Variant report

Variant	nsv455933
Chromosome Location	chr13:67392298-67437316
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:184)
CpG islands
(count:123)
Chromatin interactive
region (count:2)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:184 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67409290-67409647	K562	blood:	n/a	n/a
2	CEBPB	chr13:67421612-67422123	A549	lung:	n/a	n/a
3	CEBPB	chr13:67394952-67395122	A549	lung:	n/a	n/a
4	CEBPB	chr13:67429391-67429576	A549	lung:	n/a	n/a
5	CEBPB	chr13:67421847-67422047	A549	lung:	n/a	n/a
6	CEBPB	chr13:67394912-67395112	HepG2	liver:	n/a	n/a
7	CTCF	chr13:67424040-67424190	GM12867	blood:	n/a	n/a
8	CTCF	chr13:67405780-67405930	HRE	kidney:	n/a	n/a
9	CTCF	chr13:67409600-67409750	BE2_C	brain:	n/a	n/a
10	CTCF	chr13:67420981-67421059	LNCaP	prostate:	n/a	n/a
11	CTCF	chr13:67409340-67409490	HBMEC	blood vessel:	n/a	n/a
12	CTCF	chr13:67409240-67409390	GM12875	blood:	n/a	n/a
13	CTCF	chr13:67435100-67435250	GM12871	blood:	n/a	n/a
14	CTCF	chr13:67409600-67409750	AoAF	blood vessel:	n/a	n/a
15	CTCF	chr13:67424096-67424113	HepG2	liver:	n/a	n/a
16	CTCF	chr13:67409620-67409770	BE2_C	brain:	n/a	n/a
17	CTCF	chr13:67409620-67409770	HEK293	kidney:	n/a	n/a
18	CTCF	chr13:67409300-67409450	SK-N-SH_RA	brain:	n/a	n/a
19	CTCF	chr13:67409680-67409830	A549	lung:	n/a	n/a
20	CTCF	chr13:67409600-67409750	HPF	lung:	n/a	n/a
21	CTCF	chr13:67394999-67395078	GM10248	blood:	n/a	n/a
22	CUX1	chr13:67420153-67420166	K562	blood:	n/a	n/a
23	E2F4	chr13:67410109-67410314	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr13:67404479-67404547	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr13:67403495-67403634	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr13:67432774-67432869	MCF10A-Er-Src	breast:	n/a	n/a
27	ELK1	chr13:67405194-67405210	Hela-S3	cervix:	n/a	n/a
28	EP300	chr13:67409195-67409689	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr13:67409239-67409712	SK-N-SH_RA	brain:	n/a	n/a
30	EP300	chr13:67405609-67406005	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr13:67421533-67422102	A549	lung:	n/a	n/a
32	EP300	chr13:67409076-67409697	A549	lung:	n/a	n/a
33	EP300	chr13:67421519-67422049	A549	lung:	n/a	n/a
34	EP300	chr13:67409306-67409668	K562	blood:	n/a	n/a
35	FOS	chr13:67405588-67405940	MCF10A-Er-Src	breast:	n/a	chr13:67405887-67405897 chr13:67405888-67405897 chr13:67405887-67405897 chr13:67405635-67405643 chr13:67405887-67405897 chr13:67405887-67405897
36	FOS	chr13:67405759-67405935	MCF10A-Er-Src	breast:	n/a	chr13:67405887-67405897 chr13:67405888-67405897 chr13:67405887-67405897 chr13:67405887-67405897 chr13:67405887-67405897
37	FOS	chr13:67427742-67428162	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr13:67400469-67400887	HUVEC	blood vessel:	n/a	n/a
39	FOS	chr13:67427706-67428149	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr13:67433204-67433607	HUVEC	blood vessel:	n/a	chr13:67433435-67433446
41	FOS	chr13:67399025-67399073	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr13:67429170-67429667	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr13:67429270-67429678	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr13:67429311-67429623	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr13:67405533-67406023	MCF10A-Er-Src	breast:	n/a	chr13:67405887-67405897 chr13:67405888-67405897 chr13:67405887-67405897 chr13:67405635-67405643 chr13:67405887-67405897 chr13:67405887-67405897
46	FOS	chr13:67433270-67433604	MCF10A-Er-Src	breast:	n/a	chr13:67433435-67433446
47	FOS	chr13:67433281-67433604	MCF10A-Er-Src	breast:	n/a	chr13:67433435-67433446
48	FOS	chr13:67436862-67436893	MCF10A-Er-Src	breast:	n/a	chr13:67436880-67436889 chr13:67436881-67436888 chr13:67436881-67436889 chr13:67436879-67436891 chr13:67436881-67436890
49	FOS	chr13:67429161-67429686	MCF10A-Er-Src	breast:	n/a	n/a
50	FOS	chr13:67427826-67428165	MCF10A-Er-Src	breast:	n/a	n/a

(count:123 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67421996-67422046	GM12891	blood:	n/a
2	chr13:67421996-67422046	GM12891	blood:	n/a
3	chr13:67434423-67434473	Hela-S3	cervix:	n/a
4	chr13:67421996-67422046	HEEpiC	esophagus:	n/a
5	chr13:67421996-67422046	HCM	heart:	n/a
6	chr13:67434423-67434473	HCM	heart:	n/a
7	chr13:67434423-67434473	GM06990	blood:	n/a
8	chr13:67421996-67422046	NHDF-neo	bronchial:	n/a
9	chr13:67434423-67434473	SKMC	muscle:	n/a
10	chr13:67434423-67434473	HMEC	breast:	n/a
11	chr13:67421996-67422046	PFSK-1	brain:	n/a
12	chr13:67421996-67422046	Hepatocyte	liver:	n/a
13	chr13:67421996-67422046	AG09319	gingival:	n/a
14	chr13:67434423-67434473	K562	blood:	n/a
15	chr13:67434423-67434473	BE2_C	brain:	n/a
16	chr13:67434423-67434473	PANC-1	pancreas:	n/a
17	chr13:67434423-67434473	Jurkat	blood:	n/a
18	chr13:67421996-67422046	GM06990	blood:	n/a
19	chr13:67421996-67422046	NT2-D1	testis:	n/a
20	chr13:67421996-67422046	SK-N-MC	brain:	n/a
21	chr13:67434423-67434473	SK-N-MC	brain:	n/a
22	chr13:67421996-67422046	PrEC	prostate:	n/a
23	chr13:67434423-67434473	AoSMC	blood vessel:	n/a
24	chr13:67421996-67422046	ECC-1	luminal epithelium:	n/a
25	chr13:67421996-67422046	SAEC	small airway:	n/a
26	chr13:67421996-67422046	SK-N-SH	brain:	n/a
27	chr13:67434423-67434473	GM19239	blood:	n/a
28	chr13:67421996-67422046	T-47D	breast:	n/a
29	chr13:67421996-67422046	HRPEpiC	eye:	n/a
30	chr13:67434423-67434473	HCF	heart:	n/a
31	chr13:67421996-67422046	PANC-1	pancreas:	n/a
32	chr13:67421996-67422046	MCF-7	breast:	n/a
33	chr13:67434423-67434473	SK-N-SH_RA	brain:	n/a
34	chr13:67421996-67422046	HAEpiC	amniotic membrane:	n/a
35	chr13:67421996-67422046	HCPEpiC	choroid plexus:	n/a
36	chr13:67421996-67422046	GM19239	blood:	n/a
37	chr13:67434423-67434473	HL-60	blood:	n/a
38	chr13:67434423-67434473	NT2-D1	testis:	n/a
39	chr13:67421996-67422046	HMEC	breast:	n/a
40	chr13:67421996-67422046	AG04450	lung:	fetal
41	chr13:67434423-67434473	ProgFib	skin:	n/a
42	chr13:67421996-67422046	HCF	heart:	n/a
43	chr13:67421996-67422046	HRCEpiC	kidney:	n/a
44	chr13:67421996-67422046	HEK293	kidney:	embryo
45	chr13:67434423-67434473	ECC-1	luminal epithelium:	n/a
46	chr13:67421996-67422046	LNCaP	prostate:	n/a
47	chr13:67434423-67434473	AG04450	lung:	fetal
48	chr13:67421996-67422046	NB4	blood:	n/a
49	chr13:67421996-67422046	AG04449	skin:	fetal
50	chr13:67434423-67434473	HCT-116	colon:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:67397391..67400012-chr13:67432704..67434627,2	K562	blood:
2	chr13:67414851..67415422-chr7:70812042..70812870,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-14	chr13:67399301-67399368	ENSG00000228842.2
2	lnc-AL445989.1-14	chr13:67433120-67433252	ENSG00000228842.2
3	lnc-AL445989.1-14	chr13:67433130-67433252	ENSG00000228842.1

No data

Variant related genes	Relation type
PCDH9-AS2	TF binding region
PCDH9-AS2	CpG island
ENSG00000228842	chromatin interactions

Extended variants
information (count: 1300 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1300 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568253476	chr13:67394334-67394335	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs76713671	chr13:67394341-67394342	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542208106	chr13:67394375-67394376	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs112250425	chr13:67394376-67394377	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs75808683	chr13:67394736-67394737	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs74846074	chr13:67394743-67394744	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs80274811	chr13:67394744-67394745	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs539087775	chr13:67394915-67394916	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs551296162	chr13:67394919-67394920	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs571374553	chr13:67394957-67394958	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371248200	chr13:67394976-67394977	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs536850902	chr13:67394978-67394979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs186054741	chr13:67395002-67395003	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs148511263	chr13:67395025-67395026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs369029533	chr13:67395057-67395058	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs141868959	chr13:67395061-67395062	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs190039207	chr13:67395065-67395066	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs572870224	chr13:67395110-67395111	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs544802139	chr13:67395237-67395238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs561595501	chr13:67395250-67395251	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs530388049	chr13:67395328-67395329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs80174886	chr13:67395365-67395366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs567172595	chr13:67395372-67395373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs76066698	chr13:67395418-67395419	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs532503421	chr13:67395473-67395474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs181069528	chr13:67395499-67395500	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537305550	chr13:67395510-67395511	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs530768944	chr13:67395562-67395563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550341680	chr13:67395565-67395566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185556983	chr13:67395652-67395653	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs536110162	chr13:67395660-67395661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs552560796	chr13:67395662-67395663	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9599152	chr13:67395668-67395669	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs150647348	chr13:67395682-67395683	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs140885983	chr13:67395789-67395790	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs574048575	chr13:67395818-67395819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs541573358	chr13:67395836-67395837	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs9540924	chr13:67395856-67395857	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs544840472	chr13:67395863-67395864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs190596860	chr13:67395867-67395868	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs578236443	chr13:67395893-67395894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs116195684	chr13:67395906-67395907	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs188728285	chr13:67395948-67395949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs9592488	chr13:67395978-67395979	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs77422219	chr13:67395979-67395980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545863881	chr13:67395999-67396000	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs563027576	chr13:67396025-67396026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs531685814	chr13:67396061-67396062	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs144807498	chr13:67396086-67396087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs567085333	chr13:67396144-67396145	Enhancers	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
Prostate cancer	22341455	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:242 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67395200-67396200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
2	chr13:67400400-67401000	Enhancers	HUVEC	blood vessel
3	chr13:67400400-67401400	Enhancers	Muscle Satellite Cultured Cells	--
4	chr13:67401400-67405200	Weak transcription	Muscle Satellite Cultured Cells	--
5	chr13:67404400-67406200	Enhancers	Primary B cells from peripheral blood	blood
6	chr13:67404800-67406000	Enhancers	Brain Substantia Nigra	brain
7	chr13:67405000-67406000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:67405000-67406200	Enhancers	Primary B cells from cord blood	blood
9	chr13:67405200-67405400	Active TSS	A549	lung
10	chr13:67405200-67405600	Enhancers	Fetal Kidney	kidney
11	chr13:67405200-67406000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr13:67405200-67406000	Enhancers	Muscle Satellite Cultured Cells	--
13	chr13:67405200-67406000	Enhancers	HMEC	breast
14	chr13:67405200-67406000	Enhancers	HSMM	muscle
15	chr13:67405200-67406200	Enhancers	Brain Angular Gyrus	brain
16	chr13:67405200-67406200	Enhancers	Brain Anterior Caudate	brain
17	chr13:67405200-67406200	Enhancers	Brain Hippocampus Middle	brain
18	chr13:67405200-67406200	Enhancers	Brain Inferior Temporal Lobe	brain
19	chr13:67405400-67405800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr13:67405400-67405800	Enhancers	Cortex derived primary cultured neurospheres	brain
21	chr13:67405400-67405800	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
22	chr13:67405400-67405800	Flanking Active TSS	A549	lung
23	chr13:67405400-67406000	Enhancers	Brain Cingulate Gyrus	brain
24	chr13:67405600-67409000	Weak transcription	Fetal Kidney	kidney
25	chr13:67405800-67406200	Enhancers	A549	lung
26	chr13:67405800-67408400	Weak transcription	Cortex derived primary cultured neurospheres	brain
27	chr13:67405800-67409000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
28	chr13:67406000-67408400	Weak transcription	Brain Cingulate Gyrus	brain
29	chr13:67406000-67408600	Weak transcription	Brain Substantia Nigra	brain
30	chr13:67406000-67408800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:67406000-67409200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
32	chr13:67406000-67409200	Weak transcription	Muscle Satellite Cultured Cells	--
33	chr13:67406200-67407400	Weak transcription	Brain Anterior Caudate	brain
34	chr13:67406200-67408400	Weak transcription	Brain Hippocampus Middle	brain
35	chr13:67406200-67408400	Weak transcription	Brain Inferior Temporal Lobe	brain
36	chr13:67406200-67408800	Weak transcription	A549	lung
37	chr13:67406200-67409000	Weak transcription	Brain Angular Gyrus	brain
38	chr13:67407400-67408000	Enhancers	Brain Anterior Caudate	brain
39	chr13:67408000-67408400	Weak transcription	Brain Anterior Caudate	brain
40	chr13:67408400-67408600	Enhancers	Brain Hippocampus Middle	brain
41	chr13:67408400-67409000	Enhancers	Brain Anterior Caudate	brain
42	chr13:67408400-67409200	Enhancers	Brain Inferior Temporal Lobe	brain
43	chr13:67408400-67409400	Enhancers	Left Ventricle	heart
44	chr13:67408400-67409600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
45	chr13:67408400-67409600	Enhancers	Fetal Muscle Trunk	muscle
46	chr13:67408400-67409600	Enhancers	Fetal Muscle Leg	muscle
47	chr13:67408400-67409800	Enhancers	Brain Cingulate Gyrus	brain
48	chr13:67408400-67410000	Enhancers	Cortex derived primary cultured neurospheres	brain
49	chr13:67408600-67409000	Enhancers	Brain Germinal Matrix	brain
50	chr13:67408600-67409000	Enhancers	Skeletal Muscle Male	skeletal muscle

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