Variant report

Variant	esv3525266
Chromosome Location	chr13:69794000-69846365
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:13)
LncRNA
region (count:4)
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	BHLHE40	chr13:69839148-69839308	K562	blood:	n/a	n/a
3	CEBPB	chr13:69795373-69795654	Hela-S3	cervix:	n/a	n/a
4	CEBPB	chr13:69795374-69795674	K562	blood:	n/a	n/a
5	CEBPB	chr13:69839218-69839553	K562	blood:	n/a	n/a
6	CEBPB	chr13:69795365-69795601	HepG2	liver:	n/a	n/a
7	CEBPD	chr13:69795817-69796165	K562	blood:	n/a	n/a
8	CHD1	chr13:69808687-69808760	H1-hESC	embryonic stem cell:	n/a	n/a
9	CHD2	chr13:69838411-69838604	Hela-S3	cervix:	n/a	n/a
10	CTBP2	chr13:69808828-69809721	H1-hESC	embryonic stem cell:	n/a	n/a
11	CTCF	chr13:69832600-69832750	WI-38	lung:	n/a	n/a
12	CTCF	chr13:69809200-69809350	GM12865	blood:	n/a	n/a
13	CTCF	chr13:69798214-69798362	K562	blood:	n/a	n/a
14	CTCF	chr13:69838641-69838695	MCF-7	breast:	n/a	n/a
15	CTCF	chr13:69817605-69817738	GM12878	blood:	n/a	n/a
16	CTCF	chr13:69836756-69836786	Lung_OC	lung:	n/a	n/a
17	CTCF	chr13:69817683-69817706	MCF-7	breast:	n/a	n/a
18	CTCF	chr13:69797096-69797176	Kidney_OC	kidney:	n/a	n/a
19	CTCF	chr13:69797040-69797102	LNCaP	prostate:	n/a	n/a
20	CTCF	chr13:69817667-69817727	MCF-7	breast:	n/a	n/a
21	CTCF	chr13:69800977-69800998	GM20000	blood:	n/a	n/a
22	CTCF	chr13:69798188-69798430	K562	blood:	n/a	n/a
23	E2F4	chr13:69840640-69840815	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr13:69842781-69843022	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr13:69814207-69814362	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr13:69834597-69834619	MCF10A-Er-Src	breast:	n/a	n/a
27	EBF1	chr13:69839598-69839806	GM12878	blood:	n/a	chr13:69839659-69839670
28	ELK1	chr13:69801719-69801720	K562	blood:	n/a	n/a
29	EP300	chr13:69795806-69796108	GM12878	blood:	n/a	n/a
30	FOS	chr13:69839220-69839509	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr13:69839281-69839481	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr13:69839206-69839507	MCF10A-Er-Src	breast:	n/a	n/a
33	FOS	chr13:69805182-69805386	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr13:69839268-69839479	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr13:69834237-69834297	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr13:69814433-69814610	MCF10A-Er-Src	breast:	n/a	n/a
37	GABPA	chr13:69839144-69839364	K562	blood:	n/a	n/a
38	GATA2	chr13:69839106-69839414	K562	blood:	n/a	n/a
39	GATA3	chr13:69838751-69839105	T-47D	breast:	n/a	n/a
40	GATA3	chr13:69817346-69817745	T-47D	breast:	n/a	n/a
41	GATA3	chr13:69817360-69817806	T-47D	breast:	n/a	n/a
42	GATA3	chr13:69838346-69838806	MCF-7	breast:	n/a	chr13:69838467-69838475
43	GATA3	chr13:69838776-69839126	T-47D	breast:	n/a	n/a
44	GATA3	chr13:69838149-69838834	MCF-7	breast:	n/a	chr13:69838467-69838475
45	GATA3	chr13:69838309-69838706	T-47D	breast:	n/a	chr13:69838467-69838475
46	GATA3	chr13:69838219-69838680	T-47D	breast:	n/a	chr13:69838467-69838475
47	GTF2B	chr13:69795853-69796053	K562	blood:	n/a	n/a
48	GTF2F1	chr13:69795914-69796053	K562	blood:	n/a	n/a
49	HEY1	chr13:69795815-69796706	K562	blood:	n/a	n/a
50	HEY1	chr13:69796967-69797283	K562	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	chr13:69796857-69796907	BJ	skin:	n/a
2	chr13:69796857-69796907	BJ	skin:	n/a
3	chr13:69809293-69809343	GM19239	blood:	n/a
4	chr13:69796872-69796922	SAEC	small airway:	n/a
5	chr13:69809293-69809343	HCPEpiC	choroid plexus:	n/a
6	chr13:69809293-69809343	BJ	skin:	n/a
7	chr13:69796857-69796907	NHDF-neo	bronchial:	n/a
8	chr13:69809293-69809343	PANC-1	pancreas:	n/a
9	chr13:69809293-69809343	AG04450	lung:	fetal
10	chr13:69796872-69796922	U87	brain:	n/a
11	chr13:69796857-69796907	SKMC	muscle:	n/a
12	chr13:69796872-69796922	GM12878	blood:	n/a
13	chr13:69809293-69809343	HL-60	blood:	n/a
14	chr13:69796857-69796907	HCPEpiC	choroid plexus:	n/a
15	chr13:69809293-69809343	AoSMC	blood vessel:	n/a
16	chr13:69809293-69809343	AG10803	skin:	n/a
17	chr13:69809293-69809343	HPAEpiC	pulmonary alveolar:	n/a
18	chr13:69796857-69796907	Hepatocyte	liver:	n/a
19	chr13:69809293-69809343	HAEpiC	amniotic membrane:	n/a
20	chr13:69796872-69796922	HMEC	breast:	n/a
21	chr13:69809293-69809343	IMR90	lung:	fetal
22	chr13:69809293-69809343	Caco-2	colon:	n/a
23	chr13:69796857-69796907	U87	brain:	n/a
24	chr13:69796872-69796922	HNPCEpiC	eye:	n/a
25	chr13:69809293-69809343	NHDF-neo	bronchial:	n/a
26	chr13:69809293-69809343	AG09319	gingival:	n/a
27	chr13:69796872-69796922	NH-A	brain:	n/a
28	chr13:69796872-69796922	GM19239	blood:	n/a
29	chr13:69796857-69796907	HMEC	breast:	n/a
30	chr13:69796872-69796922	GM12892	blood:	n/a
31	chr13:69809293-69809343	HRCEpiC	kidney:	n/a
32	chr13:69796857-69796907	HAEpiC	amniotic membrane:	n/a
33	chr13:69796872-69796922	PrEC	prostate:	n/a
34	chr13:69796857-69796907	NH-A	brain:	n/a
35	chr13:69796857-69796907	K562	blood:	n/a
36	chr13:69796872-69796922	IMR90	lung:	fetal
37	chr13:69796857-69796907	Hela-S3	cervix:	n/a
38	chr13:69809293-69809343	HRPEpiC	eye:	n/a
39	chr13:69809293-69809343	HEEpiC	esophagus:	n/a
40	chr13:69809293-69809343	U87	brain:	n/a
41	chr13:69796857-69796907	PrEC	prostate:	n/a
42	chr13:69809293-69809343	HUVEC	blood vessel:	n/a
43	chr13:69809293-69809343	SK-N-MC	brain:	n/a
44	chr13:69809293-69809343	HNPCEpiC	eye:	n/a
45	chr13:69809293-69809343	CMK	blood:	n/a
46	chr13:69796872-69796922	SK-N-SH_RA	brain:	n/a
47	chr13:69809293-69809343	NB4	blood:	n/a
48	chr13:69796872-69796922	SK-N-MC	brain:	n/a
49	chr13:69796872-69796922	H1-hESC	embryonic stem cell:	embryo
50	chr13:69809293-69809343	Hela-S3	cervix:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69803907..69806465-chr13:69811377..69814161,2	K562	blood:
2	chr13:69792364..69793914-chr13:69801146..69804044,2	K562	blood:
3	chr13:69799858..69802118-chr13:69802729..69806556,4	K562	blood:
4	chr13:69795398..69798188-chr13:69884200..69887047,2	K562	blood:
5	chr13:69788123..69789818-chr13:69791504..69794154,2	K562	blood:
6	chr13:69794151..69795814-chr13:69798376..69800690,2	K562	blood:
7	chr13:69831283..69833346-chr13:69836562..69838763,2	MCF-7	breast:
8	chr13:69839216..69841490-chr13:69867661..69869798,2	K562	blood:
9	chr13:69803907..69806465-chr13:69811377..69814161,2	K562	blood:
10	chr13:69831283..69833346-chr13:69836562..69838763,2	MCF-7	breast:
11	chr13:69799858..69802118-chr13:69802729..69806556,4	K562	blood:
12	chr13:69794151..69795814-chr13:69798376..69800690,2	K562	blood:
13	chr13:69794008..69796830-chr13:69806883..69809682,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BORA-6	chr13:69844022-69844083	NONHSAT034241
2	lnc-BORA-6	chr13:69796478-69796580	XLOC_010420
3	lnc-BORA-6	chr13:69795972-69796802	NONHSAT034241
4	lnc-BORA-6	chr13:69844023-69844083	XLOC_010420

No data

Variant related genes	Relation type
LINC00383	TF binding region
LINC00383	CpG island
ENSG00000235221	chromatin interactions
ENSG00000237534	chromatin interactions
EIF4G2	miRNA target sites
EIF4G3	miRNA target sites

Extended variants
information (count: 1476 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:1476 , 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	rs148452899	chr13:69795368-69795369	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs117570961	chr13:69795369-69795370	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs562786649	chr13:69795472-69795473	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs192365892	chr13:69795508-69795509	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs548432481	chr13:69795535-69795536	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs367664838	chr13:69795544-69795545	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs561224531	chr13:69795546-69795547	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs554520744	chr13:69795555-69795556	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs530255490	chr13:69795634-69795635	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs546790033	chr13:69795650-69795651	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs566812622	chr13:69795683-69795684	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs532395203	chr13:69795736-69795737	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs552421240	chr13:69795770-69795771	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs569234673	chr13:69795784-69795785	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs183749014	chr13:69795839-69795840	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs142707030	chr13:69795845-69795846	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs189640312	chr13:69795889-69795890	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs533836137	chr13:69795910-69795911	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs146023598	chr13:69795934-69795935	Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs533701848	chr13:69795987-69795988	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
21	rs9599431	chr13:69795992-69795993	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs556475500	chr13:69796018-69796019	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
23	rs192459730	chr13:69796059-69796060	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
24	rs7323538	chr13:69796074-69796075	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs561882554	chr13:69796077-69796078	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
26	rs527500026	chr13:69796126-69796127	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
27	rs540695295	chr13:69796127-69796128	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
28	rs560401327	chr13:69796134-69796135	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
29	rs184677692	chr13:69796160-69796161	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
30	rs552198089	chr13:69796187-69796188	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
31	rs370394440	chr13:69796190-69796191	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
32	rs144185133	chr13:69796200-69796201	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
33	rs574698301	chr13:69796212-69796213	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
34	rs531842726	chr13:69796214-69796215	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
35	rs548601905	chr13:69796217-69796218	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs568610527	chr13:69796271-69796272	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs534142888	chr13:69796305-69796306	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs372489515	chr13:69796344-69796345	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs541552361	chr13:69796393-69796394	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs9599432	chr13:69796396-69796397	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs560589083	chr13:69796404-69796405	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs539437298	chr13:69796455-69796456	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs190057910	chr13:69796463-69796464	Active TSS	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs576117648	chr13:69796491-69796492	Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs542101396	chr13:69796506-69796507	Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs555398581	chr13:69796592-69796593	Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
47	rs572174373	chr13:69796599-69796600	Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
48	rs139730891	chr13:69796609-69796610	Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs181704232	chr13:69796613-69796614	Active TSS	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs200333733	chr13:69796617-69796618	Active TSS	Chromatin interactive region lncRNA	1 gene(s)	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	22037309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD

Chromatin state (count:43 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69795400-69798200	Active TSS	K562	blood
2	chr13:69797800-69798000	Enhancers	HUES64 Cell Line	embryonic stem cell
3	chr13:69798200-69799600	Weak transcription	K562	blood
4	chr13:69798200-69807400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr13:69798200-69807800	Weak transcription	HUES64 Cell Line	embryonic stem cell
6	chr13:69799600-69800200	Active TSS	Duodenum Mucosa	Duodenum
7	chr13:69799600-69800200	Enhancers	K562	blood
8	chr13:69800200-69802600	Weak transcription	K562	blood
9	chr13:69800400-69801600	Enhancers	Gastric	stomach
10	chr13:69806600-69808200	Weak transcription	HUES6 Cell Line	embryonic stem cell
11	chr13:69806800-69807000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr13:69807000-69807200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
13	chr13:69807200-69809000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:69807400-69810000	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr13:69807800-69809200	Enhancers	HUES64 Cell Line	embryonic stem cell
16	chr13:69807800-69809200	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr13:69807800-69809600	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr13:69808000-69809200	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr13:69808200-69809800	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr13:69808600-69809000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr13:69808600-69809000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:69808600-69809400	Enhancers	H9 Cell Line	embryonic stem cell
23	chr13:69808600-69809600	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chr13:69808600-69809600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr13:69808600-69809800	Enhancers	H1 Cell Line	embryonic stem cell
26	chr13:69809000-69809800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
27	chr13:69809000-69809800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr13:69809400-69810400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr13:69810600-69810800	Enhancers	H9 Cell Line	embryonic stem cell
30	chr13:69813200-69821800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr13:69821800-69822200	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr13:69822200-69822400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr13:69836800-69837000	Enhancers	K562	blood
34	chr13:69837000-69838000	Weak transcription	K562	blood
35	chr13:69837600-69839600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr13:69838000-69839600	Enhancers	K562	blood
37	chr13:69838200-69839400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr13:69838400-69839000	Enhancers	Placenta Amnion	Placenta Amnion
39	chr13:69838400-69839200	Enhancers	Gastric	stomach
40	chr13:69838600-69839200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr13:69839400-69839800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr13:69839600-69839800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr13:69839600-69856400	Weak transcription	K562	blood

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