Variant report

Variant	nsv900098
Chromosome Location	chr13:55563725-55778669
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	BACH1	chr13:55575088-55575361	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:55761085-55761087	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:55609400-55609437	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr13:55566557-55566577	GM12878	blood:	n/a	n/a
5	CEBPB	chr13:55658829-55659084	K562	blood:	n/a	chr13:55658962-55658973
6	CEBPB	chr13:55752126-55752249	HepG2	liver:	n/a	chr13:55752198-55752209
7	CEBPB	chr13:55651579-55651868	IMR90	lung:	n/a	chr13:55651706-55651723
8	CEBPB	chr13:55571000-55571200	HepG2	liver:	n/a	n/a
9	CEBPB	chr13:55603473-55603806	HepG2	liver:	n/a	chr13:55603619-55603632 chr13:55603621-55603630 chr13:55603619-55603630 chr13:55603621-55603630 chr13:55603621-55603630
10	CEBPB	chr13:55776990-55777388	HepG2	liver:	n/a	chr13:55777077-55777088 chr13:55777076-55777087 chr13:55777076-55777089 chr13:55777075-55777092
11	CEBPB	chr13:55658798-55659147	H1-hESC	embryonic stem cell:	n/a	chr13:55658962-55658973
12	CEBPB	chr13:55651572-55651871	HepG2	liver:	n/a	chr13:55651706-55651723
13	CEBPB	chr13:55603464-55603809	H1-hESC	embryonic stem cell:	n/a	chr13:55603619-55603632 chr13:55603621-55603630 chr13:55603619-55603630 chr13:55603621-55603630 chr13:55603621-55603630
14	CEBPB	chr13:55603439-55603795	IMR90	lung:	n/a	chr13:55603619-55603632 chr13:55603621-55603630 chr13:55603619-55603630 chr13:55603621-55603630 chr13:55603621-55603630
15	CEBPB	chr13:55658783-55659141	IMR90	lung:	n/a	chr13:55658962-55658973
16	CEBPB	chr13:55563190-55563968	H1-hESC	embryonic stem cell:	n/a	n/a
17	CEBPB	chr13:55745261-55745481	HepG2	liver:	n/a	chr13:55745328-55745339
18	CEBPB	chr13:55752073-55752328	H1-hESC	embryonic stem cell:	n/a	chr13:55752198-55752209
19	CEBPB	chr13:55651619-55651872	H1-hESC	embryonic stem cell:	n/a	chr13:55651706-55651723
20	CEBPB	chr13:55658778-55659120	ECC-1	luminal epithelium:	n/a	chr13:55658962-55658973
21	CEBPB	chr13:55658810-55659132	A549	lung:	n/a	chr13:55658962-55658973
22	CEBPB	chr13:55603451-55603799	K562	blood:	n/a	chr13:55603619-55603632 chr13:55603621-55603630 chr13:55603619-55603630 chr13:55603621-55603630 chr13:55603621-55603630
23	CEBPB	chr13:55658786-55659147	HepG2	liver:	n/a	chr13:55658962-55658973
24	CEBPB	chr13:55694979-55695179	HepG2	liver:	n/a	n/a
25	CHD1	chr13:55614957-55615324	H1-hESC	embryonic stem cell:	n/a	n/a
26	CHD1	chr13:55614223-55614494	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD1	chr13:55616086-55617087	H1-hESC	embryonic stem cell:	n/a	n/a
28	CHD2	chr13:55647449-55647657	H1-hESC	embryonic stem cell:	n/a	n/a
29	CTCF	chr13:55738680-55738830	GM12869	blood:	n/a	n/a
30	CTCF	chr13:55563690-55563955	MCF-7	breast:	n/a	n/a
31	CTCF	chr13:55773361-55773594	MCF-7	breast:	n/a	n/a
32	CTCF	chr13:55563700-55563850	Caco-2	colon:	n/a	n/a
33	CTCF	chr13:55773438-55773544	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr13:55773380-55773530	HEK293	kidney:	n/a	n/a
35	CTCF	chr13:55563740-55563890	Caco-2	colon:	n/a	n/a
36	CTCF	chr13:55773397-55773496	Pancreas_OC	pancreas:	n/a	n/a
37	CTCF	chr13:55773400-55773550	BE2_C	brain:	n/a	n/a
38	CTCF	chr13:55773401-55773534	LNCaP	prostate:	n/a	n/a
39	CTCF	chr13:55563740-55563890	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr13:55661360-55661510	HEK293	kidney:	n/a	n/a
41	CTCF	chr13:55563780-55563930	BE2_C	brain:	n/a	n/a
42	CTCF	chr13:55773276-55773693	MCF-7	breast:	n/a	n/a
43	CTCF	chr13:55773353-55773587	T-47D	breast:	n/a	n/a
44	CTCF	chr13:55661392-55661461	MCF-7	breast:	n/a	n/a
45	CTCF	chr13:55563680-55563830	MCF-7	breast:	n/a	n/a
46	CTCF	chr13:55563720-55563870	NHEK	skin:	n/a	n/a
47	CTCF	chr13:55773360-55773510	HRPEpiC	eye:	n/a	n/a
48	CTCF	chr13:55773394-55773544	HepG2	liver:	n/a	n/a
49	CTCF	chr13:55598645-55598692	GM10248	blood:	n/a	n/a
50	CTCF	chr13:55773330-55773620	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:55628257-55628307	AG09319	gingival:	n/a
2	chr13:55576092-55576142	PANC-1	pancreas:	n/a
3	chr13:55612647-55612697	SK-N-SH	brain:	n/a
4	chr13:55612647-55612697	HEK293	kidney:	embryo
5	chr13:55587486-55587536	Caco-2	colon:	n/a
6	chr13:55628673-55628723	HCM	heart:	n/a
7	chr13:55587486-55587536	IMR90	lung:	fetal
8	chr13:55628454-55628504	CMK	blood:	n/a
9	chr13:55628257-55628307	ovcar-3	ovarian:	n/a
10	chr13:55628673-55628723	MCF10A-Er-Src	breast:	n/a
11	chr13:55628257-55628307	GM19239	blood:	n/a
12	chr13:55628454-55628504	SKMC	muscle:	n/a
13	chr13:55628454-55628504	HEEpiC	esophagus:	n/a
14	chr13:55576092-55576142	ovcar-3	ovarian:	n/a
15	chr13:55612647-55612697	BJ	skin:	n/a
16	chr13:55628257-55628307	HPAEpiC	pulmonary alveolar:	n/a
17	chr13:55628257-55628307	HCT-116	colon:	n/a
18	chr13:55587486-55587536	AG09319	gingival:	n/a
19	chr13:55628673-55628723	NB4	blood:	n/a
20	chr13:55576092-55576142	SKMC	muscle:	n/a
21	chr13:55628673-55628723	HMEC	breast:	n/a
22	chr13:55587486-55587536	HCPEpiC	choroid plexus:	n/a
23	chr13:55628257-55628307	HCF	heart:	n/a
24	chr13:55612647-55612697	RPTEC	kidney:	n/a
25	chr13:55628454-55628504	HUVEC	blood vessel:	n/a
26	chr13:55587486-55587536	HRCEpiC	kidney:	n/a
27	chr13:55576092-55576142	CMK	blood:	n/a
28	chr13:55576092-55576142	BJ	skin:	n/a
29	chr13:55628257-55628307	BJ	skin:	n/a
30	chr13:55628257-55628307	HCM	heart:	n/a
31	chr13:55628673-55628723	AG04449	skin:	fetal
32	chr13:55628257-55628307	ECC-1	luminal epithelium:	n/a
33	chr13:55612647-55612697	K562	blood:	n/a
34	chr13:55628673-55628723	RPTEC	kidney:	n/a
35	chr13:55587486-55587536	SK-N-SH_RA	brain:	n/a
36	chr13:55628673-55628723	HL-60	blood:	n/a
37	chr13:55587486-55587536	SKMC	muscle:	n/a
38	chr13:55628673-55628723	AG09319	gingival:	n/a
39	chr13:55628454-55628504	GM19239	blood:	n/a
40	chr13:55628673-55628723	SK-N-SH	brain:	n/a
41	chr13:55628673-55628723	GM12892	blood:	n/a
42	chr13:55628673-55628723	U87	brain:	n/a
43	chr13:55628257-55628307	H1-hESC	embryonic stem cell:	embryo
44	chr13:55628257-55628307	A549	lung:	n/a
45	chr13:55628257-55628307	SK-N-SH	brain:	n/a
46	chr13:55628454-55628504	U87	brain:	n/a
47	chr13:55576092-55576142	ProgFib	skin:	n/a
48	chr13:55576092-55576142	AG04449	skin:	fetal
49	chr13:55576092-55576142	PrEC	prostate:	n/a
50	chr13:55628454-55628504	HEK293	kidney:	embryo

No.	Distal block	Cell Line	Cell type
1	chr13:55719312..55721477-chr13:55723763..55726204,2	K562	blood:
2	chr13:55588254..55589830-chr13:55591495..55593128,2	K562	blood:
3	chr13:55588254..55589830-chr13:55591495..55593128,2	K562	blood:
4	chr13:55719312..55721477-chr13:55723763..55726204,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PRR20A-10	chr13:55682117-55682626	NONHSAT034041
2	lnc-OLFM4-13	chr13:55628379-55629550	NONHSAT034038
3	lnc-OLFM4-13	chr13:55613553-55627834	NONHSAT034038
4	lnc-PRR20A-10	chr13:55682789-55682990	NONHSAT034041

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5007-3p	chr13:55748644-55748665	MIMAT0021036
hsa-miR-5007-5p	chr13:55748609-55748630	MIMAT0021035

Variant related genes	Relation type
MIR5007	TF binding region
MIR5007	CpG island

Extended variants
information (count: 5717 )
Associated
traits (count: 105 )

Variant overlapped rSNPs/rCNVs (count:5717 , 50 per page) page: 1 2 3 4 5 6 7 ... 115

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs263811	chr13:55563725-55563726	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs182120680	chr13:55563764-55563765	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148223919	chr13:55563804-55563805	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs567995313	chr13:55563826-55563827	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs143167184	chr13:55563829-55563830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556229097	chr13:55563835-55563836	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9569166	chr13:55563848-55563849	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs186804420	chr13:55563865-55563866	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539152231	chr13:55563875-55563876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs191602432	chr13:55563885-55563886	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12232053	chr13:55563903-55563904	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs373401535	chr13:55563904-55563905	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs185646732	chr13:55563989-55563990	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs574422500	chr13:55563997-55563998	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs543299394	chr13:55564027-55564028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs562560572	chr13:55564038-55564039	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs568626722	chr13:55564067-55564068	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs190514674	chr13:55564068-55564069	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543618256	chr13:55564192-55564193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs566122530	chr13:55564209-55564210	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545178254	chr13:55564296-55564297	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565417128	chr13:55564329-55564330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527778724	chr13:55564365-55564366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs147510482	chr13:55564366-55564367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs533740059	chr13:55564374-55564375	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376089008	chr13:55564391-55564392	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9563269	chr13:55564400-55564401	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs193062336	chr13:55564418-55564419	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs569672414	chr13:55564429-55564430	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145649230	chr13:55564444-55564445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs150700801	chr13:55564445-55564446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs565816895	chr13:55564612-55564613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75895423	chr13:55564635-55564636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs139678477	chr13:55564666-55564667	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs7994156	chr13:55564706-55564707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs374762146	chr13:55564749-55564750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs72623354	chr13:55564772-55564773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188401685	chr13:55564782-55564783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs149776429	chr13:55564794-55564795	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs538001440	chr13:55564809-55564810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs76830361	chr13:55564834-55564835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs565110913	chr13:55564842-55564843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs77340040	chr13:55564850-55564851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs376382615	chr13:55564853-55564854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181239201	chr13:55564857-55564858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9597070	chr13:55564871-55564872	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs263812	chr13:55564876-55564877	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs550505043	chr13:55564955-55564956	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs564013001	chr13:55564960-55564961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183474556	chr13:55565022-55565023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:105)

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
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	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
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	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
Urothelial carcinoma	21177765	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Esophageal squamous carcinoma	17470683	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:55562000-55565600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:55563000-55563800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:55563200-55563800	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr13:55563200-55563800	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr13:55563600-55563800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chr13:55563600-55563800	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:55563600-55563800	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr13:55563600-55564200	Enhancers	Adipose Nuclei	Adipose
9	chr13:55563800-55566200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:55563800-55567400	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr13:55563800-55569200	Weak transcription	HUES64 Cell Line	embryonic stem cell
12	chr13:55563800-55569200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr13:55564000-55564600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
14	chr13:55566200-55566600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr13:55567400-55567600	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chr13:55567600-55567800	Weak transcription	HUES48 Cell Line	embryonic stem cell
17	chr13:55568000-55569600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr13:55569000-55574200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:55569200-55571600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
20	chr13:55569200-55572000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
21	chr13:55569400-55572400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
22	chr13:55569600-55571600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
23	chr13:55569800-55572000	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr13:55570600-55570800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
25	chr13:55570800-55573000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
26	chr13:55570800-55575600	Weak transcription	H9 Cell Line	embryonic stem cell
27	chr13:55571600-55573200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
28	chr13:55571600-55573400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
29	chr13:55572000-55572800	Weak transcription	H1 Cell Line	embryonic stem cell
30	chr13:55572000-55573400	Weak transcription	HUES64 Cell Line	embryonic stem cell
31	chr13:55572400-55573200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr13:55572800-55576800	Enhancers	H1 Cell Line	embryonic stem cell
33	chr13:55573000-55573600	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chr13:55573200-55574000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr13:55573200-55574400	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr13:55573200-55576800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr13:55573200-55577800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr13:55573400-55573600	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:55573400-55574200	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr13:55573400-55576000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
41	chr13:55573400-55577000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr13:55573600-55574000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr13:55573600-55575200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr13:55573600-55576400	Enhancers	HUES6 Cell Line	embryonic stem cell
45	chr13:55574000-55574200	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
46	chr13:55574000-55574800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
47	chr13:55574200-55574400	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
48	chr13:55574200-55575000	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr13:55574200-55575200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr13:55574400-55574600	Enhancers	HUES64 Cell Line	embryonic stem cell

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