Variant report

Variant	nsv1006118
Chromosome Location	chr2:52764196-52815385
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	chr2:52779626-52779886	Hela-S3	cervix:	n/a	chr2:52779731-52779742
2	CEBPB	chr2:52779571-52779911	IMR90	lung:	n/a	chr2:52779731-52779742
3	CEBPB	chr2:52779693-52779886	HepG2	liver:	n/a	chr2:52779731-52779742
4	CEBPB	chr2:52766737-52766993	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:52796338-52796610	IMR90	lung:	n/a	chr2:52796497-52796508
6	CEBPB	chr2:52796324-52796609	HepG2	liver:	n/a	chr2:52796497-52796508
7	CEBPB	chr2:52779591-52779882	A549	lung:	n/a	chr2:52779731-52779742
8	CEBPB	chr2:52779600-52779788	K562	blood:	n/a	chr2:52779731-52779742
9	CEBPB	chr2:52796334-52796619	A549	lung:	n/a	chr2:52796497-52796508
10	CEBPB	chr2:52805150-52805325	HepG2	liver:	n/a	n/a
11	CTCF	chr2:52806980-52807114	H1-hESC	embryonic stem cell:	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	chr2:52807005-52807081	MCF-7	breast:	n/a	n/a
15	CTCF	chr2:52807056-52807087	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	chr2:52764105-52764433	MCF10A-Er-Src	breast:	n/a	chr2:52764278-52764286 chr2:52764278-52764285 chr2:52764279-52764290 chr2:52764276-52764288 chr2:52764277-52764286
19	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
20	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
21	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
22	FOXA1	chr2:52767163-52767340	T-47D	breast:	n/a	n/a
23	FOXA1	chr2:52766561-52767471	T-47D	breast:	n/a	n/a
24	FOXA1	chr2:52766626-52767015	T-47D	breast:	n/a	n/a
25	GATA3	chr2:52766330-52767424	T-47D	breast:	n/a	n/a
26	GATA3	chr2:52767060-52767383	T-47D	breast:	n/a	n/a
27	GATA3	chr2:52766197-52766592	T-47D	breast:	n/a	n/a
28	JUN	chr2:52802812-52802958	K562	blood:	n/a	n/a
29	MAFF	chr2:52764776-52765093	K562	blood:	n/a	chr2:52764917-52764935
30	MAFF	chr2:52764787-52765085	HepG2	liver:	n/a	chr2:52764917-52764935
31	MAFF	chr2:52796448-52796757	HepG2	liver:	n/a	n/a
32	MAFK	chr2:52796441-52796750	HepG2	liver:	n/a	n/a
33	MAFK	chr2:52764749-52765055	Hela-S3	cervix:	n/a	chr2:52764918-52764933
34	MAFK	chr2:52764754-52765103	HepG2	liver:	n/a	chr2:52764918-52764933
35	MAFK	chr2:52792756-52792907	HepG2	liver:	n/a	chr2:52792809-52792820 chr2:52792830-52792841 chr2:52792829-52792840
36	MAFK	chr2:52814012-52814267	HepG2	liver:	n/a	chr2:52814149-52814160
37	MAFK	chr2:52764755-52765076	K562	blood:	n/a	chr2:52764918-52764933
38	MAFK	chr2:52764825-52764933	H1-hESC	embryonic stem cell:	n/a	chr2:52764918-52764933
39	MAFK	chr2:52802002-52802078	HepG2	liver:	n/a	n/a
40	MAFK	chr2:52796459-52796743	IMR90	lung:	n/a	n/a
41	MAFK	chr2:52764738-52765107	IMR90	lung:	n/a	chr2:52764918-52764933
42	MAFK	chr2:52764779-52765066	HepG2	liver:	n/a	chr2:52764918-52764933
43	MAFK	chr2:52814007-52814246	HepG2	liver:	n/a	chr2:52814149-52814160
44	MAFK	chr2:52796413-52796768	HepG2	liver:	n/a	n/a
45	MAFK	chr2:52796477-52796540	Hela-S3	cervix:	n/a	n/a
46	MAX	chr2:52785285-52785662	H1-hESC	embryonic stem cell:	n/a	n/a
47	MAX	chr2:52811205-52811530	NB4	blood:	n/a	n/a
48	MAZ	chr2:52810719-52810797	HepG2	liver:	n/a	n/a
49	MAZ	chr2:52805302-52805502	HepG2	liver:	n/a	n/a
50	MYC	chr2:52764213-52764279	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:52798927-52798977	PANC-1	pancreas:	n/a
2	chr2:52798927-52798977	PANC-1	pancreas:	n/a
3	chr2:52798927-52798977	HRCEpiC	kidney:	n/a
4	chr2:52798927-52798977	HCF	heart:	n/a
5	chr2:52799518-52799568	AG09319	gingival:	n/a
6	chr2:52799378-52799428	HRE	kidney:	n/a
7	chr2:52798801-52798851	SKMC	muscle:	n/a
8	chr2:52785721-52785771	HUVEC	blood vessel:	n/a
9	chr2:52798363-52798413	HCF	heart:	n/a
10	chr2:52799378-52799428	AG09319	gingival:	n/a
11	chr2:52796128-52796178	AG09319	gingival:	n/a
12	chr2:52796128-52796178	HNPCEpiC	eye:	n/a
13	chr2:52802050-52802100	HUVEC	blood vessel:	n/a
14	chr2:52785721-52785771	AG09319	gingival:	n/a
15	chr2:52799970-52800020	HCPEpiC	choroid plexus:	n/a
16	chr2:52798801-52798851	H1-hESC	embryonic stem cell:	embryo
17	chr2:52802050-52802100	CMK	blood:	n/a
18	chr2:52799970-52800020	HCT-116	colon:	n/a
19	chr2:52802050-52802100	AG04450	lung:	fetal
20	chr2:52798363-52798413	AG09319	gingival:	n/a
21	chr2:52802050-52802100	NH-A	brain:	n/a
22	chr2:52798927-52798977	NT2-D1	testis:	n/a
23	chr2:52796128-52796178	HEK293	kidney:	embryo
24	chr2:52785721-52785771	HNPCEpiC	eye:	n/a
25	chr2:52799518-52799568	HRE	kidney:	n/a
26	chr2:52797873-52797923	HRPEpiC	eye:	n/a
27	chr2:52799518-52799568	GM12878	blood:	n/a
28	chr2:52798927-52798977	SK-N-SH	brain:	n/a
29	chr2:52799518-52799568	GM06990	blood:	n/a
30	chr2:52802050-52802100	MCF10A-Er-Src	breast:	n/a
31	chr2:52798927-52798977	AG09319	gingival:	n/a
32	chr2:52802050-52802100	HEK293	kidney:	embryo
33	chr2:52799518-52799568	AG09309	skin:	n/a
34	chr2:52799378-52799428	SAEC	small airway:	n/a
35	chr2:52796128-52796178	NT2-D1	testis:	n/a
36	chr2:52796128-52796178	GM12891	blood:	n/a
37	chr2:52785721-52785771	AoSMC	blood vessel:	n/a
38	chr2:52798801-52798851	ProgFib	skin:	n/a
39	chr2:52796128-52796178	NB4	blood:	n/a
40	chr2:52798801-52798851	Hela-S3	cervix:	n/a
41	chr2:52798927-52798977	SK-N-MC	brain:	n/a
42	chr2:52799970-52800020	HAEpiC	amniotic membrane:	n/a
43	chr2:52799518-52799568	HMEC	breast:	n/a
44	chr2:52799518-52799568	HIPEpiC	eye:	n/a
45	chr2:52798927-52798977	LNCaP	prostate:	n/a
46	chr2:52799518-52799568	HEEpiC	esophagus:	n/a
47	chr2:52785721-52785771	HCPEpiC	choroid plexus:	n/a
48	chr2:52797873-52797923	NHDF-neo	bronchial:	n/a
49	chr2:52798363-52798413	NH-A	brain:	n/a
50	chr2:52798363-52798413	NHBE	bronchial:	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	chr2:52771951-52772275	l_1835_chr2:52771950-52778840_testes
2	lnc-ASB3-9	chr2:52778477-52778840	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: 1110 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:1110 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190108114	chr2:52764208-52764209	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs573482942	chr2:52764227-52764228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs7563514	chr2:52764242-52764243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs547263954	chr2:52764243-52764244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs373730656	chr2:52764271-52764272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs573047575	chr2:52764305-52764306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs7563618	chr2:52764338-52764339	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs554265729	chr2:52764349-52764350	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs567780523	chr2:52764361-52764362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs562001701	chr2:52764396-52764397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs150838569	chr2:52764414-52764415	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs139704377	chr2:52764416-52764417	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs114107957	chr2:52764518-52764519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556762300	chr2:52764570-52764571	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573383463	chr2:52764572-52764573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs4971842	chr2:52764603-52764604	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs142920055	chr2:52764604-52764605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs553188292	chr2:52764645-52764646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs539800607	chr2:52764682-52764683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs199635220	chr2:52764724-52764725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs146160304	chr2:52764730-52764731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542212090	chr2:52764738-52764739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs182607706	chr2:52764747-52764748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs575838125	chr2:52764759-52764760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs59533946	chr2:52764774-52764775	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs187262973	chr2:52764808-52764809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs367704147	chr2:52764890-52764891	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs564565214	chr2:52764906-52764907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs57552372	chr2:52764932-52764933	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs189826603	chr2:52764948-52764949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs569332102	chr2:52765012-52765013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140170797	chr2:52765075-52765076	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs367881693	chr2:52765099-52765100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs77458663	chr2:52765138-52765139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs561761250	chr2:52765143-52765144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs547814411	chr2:52765144-52765145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371032640	chr2:52765154-52765155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs72894854	chr2:52765170-52765171	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs144888390	chr2:52765176-52765177	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550249801	chr2:52765183-52765184	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs148651163	chr2:52765186-52765187	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539594474	chr2:52765326-52765327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs553009438	chr2:52765332-52765333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs373478462	chr2:52765367-52765368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs183005762	chr2:52765406-52765407	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs142117273	chr2:52765408-52765409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs555846647	chr2:52765418-52765419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs151159315	chr2:52765464-52765465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs544728434	chr2:52765497-52765498	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564556546	chr2:52765696-52765697	Weak transcription	n/a	n/a	Overlapped CNVs	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:53 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:52761400-52764200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
2	chr2:52764200-52764800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
3	chr2:52764400-52764600	Enhancers	Breast Myoepithelial Primary Cells	Breast
4	chr2:52764800-52765800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr2:52764800-52766200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr2:52765800-52766400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr2:52766000-52766400	Enhancers	Fetal Muscle Trunk	muscle
8	chr2:52766000-52766400	Enhancers	Fetal Muscle Leg	muscle
9	chr2:52766200-52767200	Enhancers	Breast Myoepithelial Primary Cells	Breast
10	chr2:52766400-52767600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr2:52766400-52767800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
12	chr2:52766600-52767200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr2:52766800-52767400	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr2:52766800-52767400	Enhancers	NH-A	brain
15	chr2:52767600-52768000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
16	chr2:52773000-52773400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr2:52784600-52785000	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr2:52784600-52786200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr2:52784800-52786200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr2:52784800-52786400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr2:52785000-52785200	Enhancers	HUES6 Cell Line	embryonic stem cell
22	chr2:52785000-52785400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
23	chr2:52785000-52786200	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr2:52785200-52785400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr2:52785200-52785600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
26	chr2:52785200-52785800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr2:52785200-52785800	Enhancers	H9 Cell Line	embryonic stem cell
28	chr2:52785200-52786000	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr2:52785200-52786000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr2:52785400-52785600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr2:52785400-52785600	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr2:52785400-52785800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr2:52785400-52785800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr2:52785400-52785800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
35	chr2:52785600-52785800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
36	chr2:52785600-52786000	Enhancers	HUES6 Cell Line	embryonic stem cell
37	chr2:52785600-52795200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
38	chr2:52785800-52786200	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr2:52785800-52790000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr2:52786000-52786200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
41	chr2:52790000-52790200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr2:52790200-52790800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr2:52790800-52791000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr2:52791000-52791200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr2:52791200-52792400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr2:52798000-52798600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr2:52798000-52799600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr2:52798000-52800000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
49	chr2:52807400-52807800	Enhancers	Fetal Lung	lung
50	chr2:52811800-52813000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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