Variant report

Variant	esv2753335
Chromosome Location	chr2:212322858-212424019
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:280)
CpG islands
(count:184)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:280 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr2:212363692-212363815	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr2:212341207-212341417	HepG2	liver:	n/a	chr2:212341327-212341338
3	CEBPB	chr2:212342486-212342714	IMR90	lung:	n/a	chr2:212342524-212342537 chr2:212342524-212342535
4	CEBPB	chr2:212357683-212357979	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr2:212342586-212342717	H1-hESC	embryonic stem cell:	n/a	n/a
6	CEBPB	chr2:212328998-212329141	H1-hESC	embryonic stem cell:	n/a	chr2:212329055-212329066 chr2:212329055-212329068 chr2:212329056-212329067 chr2:212329055-212329066 chr2:212329055-212329068
7	CEBPB	chr2:212357692-212358007	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:212328902-212329207	A549	lung:	n/a	chr2:212329055-212329066 chr2:212329055-212329068 chr2:212329056-212329067 chr2:212329055-212329066 chr2:212329055-212329068
9	CEBPB	chr2:212328905-212329225	HepG2	liver:	n/a	chr2:212329055-212329066 chr2:212329055-212329068 chr2:212329056-212329067 chr2:212329055-212329066 chr2:212329055-212329068
10	CEBPB	chr2:212342377-212343109	HepG2	liver:	n/a	chr2:212342524-212342537 chr2:212342524-212342535
11	CEBPB	chr2:212363646-212363764	HepG2	liver:	n/a	chr2:212363681-212363692
12	CEBPB	chr2:212377956-212378135	HepG2	liver:	n/a	chr2:212378026-212378037
13	CEBPB	chr2:212357678-212358005	A549	lung:	n/a	n/a
14	CEBPB	chr2:212342461-212342725	A549	lung:	n/a	chr2:212342524-212342537 chr2:212342524-212342535
15	CEBPB	chr2:212355456-212355746	HepG2	liver:	n/a	chr2:212355578-212355589 chr2:212355580-212355591
16	CEBPB	chr2:212357657-212358022	IMR90	lung:	n/a	n/a
17	CEBPB	chr2:212375518-212375530	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr2:212372106-212372296	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:212363575-212363885	H1-hESC	embryonic stem cell:	n/a	chr2:212363681-212363692
20	CEBPB	chr2:212414722-212414939	HepG2	liver:	n/a	chr2:212414816-212414827
21	CHD2	chr2:212363638-212363823	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr2:212368687-212368856	K562	blood:	n/a	n/a
23	CTCF	chr2:212368700-212368850	NB4	blood:	n/a	n/a
24	CTCF	chr2:212368680-212368830	HPAF	blood vessel:	n/a	n/a
25	CTCF	chr2:212368720-212368870	AG09309	skin:	n/a	n/a
26	CTCF	chr2:212368707-212368832	GM10248	blood:	n/a	n/a
27	CTCF	chr2:212368700-212368850	Caco-2	colon:	n/a	n/a
28	CTCF	chr2:212368720-212368870	GM12865	blood:	n/a	n/a
29	CTCF	chr2:212368691-212368854	HepG2	liver:	n/a	n/a
30	CTCF	chr2:212368713-212368825	GM20000	blood:	n/a	n/a
31	CTCF	chr2:212368680-212368830	Hela-S3	cervix:	n/a	n/a
32	CTCF	chr2:212368633-212368869	GM12892	blood:	n/a	n/a
33	CTCF	chr2:212368691-212368835	A549	lung:	n/a	n/a
34	CTCF	chr2:212368720-212368870	SK-N-SH_RA	brain:	n/a	n/a
35	CTCF	chr2:212368682-212368877	Gliobla	brain:	n/a	n/a
36	CTCF	chr2:212368680-212368830	BE2_C	brain:	n/a	n/a
37	CTCF	chr2:212368720-212368870	WERI-Rb-1	eye:	n/a	n/a
38	CTCF	chr2:212368600-212368750	NHDF-neo	bronchial:	n/a	n/a
39	CTCF	chr2:212368700-212368850	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr2:212340360-212340510	BE2_C	brain:	n/a	chr2:212340385-212340406 chr2:212340383-212340401
41	CTCF	chr2:212368700-212368850	GM12866	blood:	n/a	n/a
42	CTCF	chr2:212368640-212368790	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr2:212368691-212368839	NHEK	skin:	n/a	n/a
44	CTCF	chr2:212340341-212340430	MCF-7	breast:	n/a	chr2:212340385-212340406 chr2:212340383-212340401
45	CTCF	chr2:212368747-212368867	LNCaP	prostate:	n/a	n/a
46	CTCF	chr2:212368720-212368870	GM06990	blood:	n/a	n/a
47	CTCF	chr2:212368480-212368630	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr2:212368640-212368790	GM12872	blood:	n/a	n/a
49	CTCF	chr2:212368720-212368870	GM12864	blood:	n/a	n/a
50	CTCF	chr2:212368720-212368870	GM12878	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:212388373-212388423	HEEpiC	esophagus:	n/a
2	chr2:212388373-212388423	HEEpiC	esophagus:	n/a
3	chr2:212389424-212389474	HCM	heart:	n/a
4	chr2:212389424-212389474	Hepatocyte	liver:	n/a
5	chr2:212389424-212389474	NB4	blood:	n/a
6	chr2:212388373-212388423	Jurkat	blood:	n/a
7	chr2:212388373-212388423	LNCaP	prostate:	n/a
8	chr2:212388373-212388423	Caco-2	colon:	n/a
9	chr2:212389424-212389474	HEEpiC	esophagus:	n/a
10	chr2:212389424-212389474	GM19239	blood:	n/a
11	chr2:212388373-212388423	GM12891	blood:	n/a
12	chr2:212388373-212388423	SK-N-MC	brain:	n/a
13	chr2:212388373-212388423	HRPEpiC	eye:	n/a
14	chr2:212388373-212388423	HCPEpiC	choroid plexus:	n/a
15	chr2:212388373-212388423	T-47D	breast:	n/a
16	chr2:212389424-212389474	GM12878	blood:	n/a
17	chr2:212363715-212363765	SK-N-SH_RA	brain:	n/a
18	chr2:212363715-212363765	ProgFib	skin:	n/a
19	chr2:212363715-212363765	HRPEpiC	eye:	n/a
20	chr2:212388373-212388423	NH-A	brain:	n/a
21	chr2:212363715-212363765	SKMC	muscle:	n/a
22	chr2:212389424-212389474	ovcar-3	ovarian:	n/a
23	chr2:212389424-212389474	AG04449	skin:	fetal
24	chr2:212363715-212363765	AG04449	skin:	fetal
25	chr2:212389424-212389474	AG09309	skin:	n/a
26	chr2:212389424-212389474	ECC-1	luminal epithelium:	n/a
27	chr2:212388373-212388423	RPTEC	kidney:	n/a
28	chr2:212389424-212389474	Caco-2	colon:	n/a
29	chr2:212389424-212389474	HIPEpiC	eye:	n/a
30	chr2:212389424-212389474	HAEpiC	amniotic membrane:	n/a
31	chr2:212388373-212388423	HCT-116	colon:	n/a
32	chr2:212388373-212388423	HCF	heart:	n/a
33	chr2:212363715-212363765	MCF-7	breast:	n/a
34	chr2:212388373-212388423	HAEpiC	amniotic membrane:	n/a
35	chr2:212389424-212389474	BE2_C	brain:	n/a
36	chr2:212363715-212363765	GM19239	blood:	n/a
37	chr2:212363715-212363765	NHBE	bronchial:	n/a
38	chr2:212389424-212389474	SK-N-SH	brain:	n/a
39	chr2:212389424-212389474	U87	brain:	n/a
40	chr2:212363715-212363765	LNCaP	prostate:	n/a
41	chr2:212388373-212388423	AG09309	skin:	n/a
42	chr2:212388373-212388423	HRE	kidney:	n/a
43	chr2:212363715-212363765	AG09309	skin:	n/a
44	chr2:212363715-212363765	HIPEpiC	eye:	n/a
45	chr2:212388373-212388423	MCF-7	breast:	n/a
46	chr2:212389424-212389474	K562	blood:	n/a
47	chr2:212388373-212388423	IMR90	lung:	fetal
48	chr2:212388373-212388423	HNPCEpiC	eye:	n/a
49	chr2:212363715-212363765	SAEC	small airway:	n/a
50	chr2:212389424-212389474	HCF	heart:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:
2	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
3	chr2:212288710..212290756-chr2:212380740..212383126,2	MCF-7	breast:
4	chr17:57933020..57935872-chr2:212325257..212328116,2	MCF-7	breast:
5	chr2:212352611..212354767-chr2:212356529..212358511,2	MCF-7	breast:
6	chr2:212328628..212332038-chr2:212332518..212335674,3	MCF-7	breast:
7	chr2:212318807..212321033-chr2:212328093..212330095,2	MCF-7	breast:
8	chr2:212408584..212410240-chr2:212416395..212418822,2	MCF-7	breast:
9	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
10	chr2:212366946..212368723-chr2:212370212..212371913,2	K562	blood:
11	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:
12	chr2:212320246..212322831-chr2:212376794..212379145,2	MCF-7	breast:
13	chr2:212328628..212332038-chr2:212332518..212335674,3	MCF-7	breast:
14	chr2:212349648..212351176-chr2:212354643..212357480,2	MCF-7	breast:
15	chr1:203274022..203274758-chr2:212363047..212363985,2	MCF-7	breast:

No data

Variant related genes	Relation type
RNA5SP119	TF binding region
RNA5SP119	CpG island
ENSG00000159388	chromatin interactions
ENSG00000233791	chromatin interactions

Extended variants
information (count: 4210 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:4210 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2033646	chr2:212322858-212322859	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs10221842	chr2:212322887-212322888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs2887993	chr2:212322909-212322910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150817178	chr2:212322911-212322912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs370990339	chr2:212322921-212322922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs4673619	chr2:212322936-212322937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs59473927	chr2:212322995-212322996	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs78126977	chr2:212322996-212322997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs544831320	chr2:212323014-212323015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs188224947	chr2:212323024-212323025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs575310414	chr2:212323077-212323078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs373113766	chr2:212323113-212323114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568916939	chr2:212323148-212323149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544505260	chr2:212323149-212323150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192554678	chr2:212323153-212323154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs536363776	chr2:212323176-212323177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547950365	chr2:212323180-212323181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs375121690	chr2:212323186-212323187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs61241208	chr2:212323211-212323212	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs566539763	chr2:212323212-212323213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532226032	chr2:212323268-212323269	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs533587212	chr2:212323269-212323270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs147755365	chr2:212323272-212323273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs35420885	chr2:212323282-212323283	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs537199131	chr2:212323293-212323294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs184484418	chr2:212323352-212323353	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs140914524	chr2:212323384-212323385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs142834751	chr2:212323401-212323402	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371735192	chr2:212323402-212323403	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs4311002	chr2:212323420-212323421	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs555739604	chr2:212323471-212323472	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs144848419	chr2:212323506-212323507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs536279016	chr2:212323591-212323592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs574423786	chr2:212323624-212323625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs539294384	chr2:212323629-212323630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552926949	chr2:212323633-212323634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs577107617	chr2:212323793-212323794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs186557481	chr2:212323819-212323820	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs374768615	chr2:212323824-212323825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538762464	chr2:212323851-212323852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192570989	chr2:212323857-212323858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs558741428	chr2:212323865-212323866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs575399850	chr2:212323878-212323879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs145505501	chr2:212323883-212323884	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs554889708	chr2:212323920-212323921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs184651401	chr2:212323923-212323924	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148842220	chr2:212323950-212323951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540262248	chr2:212324037-212324038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs560215835	chr2:212324048-212324049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs532112558	chr2:212324121-212324122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	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
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	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
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Schizophrenia	20838587	CNVD
Breast cancer	17661082	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	18990708	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:213 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:212320000-212328000	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr2:212320400-212324200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr2:212320400-212332800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr2:212322400-212327400	Weak transcription	Pancreas	Pancrea
5	chr2:212324200-212324400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr2:212324400-212330600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr2:212327800-212328800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr2:212328000-212328400	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr2:212328000-212328800	Enhancers	HUES6 Cell Line	embryonic stem cell
10	chr2:212328000-212328800	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr2:212328000-212328800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr2:212328000-212329000	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr2:212328000-212329200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
14	chr2:212328200-212328400	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr2:212328200-212328400	Enhancers	H9 Cell Line	embryonic stem cell
16	chr2:212328200-212328800	Enhancers	H1 Cell Line	embryonic stem cell
17	chr2:212328200-212328800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr2:212328400-212330400	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr2:212328600-212328800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr2:212328600-212333800	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr2:212328800-212329800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr2:212328800-212330400	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr2:212328800-212332800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
24	chr2:212328800-212333000	Weak transcription	HUES6 Cell Line	embryonic stem cell
25	chr2:212328800-212333600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr2:212328800-212333800	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr2:212329000-212333000	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr2:212329800-212331000	Enhancers	iPS-18 Cell Line	embryonic stem cell
29	chr2:212329800-212331400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr2:212330200-212331000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr2:212330400-212331000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr2:212330400-212331200	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr2:212330400-212331200	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr2:212330600-212330800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr2:212330600-212330800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr2:212330600-212331400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr2:212331000-212333200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr2:212331000-212333600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
39	chr2:212331000-212334200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr2:212331200-212333600	Weak transcription	HUES64 Cell Line	embryonic stem cell
41	chr2:212331200-212333600	Weak transcription	Cortex derived primary cultured neurospheres	brain
42	chr2:212331400-212332800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr2:212331400-212333000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr2:212332000-212332600	Enhancers	Aorta	Aorta
45	chr2:212332000-212334600	Enhancers	Fetal Heart	heart
46	chr2:212332600-212335600	Weak transcription	Aorta	Aorta
47	chr2:212332800-212333000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chr2:212332800-212334400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:212332800-212335200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr2:212332800-212335800	Enhancers	iPS-20b Cell Line	embryonic stem cell

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