Variant report

Variant	esv2757790
Chromosome Location	chr2:35237743-35404984
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:553)
CpG islands
(count:0)
Chromatin interactive
region (count:21)
LncRNA
region (count:41)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:553 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF3	chr2:35305906-35306470	A549	lung:	n/a	n/a
2	BCL11A	chr2:35401795-35402176	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr2:35399964-35400197	Hela-S3	cervix:	n/a	n/a
4	CCNT2	chr2:35338484-35338775	K562	blood:	n/a	n/a
5	CEBPB	chr2:35375163-35375530	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr2:35268498-35268587	A549	lung:	n/a	n/a
7	CEBPB	chr2:35255529-35255814	HepG2	liver:	n/a	chr2:35255644-35255655
8	CEBPB	chr2:35376002-35376339	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr2:35305797-35306568	A549	lung:	n/a	chr2:35306013-35306030
10	CEBPB	chr2:35350260-35350409	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:35306030-35306381	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr2:35367584-35367813	A549	lung:	n/a	n/a
13	CEBPB	chr2:35305751-35306362	A549	lung:	n/a	chr2:35306013-35306030
14	CEBPB	chr2:35312055-35312217	A549	lung:	n/a	n/a
15	CEBPB	chr2:35381648-35381980	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr2:35305982-35306458	A549	lung:	n/a	chr2:35306013-35306030
17	CEBPB	chr2:35305183-35305324	HepG2	liver:	n/a	chr2:35305190-35305202 chr2:35305241-35305252
18	CEBPB	chr2:35354834-35355117	A549	lung:	n/a	n/a
19	CEBPB	chr2:35268351-35268632	HepG2	liver:	n/a	chr2:35268466-35268477
20	CEBPB	chr2:35392695-35392991	HepG2	liver:	n/a	chr2:35392847-35392858
21	CEBPB	chr2:35303761-35303856	HepG2	liver:	n/a	chr2:35303788-35303799
22	CEBPB	chr2:35375309-35375511	HepG2	liver:	n/a	n/a
23	CEBPB	chr2:35354790-35355067	IMR90	lung:	n/a	n/a
24	CEBPB	chr2:35392691-35392950	A549	lung:	n/a	chr2:35392847-35392858
25	CHD2	chr2:35399982-35400231	Hela-S3	cervix:	n/a	n/a
26	CTCF	chr2:35261140-35261290	GM12872	blood:	n/a	n/a
27	CTCF	chr2:35393559-35393705	LNCaP	prostate:	n/a	chr2:35393622-35393640 chr2:35393624-35393645
28	CTCF	chr2:35261080-35261230	A549	lung:	n/a	n/a
29	CTCF	chr2:35393540-35393690	HRE	kidney:	n/a	chr2:35393622-35393640 chr2:35393624-35393645
30	CTCF	chr2:35326580-35326730	MCF-7	breast:	n/a	n/a
31	CTCF	chr2:35339993-35340099	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr2:35261067-35261193	Medullo	brain:	n/a	n/a
33	CTCF	chr2:35326702-35326779	Gliobla	brain:	n/a	n/a
34	CTCF	chr2:35261038-35261230	Pancreas_OC	pancreas:	n/a	n/a
35	CTCF	chr2:35351016-35351098	GM13976	blood:	n/a	n/a
36	CTCF	chr2:35339971-35340099	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr2:35261010-35261246	LNCaP	prostate:	n/a	n/a
38	CTCF	chr2:35324475-35324708	MCF-7	breast:	n/a	n/a
39	CTCF	chr2:35339920-35340070	WERI-Rb-1	eye:	n/a	n/a
40	CTCF	chr2:35261060-35261210	HAc	cerebellar:	n/a	n/a
41	CTCF	chr2:35339929-35340140	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr2:35393579-35393677	GM12878	blood:	n/a	chr2:35393622-35393640 chr2:35393624-35393645
43	CTCF	chr2:35337895-35337962	MCF-7	breast:	n/a	n/a
44	CTCF	chr2:35261007-35261347	SK-N-SH	brain:	n/a	n/a
45	CTCF	chr2:35261000-35261150	GM12871	blood:	n/a	n/a
46	CTCF	chr2:35326620-35326770	MCF-7	breast:	n/a	n/a
47	CTCF	chr2:35393300-35393450	HRE	kidney:	n/a	n/a
48	CTCF	chr2:35284871-35284891	GM20000	blood:	n/a	n/a
49	CTCF	chr2:35393554-35393703	MCF-7	breast:	n/a	chr2:35393622-35393640 chr2:35393624-35393645
50	CTCF	chr2:35339940-35340090	GM12867	blood:	n/a	n/a

No data

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:35324525..35325781-chr2:35339538..35340526,4	MCF-7	breast:
2	chr2:35390044..35391720-chr2:35398125..35400924,2	K562	blood:
3	chr2:35336496..35338395-chr2:35339571..35342545,2	MCF-7	breast:
4	chr2:35393157..35394354-chr2:35634679..35636139,8	MCF-7	breast:
5	chr2:35286578..35288607-chr2:35290647..35293256,2	K562	blood:
6	chr2:35385075..35387812-chr2:35387950..35390253,3	K562	blood:
7	chr2:35230910..35232963-chr2:35235828..35238432,2	K562	blood:
8	chr2:35286578..35288607-chr2:35290647..35293256,2	K562	blood:
9	chr2:35322123..35325054-chr2:35336591..35340112,3	MCF-7	breast:
10	chr2:35359597..35360193-chr6:115017299..115018148,2	MCF-7	breast:
11	chr2:35392713..35393658-chr2:35567942..35568821,2	MCF-7	breast:
12	chr2:35324525..35325781-chr2:35339538..35340526,4	MCF-7	breast:
13	chr2:35393272..35393934-chr2:35653413..35654042,2	MCF-7	breast:
14	chr2:35385075..35387812-chr2:35387950..35390253,3	K562	blood:
15	chr2:35322123..35325054-chr2:35336591..35340112,3	MCF-7	breast:
16	chr2:35336496..35338395-chr2:35339571..35342545,2	MCF-7	breast:
17	chr2:35342917..35344665-chr2:35344772..35347578,2	MCF-7	breast:
18	chr2:34237421..34238380-chr2:35339556..35340362,2	MCF-7	breast:
19	chr2:35342917..35344665-chr2:35344772..35347578,2	MCF-7	breast:
20	chr2:35390044..35391720-chr2:35398125..35400924,2	K562	blood:
21	chr2:35393099..35394069-chr2:35567966..35568823,5	MCF-7	breast:

(count:41 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CRIM1-1	chr2:35387842-35387905	ENSG00000226994.3
2	lnc-CRIM1-1	chr2:35387842-35387905	ENSG00000226994.3
3	lnc-CRIM1-1	chr2:35387842-35387905	ENSG00000226994.3
4	lnc-CRIM1-1	chr2:35387997-35388125	ENSG00000226994.3
5	lnc-CRIM1-1	chr2:35387997-35388125	ENSG00000226994.3
6	lnc-CRIM1-1	chr2:35388867-35389031	ENSG00000226994.3
7	lnc-CRIM1-1	chr2:35384613-35384694	ENSG00000226994.3
8	lnc-CRIM1-1	chr2:35387997-35388125	ENSG00000226994.3
9	lnc-CRIM1-1	chr2:35384613-35385344	ENSG00000226994.3
10	lnc-CRIM1-1	chr2:35384150-35384221	ENSG00000226994.3
11	lnc-RASGRP3-15	chr2:35238117-35238198	NONHSAT070041
12	lnc-CRIM1-1	chr2:35389194-35389308	ENSG00000226994.3
13	lnc-CRIM1-1	chr2:35387997-35388125	ENSG00000226994.3
14	lnc-CRIM1-1	chr2:35399595-35399715	ENSG00000226994.3
15	lnc-CRIM1-1	chr2:35384150-35384221	ENSG00000226994.3
16	lnc-CRIM1-1	chr2:35387997-35388125	ENSG00000226994.3
17	lnc-CRIM1-1	chr2:35397858-35398097	ENSG00000226994.3
18	lnc-CRIM1-1	chr2:35387842-35387905	ENSG00000226994.3
19	lnc-CRIM1-1	chr2:35384150-35384830	ENSG00000226994.3
20	lnc-CRIM1-1	chr2:35395244-35395415	ENSG00000226994.3
21	lnc-CRIM1-1	chr2:35387997-35388125	ENSG00000226994.3
22	lnc-CRIM1-1	chr2:35384150-35384221	XLOC_001425
23	lnc-CRIM1-1	chr2:35387855-35387905	ENSG00000226994.3
24	lnc-CRIM1-1	chr2:35384150-35384221	ENSG00000226994.3
25	lnc-CRIM1-1	chr2:35389194-35389308	ENSG00000226994.3
26	lnc-CRIM1-1	chr2:35389194-35389308	ENSG00000226994.3
27	lnc-CRIM1-1	chr2:35384665-35384694	ENSG00000226994.3
28	lnc-CRIM1-1	chr2:35384613-35384694	XLOC_001425
29	lnc-CRIM1-1	chr2:35387852-35387905	ENSG00000226994.3
30	lnc-CRIM1-1	chr2:35387842-35387905	XLOC_001425
31	lnc-CRIM1-1	chr2:35387842-35387905	ENSG00000226994.3
32	lnc-CRIM1-1	chr2:35397858-35398190	ENSG00000226994.3
33	lnc-CRIM1-1	chr2:35387997-35388178	XLOC_001425
34	lnc-CRIM1-1	chr2:35384150-35384221	ENSG00000226994.3
35	lnc-CRIM1-1	chr2:35397858-35398245	ENSG00000226994.3
36	lnc-CRIM1-1	chr2:35384613-35384694	ENSG00000226994.3
37	lnc-RASGRP3-15	chr2:35241346-35241409	NONHSAT070041
38	lnc-CRIM1-1	chr2:35384613-35384694	ENSG00000226994.3
39	lnc-CRIM1-1	chr2:35387997-35388125	ENSG00000226994.3
40	lnc-CRIM1-1	chr2:35384150-35384221	ENSG00000226994.3
41	lnc-RASGRP3-15	chr2:35241501-35241682	NONHSAT070041

No data

Variant related genes	Relation type
ENSG00000226994	TF binding region
NAPEPLD	miRNA target sites

Extended variants
information (count: 945 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:945 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs182408935	chr2:35238139-35238140	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs373182286	chr2:35238143-35238144	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs548896549	chr2:35238166-35238167	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs574008094	chr2:35241355-35241356	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs542798428	chr2:35241376-35241377	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs377327130	chr2:35241387-35241388	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs7599426	chr2:35241398-35241399	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs181293983	chr2:35241406-35241407	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs564704139	chr2:35241513-35241514	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs527315763	chr2:35241515-35241516	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs547003191	chr2:35241525-35241526	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs560384164	chr2:35241534-35241535	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs531010047	chr2:35241592-35241593	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs143793823	chr2:35241653-35241654	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs189803231	chr2:35241675-35241676	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs569473476	chr2:35241676-35241677	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs534384203	chr2:35263054-35263055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs554453076	chr2:35263066-35263067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs79958963	chr2:35263096-35263097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs536716095	chr2:35263106-35263107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs556403364	chr2:35263152-35263153	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs576338719	chr2:35263171-35263172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs77269765	chr2:35263174-35263175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141303503	chr2:35263180-35263181	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs568601551	chr2:35263274-35263275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs187507604	chr2:35263328-35263329	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536053906	chr2:35263334-35263335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs540803399	chr2:35263414-35263415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs560780949	chr2:35263434-35263435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs193195601	chr2:35263435-35263436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543479664	chr2:35263466-35263467	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs563241226	chr2:35263485-35263486	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs74529406	chr2:35263539-35263540	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs184696260	chr2:35263584-35263585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571969185	chr2:35263597-35263598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs557518537	chr2:35263602-35263603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs189969440	chr2:35263648-35263649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs144957981	chr2:35263651-35263652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs567831344	chr2:35263668-35263669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536449024	chr2:35263679-35263680	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs556578642	chr2:35263704-35263705	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570090892	chr2:35263708-35263709	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539018066	chr2:35263714-35263715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs558554669	chr2:35263725-35263726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs116771538	chr2:35263742-35263743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562985430	chr2:35263749-35263750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs530755042	chr2:35263828-35263829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs554468011	chr2:35263876-35263877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs574530684	chr2:35263879-35263880	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs79504865	chr2:35264016-35264017	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	17603634	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	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
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Bladder cancer	21909424	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Breast cancer	21364760	CNVD
Wilms tumour	21544195	CNVD
Non-small cell lung cancer	18927303	CNVD
Hereditary gingival fibromatosis	19633868	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Neurocytoma	17123091	CNVD
Autism	22495309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:64 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:35263000-35263200	Enhancers	Esophagus	oesophagus
2	chr2:35263200-35265200	Weak transcription	Esophagus	oesophagus
3	chr2:35265200-35265400	Enhancers	Esophagus	oesophagus
4	chr2:35265400-35265600	Weak transcription	Esophagus	oesophagus
5	chr2:35292400-35293200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr2:35305000-35307600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
7	chr2:35305200-35305600	Enhancers	NHDF-Ad	bronchial
8	chr2:35305200-35305800	Enhancers	Muscle Satellite Cultured Cells	--
9	chr2:35305200-35306600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr2:35305400-35305800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr2:35305400-35306000	Active TSS	A549	lung
12	chr2:35305600-35306200	Enhancers	NH-A	brain
13	chr2:35305800-35306200	Flanking Active TSS	Muscle Satellite Cultured Cells	--
14	chr2:35305800-35306400	Enhancers	Fetal Lung	lung
15	chr2:35306000-35306200	Flanking Active TSS	A549	lung
16	chr2:35306000-35306400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr2:35306200-35307200	Weak transcription	A549	lung
18	chr2:35306200-35307400	Enhancers	Muscle Satellite Cultured Cells	--
19	chr2:35306600-35307000	Enhancers	Pancreatic Islets	Pancreatic Islet
20	chr2:35307200-35307400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr2:35307200-35307600	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr2:35307200-35307600	Enhancers	H9 Cell Line	embryonic stem cell
23	chr2:35307200-35307600	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr2:35307200-35307600	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr2:35307200-35307600	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:35307200-35307600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr2:35307200-35307800	Enhancers	A549	lung
28	chr2:35307400-35307800	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr2:35307800-35309800	Weak transcription	A549	lung
30	chr2:35309800-35310200	Enhancers	A549	lung
31	chr2:35313400-35314000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr2:35314000-35314200	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:35317200-35318000	Enhancers	A549	lung
34	chr2:35317200-35318200	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr2:35317800-35318200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr2:35317800-35318400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr2:35338000-35338600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr2:35340000-35341600	Enhancers	Esophagus	oesophagus
39	chr2:35350200-35350600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr2:35365200-35365600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr2:35386000-35386400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr2:35400200-35400400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
43	chr2:35400200-35400600	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr2:35400200-35400800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
45	chr2:35400400-35400800	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
46	chr2:35400400-35400800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
47	chr2:35400400-35401000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
48	chr2:35400600-35400800	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
49	chr2:35401400-35401800	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
50	chr2:35401600-35401800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell

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