Variant report

Variant	nsv482659
Chromosome Location	chr13:64457132-64634096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:412)
CpG islands
(count:61)
Chromatin interactive
region (count:29)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:412 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:64522080-64522711	HepG2	liver:	n/a	n/a
2	CEBPB	chr13:64516511-64516897	IMR90	lung:	n/a	chr13:64516700-64516711
3	CEBPB	chr13:64574784-64575086	HepG2	liver:	n/a	chr13:64574932-64574943
4	CEBPB	chr13:64514382-64514695	HepG2	liver:	n/a	chr13:64514540-64514551 chr13:64514541-64514550 chr13:64514539-64514552 chr13:64514539-64514550
5	CEBPB	chr13:64550954-64551166	K562	blood:	n/a	chr13:64551014-64551025 chr13:64551013-64551026
6	CEBPB	chr13:64631631-64631969	HepG2	liver:	n/a	chr13:64631808-64631819 chr13:64631809-64631820 chr13:64631808-64631821
7	CEBPB	chr13:64513029-64513299	IMR90	lung:	n/a	n/a
8	CEBPB	chr13:64514442-64514720	Hela-S3	cervix:	n/a	chr13:64514540-64514551 chr13:64514541-64514550 chr13:64514539-64514552 chr13:64514539-64514550
9	CEBPB	chr13:64494229-64494429	HepG2	liver:	n/a	chr13:64494372-64494383
10	CEBPB	chr13:64631661-64631931	K562	blood:	n/a	chr13:64631808-64631819 chr13:64631809-64631820 chr13:64631808-64631821
11	CEBPB	chr13:64533697-64534023	IMR90	lung:	n/a	chr13:64533832-64533843 chr13:64533855-64533866
12	CEBPB	chr13:64461878-64462200	HepG2	liver:	n/a	chr13:64462014-64462025
13	CEBPB	chr13:64516563-64516880	ECC-1	luminal epithelium:	n/a	chr13:64516700-64516711
14	CEBPB	chr13:64514357-64514711	IMR90	lung:	n/a	chr13:64514540-64514551 chr13:64514541-64514550 chr13:64514539-64514552 chr13:64514539-64514550
15	CEBPB	chr13:64516532-64516875	HepG2	liver:	n/a	chr13:64516700-64516711
16	CEBPB	chr13:64562560-64562797	HepG2	liver:	n/a	chr13:64562678-64562689 chr13:64562678-64562691
17	CEBPB	chr13:64590178-64590414	K562	blood:	n/a	n/a
18	CEBPB	chr13:64533716-64533970	A549	lung:	n/a	chr13:64533832-64533843 chr13:64533855-64533866
19	CEBPB	chr13:64550843-64551208	HepG2	liver:	n/a	chr13:64551014-64551025 chr13:64551013-64551026
20	CEBPB	chr13:64574892-64574972	H1-hESC	embryonic stem cell:	n/a	chr13:64574932-64574943
21	CEBPB	chr13:64631725-64631858	HepG2	liver:	n/a	chr13:64631808-64631819 chr13:64631809-64631820 chr13:64631808-64631821
22	CEBPB	chr13:64516546-64516827	A549	lung:	n/a	chr13:64516700-64516711
23	CEBPB	chr13:64516525-64516869	Hela-S3	cervix:	n/a	chr13:64516700-64516711
24	CEBPB	chr13:64533704-64534019	HepG2	liver:	n/a	chr13:64533832-64533843 chr13:64533855-64533866
25	CEBPD	chr13:64626677-64626975	K562	blood:	n/a	n/a
26	CHD1	chr13:64541336-64541376	GM12878	blood:	n/a	n/a
27	CHD2	chr13:64630471-64630608	GM12878	blood:	n/a	n/a
28	CTCF	chr13:64475800-64475950	NB4	blood:	n/a	n/a
29	CTCF	chr13:64475880-64476030	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr13:64517240-64517390	HPF	lung:	n/a	n/a
31	CTCF	chr13:64528860-64529010	BE2_C	brain:	n/a	n/a
32	CTCF	chr13:64528900-64529050	HepG2	liver:	n/a	n/a
33	CTCF	chr13:64528880-64529030	Caco-2	colon:	n/a	n/a
34	CTCF	chr13:64475911-64476006	MCF-7	breast:	n/a	n/a
35	CTCF	chr13:64623900-64624050	HFF-Myc	foreskin:	n/a	n/a
36	CTCF	chr13:64475874-64476050	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr13:64558980-64559001	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr13:64475893-64476039	HepG2	liver:	n/a	n/a
39	CTCF	chr13:64626827-64626922	MCF-7	breast:	n/a	n/a
40	CTCF	chr13:64550580-64550730	GM12865	blood:	n/a	n/a
41	CTCF	chr13:64475893-64476033	MCF-7	breast:	n/a	n/a
42	CTCF	chr13:64626860-64627010	BE2_C	brain:	n/a	n/a
43	CTCF	chr13:64626780-64626930	HepG2	liver:	n/a	n/a
44	CTCF	chr13:64626821-64626939	K562	blood:	n/a	n/a
45	CTCF	chr13:64626740-64626890	HEK293	kidney:	n/a	n/a
46	CTCF	chr13:64475860-64476010	HCPEpiC	choroid plexus:	n/a	n/a
47	CTCF	chr13:64475885-64476012	K562	blood:	n/a	n/a
48	CTCF	chr13:64626759-64627015	K562	blood:	n/a	n/a
49	CTCF	chr13:64626740-64626890	K562	blood:	n/a	n/a
50	CTCF	chr13:64528920-64529070	BE2_C	brain:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:64516824-64516874	NH-A	brain:	n/a
2	chr13:64516824-64516874	SK-N-SH	brain:	n/a
3	chr13:64516824-64516874	PFSK-1	brain:	n/a
4	chr13:64516824-64516874	GM19239	blood:	n/a
5	chr13:64516824-64516874	HCT-116	colon:	n/a
6	chr13:64516824-64516874	CMK	blood:	n/a
7	chr13:64516824-64516874	GM12891	blood:	n/a
8	chr13:64516824-64516874	SK-N-SH_RA	brain:	n/a
9	chr13:64516824-64516874	K562	blood:	n/a
10	chr13:64516824-64516874	HIPEpiC	eye:	n/a
11	chr13:64516824-64516874	SKMC	muscle:	n/a
12	chr13:64516824-64516874	SAEC	small airway:	n/a
13	chr13:64516824-64516874	T-47D	breast:	n/a
14	chr13:64516824-64516874	HUVEC	blood vessel:	n/a
15	chr13:64516824-64516874	Jurkat	blood:	n/a
16	chr13:64516824-64516874	GM12892	blood:	n/a
17	chr13:64516824-64516874	Hepatocyte	liver:	n/a
18	chr13:64516824-64516874	NB4	blood:	n/a
19	chr13:64516824-64516874	HCPEpiC	choroid plexus:	n/a
20	chr13:64516824-64516874	MCF-7	breast:	n/a
21	chr13:64516824-64516874	HNPCEpiC	eye:	n/a
22	chr13:64516824-64516874	AG04450	lung:	fetal
23	chr13:64516824-64516874	IMR90	lung:	fetal
24	chr13:64516824-64516874	AG09319	gingival:	n/a
25	chr13:64516824-64516874	HEEpiC	esophagus:	n/a
26	chr13:64516824-64516874	HCM	heart:	n/a
27	chr13:64516824-64516874	ovcar-3	ovarian:	n/a
28	chr13:64516824-64516874	AG04449	skin:	fetal
29	chr13:64516824-64516874	GM12878	blood:	n/a
30	chr13:64516824-64516874	HRE	kidney:	n/a
31	chr13:64516824-64516874	NHBE	bronchial:	n/a
32	chr13:64516824-64516874	HPAEpiC	pulmonary alveolar:	n/a
33	chr13:64516824-64516874	RPTEC	kidney:	n/a
34	chr13:64516824-64516874	Hela-S3	cervix:	n/a
35	chr13:64516824-64516874	MCF10A-Er-Src	breast:	n/a
36	chr13:64516824-64516874	HCF	heart:	n/a
37	chr13:64516824-64516874	HL-60	blood:	n/a
38	chr13:64516824-64516874	SK-N-MC	brain:	n/a
39	chr13:64516824-64516874	NHDF-neo	bronchial:	n/a
40	chr13:64516824-64516874	U87	brain:	n/a
41	chr13:64516824-64516874	NT2-D1	testis:	n/a
42	chr13:64516824-64516874	PrEC	prostate:	n/a
43	chr13:64516824-64516874	HEK293	kidney:	embryo
44	chr13:64516824-64516874	HepG2	liver:	n/a
45	chr13:64516824-64516874	HMEC	breast:	n/a
46	chr13:64516824-64516874	BE2_C	brain:	n/a
47	chr13:64516824-64516874	AG10803	skin:	n/a
48	chr13:64516824-64516874	AoSMC	blood vessel:	n/a
49	chr13:64516824-64516874	H1-hESC	embryonic stem cell:	embryo
50	chr13:64516824-64516874	AG09309	skin:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:64611241..64613586-chr13:64615130..64617717,2	K562	blood:
2	chr13:64478683..64481675-chr13:64487598..64489103,2	MCF-7	breast:
3	chr13:64597503..64599019-chr13:64609269..64611005,2	K562	blood:
4	chr13:64553735..64556887-chr13:64557043..64560591,3	K562	blood:
5	chr13:64461452..64464035-chr13:64465171..64467980,2	K562	blood:
6	chr13:64573569..64576340-chr13:64627433..64629862,2	K562	blood:
7	chr13:64475617..64476410-chr13:64728809..64729366,2	MCF-7	breast:
8	chr13:64553735..64556887-chr13:64557043..64560591,3	K562	blood:
9	chr13:64569387..64571962-chr13:64582187..64583914,2	MCF-7	breast:
10	chr13:64611241..64613586-chr13:64615130..64617717,2	K562	blood:
11	chr13:64478683..64481675-chr13:64487598..64489103,2	MCF-7	breast:
12	chr13:64597503..64599019-chr13:64609269..64611005,2	K562	blood:
13	chr13:64625157..64626688-chr13:64631104..64632843,2	K562	blood:
14	chr13:64587782..64590313-chr13:64593691..64596528,2	MCF-7	breast:
15	chr13:64587782..64590313-chr13:64593691..64596528,2	MCF-7	breast:
16	chr13:64625157..64626688-chr13:64631104..64632843,2	K562	blood:
17	chr13:64589018..64592206-chr13:64593132..64595974,4	K562	blood:
18	chr13:64461452..64464035-chr13:64465171..64467980,2	K562	blood:
19	chr13:64580543..64583349-chr13:64585770..64588004,2	MCF-7	breast:
20	chr13:64600090..64601609-chr13:64604264..64606760,2	K562	blood:
21	chr13:64570537..64572050-chr13:64574035..64576915,2	K562	blood:
22	chr13:64629925..64632065-chr13:64645172..64647089,2	K562	blood:
23	chr13:64569387..64571962-chr13:64582187..64583914,2	MCF-7	breast:
24	chr13:64570537..64572050-chr13:64574035..64576915,2	K562	blood:
25	chr13:64600090..64601609-chr13:64604264..64606760,2	K562	blood:
26	chr13:64580543..64583349-chr13:64585770..64588004,2	MCF-7	breast:
27	chr13:64632651..64634373-chr13:64649799..64652213,2	K562	blood:
28	chr13:64573569..64576340-chr13:64627433..64629862,2	K562	blood:
29	chr13:64589018..64592206-chr13:64593132..64595974,4	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH9-13	chr13:64549584-64550555	NONHSAT034188
2	lnc-PCDH9-4	chr13:64608480-64608670	NONHSAT034190
3	lnc-PCDH9-4	chr13:64564229-64564333	NONHSAT034190
4	lnc-PCDH9-4	chr13:64576518-64576542	NONHSAT034190
5	lnc-PCDH9-4	chr13:64577481-64577601	NONHSAT034190

No data

Variant related genes	Relation type
NFYAP1	TF binding region
NFYAP1	CpG island
ENSG00000227674	chromatin interactions

Extended variants
information (count: 1513 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1513 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs534327834	chr13:64479961-64479962	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs550223245	chr13:64479963-64479964	Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs369386509	chr13:64479969-64479970	Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs552256851	chr13:64480091-64480092	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs570834728	chr13:64480093-64480094	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs538092126	chr13:64480128-64480129	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs556494021	chr13:64480138-64480139	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs509740	chr13:64480154-64480155	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs373321505	chr13:64480188-64480189	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs183456255	chr13:64483495-64483496	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs183919	chr13:64483504-64483505	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs1335772	chr13:64483533-64483534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs9598643	chr13:64483585-64483586	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs187947790	chr13:64483593-64483594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs372876252	chr13:64483625-64483626	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs544980073	chr13:64483666-64483667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs556960380	chr13:64483721-64483722	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs148529601	chr13:64483762-64483763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs115854440	chr13:64483765-64483766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs182803228	chr13:64483772-64483773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs561093161	chr13:64483825-64483826	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs528268682	chr13:64483845-64483846	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs540459298	chr13:64483873-64483874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78372480	chr13:64483909-64483910	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532270930	chr13:64483910-64483911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9598644	chr13:64483915-64483916	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs370749120	chr13:64484003-64484004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs568885002	chr13:64484010-64484011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs531189137	chr13:64484123-64484124	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs148081929	chr13:64484129-64484130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567991054	chr13:64484163-64484164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs372608237	chr13:64484192-64484193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs546015295	chr13:64484290-64484291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs534890700	chr13:64484325-64484326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs553560215	chr13:64484352-64484353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs571380291	chr13:64484376-64484377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs538764836	chr13:64484378-64484379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs556898748	chr13:64484398-64484399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs575239459	chr13:64484401-64484402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs375660137	chr13:64484411-64484412	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs536699798	chr13:64484423-64484424	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs371144421	chr13:64484457-64484458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536896711	chr13:64484480-64484481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs9592294	chr13:64484490-64484491	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs141381427	chr13:64484531-64484532	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs373434572	chr13:64484538-64484539	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs73495987	chr13:64484610-64484611	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs111964317	chr13:64484644-64484645	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs377637743	chr13:64484655-64484656	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs371097896	chr13:64484733-64484734	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
Melanoma	20688739	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:71 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:64479800-64480200	Active TSS	Aorta	Aorta
2	chr13:64483400-64484400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
3	chr13:64483800-64485400	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr13:64484000-64485400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:64484200-64485000	Enhancers	Fetal Muscle Leg	muscle
6	chr13:64484200-64485400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:64484400-64484600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr13:64484600-64484800	Active TSS	Brain Anterior Caudate	brain
9	chr13:64484600-64484800	Active TSS	Brain Cingulate Gyrus	brain
10	chr13:64484600-64485000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr13:64484600-64485000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr13:64484600-64485000	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr13:64484600-64485000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chr13:64484600-64485000	Enhancers	Fetal Brain Male	brain
15	chr13:64484800-64485000	Flanking Active TSS	Brain Anterior Caudate	brain
16	chr13:64484800-64485000	Flanking Active TSS	Brain Cingulate Gyrus	brain
17	chr13:64485000-64485200	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr13:64485200-64485400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr13:64494000-64494200	Enhancers	Gastric	stomach
20	chr13:64503000-64503400	Enhancers	Fetal Heart	heart
21	chr13:64512800-64513600	Enhancers	Muscle Satellite Cultured Cells	--
22	chr13:64513600-64516600	Weak transcription	Muscle Satellite Cultured Cells	--
23	chr13:64515800-64516000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr13:64516400-64516800	Enhancers	Rectal Smooth Muscle	rectum
25	chr13:64516400-64517000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:64516400-64517400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr13:64516600-64517000	Enhancers	Muscle Satellite Cultured Cells	--
28	chr13:64516800-64517000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
29	chr13:64517000-64517200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr13:64517200-64517400	Enhancers	Rectal Smooth Muscle	rectum
31	chr13:64517200-64521600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
32	chr13:64519200-64519600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:64521600-64522000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
34	chr13:64521800-64522800	Enhancers	HepG2	liver
35	chr13:64522800-64524600	Weak transcription	HepG2	liver
36	chr13:64524600-64525200	Enhancers	HepG2	liver
37	chr13:64550000-64550800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:64551800-64552000	Enhancers	HUVEC	blood vessel
39	chr13:64552000-64553400	Weak transcription	HUVEC	blood vessel
40	chr13:64553400-64558400	Enhancers	HUVEC	blood vessel
41	chr13:64554000-64554800	Enhancers	HepG2	liver
42	chr13:64569600-64571200	Enhancers	Fetal Lung	lung
43	chr13:64574200-64574800	Active TSS	Pancreatic Islets	Pancreatic Islet
44	chr13:64574800-64575200	Enhancers	Pancreatic Islets	Pancreatic Islet
45	chr13:64594600-64595200	Enhancers	Fetal Stomach	stomach
46	chr13:64594800-64595200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
47	chr13:64608200-64608600	Enhancers	Fetal Lung	lung
48	chr13:64608200-64608800	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr13:64608400-64608800	ZNF genes & repeats	Pancreas	Pancrea
50	chr13:64615400-64615800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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