Variant report

Variant	nsv900455
Chromosome Location	chr13:69484933-69579427
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:318)
CpG islands
(count:427)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:318 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CCNT2	chr13:69558900-69559144	K562	blood:	n/a	n/a
2	CHD2	chr13:69528075-69528263	H1-hESC	embryonic stem cell:	n/a	n/a
3	CHD2	chr13:69528047-69528275	HepG2	liver:	n/a	n/a
4	CTCF	chr13:69501698-69501841	GM10266	blood:	n/a	n/a
5	CTCF	chr13:69501645-69501813	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr13:69501680-69501830	Caco-2	colon:	n/a	n/a
7	CTCF	chr13:69501660-69501810	K562	blood:	n/a	n/a
8	CTCF	chr13:69501680-69501830	HPAF	blood vessel:	n/a	n/a
9	CTCF	chr13:69501551-69501987	MCF-7	breast:	n/a	n/a
10	CTCF	chr13:69501660-69501810	HMF	breast:	n/a	n/a
11	CTCF	chr13:69501681-69501843	Kidney_OC	kidney:	n/a	n/a
12	CTCF	chr13:69501706-69501792	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chr13:69501680-69501830	GM12875	blood:	n/a	n/a
14	CTCF	chr13:69501616-69501963	K562	blood:	n/a	n/a
15	CTCF	chr13:69501617-69501812	K562	blood:	n/a	n/a
16	CTCF	chr13:69501642-69501824	SK-N-SH_RA	brain:	n/a	n/a
17	CTCF	chr13:69501740-69501890	GM12878	blood:	n/a	n/a
18	CTCF	chr13:69501506-69501962	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr13:69501600-69501750	HAc	cerebellar:	n/a	n/a
20	CTCF	chr13:69501660-69501810	GM12867	blood:	n/a	n/a
21	CTCF	chr13:69501680-69501830	SAEC	small airway:	n/a	n/a
22	CTCF	chr13:69501434-69501990	A549	lung:	n/a	n/a
23	CTCF	chr13:69501680-69501830	HPF	lung:	n/a	n/a
24	CTCF	chr13:69501680-69501830	GM12872	blood:	n/a	n/a
25	CTCF	chr13:69501638-69501818	MCF-7	breast:	n/a	n/a
26	CTCF	chr13:69501700-69501850	MCF-7	breast:	n/a	n/a
27	CTCF	chr13:69501523-69501871	MCF-7	breast:	n/a	n/a
28	CTCF	chr13:69501648-69501845	GM19239	blood:	n/a	n/a
29	CTCF	chr13:69501680-69501830	NB4	blood:	n/a	n/a
30	CTCF	chr13:69501700-69501850	HMEC	breast:	n/a	n/a
31	CTCF	chr13:69501660-69501810	HA-sp	spinal cord:	n/a	n/a
32	CTCF	chr13:69501680-69501830	MCF-7	breast:	n/a	n/a
33	CTCF	chr13:69501700-69501850	BE2_C	brain:	n/a	n/a
34	CTCF	chr13:69501680-69501830	RPTEC	kidney:	n/a	n/a
35	CTCF	chr13:69501649-69501818	MCF-7	breast:	n/a	n/a
36	CTCF	chr13:69501720-69501870	HEK293	kidney:	n/a	n/a
37	CTCF	chr13:69501617-69501827	A549	lung:	n/a	n/a
38	CTCF	chr13:69536416-69536486	GM13976	blood:	n/a	n/a
39	CTCF	chr13:69501679-69501808	GM19240	blood:	n/a	n/a
40	CTCF	chr13:69501634-69501900	SK-N-SH_RA	brain:	n/a	n/a
41	CTCF	chr13:69501640-69501790	HL-60	blood:	n/a	n/a
42	CTCF	chr13:69501647-69501857	HepG2	liver:	n/a	n/a
43	CTCF	chr13:69501648-69501830	GM19238	blood:	n/a	n/a
44	CTCF	chr13:69501720-69501870	GM12871	blood:	n/a	n/a
45	CTCF	chr13:69501668-69501856	K562	blood:	n/a	n/a
46	CTCF	chr13:69501700-69501850	Hela-S3	cervix:	n/a	n/a
47	CTCF	chr13:69501660-69501810	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr13:69501660-69501810	HepG2	liver:	n/a	n/a
49	CTCF	chr13:69501660-69501810	HEEpiC	esophagus:	n/a	n/a
50	CTCF	chr13:69501680-69501830	Hela-S3	cervix:	n/a	n/a

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69557960-69558010	GM12891	blood:	n/a
2	chr13:69558928-69558978	BJ	skin:	n/a
3	chr13:69559303-69559353	HIPEpiC	eye:	n/a
4	chr13:69557960-69558010	RPTEC	kidney:	n/a
5	chr13:69557960-69558010	SK-N-SH	brain:	n/a
6	chr13:69559039-69559089	HL-60	blood:	n/a
7	chr13:69558928-69558978	HIPEpiC	eye:	n/a
8	chr13:69561352-69561402	RPTEC	kidney:	n/a
9	chr13:69561352-69561402	LNCaP	prostate:	n/a
10	chr13:69559303-69559353	HEK293	kidney:	embryo
11	chr13:69559039-69559089	HPAEpiC	pulmonary alveolar:	n/a
12	chr13:69558928-69558978	CMK	blood:	n/a
13	chr13:69559303-69559353	PrEC	prostate:	n/a
14	chr13:69559194-69559244	IMR90	lung:	fetal
15	chr13:69557960-69558010	SKMC	muscle:	n/a
16	chr13:69558928-69558978	HPAEpiC	pulmonary alveolar:	n/a
17	chr13:69559194-69559244	BE2_C	brain:	n/a
18	chr13:69558928-69558978	H1-hESC	embryonic stem cell:	embryo
19	chr13:69559039-69559089	IMR90	lung:	fetal
20	chr13:69559039-69559089	AG10803	skin:	n/a
21	chr13:69559303-69559353	BJ	skin:	n/a
22	chr13:69555907-69555957	NH-A	brain:	n/a
23	chr13:69555907-69555957	IMR90	lung:	fetal
24	chr13:69557960-69558010	Caco-2	colon:	n/a
25	chr13:69559194-69559244	T-47D	breast:	n/a
26	chr13:69559039-69559089	Caco-2	colon:	n/a
27	chr13:69558928-69558978	SK-N-SH	brain:	n/a
28	chr13:69558928-69558978	PANC-1	pancreas:	n/a
29	chr13:69559303-69559353	HUVEC	blood vessel:	n/a
30	chr13:69559194-69559244	PANC-1	pancreas:	n/a
31	chr13:69561352-69561402	Hepatocyte	liver:	n/a
32	chr13:69558928-69558978	PrEC	prostate:	n/a
33	chr13:69559303-69559353	HCF	heart:	n/a
34	chr13:69559303-69559353	HL-60	blood:	n/a
35	chr13:69559039-69559089	ProgFib	skin:	n/a
36	chr13:69561352-69561402	AG04449	skin:	fetal
37	chr13:69558928-69558978	AG04450	lung:	fetal
38	chr13:69559039-69559089	AG09309	skin:	n/a
39	chr13:69557960-69558010	ECC-1	luminal epithelium:	n/a
40	chr13:69559194-69559244	GM06990	blood:	n/a
41	chr13:69559303-69559353	SK-N-SH_RA	brain:	n/a
42	chr13:69558928-69558978	NT2-D1	testis:	n/a
43	chr13:69555907-69555957	HUVEC	blood vessel:	n/a
44	chr13:69559194-69559244	HIPEpiC	eye:	n/a
45	chr13:69555907-69555957	T-47D	breast:	n/a
46	chr13:69561352-69561402	H1-hESC	embryonic stem cell:	embryo
47	chr13:69555907-69555957	HRPEpiC	eye:	n/a
48	chr13:69561352-69561402	HCT-116	colon:	n/a
49	chr13:69559303-69559353	NT2-D1	testis:	n/a
50	chr13:69557960-69558010	GM19239	blood:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69557613..69560490-chr13:69560641..69563029,2	K562	blood:
2	chr13:69577123..69579403-chr13:69580839..69583998,3	K562	blood:
3	chr13:69514136..69516850-chr13:69517321..69519328,2	K562	blood:
4	chr13:68878193..68879007-chr13:69501325..69502164,3	MCF-7	breast:
5	chr13:69514136..69516850-chr13:69517321..69519328,2	K562	blood:
6	chr13:68308872..68310810-chr13:69501547..69503078,2	MCF-7	breast:
7	chr13:69577914..69580803-chr13:69584083..69586306,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-25	chr13:69559190-69560196	NONHSAT034239

No data

Variant related genes	Relation type
ZDHHC20P4	TF binding region
ZDHHC20P4	CpG island
ENSG00000232380	chromatin interactions

Extended variants
information (count: 1410 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1410 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2438453	chr13:69484933-69484934	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs556926183	chr13:69484963-69484964	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573552931	chr13:69484987-69484988	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs374728175	chr13:69485045-69485046	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs71196223	chr13:69485046-69485047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs542504098	chr13:69485047-69485048	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80214231	chr13:69485062-69485063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs57198543	chr13:69485063-69485064	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs77255401	chr13:69485064-69485065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140954873	chr13:69485078-69485079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs560826256	chr13:69485083-69485084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2438452	chr13:69485168-69485169	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs200833815	chr13:69485210-69485211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs528247988	chr13:69485216-69485217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs544824902	chr13:69485237-69485238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs370545159	chr13:69485266-69485267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564387386	chr13:69485270-69485271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs547249275	chr13:69485272-69485273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs138126758	chr13:69485279-69485280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552780829	chr13:69485299-69485300	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs564713880	chr13:69485314-69485315	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs143581835	chr13:69485324-69485325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs79960495	chr13:69485353-69485354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529348621	chr13:69485368-69485369	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188008707	chr13:69485417-69485418	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs373286441	chr13:69485421-69485422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs147192434	chr13:69485467-69485468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532031495	chr13:69485486-69485487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs535202678	chr13:69485489-69485490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs192387075	chr13:69485490-69485491	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs571215099	chr13:69485525-69485526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs34830226	chr13:69485563-69485564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145809639	chr13:69485564-69485565	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs76084384	chr13:69485577-69485578	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs61951408	chr13:69485581-69485582	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs397958679	chr13:69485582-69485583	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs188708198	chr13:69485583-69485584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368139529	chr13:69485597-69485598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs556818944	chr13:69485604-69485605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs550325363	chr13:69485605-69485606	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs372390003	chr13:69485609-69485610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573284959	chr13:69485611-69485612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs201583981	chr13:69485619-69485620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs375590205	chr13:69485629-69485630	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs377326634	chr13:69485645-69485646	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201506227	chr13:69485648-69485649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199837029	chr13:69485656-69485657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs61951409	chr13:69485657-69485658	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs370005653	chr13:69485658-69485659	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148707520	chr13:69485667-69485668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
Breast cancer	22737080	CNVD
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69483400-69486800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:69499800-69500200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:69499800-69500200	Active TSS	Breast Myoepithelial Primary Cells	Breast
4	chr13:69500200-69503600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
5	chr13:69503600-69504200	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr13:69512800-69515200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:69513200-69514400	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr13:69513200-69514600	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:69513200-69515000	Enhancers	HUES48 Cell Line	embryonic stem cell
10	chr13:69513600-69514600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:69513800-69514600	Enhancers	H9 Cell Line	embryonic stem cell
12	chr13:69514000-69514600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr13:69514000-69514600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chr13:69514400-69514800	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr13:69516400-69516600	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr13:69533600-69533800	Enhancers	iPS-20b Cell Line	embryonic stem cell
17	chr13:69533800-69534800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr13:69534400-69535200	Enhancers	HUES48 Cell Line	embryonic stem cell
19	chr13:69534800-69535400	Enhancers	iPS-20b Cell Line	embryonic stem cell
20	chr13:69540800-69541200	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr13:69541200-69541600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
22	chr13:69541400-69542400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
23	chr13:69541600-69541800	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chr13:69541600-69543400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
25	chr13:69541800-69542000	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr13:69541800-69542400	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr13:69541800-69542400	Enhancers	HUES64 Cell Line	embryonic stem cell
28	chr13:69541800-69544000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
29	chr13:69542000-69543800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
30	chr13:69542400-69543800	Weak transcription	HUES48 Cell Line	embryonic stem cell
31	chr13:69542400-69543800	Weak transcription	HUES64 Cell Line	embryonic stem cell
32	chr13:69543800-69545400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:69543800-69545600	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr13:69543800-69545800	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chr13:69543800-69546200	Enhancers	HUES64 Cell Line	embryonic stem cell
36	chr13:69543800-69546400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr13:69544000-69545800	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr13:69544000-69546000	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:69544200-69545600	Enhancers	H1 Cell Line	embryonic stem cell
40	chr13:69544200-69545800	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr13:69545400-69547400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr13:69547600-69547800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr13:69554000-69554400	Enhancers	iPS-20b Cell Line	embryonic stem cell
44	chr13:69557200-69557600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
45	chr13:69557200-69558000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
46	chr13:69557600-69558000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
47	chr13:69558000-69559000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr13:69558000-69570200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
49	chr13:69558800-69559000	Enhancers	Placenta	Placenta
50	chr13:69559000-69559400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell

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