Variant report

Variant	nsv1054050
Chromosome Location	chr13:66821545-66914754
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:289)
CpG islands
(count:61)
Chromatin interactive
region (count:6)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:66886857-66887028	HepG2	liver:	n/a	n/a
2	ATF3	chr13:66886740-66887227	A549	lung:	n/a	n/a
3	BCL3	chr13:66886752-66887345	A549	lung:	n/a	n/a
4	BCL3	chr13:66886608-66887994	A549	lung:	n/a	n/a
5	BHLHE40	chr13:66902776-66902779	K562	blood:	n/a	n/a
6	BRCA1	chr13:66878245-66878246	Hela-S3	cervix:	n/a	n/a
7	CBX3	chr13:66861033-66861253	K562	blood:	n/a	n/a
8	CEBPB	chr13:66872525-66872807	Hela-S3	cervix:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
9	CEBPB	chr13:66888568-66888896	A549	lung:	n/a	n/a
10	CEBPB	chr13:66898105-66898199	HepG2	liver:	n/a	chr13:66898111-66898122
11	CEBPB	chr13:66887551-66887864	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:66906331-66906484	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr13:66872470-66872807	IMR90	lung:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
14	CEBPB	chr13:66840058-66840316	IMR90	lung:	n/a	chr13:66840131-66840144 chr13:66840121-66840133
15	CEBPB	chr13:66872481-66872820	HepG2	liver:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
16	CEBPB	chr13:66887496-66887884	A549	lung:	n/a	n/a
17	CEBPB	chr13:66887481-66887890	A549	lung:	n/a	n/a
18	CEBPB	chr13:66886648-66888000	A549	lung:	n/a	n/a
19	CEBPB	chr13:66887553-66887871	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:66886928-66887166	A549	lung:	n/a	n/a
21	CEBPB	chr13:66886797-66887222	A549	lung:	n/a	n/a
22	CEBPB	chr13:66888682-66888899	HepG2	liver:	n/a	n/a
23	CEBPB	chr13:66872489-66872826	K562	blood:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
24	CEBPB	chr13:66872539-66872758	H1-hESC	embryonic stem cell:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
25	CEBPB	chr13:66891929-66892183	HepG2	liver:	n/a	chr13:66892052-66892065 chr13:66892041-66892052
26	CEBPB	chr13:66872466-66872822	A549	lung:	n/a	chr13:66872645-66872656 chr13:66872626-66872637
27	CEBPB	chr13:66840059-66840240	HepG2	liver:	n/a	chr13:66840131-66840144 chr13:66840121-66840133
28	CEBPD	chr13:66872704-66873142	K562	blood:	n/a	n/a
29	CHD2	chr13:66898349-66898352	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr13:66887670-66887940	A549	lung:	n/a	n/a
31	CREB1	chr13:66886531-66886751	A549	lung:	n/a	n/a
32	CREB1	chr13:66887558-66887926	A549	lung:	n/a	n/a
33	CTCF	chr13:66845240-66845390	AG09309	skin:	n/a	n/a
34	CTCF	chr13:66839680-66839830	RPTEC	kidney:	n/a	n/a
35	CTCF	chr13:66845277-66845309	LNCaP	prostate:	n/a	n/a
36	CTCF	chr13:66908324-66908395	GM10248	blood:	n/a	n/a
37	CTCF	chr13:66908162-66908197	Lung_OC	lung:	n/a	n/a
38	CTCF	chr13:66908200-66908204	Lung_OC	lung:	n/a	n/a
39	CTCF	chr13:66839520-66839670	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr13:66839580-66839730	HCPEpiC	choroid plexus:	n/a	n/a
41	CTCF	chr13:66845301-66845394	LNCaP	prostate:	n/a	n/a
42	CTCF	chr13:66839540-66839690	HAc	cerebellar:	n/a	n/a
43	CTCF	chr13:66888880-66889030	BE2_C	brain:	n/a	n/a
44	CTCF	chr13:66822520-66822670	GM12864	blood:	n/a	n/a
45	CTCF	chr13:66847520-66847670	WI-38	lung:	n/a	n/a
46	CTCF	chr13:66839600-66839750	HA-sp	spinal cord:	n/a	n/a
47	CTCF	chr13:66839620-66839770	HBMEC	blood vessel:	n/a	n/a
48	CTCF	chr13:66877471-66877527	GM10248	blood:	n/a	n/a
49	CTCF	chr13:66889260-66889410	GM12872	blood:	n/a	n/a
50	CTCF	chr13:66839620-66839770	HRE	kidney:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:66878738-66878788	BE2_C	brain:	n/a
2	chr13:66878738-66878788	GM12891	blood:	n/a
3	chr13:66878738-66878788	HEK293	kidney:	embryo
4	chr13:66878738-66878788	BJ	skin:	n/a
5	chr13:66878738-66878788	HEEpiC	esophagus:	n/a
6	chr13:66878738-66878788	AG09319	gingival:	n/a
7	chr13:66878738-66878788	Hela-S3	cervix:	n/a
8	chr13:66878738-66878788	ProgFib	skin:	n/a
9	chr13:66878738-66878788	PFSK-1	brain:	n/a
10	chr13:66878738-66878788	NHBE	bronchial:	n/a
11	chr13:66878738-66878788	HPAEpiC	pulmonary alveolar:	n/a
12	chr13:66878738-66878788	SK-N-SH_RA	brain:	n/a
13	chr13:66878738-66878788	AG04449	skin:	fetal
14	chr13:66878738-66878788	SK-N-SH	brain:	n/a
15	chr13:66878738-66878788	HAEpiC	amniotic membrane:	n/a
16	chr13:66878738-66878788	HRCEpiC	kidney:	n/a
17	chr13:66878738-66878788	Hepatocyte	liver:	n/a
18	chr13:66878738-66878788	GM19239	blood:	n/a
19	chr13:66878738-66878788	A549	lung:	n/a
20	chr13:66878738-66878788	Jurkat	blood:	n/a
21	chr13:66878738-66878788	HRE	kidney:	n/a
22	chr13:66878738-66878788	SK-N-MC	brain:	n/a
23	chr13:66878738-66878788	HRPEpiC	eye:	n/a
24	chr13:66878738-66878788	K562	blood:	n/a
25	chr13:66878738-66878788	RPTEC	kidney:	n/a
26	chr13:66878738-66878788	HL-60	blood:	n/a
27	chr13:66878738-66878788	GM12892	blood:	n/a
28	chr13:66878738-66878788	HCF	heart:	n/a
29	chr13:66878738-66878788	AG09309	skin:	n/a
30	chr13:66878738-66878788	HIPEpiC	eye:	n/a
31	chr13:66878738-66878788	CMK	blood:	n/a
32	chr13:66878738-66878788	HMEC	breast:	n/a
33	chr13:66878738-66878788	HCM	heart:	n/a
34	chr13:66878738-66878788	IMR90	lung:	fetal
35	chr13:66878738-66878788	HCT-116	colon:	n/a
36	chr13:66878738-66878788	T-47D	breast:	n/a
37	chr13:66878738-66878788	LNCaP	prostate:	n/a
38	chr13:66878738-66878788	SKMC	muscle:	n/a
39	chr13:66878738-66878788	AG04450	lung:	fetal
40	chr13:66878738-66878788	NH-A	brain:	n/a
41	chr13:66878738-66878788	NHDF-neo	bronchial:	n/a
42	chr13:66878738-66878788	SAEC	small airway:	n/a
43	chr13:66878738-66878788	ECC-1	luminal epithelium:	n/a
44	chr13:66878738-66878788	ovcar-3	ovarian:	n/a
45	chr13:66878738-66878788	HCPEpiC	choroid plexus:	n/a
46	chr13:66878738-66878788	NB4	blood:	n/a
47	chr13:66878738-66878788	Caco-2	colon:	n/a
48	chr13:66878738-66878788	PrEC	prostate:	n/a
49	chr13:66878738-66878788	U87	brain:	n/a
50	chr13:66878738-66878788	GM06990	blood:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
2	chr13:66879908..66881972-chr13:66902872..66904425,2	K562	blood:
3	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:
4	chr13:66909684..66911530-chr13:66916300..66919201,2	K562	blood:
5	chr13:66824109..66824810-chr16:71735977..71736631,2	MCF-7	breast:
6	chr13:66901663..66903255-chr13:66906195..66907818,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-26	chr13:66843129-66844590	NONHSAT034207
2	lnc-AL445989.1-13	chr13:66897306-66897693	ENSG00000234527.1
3	lnc-AL445989.1-26	chr13:66851684-66852109	NONHSAT034208
4	lnc-AL445989.1-26	chr13:66846998-66847098	NONHSAT034208
5	lnc-AL445989.1-13	chr13:66878003-66878146	ENSG00000234527.1
6	lnc-AL445989.1-26	chr13:66844520-66844603	NONHSAT034208

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	PCDH9	hsa-miR-155-5p	chr13:66877756-66877779
2	PCDH9	hsa-miR-155-5p	chr13:66878321-66878343
3	PCDH9	hsa-miR-155-5p	chr13:66878327-66878320

Variant related genes	Relation type
TRIM60P19	TF binding region
PCDH9-AS1	TF binding region
TRIM60P19	CpG island
PCDH9-AS1	CpG island

Extended variants
information (count: 2179 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:2179 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs562040167	chr13:66834215-66834216	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs527557360	chr13:66834255-66834256	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
3	rs75319338	chr13:66834256-66834257	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs570292616	chr13:66834271-66834272	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs566092739	chr13:66834297-66834298	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs549870306	chr13:66834313-66834314	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs112068916	chr13:66834354-66834355	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs371223195	chr13:66834358-66834359	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs187976821	chr13:66834413-66834414	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs76238788	chr13:66834464-66834465	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs192997569	chr13:66834465-66834466	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs534983042	chr13:66834560-66834561	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs184266475	chr13:66834576-66834577	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs557186453	chr13:66834579-66834580	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs188269330	chr13:66834587-66834588	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs575571767	chr13:66834589-66834590	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs543993868	chr13:66834594-66834595	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs556298278	chr13:66834595-66834596	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs576030754	chr13:66834639-66834640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs180928333	chr13:66834716-66834717	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs78210559	chr13:66834719-66834720	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs572334561	chr13:66834735-66834736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs184576668	chr13:66834765-66834766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs79438585	chr13:66834768-66834769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs151241182	chr13:66834787-66834788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs573325902	chr13:66834800-66834801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs189359542	chr13:66834825-66834826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs563819154	chr13:66834838-66834839	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs529353154	chr13:66834876-66834877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs76828220	chr13:66834895-66834896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs145432009	chr13:66834921-66834922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs111542340	chr13:66834925-66834926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs75191551	chr13:66834958-66834959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs199847715	chr13:66834994-66834995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs376965717	chr13:66835042-66835043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs571924519	chr13:66835046-66835047	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540724480	chr13:66835066-66835067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs537665995	chr13:66835088-66835089	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565480593	chr13:66835093-66835094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs371128818	chr13:66835122-66835123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374490910	chr13:66835160-66835161	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs367774850	chr13:66835163-66835164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs181373386	chr13:66835208-66835209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs78172403	chr13:66835216-66835217	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555389357	chr13:66835320-66835321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs9599100	chr13:66835378-66835379	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs112121751	chr13:66835388-66835389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs540576903	chr13:66835413-66835414	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs551320292	chr13:66835428-66835429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs139522911	chr13:66835443-66835444	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:97)

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
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:66834200-66834600	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
2	chr13:66834600-66837400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr13:66837600-66837800	Enhancers	Fetal Kidney	kidney
4	chr13:66837600-66840400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chr13:66838000-66839000	Weak transcription	Fetal Kidney	kidney
6	chr13:66838200-66839200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr13:66838400-66838600	Enhancers	Brain Hippocampus Middle	brain
8	chr13:66838600-66840000	Enhancers	Brain Germinal Matrix	brain
9	chr13:66839000-66839200	Enhancers	Brain Anterior Caudate	brain
10	chr13:66839000-66839200	Enhancers	Brain Cingulate Gyrus	brain
11	chr13:66839000-66839200	Enhancers	Fetal Brain Female	brain
12	chr13:66839000-66839200	Enhancers	Fetal Kidney	kidney
13	chr13:66839000-66839600	Active TSS	Brain Inferior Temporal Lobe	brain
14	chr13:66839000-66840000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr13:66839000-66840000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr13:66839200-66839400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr13:66839200-66839600	Active TSS	Brain Angular Gyrus	brain
18	chr13:66839200-66839600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
19	chr13:66839200-66839600	Flanking Active TSS	Fetal Brain Female	brain
20	chr13:66839200-66839800	Active TSS	Brain Substantia Nigra	brain
21	chr13:66839200-66840000	Active TSS	Brain Anterior Caudate	brain
22	chr13:66839200-66840000	Flanking Active TSS	Brain Cingulate Gyrus	brain
23	chr13:66839200-66840000	Active TSS	Brain Hippocampus Middle	brain
24	chr13:66839200-66840000	Flanking Active TSS	Fetal Kidney	kidney
25	chr13:66839200-66840200	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr13:66839400-66839600	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
27	chr13:66839400-66839600	Active TSS	Pancreatic Islets	Pancreatic Islet
28	chr13:66839400-66839800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr13:66839400-66839800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr13:66839400-66839800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr13:66839400-66839800	Enhancers	NH-A	brain
32	chr13:66839400-66839800	Active TSS	Osteobl	bone
33	chr13:66839400-66840200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr13:66839600-66839800	Enhancers	Brain Angular Gyrus	brain
35	chr13:66839600-66839800	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
36	chr13:66839600-66839800	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
37	chr13:66839600-66840000	Enhancers	Fetal Brain Female	brain
38	chr13:66839800-66840000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr13:66839800-66840000	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr13:66839800-66840000	Flanking Active TSS	Brain Substantia Nigra	brain
41	chr13:66839800-66840000	Enhancers	Pancreatic Islets	Pancreatic Islet
42	chr13:66840000-66841200	Weak transcription	Fetal Kidney	kidney
43	chr13:66840200-66841200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chr13:66841200-66841400	Enhancers	Fetal Kidney	kidney
45	chr13:66841200-66847200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr13:66847000-66847400	Enhancers	Dnd41	blood
47	chr13:66847200-66847800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr13:66847600-66848400	Active TSS	Fetal Kidney	kidney
49	chr13:66848400-66849400	Weak transcription	Fetal Kidney	kidney
50	chr13:66849400-66849800	Active TSS	Fetal Kidney	kidney

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