Variant report

Variant	nsv589855
Chromosome Location	chr3:19409153-19512074
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	ATF1	chr3:19409997-19410011	K562	blood:	n/a	n/a
2	ATF2	chr3:19426308-19426774	GM12878	blood:	n/a	n/a
3	CEBPB	chr3:19464404-19464635	A549	lung:	n/a	chr3:19464466-19464479 chr3:19464466-19464477 chr3:19464466-19464479 chr3:19464466-19464477 chr3:19464466-19464479
4	CEBPB	chr3:19464410-19464651	HepG2	liver:	n/a	chr3:19464466-19464479 chr3:19464466-19464477 chr3:19464466-19464479 chr3:19464466-19464477 chr3:19464466-19464479
5	CEBPB	chr3:19469746-19469985	A549	lung:	n/a	chr3:19469897-19469908 chr3:19469868-19469885
6	CEBPB	chr3:19469715-19469969	HepG2	liver:	n/a	chr3:19469897-19469908 chr3:19469868-19469885
7	CEBPB	chr3:19497243-19497499	A549	lung:	n/a	chr3:19497371-19497382 chr3:19497370-19497381
8	CEBPB	chr3:19497227-19497544	HepG2	liver:	n/a	chr3:19497371-19497382 chr3:19497370-19497381
9	CEBPB	chr3:19499112-19499282	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr3:19436511-19436765	MCF-7	breast:	n/a	n/a
11	CTCF	chr3:19436560-19436710	MCF-7	breast:	n/a	n/a
12	CTCF	chr3:19436473-19436766	MCF-7	breast:	n/a	n/a
13	CTCF	chr3:19434660-19434810	AoAF	blood vessel:	n/a	n/a
14	CTCF	chr3:19436560-19436710	Caco-2	colon:	n/a	n/a
15	CTCF	chr3:19469360-19469510	K562	blood:	n/a	n/a
16	CTCF	chr3:19436548-19436737	MCF-7	breast:	n/a	n/a
17	CTCF	chr3:19436544-19436706	A549	lung:	n/a	n/a
18	CTCF	chr3:19436503-19436724	T-47D	breast:	n/a	n/a
19	CTCF	chr3:19436575-19436660	Gliobla	brain:	n/a	n/a
20	CTCF	chr3:19436540-19436690	MCF-7	breast:	n/a	n/a
21	CTCF	chr3:19436532-19436695	HepG2	liver:	n/a	n/a
22	CTCF	chr3:19412191-19412251	GM20000	blood:	n/a	n/a
23	CTCF	chr3:19436539-19436735	MCF-7	breast:	n/a	n/a
24	CTCF	chr3:19436564-19436650	K562	blood:	n/a	n/a
25	CTCF	chr3:19436521-19436766	MCF-7	breast:	n/a	n/a
26	CTCF	chr3:19436539-19436756	MCF-7	breast:	n/a	n/a
27	CTCF	chr3:19473338-19473378	Kidney_OC	kidney:	n/a	n/a
28	CTCF	chr3:19467620-19467770	GM12864	blood:	n/a	n/a
29	CUX1	chr3:19488447-19488455	GM12878	blood:	n/a	n/a
30	E2F4	chr3:19475469-19475765	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr3:19438402-19438803	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr3:19469813-19469903	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr3:19459148-19459348	MCF10A-Er-Src	breast:	n/a	n/a
34	EP300	chr3:19451804-19451939	GM12878	blood:	n/a	n/a
35	FOS	chr3:19498908-19499417	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr3:19468965-19469291	MCF10A-Er-Src	breast:	n/a	chr3:19469112-19469121 chr3:19469112-19469120 chr3:19469111-19469121 chr3:19469113-19469120
37	FOS	chr3:19440943-19441105	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr3:19440931-19441071	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr3:19498899-19499389	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr3:19468963-19469271	MCF10A-Er-Src	breast:	n/a	chr3:19469112-19469121 chr3:19469112-19469120 chr3:19469111-19469121 chr3:19469113-19469120
41	FOS	chr3:19441414-19441593	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr3:19444944-19445090	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr3:19441395-19441693	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr3:19509011-19509084	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr3:19498962-19499329	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr3:19468988-19469262	MCF10A-Er-Src	breast:	n/a	chr3:19469112-19469121 chr3:19469112-19469120 chr3:19469111-19469121 chr3:19469113-19469120
47	FOS	chr3:19508885-19509178	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr3:19468955-19469285	MCF10A-Er-Src	breast:	n/a	chr3:19469112-19469121 chr3:19469112-19469120 chr3:19469111-19469121 chr3:19469113-19469120
49	FOS	chr3:19441426-19441607	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr3:19498931-19499344	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:19440409-19440459	GM06990	blood:	n/a
2	chr3:19440409-19440459	SK-N-SH	brain:	n/a
3	chr3:19440409-19440459	AoSMC	blood vessel:	n/a
4	chr3:19440409-19440459	GM12878	blood:	n/a
5	chr3:19440409-19440459	CMK	blood:	n/a
6	chr3:19440409-19440459	GM19239	blood:	n/a
7	chr3:19440409-19440459	AG09309	skin:	n/a
8	chr3:19440409-19440459	HUVEC	blood vessel:	n/a
9	chr3:19440409-19440459	PrEC	prostate:	n/a
10	chr3:19440409-19440459	Caco-2	colon:	n/a
11	chr3:19440409-19440459	NH-A	brain:	n/a
12	chr3:19440409-19440459	PANC-1	pancreas:	n/a
13	chr3:19440409-19440459	AG10803	skin:	n/a
14	chr3:19440409-19440459	HEK293	kidney:	embryo
15	chr3:19440409-19440459	HRE	kidney:	n/a
16	chr3:19440409-19440459	SK-N-MC	brain:	n/a
17	chr3:19440409-19440459	ovcar-3	ovarian:	n/a
18	chr3:19440409-19440459	HMEC	breast:	n/a
19	chr3:19440409-19440459	LNCaP	prostate:	n/a
20	chr3:19440409-19440459	HNPCEpiC	eye:	n/a
21	chr3:19440409-19440459	NT2-D1	testis:	n/a
22	chr3:19440409-19440459	SK-N-SH_RA	brain:	n/a
23	chr3:19440409-19440459	U87	brain:	n/a
24	chr3:19440409-19440459	RPTEC	kidney:	n/a
25	chr3:19440409-19440459	HIPEpiC	eye:	n/a
26	chr3:19440409-19440459	Hela-S3	cervix:	n/a
27	chr3:19440409-19440459	HCM	heart:	n/a
28	chr3:19440409-19440459	NHDF-neo	bronchial:	n/a
29	chr3:19440409-19440459	HepG2	liver:	n/a
30	chr3:19440409-19440459	AG09319	gingival:	n/a
31	chr3:19440409-19440459	HCT-116	colon:	n/a
32	chr3:19440409-19440459	HAEpiC	amniotic membrane:	n/a
33	chr3:19440409-19440459	HCPEpiC	choroid plexus:	n/a
34	chr3:19440409-19440459	HPAEpiC	pulmonary alveolar:	n/a
35	chr3:19440409-19440459	BJ	skin:	n/a
36	chr3:19440409-19440459	HRPEpiC	eye:	n/a
37	chr3:19440409-19440459	NB4	blood:	n/a
38	chr3:19440409-19440459	H1-hESC	embryonic stem cell:	embryo
39	chr3:19440409-19440459	ProgFib	skin:	n/a
40	chr3:19440409-19440459	Jurkat	blood:	n/a
41	chr3:19440409-19440459	GM12891	blood:	n/a
42	chr3:19440409-19440459	A549	lung:	n/a
43	chr3:19440409-19440459	ECC-1	luminal epithelium:	n/a
44	chr3:19440409-19440459	AG04449	skin:	fetal
45	chr3:19440409-19440459	SKMC	muscle:	n/a
46	chr3:19440409-19440459	NHBE	bronchial:	n/a
47	chr3:19440409-19440459	K562	blood:	n/a
48	chr3:19440409-19440459	SAEC	small airway:	n/a
49	chr3:19440409-19440459	BE2_C	brain:	n/a
50	chr3:19440409-19440459	PFSK-1	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:105766716..105768972-chr3:19479211..19481306,2	MCF-7	breast:
2	chr3:19443170..19445320-chr3:19453492..19455526,2	K562	blood:
3	chr3:19443170..19445320-chr3:19453492..19455526,2	K562	blood:
4	chr3:19489514..19491858-chr3:19516874..19519279,2	K562	blood:

Variant related genes	Relation type
KCNH8	TF binding region
KCNH8	CpG island

Extended variants
information (count: 3443 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:3443 , 50 per page) page: 1 2 3 4 5 6 7 ... 69

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7645658	chr3:19409153-19409154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs374763858	chr3:19409158-19409159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556106667	chr3:19409195-19409196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs368236992	chr3:19409196-19409197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs552956107	chr3:19409199-19409200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs188755311	chr3:19409343-19409344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs541844272	chr3:19409348-19409349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs563714992	chr3:19409365-19409366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs531023999	chr3:19409416-19409417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs546272414	chr3:19409463-19409464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs182014850	chr3:19409505-19409506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs372510940	chr3:19409583-19409584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs144929059	chr3:19409620-19409621	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs547192899	chr3:19409643-19409644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs568635878	chr3:19409675-19409676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs185334020	chr3:19409678-19409679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs538067140	chr3:19409689-19409690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs568863438	chr3:19409731-19409732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs547865458	chr3:19409732-19409733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370089586	chr3:19409805-19409806	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs557937558	chr3:19409848-19409849	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs578075144	chr3:19409860-19409861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536660751	chr3:19409882-19409883	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs9875843	chr3:19409996-19409997	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570237460	chr3:19410050-19410051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58151720	chr3:19410095-19410096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs534497920	chr3:19410098-19410099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs554285969	chr3:19410099-19410100	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs574637095	chr3:19410103-19410104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs79175834	chr3:19410120-19410121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9310595	chr3:19410169-19410170	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs574380917	chr3:19410189-19410190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs546233648	chr3:19410236-19410237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564543356	chr3:19410249-19410250	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs528612764	chr3:19410309-19410310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs371273834	chr3:19410335-19410336	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115983750	chr3:19410342-19410343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs2119804	chr3:19410346-19410347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs529554585	chr3:19410355-19410356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543294105	chr3:19410465-19410466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550812415	chr3:19410496-19410497	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs201473104	chr3:19410498-19410499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs7630441	chr3:19410579-19410580	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs199949305	chr3:19410581-19410582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373435060	chr3:19410585-19410586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs75475353	chr3:19410686-19410687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570198367	chr3:19410687-19410688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs17511437	chr3:19410738-19410739	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs552888884	chr3:19410793-19410794	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs9821751	chr3:19410829-19410830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Medulloblastoma	21979893	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Neuroblastoma	17327916	CNVD
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	18923191	CNVD
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	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
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
lymphocytic leukemia	21291569	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Esophageal cancer	20955586	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Squamous cell cancer	20885788	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Breast cancer	17133270	CNVD
Developmental delay	21147756	CNVD
Uveal melanoma	20484589	CNVD
Autism	20531469	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:215 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:19395200-19423800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr3:19417600-19418400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr3:19417800-19418200	Active TSS	HUES6 Cell Line	embryonic stem cell
4	chr3:19423800-19424600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr3:19424600-19436200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr3:19425800-19427400	Enhancers	GM12878-XiMat	blood
7	chr3:19426400-19426600	Enhancers	Primary B cells from peripheral blood	blood
8	chr3:19426600-19435800	Weak transcription	Primary B cells from peripheral blood	blood
9	chr3:19428800-19429600	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr3:19429600-19430000	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr3:19429800-19430000	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chr3:19430200-19440800	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr3:19430800-19431400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr3:19430800-19434000	Weak transcription	Primary B cells from cord blood	blood
15	chr3:19433800-19434400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr3:19434000-19434400	Enhancers	Primary B cells from cord blood	blood
17	chr3:19434400-19436400	Weak transcription	Primary B cells from cord blood	blood
18	chr3:19435200-19449000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chr3:19435600-19441000	Weak transcription	Primary hematopoietic stem cells	blood
20	chr3:19435800-19436600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr3:19435800-19438800	Enhancers	Primary B cells from peripheral blood	blood
22	chr3:19436200-19438000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr3:19436400-19436800	Enhancers	Primary B cells from cord blood	blood
24	chr3:19436600-19436800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr3:19436600-19436800	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr3:19436600-19436800	Enhancers	Aorta	Aorta
27	chr3:19436600-19436800	Enhancers	Gastric	stomach
28	chr3:19436800-19437800	Weak transcription	Primary B cells from cord blood	blood
29	chr3:19436800-19441800	Weak transcription	Aorta	Aorta
30	chr3:19436800-19448800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr3:19437800-19438600	Enhancers	Primary B cells from cord blood	blood
32	chr3:19438000-19443800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr3:19438600-19446200	Weak transcription	Primary B cells from cord blood	blood
34	chr3:19438800-19445600	Weak transcription	Primary B cells from peripheral blood	blood
35	chr3:19440000-19441600	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr3:19440000-19441800	Enhancers	ES-I3 Cell Line	embryonic stem cell
37	chr3:19440200-19441600	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr3:19440200-19441600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr3:19440200-19441600	Enhancers	iPS-20b Cell Line	embryonic stem cell
40	chr3:19440200-19441800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr3:19440400-19441600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr3:19440800-19441600	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chr3:19441000-19441600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr3:19441000-19441600	Enhancers	H9 Cell Line	embryonic stem cell
45	chr3:19441000-19441600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr3:19441200-19441800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr3:19441400-19441800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr3:19443800-19444600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr3:19444600-19445400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr3:19445400-19445600	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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