Variant report

Variant	nsv1004771
Chromosome Location	chr2:52754456-52812175
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	CEBPB	chr2:52796334-52796619	A549	lung:	n/a	chr2:52796497-52796508
2	CEBPB	chr2:52779693-52779886	HepG2	liver:	n/a	chr2:52779731-52779742
3	CEBPB	chr2:52779591-52779882	A549	lung:	n/a	chr2:52779731-52779742
4	CEBPB	chr2:52779571-52779911	IMR90	lung:	n/a	chr2:52779731-52779742
5	CEBPB	chr2:52766737-52766993	IMR90	lung:	n/a	n/a
6	CEBPB	chr2:52796338-52796610	IMR90	lung:	n/a	chr2:52796497-52796508
7	CEBPB	chr2:52796324-52796609	HepG2	liver:	n/a	chr2:52796497-52796508
8	CEBPB	chr2:52805150-52805325	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:52779626-52779886	Hela-S3	cervix:	n/a	chr2:52779731-52779742
10	CEBPB	chr2:52779600-52779788	K562	blood:	n/a	chr2:52779731-52779742
11	CTCF	chr2:52807056-52807087	MCF-7	breast:	n/a	n/a
12	CTCF	chr2:52785300-52785450	GM12866	blood:	n/a	n/a
13	CTCF	chr2:52806920-52807070	HEK293	kidney:	n/a	n/a
14	CTCF	chr2:52806980-52807114	H1-hESC	embryonic stem cell:	n/a	n/a
15	CTCF	chr2:52807005-52807081	MCF-7	breast:	n/a	n/a
16	E2F6	chr2:52785333-52785717	H1-hESC	embryonic stem cell:	n/a	n/a
17	EP300	chr2:52766648-52767467	T-47D	breast:	n/a	chr2:52766962-52766972 chr2:52766715-52766729
18	FOS	chr2:52764103-52764447	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
19	FOS	chr2:52764103-52764432	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
20	FOS	chr2:52764107-52764446	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
21	FOS	chr2:52764105-52764433	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
22	FOXA1	chr2:52766626-52767015	T-47D	breast:	n/a	n/a
23	FOXA1	chr2:52766561-52767471	T-47D	breast:	n/a	n/a
24	FOXA1	chr2:52767163-52767340	T-47D	breast:	n/a	n/a
25	FOXA1	chr2:52760908-52761212	T-47D	breast:	n/a	chr2:52761022-52761037
26	GATA3	chr2:52766197-52766592	T-47D	breast:	n/a	n/a
27	GATA3	chr2:52766330-52767424	T-47D	breast:	n/a	n/a
28	GATA3	chr2:52767060-52767383	T-47D	breast:	n/a	n/a
29	JUN	chr2:52802812-52802958	K562	blood:	n/a	n/a
30	MAFF	chr2:52764776-52765093	K562	blood:	n/a	chr2:52764917-52764935
31	MAFF	chr2:52796448-52796757	HepG2	liver:	n/a	n/a
32	MAFF	chr2:52764787-52765085	HepG2	liver:	n/a	chr2:52764917-52764935
33	MAFK	chr2:52764738-52765107	IMR90	lung:	n/a	chr2:52764918-52764933
34	MAFK	chr2:52764755-52765076	K562	blood:	n/a	chr2:52764918-52764933
35	MAFK	chr2:52796459-52796743	IMR90	lung:	n/a	n/a
36	MAFK	chr2:52796441-52796750	HepG2	liver:	n/a	n/a
37	MAFK	chr2:52796477-52796540	Hela-S3	cervix:	n/a	n/a
38	MAFK	chr2:52764779-52765066	HepG2	liver:	n/a	chr2:52764918-52764933
39	MAFK	chr2:52764825-52764933	H1-hESC	embryonic stem cell:	n/a	chr2:52764918-52764933
40	MAFK	chr2:52792756-52792907	HepG2	liver:	n/a	chr2:52792809-52792820 chr2:52792830-52792841 chr2:52792829-52792840
41	MAFK	chr2:52764749-52765055	Hela-S3	cervix:	n/a	chr2:52764918-52764933
42	MAFK	chr2:52764754-52765103	HepG2	liver:	n/a	chr2:52764918-52764933
43	MAFK	chr2:52802002-52802078	HepG2	liver:	n/a	n/a
44	MAFK	chr2:52796413-52796768	HepG2	liver:	n/a	n/a
45	MAX	chr2:52785285-52785662	H1-hESC	embryonic stem cell:	n/a	n/a
46	MAX	chr2:52811205-52811530	NB4	blood:	n/a	n/a
47	MAZ	chr2:52810719-52810797	HepG2	liver:	n/a	n/a
48	MAZ	chr2:52805302-52805502	HepG2	liver:	n/a	n/a
49	MYC	chr2:52799139-52799240	MCF-7	breast:	n/a	n/a
50	MYC	chr2:52811317-52811485	NB4	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52802050-52802100	SAEC	small airway:	n/a
2	chr2:52796128-52796178	GM12891	blood:	n/a
3	chr2:52802050-52802100	U87	brain:	n/a
4	chr2:52802050-52802100	GM12892	blood:	n/a
5	chr2:52799518-52799568	MCF-7	breast:	n/a
6	chr2:52798927-52798977	HCPEpiC	choroid plexus:	n/a
7	chr2:52798927-52798977	SK-N-SH_RA	brain:	n/a
8	chr2:52802050-52802100	HRCEpiC	kidney:	n/a
9	chr2:52785721-52785771	GM06990	blood:	n/a
10	chr2:52799518-52799568	HUVEC	blood vessel:	n/a
11	chr2:52798801-52798851	GM12891	blood:	n/a
12	chr2:52798801-52798851	GM12892	blood:	n/a
13	chr2:52799518-52799568	BE2_C	brain:	n/a
14	chr2:52785721-52785771	GM12891	blood:	n/a
15	chr2:52799378-52799428	HAEpiC	amniotic membrane:	n/a
16	chr2:52797873-52797923	NT2-D1	testis:	n/a
17	chr2:52802050-52802100	GM06990	blood:	n/a
18	chr2:52796128-52796178	HL-60	blood:	n/a
19	chr2:52797873-52797923	HepG2	liver:	n/a
20	chr2:52802050-52802100	GM19239	blood:	n/a
21	chr2:52798927-52798977	RPTEC	kidney:	n/a
22	chr2:52797873-52797923	HIPEpiC	eye:	n/a
23	chr2:52798363-52798413	HL-60	blood:	n/a
24	chr2:52799970-52800020	NHBE	bronchial:	n/a
25	chr2:52799970-52800020	SKMC	muscle:	n/a
26	chr2:52799970-52800020	HCT-116	colon:	n/a
27	chr2:52802050-52802100	AG09309	skin:	n/a
28	chr2:52798363-52798413	NB4	blood:	n/a
29	chr2:52798363-52798413	RPTEC	kidney:	n/a
30	chr2:52799518-52799568	IMR90	lung:	fetal
31	chr2:52799518-52799568	T-47D	breast:	n/a
32	chr2:52798801-52798851	U87	brain:	n/a
33	chr2:52802050-52802100	AoSMC	blood vessel:	n/a
34	chr2:52798927-52798977	IMR90	lung:	fetal
35	chr2:52798363-52798413	HepG2	liver:	n/a
36	chr2:52799378-52799428	HNPCEpiC	eye:	n/a
37	chr2:52797873-52797923	GM19239	blood:	n/a
38	chr2:52796128-52796178	HAEpiC	amniotic membrane:	n/a
39	chr2:52799518-52799568	HRE	kidney:	n/a
40	chr2:52796128-52796178	HCPEpiC	choroid plexus:	n/a
41	chr2:52785721-52785771	MCF-7	breast:	n/a
42	chr2:52802050-52802100	T-47D	breast:	n/a
43	chr2:52799970-52800020	HCPEpiC	choroid plexus:	n/a
44	chr2:52796128-52796178	GM19239	blood:	n/a
45	chr2:52798927-52798977	Jurkat	blood:	n/a
46	chr2:52785721-52785771	AG04450	lung:	fetal
47	chr2:52759434-52759484	RPTEC	kidney:	n/a
48	chr2:52799970-52800020	NHDF-neo	bronchial:	n/a
49	chr2:52798927-52798977	BE2_C	brain:	n/a
50	chr2:52796128-52796178	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr2:52796228..52798842-chr2:52811268..52813785,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ASB3-9	chr2:52778477-52778840	l_1835_chr2:52771950-52778840_testes
2	lnc-ASB3-9	chr2:52771951-52772275	l_1835_chr2:52771950-52778840_testes

Variant related genes	Relation type
ENSG00000204993	TF binding region
ENSG00000204993	CpG island
ENSG00000204993	chromatin interactions

Extended variants
information (count: 1393 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1393 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549086556	chr2:52754458-52754459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568907364	chr2:52754473-52754474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs189618321	chr2:52754478-52754479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs116624056	chr2:52754485-52754486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571459052	chr2:52754491-52754492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs138025848	chr2:52754504-52754505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs200589686	chr2:52754553-52754554	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562463259	chr2:52754650-52754651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs554091030	chr2:52754655-52754656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59727652	chr2:52754665-52754666	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs12471695	chr2:52754672-52754673	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs72894838	chr2:52754696-52754697	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs368412782	chr2:52754698-52754699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533880354	chr2:52754773-52754774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs547181686	chr2:52754803-52754804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs12463745	chr2:52754844-52754845	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs368384656	chr2:52754847-52754848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs564078348	chr2:52754855-52754856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs34246098	chr2:52754898-52754899	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs181466709	chr2:52754899-52754900	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs186106376	chr2:52754901-52754902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141714886	chr2:52754904-52754905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12467933	chr2:52754952-52754953	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs189721415	chr2:52754968-52754969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566795496	chr2:52754974-52754975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs12463812	chr2:52754986-52754987	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs538985592	chr2:52754991-52754992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12467957	chr2:52754996-52754997	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs568856308	chr2:52755030-52755031	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs369151234	chr2:52755039-52755040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12463822	chr2:52755042-52755043	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs150593599	chr2:52755053-52755054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs12464625	chr2:52755076-52755077	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs556560165	chr2:52755153-52755154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs139609349	chr2:52755192-52755193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs538774983	chr2:52755193-52755194	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs571575339	chr2:52755269-52755270	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs149358854	chr2:52755273-52755274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs58479536	chr2:52755298-52755299	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs541199653	chr2:52755403-52755404	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs60687599	chr2:52755434-52755435	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs575039248	chr2:52755438-52755439	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181324884	chr2:52755441-52755442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs112544268	chr2:52755456-52755457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531309722	chr2:52755458-52755459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs77625354	chr2:52755464-52755465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72894841	chr2:52755503-52755504	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs527566462	chr2:52755561-52755562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs148568506	chr2:52755575-52755576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs58294011	chr2:52755576-52755577	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:75)

Disease	PMID	Source
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
Breast cancer	17603634	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Ependymoma	16718352	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Medulloblastoma	20607354	CNVD
Leukemia	18628472	CNVD
Autism	22495311	CNVD
Autism	18522746	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Neuroblastoma	21508638	CNVD
Neurodevelopmental disorder	22521361	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	16272173	CNVD
Lung cancer	17297452	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Lung adenocarcinoma	17086460	CNVD
Retinoblastoma	22278416	CNVD
Cancer	21183584	CNVD
Breast cancer	16397240	CNVD
Acute lymphoblastic leukemia	18768390	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	18940311	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18945720	CNVD
Schizophrenia	19571808	CNVD
Prostate cancer	16573809	CNVD
Neuroticism	17667963	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19546859	CNVD
Autism	17322880	CNVD
Lung cancer	17086460	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Hereditary non-polyposis colorectal cancer	19566914	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:56 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52754000-52754600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:52754600-52758600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:52758600-52760000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
4	chr2:52759400-52760600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr2:52760000-52760400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
6	chr2:52760400-52761400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:52761400-52764200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
8	chr2:52764200-52764800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr2:52764400-52764600	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr2:52764800-52765800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr2:52764800-52766200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr2:52765800-52766400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr2:52766000-52766400	Enhancers	Fetal Muscle Trunk	muscle
14	chr2:52766000-52766400	Enhancers	Fetal Muscle Leg	muscle
15	chr2:52766200-52767200	Enhancers	Breast Myoepithelial Primary Cells	Breast
16	chr2:52766400-52767600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr2:52766400-52767800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
18	chr2:52766600-52767200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
19	chr2:52766800-52767400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr2:52766800-52767400	Enhancers	NH-A	brain
21	chr2:52767600-52768000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
22	chr2:52773000-52773400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr2:52784600-52785000	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr2:52784600-52786200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr2:52784800-52786200	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr2:52784800-52786400	Enhancers	HUES64 Cell Line	embryonic stem cell
27	chr2:52785000-52785200	Enhancers	HUES6 Cell Line	embryonic stem cell
28	chr2:52785000-52785400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
29	chr2:52785000-52786200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr2:52785200-52785400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chr2:52785200-52785600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
32	chr2:52785200-52785800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr2:52785200-52785800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr2:52785200-52786000	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chr2:52785200-52786000	Enhancers	Cortex derived primary cultured neurospheres	brain
36	chr2:52785400-52785600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
37	chr2:52785400-52785600	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr2:52785400-52785800	Enhancers	H1 Cell Line	embryonic stem cell
39	chr2:52785400-52785800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:52785400-52785800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr2:52785600-52785800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
42	chr2:52785600-52786000	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr2:52785600-52795200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr2:52785800-52786200	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr2:52785800-52790000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:52786000-52786200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
47	chr2:52790000-52790200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr2:52790200-52790800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr2:52790800-52791000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr2:52791000-52791200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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