Variant report

Variant	nsv900453
Chromosome Location	chr13:69449431-69757982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:693)
CpG islands
(count:734)
Chromatin interactive
region (count:33)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:693 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:69584667-69584945	K562	blood:	n/a	n/a
2	BATF	chr13:69463008-69463335	GM12878	blood:	n/a	chr13:69463154-69463165 chr13:69463182-69463193 chr13:69463126-69463137
3	BCL3	chr13:69713198-69713412	GM12878	blood:	n/a	n/a
4	BHLHE40	chr13:69471792-69471824	HepG2	liver:	n/a	n/a
5	BRCA1	chr13:69471570-69471717	H1-hESC	embryonic stem cell:	n/a	n/a
6	CCNT2	chr13:69558900-69559144	K562	blood:	n/a	n/a
7	CEBPB	chr13:69744343-69744543	HepG2	liver:	n/a	chr13:69744403-69744416 chr13:69744414-69744427 chr13:69744414-69744425
8	CEBPB	chr13:69456603-69456800	A549	lung:	n/a	chr13:69456701-69456712
9	CEBPB	chr13:69659890-69660227	A549	lung:	n/a	n/a
10	CEBPB	chr13:69621157-69621357	K562	blood:	n/a	n/a
11	CEBPB	chr13:69603498-69603621	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:69720588-69720825	HepG2	liver:	n/a	chr13:69720689-69720700
13	CEBPB	chr13:69733575-69733858	HepG2	liver:	n/a	chr13:69733710-69733721
14	CEBPB	chr13:69454041-69454489	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr13:69456526-69456831	HepG2	liver:	n/a	chr13:69456701-69456712
16	CEBPB	chr13:69659461-69660073	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:69643875-69643893	H1-hESC	embryonic stem cell:	n/a	n/a
18	CEBPB	chr13:69471628-69471847	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr13:69639602-69639802	HepG2	liver:	n/a	chr13:69639729-69639742 chr13:69639730-69639741
20	CEBPB	chr13:69680041-69680394	HepG2	liver:	n/a	chr13:69680205-69680216
21	CHD2	chr13:69528075-69528263	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr13:69528047-69528275	HepG2	liver:	n/a	n/a
23	CTCF	chr13:69749083-69749169	K562	blood:	n/a	n/a
24	CTCF	chr13:69501620-69501879	MCF-7	breast:	n/a	n/a
25	CTCF	chr13:69501660-69501810	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr13:69501640-69501790	GM12868	blood:	n/a	n/a
27	CTCF	chr13:69501633-69501902	HUVEC	blood vessel:	n/a	n/a
28	CTCF	chr13:69501698-69501841	GM10266	blood:	n/a	n/a
29	CTCF	chr13:69501720-69501870	RPTEC	kidney:	n/a	n/a
30	CTCF	chr13:69501617-69501812	K562	blood:	n/a	n/a
31	CTCF	chr13:69501539-69501955	GM12878	blood:	n/a	n/a
32	CTCF	chr13:69501600-69501750	GM12873	blood:	n/a	n/a
33	CTCF	chr13:69501640-69501790	NHEK	skin:	n/a	n/a
34	CTCF	chr13:69501596-69501885	Gliobla	brain:	n/a	n/a
35	CTCF	chr13:69677225-69677404	Medullo	brain:	n/a	n/a
36	CTCF	chr13:69667160-69667310	Caco-2	colon:	n/a	n/a
37	CTCF	chr13:69667220-69667370	RPTEC	kidney:	n/a	n/a
38	CTCF	chr13:69501680-69501830	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr13:69501680-69501830	RPTEC	kidney:	n/a	n/a
40	CTCF	chr13:69501680-69501830	GM12872	blood:	n/a	n/a
41	CTCF	chr13:69667140-69667290	MCF-7	breast:	n/a	n/a
42	CTCF	chr13:69501680-69501830	SAEC	small airway:	n/a	n/a
43	CTCF	chr13:69501680-69501830	GM12878	blood:	n/a	n/a
44	CTCF	chr13:69501680-69501830	HPF	lung:	n/a	n/a
45	CTCF	chr13:69501700-69501850	GM12873	blood:	n/a	n/a
46	CTCF	chr13:69501679-69501842	GM10248	blood:	n/a	n/a
47	CTCF	chr13:69732120-69732177	ProgFib	skin:	n/a	n/a
48	CTCF	chr13:69501680-69501830	HRPEpiC	eye:	n/a	n/a
49	CTCF	chr13:69501660-69501810	GM12865	blood:	n/a	n/a
50	CTCF	chr13:69667128-69667390	GM12878	blood:	n/a	n/a

(count:734 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:69559303-69559353	CMK	blood:	n/a
2	chr13:69459533-69459583	AoSMC	blood vessel:	n/a
3	chr13:69559303-69559353	CMK	blood:	n/a
4	chr13:69459533-69459583	AoSMC	blood vessel:	n/a
5	chr13:69559194-69559244	HepG2	liver:	n/a
6	chr13:69559194-69559244	A549	lung:	n/a
7	chr13:69559194-69559244	AG04450	lung:	fetal
8	chr13:69587760-69587810	GM12878	blood:	n/a
9	chr13:69587760-69587810	GM06990	blood:	n/a
10	chr13:69561352-69561402	PANC-1	pancreas:	n/a
11	chr13:69459913-69459963	AG04450	lung:	fetal
12	chr13:69555907-69555957	HEEpiC	esophagus:	n/a
13	chr13:69558928-69558978	K562	blood:	n/a
14	chr13:69555907-69555957	HAEpiC	amniotic membrane:	n/a
15	chr13:69459913-69459963	ovcar-3	ovarian:	n/a
16	chr13:69459742-69459792	AG10803	skin:	n/a
17	chr13:69459607-69459657	HEEpiC	esophagus:	n/a
18	chr13:69559194-69559244	AG04449	skin:	fetal
19	chr13:69587760-69587810	BE2_C	brain:	n/a
20	chr13:69559194-69559244	SK-N-SH_RA	brain:	n/a
21	chr13:69559039-69559089	HPAEpiC	pulmonary alveolar:	n/a
22	chr13:69561352-69561402	NB4	blood:	n/a
23	chr13:69559303-69559353	NB4	blood:	n/a
24	chr13:69459533-69459583	Hela-S3	cervix:	n/a
25	chr13:69559039-69559089	BJ	skin:	n/a
26	chr13:69559039-69559089	PANC-1	pancreas:	n/a
27	chr13:69459533-69459583	PrEC	prostate:	n/a
28	chr13:69561352-69561402	SK-N-MC	brain:	n/a
29	chr13:69558928-69558978	GM19239	blood:	n/a
30	chr13:69459742-69459792	HAEpiC	amniotic membrane:	n/a
31	chr13:69459913-69459963	HCT-116	colon:	n/a
32	chr13:69559194-69559244	SK-N-MC	brain:	n/a
33	chr13:69558928-69558978	HRCEpiC	kidney:	n/a
34	chr13:69459533-69459583	HAEpiC	amniotic membrane:	n/a
35	chr13:69459607-69459657	NT2-D1	testis:	n/a
36	chr13:69555907-69555957	Caco-2	colon:	n/a
37	chr13:69558928-69558978	AG09309	skin:	n/a
38	chr13:69587760-69587810	HCF	heart:	n/a
39	chr13:69459742-69459792	MCF-7	breast:	n/a
40	chr13:69559194-69559244	BJ	skin:	n/a
41	chr13:69587760-69587810	SAEC	small airway:	n/a
42	chr13:69459607-69459657	HAEpiC	amniotic membrane:	n/a
43	chr13:69587760-69587810	K562	blood:	n/a
44	chr13:69557960-69558010	HCM	heart:	n/a
45	chr13:69555907-69555957	NT2-D1	testis:	n/a
46	chr13:69587760-69587810	AG04449	skin:	fetal
47	chr13:69459742-69459792	HIPEpiC	eye:	n/a
48	chr13:69561352-69561402	HIPEpiC	eye:	n/a
49	chr13:69559194-69559244	ProgFib	skin:	n/a
50	chr13:69459913-69459963	HAEpiC	amniotic membrane:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:69577914..69580803-chr13:69584083..69586306,2	K562	blood:
2	chr13:52026657..52027294-chr13:69594051..69594992,2	Hela-S3	cervix:
3	chr13:69577914..69580803-chr13:69584083..69586306,2	K562	blood:
4	chr13:68878193..68879007-chr13:69501325..69502164,3	MCF-7	breast:
5	chr13:69583714..69586393-chr13:69587871..69590253,3	K562	blood:
6	chr13:69583714..69586393-chr13:69587871..69590253,3	K562	blood:
7	chr13:69588937..69591463-chr13:69592795..69594701,2	MCF-7	breast:
8	chr13:68308872..68310810-chr13:69501547..69503078,2	MCF-7	breast:
9	chr13:69676877..69679728-chr13:69680148..69683095,2	K562	blood:
10	chr13:69514136..69516850-chr13:69517321..69519328,2	K562	blood:
11	chr13:69577123..69579403-chr13:69580839..69583998,3	K562	blood:
12	chr13:69557613..69560490-chr13:69560641..69563029,2	K562	blood:
13	chr13:69676877..69679728-chr13:69680148..69683095,2	K562	blood:
14	chr13:69682184..69685154-chr13:69690217..69692966,2	MCF-7	breast:
15	chr13:69584341..69586393-chr13:69588333..69590253,2	K562	blood:
16	chr13:69468479..69470579-chr13:69472768..69475321,2	MCF-7	breast:
17	chr13:69342465..69344656-chr13:69450218..69452422,2	K562	blood:
18	chr13:69745232..69748502-chr13:69749716..69752165,3	K562	blood:
19	chr13:69468479..69470579-chr13:69472768..69475321,2	MCF-7	breast:
20	chr13:69613880..69614380-chr3:73159953..73160630,2	HCT-116	colon:
21	chr13:69577123..69579403-chr13:69580839..69583998,3	K562	blood:
22	chr13:69443623..69445703-chr13:69462131..69463652,2	K562	blood:
23	chr13:69682184..69685154-chr13:69690217..69692966,2	MCF-7	breast:
24	chr13:69588937..69591463-chr13:69592795..69594701,2	MCF-7	breast:
25	chr13:69591603..69593208-chr13:69593619..69596259,2	K562	blood:
26	chr13:69714056..69716276-chr13:69718003..69720076,2	K562	blood:
27	chr13:69514136..69516850-chr13:69517321..69519328,2	K562	blood:
28	chr13:69745232..69748502-chr13:69749716..69752165,3	K562	blood:
29	chr13:69584341..69586393-chr13:69588333..69590253,2	K562	blood:
30	chr13:69591603..69593208-chr13:69593619..69596259,2	K562	blood:
31	chr13:69745779..69747312-chr13:69749716..69751908,2	K562	blood:
32	chr13:69745779..69747312-chr13:69749716..69751908,2	K562	blood:
33	chr13:69714056..69716276-chr13:69718003..69720076,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KLHL1-1	chr13:69459309-69459457	XLOC_010651
2	lnc-KLHL1-1	chr13:69459309-69459457	NONHSAT034238
3	lnc-KLHL1-7	chr13:69675964-69676188	NONHSAT034240
4	lnc-BORA-25	chr13:69559190-69560196	NONHSAT034239

No data

Variant related genes	Relation type
ZDHHC20P4	TF binding region
SNRPFP3	TF binding region
ZDHHC20P4	CpG island
SNRPFP3	CpG island
ENSG00000223247	chromatin interactions
ENSG00000102786	chromatin interactions
ENSG00000232380	chromatin interactions

Extended variants
information (count: 4398 )
Associated
traits (count: 106 )

Variant overlapped rSNPs/rCNVs (count:4398 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549609733	chr13:69453000-69453001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs532391730	chr13:69453006-69453007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs568398053	chr13:69453032-69453033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565552727	chr13:69453044-69453045	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs534570795	chr13:69453095-69453096	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs386771990	chr13:69453106-69453107	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565079479	chr13:69453114-69453115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs9541601	chr13:69453116-69453117	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs371712526	chr13:69453128-69453129	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs193232773	chr13:69453177-69453178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs9592571	chr13:69453186-69453187	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs573733150	chr13:69453188-69453189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2438448	chr13:69453218-69453219	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs558347493	chr13:69453230-69453231	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9599344	chr13:69453242-69453243	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs572130463	chr13:69453264-69453265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs183726272	chr13:69453276-69453277	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs564276968	chr13:69453288-69453289	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs575753086	chr13:69453310-69453311	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs368806952	chr13:69453369-69453370	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139359795	chr13:69453373-69453374	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs9592572	chr13:69453400-69453401	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs114717141	chr13:69453410-69453411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs149626646	chr13:69453432-69453433	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs544484167	chr13:69453446-69453447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs566338933	chr13:69453478-69453479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs144332825	chr13:69453485-69453486	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188719365	chr13:69453535-69453536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs374305091	chr13:69453546-69453547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs555982120	chr13:69453581-69453582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9592573	chr13:69453590-69453591	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs6562539	chr13:69453591-69453592	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs56353826	chr13:69453623-69453624	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs567364502	chr13:69453685-69453686	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs536419378	chr13:69453686-69453687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs76270248	chr13:69453700-69453701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs572787605	chr13:69453706-69453707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs74493106	chr13:69453729-69453730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs571982123	chr13:69453730-69453731	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs373125811	chr13:69453743-69453744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs557730694	chr13:69453765-69453766	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577571112	chr13:69453769-69453770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11371960	chr13:69453774-69453775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs34002510	chr13:69453775-69453776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs539455138	chr13:69453782-69453783	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563771513	chr13:69453790-69453791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs376593927	chr13:69453831-69453832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs574177627	chr13:69453870-69453871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs545610833	chr13:69453898-69453899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs191915480	chr13:69453956-69453957	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:106)

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
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Bipolar disorder	19114987	CNVD

Chromatin state (count:208 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:69453000-69454800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:69458200-69458400	Enhancers	Fetal Brain Male	brain
3	chr13:69458200-69458600	Enhancers	Cortex derived primary cultured neurospheres	brain
4	chr13:69458200-69458600	Enhancers	Fetal Brain Female	brain
5	chr13:69458600-69459600	Weak transcription	Fetal Brain Male	brain
6	chr13:69459200-69459600	Enhancers	Brain Hippocampus Middle	brain
7	chr13:69459400-69459600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:69459400-69459800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
9	chr13:69459600-69460000	Enhancers	Fetal Brain Male	brain
10	chr13:69459600-69460400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:69459600-69466800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr13:69462800-69463200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr13:69463200-69472600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr13:69464000-69467400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr13:69465600-69465800	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr13:69465800-69471400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
17	chr13:69466600-69467000	Enhancers	HUES64 Cell Line	embryonic stem cell
18	chr13:69466600-69467400	Enhancers	iPS-15b Cell Line	embryonic stem cell
19	chr13:69466800-69467000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:69466800-69467600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chr13:69467000-69467200	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr13:69467000-69467600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:69467000-69467800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr13:69467000-69471800	Weak transcription	HUES64 Cell Line	embryonic stem cell
25	chr13:69467200-69471200	Weak transcription	HUES48 Cell Line	embryonic stem cell
26	chr13:69467200-69471400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
27	chr13:69467400-69467800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr13:69467400-69471600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
29	chr13:69467600-69468200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
30	chr13:69467600-69468600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr13:69467800-69468200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr13:69467800-69471600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:69468600-69469000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:69471200-69472200	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr13:69471400-69472000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr13:69471400-69472200	Enhancers	iPS-20b Cell Line	embryonic stem cell
37	chr13:69471600-69472000	Enhancers	H1 Cell Line	embryonic stem cell
38	chr13:69471600-69472000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr13:69471600-69472000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr13:69471600-69472200	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr13:69471800-69472200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr13:69472000-69478800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr13:69472200-69472400	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr13:69472200-69472600	Weak transcription	HUES48 Cell Line	embryonic stem cell
45	chr13:69472400-69473200	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
46	chr13:69472600-69472800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
47	chr13:69472600-69473400	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
48	chr13:69478800-69479800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
49	chr13:69483000-69483400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
50	chr13:69483400-69486800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell

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