Variant report

Variant	nsv1054431
Chromosome Location	chr13:76460431-76885094
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1649)
CpG islands
(count:610)
Chromatin interactive
region (count:21)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:76593602-76593887	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:76579598-76579908	K562	blood:	n/a	n/a
3	ARID3A	chr13:76522818-76522965	K562	blood:	n/a	n/a
4	ARID3A	chr13:76602372-76602523	K562	blood:	n/a	n/a
5	ARID3A	chr13:76537499-76537752	K562	blood:	n/a	n/a
6	ARID3A	chr13:76559284-76559897	K562	blood:	n/a	n/a
7	ARID3A	chr13:76603056-76603834	K562	blood:	n/a	n/a
8	ATF1	chr13:76711905-76712094	K562	blood:	n/a	n/a
9	ATF2	chr13:76534509-76535156	GM12878	blood:	n/a	n/a
10	ATF2	chr13:76560824-76561287	GM12878	blood:	n/a	n/a
11	ATF2	chr13:76534622-76535151	GM12878	blood:	n/a	n/a
12	BACH1	chr13:76463615-76464005	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr13:76463777-76463874	K562	blood:	n/a	n/a
14	BACH1	chr13:76537448-76537842	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr13:76537470-76537809	K562	blood:	n/a	n/a
16	BATF	chr13:76867565-76867840	GM12878	blood:	n/a	chr13:76867692-76867703
17	BATF	chr13:76560991-76561290	GM12878	blood:	n/a	n/a
18	BATF	chr13:76534633-76534979	GM12878	blood:	n/a	n/a
19	BATF	chr13:76867599-76867759	GM12878	blood:	n/a	chr13:76867692-76867703
20	BATF	chr13:76534611-76535247	GM12878	blood:	n/a	n/a
21	BCL11A	chr13:76534599-76535183	GM12878	blood:	n/a	n/a
22	BCL11A	chr13:76534761-76534990	GM12878	blood:	n/a	n/a
23	BCL3	chr13:76583328-76584299	A549	lung:	n/a	n/a
24	BHLHE40	chr13:76591133-76591336	K562	blood:	n/a	n/a
25	BHLHE40	chr13:76570830-76570995	GM12878	blood:	n/a	n/a
26	BHLHE40	chr13:76536089-76536327	K562	blood:	n/a	n/a
27	BHLHE40	chr13:76537516-76537890	K562	blood:	n/a	n/a
28	BHLHE40	chr13:76871542-76871741	HepG2	liver:	n/a	n/a
29	BHLHE40	chr13:76591086-76591286	GM12878	blood:	n/a	n/a
30	BHLHE40	chr13:76579770-76579771	K562	blood:	n/a	n/a
31	BHLHE40	chr13:76559381-76559682	K562	blood:	n/a	n/a
32	BRCA1	chr13:76461975-76461988	GM12878	blood:	n/a	n/a
33	CBX3	chr13:76660872-76661247	K562	blood:	n/a	n/a
34	CBX3	chr13:76590994-76591244	K562	blood:	n/a	n/a
35	CBX3	chr13:76559263-76559793	K562	blood:	n/a	n/a
36	CBX3	chr13:76660989-76661195	K562	blood:	n/a	n/a
37	CBX3	chr13:76603174-76603645	K562	blood:	n/a	n/a
38	CCNT2	chr13:76536196-76536396	K562	blood:	n/a	n/a
39	CCNT2	chr13:76673714-76673907	K562	blood:	n/a	n/a
40	CCNT2	chr13:76603230-76603534	K562	blood:	n/a	n/a
41	CCNT2	chr13:76577864-76578064	K562	blood:	n/a	n/a
42	CCNT2	chr13:76579693-76579959	K562	blood:	n/a	n/a
43	CCNT2	chr13:76559391-76559719	K562	blood:	n/a	chr13:76559513-76559533
44	CEBPB	chr13:76698248-76698479	HepG2	liver:	n/a	chr13:76698389-76698400
45	CEBPB	chr13:76583356-76584105	A549	lung:	n/a	chr13:76583384-76583397
46	CEBPB	chr13:76542244-76542579	A549	lung:	n/a	chr13:76542402-76542413
47	CEBPB	chr13:76553063-76553144	HepG2	liver:	n/a	n/a
48	CEBPB	chr13:76542274-76542441	K562	blood:	n/a	chr13:76542402-76542413
49	CEBPB	chr13:76621172-76621223	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr13:76553023-76553249	K562	blood:	n/a	n/a

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:76723380-76723430	HepG2	liver:	n/a
2	chr13:76508987-76509037	HepG2	liver:	n/a
3	chr13:76508987-76509037	HUVEC	blood vessel:	n/a
4	chr13:76764376-76764426	HRE	kidney:	n/a
5	chr13:76764321-76764371	HRE	kidney:	n/a
6	chr13:76508987-76509037	AG04449	skin:	fetal
7	chr13:76462678-76462728	AG09309	skin:	n/a
8	chr13:76869281-76869331	SAEC	small airway:	n/a
9	chr13:76723380-76723430	HNPCEpiC	eye:	n/a
10	chr13:76764376-76764426	HCM	heart:	n/a
11	chr13:76723380-76723430	HEEpiC	esophagus:	n/a
12	chr13:76869436-76869486	HCT-116	colon:	n/a
13	chr13:76508987-76509037	HEEpiC	esophagus:	n/a
14	chr13:76508987-76509037	NB4	blood:	n/a
15	chr13:76800180-76800230	U87	brain:	n/a
16	chr13:76464782-76464832	T-47D	breast:	n/a
17	chr13:76464782-76464832	HUVEC	blood vessel:	n/a
18	chr13:76869436-76869486	SK-N-MC	brain:	n/a
19	chr13:76764376-76764426	H1-hESC	embryonic stem cell:	embryo
20	chr13:76764376-76764426	AG04449	skin:	fetal
21	chr13:76508987-76509037	T-47D	breast:	n/a
22	chr13:76508987-76509037	ECC-1	luminal epithelium:	n/a
23	chr13:76723380-76723430	MCF-7	breast:	n/a
24	chr13:76536939-76536989	Hepatocyte	liver:	n/a
25	chr13:76462678-76462728	GM12878	blood:	n/a
26	chr13:76508987-76509037	HCM	heart:	n/a
27	chr13:76800180-76800230	MCF10A-Er-Src	breast:	n/a
28	chr13:76869281-76869331	AG09309	skin:	n/a
29	chr13:76536939-76536989	HCM	heart:	n/a
30	chr13:76800180-76800230	HIPEpiC	eye:	n/a
31	chr13:76536939-76536989	HPAEpiC	pulmonary alveolar:	n/a
32	chr13:76764376-76764426	HAEpiC	amniotic membrane:	n/a
33	chr13:76764376-76764426	HL-60	blood:	n/a
34	chr13:76464782-76464832	HNPCEpiC	eye:	n/a
35	chr13:76800180-76800230	HRCEpiC	kidney:	n/a
36	chr13:76800180-76800230	GM19239	blood:	n/a
37	chr13:76869436-76869486	RPTEC	kidney:	n/a
38	chr13:76800180-76800230	AoSMC	blood vessel:	n/a
39	chr13:76508987-76509037	K562	blood:	n/a
40	chr13:76869281-76869331	SK-N-SH	brain:	n/a
41	chr13:76723380-76723430	BJ	skin:	n/a
42	chr13:76462678-76462728	IMR90	lung:	fetal
43	chr13:76464782-76464832	H1-hESC	embryonic stem cell:	embryo
44	chr13:76764321-76764371	ProgFib	skin:	n/a
45	chr13:76764321-76764371	NB4	blood:	n/a
46	chr13:76869436-76869486	Jurkat	blood:	n/a
47	chr13:76464782-76464832	Jurkat	blood:	n/a
48	chr13:76764321-76764371	RPTEC	kidney:	n/a
49	chr13:76536939-76536989	HEEpiC	esophagus:	n/a
50	chr13:76764376-76764426	HIPEpiC	eye:	n/a

(count:21 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:76505508..76507844-chr13:76509844..76512114,2	K562	blood:
2	chr13:76540838..76542386-chr13:76542518..76545047,2	MCF-7	breast:
3	chr13:76613524..76614133-chr13:77047364..77048499,5	MCF-7	breast:
4	chr13:76444149..76445101-chr13:76593232..76594146,4	MCF-7	breast:
5	chr13:76515246..76517813-chr7:2394882..2397172,2	MCF-7	breast:
6	chr13:76540838..76542386-chr13:76542518..76545047,2	MCF-7	breast:
7	chr13:76450462..76451207-chr13:76591002..76591569,2	MCF-7	breast:
8	chr13:76569777..76571605-chr13:76572909..76574640,2	K562	blood:
9	chr13:76547458..76549080-chr13:76550616..76553437,2	K562	blood:
10	chr13:76876047..76878935-chr13:77566060..77567792,2	K562	blood:
11	chr13:76569777..76571605-chr13:76572909..76574640,2	K562	blood:
12	chr11:34379701..34380202-chr13:76805632..76806132,2	NB4	blood:
13	chr13:76438174..76440869-chr13:76485798..76487391,2	K562	blood:
14	chr13:76596252..76598622-chr13:76601248..76603382,2	K562	blood:
15	chr13:76450119..76450751-chr13:76590749..76591620,4	MCF-7	breast:
16	chr13:76450221..76451145-chr13:76590691..76591575,2	K562	blood:
17	chr13:76547458..76549080-chr13:76550616..76553437,2	K562	blood:
18	chr13:76596252..76598622-chr13:76601248..76603382,2	K562	blood:
19	chr12:83286167..83286675-chr13:76878102..76878843,2	MCF-7	breast:
20	chr13:76613162..76614105-chr13:77047335..77048422,4	MCF-7	breast:
21	chr13:76505508..76507844-chr13:76509844..76512114,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AL359392.1-2	chr13:76587159-76587292	XLOC_010435
2	lnc-COMMD6-3	chr13:76506531-76509268	ENSG00000261206.1
3	lnc-AL359392.1-2	chr13:76588495-76588637	XLOC_010435
4	lnc-COMMD6-11	chr13:76587159-76587292	ENSG00000224933.2
5	lnc-COMMD6-11	chr13:76588495-76588637	ENSG00000224933.2
6	lnc-AL359392.1-5	chr13:76709067-76709360	NONHSAT034379

No data

Variant related genes	Relation type
RN7SL571P	TF binding region
LINC01034	TF binding region
LINC00561	TF binding region
RN7SL571P	CpG island
LINC01034	CpG island
LINC00561	CpG island
ENSG00000102805	chromatin interactions

Extended variants
information (count: 9167 )
Associated
traits (count: 103 )

Variant overlapped rSNPs/rCNVs (count:9167 , 50 per page) page: 1 2 3 4 5 6 7 ... 184

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563264231	chr13:76460431-76460432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs142098088	chr13:76460452-76460453	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs192630112	chr13:76460460-76460461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs112427374	chr13:76460534-76460535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs555385445	chr13:76460548-76460549	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs547019324	chr13:76460580-76460581	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs80260947	chr13:76460606-76460607	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs367611147	chr13:76460664-76460665	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs560938755	chr13:76460698-76460699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs12429274	chr13:76460707-76460708	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs17065215	chr13:76460733-76460734	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs35986631	chr13:76460755-76460756	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs200165276	chr13:76460756-76460757	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs527892690	chr13:76460774-76460775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs528685438	chr13:76460781-76460782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs573328654	chr13:76460842-76460843	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs9530483	chr13:76460888-76460889	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
18	rs112927730	chr13:76460933-76460934	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115673036	chr13:76460992-76460993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529259030	chr13:76461097-76461098	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551286838	chr13:76461112-76461113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs562816673	chr13:76461118-76461119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs533357127	chr13:76461174-76461175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs185093598	chr13:76461175-76461176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs566717032	chr13:76461182-76461183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs533925439	chr13:76461246-76461247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548788102	chr13:76461262-76461263	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567282322	chr13:76461288-76461289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs115996546	chr13:76461295-76461296	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs140086343	chr13:76461319-76461320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs572396749	chr13:76461334-76461335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4885362	chr13:76461376-76461377	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs543349798	chr13:76461379-76461380	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs190423452	chr13:76461411-76461412	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs181242345	chr13:76461441-76461442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145612221	chr13:76461444-76461445	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs540757776	chr13:76461459-76461460	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34440314	chr13:76461470-76461471	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs7991366	chr13:76461471-76461472	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs563283627	chr13:76461543-76461544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs562844050	chr13:76461552-76461553	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs184926931	chr13:76461595-76461596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs187968072	chr13:76461601-76461602	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs545285338	chr13:76461629-76461630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs114657918	chr13:76461656-76461657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs534148253	chr13:76461667-76461668	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs115007054	chr13:76461691-76461692	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138132675	chr13:76461715-76461716	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs7997894	chr13:76461736-76461737	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs180922359	chr13:76461827-76461828	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:103)

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
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
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	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
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
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
Hodgkin''s lymphoma	18641027	CNVD
Hirschsprung''s Disease	21712996	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Intracranial aneurysm	16715129	CNVD
Non-small cell lung cancer	19010865	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Breast cancer	21364760	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Osteosarcoma	21215367	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:925 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:76440000-76469200	Weak transcription	HSMM	muscle
2	chr13:76451800-76463600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:76461600-76462600	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr13:76461600-76462600	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr13:76461600-76464400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr13:76461600-76466400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr13:76461800-76462600	Enhancers	HUES64 Cell Line	embryonic stem cell
8	chr13:76462000-76462200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
9	chr13:76462000-76462400	Enhancers	H1 Cell Line	embryonic stem cell
10	chr13:76462000-76464400	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:76462200-76462800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:76462200-76465400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
13	chr13:76462400-76463400	Weak transcription	H1 Cell Line	embryonic stem cell
14	chr13:76462600-76463000	Weak transcription	HUES64 Cell Line	embryonic stem cell
15	chr13:76462600-76463200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chr13:76462600-76465600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
17	chr13:76462800-76464000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:76463000-76464200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr13:76463200-76464400	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr13:76463200-76464400	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr13:76463400-76463600	Enhancers	H1 Cell Line	embryonic stem cell
22	chr13:76463400-76464000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
23	chr13:76463400-76464600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr13:76463600-76463800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr13:76463600-76463800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr13:76463600-76464000	Weak transcription	H1 Cell Line	embryonic stem cell
27	chr13:76463600-76464200	Enhancers	Fetal Heart	heart
28	chr13:76463600-76464600	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chr13:76463600-76464600	Enhancers	H9 Cell Line	embryonic stem cell
30	chr13:76463600-76464600	Enhancers	K562	blood
31	chr13:76463800-76464400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr13:76463800-76466000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:76464000-76464400	Enhancers	H1 Cell Line	embryonic stem cell
34	chr13:76464000-76464600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:76464200-76465800	Weak transcription	HUES64 Cell Line	embryonic stem cell
36	chr13:76464400-76465600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr13:76464400-76465800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
38	chr13:76464400-76466000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chr13:76464400-76468200	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr13:76464600-76465200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
41	chr13:76464600-76465600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr13:76464600-76465800	Weak transcription	H9 Cell Line	embryonic stem cell
43	chr13:76464600-76478200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:76465200-76466400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:76465400-76466400	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
46	chr13:76465600-76466400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr13:76465600-76466600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr13:76465600-76468000	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chr13:76465800-76466200	Enhancers	H9 Cell Line	embryonic stem cell
50	chr13:76465800-76466400	Enhancers	HUES64 Cell Line	embryonic stem cell

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