Variant report

Variant	nsv584042
Chromosome Location	chr2:188678973-188793238
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:188684551-188684613	HepG2	liver:	n/a	n/a
2	ARID3A	chr2:188729881-188730106	HepG2	liver:	n/a	n/a
3	ARID3A	chr2:188707985-188708297	HepG2	liver:	n/a	n/a
4	BACH1	chr2:188689902-188690134	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr2:188782257-188782549	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr2:188733916-188734173	GM12878	blood:	n/a	n/a
7	CEBPB	chr2:188705494-188705694	HepG2	liver:	n/a	n/a
8	CEBPB	chr2:188786896-188787007	Hela-S3	cervix:	n/a	chr2:188786933-188786944
9	CEBPB	chr2:188776944-188777121	K562	blood:	n/a	chr2:188777047-188777060 chr2:188776985-188776996 chr2:188777047-188777060
10	CEBPB	chr2:188697541-188697879	K562	blood:	n/a	chr2:188697730-188697739 chr2:188697728-188697741 chr2:188697728-188697739
11	CEBPB	chr2:188777758-188777958	IMR90	lung:	n/a	n/a
12	CEBPB	chr2:188697226-188697904	HepG2	liver:	n/a	chr2:188697730-188697739 chr2:188697728-188697741 chr2:188697728-188697739
13	CEBPB	chr2:188786769-188787111	HepG2	liver:	n/a	chr2:188786933-188786944
14	CEBPB	chr2:188782297-188782583	IMR90	lung:	n/a	n/a
15	CEBPB	chr2:188786784-188787094	IMR90	lung:	n/a	chr2:188786933-188786944
16	CEBPB	chr2:188776975-188777410	H1-hESC	embryonic stem cell:	n/a	chr2:188777047-188777060 chr2:188776985-188776996 chr2:188777047-188777060
17	CEBPB	chr2:188776902-188777154	HepG2	liver:	n/a	chr2:188777047-188777060 chr2:188776985-188776996 chr2:188777047-188777060
18	CEBPB	chr2:188777330-188777442	A549	lung:	n/a	n/a
19	CEBPB	chr2:188762259-188762509	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr2:188691096-188691299	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr2:188697561-188697865	IMR90	lung:	n/a	chr2:188697730-188697739 chr2:188697728-188697741 chr2:188697728-188697739
22	CEBPB	chr2:188776944-188777152	IMR90	lung:	n/a	chr2:188777047-188777060 chr2:188776985-188776996 chr2:188777047-188777060
23	CEBPB	chr2:188786821-188787055	A549	lung:	n/a	chr2:188786933-188786944
24	CEBPB	chr2:188788958-188789299	MCF-7	breast:	n/a	n/a
25	CEBPB	chr2:188724170-188724362	HepG2	liver:	n/a	chr2:188724258-188724269
26	CEBPB	chr2:188683622-188683880	HepG2	liver:	n/a	chr2:188683751-188683762
27	CHD1	chr2:188707846-188708434	IMR90	lung:	n/a	n/a
28	CTCF	chr2:188708014-188708270	Pancreas_OC	pancreas:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
29	CTCF	chr2:188708020-188708170	GM12873	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
30	CTCF	chr2:188708128-188708177	NHEK	skin:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
31	CTCF	chr2:188707325-188708634	A549	lung:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
32	CTCF	chr2:188708080-188708230	GM12866	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
33	CTCF	chr2:188708060-188708210	AG04449	skin:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
34	CTCF	chr2:188708050-188708269	Lung_OC	lung:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
35	CTCF	chr2:188708080-188708230	GM12869	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
36	CTCF	chr2:188707961-188708361	GM12878	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
37	CTCF	chr2:188708080-188708230	Hela-S3	cervix:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
38	CTCF	chr2:188705560-188705710	AoAF	blood vessel:	n/a	n/a
39	CTCF	chr2:188708340-188708490	GM12869	blood:	n/a	n/a
40	CTCF	chr2:188708091-188708227	LNCaP	prostate:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
41	CTCF	chr2:188708035-188708261	MCF-7	breast:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
42	CTCF	chr2:188708020-188708170	AG04450	lung:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
43	CTCF	chr2:188708060-188708210	HMEC	breast:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
44	CTCF	chr2:188708100-188708250	GM12801	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
45	CTCF	chr2:188708080-188708230	GM12868	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
46	CTCF	chr2:188708059-188708275	GM10248	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
47	CTCF	chr2:188707979-188708239	ECC-1	luminal epithelium:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
48	CTCF	chr2:188708101-188708229	GM20000	blood:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
49	CTCF	chr2:188708060-188708210	HFF-Myc	foreskin:	n/a	chr2:188708144-188708165 chr2:188708151-188708164 chr2:188708149-188708167
50	CTCF	chr2:188708415-188708452	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:188782251-188782301	K562	blood:	n/a
2	chr2:188782251-188782301	K562	blood:	n/a
3	chr2:188754840-188754890	GM06990	blood:	n/a
4	chr2:188782251-188782301	Hela-S3	cervix:	n/a
5	chr2:188782251-188782301	PrEC	prostate:	n/a
6	chr2:188782251-188782301	H1-hESC	embryonic stem cell:	embryo
7	chr2:188754840-188754890	Hepatocyte	liver:	n/a
8	chr2:188689981-188690031	HRPEpiC	eye:	n/a
9	chr2:188689981-188690031	AG09309	skin:	n/a
10	chr2:188754840-188754890	GM12892	blood:	n/a
11	chr2:188782251-188782301	GM12878	blood:	n/a
12	chr2:188782251-188782301	HPAEpiC	pulmonary alveolar:	n/a
13	chr2:188754840-188754890	GM12878	blood:	n/a
14	chr2:188754840-188754890	HCF	heart:	n/a
15	chr2:188754840-188754890	HRCEpiC	kidney:	n/a
16	chr2:188754840-188754890	GM19239	blood:	n/a
17	chr2:188754840-188754890	A549	lung:	n/a
18	chr2:188689981-188690031	GM12878	blood:	n/a
19	chr2:188782251-188782301	SK-N-SH	brain:	n/a
20	chr2:188754840-188754890	PrEC	prostate:	n/a
21	chr2:188782251-188782301	HepG2	liver:	n/a
22	chr2:188754840-188754890	PFSK-1	brain:	n/a
23	chr2:188689981-188690031	SKMC	muscle:	n/a
24	chr2:188782251-188782301	GM06990	blood:	n/a
25	chr2:188689981-188690031	Caco-2	colon:	n/a
26	chr2:188782251-188782301	U87	brain:	n/a
27	chr2:188689981-188690031	HRE	kidney:	n/a
28	chr2:188782251-188782301	BE2_C	brain:	n/a
29	chr2:188689981-188690031	NH-A	brain:	n/a
30	chr2:188782251-188782301	LNCaP	prostate:	n/a
31	chr2:188689981-188690031	NB4	blood:	n/a
32	chr2:188689981-188690031	NHBE	bronchial:	n/a
33	chr2:188689981-188690031	PANC-1	pancreas:	n/a
34	chr2:188689981-188690031	IMR90	lung:	fetal
35	chr2:188782251-188782301	PFSK-1	brain:	n/a
36	chr2:188782251-188782301	NT2-D1	testis:	n/a
37	chr2:188782251-188782301	HEEpiC	esophagus:	n/a
38	chr2:188754840-188754890	AG09319	gingival:	n/a
39	chr2:188782251-188782301	T-47D	breast:	n/a
40	chr2:188782251-188782301	NHBE	bronchial:	n/a
41	chr2:188754840-188754890	HIPEpiC	eye:	n/a
42	chr2:188754840-188754890	HCPEpiC	choroid plexus:	n/a
43	chr2:188782251-188782301	SK-N-MC	brain:	n/a
44	chr2:188754840-188754890	HL-60	blood:	n/a
45	chr2:188782251-188782301	RPTEC	kidney:	n/a
46	chr2:188754840-188754890	HPAEpiC	pulmonary alveolar:	n/a
47	chr2:188754840-188754890	LNCaP	prostate:	n/a
48	chr2:188689981-188690031	HCM	heart:	n/a
49	chr2:188782251-188782301	HIPEpiC	eye:	n/a
50	chr2:188754840-188754890	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:188778237..188780956-chr2:188785376..188787506,2	MCF-7	breast:
2	chr2:188717832..188720223-chr2:188721480..188723340,2	K562	blood:
3	chr2:188776029..188778640-chr2:188796709..188799566,2	MCF-7	breast:
4	chr2:188747783..188749370-chr2:188752482..188755177,2	K562	blood:
5	chr2:188707921..188708505-chr2:189376811..189377638,2	MCF-7	breast:
6	chr2:188445739..188446515-chr2:188708197..188708735,2	MCF-7	breast:
7	chr2:188445783..188446859-chr2:188707667..188708674,8	MCF-7	breast:
8	chr2:188736660..188738467-chr2:188741573..188744493,2	MCF-7	breast:
9	chr2:188710121..188711814-chr2:188979120..188982025,2	MCF-7	breast:
10	chr2:188364379..188365187-chr2:188708060..188708991,2	MCF-7	breast:
11	chr2:188704815..188707426-chr2:188716735..188719605,2	MCF-7	breast:
12	chr2:188736660..188738467-chr2:188741573..188744493,2	MCF-7	breast:
13	chr2:188711161..188713691-chr2:188716532..188718506,2	MCF-7	breast:
14	chr2:188364448..188365318-chr2:188707678..188708407,3	K562	blood:
15	chr2:188523465..188524329-chr2:188707490..188708173,2	MCF-7	breast:
16	chr2:188717832..188720223-chr2:188721480..188723340,2	K562	blood:
17	chr10:79342547..79345269-chr2:188716021..188718292,2	MCF-7	breast:
18	chr2:188695020..188696926-chr2:188699233..188701652,2	K562	blood:
19	chr2:188747783..188749370-chr2:188752482..188755177,2	K562	blood:
20	chr2:188695020..188696926-chr2:188699233..188701652,2	K562	blood:
21	chr2:188778237..188780956-chr2:188785376..188787506,2	MCF-7	breast:
22	chr2:188711161..188713691-chr2:188716532..188718506,2	MCF-7	breast:
23	chr2:188704815..188707426-chr2:188716735..188719605,2	MCF-7	breast:
24	chr2:188712201..188714788-chr2:189156773..189159131,2	MCF-7	breast:
25	chr2:188707924..188708424-chr2:189233846..189234774,2	MCF-7	breast:

Variant related genes	Relation type
ST13P2	TF binding region
ST13P2	CpG island
ENSG00000144366	chromatin interactions

Extended variants
information (count: 2898 )
Associated
traits (count: 51 )

Variant overlapped rSNPs/rCNVs (count:2898 , 50 per page) page: 1 2 3 4 5 6 7 ... 58

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6742191	chr2:188678973-188678974	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs138315588	chr2:188679012-188679013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs6713430	chr2:188679064-188679065	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547786829	chr2:188679076-188679077	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs533452001	chr2:188679135-188679136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs566406028	chr2:188679182-188679183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs34258832	chr2:188679241-188679242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs188609261	chr2:188679271-188679272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547814313	chr2:188679365-188679366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs569374143	chr2:188679412-188679413	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs551604134	chr2:188679453-188679454	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs536769683	chr2:188679502-188679503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs569997844	chr2:188679505-188679506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs76469611	chr2:188679518-188679519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs558670011	chr2:188679617-188679618	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12618942	chr2:188679626-188679627	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs534857501	chr2:188679630-188679631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112065620	chr2:188679659-188679660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556047057	chr2:188679692-188679693	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs145107899	chr2:188679714-188679715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs543027630	chr2:188679715-188679716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs561283262	chr2:188679735-188679736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs576578368	chr2:188679756-188679757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192963624	chr2:188679772-188679773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535381130	chr2:188679864-188679865	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs532589307	chr2:188679893-188679894	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs553587774	chr2:188679895-188679896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs548019361	chr2:188679899-188679900	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs559776079	chr2:188679912-188679913	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs530339501	chr2:188679919-188679920	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs547752601	chr2:188679937-188679938	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs34347770	chr2:188679944-188679945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs569311681	chr2:188679987-188679988	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs185336714	chr2:188680037-188680038	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs551975256	chr2:188680054-188680055	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs570571885	chr2:188680082-188680083	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs138920076	chr2:188680091-188680092	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs553165837	chr2:188680119-188680120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs568327255	chr2:188680146-188680147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs535771519	chr2:188680151-188680152	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs377119230	chr2:188680175-188680176	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs114303908	chr2:188680177-188680178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543840975	chr2:188680184-188680185	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs558782392	chr2:188680202-188680203	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs577297345	chr2:188680220-188680221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs188506838	chr2:188680302-188680303	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs73038565	chr2:188680315-188680316	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs75191025	chr2:188680373-188680374	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs542125038	chr2:188680391-188680392	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563678709	chr2:188680393-188680394	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:51)

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
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
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
Urothelial carcinoma	21177765	CNVD
Intellectual disability	22102821	CNVD
Tetralogy of Fallot	22912587	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:256 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:188677200-188681400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:188679800-188680200	Enhancers	HepG2	liver
3	chr2:188680000-188680200	Enhancers	Stomach Mucosa	stomach
4	chr2:188680000-188680400	Enhancers	A549	lung
5	chr2:188680200-188682000	Weak transcription	HepG2	liver
6	chr2:188680400-188684000	Weak transcription	A549	lung
7	chr2:188681400-188682000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
8	chr2:188681400-188682200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr2:188681400-188682600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chr2:188682000-188682600	Enhancers	HepG2	liver
11	chr2:188684000-188684200	Enhancers	A549	lung
12	chr2:188684200-188685000	Weak transcription	A549	lung
13	chr2:188685000-188685400	Enhancers	A549	lung
14	chr2:188690000-188691200	Enhancers	Psoas Muscle	Psoas
15	chr2:188690200-188691200	Enhancers	Skeletal Muscle Male	skeletal muscle
16	chr2:188690400-188691200	Enhancers	Skeletal Muscle Female	skeletal muscle
17	chr2:188690600-188691000	Enhancers	Muscle Satellite Cultured Cells	--
18	chr2:188690600-188691000	Enhancers	Hela-S3	cervix
19	chr2:188690600-188691200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr2:188692200-188692800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr2:188694800-188695600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr2:188699800-188700200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr2:188703400-188704000	Enhancers	Stomach Mucosa	stomach
24	chr2:188703600-188703800	Enhancers	Aorta	Aorta
25	chr2:188703600-188704400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr2:188703800-188716800	Weak transcription	Aorta	Aorta
27	chr2:188707600-188708000	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chr2:188707800-188708200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr2:188708000-188713400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
30	chr2:188709200-188709400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:188709400-188710200	Enhancers	Fetal Lung	lung
32	chr2:188709400-188711400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr2:188710200-188716000	Weak transcription	Fetal Lung	lung
34	chr2:188711400-188711600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr2:188711400-188711800	Enhancers	Liver	Liver
36	chr2:188711600-188712200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:188711800-188712000	Flanking Active TSS	Liver	Liver
38	chr2:188711800-188713400	Enhancers	Fetal Intestine Large	intestine
39	chr2:188712000-188712200	Enhancers	Liver	Liver
40	chr2:188712000-188712600	Enhancers	Duodenum Mucosa	Duodenum
41	chr2:188712200-188712400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr2:188712200-188712400	Flanking Active TSS	Liver	Liver
43	chr2:188712200-188712600	Enhancers	Fetal Kidney	kidney
44	chr2:188712200-188713400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:188712400-188713200	Enhancers	Liver	Liver
46	chr2:188712400-188717200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
47	chr2:188712600-188713000	Weak transcription	Fetal Kidney	kidney
48	chr2:188713000-188713200	Enhancers	Fetal Kidney	kidney
49	chr2:188713000-188713400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr2:188713200-188713800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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