal
45	chr2:76880863-76880913	Hepatocyte	liver:	n/a
46	chr2:76880863-76880913	GM12892	blood:	n/a
47	chr2:76806361-76806411	LNCaP	prostate:	n/a
48	chr2:76806361-76806411	HCF	heart:	n/a
49	chr2:76806361-76806411	GM06990	blood:	n/a
50	chr2:76806361-76806411	HL-60	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:76837968..76839669-chr2:76845469..76848246,2	MCF-7	breast:
2	chr2:76837968..76839669-chr2:76845469..76848246,2	MCF-7	breast:
3	chr2:76014514..76015446-chr2:76826422..76827585,4	MCF-7	breast:
4	chr2:76123697..76124563-chr2:76826531..76827162,2	MCF-7	breast:
5	chr2:76424788..76425711-chr2:76826568..76827565,9	MCF-7	breast:
6	chr2:75957100..75957649-chr2:76826627..76827405,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-LRRTM4-5	chr2:76822539-76822804	NONHSAT071821
2	lnc-MRPL19-18	chr2:76807165-76807212	NONHSAT071820
3	lnc-MRPL19-18	chr2:76814741-76814827	NONHSAT071820
4	lnc-MRPL19-17	chr2:76802439-76802582	NONHSAT071819
5	lnc-MRPL19-18	chr2:76806776-76806856	NONHSAT071820
6	lnc-MRPL19-18	chr2:76802723-76802739	NONHSAT071820
7	lnc-MRPL19-17	chr2:76805608-76805913	NONHSAT071819

No data

Variant related genes	Relation type
RN7SKP164	TF binding region
RN7SKP164	CpG island

Extended variants
information (count: 4719 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:4719 , 50 per page) page: 1 2 3 4 5 6 7 ... 95

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7592517	chr2:76777279-76777280	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs6547091	chr2:76777301-76777302	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs182089462	chr2:76777316-76777317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372395790	chr2:76777432-76777433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142989065	chr2:76777439-76777440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77614603	chr2:76777449-76777450	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs573710256	chr2:76777462-76777463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs570273291	chr2:76777493-76777494	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs146114471	chr2:76777513-76777514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs558687139	chr2:76777530-76777531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs577158737	chr2:76777569-76777570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185137444	chr2:76777581-76777582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs77575832	chr2:76777616-76777617	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs141599702	chr2:76777667-76777668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs115977291	chr2:76777672-76777673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs189883395	chr2:76777683-76777684	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs563470063	chr2:76777703-76777704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs150720937	chr2:76777768-76777769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138987378	chr2:76777794-76777795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs563968723	chr2:76777803-76777804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs528093195	chr2:76777843-76777844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs541458189	chr2:76777887-76777888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs546747919	chr2:76777912-76777913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs199772351	chr2:76777917-76777918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs367789475	chr2:76777947-76777948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs149456937	chr2:76777976-76777977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs181151031	chr2:76778004-76778005	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs528968032	chr2:76778061-76778062	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79278045	chr2:76778108-76778109	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs144187360	chr2:76778115-76778116	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs537384341	chr2:76778196-76778197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs186463877	chr2:76778205-76778206	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191540236	chr2:76778206-76778207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs534681743	chr2:76778222-76778223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs577486151	chr2:76778232-76778233	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs4853259	chr2:76778258-76778259	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs559933932	chr2:76778274-76778275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs183358684	chr2:76778290-76778291	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs535896446	chr2:76778291-76778292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs556888047	chr2:76778297-76778298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72810862	chr2:76778461-76778462	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs545829043	chr2:76778474-76778475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs116534283	chr2:76778475-76778476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs563892388	chr2:76778533-76778534	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531386409	chr2:76778590-76778591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs572911842	chr2:76778635-76778636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187508687	chr2:76778644-76778645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540251863	chr2:76778705-76778706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs561619902	chr2:76778729-76778730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs374966128	chr2:76778790-76778791	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Lung cancer	18438408	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Seminomas	18059402	CNVD
Testicular germ cell tumor	18059402	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Renal cell carcinoma	18765545	CNVD
Myxofibrosarcoma	16751306	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	21251322	CNVD
Mental retardation	17124404	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17440070	CNVD
Myelofibrosis	22110671	CNVD
Attention deficit hyperactivity disorder	21324949	CNVD
Breast cancer	16272173	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	20531469	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:76776000-76807000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr2:76778000-76780600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr2:76780600-76781000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr2:76783000-76783600	Enhancers	Liver	Liver
5	chr2:76788800-76789400	Enhancers	ES-I3 Cell Line	embryonic stem cell
6	chr2:76789400-76793800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr2:76790800-76793000	Enhancers	Liver	Liver
8	chr2:76792000-76792400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr2:76792000-76792400	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr2:76792000-76792400	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr2:76793000-76796600	Weak transcription	Liver	Liver
12	chr2:76793400-76793800	Weak transcription	HUES48 Cell Line	embryonic stem cell
13	chr2:76793800-76794200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr2:76793800-76795200	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
15	chr2:76793800-76798800	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr2:76794200-76794800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
17	chr2:76794800-76795400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
18	chr2:76795000-76797200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr2:76795200-76797000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:76795400-76796800	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr2:76796600-76796800	Enhancers	Liver	Liver
22	chr2:76796800-76797200	Active TSS	Pancreatic Islets	Pancreatic Islet
23	chr2:76796800-76797600	Flanking Active TSS	Liver	Liver
24	chr2:76796800-76797800	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr2:76796800-76800000	Enhancers	HUES6 Cell Line	embryonic stem cell
26	chr2:76796800-76800600	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr2:76797000-76797600	Enhancers	Pancreas	Pancrea
28	chr2:76797000-76797800	Enhancers	Fetal Heart	heart
29	chr2:76797000-76800800	Enhancers	ES-I3 Cell Line	embryonic stem cell
30	chr2:76797200-76797600	Enhancers	H9 Cell Line	embryonic stem cell
31	chr2:76797200-76797600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr2:76797400-76797600	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr2:76797600-76798600	Weak transcription	H9 Cell Line	embryonic stem cell
34	chr2:76797600-76798800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr2:76797600-76800000	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:76797800-76798200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr2:76798200-76799000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
38	chr2:76798200-76799400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr2:76798200-76800000	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr2:76798600-76799200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:76798600-76799200	Enhancers	H9 Cell Line	embryonic stem cell
42	chr2:76798600-76799800	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr2:76798800-76799000	Enhancers	H1 Cell Line	embryonic stem cell
44	chr2:76798800-76800000	Enhancers	iPS-18 Cell Line	embryonic stem cell
45	chr2:76798800-76800600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr2:76799000-76799800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
47	chr2:76799000-76799800	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr2:76799200-76799600	Weak transcription	H9 Cell Line	embryonic stem cell
49	chr2:76799200-76800000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr2:76799600-76800200	Enhancers	H9 Cell Line	embryonic stem cell

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