Variant report

Variant	nsv900412
Chromosome Location	chr13:67512877-67572221
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:469)
CpG islands
(count:244)
Chromatin interactive
region (count:6)
LncRNA
region (count:11)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:469 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:67568448-67568775	K562	blood:	n/a	n/a
2	ATF2	chr13:67568271-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF3	chr13:67514291-67514517	K562	blood:	n/a	n/a
4	ATF3	chr13:67513673-67513979	K562	blood:	n/a	n/a
5	ATF3	chr13:67568179-67568725	A549	lung:	n/a	n/a
6	BCL3	chr13:67568092-67568724	A549	lung:	n/a	chr13:67568680-67568687
7	BHLHE40	chr13:67569138-67569828	GM12878	blood:	n/a	n/a
8	BHLHE40	chr13:67568386-67568547	K562	blood:	n/a	n/a
9	CEBPB	chr13:67568953-67569159	A549	lung:	n/a	n/a
10	CEBPB	chr13:67570660-67571082	A549	lung:	n/a	chr13:67570842-67570855
11	CEBPB	chr13:67566342-67567192	IMR90	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
12	CEBPB	chr13:67551323-67551595	IMR90	lung:	n/a	n/a
13	CEBPB	chr13:67568192-67568523	A549	lung:	n/a	n/a
14	CEBPB	chr13:67516734-67517339	IMR90	lung:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
15	CEBPB	chr13:67533828-67533837	K562	blood:	n/a	n/a
16	CEBPB	chr13:67568038-67568652	A549	lung:	n/a	n/a
17	CEBPB	chr13:67516745-67517360	Hela-S3	cervix:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
18	CEBPB	chr13:67558401-67558722	IMR90	lung:	n/a	chr13:67558552-67558563
19	CEBPB	chr13:67566346-67566737	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
20	CEBPB	chr13:67525177-67525315	H1-hESC	embryonic stem cell:	n/a	chr13:67525201-67525214
21	CEBPB	chr13:67566898-67567137	A549	lung:	n/a	n/a
22	CEBPB	chr13:67566839-67567157	K562	blood:	n/a	n/a
23	CEBPB	chr13:67566763-67567107	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr13:67515155-67515402	K562	blood:	n/a	chr13:67515279-67515290
25	CEBPB	chr13:67566840-67567107	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chr13:67536801-67536984	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:67516781-67517023	K562	blood:	n/a	chr13:67516868-67516877 chr13:67516868-67516877 chr13:67516866-67516879 chr13:67516868-67516877 chr13:67516868-67516879 chr13:67516868-67516877
28	CEBPB	chr13:67568217-67568468	HepG2	liver:	n/a	n/a
29	CEBPB	chr13:67558407-67558682	A549	lung:	n/a	chr13:67558552-67558563
30	CEBPB	chr13:67566236-67566719	A549	lung:	n/a	chr13:67566693-67566704 chr13:67566693-67566704
31	CEBPB	chr13:67568307-67568516	K562	blood:	n/a	n/a
32	CEBPB	chr13:67558478-67558699	HepG2	liver:	n/a	chr13:67558552-67558563
33	CEBPB	chr13:67568217-67568658	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr13:67566342-67566648	A549	lung:	n/a	n/a
35	CEBPB	chr13:67568171-67568602	A549	lung:	n/a	n/a
36	CEBPB	chr13:67515187-67515415	HepG2	liver:	n/a	chr13:67515279-67515290
37	CEBPB	chr13:67566854-67567179	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr13:67525159-67525306	A549	lung:	n/a	chr13:67525201-67525214
39	CHD2	chr13:67568389-67568563	K562	blood:	n/a	n/a
40	CHD2	chr13:67569170-67569763	GM12878	blood:	n/a	n/a
41	CHD2	chr13:67568285-67568652	H1-hESC	embryonic stem cell:	n/a	n/a
42	CREB1	chr13:67568282-67568593	A549	lung:	n/a	n/a
43	CTCF	chr13:67568434-67568617	GM20000	blood:	n/a	n/a
44	CTCF	chr13:67568460-67568611	LNCaP	prostate:	n/a	n/a
45	CTCF	chr13:67568460-67568610	GM12872	blood:	n/a	n/a
46	CTCF	chr13:67568408-67568631	LNCaP	prostate:	n/a	n/a
47	CTCF	chr13:67568378-67568641	ProgFib	skin:	n/a	n/a
48	CTCF	chr13:67568416-67568652	K562	blood:	n/a	n/a
49	CTCF	chr13:67526771-67526910	H1-hESC	embryonic stem cell:	n/a	chr13:67526830-67526839
50	CTCF	chr13:67568460-67568610	NHDF-neo	bronchial:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:67568518-67568568	ECC-1	luminal epithelium:	n/a
2	chr13:67568473-67568523	NB4	blood:	n/a
3	chr13:67568473-67568523	T-47D	breast:	n/a
4	chr13:67568473-67568523	ECC-1	luminal epithelium:	n/a
5	chr13:67568518-67568568	PFSK-1	brain:	n/a
6	chr13:67548536-67548586	LNCaP	prostate:	n/a
7	chr13:67568518-67568568	NB4	blood:	n/a
8	chr13:67568518-67568568	HCM	heart:	n/a
9	chr13:67568518-67568568	AG04450	lung:	fetal
10	chr13:67568518-67568568	HRE	kidney:	n/a
11	chr13:67568518-67568568	IMR90	lung:	fetal
12	chr13:67568473-67568523	A549	lung:	n/a
13	chr13:67570127-67570177	Hepatocyte	liver:	n/a
14	chr13:67548536-67548586	GM12891	blood:	n/a
15	chr13:67570127-67570177	K562	blood:	n/a
16	chr13:67568518-67568568	GM12892	blood:	n/a
17	chr13:67548536-67548586	HCM	heart:	n/a
18	chr13:67548536-67548586	GM12892	blood:	n/a
19	chr13:67548536-67548586	AG04450	lung:	fetal
20	chr13:67570127-67570177	HCPEpiC	choroid plexus:	n/a
21	chr13:67570127-67570177	IMR90	lung:	fetal
22	chr13:67568473-67568523	HRE	kidney:	n/a
23	chr13:67548536-67548586	NT2-D1	testis:	n/a
24	chr13:67570127-67570177	NH-A	brain:	n/a
25	chr13:67570127-67570177	HEK293	kidney:	embryo
26	chr13:67568518-67568568	HCF	heart:	n/a
27	chr13:67568473-67568523	CMK	blood:	n/a
28	chr13:67568518-67568568	Jurkat	blood:	n/a
29	chr13:67570127-67570177	HEEpiC	esophagus:	n/a
30	chr13:67570127-67570177	HL-60	blood:	n/a
31	chr13:67568473-67568523	HL-60	blood:	n/a
32	chr13:67568473-67568523	RPTEC	kidney:	n/a
33	chr13:67568473-67568523	AoSMC	blood vessel:	n/a
34	chr13:67570127-67570177	ovcar-3	ovarian:	n/a
35	chr13:67570127-67570177	MCF10A-Er-Src	breast:	n/a
36	chr13:67568518-67568568	HNPCEpiC	eye:	n/a
37	chr13:67568518-67568568	BJ	skin:	n/a
38	chr13:67568518-67568568	HPAEpiC	pulmonary alveolar:	n/a
39	chr13:67568518-67568568	GM12878	blood:	n/a
40	chr13:67570127-67570177	HRE	kidney:	n/a
41	chr13:67568473-67568523	MCF10A-Er-Src	breast:	n/a
42	chr13:67568518-67568568	HCPEpiC	choroid plexus:	n/a
43	chr13:67568518-67568568	NHBE	bronchial:	n/a
44	chr13:67570127-67570177	GM06990	blood:	n/a
45	chr13:67568473-67568523	BE2_C	brain:	n/a
46	chr13:67568518-67568568	HEK293	kidney:	embryo
47	chr13:67568518-67568568	SK-N-SH_RA	brain:	n/a
48	chr13:67570127-67570177	NHBE	bronchial:	n/a
49	chr13:67568473-67568523	Hepatocyte	liver:	n/a
50	chr13:67548536-67548586	HRCEpiC	kidney:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:67497444..67500061-chr13:67515647..67517481,2	K562	blood:
2	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:
3	chr13:67509668..67511474-chr13:67514101..67516252,2	K562	blood:
4	chr13:67562882..67565273-chr13:67566706..67568513,2	K562	blood:
5	chr13:67542691..67545017-chr13:67591674..67594006,2	K562	blood:
6	chr13:67517858..67520029-chr13:67533541..67536022,2	K562	blood:

(count:11 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL445989.1-15	chr13:67559629-67559908	NONHSAT034215
2	lnc-AL445989.1-16	chr13:67570354-67570413	NR_046637
3	lnc-AL445989.1-15	chr13:67551521-67551663	NONHSAT034215
4	lnc-AL445989.1-16	chr13:67565018-67565231	NR_046637
5	lnc-AL445989.1-15	chr13:67551564-67551663	ENSG00000225263.1
6	lnc-AL445989.1-15	chr13:67559629-67559908	ENSG00000225263.1
7	lnc-AL445989.1-16	chr13:67570354-67570413	ENSG00000233840.1
8	lnc-AL445989.1-15	chr13:67552505-67552603	NONHSAT034215
9	lnc-AL445989.1-15	chr13:67552505-67552603	ENSG00000225263.1
10	lnc-AL445989.1-16	chr13:67565018-67565231	ENSG00000233840.1
11	lnc-AL445989.1-14	chr13:67517880-67518119	NONHSAT034214

No data

Variant related genes	Relation type
PCDH9-AS4	TF binding region
PCDH9-AS3	TF binding region
PCDH9-AS4	CpG island
PCDH9-AS3	CpG island
ENSG00000233840	chromatin interactions

Extended variants
information (count: 1885 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1885 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1323910	chr13:67512877-67512878	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs143302826	chr13:67512906-67512907	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs186825952	chr13:67512916-67512917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs574332204	chr13:67512958-67512959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9540949	chr13:67512968-67512969	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs190007379	chr13:67512994-67512995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs181187736	chr13:67513023-67513024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs115916145	chr13:67513055-67513056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs540443937	chr13:67513070-67513071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565462231	chr13:67513083-67513084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs9540950	chr13:67513090-67513091	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs562504041	chr13:67513091-67513092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs148342672	chr13:67513100-67513101	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs140538278	chr13:67513106-67513107	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs185538025	chr13:67513140-67513141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs112940951	chr13:67513214-67513215	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs564826448	chr13:67513231-67513232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs574635836	chr13:67513250-67513251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs550037118	chr13:67513252-67513253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs35385470	chr13:67513257-67513258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs34654816	chr13:67513282-67513283	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569760681	chr13:67513283-67513284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs112404570	chr13:67513297-67513298	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs201732999	chr13:67513315-67513316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs371794475	chr13:67513339-67513340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs549073242	chr13:67513348-67513349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs565991386	chr13:67513355-67513356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs534012853	chr13:67513416-67513417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs78705270	chr13:67513445-67513446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374874291	chr13:67513448-67513449	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs576953158	chr13:67513467-67513468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539774175	chr13:67513468-67513469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs35492055	chr13:67513502-67513503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs556495736	chr13:67513506-67513507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs370276859	chr13:67513556-67513557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs141256412	chr13:67513557-67513558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs59727350	chr13:67513583-67513584	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs59199272	chr13:67513589-67513590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs57997772	chr13:67513590-67513591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs576150239	chr13:67513609-67513610	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs189660174	chr13:67513618-67513619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs561772509	chr13:67513655-67513656	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs536667354	chr13:67513693-67513694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554653284	chr13:67513694-67513695	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs199850240	chr13:67513696-67513697	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs572020239	chr13:67513737-67513738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs541102938	chr13:67513741-67513742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs369611135	chr13:67513744-67513745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs569409798	chr13:67513754-67513755	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs533568025	chr13:67513759-67513760	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:417 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:67508600-67513600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr13:67513600-67514400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr13:67513600-67514400	Enhancers	HMEC	breast
4	chr13:67513600-67514800	Enhancers	HUVEC	blood vessel
5	chr13:67514200-67514600	Enhancers	A549	lung
6	chr13:67518200-67519200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
7	chr13:67518600-67519600	Enhancers	Primary B cells from peripheral blood	blood
8	chr13:67518600-67519600	Enhancers	Dnd41	blood
9	chr13:67518800-67519400	Enhancers	Primary B cells from cord blood	blood
10	chr13:67519400-67520000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr13:67521600-67523400	Enhancers	A549	lung
12	chr13:67521800-67526400	Enhancers	iPS-20b Cell Line	embryonic stem cell
13	chr13:67522000-67522200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr13:67522400-67525400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr13:67522400-67526800	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr13:67522600-67523000	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr13:67522600-67526400	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chr13:67522800-67523000	Enhancers	Brain Anterior Caudate	brain
19	chr13:67522800-67523200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr13:67522800-67526400	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr13:67522800-67526600	Enhancers	Brain Hippocampus Middle	brain
22	chr13:67523000-67523400	Flanking Active TSS	Brain Anterior Caudate	brain
23	chr13:67523000-67523400	Active TSS	Brain Inferior Temporal Lobe	brain
24	chr13:67523000-67524600	Enhancers	Brain Cingulate Gyrus	brain
25	chr13:67523000-67525800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr13:67523000-67526400	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr13:67523200-67523600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr13:67523200-67523800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
29	chr13:67523200-67523800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr13:67523200-67524600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr13:67523400-67523600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr13:67523400-67523600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr13:67523400-67523800	Enhancers	H9 Cell Line	embryonic stem cell
34	chr13:67523400-67523800	Enhancers	Brain Angular Gyrus	brain
35	chr13:67523400-67523800	Enhancers	Fetal Brain Male	brain
36	chr13:67523400-67526400	Enhancers	Brain Anterior Caudate	brain
37	chr13:67523400-67531200	Weak transcription	A549	lung
38	chr13:67523600-67523800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr13:67523600-67524400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
40	chr13:67523600-67525400	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr13:67523800-67524200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
42	chr13:67523800-67524800	Weak transcription	Brain Angular Gyrus	brain
43	chr13:67523800-67525200	Weak transcription	H1 Cell Line	embryonic stem cell
44	chr13:67523800-67525200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr13:67523800-67526600	Enhancers	Brain Substantia Nigra	brain
46	chr13:67524200-67524400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
47	chr13:67524400-67524800	Enhancers	Brain Germinal Matrix	brain
48	chr13:67524400-67525200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
49	chr13:67524400-67526400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
50	chr13:67524400-67526400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain

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