Variant report

Variant	nsv899994
Chromosome Location	chr13:37816086-38087145
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	chr13:37978398-37978457	HepG2	liver:	n/a	chr13:37978409-37978425
2	ATF2	chr13:37988805-37989143	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr13:38069316-38069453	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr13:37868854-37868872	GM12878	blood:	n/a	n/a
5	CEBPB	chr13:37992645-37993031	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:37977802-37978307	IMR90	lung:	n/a	n/a
7	CEBPB	chr13:38073811-38074011	HepG2	liver:	n/a	chr13:38073935-38073946
8	CEBPB	chr13:38000250-38000447	A549	lung:	n/a	n/a
9	CEBPB	chr13:37900464-37900804	IMR90	lung:	n/a	n/a
10	CEBPB	chr13:38055361-38055984	IMR90	lung:	n/a	n/a
11	CEBPB	chr13:37971416-37971706	IMR90	lung:	n/a	n/a
12	CEBPB	chr13:37851901-37852268	IMR90	lung:	n/a	n/a
13	CEBPB	chr13:37901963-37902181	HepG2	liver:	n/a	chr13:37902037-37902048
14	CEBPB	chr13:37847012-37847080	H1-hESC	embryonic stem cell:	n/a	chr13:37847026-37847037
15	CEBPB	chr13:38031814-38032120	Hela-S3	cervix:	n/a	chr13:38031952-38031963
16	CEBPB	chr13:38031786-38032118	IMR90	lung:	n/a	chr13:38031952-38031963
17	CEBPB	chr13:38000130-38000400	IMR90	lung:	n/a	n/a
18	CEBPB	chr13:38073908-38073913	K562	blood:	n/a	n/a
19	CEBPB	chr13:38004006-38004558	IMR90	lung:	n/a	n/a
20	CEBPB	chr13:37851627-37852275	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chr13:37831389-37831693	A549	lung:	n/a	chr13:37831531-37831540 chr13:37831529-37831540 chr13:37831529-37831542 chr13:37831530-37831541 chr13:37831531-37831540 chr13:37831529-37831542 chr13:37831531-37831540 chr13:37831531-37831540 chr13:37831529-37831540
22	CEBPB	chr13:37880896-37881440	IMR90	lung:	n/a	n/a
23	CEBPB	chr13:37949870-37950225	IMR90	lung:	n/a	n/a
24	CEBPB	chr13:38000134-38000356	HepG2	liver:	n/a	n/a
25	CEBPB	chr13:37846893-37847199	HepG2	liver:	n/a	chr13:37847026-37847037
26	CEBPB	chr13:37991202-37991508	IMR90	lung:	n/a	n/a
27	CEBPB	chr13:38031822-38032042	A549	lung:	n/a	chr13:38031952-38031963
28	CEBPB	chr13:37986507-37987218	IMR90	lung:	n/a	chr13:37986698-37986711 chr13:37986698-37986709 chr13:37987043-37987056 chr13:37986700-37986709 chr13:37986698-37986711 chr13:37987043-37987056 chr13:37986700-37986709 chr13:37986700-37986709 chr13:37986698-37986711 chr13:37986700-37986709 chr13:37986698-37986709
29	CEBPB	chr13:37971471-37971590	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr13:37831409-37831678	H1-hESC	embryonic stem cell:	n/a	chr13:37831531-37831540 chr13:37831529-37831540 chr13:37831529-37831542 chr13:37831530-37831541 chr13:37831531-37831540 chr13:37831529-37831542 chr13:37831531-37831540 chr13:37831531-37831540 chr13:37831529-37831540
31	CEBPB	chr13:38017814-38018021	HepG2	liver:	n/a	chr13:38017896-38017907 chr13:38017896-38017909
32	CEBPB	chr13:38069178-38069527	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr13:37934830-37935158	IMR90	lung:	n/a	n/a
34	CEBPB	chr13:37879321-37879482	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr13:37851670-37852091	HepG2	liver:	n/a	n/a
36	CEBPB	chr13:37900516-37900790	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr13:37929667-37929768	H1-hESC	embryonic stem cell:	n/a	chr13:37929736-37929745 chr13:37929736-37929745 chr13:37929736-37929745
38	CEBPB	chr13:37831356-37831715	IMR90	lung:	n/a	chr13:37831531-37831540 chr13:37831529-37831540 chr13:37831529-37831542 chr13:37831530-37831541 chr13:37831531-37831540 chr13:37831529-37831542 chr13:37831531-37831540 chr13:37831531-37831540 chr13:37831529-37831540
39	CEBPB	chr13:38017210-38018156	IMR90	lung:	n/a	chr13:38017896-38017907 chr13:38017896-38017909
40	CEBPB	chr13:38073753-38074121	IMR90	lung:	n/a	chr13:38073935-38073946
41	CEBPB	chr13:37831375-37831705	HepG2	liver:	n/a	chr13:37831531-37831540 chr13:37831529-37831540 chr13:37831529-37831542 chr13:37831530-37831541 chr13:37831531-37831540 chr13:37831529-37831542 chr13:37831531-37831540 chr13:37831531-37831540 chr13:37831529-37831540
42	CEBPB	chr13:38066918-38067554	IMR90	lung:	n/a	n/a
43	CHD2	chr13:38047200-38047523	H1-hESC	embryonic stem cell:	n/a	n/a
44	CTCF	chr13:38047308-38047446	MCF-7	breast:	n/a	n/a
45	CTCF	chr13:37879420-37879570	RPTEC	kidney:	n/a	n/a
46	CTCF	chr13:38047240-38047454	K562	blood:	n/a	n/a
47	CTCF	chr13:37844820-37844970	HUVEC	blood vessel:	n/a	n/a
48	CTCF	chr13:37879340-37879490	NHEK	skin:	n/a	n/a
49	CTCF	chr13:37844956-37845047	MCF-7	breast:	n/a	n/a
50	CTCF	chr13:37879340-37879490	SK-N-SH_RA	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:38021368-38021418	PANC-1	pancreas:	n/a
2	chr13:38004268-38004318	NHDF-neo	bronchial:	n/a
3	chr13:38021368-38021418	HNPCEpiC	eye:	n/a
4	chr13:37838311-37838361	BE2_C	brain:	n/a
5	chr13:37992174-37992224	GM12878	blood:	n/a
6	chr13:37881008-37881058	U87	brain:	n/a
7	chr13:37992174-37992224	HRE	kidney:	n/a
8	chr13:38004268-38004318	AG10803	skin:	n/a
9	chr13:38021368-38021418	K562	blood:	n/a
10	chr13:38066983-38067033	ECC-1	luminal epithelium:	n/a
11	chr13:37881008-37881058	A549	lung:	n/a
12	chr13:37961201-37961251	HIPEpiC	eye:	n/a
13	chr13:37961201-37961251	HNPCEpiC	eye:	n/a
14	chr13:37824788-37824838	Caco-2	colon:	n/a
15	chr13:37824788-37824838	PANC-1	pancreas:	n/a
16	chr13:38066983-38067033	NHDF-neo	bronchial:	n/a
17	chr13:37824788-37824838	HCT-116	colon:	n/a
18	chr13:37838311-37838361	HAEpiC	amniotic membrane:	n/a
19	chr13:37881008-37881058	HEK293	kidney:	embryo
20	chr13:37838311-37838361	NB4	blood:	n/a
21	chr13:38004268-38004318	HPAEpiC	pulmonary alveolar:	n/a
22	chr13:37986386-37986436	T-47D	breast:	n/a
23	chr13:38004268-38004318	AG09319	gingival:	n/a
24	chr13:38066983-38067033	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:37961201-37961251	GM19239	blood:	n/a
26	chr13:37986386-37986436	IMR90	lung:	fetal
27	chr13:38066983-38067033	GM12892	blood:	n/a
28	chr13:37961201-37961251	HCT-116	colon:	n/a
29	chr13:38021368-38021418	HIPEpiC	eye:	n/a
30	chr13:37992174-37992224	U87	brain:	n/a
31	chr13:38004268-38004318	HUVEC	blood vessel:	n/a
32	chr13:38066983-38067033	HCPEpiC	choroid plexus:	n/a
33	chr13:38066983-38067033	AoSMC	blood vessel:	n/a
34	chr13:38004268-38004318	Hela-S3	cervix:	n/a
35	chr13:37838311-37838361	ECC-1	luminal epithelium:	n/a
36	chr13:37986386-37986436	HPAEpiC	pulmonary alveolar:	n/a
37	chr13:37986386-37986436	SK-N-MC	brain:	n/a
38	chr13:37824788-37824838	HIPEpiC	eye:	n/a
39	chr13:38066983-38067033	SK-N-MC	brain:	n/a
40	chr13:37838311-37838361	K562	blood:	n/a
41	chr13:37992174-37992224	HAEpiC	amniotic membrane:	n/a
42	chr13:37824788-37824838	HRE	kidney:	n/a
43	chr13:37961201-37961251	GM12878	blood:	n/a
44	chr13:37986386-37986436	GM19239	blood:	n/a
45	chr13:37838311-37838361	HL-60	blood:	n/a
46	chr13:37961201-37961251	AoSMC	blood vessel:	n/a
47	chr13:37838311-37838361	HRE	kidney:	n/a
48	chr13:37961201-37961251	MCF10A-Er-Src	breast:	n/a
49	chr13:37992174-37992224	PrEC	prostate:	n/a
50	chr13:37992174-37992224	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:37846547..37848688-chr13:37852858..37855009,2	MCF-7	breast:
2	chr13:37985346..37987994-chr13:37989139..37991026,2	K562	blood:
3	chr13:37978373..37981171-chr13:37983572..37986304,2	MCF-7	breast:
4	chr13:37911752..37912689-chr17:64378852..64379473,2	MCF-7	breast:
5	chr12:126015648..126016148-chr13:37878876..37879768,2	K562	blood:
6	chr13:37989930..37990641-chr3:175337726..175338710,2	MCF-7	breast:
7	chr13:37985346..37987994-chr13:37989139..37991026,2	K562	blood:
8	chr13:37846547..37848688-chr13:37852858..37855009,2	MCF-7	breast:
9	chr13:37978373..37981171-chr13:37983572..37986304,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-EXOSC8-1	chr13:38064564-38064928	XLOC_010348
2	lnc-EXOSC8-5	chr13:38050866-38051088	l_812_chr13:38039862-38051088_testes
3	lnc-EXOSC8-1	chr13:38052747-38052840	XLOC_010348
4	lnc-POSTN-3	chr13:38017324-38017436	NONHSAT033246
5	lnc-EXOSC8-5	chr13:38050866-38051131	NONHSAT033247
6	lnc-POSTN-1	chr13:38058607-38058682	XLOC_010570
7	lnc-EXOSC8-5	chr13:38049742-38049847	NONHSAT033247
8	lnc-POSTN-3	chr13:38005480-38006157	NONHSAT033246
9	lnc-POSTN-1	chr13:38058842-38058906	XLOC_010570
10	lnc-EXOSC8-5	chr13:38039863-38039932	l_812_chr13:38039862-38051088_testes
11	lnc-EXOSC8-5	chr13:38048777-38048839	NONHSAT033247
12	lnc-EXOSC8-5	chr13:38048795-38048839	l_812_chr13:38039862-38051088_testes
13	lnc-POSTN-1	chr13:38058422-38058530	XLOC_010570
14	lnc-POSTN-1	chr13:38055604-38055864	XLOC_010570

Variant related genes	Relation type
LINC01048	TF binding region
LINC01048	CpG island

Extended variants
information (count: 8189 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:8189 , 50 per page) page: 1 2 3 4 5 6 7 ... 164

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1980733	chr13:37816086-37816087	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs9547757	chr13:37816147-37816148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192954456	chr13:37816172-37816173	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs150531157	chr13:37816174-37816175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9576227	chr13:37816214-37816215	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs577179973	chr13:37816217-37816218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185380219	chr13:37816222-37816223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs1980732	chr13:37816223-37816224	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs567010879	chr13:37816238-37816239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs576193417	chr13:37816279-37816280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs35141258	chr13:37816300-37816301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs188942518	chr13:37816327-37816328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373091288	chr13:37816340-37816341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs561971935	chr13:37816373-37816374	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs376384899	chr13:37816527-37816528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs527974947	chr13:37816550-37816551	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs547815073	chr13:37816558-37816559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs544423345	chr13:37816559-37816560	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs532034237	chr13:37816628-37816629	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs552216984	chr13:37816651-37816652	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs534511220	chr13:37816667-37816668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs568958942	chr13:37816684-37816685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs370241655	chr13:37816687-37816688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs181318421	chr13:37816688-37816689	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555967665	chr13:37816731-37816732	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs548403849	chr13:37816735-37816736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs9547758	chr13:37816768-37816769	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs534053948	chr13:37816795-37816796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183992156	chr13:37816798-37816799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs373370536	chr13:37816801-37816802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs539463935	chr13:37816802-37816803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs556170752	chr13:37816851-37816852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544699786	chr13:37816863-37816864	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188468290	chr13:37816875-37816876	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs542563487	chr13:37816878-37816879	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs541965753	chr13:37816950-37816951	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs561935963	chr13:37816975-37816976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs556421636	chr13:37817053-37817054	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs377722314	chr13:37817109-37817110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs572561109	chr13:37817148-37817149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs541662478	chr13:37817170-37817171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs370732903	chr13:37817217-37817218	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs577965596	chr13:37817276-37817277	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs180850984	chr13:37817345-37817346	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs368050971	chr13:37817382-37817383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs67753482	chr13:37817393-37817394	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs3084235	chr13:37817394-37817395	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs375175077	chr13:37817398-37817399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs60002579	chr13:37817399-37817400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs201007889	chr13:37817400-37817401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:98)

Disease	PMID	Source
Cancer	20164920	CNVD
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
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	18698080	CNVD
Chordoma	21602918	CNVD
Bladder cancer	21949216	CNVD
Acute myeloid leukemia	16864856	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
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	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
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	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	17899364	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Trisomy	24170809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Alveolar rhabdomyosarcoma	16790082	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Prostate cancer	21965145	CNVD
Hirschsprung''s Disease	21712996	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Monoclonal gammopathy of undetermined significance	19135901	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Colorectal cancer	21645411	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Melanoma	18172304	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Urothelial carcinoma	21177765	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Cancer	17440070	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:963 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:37814400-37816800	Weak transcription	Osteobl	bone
2	chr13:37816000-37817800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr13:37817800-37819400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr13:37818200-37819000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr13:37824400-37824800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
6	chr13:37824400-37824800	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
7	chr13:37824400-37824800	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:37824400-37824800	Active TSS	H9 Cell Line	embryonic stem cell
9	chr13:37834200-37834600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
10	chr13:37837200-37837600	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr13:37837600-37845400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
12	chr13:37843200-37843600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr13:37843200-37843600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr13:37843200-37843600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr13:37843200-37843600	Enhancers	NH-A	brain
16	chr13:37843200-37843600	Enhancers	NHDF-Ad	bronchial
17	chr13:37843200-37843800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr13:37843200-37843800	Enhancers	HMEC	breast
19	chr13:37845400-37848200	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr13:37847400-37847800	Enhancers	Fetal Muscle Leg	muscle
21	chr13:37847800-37848200	Weak transcription	Fetal Muscle Leg	muscle
22	chr13:37848200-37848400	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
23	chr13:37848200-37848400	Enhancers	Fetal Muscle Leg	muscle
24	chr13:37848400-37848800	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr13:37848400-37849800	Weak transcription	Fetal Muscle Leg	muscle
26	chr13:37848800-37849200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr13:37849000-37849200	Enhancers	NHDF-Ad	bronchial
28	chr13:37849200-37852000	Enhancers	Breast Myoepithelial Primary Cells	Breast
29	chr13:37849800-37850000	Enhancers	Fetal Muscle Leg	muscle
30	chr13:37849800-37850000	Enhancers	NHDF-Ad	bronchial
31	chr13:37850800-37851200	Enhancers	Colon Smooth Muscle	Colon
32	chr13:37851000-37851800	Enhancers	HMEC	breast
33	chr13:37851200-37851600	Enhancers	Fetal Heart	heart
34	chr13:37851200-37851800	Enhancers	Osteobl	bone
35	chr13:37851200-37852000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr13:37851200-37852200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr13:37851400-37852000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr13:37851800-37852200	Enhancers	NHEK	skin
39	chr13:37852200-37860200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr13:37859000-37859800	Enhancers	Muscle Satellite Cultured Cells	--
41	chr13:37859000-37863400	Enhancers	HUVEC	blood vessel
42	chr13:37860200-37861400	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr13:37861400-37862200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr13:37861400-37877200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr13:37862200-37862400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr13:37862200-37862600	Enhancers	Fetal Muscle Leg	muscle
47	chr13:37862400-37862600	Enhancers	Adipose Nuclei	Adipose
48	chr13:37862400-37863400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr13:37863200-37864200	Enhancers	Brain Substantia Nigra	brain
50	chr13:37863400-37863800	Enhancers	Fetal Heart	heart

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