Variant report

Variant	nsv561955
Chromosome Location	chr13:64259484-64348759
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:176)
CpG islands
(count:183)
Chromatin interactive
region (count:2)
LncRNA
region (count:20)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:176 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr13:64282710-64282910	H1-hESC	embryonic stem cell:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
2	CEBPB	chr13:64282619-64282952	IMR90	lung:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
3	CEBPB	chr13:64262408-64262608	HepG2	liver:	n/a	chr13:64262502-64262513
4	CEBPB	chr13:64282631-64282951	HepG2	liver:	n/a	chr13:64282778-64282789 chr13:64282778-64282791 chr13:64282779-64282790
5	CEBPB	chr13:64313524-64313659	HepG2	liver:	n/a	chr13:64313555-64313566
6	CTCF	chr13:64324024-64324308	K562	blood:	n/a	n/a
7	CTCF	chr13:64324094-64324161	K562	blood:	n/a	n/a
8	CTCF	chr13:64324125-64324255	Fibrobl	skin:	n/a	n/a
9	CTCF	chr13:64324128-64324253	GM19239	blood:	n/a	n/a
10	CTCF	chr13:64338496-64338540	ProgFib	skin:	n/a	n/a
11	CTCF	chr13:64334444-64334532	Spleen_OC	spleen:	n/a	n/a
12	CTCF	chr13:64324072-64324260	Hela-S3	cervix:	n/a	n/a
13	CTCF	chr13:64324133-64324259	MCF-7	breast:	n/a	n/a
14	CTCF	chr13:64320948-64321033	LNCaP	prostate:	n/a	n/a
15	CTCF	chr13:64324097-64324217	Spleen_OC	spleen:	n/a	n/a
16	CTCF	chr13:64281020-64281170	HCPEpiC	choroid plexus:	n/a	n/a
17	CTCF	chr13:64324050-64324261	MCF-7	breast:	n/a	n/a
18	CTCF	chr13:64324047-64324270	Medullo	brain:	n/a	n/a
19	CTCF	chr13:64324133-64324244	ProgFib	skin:	n/a	n/a
20	CTCF	chr13:64330862-64330927	Medullo	brain:	n/a	n/a
21	CTCF	chr13:64324117-64324248	GM10266	blood:	n/a	n/a
22	CTCF	chr13:64324119-64324214	GM10248	blood:	n/a	n/a
23	CTCF	chr13:64324079-64324211	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr13:64338485-64338489	ProgFib	skin:	n/a	n/a
25	CTCF	chr13:64324126-64324196	HUVEC	blood vessel:	n/a	n/a
26	CTCF	chr13:64324173-64324251	GM12878	blood:	n/a	n/a
27	CTCF	chr13:64312774-64312800	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr13:64324028-64324296	A549	lung:	n/a	n/a
29	CTCF	chr13:64324188-64324191	GM19240	blood:	n/a	n/a
30	CTCF	chr13:64339091-64339163	Lung_OC	lung:	n/a	n/a
31	CTCF	chr13:64313949-64314007	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr13:64324142-64324254	A549	lung:	n/a	n/a
33	CTCF	chr13:64281060-64281210	HCT-116	colon:	n/a	n/a
34	CTCF	chr13:64297739-64297766	LNCaP	prostate:	n/a	n/a
35	CTCF	chr13:64338203-64338280	GM13976	blood:	n/a	n/a
36	CTCF	chr13:64324118-64324236	GM13977	blood:	n/a	n/a
37	CTCF	chr13:64296335-64296399	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr13:64324108-64324265	MCF-7	breast:	n/a	n/a
39	CTCF	chr13:64338648-64338715	Kidney_OC	kidney:	n/a	n/a
40	CTCF	chr13:64324042-64324308	LNCaP	prostate:	n/a	n/a
41	CTCF	chr13:64324080-64324269	Kidney_OC	kidney:	n/a	n/a
42	CTCF	chr13:64320841-64320933	LNCaP	prostate:	n/a	n/a
43	CTCF	chr13:64324034-64324271	MCF-7	breast:	n/a	n/a
44	CTCF	chr13:64324052-64324317	LNCaP	prostate:	n/a	n/a
45	CTCF	chr13:64324030-64324275	Gliobla	brain:	n/a	n/a
46	CTCF	chr13:64292407-64292528	Lung_OC	lung:	n/a	n/a
47	CTCF	chr13:64330314-64330384	Kidney_OC	kidney:	n/a	n/a
48	CTCF	chr13:64292400-64292402	Lung_OC	lung:	n/a	n/a
49	CTCF	chr13:64324040-64324265	HepG2	liver:	n/a	n/a
50	CTCF	chr13:64324183-64324225	H1-hESC	embryonic stem cell:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64315383-64315433	AoSMC	blood vessel:	n/a
2	chr13:64311555-64311605	AG04449	skin:	fetal
3	chr13:64311555-64311605	U87	brain:	n/a
4	chr13:64311397-64311447	NH-A	brain:	n/a
5	chr13:64311555-64311605	A549	lung:	n/a
6	chr13:64315383-64315433	HIPEpiC	eye:	n/a
7	chr13:64311555-64311605	HRE	kidney:	n/a
8	chr13:64311555-64311605	HCPEpiC	choroid plexus:	n/a
9	chr13:64315383-64315433	HCM	heart:	n/a
10	chr13:64311555-64311605	Hela-S3	cervix:	n/a
11	chr13:64311397-64311447	SAEC	small airway:	n/a
12	chr13:64311397-64311447	HEK293	kidney:	embryo
13	chr13:64315383-64315433	AG09319	gingival:	n/a
14	chr13:64311397-64311447	SK-N-SH_RA	brain:	n/a
15	chr13:64311555-64311605	SKMC	muscle:	n/a
16	chr13:64311397-64311447	IMR90	lung:	fetal
17	chr13:64311555-64311605	HRPEpiC	eye:	n/a
18	chr13:64315383-64315433	SAEC	small airway:	n/a
19	chr13:64311555-64311605	NHDF-neo	bronchial:	n/a
20	chr13:64311555-64311605	SK-N-SH	brain:	n/a
21	chr13:64315383-64315433	Hepatocyte	liver:	n/a
22	chr13:64311397-64311447	PrEC	prostate:	n/a
23	chr13:64311555-64311605	BJ	skin:	n/a
24	chr13:64311555-64311605	Hepatocyte	liver:	n/a
25	chr13:64311397-64311447	AG04449	skin:	fetal
26	chr13:64311555-64311605	Jurkat	blood:	n/a
27	chr13:64315383-64315433	HCF	heart:	n/a
28	chr13:64315383-64315433	NH-A	brain:	n/a
29	chr13:64315383-64315433	PrEC	prostate:	n/a
30	chr13:64315383-64315433	A549	lung:	n/a
31	chr13:64311555-64311605	ECC-1	luminal epithelium:	n/a
32	chr13:64315383-64315433	HL-60	blood:	n/a
33	chr13:64315383-64315433	NT2-D1	testis:	n/a
34	chr13:64311555-64311605	HMEC	breast:	n/a
35	chr13:64315383-64315433	MCF-7	breast:	n/a
36	chr13:64311555-64311605	HCT-116	colon:	n/a
37	chr13:64315383-64315433	HRPEpiC	eye:	n/a
38	chr13:64311397-64311447	ECC-1	luminal epithelium:	n/a
39	chr13:64311555-64311605	HCF	heart:	n/a
40	chr13:64311555-64311605	HCM	heart:	n/a
41	chr13:64315383-64315433	CMK	blood:	n/a
42	chr13:64311555-64311605	ovcar-3	ovarian:	n/a
43	chr13:64311397-64311447	HAEpiC	amniotic membrane:	n/a
44	chr13:64315383-64315433	HPAEpiC	pulmonary alveolar:	n/a
45	chr13:64315383-64315433	GM12892	blood:	n/a
46	chr13:64311397-64311447	PANC-1	pancreas:	n/a
47	chr13:64311555-64311605	Caco-2	colon:	n/a
48	chr13:64311555-64311605	HL-60	blood:	n/a
49	chr13:64311555-64311605	GM06990	blood:	n/a
50	chr13:64315383-64315433	GM19239	blood:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:
2	chr13:64303686..64305846-chr13:64306387..64309282,2	MCF-7	breast:

(count:20 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-1	chr13:64322132-64322530	ENSG00000237378
2	lnc-PCDH20-9	chr13:64261535-64261688	XLOC_010643
3	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034173
4	lnc-PCDH20-9	chr13:64303522-64303895	XLOC_010643
5	lnc-AL445989.1-20	chr13:64311843-64312482	NONHSAT034172
6	lnc-AL445989.1-20	chr13:64316498-64316945	NONHSAT034176
7	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034172
8	lnc-PCDH20-9	chr13:64303522-64303642	XLOC_010643
9	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034174
10	lnc-PCDH20-9	chr13:64312042-64312151	XLOC_010643
11	lnc-AL445989.1-20	chr13:64313246-64314310	NONHSAT034174
12	lnc-PCDH20-9	chr13:64301184-64301215	XLOC_010643
13	lnc-AL445989.1-20	chr13:64316485-64316936	NONHSAT034175
14	lnc-AL445989.1-1	chr13:64324837-64325213	ENSG00000237378
15	lnc-PCDH20-9	chr13:64288485-64288508	XLOC_010643
16	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034173
17	lnc-PCDH20-9	chr13:64291083-64291151	XLOC_010643
18	lnc-AL445989.1-20	chr13:64313246-64314376	NONHSAT034175
19	lnc-AL445989.1-20	chr13:64314899-64315042	NONHSAT034174
20	lnc-AL445989.1-20	chr13:64311843-64312416	NONHSAT034173

No data

Variant related genes	Relation type
ENSG00000226974	TF binding region
LINC00395	TF binding region
ENSG00000237378	TF binding region
OR7E156P	TF binding region
ENSG00000226974	CpG island
LINC00395	CpG island
ENSG00000237378	CpG island
OR7E156P	CpG island
DUSP3	miRNA target sites
DUSP2	miRNA target sites

Extended variants
information (count: 909 )
Associated
traits (count: 95 )

Variant overlapped rSNPs/rCNVs (count:909 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17088704	chr13:64259484-64259485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs76696476	chr13:64259513-64259514	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562050949	chr13:64259526-64259527	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs376164010	chr13:64259545-64259546	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs529453076	chr13:64259566-64259567	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs547862435	chr13:64259571-64259572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565873931	chr13:64259594-64259595	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs539222518	chr13:64259658-64259659	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs140230537	chr13:64259696-64259697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs12864820	chr13:64259703-64259704	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551674168	chr13:64259764-64259765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9570989	chr13:64259767-64259768	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs536932504	chr13:64259786-64259787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs532120253	chr13:64261536-64261537	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs550433051	chr13:64261570-64261571	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs568997710	chr13:64261571-64261572	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs144637604	chr13:64261619-64261620	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs549609083	chr13:64261621-64261622	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs567813181	chr13:64261643-64261644	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs9570993	chr13:64261656-64261657	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs181124499	chr13:64261665-64261666	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs115344933	chr13:64261678-64261679	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs367965293	chr13:64262804-64262805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76271555	chr13:64262815-64262816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs78912187	chr13:64262834-64262835	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs17088713	chr13:64262893-64262894	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs9570996	chr13:64262939-64262940	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547185114	chr13:64262940-64262941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs76150451	chr13:64262945-64262946	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9570997	chr13:64262946-64262947	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs180861980	chr13:64262982-64262983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs543667892	chr13:64262991-64262992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs386771710	chr13:64262999-64263000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs568947488	chr13:64263001-64263002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140249795	chr13:64263009-64263010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs150293076	chr13:64263061-64263062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs375488314	chr13:64263075-64263076	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533997621	chr13:64263077-64263078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs185911827	chr13:64263106-64263107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs145416774	chr13:64263118-64263119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs149211079	chr13:64263236-64263237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs143342747	chr13:64263279-64263280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs191234744	chr13:64263322-64263323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs183170281	chr13:64263329-64263330	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs185628149	chr13:64263342-64263343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs9570998	chr13:64263345-64263346	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs371999265	chr13:64263379-64263380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571403957	chr13:64263381-64263382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs9570999	chr13:64263419-64263420	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs565518922	chr13:64263430-64263431	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:95)

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
Multiple myeloma	17550852	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	15273396	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Non-syndromic sensorineural hearing loss	19036926	CNVD

Chromatin state (count:29 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64259000-64259800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr13:64259000-64259800	Enhancers	iPS-20b Cell Line	embryonic stem cell
3	chr13:64259200-64259600	Enhancers	HUES64 Cell Line	embryonic stem cell
4	chr13:64262800-64263600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr13:64274200-64275000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:64274400-64274800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr13:64274400-64275000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr13:64274600-64275200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
9	chr13:64279200-64279600	Enhancers	Fetal Brain Male	brain
10	chr13:64302400-64302800	Enhancers	Fetal Intestine Small	intestine
11	chr13:64302400-64303200	Enhancers	Fetal Intestine Large	intestine
12	chr13:64302800-64303800	Weak transcription	Fetal Intestine Small	intestine
13	chr13:64303200-64303600	Weak transcription	Fetal Intestine Large	intestine
14	chr13:64303600-64303800	Enhancers	Fetal Intestine Large	intestine
15	chr13:64303800-64304400	Enhancers	Fetal Intestine Small	intestine
16	chr13:64303800-64305800	Weak transcription	Fetal Intestine Large	intestine
17	chr13:64304400-64305800	Weak transcription	Fetal Intestine Small	intestine
18	chr13:64305600-64306000	Enhancers	Pancreatic Islets	Pancreatic Islet
19	chr13:64305800-64306200	Enhancers	HepG2	liver
20	chr13:64305800-64306600	Enhancers	Fetal Intestine Large	intestine
21	chr13:64305800-64306600	Enhancers	Stomach Mucosa	stomach
22	chr13:64305800-64307200	Enhancers	Fetal Intestine Small	intestine
23	chr13:64306000-64307800	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr13:64306200-64307000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr13:64307800-64308200	Enhancers	Pancreatic Islets	Pancreatic Islet
26	chr13:64308200-64310200	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr13:64310200-64310600	Enhancers	Pancreatic Islets	Pancreatic Islet
28	chr13:64315400-64316200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
29	chr13:64347400-64348200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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