Variant report

Variant	nsv876814
Chromosome Location	chr3:55802749-55860526
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:122)
Chromatin interactive
region (count:3)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 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	chr3:55824891-55824942	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr3:55827490-55827662	HepG2	liver:	n/a	chr3:55827589-55827600
3	CEBPB	chr3:55826055-55826352	HepG2	liver:	n/a	chr3:55826204-55826217 chr3:55826204-55826215 chr3:55826205-55826216 chr3:55826204-55826217
4	CEBPB	chr3:55827595-55827601	IMR90	lung:	n/a	n/a
5	CEBPB	chr3:55829713-55830032	A549	lung:	n/a	n/a
6	CEBPB	chr3:55826029-55826371	MCF-7	breast:	n/a	chr3:55826204-55826217 chr3:55826204-55826215 chr3:55826205-55826216 chr3:55826204-55826217
7	CEBPB	chr3:55824987-55825343	MCF-7	breast:	n/a	n/a
8	CEBPB	chr3:55829765-55829902	K562	blood:	n/a	n/a
9	CEBPB	chr3:55826105-55826278	A549	lung:	n/a	chr3:55826204-55826217 chr3:55826204-55826215 chr3:55826205-55826216 chr3:55826204-55826217
10	CEBPB	chr3:55824919-55825208	MCF-7	breast:	n/a	n/a
11	CEBPB	chr3:55826157-55826319	Hela-S3	cervix:	n/a	chr3:55826204-55826217 chr3:55826204-55826215 chr3:55826205-55826216 chr3:55826204-55826217
12	CEBPB	chr3:55829709-55830051	HepG2	liver:	n/a	n/a
13	CEBPB	chr3:55829655-55830026	MCF-7	breast:	n/a	n/a
14	CTCF	chr3:55804140-55804290	AG09319	gingival:	n/a	n/a
15	CTCF	chr3:55852608-55852796	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr3:55838353-55838415	K562	blood:	n/a	chr3:55838374-55838383
17	CTCF	chr3:55852640-55852790	SK-N-SH_RA	brain:	n/a	n/a
18	CTCF	chr3:55852644-55852790	Medullo	brain:	n/a	n/a
19	CTCF	chr3:55852640-55852790	HFF-Myc	foreskin:	n/a	n/a
20	CTCF	chr3:55852620-55852770	SK-N-SH_RA	brain:	n/a	n/a
21	CTCF	chr3:55852720-55852870	GM12873	blood:	n/a	n/a
22	CTCF	chr3:55851398-55851458	GM19240	blood:	n/a	chr3:55851400-55851413
23	CTCF	chr3:55852588-55852791	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr3:55851360-55851510	HBMEC	blood vessel:	n/a	chr3:55851400-55851413
25	CTCF	chr3:55851388-55851502	MCF-7	breast:	n/a	chr3:55851400-55851413
26	CTCF	chr3:55852640-55852790	HVMF	connective:	n/a	n/a
27	CTCF	chr3:55852600-55852750	AG04449	skin:	n/a	n/a
28	CTCF	chr3:55852620-55852770	GM12878	blood:	n/a	n/a
29	CTCF	chr3:55852653-55852758	MCF-7	breast:	n/a	n/a
30	CTCF	chr3:55851373-55851509	GM12892	blood:	n/a	chr3:55851400-55851413
31	CTCF	chr3:55852680-55852830	HBMEC	blood vessel:	n/a	n/a
32	CTCF	chr3:55852600-55852750	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr3:55804239-55804281	K562	blood:	n/a	n/a
34	CTCF	chr3:55852620-55852770	NHLF	lung:	n/a	n/a
35	CTCF	chr3:55852620-55852770	GM12871	blood:	n/a	n/a
36	CTCF	chr3:55819559-55819589	GM20000	blood:	n/a	n/a
37	CTCF	chr3:55852631-55852765	GM12892	blood:	n/a	n/a
38	CTCF	chr3:55852543-55852832	GM12878	blood:	n/a	n/a
39	CTCF	chr3:55851300-55851450	GM12864	blood:	n/a	chr3:55851400-55851413
40	CTCF	chr3:55852700-55852850	HUVEC	blood vessel:	n/a	n/a
41	CTCF	chr3:55843333-55843400	GM20000	blood:	n/a	n/a
42	CTCF	chr3:55851412-55851490	GM19238	blood:	n/a	n/a
43	CTCF	chr3:55852560-55852710	HVMF	connective:	n/a	n/a
44	CTCF	chr3:55852666-55852745	GM12891	blood:	n/a	n/a
45	CTCF	chr3:55852640-55852790	HEEpiC	esophagus:	n/a	n/a
46	CTCF	chr3:55806549-55806578	LNCaP	prostate:	n/a	n/a
47	CTCF	chr3:55858015-55858095	GM13976	blood:	n/a	n/a
48	CTCF	chr3:55852600-55852750	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr3:55851325-55851587	GM12878	blood:	n/a	chr3:55851400-55851413
50	CTCF	chr3:55852620-55852770	HEK293	kidney:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:55824354-55824404	BJ	skin:	n/a
2	chr3:55824354-55824404	SK-N-SH	brain:	n/a
3	chr3:55809537-55809587	T-47D	breast:	n/a
4	chr3:55824354-55824404	HEK293	kidney:	embryo
5	chr3:55824354-55824404	MCF10A-Er-Src	breast:	n/a
6	chr3:55809537-55809587	AG09309	skin:	n/a
7	chr3:55809537-55809587	PrEC	prostate:	n/a
8	chr3:55824354-55824404	H1-hESC	embryonic stem cell:	embryo
9	chr3:55809537-55809587	AG04450	lung:	fetal
10	chr3:55809537-55809587	HCM	heart:	n/a
11	chr3:55809537-55809587	ProgFib	skin:	n/a
12	chr3:55809537-55809587	NHDF-neo	bronchial:	n/a
13	chr3:55824354-55824404	HRCEpiC	kidney:	n/a
14	chr3:55809537-55809587	Hela-S3	cervix:	n/a
15	chr3:55809537-55809587	NT2-D1	testis:	n/a
16	chr3:55809537-55809587	HCT-116	colon:	n/a
17	chr3:55809537-55809587	GM06990	blood:	n/a
18	chr3:55824354-55824404	GM19239	blood:	n/a
19	chr3:55809537-55809587	RPTEC	kidney:	n/a
20	chr3:55809537-55809587	HCPEpiC	choroid plexus:	n/a
21	chr3:55824354-55824404	HIPEpiC	eye:	n/a
22	chr3:55824354-55824404	NH-A	brain:	n/a
23	chr3:55809537-55809587	NB4	blood:	n/a
24	chr3:55824354-55824404	AG04449	skin:	fetal
25	chr3:55809537-55809587	HCF	heart:	n/a
26	chr3:55824354-55824404	GM06990	blood:	n/a
27	chr3:55824354-55824404	HCPEpiC	choroid plexus:	n/a
28	chr3:55824354-55824404	HAEpiC	amniotic membrane:	n/a
29	chr3:55809537-55809587	HUVEC	blood vessel:	n/a
30	chr3:55809537-55809587	AG04449	skin:	fetal
31	chr3:55824354-55824404	Jurkat	blood:	n/a
32	chr3:55809537-55809587	CMK	blood:	n/a
33	chr3:55824354-55824404	SK-N-MC	brain:	n/a
34	chr3:55824354-55824404	T-47D	breast:	n/a
35	chr3:55809537-55809587	BE2_C	brain:	n/a
36	chr3:55824354-55824404	LNCaP	prostate:	n/a
37	chr3:55809537-55809587	HMEC	breast:	n/a
38	chr3:55824354-55824404	HNPCEpiC	eye:	n/a
39	chr3:55809537-55809587	ovcar-3	ovarian:	n/a
40	chr3:55824354-55824404	HL-60	blood:	n/a
41	chr3:55809537-55809587	AoSMC	blood vessel:	n/a
42	chr3:55809537-55809587	HIPEpiC	eye:	n/a
43	chr3:55809537-55809587	SKMC	muscle:	n/a
44	chr3:55809537-55809587	HAEpiC	amniotic membrane:	n/a
45	chr3:55809537-55809587	HL-60	blood:	n/a
46	chr3:55824354-55824404	HUVEC	blood vessel:	n/a
47	chr3:55809537-55809587	NH-A	brain:	n/a
48	chr3:55809537-55809587	SAEC	small airway:	n/a
49	chr3:55824354-55824404	HCT-116	colon:	n/a
50	chr3:55809537-55809587	HEK293	kidney:	embryo

(count:3 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr3:55850876..55853376-chr3:55857822..55860534,2	MCF-7	breast:
2	chr1:19587574..19589877-chr3:55844063..55845564,2	K562	blood:
3	chr3:55850876..55853376-chr3:55857822..55860534,2	MCF-7	breast:

No data

Variant related genes	Relation type
ERC2	TF binding region
ERC2	CpG island

Extended variants
information (count: 1991 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1991 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1495366	chr3:55802749-55802750	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs545498502	chr3:55802757-55802758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs181440530	chr3:55802762-55802763	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs534031122	chr3:55802764-55802765	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs140641795	chr3:55802784-55802785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs58315468	chr3:55802802-55802803	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs113514449	chr3:55802820-55802821	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs6445753	chr3:55802827-55802828	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs570815898	chr3:55802838-55802839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs187189784	chr3:55802840-55802841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs563674248	chr3:55802846-55802847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs145798983	chr3:55802851-55802852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs146620189	chr3:55802856-55802857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs566264511	chr3:55802857-55802858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528714008	chr3:55802869-55802870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs576706558	chr3:55802908-55802909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs548597972	chr3:55802913-55802914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs192119376	chr3:55802957-55802958	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537355599	chr3:55802963-55802964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537881418	chr3:55802968-55802969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs141293220	chr3:55802971-55802972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs544106208	chr3:55802973-55802974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9815001	chr3:55802982-55802983	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
24	rs182724845	chr3:55803028-55803029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs186064017	chr3:55803072-55803073	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs577798827	chr3:55803078-55803079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs76573765	chr3:55803079-55803080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9815155	chr3:55803101-55803102	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs575446723	chr3:55803114-55803115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs544199914	chr3:55803130-55803131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs72875449	chr3:55803159-55803160	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs577347554	chr3:55803168-55803169	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546300679	chr3:55803243-55803244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs35408044	chr3:55803244-55803245	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371437895	chr3:55803273-55803274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569310727	chr3:55803288-55803289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9835091	chr3:55803291-55803292	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs528669666	chr3:55803292-55803293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554411866	chr3:55803316-55803317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9852746	chr3:55803332-55803333	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs531209018	chr3:55803338-55803339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs9815229	chr3:55803349-55803350	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs143304773	chr3:55803372-55803373	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539092676	chr3:55803378-55803379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs9852888	chr3:55803435-55803436	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
46	rs566187705	chr3:55803448-55803449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs148291828	chr3:55803451-55803452	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555507794	chr3:55803475-55803476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575366549	chr3:55803492-55803493	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs540418422	chr3:55803521-55803522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Acute myeloid leukemia	20729466	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Breast cancer	21785460	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Squamous cell cancer	20885788	CNVD
Breast cancer	16608533	CNVD
Prostate cancer	21965145	CNVD
Cancer	21129771	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Renal cell carcinoma	18765545	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21509527	CNVD
Prostate cancer	18632612	CNVD
Cancer	20164919	CNVD
Myelofibrosis	22110671	CNVD
Urothelial cell carcinoma	18451213	CNVD
Breast cancer	19490591	CNVD
Autism	18414403	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-small cell lung cancer	20864512	CNVD
Metastatic melanoma	17975146	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:55801800-55804000	Weak transcription	Pancreas	Pancrea
2	chr3:55804000-55804200	Enhancers	Pancreas	Pancrea
3	chr3:55804000-55804400	Enhancers	Ovary	ovary
4	chr3:55805600-55805800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr3:55805800-55808000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr3:55807200-55807400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr3:55807400-55809800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr3:55809000-55809400	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chr3:55809200-55810400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
10	chr3:55809200-55810600	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr3:55809400-55809800	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr3:55809400-55810000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr3:55809800-55810400	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr3:55809800-55810400	Enhancers	HUES64 Cell Line	embryonic stem cell
15	chr3:55809800-55810400	Enhancers	iPS-18 Cell Line	embryonic stem cell
16	chr3:55809800-55810600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr3:55810600-55816200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr3:55811000-55811400	Enhancers	Fetal Stomach	stomach
19	chr3:55811400-55814800	Weak transcription	Fetal Stomach	stomach
20	chr3:55813600-55813800	Enhancers	Fetal Lung	lung
21	chr3:55813800-55814800	Weak transcription	Fetal Lung	lung
22	chr3:55814600-55815600	Enhancers	Fetal Heart	heart
23	chr3:55814800-55815000	Enhancers	Pancreas	Pancrea
24	chr3:55814800-55815200	Enhancers	Fetal Lung	lung
25	chr3:55814800-55815400	Enhancers	Fetal Stomach	stomach
26	chr3:55814800-55817400	Enhancers	Spleen	Spleen
27	chr3:55815000-55815200	Bivalent Enhancer	Fetal Kidney	kidney
28	chr3:55815000-55816200	Weak transcription	Pancreas	Pancrea
29	chr3:55815200-55816600	Enhancers	Gastric	stomach
30	chr3:55815600-55816600	Weak transcription	Fetal Heart	heart
31	chr3:55816000-55816800	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr3:55816200-55816800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr3:55816200-55817200	Enhancers	Pancreas	Pancrea
34	chr3:55816400-55816600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr3:55816600-55817000	Weak transcription	Gastric	stomach
36	chr3:55816600-55817200	Enhancers	Dnd41	blood
37	chr3:55816800-55817000	Enhancers	Fetal Heart	heart
38	chr3:55816800-55817200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr3:55816800-55819000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr3:55817000-55817400	Enhancers	Gastric	stomach
41	chr3:55817200-55817400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
42	chr3:55817200-55830600	Weak transcription	Pancreas	Pancrea
43	chr3:55817400-55818800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr3:55818800-55819600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr3:55819000-55820200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr3:55819000-55820600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr3:55819600-55821800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
48	chr3:55820200-55822200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr3:55820600-55821600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:55821600-55825200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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