Variant report

Variant	nsv562141
Chromosome Location	chr13:67842588-67878422
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67857713-67858283	HepG2	liver:	n/a	n/a
2	BACH1	chr13:67847366-67847439	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr13:67877967-67878020	A549	lung:	n/a	n/a
4	CEBPB	chr13:67852389-67852895	IMR90	lung:	n/a	n/a
5	CEBPB	chr13:67857846-67857971	HepG2	liver:	n/a	n/a
6	CEBPB	chr13:67873385-67873803	IMR90	lung:	n/a	n/a
7	CEBPB	chr13:67857728-67858180	HepG2	liver:	n/a	chr13:67857737-67857746
8	CEBPB	chr13:67860708-67860903	IMR90	lung:	n/a	n/a
9	CEBPZ	chr13:67864635-67864704	HepG2	liver:	n/a	n/a
10	E2F4	chr13:67873432-67873707	MCF10A-Er-Src	breast:	n/a	n/a
11	EP300	chr13:67852208-67852848	SK-N-SH	brain:	n/a	n/a
12	EP300	chr13:67852297-67852724	SK-N-SH_RA	brain:	n/a	n/a
13	EP300	chr13:67857855-67857967	Hela-S3	cervix:	n/a	n/a
14	EP300	chr13:67873493-67873717	Hela-S3	cervix:	n/a	n/a
15	EP300	chr13:67857731-67858296	HepG2	liver:	n/a	chr13:67858023-67858037 chr13:67857792-67857806
16	EP300	chr13:67857655-67858251	HepG2	liver:	n/a	chr13:67858023-67858037 chr13:67857792-67857806
17	EP300	chr13:67873111-67873964	ECC-1	luminal epithelium:	n/a	n/a
18	EP300	chr13:67852407-67852717	SK-N-SH_RA	brain:	n/a	n/a
19	EP300	chr13:67873405-67873736	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chr13:67877534-67879028	SK-N-SH	brain:	n/a	n/a
21	EP300	chr13:67873206-67873918	SK-N-SH	brain:	n/a	n/a
22	EP300	chr13:67873348-67873765	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chr13:67877837-67878333	SK-N-SH_RA	brain:	n/a	n/a
24	FOS	chr13:67873374-67874135	HUVEC	blood vessel:	n/a	n/a
25	FOS	chr13:67847177-67847462	MCF10A-Er-Src	breast:	n/a	chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290
26	FOS	chr13:67857735-67858022	MCF10A-Er-Src	breast:	n/a	chr13:67857848-67857860 chr13:67857850-67857858
27	FOS	chr13:67870780-67870937	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr13:67878003-67878010	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr13:67851924-67851936	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr13:67852450-67852603	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr13:67870710-67871007	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr13:67856024-67856142	MCF10A-Er-Src	breast:	n/a	chr13:67856102-67856111 chr13:67856101-67856112
33	FOS	chr13:67857725-67857968	MCF10A-Er-Src	breast:	n/a	chr13:67857848-67857860 chr13:67857850-67857858
34	FOS	chr13:67847125-67847462	MCF10A-Er-Src	breast:	n/a	chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290
35	FOS	chr13:67870701-67870899	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr13:67857757-67857925	MCF10A-Er-Src	breast:	n/a	chr13:67857848-67857860 chr13:67857850-67857858
37	FOS	chr13:67847140-67847479	MCF10A-Er-Src	breast:	n/a	chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290
38	FOS	chr13:67873402-67874238	MCF10A-Er-Src	breast:	n/a	n/a
39	FOS	chr13:67873365-67874273	MCF10A-Er-Src	breast:	n/a	n/a
40	FOS	chr13:67847156-67847511	MCF10A-Er-Src	breast:	n/a	chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290 chr13:67847280-67847290
41	FOS	chr13:67873371-67874246	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr13:67857731-67858022	MCF10A-Er-Src	breast:	n/a	chr13:67857848-67857860 chr13:67857850-67857858
43	FOS	chr13:67852459-67852650	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr13:67873425-67874246	MCF10A-Er-Src	breast:	n/a	n/a
45	FOSL1	chr13:67857670-67858145	HCT-116	colon:	n/a	chr13:67857848-67857860 chr13:67857850-67857858
46	FOSL2	chr13:67857744-67858083	HepG2	liver:	n/a	chr13:67857848-67857860 chr13:67857849-67857860 chr13:67857850-67857858
47	FOSL2	chr13:67857676-67858103	HepG2	liver:	n/a	chr13:67857848-67857860 chr13:67857849-67857860 chr13:67857850-67857858
48	FOSL2	chr13:67873379-67873875	SK-N-SH	brain:	n/a	n/a
49	FOXA1	chr13:67857738-67858165	HepG2	liver:	n/a	n/a
50	FOXA1	chr13:67857718-67858202	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67872416-67872466	HL-60	blood:	n/a
2	chr13:67872416-67872466	SK-N-SH	brain:	n/a
3	chr13:67872416-67872466	MCF-7	breast:	n/a
4	chr13:67872416-67872466	IMR90	lung:	fetal
5	chr13:67872416-67872466	HRPEpiC	eye:	n/a
6	chr13:67872416-67872466	RPTEC	kidney:	n/a
7	chr13:67872416-67872466	HPAEpiC	pulmonary alveolar:	n/a
8	chr13:67872416-67872466	Hepatocyte	liver:	n/a
9	chr13:67872416-67872466	GM12892	blood:	n/a
10	chr13:67872416-67872466	PFSK-1	brain:	n/a
11	chr13:67872416-67872466	SK-N-MC	brain:	n/a
12	chr13:67872416-67872466	Jurkat	blood:	n/a
13	chr13:67872416-67872466	A549	lung:	n/a
14	chr13:67872416-67872466	HepG2	liver:	n/a
15	chr13:67872416-67872466	HIPEpiC	eye:	n/a
16	chr13:67872416-67872466	SK-N-SH_RA	brain:	n/a
17	chr13:67872416-67872466	Caco-2	colon:	n/a
18	chr13:67872416-67872466	ProgFib	skin:	n/a
19	chr13:67872416-67872466	HCF	heart:	n/a
20	chr13:67872416-67872466	HEK293	kidney:	embryo
21	chr13:67872416-67872466	GM12891	blood:	n/a
22	chr13:67872416-67872466	NT2-D1	testis:	n/a
23	chr13:67872416-67872466	NHDF-neo	bronchial:	n/a
24	chr13:67872416-67872466	ovcar-3	ovarian:	n/a
25	chr13:67872416-67872466	PANC-1	pancreas:	n/a
26	chr13:67872416-67872466	H1-hESC	embryonic stem cell:	embryo
27	chr13:67872416-67872466	AoSMC	blood vessel:	n/a
28	chr13:67872416-67872466	AG04450	lung:	fetal
29	chr13:67872416-67872466	HCPEpiC	choroid plexus:	n/a
30	chr13:67872416-67872466	NHBE	bronchial:	n/a
31	chr13:67872416-67872466	CMK	blood:	n/a
32	chr13:67872416-67872466	AG09319	gingival:	n/a
33	chr13:67872416-67872466	T-47D	breast:	n/a
34	chr13:67872416-67872466	HRCEpiC	kidney:	n/a
35	chr13:67872416-67872466	SKMC	muscle:	n/a
36	chr13:67872416-67872466	AG04449	skin:	fetal
37	chr13:67872416-67872466	MCF10A-Er-Src	breast:	n/a
38	chr13:67872416-67872466	Hela-S3	cervix:	n/a
39	chr13:67872416-67872466	HRE	kidney:	n/a
40	chr13:67872416-67872466	HAEpiC	amniotic membrane:	n/a
41	chr13:67872416-67872466	NH-A	brain:	n/a
42	chr13:67872416-67872466	ECC-1	luminal epithelium:	n/a
43	chr13:67872416-67872466	HEEpiC	esophagus:	n/a
44	chr13:67872416-67872466	SAEC	small airway:	n/a
45	chr13:67872416-67872466	GM12878	blood:	n/a
46	chr13:67872416-67872466	GM19239	blood:	n/a
47	chr13:67872416-67872466	K562	blood:	n/a
48	chr13:67872416-67872466	HUVEC	blood vessel:	n/a
49	chr13:67872416-67872466	HNPCEpiC	eye:	n/a
50	chr13:67872416-67872466	GM06990	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:67844700..67846615-chr13:67859322..67861875,2	K562	blood:
2	chr13:67844700..67846615-chr13:67859322..67861875,2	K562	blood:
3	chr13:67839825..67842452-chr13:67857701..67859414,2	MCF-7	breast:

Variant related genes	Relation type
RPSAP53	TF binding region
RPSAP53	CpG island
ENSG00000214263	chromatin interactions

Extended variants
information (count: 895 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:895 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs149290846	chr13:67842616-67842617	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs185389092	chr13:67842644-67842645	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs542396837	chr13:67842659-67842660	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs559282798	chr13:67842708-67842709	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs552085160	chr13:67845170-67845171	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs560069224	chr13:67845183-67845184	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs537932090	chr13:67845678-67845679	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs561921660	chr13:67845729-67845730	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs9592507	chr13:67845755-67845756	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs189563637	chr13:67846446-67846447	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs145410989	chr13:67846447-67846448	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555852049	chr13:67846497-67846498	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs572317742	chr13:67846498-67846499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs564511077	chr13:67846532-67846533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs149023533	chr13:67846538-67846539	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs377624993	chr13:67846549-67846550	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs112987474	chr13:67846562-67846563	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs576715995	chr13:67846585-67846586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs202112802	chr13:67846715-67846716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs373349748	chr13:67846722-67846723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371027392	chr13:67846744-67846745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143038160	chr13:67846768-67846769	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs531422387	chr13:67846832-67846833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs541523817	chr13:67846850-67846851	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs561828720	chr13:67846901-67846902	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs527237511	chr13:67846927-67846928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148201617	chr13:67846959-67846960	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs141196439	chr13:67846964-67846965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs113934357	chr13:67846979-67846980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs531942070	chr13:67846980-67846981	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs377031359	chr13:67847056-67847057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs550525393	chr13:67847093-67847094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs544296894	chr13:67847108-67847109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs145391121	chr13:67847132-67847133	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs80132596	chr13:67847156-67847157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs182919440	chr13:67847221-67847222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs561778338	chr13:67847298-67847299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377156286	chr13:67847316-67847317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1033939	chr13:67847357-67847358	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs138024381	chr13:67847387-67847388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1033940	chr13:67847391-67847392	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs188669473	chr13:67847432-67847433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556052164	chr13:67847484-67847485	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs575790533	chr13:67847513-67847514	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs527584007	chr13:67847518-67847519	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs542008959	chr13:67847567-67847568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs17521186	chr13:67847590-67847591	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs570288316	chr13:67847608-67847609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs376478577	chr13:67847611-67847612	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537668772	chr13:67847632-67847633	Enhancers 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
Myelofibrosis	22110671	CNVD
Schizophrenia	23813976	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:126 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67846400-67847800	Enhancers	Muscle Satellite Cultured Cells	--
2	chr13:67846400-67848400	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr13:67846600-67848200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr13:67846800-67847400	Enhancers	HSMM	muscle
5	chr13:67846800-67848200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:67847000-67848400	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:67847200-67848000	Enhancers	iPS-20b Cell Line	embryonic stem cell
8	chr13:67847400-67848400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:67847400-67850200	Weak transcription	HSMM	muscle
10	chr13:67847600-67848000	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chr13:67847800-67848200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr13:67847800-67848200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr13:67847800-67848200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr13:67847800-67848400	Enhancers	H9 Cell Line	embryonic stem cell
15	chr13:67847800-67851600	Weak transcription	Muscle Satellite Cultured Cells	--
16	chr13:67848000-67848200	Enhancers	Fetal Thymus	thymus
17	chr13:67848000-67848400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
18	chr13:67848000-67848400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr13:67848200-67851600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
20	chr13:67848400-67849400	Weak transcription	Fetal Thymus	thymus
21	chr13:67849400-67850600	Enhancers	Primary hematopoietic stem cells	blood
22	chr13:67849400-67851000	Enhancers	Fetal Thymus	thymus
23	chr13:67849600-67850000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr13:67849600-67850200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr13:67849600-67850200	Enhancers	HSMMtube	muscle
26	chr13:67849800-67850600	Enhancers	Dnd41	blood
27	chr13:67850200-67850800	Enhancers	HSMM	muscle
28	chr13:67850200-67851600	Weak transcription	HSMMtube	muscle
29	chr13:67850800-67851600	Weak transcription	HSMM	muscle
30	chr13:67851600-67853200	Enhancers	HSMMtube	muscle
31	chr13:67851600-67853400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr13:67851600-67853400	Enhancers	Osteobl	bone
33	chr13:67851600-67853800	Enhancers	HSMM	muscle
34	chr13:67851600-67854000	Enhancers	Muscle Satellite Cultured Cells	--
35	chr13:67851800-67853000	Enhancers	NH-A	brain
36	chr13:67851800-67853200	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr13:67851800-67853400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
38	chr13:67852400-67853000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chr13:67853000-67857800	Weak transcription	NH-A	brain
40	chr13:67853200-67855600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr13:67853400-67855600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
42	chr13:67853600-67853800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
43	chr13:67853800-67855200	Weak transcription	HSMM	muscle
44	chr13:67854000-67855800	Weak transcription	Muscle Satellite Cultured Cells	--
45	chr13:67854400-67856400	Enhancers	Cortex derived primary cultured neurospheres	brain
46	chr13:67854400-67856600	Enhancers	Brain Germinal Matrix	brain
47	chr13:67855200-67855800	Enhancers	HUES48 Cell Line	embryonic stem cell
48	chr13:67855200-67856000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
49	chr13:67855200-67856200	Enhancers	HSMM	muscle
50	chr13:67855400-67855800	Enhancers	iPS-18 Cell Line	embryonic stem cell

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