Variant report

Variant	nsv832676
Chromosome Location	chr13:89941212-90090424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:452)
CpG islands
(count:488)
Chromatin interactive
region (count:8)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:452 , 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	BACH1	chr13:90023891-90023904	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr13:89959518-89959795	GM12878	blood:	n/a	n/a
4	BATF	chr13:89959469-89959854	GM12878	blood:	n/a	n/a
5	BCL11A	chr13:89959576-89959854	GM12878	blood:	n/a	n/a
6	CEBPB	chr13:90053432-90053763	MCF-7	breast:	n/a	chr13:90053581-90053592
7	CEBPB	chr13:90030039-90030322	IMR90	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
8	CEBPB	chr13:89958754-89959095	HepG2	liver:	n/a	chr13:89958917-89958928
9	CEBPB	chr13:89958778-89959043	A549	lung:	n/a	chr13:89958917-89958928
10	CEBPB	chr13:90053319-90053891	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
11	CEBPB	chr13:90032305-90032917	ECC-1	luminal epithelium:	n/a	n/a
12	CEBPB	chr13:90053338-90053860	A549	lung:	n/a	chr13:90053581-90053592
13	CEBPB	chr13:90032538-90032854	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr13:90053471-90053879	HCT-116	colon:	n/a	chr13:90053581-90053592
15	CEBPB	chr13:89958803-89959062	IMR90	lung:	n/a	chr13:89958917-89958928
16	CEBPB	chr13:90053451-90053803	HepG2	liver:	n/a	chr13:90053581-90053592
17	CEBPB	chr13:90053216-90053959	A549	lung:	n/a	chr13:90053581-90053592
18	CEBPB	chr13:90032305-90032732	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr13:90053390-90054036	A549	lung:	n/a	chr13:90053581-90053592
20	CEBPB	chr13:89994770-89995032	HepG2	liver:	n/a	n/a
21	CEBPB	chr13:90076020-90076326	IMR90	lung:	n/a	n/a
22	CEBPB	chr13:90005411-90005608	HepG2	liver:	n/a	n/a
23	CEBPB	chr13:90010585-90010905	HepG2	liver:	n/a	chr13:90010757-90010768 chr13:90010755-90010766 chr13:90010755-90010768
24	CEBPB	chr13:90053370-90053798	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
25	CEBPB	chr13:89946872-89947134	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr13:90030123-90030303	A549	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
27	CEBPB	chr13:90061206-90061460	HepG2	liver:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
28	CEBPB	chr13:90016763-90017043	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr13:90053399-90053954	IMR90	lung:	n/a	chr13:90053581-90053592
30	CEBPB	chr13:90076016-90076314	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:90053368-90054010	Hela-S3	cervix:	n/a	chr13:90053581-90053592
32	CEBPB	chr13:90061199-90061485	A549	lung:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
33	CEBPB	chr13:90053453-90053969	H1-hESC	embryonic stem cell:	n/a	chr13:90053581-90053592
34	CEBPB	chr13:90053490-90053648	K562	blood:	n/a	chr13:90053581-90053592
35	CEBPB	chr13:90046959-90047120	HepG2	liver:	n/a	n/a
36	CEBPB	chr13:90032530-90032817	A549	lung:	n/a	n/a
37	CEBPB	chr13:90005361-90005601	A549	lung:	n/a	n/a
38	CTCF	chr13:90086960-90087110	AG10803	skin:	n/a	n/a
39	CTCF	chr13:90014280-90014430	HCFaa	heart:	n/a	n/a
40	CTCF	chr13:90014296-90014419	MCF-7	breast:	n/a	n/a
41	CTCF	chr13:90014240-90014390	HPAF	blood vessel:	n/a	n/a
42	CTCF	chr13:90014300-90014450	A549	lung:	n/a	n/a
43	CTCF	chr13:90014291-90014454	HepG2	liver:	n/a	n/a
44	CTCF	chr13:90086980-90087130	HRPEpiC	eye:	n/a	n/a
45	CTCF	chr13:90086979-90087143	Gliobla	brain:	n/a	n/a
46	CTCF	chr13:90014220-90014370	HRPEpiC	eye:	n/a	n/a
47	CTCF	chr13:90054530-90054573	GM20000	blood:	n/a	n/a
48	CTCF	chr13:90082948-90083071	Kidney_OC	kidney:	n/a	n/a
49	CTCF	chr13:90014340-90014490	BE2_C	brain:	n/a	n/a
50	CTCF	chr13:90014160-90014310	HMEC	breast:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90045847-90045897	IMR90	lung:	fetal
2	chr13:90014513-90014563	SK-N-SH_RA	brain:	n/a
3	chr13:90015912-90015962	BJ	skin:	n/a
4	chr13:90015774-90015824	HPAEpiC	pulmonary alveolar:	n/a
5	chr13:90015633-90015683	NB4	blood:	n/a
6	chr13:90045847-90045897	ECC-1	luminal epithelium:	n/a
7	chr13:90014513-90014563	HPAEpiC	pulmonary alveolar:	n/a
8	chr13:90053523-90053573	MCF10A-Er-Src	breast:	n/a
9	chr13:90053523-90053573	GM12891	blood:	n/a
10	chr13:90014813-90014863	HUVEC	blood vessel:	n/a
11	chr13:90015518-90015568	HCM	heart:	n/a
12	chr13:90014513-90014563	SK-N-MC	brain:	n/a
13	chr13:90015518-90015568	H1-hESC	embryonic stem cell:	embryo
14	chr13:90015912-90015962	K562	blood:	n/a
15	chr13:90015774-90015824	GM12878	blood:	n/a
16	chr13:90014513-90014563	Hela-S3	cervix:	n/a
17	chr13:90014513-90014563	GM06990	blood:	n/a
18	chr13:90053523-90053573	GM06990	blood:	n/a
19	chr13:90015774-90015824	HRCEpiC	kidney:	n/a
20	chr13:90015633-90015683	RPTEC	kidney:	n/a
21	chr13:90015518-90015568	U87	brain:	n/a
22	chr13:90014813-90014863	HL-60	blood:	n/a
23	chr13:90015518-90015568	NT2-D1	testis:	n/a
24	chr13:90015912-90015962	HNPCEpiC	eye:	n/a
25	chr13:90014813-90014863	HEEpiC	esophagus:	n/a
26	chr13:90015518-90015568	ECC-1	luminal epithelium:	n/a
27	chr13:90045847-90045897	U87	brain:	n/a
28	chr13:90015774-90015824	RPTEC	kidney:	n/a
29	chr13:90053523-90053573	HEEpiC	esophagus:	n/a
30	chr13:90014513-90014563	HL-60	blood:	n/a
31	chr13:90015912-90015962	HEEpiC	esophagus:	n/a
32	chr13:90014813-90014863	ProgFib	skin:	n/a
33	chr13:90045847-90045897	A549	lung:	n/a
34	chr13:90015774-90015824	BE2_C	brain:	n/a
35	chr13:90015912-90015962	HRPEpiC	eye:	n/a
36	chr13:90045847-90045897	HRPEpiC	eye:	n/a
37	chr13:90015518-90015568	SAEC	small airway:	n/a
38	chr13:90015774-90015824	HNPCEpiC	eye:	n/a
39	chr13:90015518-90015568	HMEC	breast:	n/a
40	chr13:90014813-90014863	Caco-2	colon:	n/a
41	chr13:90015912-90015962	Jurkat	blood:	n/a
42	chr13:90015518-90015568	HRCEpiC	kidney:	n/a
43	chr13:90045847-90045897	AG04450	lung:	fetal
44	chr13:90015518-90015568	ovcar-3	ovarian:	n/a
45	chr13:90014513-90014563	BJ	skin:	n/a
46	chr13:90014813-90014863	PANC-1	pancreas:	n/a
47	chr13:90045847-90045897	MCF-7	breast:	n/a
48	chr13:90015518-90015568	T-47D	breast:	n/a
49	chr13:90014513-90014563	HCT-116	colon:	n/a
50	chr13:90014813-90014863	AG04449	skin:	fetal

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
2	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
3	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
4	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
5	chr1:28837703..28838287-chr13:89988449..89988969,2	Hela-S3	cervix:
6	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
7	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
8	chr13:90015162..90016936-chr13:90019494..90021362,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-23	chr13:89963743-89963827	NONHSAT034627
2	lnc-SLITRK5-23	chr13:89943542-89943672	NONHSAT034627
3	lnc-SLITRK5-23	chr13:89985010-89985335	NONHSAT034627
4	lnc-SLITRK5-23	chr13:89977655-89977753	NONHSAT034627
5	lnc-SLITRK5-23	chr13:89983031-89983075	NONHSAT034627
6	lnc-SLITRK5-23	chr13:89985010-89985594	ucscGeneNc_uc001vlo_2
7	lnc-SLITRK5-23	chr13:89983031-89983075	ucscGeneNc_uc001vlo_2
8	lnc-SLITRK5-24	chr13:89988809-89989762	NONHSAT034628
9	lnc-SLITRK5-23	chr13:89943543-89943672	ucscGeneNc_uc001vlo_2
10	lnc-SLITRK5-24	chr13:89997201-89997338	NONHSAT034628
11	lnc-SLITRK5-23	chr13:89963743-89963827	ucscGeneNc_uc001vlo_2
12	lnc-SLITRK5-23	chr13:89948465-89948520	ucscGeneNc_uc001vlo_2
13	lnc-SLITRK5-23	chr13:89977655-89977753	ucscGeneNc_uc001vlo_2
14	lnc-SLITRK5-23	chr13:89948465-89948520	NONHSAT034627

No data

Variant related genes	Relation type
SP3P	TF binding region
SP3P	CpG island
ENSG00000225530	chromatin interactions

Extended variants
information (count: 2934 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:2934 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115033135	chr13:89943564-89943565	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs530712753	chr13:89943588-89943589	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs149084987	chr13:89943589-89943590	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs190984013	chr13:89943606-89943607	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs183144008	chr13:89943616-89943617	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs143107764	chr13:89943634-89943635	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs186651494	chr13:89943658-89943659	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs536350563	chr13:89946406-89946407	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs79413324	chr13:89946407-89946408	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs375848939	chr13:89946408-89946409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs75776046	chr13:89946409-89946410	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs12428874	chr13:89946442-89946443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs2348654	chr13:89946444-89946445	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs372257233	chr13:89946468-89946469	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs184827130	chr13:89946476-89946477	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs2348655	chr13:89946493-89946494	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs150932115	chr13:89946515-89946516	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs188502879	chr13:89946612-89946613	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs139494694	chr13:89946614-89946615	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs9555866	chr13:89946615-89946616	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs548790877	chr13:89946636-89946637	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs560335645	chr13:89946637-89946638	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144323765	chr13:89946702-89946703	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs552235981	chr13:89946704-89946705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs181007706	chr13:89946773-89946774	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs183715856	chr13:89946780-89946781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs147817296	chr13:89946876-89946877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs575543702	chr13:89946879-89946880	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs367647216	chr13:89946934-89946935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs536642517	chr13:89946993-89946994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs9560285	chr13:89947058-89947059	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs141364271	chr13:89947060-89947061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs573031594	chr13:89947064-89947065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs78729766	chr13:89947101-89947102	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs147006715	chr13:89947138-89947139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs9555867	chr13:89947192-89947193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs544584620	chr13:89947198-89947199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs145136987	chr13:89947238-89947239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs369017128	chr13:89947353-89947354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs575206603	chr13:89947364-89947365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs542470753	chr13:89947458-89947459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs560652503	chr13:89947477-89947478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs527398943	chr13:89947483-89947484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs189568469	chr13:89947492-89947493	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs545855419	chr13:89947531-89947532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372663983	chr13:89947554-89947555	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs561299908	chr13:89948497-89948498	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs533407039	chr13:89961000-89961001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs370420759	chr13:89961025-89961026	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs557500891	chr13:89961039-89961040	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Non-small cell lung cancer	16651412	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:179 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89946400-89947200	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chr13:89946600-89947000	Enhancers	H1 Cell Line	embryonic stem cell
3	chr13:89946800-89947400	Enhancers	HUES48 Cell Line	embryonic stem cell
4	chr13:89947000-89947600	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr13:89961000-89961400	Enhancers	Fetal Heart	heart
6	chr13:89963000-89964000	Enhancers	Muscle Satellite Cultured Cells	--
7	chr13:89970200-89972600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr13:89972200-89972400	ZNF genes & repeats	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:89972400-89979400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr13:89974200-89974800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:89974800-89975200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr13:89974800-89976200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr13:89975200-89976200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:89975600-89975800	Enhancers	H9 Cell Line	embryonic stem cell
15	chr13:89975600-89976200	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chr13:89975600-89977400	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr13:89975600-89977400	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chr13:89975800-89982200	Weak transcription	H9 Cell Line	embryonic stem cell
19	chr13:89976200-89976400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:89976200-89977000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr13:89976200-89977200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:89976400-89977800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:89977200-89977400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
24	chr13:89995200-89995600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr13:89995200-89995600	Enhancers	NHEK	skin
26	chr13:90002600-90004000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:90003000-90003200	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr13:90003000-90003600	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:90003000-90004000	Enhancers	H1 Cell Line	embryonic stem cell
30	chr13:90003200-90003800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chr13:90003800-90004000	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr13:90004000-90004800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr13:90004800-90005000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
34	chr13:90005000-90010600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr13:90010600-90010800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr13:90014800-90015600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
37	chr13:90015200-90015800	Active TSS	HUES6 Cell Line	embryonic stem cell
38	chr13:90015600-90015800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr13:90015800-90016000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr13:90015800-90017000	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chr13:90016600-90017200	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr13:90016600-90017600	Enhancers	HUES48 Cell Line	embryonic stem cell
43	chr13:90016800-90017400	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chr13:90016800-90017400	Enhancers	iPS-20b Cell Line	embryonic stem cell
45	chr13:90017000-90017200	Enhancers	iPS-15b Cell Line	embryonic stem cell
46	chr13:90017000-90017400	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr13:90017000-90017400	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr13:90017000-90017400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr13:90023400-90023800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
50	chr13:90023800-90025400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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