Variant report

Variant	nsv900793
Chromosome Location	chr13:88711960-88871759
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	CEBPB	chr13:88727050-88727357	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chr13:88727036-88727372	A549	lung:	n/a	n/a
3	CEBPB	chr13:88762183-88762523	HepG2	liver:	n/a	chr13:88762352-88762363
4	CEBPB	chr13:88863340-88863614	A549	lung:	n/a	chr13:88863466-88863477 chr13:88863464-88863477 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863464-88863475 chr13:88863466-88863475
5	CEBPB	chr13:88727043-88727561	IMR90	lung:	n/a	chr13:88727502-88727515
6	CEBPB	chr13:88727076-88727400	HepG2	liver:	n/a	n/a
7	CEBPB	chr13:88767434-88767754	IMR90	lung:	n/a	chr13:88767584-88767593 chr13:88767583-88767594 chr13:88767582-88767595 chr13:88767584-88767593 chr13:88767582-88767595 chr13:88767584-88767593 chr13:88767584-88767593 chr13:88767582-88767593
8	CEBPB	chr13:88767433-88767752	HepG2	liver:	n/a	chr13:88767584-88767593 chr13:88767583-88767594 chr13:88767582-88767595 chr13:88767584-88767593 chr13:88767582-88767595 chr13:88767584-88767593 chr13:88767584-88767593 chr13:88767582-88767593
9	CEBPB	chr13:88835698-88836071	IMR90	lung:	n/a	chr13:88835878-88835889
10	CEBPB	chr13:88835716-88836061	HepG2	liver:	n/a	chr13:88835878-88835889
11	CEBPB	chr13:88738895-88739283	IMR90	lung:	n/a	n/a
12	CEBPB	chr13:88762241-88762489	H1-hESC	embryonic stem cell:	n/a	chr13:88762352-88762363
13	CEBPB	chr13:88762182-88762525	IMR90	lung:	n/a	chr13:88762352-88762363
14	CEBPB	chr13:88767478-88767700	ECC-1	luminal epithelium:	n/a	chr13:88767584-88767593 chr13:88767583-88767594 chr13:88767582-88767595 chr13:88767584-88767593 chr13:88767582-88767595 chr13:88767584-88767593 chr13:88767584-88767593 chr13:88767582-88767593
15	CEBPB	chr13:88776105-88776217	HepG2	liver:	n/a	chr13:88776141-88776152
16	CEBPB	chr13:88835729-88836054	ECC-1	luminal epithelium:	n/a	chr13:88835878-88835889
17	CEBPB	chr13:88863398-88863506	H1-hESC	embryonic stem cell:	n/a	chr13:88863466-88863477 chr13:88863464-88863477 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863464-88863475 chr13:88863466-88863475
18	CEBPB	chr13:88863332-88863622	HepG2	liver:	n/a	chr13:88863466-88863477 chr13:88863464-88863477 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863466-88863475 chr13:88863464-88863475 chr13:88863466-88863475
19	CEBPB	chr13:88727025-88727639	Hela-S3	cervix:	n/a	chr13:88727502-88727515
20	CEBPB	chr13:88870153-88870512	Hela-S3	cervix:	n/a	chr13:88870385-88870397 chr13:88870291-88870304 chr13:88870291-88870302 chr13:88870291-88870302 chr13:88870291-88870304
21	CEBPB	chr13:88762210-88762467	A549	lung:	n/a	chr13:88762352-88762363
22	CEBPB	chr13:88862412-88862495	H1-hESC	embryonic stem cell:	n/a	n/a
23	CEBPB	chr13:88835715-88836040	A549	lung:	n/a	chr13:88835878-88835889
24	CEBPB	chr13:88835735-88836046	Hela-S3	cervix:	n/a	chr13:88835878-88835889
25	CEBPB	chr13:88835698-88836053	H1-hESC	embryonic stem cell:	n/a	chr13:88835878-88835889
26	CTCF	chr13:88848517-88848575	LNCaP	prostate:	n/a	n/a
27	CTCF	chr13:88796960-88797110	MCF-7	breast:	n/a	n/a
28	CTCF	chr13:88721341-88721529	MCF-7	breast:	n/a	n/a
29	CTCF	chr13:88721258-88721610	H1-hESC	embryonic stem cell:	n/a	n/a
30	CTCF	chr13:88721297-88721492	T-47D	breast:	n/a	n/a
31	CTCF	chr13:88797020-88797170	BE2_C	brain:	n/a	n/a
32	CTCF	chr13:88848440-88848590	HCT-116	colon:	n/a	n/a
33	CTCF	chr13:88721269-88721542	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTCF	chr13:88796942-88797174	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr13:88848477-88848609	Gliobla	brain:	n/a	n/a
36	CTCF	chr13:88721328-88721477	LNCaP	prostate:	n/a	n/a
37	CTCF	chr13:88838293-88838314	GM13976	blood:	n/a	n/a
38	CTCF	chr13:88721407-88721443	GM12878	blood:	n/a	n/a
39	CTCF	chr13:88721357-88721496	NHEK	skin:	n/a	n/a
40	CTCF	chr13:88721220-88721370	A549	lung:	n/a	n/a
41	CTCF	chr13:88721331-88721521	HepG2	liver:	n/a	n/a
42	CTCF	chr13:88799060-88799210	NHLF	lung:	n/a	n/a
43	CTCF	chr13:88721300-88721450	HCT-116	colon:	n/a	n/a
44	CTCF	chr13:88784712-88784735	GM10248	blood:	n/a	n/a
45	CTCF	chr13:88838322-88838326	GM13976	blood:	n/a	n/a
46	CTCF	chr13:88848512-88848580	GM19238	blood:	n/a	n/a
47	CTCF	chr13:88797019-88797061	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chr13:88796900-88797050	BE2_C	brain:	n/a	n/a
49	CTCF	chr13:88721340-88721490	GM12878	blood:	n/a	n/a
50	CTCF	chr13:88848440-88848590	HEK293	kidney:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:88788898-88788948	SKMC	muscle:	n/a
2	chr13:88788898-88788948	H1-hESC	embryonic stem cell:	embryo
3	chr13:88788898-88788948	GM12891	blood:	n/a
4	chr13:88788987-88789037	IMR90	lung:	fetal
5	chr13:88788898-88788948	PrEC	prostate:	n/a
6	chr13:88788987-88789037	HAEpiC	amniotic membrane:	n/a
7	chr13:88788898-88788948	NH-A	brain:	n/a
8	chr13:88788987-88789037	SK-N-MC	brain:	n/a
9	chr13:88788898-88788948	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:88788987-88789037	GM19239	blood:	n/a
11	chr13:88788987-88789037	HIPEpiC	eye:	n/a
12	chr13:88788987-88789037	A549	lung:	n/a
13	chr13:88788987-88789037	NHBE	bronchial:	n/a
14	chr13:88788898-88788948	HEK293	kidney:	embryo
15	chr13:88788898-88788948	HRPEpiC	eye:	n/a
16	chr13:88788987-88789037	SAEC	small airway:	n/a
17	chr13:88788898-88788948	HepG2	liver:	n/a
18	chr13:88788987-88789037	K562	blood:	n/a
19	chr13:88788987-88789037	NT2-D1	testis:	n/a
20	chr13:88788898-88788948	SK-N-SH	brain:	n/a
21	chr13:88788987-88789037	T-47D	breast:	n/a
22	chr13:88788987-88789037	ECC-1	luminal epithelium:	n/a
23	chr13:88788898-88788948	RPTEC	kidney:	n/a
24	chr13:88788987-88789037	HRE	kidney:	n/a
25	chr13:88788987-88789037	MCF-7	breast:	n/a
26	chr13:88788987-88789037	PANC-1	pancreas:	n/a
27	chr13:88788987-88789037	HNPCEpiC	eye:	n/a
28	chr13:88788898-88788948	HNPCEpiC	eye:	n/a
29	chr13:88788898-88788948	NHDF-neo	bronchial:	n/a
30	chr13:88788987-88789037	PrEC	prostate:	n/a
31	chr13:88788987-88789037	NB4	blood:	n/a
32	chr13:88788987-88789037	GM06990	blood:	n/a
33	chr13:88788898-88788948	HCM	heart:	n/a
34	chr13:88788898-88788948	AoSMC	blood vessel:	n/a
35	chr13:88788898-88788948	HCT-116	colon:	n/a
36	chr13:88788898-88788948	PANC-1	pancreas:	n/a
37	chr13:88788987-88789037	BJ	skin:	n/a
38	chr13:88788898-88788948	Hela-S3	cervix:	n/a
39	chr13:88788987-88789037	H1-hESC	embryonic stem cell:	embryo
40	chr13:88788898-88788948	GM12892	blood:	n/a
41	chr13:88788898-88788948	K562	blood:	n/a
42	chr13:88788898-88788948	SAEC	small airway:	n/a
43	chr13:88788898-88788948	AG09309	skin:	n/a
44	chr13:88788898-88788948	HEEpiC	esophagus:	n/a
45	chr13:88788898-88788948	SK-N-MC	brain:	n/a
46	chr13:88788898-88788948	GM06990	blood:	n/a
47	chr13:88788987-88789037	HL-60	blood:	n/a
48	chr13:88788898-88788948	HRCEpiC	kidney:	n/a
49	chr13:88788987-88789037	RPTEC	kidney:	n/a
50	chr13:88788987-88789037	HEK293	kidney:	embryo

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-15	chr13:88723458-88723617	NONHSAT034607
2	lnc-SLITRK5-15	chr13:88729922-88730495	NONHSAT034607
3	lnc-SLITRK5-5	chr13:88795122-88795355	ENSG00000231019
4	lnc-SLITRK5-5	chr13:88866524-88866575	ENSG00000231019
5	lnc-SLITRK5-5	chr13:88864596-88864694	ENSG00000231019

Variant related genes	Relation type
ENSG00000223059	TF binding region
ENSG00000231019	TF binding region
ENSG00000223059	CpG island
ENSG00000231019	CpG island

Extended variants
information (count: 1657 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1657 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9519267	chr13:88711960-88711961	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs564917076	chr13:88711982-88711983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs9519269	chr13:88712059-88712060	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs550235984	chr13:88712077-88712078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs571198486	chr13:88712087-88712088	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs192759891	chr13:88712088-88712089	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs74104435	chr13:88712096-88712097	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs548050773	chr13:88712097-88712098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs566337994	chr13:88712160-88712161	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs538493656	chr13:88712177-88712178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184779216	chr13:88712215-88712216	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs74104436	chr13:88712254-88712255	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569649244	chr13:88712290-88712291	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536682623	chr13:88712305-88712306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs112867107	chr13:88712324-88712325	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs573445862	chr13:88712376-88712377	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs9586457	chr13:88712411-88712412	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs374894679	chr13:88712423-88712424	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs552756866	chr13:88712470-88712471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs577488401	chr13:88712525-88712526	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545305564	chr13:88712556-88712557	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs370471888	chr13:88712565-88712566	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189229870	chr13:88712585-88712586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs531712865	chr13:88712614-88712615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs145582633	chr13:88712674-88712675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs74104437	chr13:88712680-88712681	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs150465118	chr13:88712691-88712692	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529416579	chr13:88712706-88712707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs554342824	chr13:88712729-88712730	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs138315623	chr13:88712741-88712742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs566297308	chr13:88712743-88712744	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs369549045	chr13:88712775-88712776	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs533424075	chr13:88712776-88712777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs149631584	chr13:88712784-88712785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12874551	chr13:88712808-88712809	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs12874648	chr13:88712832-88712833	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs373039104	chr13:88712881-88712882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs180710054	chr13:88712893-88712894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs537043777	chr13:88712916-88712917	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs572826815	chr13:88712951-88712952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs555106987	chr13:88712976-88712977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs186451397	chr13:88712995-88712996	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1529361	chr13:88720825-88720826	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs536409351	chr13:88720826-88720827	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs574739209	chr13:88720855-88720856	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs555150494	chr13:88720885-88720886	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs180677968	chr13:88720886-88720887	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs560459992	chr13:88720976-88720977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534520783	chr13:88721010-88721011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs563092794	chr13:88721029-88721030	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:89)

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
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	18496225	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
abnormal development	18461090	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
coloboma	21285886	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:82 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:88711400-88713000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr13:88720800-88721200	Enhancers	HSMM	muscle
3	chr13:88721000-88721400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
4	chr13:88721400-88723800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr13:88723800-88724400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
6	chr13:88726200-88726600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr13:88726600-88727000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
8	chr13:88727000-88727200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
9	chr13:88727200-88727600	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr13:88727200-88727600	Enhancers	Muscle Satellite Cultured Cells	--
11	chr13:88727200-88727600	Enhancers	Adipose Nuclei	Adipose
12	chr13:88727200-88727600	Enhancers	Monocytes-CD14+_RO01746	blood
13	chr13:88727400-88727800	Enhancers	Primary monocytes fromperipheralblood	blood
14	chr13:88727600-88728000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
15	chr13:88737400-88737600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr13:88737400-88737800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr13:88737800-88738800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr13:88737800-88738800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr13:88738200-88739400	Enhancers	Muscle Satellite Cultured Cells	--
20	chr13:88738800-88739200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:88738800-88739200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr13:88749800-88750400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr13:88755200-88756600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr13:88755800-88756000	Enhancers	Aorta	Aorta
25	chr13:88755800-88756800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr13:88756200-88757000	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr13:88756800-88758600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr13:88757000-88761600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
29	chr13:88758600-88758800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
30	chr13:88761600-88762400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr13:88764200-88764400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:88764600-88765000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr13:88764600-88765400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr13:88764600-88765600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:88764800-88765400	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr13:88764800-88765400	Enhancers	Primary hematopoietic stem cells	blood
37	chr13:88765000-88765400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr13:88765600-88766000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr13:88766000-88766400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr13:88768600-88768800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr13:88775400-88775600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
42	chr13:88775400-88775600	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr13:88775600-88776200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
44	chr13:88775600-88777200	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr13:88776200-88776400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr13:88776200-88776600	Active TSS	iPS-20b Cell Line	embryonic stem cell
47	chr13:88776200-88777200	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr13:88776200-88777200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr13:88776400-88777000	Enhancers	H1 Cell Line	embryonic stem cell
50	chr13:88776400-88777000	Enhancers	HUES64 Cell Line	embryonic stem cell

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