Variant report

Variant	nsv456071
Chromosome Location	chr13:93279563-93377562
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr13:93302341-93302541	K562	blood:	n/a	n/a
2	ATF1	chr13:93305188-93305345	K562	blood:	n/a	n/a
3	ATF1	chr13:93336321-93336388	K562	blood:	n/a	n/a
4	ATF1	chr13:93301882-93301984	K562	blood:	n/a	n/a
5	ATF1	chr13:93345167-93345525	K562	blood:	n/a	n/a
6	ATF1	chr13:93317780-93317980	K562	blood:	n/a	n/a
7	ATF1	chr13:93297789-93297885	K562	blood:	n/a	n/a
8	ATF1	chr13:93335377-93335726	K562	blood:	n/a	n/a
9	ATF1	chr13:93314048-93314049	K562	blood:	n/a	n/a
10	ATF1	chr13:93304196-93304297	K562	blood:	n/a	n/a
11	ATF1	chr13:93336920-93337114	K562	blood:	n/a	n/a
12	ATF1	chr13:93303220-93303254	K562	blood:	n/a	n/a
13	ATF1	chr13:93280118-93280318	K562	blood:	n/a	n/a
14	ATF1	chr13:93291305-93291356	K562	blood:	n/a	n/a
15	BACH1	chr13:93319464-93319533	K562	blood:	n/a	n/a
16	BACH1	chr13:93334020-93334103	K562	blood:	n/a	n/a
17	BACH1	chr13:93322619-93322694	K562	blood:	n/a	n/a
18	BACH1	chr13:93331202-93331293	K562	blood:	n/a	n/a
19	BACH1	chr13:93300172-93300291	K562	blood:	n/a	n/a
20	BACH1	chr13:93279443-93279716	K562	blood:	n/a	n/a
21	BACH1	chr13:93289014-93289045	K562	blood:	n/a	n/a
22	BHLHE40	chr13:93322531-93322585	K562	blood:	n/a	n/a
23	BHLHE40	chr13:93289058-93289064	K562	blood:	n/a	n/a
24	BHLHE40	chr13:93317935-93318081	K562	blood:	n/a	n/a
25	BHLHE40	chr13:93334909-93334911	K562	blood:	n/a	n/a
26	BHLHE40	chr13:93333986-93334288	K562	blood:	n/a	n/a
27	BHLHE40	chr13:93308372-93308496	K562	blood:	n/a	n/a
28	BHLHE40	chr13:93335144-93335360	K562	blood:	n/a	n/a
29	BHLHE40	chr13:93309553-93309697	K562	blood:	n/a	n/a
30	CCNT2	chr13:93280140-93280382	K562	blood:	n/a	n/a
31	CCNT2	chr13:93294284-93294516	K562	blood:	n/a	n/a
32	CCNT2	chr13:93302999-93303032	K562	blood:	n/a	n/a
33	CCNT2	chr13:93283539-93283594	K562	blood:	n/a	n/a
34	CCNT2	chr13:93281187-93281700	K562	blood:	n/a	n/a
35	CEBPB	chr13:93317868-93318078	IMR90	lung:	n/a	n/a
36	CEBPB	chr13:93305127-93305327	K562	blood:	n/a	chr13:93305218-93305229
37	CEBPB	chr13:93286025-93286225	K562	blood:	n/a	n/a
38	CEBPB	chr13:93305087-93305365	HepG2	liver:	n/a	chr13:93305218-93305229
39	CEBPB	chr13:93333824-93333829	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr13:93299536-93299567	K562	blood:	n/a	n/a
41	CEBPB	chr13:93313698-93314077	K562	blood:	n/a	chr13:93313877-93313888
42	CEBPB	chr13:93313787-93314014	HepG2	liver:	n/a	chr13:93313877-93313888
43	CEBPB	chr13:93300745-93300759	K562	blood:	n/a	n/a
44	CHD2	chr13:93283909-93284105	K562	blood:	n/a	n/a
45	CHD2	chr13:93307322-93307327	K562	blood:	n/a	n/a
46	CHD2	chr13:93335558-93335640	K562	blood:	n/a	n/a
47	CHD2	chr13:93323108-93323117	K562	blood:	n/a	n/a
48	CHD2	chr13:93308480-93308509	K562	blood:	n/a	n/a
49	CHD2	chr13:93294800-93294821	K562	blood:	n/a	n/a
50	CHD2	chr13:93331238-93331240	K562	blood:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:93293174-93293224	HCM	heart:	n/a
2	chr13:93293174-93293224	AG09319	gingival:	n/a
3	chr13:93293174-93293224	GM19239	blood:	n/a
4	chr13:93293174-93293224	AG09309	skin:	n/a
5	chr13:93293174-93293224	Hepatocyte	liver:	n/a
6	chr13:93293174-93293224	NT2-D1	testis:	n/a
7	chr13:93293174-93293224	PFSK-1	brain:	n/a
8	chr13:93293174-93293224	SK-N-MC	brain:	n/a
9	chr13:93293174-93293224	HCPEpiC	choroid plexus:	n/a
10	chr13:93293174-93293224	HEEpiC	esophagus:	n/a
11	chr13:93293174-93293224	PANC-1	pancreas:	n/a
12	chr13:93293174-93293224	GM12892	blood:	n/a
13	chr13:93293174-93293224	GM12878	blood:	n/a
14	chr13:93293174-93293224	HepG2	liver:	n/a
15	chr13:93293174-93293224	SK-N-SH	brain:	n/a
16	chr13:93293174-93293224	ProgFib	skin:	n/a
17	chr13:93293174-93293224	HRPEpiC	eye:	n/a
18	chr13:93293174-93293224	HUVEC	blood vessel:	n/a
19	chr13:93293174-93293224	NH-A	brain:	n/a
20	chr13:93293174-93293224	GM06990	blood:	n/a
21	chr13:93293174-93293224	AG04449	skin:	fetal
22	chr13:93293174-93293224	HRCEpiC	kidney:	n/a
23	chr13:93293174-93293224	NHBE	bronchial:	n/a
24	chr13:93293174-93293224	HL-60	blood:	n/a
25	chr13:93293174-93293224	AG04450	lung:	fetal
26	chr13:93293174-93293224	CMK	blood:	n/a
27	chr13:93293174-93293224	LNCaP	prostate:	n/a
28	chr13:93293174-93293224	K562	blood:	n/a
29	chr13:93293174-93293224	PrEC	prostate:	n/a
30	chr13:93293174-93293224	HCT-116	colon:	n/a
31	chr13:93293174-93293224	MCF10A-Er-Src	breast:	n/a
32	chr13:93293174-93293224	HCF	heart:	n/a
33	chr13:93293174-93293224	BE2_C	brain:	n/a
34	chr13:93293174-93293224	AG10803	skin:	n/a
35	chr13:93293174-93293224	BJ	skin:	n/a
36	chr13:93293174-93293224	NHDF-neo	bronchial:	n/a
37	chr13:93293174-93293224	HIPEpiC	eye:	n/a
38	chr13:93293174-93293224	HRE	kidney:	n/a
39	chr13:93293174-93293224	SKMC	muscle:	n/a
40	chr13:93293174-93293224	T-47D	breast:	n/a
41	chr13:93293174-93293224	RPTEC	kidney:	n/a
42	chr13:93293174-93293224	HEK293	kidney:	embryo
43	chr13:93293174-93293224	IMR90	lung:	fetal
44	chr13:93293174-93293224	ECC-1	luminal epithelium:	n/a
45	chr13:93293174-93293224	GM12891	blood:	n/a
46	chr13:93293174-93293224	HPAEpiC	pulmonary alveolar:	n/a
47	chr13:93293174-93293224	MCF-7	breast:	n/a
48	chr13:93293174-93293224	SAEC	small airway:	n/a
49	chr13:93293174-93293224	HMEC	breast:	n/a
50	chr13:93293174-93293224	A549	lung:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:93294782..93296339-chr13:93300831..93303827,2	K562	blood:
2	chr13:93282740..93284834-chr13:93292372..93295262,2	K562	blood:
3	chr13:93273565..93275708-chr13:93279729..93281510,2	K562	blood:
4	chr13:93281680..93284628-chr13:93314114..93316635,2	K562	blood:
5	chr13:93294782..93296339-chr13:93300831..93303827,2	K562	blood:
6	chr13:93281680..93284628-chr13:93314114..93316635,2	K562	blood:
7	chr13:93316466..93319082-chr13:93326794..93329759,2	K562	blood:
8	chr13:93289108..93290701-chr13:93292511..93295289,2	K562	blood:
9	chr13:93282740..93284834-chr13:93292372..93295262,2	K562	blood:
10	chr13:93281728..93283800-chr13:93286450..93288614,2	K562	blood:
11	chr13:93316466..93319082-chr13:93326794..93329759,2	K562	blood:
12	chr13:93281728..93283800-chr13:93286450..93288614,2	K562	blood:
13	chr13:93369459..93371905-chr13:93878761..93880534,2	MCF-7	breast:
14	chr13:93289108..93290701-chr13:93292511..93295289,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DCT-4	chr13:93372161-93372227	NR_049775
2	lnc-DCT-4	chr13:93372161-93372208	NONHSAT034706
3	lnc-DCT-4	chr13:93361742-93361826	ENSG00000235984.1
4	lnc-DCT-4	chr13:93353643-93353769	NR_049775
5	lnc-DCT-4	chr13:93358214-93358312	ENSG00000235984.1
6	lnc-DCT-4	chr13:93358214-93358312	NR_049775
7	lnc-DCT-4	chr13:93361742-93361826	NR_049775
8	lnc-DCT-4	chr13:93372161-93372228	ENSG00000235984.1
9	lnc-DCT-4	chr13:93353642-93353769	ENSG00000235984.1
10	lnc-DCT-4	chr13:93361742-93361826	NONHSAT034706
11	lnc-DCT-4	chr13:93353642-93353900	NONHSAT034706
12	lnc-DCT-4	chr13:93358214-93358312	NONHSAT034706

No data

Variant related genes	Relation type
GPC5-AS1	TF binding region
GPC5-AS1	CpG island
ENSG00000183098	chromatin interactions

Extended variants
information (count: 1802 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:1802 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs543386679	chr13:93287804-93287805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553282145	chr13:93287917-93287918	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs573034611	chr13:93287962-93287963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369736030	chr13:93287997-93287998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs557200795	chr13:93288033-93288034	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs148111329	chr13:93288098-93288099	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs9556198	chr13:93288119-93288120	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs532933223	chr13:93288229-93288230	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs577181275	chr13:93288270-93288271	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs575483970	chr13:93288274-93288275	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182769886	chr13:93288293-93288294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs561326346	chr13:93288407-93288408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs574926535	chr13:93288448-93288449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376897415	chr13:93288456-93288457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs560867427	chr13:93288498-93288499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs532678929	chr13:93288504-93288505	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs542379319	chr13:93288521-93288522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs552800158	chr13:93288536-93288537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs9584052	chr13:93288565-93288566	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs144565041	chr13:93288575-93288576	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs202056700	chr13:93288587-93288588	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs141897406	chr13:93288654-93288655	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs550268252	chr13:93288661-93288662	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs187451507	chr13:93288678-93288679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs117395302	chr13:93288745-93288746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs116180609	chr13:93288776-93288777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs192411855	chr13:93288797-93288798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs185833801	chr13:93288811-93288812	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs56318693	chr13:93288895-93288896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs397715937	chr13:93288897-93288898	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9516104	chr13:93288934-93288935	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs373288101	chr13:93288936-93288937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs187575288	chr13:93288946-93288947	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551016371	chr13:93288957-93288958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs192812103	chr13:93288962-93288963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538030677	chr13:93288984-93288985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4435099	chr13:93288992-93288993	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs143981054	chr13:93291620-93291621	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561870068	chr13:93291698-93291699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs536651337	chr13:93291700-93291701	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs144341887	chr13:93291724-93291725	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs547349068	chr13:93291744-93291745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11840527	chr13:93291840-93291841	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs550501522	chr13:93291924-93291925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs532921543	chr13:93292031-93292032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549902984	chr13:93292073-93292074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112084293	chr13:93292082-93292083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs11840554	chr13:93292107-93292108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs34010497	chr13:93292130-93292131	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs549341956	chr13:93292139-93292140	Weak transcription	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
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
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
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Melanoma	20688739	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:70 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:93287800-93289000	Enhancers	Fetal Heart	heart
2	chr13:93288400-93288800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:93291600-93291800	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr13:93291800-93296400	Weak transcription	Pancreatic Islets	Pancreatic Islet
5	chr13:93296400-93296800	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr13:93299600-93299800	Enhancers	Fetal Intestine Large	intestine
7	chr13:93300000-93301200	Weak transcription	Fetal Intestine Large	intestine
8	chr13:93301200-93301800	Enhancers	Fetal Intestine Large	intestine
9	chr13:93307400-93321800	Weak transcription	Right Atrium	heart
10	chr13:93309000-93309800	Enhancers	Fetal Intestine Large	intestine
11	chr13:93309000-93310600	Enhancers	Fetal Intestine Small	intestine
12	chr13:93309600-93310000	Enhancers	Duodenum Mucosa	Duodenum
13	chr13:93309800-93310600	Weak transcription	Fetal Intestine Large	intestine
14	chr13:93310600-93310800	Enhancers	Fetal Intestine Large	intestine
15	chr13:93321600-93322200	Enhancers	Fetal Brain Male	brain
16	chr13:93321800-93322600	Enhancers	Right Atrium	heart
17	chr13:93322600-93326200	Weak transcription	Right Atrium	heart
18	chr13:93326200-93326800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr13:93326200-93327000	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr13:93326200-93327000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr13:93326200-93330000	Active TSS	Right Atrium	heart
22	chr13:93327000-93329800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr13:93329600-93330000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:93329600-93330400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr13:93329800-93330200	Enhancers	H1 Cell Line	embryonic stem cell
26	chr13:93329800-93330200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:93329800-93330200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr13:93330000-93333200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:93330000-93335400	Weak transcription	Right Atrium	heart
30	chr13:93331600-93331800	Enhancers	Pancreatic Islets	Pancreatic Islet
31	chr13:93331800-93332000	Flanking Active TSS	Pancreatic Islets	Pancreatic Islet
32	chr13:93332000-93332200	Active TSS	Pancreatic Islets	Pancreatic Islet
33	chr13:93333200-93333400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:93333600-93334200	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr13:93335400-93335600	Enhancers	Right Atrium	heart
36	chr13:93352800-93353000	Enhancers	Aorta	Aorta
37	chr13:93353400-93354200	Weak transcription	Aorta	Aorta
38	chr13:93354200-93354600	Enhancers	Aorta	Aorta
39	chr13:93354600-93354800	Weak transcription	Aorta	Aorta
40	chr13:93354800-93355200	Enhancers	Aorta	Aorta
41	chr13:93367600-93368200	Enhancers	Fetal Intestine Small	intestine
42	chr13:93367600-93369400	Enhancers	Fetal Lung	lung
43	chr13:93367800-93368200	Enhancers	Fetal Heart	heart
44	chr13:93368000-93369000	Enhancers	Fetal Stomach	stomach
45	chr13:93368600-93369400	Enhancers	Ovary	ovary
46	chr13:93369200-93369400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr13:93369200-93369600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr13:93370200-93370400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr13:93370600-93371600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
50	chr13:93371600-93372200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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