Variant report

Variant	nsv900092
Chromosome Location	chr13:54362624-54419426
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	chr13:54376269-54376545	HepG2	liver:	n/a	chr13:54376521-54376534 chr13:54376318-54376331
2	CEBPB	chr13:54404485-54404673	HepG2	liver:	n/a	chr13:54404618-54404629
3	CTCF	chr13:54372380-54372530	AG10803	skin:	n/a	n/a
4	CTCF	chr13:54362480-54362630	NHDF-neo	bronchial:	n/a	n/a
5	E2F4	chr13:54407306-54407506	MCF10A-Er-Src	breast:	n/a	n/a
6	E2F4	chr13:54380624-54380814	MCF10A-Er-Src	breast:	n/a	n/a
7	E2F4	chr13:54408713-54408913	MCF10A-Er-Src	breast:	n/a	n/a
8	EP300	chr13:54395604-54396376	T-47D	breast:	n/a	chr13:54395651-54395665 chr13:54395851-54395861 chr13:54395655-54395664
9	ESR1	chr13:54395738-54395970	T-47D	breast:	n/a	n/a
10	ESR1	chr13:54374054-54374610	T-47D	breast:	n/a	n/a
11	ESR1	chr13:54374069-54374615	T-47D	breast:	n/a	n/a
12	ESR1	chr13:54374018-54374677	T-47D	breast:	n/a	n/a
13	ESR1	chr13:54374055-54374660	T-47D	breast:	n/a	n/a
14	ESR1	chr13:54374061-54374618	T-47D	breast:	n/a	n/a
15	ESR1	chr13:54374014-54374655	T-47D	breast:	n/a	n/a
16	FAM48A	chr13:54381574-54381731	GM12878	blood:	n/a	n/a
17	FAM48A	chr13:54365348-54365548	GM12878	blood:	n/a	n/a
18	FOS	chr13:54406435-54406677	MCF10A-Er-Src	breast:	n/a	n/a
19	FOS	chr13:54406439-54406570	MCF10A-Er-Src	breast:	n/a	n/a
20	FOS	chr13:54419030-54419132	MCF10A-Er-Src	breast:	n/a	chr13:54419100-54419112 chr13:54419102-54419110
21	FOS	chr13:54406410-54406712	MCF10A-Er-Src	breast:	n/a	n/a
22	FOS	chr13:54400913-54401166	MCF10A-Er-Src	breast:	n/a	chr13:54401096-54401105 chr13:54401096-54401104 chr13:54401097-54401104
23	FOS	chr13:54419078-54419230	MCF10A-Er-Src	breast:	n/a	chr13:54419100-54419112 chr13:54419200-54419209 chr13:54419102-54419110
24	FOXA1	chr13:54362281-54362764	T-47D	breast:	n/a	n/a
25	FOXA1	chr13:54395678-54396069	T-47D	breast:	n/a	n/a
26	FOXA1	chr13:54396204-54396547	T-47D	breast:	n/a	n/a
27	FOXA1	chr13:54395660-54396140	T-47D	breast:	n/a	n/a
28	FOXA1	chr13:54374104-54374524	T-47D	breast:	n/a	n/a
29	FOXA1	chr13:54362388-54362672	T-47D	breast:	n/a	n/a
30	FOXP2	chr13:54362404-54362743	SK-N-MC	brain:	n/a	n/a
31	GATA3	chr13:54362473-54362790	T-47D	breast:	n/a	n/a
32	GATA3	chr13:54388352-54388617	T-47D	breast:	n/a	n/a
33	GATA3	chr13:54395763-54396039	T-47D	breast:	n/a	n/a
34	GATA3	chr13:54390049-54390416	T-47D	breast:	n/a	n/a
35	GATA3	chr13:54398289-54398468	SH-SY5Y	brain:	n/a	n/a
36	GATA3	chr13:54395678-54396602	T-47D	breast:	n/a	n/a
37	GATA3	chr13:54396064-54396556	T-47D	breast:	n/a	n/a
38	GATA3	chr13:54374256-54374569	T-47D	breast:	n/a	chr13:54374295-54374302 chr13:54374265-54374278
39	GATA3	chr13:54374081-54374551	T-47D	breast:	n/a	chr13:54374295-54374302 chr13:54374265-54374278
40	JUND	chr13:54401041-54401166	HepG2	liver:	n/a	chr13:54401096-54401105 chr13:54401096-54401104 chr13:54401094-54401105 chr13:54401097-54401104
41	JUND	chr13:54374161-54374581	T-47D	breast:	n/a	n/a
42	MAFF	chr13:54366521-54366672	HepG2	liver:	n/a	n/a
43	MAFF	chr13:54418965-54419147	K562	blood:	n/a	chr13:54419093-54419111
44	MAFF	chr13:54418923-54419256	HepG2	liver:	n/a	chr13:54419093-54419111
45	MAFF	chr13:54371411-54371712	HepG2	liver:	n/a	chr13:54371572-54371590
46	MAFK	chr13:54418925-54419260	IMR90	lung:	n/a	chr13:54419100-54419109 chr13:54419100-54419110 chr13:54419095-54419110
47	MAFK	chr13:54418967-54419135	K562	blood:	n/a	chr13:54419100-54419109 chr13:54419100-54419110 chr13:54419095-54419110
48	MAFK	chr13:54371411-54371735	IMR90	lung:	n/a	chr13:54371574-54371589
49	MAFK	chr13:54367418-54367426	H1-hESC	embryonic stem cell:	n/a	n/a
50	MAFK	chr13:54370035-54370197	HepG2	liver:	n/a	chr13:54370096-54370112 chr13:54370100-54370111 chr13:54370099-54370113

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:54362844-54362894	U87	brain:	n/a
2	chr13:54362844-54362894	U87	brain:	n/a
3	chr13:54362844-54362894	HAEpiC	amniotic membrane:	n/a
4	chr13:54362844-54362894	HUVEC	blood vessel:	n/a
5	chr13:54362844-54362894	K562	blood:	n/a
6	chr13:54362844-54362894	ProgFib	skin:	n/a
7	chr13:54362844-54362894	SK-N-SH_RA	brain:	n/a
8	chr13:54362844-54362894	NHBE	bronchial:	n/a
9	chr13:54362844-54362894	HPAEpiC	pulmonary alveolar:	n/a
10	chr13:54362844-54362894	GM12878	blood:	n/a
11	chr13:54362844-54362894	HCT-116	colon:	n/a
12	chr13:54362844-54362894	NT2-D1	testis:	n/a
13	chr13:54362844-54362894	NB4	blood:	n/a
14	chr13:54362844-54362894	NH-A	brain:	n/a
15	chr13:54362844-54362894	HCM	heart:	n/a
16	chr13:54362844-54362894	HL-60	blood:	n/a
17	chr13:54362844-54362894	GM12892	blood:	n/a
18	chr13:54362844-54362894	ovcar-3	ovarian:	n/a
19	chr13:54362844-54362894	HEEpiC	esophagus:	n/a
20	chr13:54362844-54362894	A549	lung:	n/a
21	chr13:54362844-54362894	PFSK-1	brain:	n/a
22	chr13:54362844-54362894	CMK	blood:	n/a
23	chr13:54362844-54362894	AG04449	skin:	fetal
24	chr13:54362844-54362894	HepG2	liver:	n/a
25	chr13:54362844-54362894	LNCaP	prostate:	n/a
26	chr13:54362844-54362894	BJ	skin:	n/a
27	chr13:54362844-54362894	HRPEpiC	eye:	n/a
28	chr13:54362844-54362894	AG04450	lung:	fetal
29	chr13:54362844-54362894	H1-hESC	embryonic stem cell:	embryo
30	chr13:54362844-54362894	PANC-1	pancreas:	n/a
31	chr13:54362844-54362894	BE2_C	brain:	n/a
32	chr13:54362844-54362894	SAEC	small airway:	n/a
33	chr13:54362844-54362894	T-47D	breast:	n/a
34	chr13:54362844-54362894	MCF10A-Er-Src	breast:	n/a
35	chr13:54362844-54362894	GM19239	blood:	n/a
36	chr13:54362844-54362894	AG10803	skin:	n/a
37	chr13:54362844-54362894	HRCEpiC	kidney:	n/a
38	chr13:54362844-54362894	Hepatocyte	liver:	n/a
39	chr13:54362844-54362894	Jurkat	blood:	n/a
40	chr13:54362844-54362894	HCPEpiC	choroid plexus:	n/a
41	chr13:54362844-54362894	MCF-7	breast:	n/a
42	chr13:54362844-54362894	ECC-1	luminal epithelium:	n/a
43	chr13:54362844-54362894	HCF	heart:	n/a
44	chr13:54362844-54362894	IMR90	lung:	fetal
45	chr13:54362844-54362894	HNPCEpiC	eye:	n/a
46	chr13:54362844-54362894	HEK293	kidney:	embryo
47	chr13:54362844-54362894	HMEC	breast:	n/a
48	chr13:54362844-54362894	SK-N-MC	brain:	n/a
49	chr13:54362844-54362894	AG09309	skin:	n/a
50	chr13:54362844-54362894	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:54411879..54413790-chr13:54440349..54442010,2	K562	blood:
2	chr13:54359558..54362515-chr13:54378341..54380305,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-3	chr13:54389554-54389628	ENSG00000261517.1
2	lnc-OLFM4-3	chr13:54418480-54418657	ENSG00000261517.1
3	lnc-OLFM4-3	chr13:54412874-54412924	ENSG00000261517.1
4	lnc-OLFM4-3	chr13:54414818-54414945	ENSG00000261517.1

Variant related genes	Relation type
LINC00558	TF binding region
LINC00558	CpG island

Extended variants
information (count: 436 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:436 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9568925	chr13:54362624-54362625	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs139372714	chr13:54362684-54362685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs546936099	chr13:54362726-54362727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs541486163	chr13:54362747-54362748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs189612612	chr13:54362784-54362785	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs529083198	chr13:54362804-54362805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs549238119	chr13:54362806-54362807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs370085187	chr13:54362820-54362821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs111256387	chr13:54362829-54362830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs372281510	chr13:54362844-54362845	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537950069	chr13:54362934-54362935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs183342557	chr13:54362948-54362949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs28757859	chr13:54362972-54362973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs571238279	chr13:54362985-54362986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs9568926	chr13:54363002-54363003	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554024593	chr13:54363022-54363023	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs574030365	chr13:54363049-54363050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs536442029	chr13:54363054-54363055	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs556766524	chr13:54363071-54363072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs143282051	chr13:54363077-54363078	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs545497409	chr13:54363082-54363083	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537754224	chr13:54363120-54363121	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187830769	chr13:54363136-54363137	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572447670	chr13:54363248-54363249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs562136959	chr13:54363255-54363256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541471234	chr13:54363339-54363340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs560463027	chr13:54363341-54363342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs529251683	chr13:54363387-54363388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs564827178	chr13:54377601-54377602	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs188429882	chr13:54377606-54377607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs193027417	chr13:54377635-54377636	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs185562897	chr13:54377663-54377664	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs9591536	chr13:54377682-54377683	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs114648601	chr13:54377816-54377817	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs151024974	chr13:54377841-54377842	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141098862	chr13:54377864-54377865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570168130	chr13:54377894-54377895	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs117606388	chr13:54377895-54377896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190623019	chr13:54377958-54377959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs567466640	chr13:54377965-54377966	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs969498	chr13:54377966-54377967	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs368054042	chr13:54377998-54377999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs530770795	chr13:54380606-54380607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs550562986	chr13:54380630-54380631	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs9563181	chr13:54380670-54380671	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs532473382	chr13:54380686-54380687	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs117994986	chr13:54380755-54380756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565843305	chr13:54380762-54380763	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs534533602	chr13:54380779-54380780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs183040252	chr13:54380793-54380794	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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
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
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	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
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	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
Urothelial carcinoma	21177765	CNVD
Schizophrenia	20967226	CNVD
Schizophrenia	23813976	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:47 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:54361400-54363000	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr13:54361400-54363400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:54361400-54363400	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr13:54361600-54363200	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr13:54361600-54363200	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr13:54362000-54363400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr13:54362200-54363000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:54362200-54363000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
9	chr13:54362200-54363000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr13:54362200-54363000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
11	chr13:54362200-54363400	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr13:54362400-54363000	Enhancers	H1 Cell Line	embryonic stem cell
13	chr13:54377600-54378000	Enhancers	HUES48 Cell Line	embryonic stem cell
14	chr13:54380600-54381600	Enhancers	Fetal Heart	heart
15	chr13:54380800-54381200	Enhancers	Fetal Lung	lung
16	chr13:54381200-54381600	Weak transcription	Fetal Lung	lung
17	chr13:54381600-54382000	Flanking Active TSS	Fetal Heart	heart
18	chr13:54381600-54382600	Enhancers	Fetal Lung	lung
19	chr13:54382000-54382600	Enhancers	Fetal Heart	heart
20	chr13:54390600-54390800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:54390800-54391000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr13:54391000-54391200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:54391200-54391600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:54391600-54396400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr13:54395000-54396000	Enhancers	Fetal Heart	heart
26	chr13:54395200-54396600	Enhancers	Fetal Brain Male	brain
27	chr13:54395400-54395800	Enhancers	Brain Substantia Nigra	brain
28	chr13:54395400-54396600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
29	chr13:54395600-54396200	Active TSS	Stomach Smooth Muscle	stomach
30	chr13:54395600-54396400	Enhancers	Breast Myoepithelial Primary Cells	Breast
31	chr13:54395800-54396000	Active TSS	Brain Substantia Nigra	brain
32	chr13:54395800-54396400	Active TSS	Brain Angular Gyrus	brain
33	chr13:54395800-54396400	Active TSS	Brain Anterior Caudate	brain
34	chr13:54395800-54396400	Active TSS	Brain Hippocampus Middle	brain
35	chr13:54395800-54396400	Active TSS	Brain Inferior Temporal Lobe	brain
36	chr13:54395800-54396600	Active TSS	Brain Cingulate Gyrus	brain
37	chr13:54395800-54396600	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr13:54396000-54396400	Bivalent/Poised TSS	Brain Substantia Nigra	brain
39	chr13:54396000-54396400	Flanking Active TSS	Fetal Heart	heart
40	chr13:54396400-54396600	Flanking Active TSS	Brain Angular Gyrus	brain
41	chr13:54396400-54397200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr13:54396400-54397200	Enhancers	Fetal Heart	heart
43	chr13:54396800-54397000	Bivalent Enhancer	Brain Substantia Nigra	brain
44	chr13:54397200-54398200	Weak transcription	Fetal Heart	heart
45	chr13:54398200-54398400	Enhancers	Fetal Heart	heart
46	chr13:54405400-54405800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr13:54405400-54405800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived

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