Variant report

Variant	nsv1039775
Chromosome Location	chr13:89995537-90260944
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:845)
CpG islands
(count:490)
Chromatin interactive
region (count:9)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:845 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:90166877-90167409	HepG2	liver:	n/a	n/a
2	ATF3	chr13:90166748-90167411	A549	lung:	n/a	n/a
3	BACH1	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr13:90023891-90023904	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
6	BCL3	chr13:90166802-90167246	A549	lung:	n/a	n/a
7	BCL3	chr13:90166728-90167467	A549	lung:	n/a	n/a
8	BRCA1	chr13:90166960-90167339	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr13:90120640-90120770	K562	blood:	n/a	chr13:90120722-90120733
10	CEBPB	chr13:90190414-90190730	A549	lung:	n/a	chr13:90190558-90190569
11	CEBPB	chr13:90053471-90053879	HCT-116	colon:	n/a	chr13:90053581-90053592
12	CEBPB	chr13:90010585-90010905	HepG2	liver:	n/a	chr13:90010757-90010768 chr13:90010755-90010766 chr13:90010755-90010768
13	CEBPB	chr13:90053399-90053954	IMR90	lung:	n/a	chr13:90053581-90053592
14	CEBPB	chr13:90216095-90216295	HepG2	liver:	n/a	chr13:90216249-90216262 chr13:90216250-90216261
15	CEBPB	chr13:90030123-90030303	A549	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
16	CEBPB	chr13:90032305-90032732	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr13:90242215-90242403	HepG2	liver:	n/a	chr13:90242323-90242334
18	CEBPB	chr13:90053390-90054036	A549	lung:	n/a	chr13:90053581-90053592
19	CEBPB	chr13:90190489-90190619	K562	blood:	n/a	chr13:90190558-90190569
20	CEBPB	chr13:90053319-90053891	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
21	CEBPB	chr13:90053432-90053763	MCF-7	breast:	n/a	chr13:90053581-90053592
22	CEBPB	chr13:90005361-90005601	A549	lung:	n/a	n/a
23	CEBPB	chr13:90127861-90128178	HepG2	liver:	n/a	chr13:90128018-90128029
24	CEBPB	chr13:90166838-90167348	A549	lung:	n/a	n/a
25	CEBPB	chr13:90061206-90061460	HepG2	liver:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
26	CEBPB	chr13:90053338-90053860	A549	lung:	n/a	chr13:90053581-90053592
27	CEBPB	chr13:90053490-90053648	K562	blood:	n/a	chr13:90053581-90053592
28	CEBPB	chr13:90127840-90128138	A549	lung:	n/a	chr13:90128018-90128029
29	CEBPB	chr13:90166633-90167478	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chr13:90076016-90076314	HepG2	liver:	n/a	n/a
31	CEBPB	chr13:90224834-90224951	HepG2	liver:	n/a	n/a
32	CEBPB	chr13:90127859-90128113	Hela-S3	cervix:	n/a	chr13:90128018-90128029
33	CEBPB	chr13:90046959-90047120	HepG2	liver:	n/a	n/a
34	CEBPB	chr13:90166942-90167297	MCF-7	breast:	n/a	n/a
35	CEBPB	chr13:90177810-90178090	A549	lung:	n/a	n/a
36	CEBPB	chr13:90190494-90190716	HepG2	liver:	n/a	chr13:90190558-90190569
37	CEBPB	chr13:90120635-90120885	H1-hESC	embryonic stem cell:	n/a	chr13:90120722-90120733
38	CEBPB	chr13:90110265-90110690	ECC-1	luminal epithelium:	n/a	n/a
39	CEBPB	chr13:90120562-90120885	HepG2	liver:	n/a	chr13:90120722-90120733
40	CEBPB	chr13:90053451-90053803	HepG2	liver:	n/a	chr13:90053581-90053592
41	CEBPB	chr13:90053370-90053798	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
42	CEBPB	chr13:90053453-90053969	H1-hESC	embryonic stem cell:	n/a	chr13:90053581-90053592
43	CEBPB	chr13:90120552-90120888	IMR90	lung:	n/a	chr13:90120722-90120733
44	CEBPB	chr13:90076020-90076326	IMR90	lung:	n/a	n/a
45	CEBPB	chr13:90127850-90128161	IMR90	lung:	n/a	chr13:90128018-90128029
46	CEBPB	chr13:90032538-90032854	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr13:90166579-90167503	A549	lung:	n/a	n/a
48	CEBPB	chr13:90030039-90030322	IMR90	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
49	CEBPB	chr13:90110184-90110994	Hela-S3	cervix:	n/a	n/a
50	CEBPB	chr13:90177917-90178057	Hela-S3	cervix:	n/a	n/a

(count:490 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90014813-90014863	HEK293	kidney:	embryo
2	chr13:90014513-90014563	PrEC	prostate:	n/a
3	chr13:90014813-90014863	HEK293	kidney:	embryo
4	chr13:90014513-90014563	PrEC	prostate:	n/a
5	chr13:90015633-90015683	HepG2	liver:	n/a
6	chr13:90014813-90014863	SK-N-SH_RA	brain:	n/a
7	chr13:90014513-90014563	NB4	blood:	n/a
8	chr13:90014813-90014863	GM12892	blood:	n/a
9	chr13:90015912-90015962	SK-N-SH	brain:	n/a
10	chr13:90045847-90045897	GM19239	blood:	n/a
11	chr13:90015633-90015683	HCF	heart:	n/a
12	chr13:90015518-90015568	GM12878	blood:	n/a
13	chr13:90014513-90014563	AG09309	skin:	n/a
14	chr13:90015633-90015683	AG04450	lung:	fetal
15	chr13:90014513-90014563	BJ	skin:	n/a
16	chr13:90014513-90014563	HL-60	blood:	n/a
17	chr13:90053523-90053573	A549	lung:	n/a
18	chr13:90015633-90015683	BE2_C	brain:	n/a
19	chr13:90015518-90015568	HAEpiC	amniotic membrane:	n/a
20	chr13:90015633-90015683	GM19239	blood:	n/a
21	chr13:90015518-90015568	HCT-116	colon:	n/a
22	chr13:90015633-90015683	IMR90	lung:	fetal
23	chr13:90015774-90015824	IMR90	lung:	fetal
24	chr13:90015774-90015824	HCF	heart:	n/a
25	chr13:90045847-90045897	MCF10A-Er-Src	breast:	n/a
26	chr13:90015774-90015824	GM12892	blood:	n/a
27	chr13:90045847-90045897	Jurkat	blood:	n/a
28	chr13:90015518-90015568	U87	brain:	n/a
29	chr13:90015518-90015568	SK-N-SH	brain:	n/a
30	chr13:90045847-90045897	HCPEpiC	choroid plexus:	n/a
31	chr13:90053523-90053573	H1-hESC	embryonic stem cell:	embryo
32	chr13:90015912-90015962	NH-A	brain:	n/a
33	chr13:90014813-90014863	SAEC	small airway:	n/a
34	chr13:90053523-90053573	GM12892	blood:	n/a
35	chr13:90015518-90015568	SK-N-SH_RA	brain:	n/a
36	chr13:90045847-90045897	U87	brain:	n/a
37	chr13:90014513-90014563	SK-N-SH	brain:	n/a
38	chr13:90015633-90015683	PrEC	prostate:	n/a
39	chr13:90015633-90015683	ECC-1	luminal epithelium:	n/a
40	chr13:90015774-90015824	ECC-1	luminal epithelium:	n/a
41	chr13:90015633-90015683	NT2-D1	testis:	n/a
42	chr13:90014513-90014563	AoSMC	blood vessel:	n/a
43	chr13:90015774-90015824	SAEC	small airway:	n/a
44	chr13:90014513-90014563	PFSK-1	brain:	n/a
45	chr13:90014513-90014563	GM06990	blood:	n/a
46	chr13:90045847-90045897	AoSMC	blood vessel:	n/a
47	chr13:90015774-90015824	H1-hESC	embryonic stem cell:	embryo
48	chr13:90015912-90015962	HIPEpiC	eye:	n/a
49	chr13:90015912-90015962	AG09319	gingival:	n/a
50	chr13:90015774-90015824	HEEpiC	esophagus:	n/a

(count:9 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
2	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
3	chr13:90045131..90046712-chr13:90048307..90050630,2	K562	blood:
4	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
5	chr13:90015162..90016936-chr13:90019494..90021362,2	MCF-7	breast:
6	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:
7	chr13:90007666..90009633-chr13:90010115..90012279,2	MCF-7	breast:
8	chr13:90172699..90174465-chr13:90182640..90184619,2	MCF-7	breast:
9	chr13:90066931..90069093-chr13:90072518..90074200,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPC5-4	chr13:90203487-90203531	ENSG00000271395.1
2	lnc-GPC5-4	chr13:90204359-90204606	XLOC_010468
3	lnc-GPC5-4	chr13:90204359-90204643	ENSG00000271395.1
4	lnc-SLITRK5-28	chr13:90186815-90187120	NONHSAT034630
5	lnc-SLITRK6-12	chr13:90200945-90201465	XLOC_010686
6	lnc-SLITRK5-24	chr13:89997201-89997338	NONHSAT034628
7	lnc-SLITRK6-12	chr13:90205985-90206058	XLOC_010686
8	lnc-SLITRK6-12	chr13:90204359-90204643	XLOC_010686
9	lnc-SLITRK6-12	chr13:90201048-90201465	NONHSAT034632
10	lnc-SLITRK6-11	chr13:90129862-90130391	XLOC_010685
11	lnc-SLITRK6-12	chr13:90203455-90203544	NONHSAT034632
12	lnc-SLITRK6-12	chr13:90205985-90206049	NONHSAT034632
13	lnc-SLITRK6-12	chr13:90216586-90216667	NONHSAT034632
14	lnc-GPC5-4	chr13:90203039-90203531	XLOC_010468
15	lnc-SLITRK6-12	chr13:90203487-90203531	XLOC_010686
16	lnc-SLITRK6-12	chr13:90203455-90203544	XLOC_010686
17	lnc-SLITRK5-28	chr13:90186444-90186646	NONHSAT034630
18	lnc-SLITRK6-11	chr13:90152628-90152763	XLOC_010685

No data

Variant related genes	Relation type
SP3P	TF binding region
LINC01040	TF binding region
LINC00353	TF binding region
ENSG00000271395	TF binding region
SP3P	CpG island
LINC01040	CpG island
LINC00353	CpG island
ENSG00000271395	CpG island
ENSG00000225530	chromatin interactions
MBNL1	miRNA target sites
HSP90B1	miRNA target sites

Extended variants
information (count: 5443 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:5443 , 50 per page) page: 1 2 3 4 5 6 7 ... 109

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs558207034	chr13:89995599-89995600	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs566271243	chr13:89997206-89997207	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs532314254	chr13:89997218-89997219	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs557856108	chr13:89997241-89997242	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs1360716	chr13:89997275-89997276	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs537128408	chr13:89997293-89997294	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs59241945	chr13:89997308-89997309	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs553856160	chr13:90002668-90002669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs565667810	chr13:90002677-90002678	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs539527002	chr13:90002693-90002694	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181706135	chr13:90002701-90002702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs9515566	chr13:90002708-90002709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs543744710	chr13:90002709-90002710	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs35360027	chr13:90002722-90002723	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs35603078	chr13:90002741-90002742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs561643948	chr13:90002777-90002778	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs555659539	chr13:90002795-90002796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141778151	chr13:90002806-90002807	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs540839701	chr13:90002865-90002866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs112852788	chr13:90002899-90002900	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs207474191	chr13:90002967-90002968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199529588	chr13:90002973-90002974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs527543225	chr13:90002983-90002984	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs377066803	chr13:90003019-90003020	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs186153509	chr13:90003029-90003030	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs72630554	chr13:90003071-90003072	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs72630556	chr13:90003123-90003124	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs539839380	chr13:90003135-90003136	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs550080144	chr13:90003150-90003151	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs562218635	chr13:90003163-90003164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs75696783	chr13:90003181-90003182	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs547710809	chr13:90003182-90003183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566255407	chr13:90003188-90003189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115474397	chr13:90003237-90003238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs111576647	chr13:90003260-90003261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs569678574	chr13:90003268-90003269	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528251594	chr13:90003269-90003270	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs555656568	chr13:90003298-90003299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs116112603	chr13:90003346-90003347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs534901498	chr13:90003352-90003353	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs552929795	chr13:90003362-90003363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs190520073	chr13:90003381-90003382	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs545893448	chr13:90003454-90003455	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs564198051	chr13:90003462-90003463	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs183008658	chr13:90003533-90003534	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs570160605	chr13:90003540-90003541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs562099188	chr13:90003576-90003577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs111970277	chr13:90003611-90003612	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs537561622	chr13:90003622-90003623	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs375364703	chr13:90003636-90003637	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
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89995200-89995600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr13:89995200-89995600	Enhancers	NHEK	skin
3	chr13:90002600-90004000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr13:90003000-90003200	Enhancers	HUES48 Cell Line	embryonic stem cell
5	chr13:90003000-90003600	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chr13:90003000-90004000	Enhancers	H1 Cell Line	embryonic stem cell
7	chr13:90003200-90003800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
8	chr13:90003800-90004000	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chr13:90004000-90004800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
10	chr13:90004800-90005000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr13:90005000-90010600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr13:90010600-90010800	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
13	chr13:90014800-90015600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
14	chr13:90015200-90015800	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr13:90015600-90015800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr13:90015800-90016000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr13:90015800-90017000	Weak transcription	HUES6 Cell Line	embryonic stem cell
18	chr13:90016600-90017200	Enhancers	HUES64 Cell Line	embryonic stem cell
19	chr13:90016600-90017600	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr13:90016800-90017400	Enhancers	iPS-18 Cell Line	embryonic stem cell
21	chr13:90016800-90017400	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr13:90017000-90017200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr13:90017000-90017400	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr13:90017000-90017400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr13:90017000-90017400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
26	chr13:90023400-90023800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
27	chr13:90023800-90025400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr13:90027400-90028200	Enhancers	Fetal Muscle Leg	muscle
29	chr13:90027600-90028800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr13:90027600-90028800	Enhancers	HUVEC	blood vessel
31	chr13:90027600-90029000	Enhancers	Fetal Lung	lung
32	chr13:90027800-90028200	Enhancers	Adipose Nuclei	Adipose
33	chr13:90027800-90028400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr13:90027800-90028600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr13:90027800-90028600	Enhancers	Fetal Heart	heart
36	chr13:90027800-90028600	Enhancers	Fetal Stomach	stomach
37	chr13:90027800-90028800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr13:90027800-90028800	Enhancers	Muscle Satellite Cultured Cells	--
39	chr13:90027800-90028800	Enhancers	Stomach Mucosa	stomach
40	chr13:90028000-90028400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr13:90028000-90028400	Enhancers	Fetal Brain Male	brain
42	chr13:90028000-90028600	Enhancers	Colon Smooth Muscle	Colon
43	chr13:90028200-90028800	Enhancers	NHEK	skin
44	chr13:90028400-90032200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr13:90028400-90032600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr13:90028800-90029800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr13:90028800-90030000	Weak transcription	Stomach Mucosa	stomach
48	chr13:90028800-90032200	Weak transcription	NHEK	skin
49	chr13:90030000-90030200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr13:90030000-90030200	Enhancers	Stomach Mucosa	stomach

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