Variant report

Variant	nsv900478
Chromosome Location	chr13:69759676-69812252
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:145)
CpG islands
(count:184)
Chromatin interactive
region (count:14)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:145 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:69796023-69796174	K562	blood:	n/a	n/a
2	CEBPB	chr13:69795365-69795601	HepG2	liver:	n/a	n/a
3	CEBPB	chr13:69795373-69795654	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr13:69768102-69768453	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr13:69795374-69795674	K562	blood:	n/a	n/a
6	CEBPD	chr13:69795817-69796165	K562	blood:	n/a	n/a
7	CHD1	chr13:69808687-69808760	H1-hESC	embryonic stem cell:	n/a	n/a
8	CTBP2	chr13:69808828-69809721	H1-hESC	embryonic stem cell:	n/a	n/a
9	CTCF	chr13:69798188-69798430	K562	blood:	n/a	n/a
10	CTCF	chr13:69797040-69797102	LNCaP	prostate:	n/a	n/a
11	CTCF	chr13:69809200-69809350	GM12865	blood:	n/a	n/a
12	CTCF	chr13:69797096-69797176	Kidney_OC	kidney:	n/a	n/a
13	CTCF	chr13:69798214-69798362	K562	blood:	n/a	n/a
14	CTCF	chr13:69800977-69800998	GM20000	blood:	n/a	n/a
15	E2F4	chr13:69781045-69781236	MCF10A-Er-Src	breast:	n/a	n/a
16	E2F4	chr13:69785870-69785881	MCF10A-Er-Src	breast:	n/a	n/a
17	E2F4	chr13:69786236-69786418	MCF10A-Er-Src	breast:	n/a	n/a
18	ELK1	chr13:69801719-69801720	K562	blood:	n/a	n/a
19	EP300	chr13:69772636-69773294	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr13:69772389-69774420	SK-N-SH	brain:	n/a	chr13:69773490-69773500
21	EP300	chr13:69773820-69774135	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chr13:69773858-69774136	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr13:69772590-69773228	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chr13:69795806-69796108	GM12878	blood:	n/a	n/a
25	FOS	chr13:69788210-69788542	MCF10A-Er-Src	breast:	n/a	n/a
26	FOS	chr13:69788204-69788550	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr13:69788203-69788543	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr13:69805182-69805386	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr13:69788343-69788479	MCF10A-Er-Src	breast:	n/a	n/a
30	FOSL2	chr13:69768328-69768610	A549	lung:	n/a	n/a
31	GATA2	chr13:69773713-69774245	SH-SY5Y	brain:	n/a	n/a
32	GATA2	chr13:69772572-69773281	SH-SY5Y	brain:	n/a	n/a
33	GATA3	chr13:69772699-69773391	SK-N-SH	brain:	n/a	n/a
34	GATA3	chr13:69773773-69774309	SK-N-SH	brain:	n/a	n/a
35	GATA3	chr13:69784976-69785172	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr13:69775546-69775710	SH-SY5Y	brain:	n/a	n/a
37	GATA3	chr13:69767774-69768560	SH-SY5Y	brain:	n/a	n/a
38	GATA3	chr13:69772776-69773432	SK-N-SH	brain:	n/a	n/a
39	GATA3	chr13:69772658-69773379	SH-SY5Y	brain:	n/a	n/a
40	GATA3	chr13:69792733-69792913	SH-SY5Y	brain:	n/a	n/a
41	GATA3	chr13:69773872-69774185	SH-SY5Y	brain:	n/a	n/a
42	GTF2B	chr13:69795853-69796053	K562	blood:	n/a	n/a
43	GTF2F1	chr13:69795914-69796053	K562	blood:	n/a	n/a
44	HEY1	chr13:69795815-69796706	K562	blood:	n/a	n/a
45	HEY1	chr13:69795814-69796874	K562	blood:	n/a	n/a
46	HEY1	chr13:69796967-69797283	K562	blood:	n/a	n/a
47	IRF1	chr13:69795905-69796139	K562	blood:	n/a	n/a
48	IRF1	chr13:69795726-69796161	K562	blood:	n/a	n/a
49	IRF1	chr13:69796409-69796516	K562	blood:	n/a	n/a
50	IRF3	chr13:69774018-69774044	GM12878	blood:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69809293-69809343	NHBE	bronchial:	n/a
2	chr13:69809293-69809343	NHBE	bronchial:	n/a
3	chr13:69809293-69809343	HMEC	breast:	n/a
4	chr13:69796872-69796922	HRPEpiC	eye:	n/a
5	chr13:69796872-69796922	HUVEC	blood vessel:	n/a
6	chr13:69796857-69796907	SK-N-SH_RA	brain:	n/a
7	chr13:69796872-69796922	T-47D	breast:	n/a
8	chr13:69809293-69809343	HAEpiC	amniotic membrane:	n/a
9	chr13:69796872-69796922	K562	blood:	n/a
10	chr13:69796857-69796907	HIPEpiC	eye:	n/a
11	chr13:69796872-69796922	HAEpiC	amniotic membrane:	n/a
12	chr13:69796857-69796907	Hepatocyte	liver:	n/a
13	chr13:69796857-69796907	AoSMC	blood vessel:	n/a
14	chr13:69796872-69796922	RPTEC	kidney:	n/a
15	chr13:69796872-69796922	SK-N-SH_RA	brain:	n/a
16	chr13:69796872-69796922	MCF10A-Er-Src	breast:	n/a
17	chr13:69809293-69809343	PFSK-1	brain:	n/a
18	chr13:69796872-69796922	Caco-2	colon:	n/a
19	chr13:69809293-69809343	HepG2	liver:	n/a
20	chr13:69809293-69809343	HCPEpiC	choroid plexus:	n/a
21	chr13:69796872-69796922	LNCaP	prostate:	n/a
22	chr13:69809293-69809343	GM12892	blood:	n/a
23	chr13:69809293-69809343	GM12878	blood:	n/a
24	chr13:69809293-69809343	NB4	blood:	n/a
25	chr13:69809293-69809343	AG09309	skin:	n/a
26	chr13:69796857-69796907	LNCaP	prostate:	n/a
27	chr13:69796857-69796907	HNPCEpiC	eye:	n/a
28	chr13:69796857-69796907	PANC-1	pancreas:	n/a
29	chr13:69796872-69796922	BE2_C	brain:	n/a
30	chr13:69796857-69796907	IMR90	lung:	fetal
31	chr13:69796857-69796907	AG10803	skin:	n/a
32	chr13:69796872-69796922	Hepatocyte	liver:	n/a
33	chr13:69796857-69796907	HEK293	kidney:	embryo
34	chr13:69796857-69796907	HCF	heart:	n/a
35	chr13:69796857-69796907	HRE	kidney:	n/a
36	chr13:69796872-69796922	HNPCEpiC	eye:	n/a
37	chr13:69796872-69796922	ovcar-3	ovarian:	n/a
38	chr13:69809293-69809343	H1-hESC	embryonic stem cell:	embryo
39	chr13:69796857-69796907	NH-A	brain:	n/a
40	chr13:69796872-69796922	SAEC	small airway:	n/a
41	chr13:69809293-69809343	HIPEpiC	eye:	n/a
42	chr13:69796857-69796907	ovcar-3	ovarian:	n/a
43	chr13:69796857-69796907	HUVEC	blood vessel:	n/a
44	chr13:69809293-69809343	ProgFib	skin:	n/a
45	chr13:69809293-69809343	GM06990	blood:	n/a
46	chr13:69809293-69809343	NT2-D1	testis:	n/a
47	chr13:69796857-69796907	AG09309	skin:	n/a
48	chr13:69796857-69796907	CMK	blood:	n/a
49	chr13:69796872-69796922	PANC-1	pancreas:	n/a
50	chr13:69796872-69796922	Hela-S3	cervix:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69792364..69793914-chr13:69801146..69804044,2	K562	blood:
2	chr13:69799858..69802118-chr13:69802729..69806556,4	K562	blood:
3	chr13:69792364..69793914-chr13:69801146..69804044,2	K562	blood:
4	chr13:69788123..69789818-chr13:69791504..69794154,2	K562	blood:
5	chr13:69799858..69802118-chr13:69802729..69806556,4	K562	blood:
6	chr13:69803907..69806465-chr13:69811377..69814161,2	K562	blood:
7	chr13:69794151..69795814-chr13:69798376..69800690,2	K562	blood:
8	chr13:69761351..69764047-chr13:69765452..69767697,2	K562	blood:
9	chr13:69788123..69789818-chr13:69791504..69794154,2	K562	blood:
10	chr13:69795398..69798188-chr13:69884200..69887047,2	K562	blood:
11	chr13:69794151..69795814-chr13:69798376..69800690,2	K562	blood:
12	chr13:69761351..69764047-chr13:69765452..69767697,2	K562	blood:
13	chr13:69803907..69806465-chr13:69811377..69814161,2	K562	blood:
14	chr13:69794008..69796830-chr13:69806883..69809682,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-6	chr13:69795972-69796802	NONHSAT034241
2	lnc-BORA-6	chr13:69796478-69796580	XLOC_010420

No data

Variant related genes	Relation type
LINC00383	TF binding region
LINC00383	CpG island
ENSG00000237534	chromatin interactions
ENSG00000235221	chromatin interactions
EIF4G2	miRNA target sites

Extended variants
information (count: 1676 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1676 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1992744	chr13:69759676-69759677	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181661210	chr13:69759690-69759691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs565179543	chr13:69759755-69759756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs369169621	chr13:69759773-69759774	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs373927988	chr13:69759778-69759779	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186458892	chr13:69759812-69759813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs560894491	chr13:69759862-69759863	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs542180745	chr13:69759881-69759882	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555358381	chr13:69759932-69759933	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs377368235	chr13:69759935-69759936	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs541355535	chr13:69759964-69759965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs144786930	chr13:69760020-69760021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs189919806	chr13:69760028-69760029	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180870973	chr13:69760032-69760033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376456967	chr13:69760058-69760059	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs563349547	chr13:69760071-69760072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529000766	chr13:69760114-69760115	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs562655919	chr13:69760130-69760131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs548964056	chr13:69760150-69760151	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs530165260	chr13:69760189-69760190	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs185071612	chr13:69760304-69760305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs528372509	chr13:69760368-69760369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs551744868	chr13:69760429-69760430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191003686	chr13:69760432-69760433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs183808015	chr13:69760446-69760447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs147962326	chr13:69760447-69760448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9541812	chr13:69760448-69760449	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs140577710	chr13:69760480-69760481	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs17659754	chr13:69760513-69760514	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs376985321	chr13:69760530-69760531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572157029	chr13:69760582-69760583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs534977987	chr13:69760595-69760596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs558389268	chr13:69760622-69760623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs564701861	chr13:69760626-69760627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs201929568	chr13:69760684-69760685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201606026	chr13:69760691-69760692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs77533803	chr13:69760693-69760694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs139722707	chr13:69760695-69760696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs35830839	chr13:69760696-69760697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs555743494	chr13:69760701-69760702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs386379630	chr13:69760703-69760704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs386379631	chr13:69760707-69760708	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs10671537	chr13:69760710-69760711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs543967447	chr13:69760722-69760723	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs202002522	chr13:69760736-69760737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188919091	chr13:69760784-69760785	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs552604873	chr13:69760791-69760792	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs149880143	chr13:69760904-69760905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7988095	chr13:69760929-69760930	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs34681197	chr13:69760939-69760940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
HIV/AIDS	22032296	CNVD
Prostate cancer	16705090	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Autism	22495311	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	CNVD
Burkitt''s lymphoma	18698080	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	21518781	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Colorectal cancer	20709793	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Ovarian cancer	20844748	CNVD
Colorectal cancer	19359472	CNVD
Intracranial aneurysm	19064780	CNVD
Breast cancer	19287154	CNVD
Acute myeloid leukemia	18379011	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Multiple myeloma	17077331	CNVD
Ependymoma	16718352	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16272173	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69742600-69770200	Weak transcription	H9 Cell Line	embryonic stem cell
2	chr13:69754600-69761600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:69761600-69762000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr13:69761600-69762200	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr13:69761800-69762200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
6	chr13:69762000-69766600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
7	chr13:69762200-69762600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr13:69762600-69762800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr13:69762800-69773800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:69766400-69766800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:69766600-69767000	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr13:69766800-69767200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr13:69766800-69769000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
14	chr13:69767000-69768200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chr13:69767200-69768400	Weak transcription	HUES64 Cell Line	embryonic stem cell
16	chr13:69767600-69768200	Enhancers	A549	lung
17	chr13:69768200-69769200	Weak transcription	A549	lung
18	chr13:69768200-69773200	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr13:69768400-69769600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
20	chr13:69768400-69771200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chr13:69768400-69775000	Enhancers	HUES64 Cell Line	embryonic stem cell
22	chr13:69768800-69770200	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr13:69768800-69774200	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:69769000-69770000	Enhancers	iPS-18 Cell Line	embryonic stem cell
25	chr13:69769200-69769400	Enhancers	A549	lung
26	chr13:69769200-69769800	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr13:69769600-69770200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
28	chr13:69769800-69773800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
29	chr13:69770000-69773800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr13:69770200-69770400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr13:69770200-69770600	Weak transcription	HUES6 Cell Line	embryonic stem cell
32	chr13:69770200-69771000	Enhancers	H9 Cell Line	embryonic stem cell
33	chr13:69770400-69773800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr13:69770600-69772000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr13:69771000-69782600	Weak transcription	H9 Cell Line	embryonic stem cell
36	chr13:69771200-69773200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
37	chr13:69772000-69772600	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr13:69772000-69774200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:69772600-69772800	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr13:69772800-69773600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr13:69773000-69773600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr13:69773200-69774400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr13:69773200-69775600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr13:69773600-69774200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:69773600-69774200	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chr13:69773600-69774400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr13:69773600-69776600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr13:69773800-69774200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
49	chr13:69773800-69774200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chr13:69773800-69774200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell

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