Variant report

Variant	nsv875761
Chromosome Location	chr2:209912108-210222004
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1369)
CpG islands
(count:1099)
Chromatin interactive
region (count:23)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1369 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:210124579-210124799	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:210072884-210073171	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:210199194-210199529	HepG2	liver:	n/a	n/a
4	ATF2	chr2:210186318-210186834	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr2:210169543-210170102	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr2:210171807-210172894	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr2:210170292-210170919	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr2:210184445-210184782	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr2:210173019-210173382	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr2:210187849-210188112	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr2:209986398-209986748	GM12878	blood:	n/a	n/a
12	BCL11A	chr2:210002834-210003125	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr2:209986484-209986694	GM12878	blood:	n/a	chr2:209986623-209986632
14	BHLHE40	chr2:210044277-210044280	K562	blood:	n/a	n/a
15	BHLHE40	chr2:209954270-209954587	K562	blood:	n/a	n/a
16	BRCA1	chr2:210187552-210187641	H1-hESC	embryonic stem cell:	n/a	n/a
17	CCNT2	chr2:210209564-210209759	K562	blood:	n/a	n/a
18	CEBPB	chr2:209925339-209925581	HepG2	liver:	n/a	chr2:209925520-209925531 chr2:209925518-209925529
19	CEBPB	chr2:210012758-210013109	MCF-7	breast:	n/a	chr2:210012850-210012861
20	CEBPB	chr2:210124019-210124022	H1-hESC	embryonic stem cell:	n/a	n/a
21	CEBPB	chr2:210012736-210013044	MCF-7	breast:	n/a	chr2:210012850-210012861
22	CEBPB	chr2:210101138-210101177	A549	lung:	n/a	n/a
23	CEBPB	chr2:210142577-210142657	H1-hESC	embryonic stem cell:	n/a	chr2:210142597-210142608
24	CEBPB	chr2:209935544-209935609	HepG2	liver:	n/a	chr2:209935580-209935591
25	CEBPB	chr2:210142593-210142635	HepG2	liver:	n/a	chr2:210142597-210142608
26	CEBPB	chr2:210037462-210037833	MCF-7	breast:	n/a	n/a
27	CEBPB	chr2:210012739-210013035	A549	lung:	n/a	chr2:210012850-210012861
28	CEBPB	chr2:210124464-210124933	HepG2	liver:	n/a	chr2:210124634-210124645
29	CEBPB	chr2:210012705-210013038	HepG2	liver:	n/a	chr2:210012850-210012861
30	CEBPB	chr2:209955124-209955199	A549	lung:	n/a	chr2:209955162-209955175 chr2:209955162-209955173
31	CEBPB	chr2:210012759-210013067	Hela-S3	cervix:	n/a	chr2:210012850-210012861
32	CEBPB	chr2:210101027-210101431	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr2:210123893-210124124	HepG2	liver:	n/a	chr2:210123953-210123966
34	CEBPB	chr2:210040328-210040574	HepG2	liver:	n/a	n/a
35	CEBPB	chr2:210011134-210011376	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr2:210076466-210076728	K562	blood:	n/a	n/a
37	CEBPB	chr2:209925435-209925658	A549	lung:	n/a	chr2:209925520-209925531 chr2:209925518-209925529
38	CEBPB	chr2:210012714-210013010	IMR90	lung:	n/a	chr2:210012850-210012861
39	CHD1	chr2:210169887-210170251	H1-hESC	embryonic stem cell:	n/a	n/a
40	CHD2	chr2:210190951-210191138	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chr2:210187594-210187825	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD2	chr2:210187850-210187855	GM12878	blood:	n/a	n/a
43	CHD2	chr2:210185992-210186034	H1-hESC	embryonic stem cell:	n/a	n/a
44	CHD2	chr2:210170260-210170826	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr2:210188420-210189235	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chr2:210171614-210172789	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chr2:210184578-210184634	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr2:210189745-210190235	H1-hESC	embryonic stem cell:	n/a	n/a
49	CHD2	chr2:210025669-210025708	HepG2	liver:	n/a	n/a
50	CREB1	chr2:210172211-210172743	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:210010124-210010174	ECC-1	luminal epithelium:	n/a
2	chr2:210010124-210010174	ECC-1	luminal epithelium:	n/a
3	chr2:210010124-210010174	GM12878	blood:	n/a
4	chr2:209981979-209982029	GM12878	blood:	n/a
5	chr2:210010124-210010174	HL-60	blood:	n/a
6	chr2:210003746-210003796	AG04450	lung:	fetal
7	chr2:209981979-209982029	HCF	heart:	n/a
8	chr2:210187995-210188045	HRE	kidney:	n/a
9	chr2:210074276-210074326	HL-60	blood:	n/a
10	chr2:210074359-210074409	HAEpiC	amniotic membrane:	n/a
11	chr2:210187995-210188045	NB4	blood:	n/a
12	chr2:210074020-210074070	AG04450	lung:	fetal
13	chr2:210010193-210010243	NT2-D1	testis:	n/a
14	chr2:210008092-210008142	GM12892	blood:	n/a
15	chr2:210010193-210010243	NHBE	bronchial:	n/a
16	chr2:210010325-210010375	GM12892	blood:	n/a
17	chr2:210187995-210188045	HRPEpiC	eye:	n/a
18	chr2:210077015-210077065	NH-A	brain:	n/a
19	chr2:210077015-210077065	SK-N-SH	brain:	n/a
20	chr2:210010228-210010278	HEK293	kidney:	embryo
21	chr2:210074020-210074070	BE2_C	brain:	n/a
22	chr2:210179077-210179127	H1-hESC	embryonic stem cell:	embryo
23	chr2:210187995-210188045	GM19239	blood:	n/a
24	chr2:210074276-210074326	CMK	blood:	n/a
25	chr2:210074276-210074326	NHDF-neo	bronchial:	n/a
26	chr2:210010325-210010375	K562	blood:	n/a
27	chr2:210171336-210171386	NB4	blood:	n/a
28	chr2:209981979-209982029	BJ	skin:	n/a
29	chr2:210171336-210171386	PrEC	prostate:	n/a
30	chr2:210221981-210222031	HCPEpiC	choroid plexus:	n/a
31	chr2:210195731-210195781	BJ	skin:	n/a
32	chr2:210010325-210010375	ECC-1	luminal epithelium:	n/a
33	chr2:210187995-210188045	MCF-7	breast:	n/a
34	chr2:210221981-210222031	CMK	blood:	n/a
35	chr2:210011147-210011197	HCPEpiC	choroid plexus:	n/a
36	chr2:210010325-210010375	HCT-116	colon:	n/a
37	chr2:210003746-210003796	MCF-7	breast:	n/a
38	chr2:210187995-210188045	BE2_C	brain:	n/a
39	chr2:210074276-210074326	HPAEpiC	pulmonary alveolar:	n/a
40	chr2:210074276-210074326	HCT-116	colon:	n/a
41	chr2:209981979-209982029	H1-hESC	embryonic stem cell:	embryo
42	chr2:210187995-210188045	GM06990	blood:	n/a
43	chr2:210003746-210003796	AG09309	skin:	n/a
44	chr2:210195731-210195781	AG09319	gingival:	n/a
45	chr2:210074276-210074326	HCM	heart:	n/a
46	chr2:210010325-210010375	BE2_C	brain:	n/a
47	chr2:210008092-210008142	AG04449	skin:	fetal
48	chr2:210074020-210074070	HEK293	kidney:	embryo
49	chr2:210010124-210010174	Hepatocyte	liver:	n/a
50	chr2:210195731-210195781	ECC-1	luminal epithelium:	n/a

(count:23 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr2:209684819..209685719-chr2:210072640..210073642,4	MCF-7	breast:
2	chr2:209923719..209926042-chr2:209927287..209929588,2	K562	blood:
3	chr2:209962059..209962630-chr8:88609274..88609836,2	MCF-7	breast:
4	chr2:209911421..209913579-chr2:209913671..209915928,2	MCF-7	breast:
5	chr2:210218244..210221102-chr2:210263734..210265265,2	MCF-7	breast:
6	chr2:209272192..209273114-chr2:210195894..210196720,4	MCF-7	breast:
7	chr2:209331311..209331890-chr2:209961645..209962198,2	MCF-7	breast:
8	chr2:210209759..210211803-chr2:210221775..210224209,2	MCF-7	breast:
9	chr2:209911421..209913579-chr2:209913671..209915928,2	MCF-7	breast:
10	chr2:210200748..210201382-chr2:210288131..210289052,2	MCF-7	breast:
11	chr2:209330724..209331762-chr2:210072595..210073780,7	MCF-7	breast:
12	chr2:210199940..210202124-chr2:210287908..210290540,2	MCF-7	breast:
13	chr2:209685011..209685630-chr2:210072613..210073438,3	MCF-7	breast:
14	chr2:209684682..209685324-chr2:209961529..209962479,2	MCF-7	breast:
15	chr2:209272322..209273071-chr2:210072607..210073525,2	K562	blood:
16	chr2:209521522..209522845-chr2:210072588..210073484,4	MCF-7	breast:
17	chr2:210198810..210200359-chr2:210287858..210289386,45	MCF-7	breast:
18	chr2:210209759..210211803-chr2:210221775..210224209,2	MCF-7	breast:
19	chr2:210198908..210199771-chr2:210420683..210421740,3	MCF-7	breast:
20	chr2:209923719..209926042-chr2:209927287..209929588,2	K562	blood:
21	chr2:209984149..209984947-chr8:69366893..69367419,2	MCF-7	breast:
22	chr2:210198604..210199864-chr2:210288126..210289099,23	MCF-7	breast:
23	chr2:209736383..209738259-chr2:210013383..210015250,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-IDH1-4	chr2:210074012-210074172	NONHSAT076653
2	lnc-IDH1-4	chr2:210044077-210044193	NONHSAT076653
3	lnc-MAP2-1	chr2:210175597-210175857	NONHSAT076656
4	lnc-IDH1-4	chr2:209914528-209914662	NONHSAT076653
5	lnc-MAP2-1	chr2:210169839-210169985	NONHSAT076656
6	lnc-MAP2-1	chr2:210164256-210164664	NONHSAT076656
7	lnc-MAP2-1	chr2:210188124-210190281	NONHSAT076656
8	lnc-IDH1-4	chr2:210016969-210017110	NONHSAT076653
9	lnc-MAP2-3	chr2:210043690-210045847	NONHSAT076655
10	lnc-MAP2-1	chr2:210186322-210186519	NONHSAT076656

No data

Variant related genes	Relation type
HSPA8P6	TF binding region
MEAF6P1	TF binding region
CRYGFP	TF binding region
PKP4P1	TF binding region
HSPA8P6	CpG island
MEAF6P1	CpG island
CRYGFP	CpG island
PKP4P1	CpG island
ENSG00000227430	chromatin interactions
ENSG00000078018	chromatin interactions

Extended variants
information (count: 7165 )
Associated
traits (count: 57 )

Variant overlapped rSNPs/rCNVs (count:7165 , 50 per page) page: 1 2 3 4 5 6 7 ... 144

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545832864	chr2:209912251-209912252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs147901106	chr2:209912332-209912333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs369632365	chr2:209912368-209912369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs545048062	chr2:209912424-209912425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574873256	chr2:209912455-209912456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs201550606	chr2:209912464-209912465	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs373694452	chr2:209912466-209912467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs187398203	chr2:209912489-209912490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs542133326	chr2:209912537-209912538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562016898	chr2:209912606-209912607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs527915956	chr2:209912642-209912643	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141598857	chr2:209912679-209912680	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs570964673	chr2:209912716-209912717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs10195762	chr2:209912729-209912730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs533263544	chr2:209912762-209912763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs550201418	chr2:209912769-209912770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570072035	chr2:209912854-209912855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs535811256	chr2:209912863-209912864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs576822130	chr2:209912907-209912908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs192816204	chr2:209912963-209912964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs184857778	chr2:209912972-209912973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs79065442	chr2:209912990-209912991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs189311958	chr2:209913000-209913001	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs577272783	chr2:209913013-209913014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs576925007	chr2:209913024-209913025	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs545592310	chr2:209913032-209913033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs543951493	chr2:209913085-209913086	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555805607	chr2:209913106-209913107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs181021978	chr2:209913124-209913125	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs185610065	chr2:209913196-209913197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs562077834	chr2:209913200-209913201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs189649051	chr2:209913204-209913205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs181581192	chr2:209913250-209913251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs544704666	chr2:209913298-209913299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs150458153	chr2:209913308-209913309	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs529534348	chr2:209913336-209913337	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs533525773	chr2:209913369-209913370	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs58821250	chr2:209913465-209913466	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs185937026	chr2:209913495-209913496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529331638	chr2:209913543-209913544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs549390089	chr2:209913578-209913579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs138252182	chr2:209913585-209913586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs533850348	chr2:209913600-209913601	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs116424715	chr2:209913605-209913606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368889958	chr2:209913681-209913682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs190652179	chr2:209913701-209913702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs149645524	chr2:209913718-209913719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs199866413	chr2:209913740-209913741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs57800601	chr2:209913741-209913742	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs73986694	chr2:209913742-209913743	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:57)

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
Acute lymphoblastic leukemia	22237106	CNVD
Developmental delay	21147756	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:209912200-209912600	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr2:209912600-209912800	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr2:209912800-209916200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr2:209916200-209916600	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr2:209928600-209929200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr2:209929000-209929200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr2:209929400-209932200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
8	chr2:209932200-209932400	Enhancers	iPS-15b Cell Line	embryonic stem cell
9	chr2:209932400-209932800	Enhancers	H1 Cell Line	embryonic stem cell
10	chr2:209932400-209933000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr2:209932400-209933200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr2:209934600-209934800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr2:209941600-209942600	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr2:209941800-209942400	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr2:209942200-209942400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr2:209943200-209943600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr2:209944800-209945000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr2:209945200-209945400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr2:209945400-209949000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chr2:209945400-209949200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr2:209947800-209949200	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr2:209949000-209950000	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr2:209949200-209949600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr2:209949200-209950000	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:209949200-209950200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr2:209950000-209951400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
27	chr2:209950000-209955600	Weak transcription	HUES48 Cell Line	embryonic stem cell
28	chr2:209950200-209955800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr2:209951000-209952000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr2:209951400-209951800	Enhancers	Placenta Amnion	Placenta Amnion
31	chr2:209951400-209952200	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr2:209951600-209952000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr2:209952400-209953400	Enhancers	Pancreatic Islets	Pancreatic Islet
34	chr2:209955600-209956200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr2:209955600-209956600	Enhancers	NHEK	skin
36	chr2:209955800-209956200	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chr2:209955800-209956200	Enhancers	Fetal Brain Female	brain
38	chr2:209958800-209959200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr2:209958800-209959200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr2:209958800-209959200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr2:209958800-209959600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
42	chr2:209959000-209959200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chr2:209959200-209962000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr2:209959200-209962000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
45	chr2:209962000-209962200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr2:209962000-209962200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr2:209962200-209962400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr2:209975400-209976400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr2:209975400-209977000	Enhancers	HUES6 Cell Line	embryonic stem cell
50	chr2:209975400-209977200	Enhancers	iPS-18 Cell Line	embryonic stem cell

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