Variant report

Variant	esv2757843
Chromosome Location	chr2:184368473-184558908
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:480)
CpG islands
(count:305)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:480 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr2:184397205-184397664	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr2:184395190-184395495	GM12878	blood:	n/a	n/a
3	BATF	chr2:184395172-184395470	GM12878	blood:	n/a	n/a
4	BCL11A	chr2:184397325-184397593	H1-hESC	embryonic stem cell:	n/a	n/a
5	BCL11A	chr2:184543663-184543896	H1-hESC	embryonic stem cell:	n/a	n/a
6	BCL11A	chr2:184543626-184543951	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr2:184406481-184406835	HepG2	liver:	n/a	n/a
8	BHLHE40	chr2:184395173-184395644	GM12878	blood:	n/a	n/a
9	CEBPB	chr2:184495787-184496126	HepG2	liver:	n/a	chr2:184495965-184495976 chr2:184495888-184495901
10	CEBPB	chr2:184507144-184507344	IMR90	lung:	n/a	chr2:184507200-184507211
11	CEBPB	chr2:184406844-184407126	A549	lung:	n/a	n/a
12	CEBPB	chr2:184507062-184507394	HepG2	liver:	n/a	chr2:184507200-184507211
13	CEBPB	chr2:184431871-184432245	IMR90	lung:	n/a	chr2:184432078-184432089
14	CEBPB	chr2:184406466-184407109	HepG2	liver:	n/a	n/a
15	CEBPB	chr2:184431896-184432225	HepG2	liver:	n/a	chr2:184432078-184432089
16	CEBPB	chr2:184398647-184398825	HepG2	liver:	n/a	chr2:184398671-184398682
17	CEBPB	chr2:184387339-184387348	HepG2	liver:	n/a	n/a
18	CEBPB	chr2:184533456-184533671	HepG2	liver:	n/a	n/a
19	CEBPB	chr2:184431962-184432233	A549	lung:	n/a	chr2:184432078-184432089
20	CEBPB	chr2:184495812-184496080	A549	lung:	n/a	chr2:184495965-184495976 chr2:184495888-184495901
21	CEBPB	chr2:184406790-184407126	IMR90	lung:	n/a	n/a
22	CEBPB	chr2:184507035-184507391	H1-hESC	embryonic stem cell:	n/a	chr2:184507200-184507211
23	CEBPB	chr2:184495870-184496106	IMR90	lung:	n/a	chr2:184495965-184495976 chr2:184495888-184495901
24	CEBPB	chr2:184507110-184507516	A549	lung:	n/a	chr2:184507200-184507211
25	CEBPB	chr2:184431962-184432138	K562	blood:	n/a	chr2:184432078-184432089
26	CEBPB	chr2:184526429-184526718	HepG2	liver:	n/a	n/a
27	CHD2	chr2:184470101-184470122	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr2:184543632-184543942	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr2:184375942-184375997	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr2:184397195-184397670	H1-hESC	embryonic stem cell:	n/a	n/a
31	CTCF	chr2:184382960-184383110	HMEC	breast:	n/a	n/a
32	CTCF	chr2:184416300-184416450	A549	lung:	n/a	n/a
33	CTCF	chr2:184475540-184475690	HRE	kidney:	n/a	n/a
34	CTCF	chr2:184548923-184549018	GM13977	blood:	n/a	n/a
35	CTCF	chr2:184478499-184478574	LNCaP	prostate:	n/a	n/a
36	CTCF	chr2:184475600-184475750	MCF-7	breast:	n/a	n/a
37	CTCF	chr2:184473708-184473734	MCF-7	breast:	n/a	n/a
38	CTCF	chr2:184382985-184383083	LNCaP	prostate:	n/a	n/a
39	CTCF	chr2:184475620-184475770	HCT-116	colon:	n/a	n/a
40	CTCF	chr2:184475614-184475691	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chr2:184473640-184473790	Caco-2	colon:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
42	CTCF	chr2:184473670-184473703	GM19238	blood:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
43	CTCF	chr2:184475580-184475730	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr2:184473571-184473788	HepG2	liver:	n/a	chr2:184473684-184473702 chr2:184473679-184473700
45	CTCF	chr2:184373002-184373093	LNCaP	prostate:	n/a	n/a
46	CTCF	chr2:184382905-184383194	GM12878	blood:	n/a	n/a
47	CTCF	chr2:184481883-184481966	GM13976	blood:	n/a	n/a
48	CTCF	chr2:184397400-184397550	HEEpiC	esophagus:	n/a	n/a
49	CTCF	chr2:184464920-184465070	HRE	kidney:	n/a	n/a
50	CTCF	chr2:184415579-184415594	GM20000	blood:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:184475542-184475592	HCT-116	colon:	n/a
2	chr2:184395412-184395462	NHDF-neo	bronchial:	n/a
3	chr2:184472883-184472933	A549	lung:	n/a
4	chr2:184475542-184475592	MCF10A-Er-Src	breast:	n/a
5	chr2:184475542-184475592	BE2_C	brain:	n/a
6	chr2:184531153-184531203	Hepatocyte	liver:	n/a
7	chr2:184472883-184472933	LNCaP	prostate:	n/a
8	chr2:184475542-184475592	Jurkat	blood:	n/a
9	chr2:184402122-184402172	HEEpiC	esophagus:	n/a
10	chr2:184395412-184395462	HPAEpiC	pulmonary alveolar:	n/a
11	chr2:184395412-184395462	AG09319	gingival:	n/a
12	chr2:184472883-184472933	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:184472883-184472933	AG04450	lung:	fetal
14	chr2:184402122-184402172	MCF10A-Er-Src	breast:	n/a
15	chr2:184472883-184472933	HUVEC	blood vessel:	n/a
16	chr2:184475542-184475592	PANC-1	pancreas:	n/a
17	chr2:184472883-184472933	Hela-S3	cervix:	n/a
18	chr2:184472883-184472933	HEEpiC	esophagus:	n/a
19	chr2:184531153-184531203	HEEpiC	esophagus:	n/a
20	chr2:184531153-184531203	SK-N-MC	brain:	n/a
21	chr2:184395412-184395462	Jurkat	blood:	n/a
22	chr2:184475542-184475592	HCF	heart:	n/a
23	chr2:184472883-184472933	GM19239	blood:	n/a
24	chr2:184531153-184531203	GM19239	blood:	n/a
25	chr2:184475542-184475592	GM12878	blood:	n/a
26	chr2:184395412-184395462	CMK	blood:	n/a
27	chr2:184531153-184531203	SAEC	small airway:	n/a
28	chr2:184531153-184531203	HUVEC	blood vessel:	n/a
29	chr2:184531153-184531203	HEK293	kidney:	embryo
30	chr2:184395412-184395462	MCF10A-Er-Src	breast:	n/a
31	chr2:184395412-184395462	HRCEpiC	kidney:	n/a
32	chr2:184472883-184472933	AG10803	skin:	n/a
33	chr2:184395412-184395462	PrEC	prostate:	n/a
34	chr2:184531153-184531203	AG10803	skin:	n/a
35	chr2:184531153-184531203	HepG2	liver:	n/a
36	chr2:184402122-184402172	SK-N-MC	brain:	n/a
37	chr2:184395412-184395462	ovcar-3	ovarian:	n/a
38	chr2:184475542-184475592	NT2-D1	testis:	n/a
39	chr2:184395412-184395462	BJ	skin:	n/a
40	chr2:184402122-184402172	AG10803	skin:	n/a
41	chr2:184531153-184531203	NH-A	brain:	n/a
42	chr2:184531153-184531203	HPAEpiC	pulmonary alveolar:	n/a
43	chr2:184402122-184402172	GM12891	blood:	n/a
44	chr2:184395412-184395462	ProgFib	skin:	n/a
45	chr2:184402122-184402172	NB4	blood:	n/a
46	chr2:184472883-184472933	GM12878	blood:	n/a
47	chr2:184475542-184475592	SAEC	small airway:	n/a
48	chr2:184472883-184472933	HCPEpiC	choroid plexus:	n/a
49	chr2:184472883-184472933	BJ	skin:	n/a
50	chr2:184531153-184531203	BJ	skin:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:184533926..184535731-chr2:184543881..184546242,2	MCF-7	breast:
2	chr2:184533926..184535731-chr2:184543881..184546242,2	MCF-7	breast:
3	chr2:184476716..184479514-chr2:184486721..184488223,2	K562	blood:
4	chr2:184441021..184443496-chr2:184443583..184445745,2	MCF-7	breast:
5	chr2:184420912..184422678-chr2:184425750..184427792,2	K562	blood:
6	chr2:184441021..184443496-chr2:184443583..184445745,2	MCF-7	breast:
7	chr2:184420912..184422678-chr2:184425750..184427792,2	K562	blood:
8	chr2:184476716..184479514-chr2:184486721..184488223,2	K562	blood:
9	chr2:184416367..184418824-chr2:184421256..184423003,2	K562	blood:
10	chr2:184387652..184388652-chr5:19684075..19684575,2	MCF-7	breast:
11	chr2:184357852..184360567-chr2:184368359..184370734,2	K562	blood:
12	chr18:21061627..21062127-chr2:184416573..184417102,2	MCF-7	breast:
13	chr2:184416367..184418824-chr2:184421256..184423003,2	K562	blood:

No data

Variant related genes	Relation type
CACYBPP2	TF binding region
CACYBPP2	CpG island

Extended variants
information (count: 3762 )
Associated
traits (count: 54 )

Variant overlapped rSNPs/rCNVs (count:3762 , 50 per page) page: 1 2 3 4 5 6 7 ... 76

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs34017793	chr2:184372037-184372038	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10931084	chr2:184372041-184372042	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs578024994	chr2:184372053-184372054	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs368649044	chr2:184372061-184372062	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs529862192	chr2:184372069-184372070	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs563833248	chr2:184372076-184372077	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs137946707	chr2:184372096-184372097	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs188005396	chr2:184372098-184372099	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs559179179	chr2:184372142-184372143	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs180917250	chr2:184372157-184372158	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs185368580	chr2:184372158-184372159	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs142417609	chr2:184372159-184372160	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs530770908	chr2:184372164-184372165	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs550385728	chr2:184372183-184372184	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs546969657	chr2:184372251-184372252	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs567403580	chr2:184372271-184372272	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs536246628	chr2:184372293-184372294	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs546629739	chr2:184372310-184372311	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs189768479	chr2:184372326-184372327	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs374770322	chr2:184372351-184372352	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs548375143	chr2:184372386-184372387	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs181880722	chr2:184372391-184372392	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs537694764	chr2:184372414-184372415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs535651803	chr2:184372463-184372464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs13386376	chr2:184372478-184372479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs574086865	chr2:184372513-184372514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs13386454	chr2:184372514-184372515	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs555901201	chr2:184372539-184372540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs143572106	chr2:184372561-184372562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs112909407	chr2:184372567-184372568	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572764869	chr2:184372596-184372597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13414287	chr2:184372598-184372599	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs538303709	chr2:184372599-184372600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs191921633	chr2:184372600-184372601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530617912	chr2:184372635-184372636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183268807	chr2:184372641-184372642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs560782049	chr2:184372661-184372662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs529817568	chr2:184372671-184372672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs558188978	chr2:184372678-184372679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs112147576	chr2:184372781-184372782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186509794	chr2:184372792-184372793	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189761750	chr2:184372809-184372810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs13402618	chr2:184372817-184372818	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs537207161	chr2:184372871-184372872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6748303	chr2:184372910-184372911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147238186	chr2:184372916-184372917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs377249390	chr2:184372917-184372918	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs553758745	chr2:184372921-184372922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs553082489	chr2:184372942-184372943	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs572881660	chr2:184372962-184372963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:54)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	18522746	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Lung cancer	18438408	CNVD
Glioblastoma	21080181	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Facial dysmorphism	20548289	CNVD
Mental retardation	20548289	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
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Sudden cardiac death	19188705	CNVD
Autism	19329560	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Obesity	21131291	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:330 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:184372000-184372400	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
2	chr2:184372400-184374800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:184373400-184374400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:184374200-184375400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
5	chr2:184374400-184376800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:184375000-184375400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr2:184376400-184377000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
8	chr2:184376800-184378200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr2:184378200-184385000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr2:184381200-184381400	Enhancers	Rectal Mucosa Donor 31	rectum
11	chr2:184382800-184383200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr2:184383200-184383600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr2:184383400-184383800	Enhancers	Pancreas	Pancrea
14	chr2:184383400-184385200	Enhancers	Fetal Intestine Small	intestine
15	chr2:184383600-184383800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr2:184383800-184385000	Weak transcription	Pancreas	Pancrea
17	chr2:184383800-184393800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr2:184384000-184384600	Enhancers	Psoas Muscle	Psoas
19	chr2:184384000-184385200	Enhancers	Fetal Intestine Large	intestine
20	chr2:184385000-184385200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr2:184385000-184385800	Enhancers	Pancreas	Pancrea
22	chr2:184385200-184385600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr2:184385600-184386000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr2:184386400-184387800	Enhancers	Pancreatic Islets	Pancreatic Islet
25	chr2:184387400-184387800	Enhancers	Fetal Heart	heart
26	chr2:184392600-184392800	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
27	chr2:184392800-184393600	Weak transcription	HUES6 Cell Line	embryonic stem cell
28	chr2:184393200-184394200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr2:184393600-184394400	Enhancers	H9 Cell Line	embryonic stem cell
30	chr2:184393600-184395000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr2:184393600-184397600	Enhancers	HUES6 Cell Line	embryonic stem cell
32	chr2:184393600-184398200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr2:184393800-184394400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr2:184393800-184394800	Enhancers	H1 Cell Line	embryonic stem cell
35	chr2:184393800-184395600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr2:184393800-184395600	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr2:184393800-184397200	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:184393800-184397600	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chr2:184394200-184394600	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
40	chr2:184394400-184395000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr2:184394400-184397800	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr2:184394600-184397200	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr2:184394800-184397600	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr2:184395000-184395200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr2:184395000-184395200	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
46	chr2:184395200-184395400	Enhancers	HUES48 Cell Line	embryonic stem cell
47	chr2:184395200-184397400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr2:184395400-184397000	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
49	chr2:184395600-184396800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
50	chr2:184395600-184397200	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell

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