Variant report

Variant	nsv916039
Chromosome Location	chr13:94035909-94191105
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	chr13:94132841-94133293	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:94157465-94158176	HepG2	liver:	n/a	n/a
3	CEBPB	chr13:94050505-94050875	IMR90	lung:	n/a	chr13:94050685-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050685-94050698 chr13:94050685-94050698 chr13:94050686-94050697
4	CEBPB	chr13:94182280-94182474	A549	lung:	n/a	n/a
5	CEBPB	chr13:94118634-94119078	A549	lung:	n/a	n/a
6	CEBPB	chr13:94157408-94157597	HepG2	liver:	n/a	chr13:94157529-94157540
7	CEBPB	chr13:94128532-94128817	A549	lung:	n/a	n/a
8	CEBPB	chr13:94182244-94182557	HepG2	liver:	n/a	chr13:94182470-94182481 chr13:94182468-94182481 chr13:94182470-94182481
9	CEBPB	chr13:94048905-94049264	A549	lung:	n/a	chr13:94049142-94049153 chr13:94049142-94049155 chr13:94049161-94049172 chr13:94049160-94049173
10	CEBPB	chr13:94075501-94075743	A549	lung:	n/a	chr13:94075661-94075672 chr13:94075661-94075674
11	CEBPB	chr13:94128557-94128780	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:94047276-94047512	A549	lung:	n/a	chr13:94047341-94047352
13	CEBPB	chr13:94182240-94182524	IMR90	lung:	n/a	chr13:94182470-94182481 chr13:94182468-94182481 chr13:94182470-94182481
14	CEBPB	chr13:94128549-94128815	MCF-7	breast:	n/a	n/a
15	CEBPB	chr13:94072192-94072317	A549	lung:	n/a	chr13:94072250-94072263 chr13:94072250-94072263 chr13:94072252-94072263
16	CEBPB	chr13:94048957-94049257	IMR90	lung:	n/a	chr13:94049142-94049153 chr13:94049142-94049155 chr13:94049161-94049172 chr13:94049160-94049173
17	CEBPB	chr13:94075480-94075800	IMR90	lung:	n/a	chr13:94075661-94075672 chr13:94075661-94075674
18	CEBPB	chr13:94118813-94119121	HepG2	liver:	n/a	n/a
19	CEBPB	chr13:94118661-94119148	A549	lung:	n/a	n/a
20	CEBPB	chr13:94152951-94153252	A549	lung:	n/a	chr13:94153092-94153103
21	CEBPB	chr13:94128471-94128896	IMR90	lung:	n/a	chr13:94128868-94128880
22	CEBPB	chr13:94102362-94102869	IMR90	lung:	n/a	chr13:94102474-94102487
23	CEBPB	chr13:94152950-94153307	MCF-7	breast:	n/a	chr13:94153092-94153103
24	CEBPB	chr13:94050523-94050763	HepG2	liver:	n/a	chr13:94050685-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050687-94050696 chr13:94050685-94050698 chr13:94050685-94050698 chr13:94050686-94050697
25	CEBPB	chr13:94049002-94049202	HepG2	liver:	n/a	chr13:94049142-94049153 chr13:94049142-94049155 chr13:94049161-94049172 chr13:94049160-94049173
26	CEBPB	chr13:94132866-94133216	HepG2	liver:	n/a	chr13:94133040-94133051
27	CEBPB	chr13:94100438-94100616	IMR90	lung:	n/a	n/a
28	CEBPB	chr13:94128467-94128903	A549	lung:	n/a	chr13:94128868-94128880
29	CEBPB	chr13:94183711-94183877	H1-hESC	embryonic stem cell:	n/a	n/a
30	CEBPB	chr13:94047341-94047401	HepG2	liver:	n/a	chr13:94047341-94047352
31	CEBPB	chr13:94075512-94075720	HepG2	liver:	n/a	chr13:94075661-94075672 chr13:94075661-94075674
32	CEBPB	chr13:94152998-94153238	IMR90	lung:	n/a	chr13:94153092-94153103
33	CEBPB	chr13:94066559-94066863	IMR90	lung:	n/a	n/a
34	CEBPB	chr13:94187588-94187874	IMR90	lung:	n/a	n/a
35	CEBPB	chr13:94159632-94159836	HepG2	liver:	n/a	chr13:94159710-94159721
36	CEBPB	chr13:94157361-94157716	HepG2	liver:	n/a	chr13:94157529-94157540
37	CEBPB	chr13:94188430-94188653	HepG2	liver:	n/a	chr13:94188557-94188568
38	CTCF	chr13:94170800-94170950	HRPEpiC	eye:	n/a	chr13:94170875-94170893
39	CTCF	chr13:94063400-94063550	GM12869	blood:	n/a	chr13:94063493-94063501
40	CTCF	chr13:94084180-94084330	BE2_C	brain:	n/a	chr13:94084292-94084310 chr13:94084294-94084315
41	CTCF	chr13:94149200-94149350	BE2_C	brain:	n/a	n/a
42	CTCF	chr13:94120112-94120196	GM10248	blood:	n/a	n/a
43	CTCF	chr13:94163780-94163930	AG04450	lung:	n/a	n/a
44	CTCF	chr13:94158200-94158350	HepG2	liver:	n/a	n/a
45	CTCF	chr13:94163046-94163135	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chr13:94170830-94170949	Medullo	brain:	n/a	chr13:94170875-94170893
47	CTCF	chr13:94114420-94114570	HCPEpiC	choroid plexus:	n/a	n/a
48	CTCF	chr13:94084231-94084353	Medullo	brain:	n/a	chr13:94084292-94084310 chr13:94084294-94084315
49	CTCF	chr13:94125920-94126070	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr13:94085380-94085530	BE2_C	brain:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:94152384-94152434	HL-60	blood:	n/a
2	chr13:94152384-94152434	HL-60	blood:	n/a
3	chr13:94107224-94107274	SK-N-SH	brain:	n/a
4	chr13:94075842-94075892	PFSK-1	brain:	n/a
5	chr13:94176949-94176999	SK-N-SH	brain:	n/a
6	chr13:94126074-94126124	NHBE	bronchial:	n/a
7	chr13:94051470-94051520	HEEpiC	esophagus:	n/a
8	chr13:94176949-94176999	T-47D	breast:	n/a
9	chr13:94107224-94107274	Jurkat	blood:	n/a
10	chr13:94051470-94051520	HMEC	breast:	n/a
11	chr13:94126074-94126124	SK-N-SH	brain:	n/a
12	chr13:94075842-94075892	GM12878	blood:	n/a
13	chr13:94161642-94161692	SAEC	small airway:	n/a
14	chr13:94176949-94176999	HNPCEpiC	eye:	n/a
15	chr13:94075842-94075892	AoSMC	blood vessel:	n/a
16	chr13:94149273-94149323	PrEC	prostate:	n/a
17	chr13:94075842-94075892	PrEC	prostate:	n/a
18	chr13:94176949-94176999	PFSK-1	brain:	n/a
19	chr13:94107224-94107274	PFSK-1	brain:	n/a
20	chr13:94075842-94075892	NHDF-neo	bronchial:	n/a
21	chr13:94051470-94051520	SAEC	small airway:	n/a
22	chr13:94161642-94161692	GM12891	blood:	n/a
23	chr13:94152384-94152434	HIPEpiC	eye:	n/a
24	chr13:94051470-94051520	ovcar-3	ovarian:	n/a
25	chr13:94075842-94075892	HRE	kidney:	n/a
26	chr13:94176949-94176999	HMEC	breast:	n/a
27	chr13:94149273-94149323	T-47D	breast:	n/a
28	chr13:94126074-94126124	NB4	blood:	n/a
29	chr13:94161642-94161692	HPAEpiC	pulmonary alveolar:	n/a
30	chr13:94126074-94126124	Caco-2	colon:	n/a
31	chr13:94176949-94176999	HPAEpiC	pulmonary alveolar:	n/a
32	chr13:94176949-94176999	HRE	kidney:	n/a
33	chr13:94051470-94051520	Caco-2	colon:	n/a
34	chr13:94152384-94152434	HUVEC	blood vessel:	n/a
35	chr13:94152384-94152434	HRE	kidney:	n/a
36	chr13:94126074-94126124	GM12891	blood:	n/a
37	chr13:94161642-94161692	AG04450	lung:	fetal
38	chr13:94161642-94161692	Hela-S3	cervix:	n/a
39	chr13:94161642-94161692	NT2-D1	testis:	n/a
40	chr13:94176949-94176999	ovcar-3	ovarian:	n/a
41	chr13:94149273-94149323	NH-A	brain:	n/a
42	chr13:94107224-94107274	HEK293	kidney:	embryo
43	chr13:94152384-94152434	GM12878	blood:	n/a
44	chr13:94075842-94075892	Jurkat	blood:	n/a
45	chr13:94152384-94152434	AG04449	skin:	fetal
46	chr13:94152384-94152434	Jurkat	blood:	n/a
47	chr13:94149273-94149323	NHBE	bronchial:	n/a
48	chr13:94051470-94051520	HIPEpiC	eye:	n/a
49	chr13:94152384-94152434	CMK	blood:	n/a
50	chr13:94107224-94107274	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:94115203..94116046-chr5:54736109..54737038,2	MCF-7	breast:
2	chr13:94173270..94175976-chr13:94179967..94182735,2	MCF-7	breast:
3	chr13:94151315..94153018-chr13:94160965..94162525,2	MCF-7	breast:
4	chr13:94151315..94153018-chr13:94160965..94162525,2	MCF-7	breast:
5	chr13:94130713..94132921-chr13:94134439..94135999,2	K562	blood:
6	chr13:94130713..94132921-chr13:94134439..94135999,2	K562	blood:
7	chr13:94173270..94175976-chr13:94179967..94182735,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCT-15	chr13:94149949-94150144	NONHSAT034712
2	lnc-GPC5-6	chr13:94163893-94166198	ucscGeneNc_uc001vmb_1
3	lnc-GPC5-6	chr13:94162971-94163648	ucscGeneNc_uc001vmb_1
4	lnc-DCT-15	chr13:94150943-94150992	NONHSAT034712
5	lnc-DCT-15	chr13:94151520-94153117	NONHSAT034712

Variant related genes	Relation type
HNRNPA1P29	TF binding region
HNRNPA1P29	CpG island

Extended variants
information (count: 5575 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:5575 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553551008	chr13:94035961-94035962	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs566923866	chr13:94035983-94035984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs11326667	chr13:94035986-94035987	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201593680	chr13:94035999-94036000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs534820545	chr13:94036014-94036015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186239571	chr13:94036038-94036039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs16948746	chr13:94036056-94036057	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs191495105	chr13:94036083-94036084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs373734281	chr13:94036126-94036127	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs4773743	chr13:94036176-94036177	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs372387787	chr13:94036187-94036188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs377074814	chr13:94036190-94036191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs376694467	chr13:94036230-94036231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs2813611	chr13:94036251-94036252	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs573619056	chr13:94036265-94036266	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs542216317	chr13:94036271-94036272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs559028504	chr13:94036311-94036312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372387532	chr13:94036362-94036363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2762122	chr13:94036398-94036399	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs137894474	chr13:94036426-94036427	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs530991737	chr13:94036447-94036448	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs551292640	chr13:94036473-94036474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567859591	chr13:94036513-94036514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs528121562	chr13:94036524-94036525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs117897870	chr13:94036602-94036603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs10640733	chr13:94036637-94036638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs34837574	chr13:94036638-94036639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs140503970	chr13:94036648-94036649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs184238947	chr13:94036649-94036650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs56183083	chr13:94036650-94036651	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9589725	chr13:94036652-94036653	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs561955171	chr13:94036659-94036660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539105438	chr13:94036694-94036695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs188740649	chr13:94036735-94036736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571451686	chr13:94036740-94036741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs536840864	chr13:94036753-94036754	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs557272523	chr13:94036829-94036830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs386773441	chr13:94036830-94036831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138559860	chr13:94036831-94036832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149310093	chr13:94036842-94036843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs144729309	chr13:94036847-94036848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs546606037	chr13:94036892-94036893	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs74765366	chr13:94036941-94036942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs191072019	chr13:94036994-94036995	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs547793813	chr13:94037012-94037013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs571199733	chr13:94037036-94037037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551069540	chr13:94037064-94037065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564813440	chr13:94037066-94037067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575835365	chr13:94037094-94037095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs148543721	chr13:94037125-94037126	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:681 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:94008800-94042400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr13:94009400-94040400	Weak transcription	Aorta	Aorta
3	chr13:94014200-94038800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:94030800-94038600	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr13:94036800-94037600	Weak transcription	Fetal Intestine Small	intestine
6	chr13:94038600-94039400	Enhancers	HUES48 Cell Line	embryonic stem cell
7	chr13:94038800-94039200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:94039200-94040800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr13:94039400-94042200	Weak transcription	HUES48 Cell Line	embryonic stem cell
10	chr13:94040400-94040800	Enhancers	Aorta	Aorta
11	chr13:94040800-94041400	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:94041200-94041600	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr13:94041400-94047000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:94042200-94043400	Enhancers	HUES48 Cell Line	embryonic stem cell
15	chr13:94042400-94042600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
16	chr13:94042400-94043400	Enhancers	iPS-18 Cell Line	embryonic stem cell
17	chr13:94044400-94045000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr13:94046600-94052400	Weak transcription	Fetal Brain Male	brain
19	chr13:94047000-94047800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:94047800-94057200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:94049600-94050200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
22	chr13:94049600-94051400	Enhancers	Osteobl	bone
23	chr13:94049800-94050600	Enhancers	Fetal Lung	lung
24	chr13:94049800-94050800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr13:94050000-94050200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr13:94050000-94050800	Enhancers	Fetal Stomach	stomach
27	chr13:94050000-94051000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr13:94050200-94050600	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chr13:94050200-94050800	Enhancers	Colon Smooth Muscle	Colon
30	chr13:94050200-94050800	Enhancers	HSMM	muscle
31	chr13:94050200-94051000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
32	chr13:94050200-94051000	Enhancers	Muscle Satellite Cultured Cells	--
33	chr13:94050200-94051000	Enhancers	Fetal Heart	heart
34	chr13:94050200-94051800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr13:94050600-94050800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:94050600-94050800	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr13:94050600-94051400	Enhancers	Adipose Nuclei	Adipose
38	chr13:94050600-94051600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr13:94050600-94052000	Enhancers	A549	lung
40	chr13:94050800-94051600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
41	chr13:94050800-94053000	Weak transcription	HUES48 Cell Line	embryonic stem cell
42	chr13:94051200-94051600	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chr13:94051200-94052200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr13:94051200-94052200	Enhancers	HepG2	liver
45	chr13:94051400-94051600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr13:94051600-94051800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr13:94051600-94052200	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr13:94051600-94055600	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr13:94052400-94052600	Enhancers	Fetal Brain Male	brain
50	chr13:94052600-94053000	Weak transcription	Fetal Brain Male	brain

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