Variant report

Variant	nsv1027959
Chromosome Location	chr5:104541551-104661834
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:224)
CpG islands
(count:0)
Chromatin interactive
region (count:35)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:224 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:104599139-104599705	K562	blood:	n/a	n/a
2	ARID3A	chr5:104565880-104566023	K562	blood:	n/a	n/a
3	ARID3A	chr5:104574137-104574841	K562	blood:	n/a	n/a
4	ATF1	chr5:104599299-104599581	K562	blood:	n/a	n/a
5	ATF1	chr5:104566225-104566645	K562	blood:	n/a	n/a
6	CCNT2	chr5:104566220-104566624	K562	blood:	n/a	n/a
7	CCNT2	chr5:104599218-104599525	K562	blood:	n/a	n/a
8	CEBPB	chr5:104593448-104593544	K562	blood:	n/a	chr5:104593456-104593469 chr5:104593456-104593469 chr5:104593458-104593469 chr5:104593456-104593469 chr5:104593458-104593469
9	CEBPB	chr5:104575874-104575947	HepG2	liver:	n/a	chr5:104575897-104575908 chr5:104575896-104575907
10	CEBPB	chr5:104660073-104660304	HepG2	liver:	n/a	chr5:104660167-104660178 chr5:104660226-104660237 chr5:104660267-104660279 chr5:104660224-104660237
11	CEBPB	chr5:104626968-104627293	HepG2	liver:	n/a	chr5:104627123-104627134
12	CEBPB	chr5:104575759-104576055	K562	blood:	n/a	chr5:104575897-104575908 chr5:104575896-104575907
13	CEBPB	chr5:104613257-104613341	K562	blood:	n/a	n/a
14	CEBPB	chr5:104647437-104647690	K562	blood:	n/a	chr5:104647455-104647466 chr5:104647453-104647466 chr5:104647453-104647466
15	CEBPB	chr5:104613163-104613370	HepG2	liver:	n/a	n/a
16	CEBPD	chr5:104566271-104566739	K562	blood:	n/a	n/a
17	CTCF	chr5:104640740-104640890	HCT-116	colon:	n/a	n/a
18	CTCF	chr5:104570902-104570953	GM20000	blood:	n/a	n/a
19	CTCF	chr5:104640620-104640770	MCF-7	breast:	n/a	n/a
20	CTCF	chr5:104640700-104640850	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr5:104640620-104640770	HPF	lung:	n/a	n/a
22	CTCF	chr5:104646160-104646310	AoAF	blood vessel:	n/a	n/a
23	CTCF	chr5:104640700-104640850	HepG2	liver:	n/a	n/a
24	CTCF	chr5:104640640-104640790	HEK293	kidney:	n/a	n/a
25	CTCF	chr5:104640660-104640810	HPF	lung:	n/a	n/a
26	CTCF	chr5:104640720-104640870	HRE	kidney:	n/a	n/a
27	CTCF	chr5:104640700-104640850	K562	blood:	n/a	n/a
28	CTCF	chr5:104640700-104640850	HEK293	kidney:	n/a	n/a
29	CTCF	chr5:104652352-104652458	Kidney_OC	kidney:	n/a	n/a
30	CTCF	chr5:104640740-104640890	GM12865	blood:	n/a	n/a
31	CTCF	chr5:104640660-104640810	HCT-116	colon:	n/a	n/a
32	CTCF	chr5:104640640-104640790	HCPEpiC	choroid plexus:	n/a	n/a
33	CTCF	chr5:104640680-104640830	RPTEC	kidney:	n/a	n/a
34	CTCF	chr5:104640680-104640830	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr5:104640680-104640830	HCFaa	heart:	n/a	n/a
36	CTCF	chr5:104640640-104640790	HMEC	breast:	n/a	n/a
37	CTCF	chr5:104640660-104640810	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr5:104640640-104640790	AG04450	lung:	n/a	n/a
39	CTCF	chr5:104640680-104640830	GM12878	blood:	n/a	n/a
40	CTCF	chr5:104640760-104640910	HEEpiC	esophagus:	n/a	n/a
41	CTCF	chr5:104640760-104640910	BE2_C	brain:	n/a	n/a
42	CTCF	chr5:104640780-104640930	NB4	blood:	n/a	n/a
43	CTCF	chr5:104579200-104579350	HCM	heart:	n/a	n/a
44	CTCF	chr5:104640620-104640770	HMF	breast:	n/a	n/a
45	CUX1	chr5:104599207-104599670	K562	blood:	n/a	n/a
46	E2F4	chr5:104542391-104542591	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr5:104659807-104660153	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr5:104643458-104643698	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr5:104607982-104608230	MCF10A-Er-Src	breast:	n/a	n/a
50	EP300	chr5:104550054-104550320	SK-N-SH_RA	brain:	n/a	n/a

No data

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
2	chr5:104660610..104663385-chr5:104663843..104665843,2	K562	blood:
3	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
4	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
5	chr5:104545106..104548123-chr5:104549429..104551527,3	K562	blood:
6	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
7	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
8	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
9	chr5:104574990..104577042-chr5:104578460..104580211,2	K562	blood:
10	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
11	chr5:104565194..104566957-chr5:104571048..104573999,2	K562	blood:
12	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
13	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:
14	chr5:104551002..104553954-chr5:104571477..104574357,2	MCF-7	breast:
15	chr5:104586940..104589611-chr5:104727738..104729575,2	K562	blood:
16	chr5:104649160..104650852-chr5:104651591..104654211,3	K562	blood:
17	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
18	chr5:104545961..104548123-chr5:104549429..104551527,2	K562	blood:
19	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
20	chr5:104604624..104606834-chr5:104613480..104615859,2	K562	blood:
21	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
22	chr5:104584886..104590168-chr5:104590478..104594256,4	K562	blood:
23	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
24	chr5:104582906..104584797-chr5:104601356..104603170,2	K562	blood:
25	chr19:12903711..12905991-chr5:104578289..104580216,2	MCF-7	breast:
26	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
27	chr5:104567163..104569932-chr5:104572220..104574679,2	MCF-7	breast:
28	chr5:104540117..104542340-chr5:104543485..104546477,2	MCF-7	breast:
29	chr5:104512964..104515332-chr5:104570864..104572424,2	K562	blood:
30	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
31	chr5:104564496..104566595-chr5:104574532..104577348,2	K562	blood:
32	chr5:104576197..104577737-chr5:104582724..104585208,2	K562	blood:
33	chr5:104542507..104545042-chr5:104552566..104554250,2	K562	blood:
34	chr5:103843512..103846064-chr5:104654970..104657716,2	K562	blood:
35	chr5:104645770..104648035-chr5:104661663..104663662,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NUDT12-7	chr5:104581998-104582065	ENSG00000253584
2	lnc-NUDT12-7	chr5:104582013-104582067	NONHSAT103097

No data

Variant related genes	Relation type
ENSG00000253584	TF binding region
ENSG00000251574	chromatin interactions

Extended variants
information (count: 1470 )
Associated
traits (count: 86 )

Variant overlapped rSNPs/rCNVs (count:1470 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369069280	chr5:104541842-104541843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs559543363	chr5:104541859-104541860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs528628388	chr5:104541868-104541869	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs551814227	chr5:104541873-104541874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs73779230	chr5:104541892-104541893	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544117674	chr5:104541936-104541937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs114268170	chr5:104541946-104541947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532913052	chr5:104541957-104541958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs28431119	chr5:104541970-104541971	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs142362487	chr5:104541990-104541991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs547079007	chr5:104542072-104542073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs34972132	chr5:104542074-104542075	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs183485025	chr5:104542080-104542081	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs565914513	chr5:104542093-104542094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs534791119	chr5:104542102-104542103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs186802252	chr5:104542111-104542112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577861322	chr5:104542113-104542114	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs192064068	chr5:104542145-104542146	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556920089	chr5:104542157-104542158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs151238382	chr5:104542159-104542160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs542330302	chr5:104542171-104542172	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs552634930	chr5:104542190-104542191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs551466235	chr5:104542201-104542202	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs28449770	chr5:104542202-104542203	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs183292547	chr5:104542203-104542204	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs139243796	chr5:104542235-104542236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149990234	chr5:104542257-104542258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs79130835	chr5:104542268-104542269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs117606604	chr5:104542273-104542274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs7721307	chr5:104542383-104542384	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs188020535	chr5:104542400-104542401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146755003	chr5:104542402-104542403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191285410	chr5:104542405-104542406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs560143196	chr5:104542422-104542423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs182367424	chr5:104542431-104542432	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs931738	chr5:104542488-104542489	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs188076222	chr5:104542507-104542508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs140450443	chr5:104542525-104542526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs566958118	chr5:104542528-104542529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs116287196	chr5:104542580-104542581	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs549338003	chr5:104542595-104542596	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs575135012	chr5:104550072-104550073	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372509152	chr5:104550073-104550074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544008146	chr5:104550155-104550156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs560699845	chr5:104550193-104550194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs529966605	chr5:104550226-104550227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs549907543	chr5:104550231-104550232	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs115092884	chr5:104550254-104550255	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs532109575	chr5:104550287-104550288	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572215320	chr5:104550299-104550300	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:86)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Breast cancer	17393978	CNVD
Cancer	21359685	CNVD
Non-small cell lung cancer	21829676	CNVD
adenomatous polyposis	22470819	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Retinoblastoma	22278416	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16272173	CNVD
Prostate cancer	16573809	CNVD
Renal cell carcinoma	18194544	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
abnormal development	18461090	CNVD
Colorectal cancer	16774939	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Ovarian cancer	21720365	CNVD
Neurocytoma	17123091	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	21509527	CNVD
Breast cancer	16608533	CNVD
Myelofibrosis	22110671	CNVD
Obesity	20622171	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Lung cancer	16773561	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Schizophrenia	21346763	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:57 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:104541800-104542600	Enhancers	Brain Germinal Matrix	brain
2	chr5:104550000-104550400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr5:104550200-104550600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr5:104550200-104550600	Enhancers	HUES6 Cell Line	embryonic stem cell
5	chr5:104550200-104550600	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr5:104550200-104550800	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr5:104550400-104550600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
8	chr5:104550600-104552600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr5:104550800-104554800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr5:104552600-104553600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr5:104553000-104553800	Enhancers	Brain Germinal Matrix	brain
12	chr5:104553200-104554200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr5:104553600-104555200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr5:104554200-104554600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr5:104554600-104555400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
16	chr5:104554800-104555200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
17	chr5:104555000-104556600	Enhancers	Primary hematopoietic stem cells	blood
18	chr5:104555200-104555400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr5:104555400-104555800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr5:104555800-104557400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr5:104556200-104556600	Active TSS	Primary T helper cells PMA-I stimulated	--
22	chr5:104565200-104565400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr5:104565400-104565800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr5:104565600-104566600	Enhancers	K562	blood
25	chr5:104565800-104566800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chr5:104565800-104566800	Enhancers	Colon Smooth Muscle	Colon
27	chr5:104566000-104566400	Enhancers	Primary hematopoietic stem cells short term culture	blood
28	chr5:104566200-104566800	Enhancers	Fetal Lung	lung
29	chr5:104566800-104567600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr5:104567600-104567800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr5:104575600-104576000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr5:104576000-104581000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr5:104581000-104581200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr5:104581200-104581400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr5:104581200-104581600	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr5:104594000-104594200	ZNF genes & repeats	K562	blood
37	chr5:104594200-104597600	Weak transcription	K562	blood
38	chr5:104595000-104596000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr5:104595200-104595800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr5:104595200-104595800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr5:104595200-104596000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr5:104597600-104598400	Enhancers	K562	blood
43	chr5:104598400-104598800	Weak transcription	K562	blood
44	chr5:104598800-104599600	Enhancers	K562	blood
45	chr5:104626800-104627600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr5:104627600-104628400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chr5:104628400-104629200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr5:104629200-104629600	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr5:104629600-104630000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr5:104630000-104630200	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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