Variant report

Variant	nsv428613
Chromosome Location	chr13:90012119-90165711
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:496)
CpG islands
(count:489)
Chromatin interactive
region (count:6)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:496 , 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	chr13:90053404-90053812	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:90023891-90023904	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr13:90117655-90117965	GM12878	blood:	n/a	chr13:90117764-90117775
4	CEBPB	chr13:90030123-90030303	A549	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
5	CEBPB	chr13:90053338-90053860	A549	lung:	n/a	chr13:90053581-90053592
6	CEBPB	chr13:90053390-90054036	A549	lung:	n/a	chr13:90053581-90053592
7	CEBPB	chr13:90127861-90128178	HepG2	liver:	n/a	chr13:90128018-90128029
8	CEBPB	chr13:90127859-90128113	Hela-S3	cervix:	n/a	chr13:90128018-90128029
9	CEBPB	chr13:90110164-90110667	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr13:90076016-90076314	HepG2	liver:	n/a	n/a
11	CEBPB	chr13:90061199-90061485	A549	lung:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
12	CEBPB	chr13:90053451-90053803	HepG2	liver:	n/a	chr13:90053581-90053592
13	CEBPB	chr13:90053319-90053891	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
14	CEBPB	chr13:90053432-90053763	MCF-7	breast:	n/a	chr13:90053581-90053592
15	CEBPB	chr13:90053368-90054010	Hela-S3	cervix:	n/a	chr13:90053581-90053592
16	CEBPB	chr13:90032305-90032917	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr13:90053471-90053879	HCT-116	colon:	n/a	chr13:90053581-90053592
18	CEBPB	chr13:90053490-90053648	K562	blood:	n/a	chr13:90053581-90053592
19	CEBPB	chr13:90053399-90053954	IMR90	lung:	n/a	chr13:90053581-90053592
20	CEBPB	chr13:90046959-90047120	HepG2	liver:	n/a	n/a
21	CEBPB	chr13:90120635-90120885	H1-hESC	embryonic stem cell:	n/a	chr13:90120722-90120733
22	CEBPB	chr13:90120640-90120770	K562	blood:	n/a	chr13:90120722-90120733
23	CEBPB	chr13:90120558-90120849	A549	lung:	n/a	chr13:90120722-90120733
24	CEBPB	chr13:90053216-90053959	A549	lung:	n/a	chr13:90053581-90053592
25	CEBPB	chr13:90076020-90076326	IMR90	lung:	n/a	n/a
26	CEBPB	chr13:90110184-90110994	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr13:90061206-90061460	HepG2	liver:	n/a	chr13:90061301-90061312 chr13:90061341-90061352
28	CEBPB	chr13:90030039-90030322	IMR90	lung:	n/a	chr13:90030207-90030224 chr13:90030208-90030221 chr13:90030208-90030219
29	CEBPB	chr13:90032305-90032732	ECC-1	luminal epithelium:	n/a	n/a
30	CEBPB	chr13:90127850-90128161	IMR90	lung:	n/a	chr13:90128018-90128029
31	CEBPB	chr13:90120562-90120885	HepG2	liver:	n/a	chr13:90120722-90120733
32	CEBPB	chr13:90032530-90032817	A549	lung:	n/a	n/a
33	CEBPB	chr13:90032538-90032854	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr13:90053453-90053969	H1-hESC	embryonic stem cell:	n/a	chr13:90053581-90053592
35	CEBPB	chr13:90127840-90128138	A549	lung:	n/a	chr13:90128018-90128029
36	CEBPB	chr13:90120552-90120888	IMR90	lung:	n/a	chr13:90120722-90120733
37	CEBPB	chr13:90053370-90053798	ECC-1	luminal epithelium:	n/a	chr13:90053581-90053592
38	CEBPB	chr13:90016763-90017043	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr13:90110265-90110690	ECC-1	luminal epithelium:	n/a	n/a
40	CTCF	chr13:90014300-90014450	HA-sp	spinal cord:	n/a	n/a
41	CTCF	chr13:90086960-90087110	AG09319	gingival:	n/a	n/a
42	CTCF	chr13:90014260-90014410	WERI-Rb-1	eye:	n/a	n/a
43	CTCF	chr13:90014240-90014390	HEK293	kidney:	n/a	n/a
44	CTCF	chr13:90087000-90087150	A549	lung:	n/a	n/a
45	CTCF	chr13:90014240-90014390	Hela-S3	cervix:	n/a	n/a
46	CTCF	chr13:90087000-90087150	MCF-7	breast:	n/a	n/a
47	CTCF	chr13:90087073-90087104	LNCaP	prostate:	n/a	n/a
48	CTCF	chr13:90017273-90017330	Hela-S3	cervix:	n/a	n/a
49	CTCF	chr13:90086940-90087090	SAEC	small airway:	n/a	n/a
50	CTCF	chr13:90014280-90014430	HRPEpiC	eye:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:90014513-90014563	HCT-116	colon:	n/a
2	chr13:90014513-90014563	HCT-116	colon:	n/a
3	chr13:90015633-90015683	LNCaP	prostate:	n/a
4	chr13:90045847-90045897	Hepatocyte	liver:	n/a
5	chr13:90015774-90015824	BJ	skin:	n/a
6	chr13:90015774-90015824	MCF-7	breast:	n/a
7	chr13:90045847-90045897	HRE	kidney:	n/a
8	chr13:90015518-90015568	ECC-1	luminal epithelium:	n/a
9	chr13:90053523-90053573	Caco-2	colon:	n/a
10	chr13:90015774-90015824	GM06990	blood:	n/a
11	chr13:90015633-90015683	NT2-D1	testis:	n/a
12	chr13:90015912-90015962	HRE	kidney:	n/a
13	chr13:90045847-90045897	HAEpiC	amniotic membrane:	n/a
14	chr13:90015912-90015962	HMEC	breast:	n/a
15	chr13:90015633-90015683	CMK	blood:	n/a
16	chr13:90015912-90015962	PrEC	prostate:	n/a
17	chr13:90014813-90014863	AG09309	skin:	n/a
18	chr13:90015518-90015568	NB4	blood:	n/a
19	chr13:90015518-90015568	HMEC	breast:	n/a
20	chr13:90015912-90015962	HCT-116	colon:	n/a
21	chr13:90015633-90015683	SAEC	small airway:	n/a
22	chr13:90053523-90053573	HCT-116	colon:	n/a
23	chr13:90015774-90015824	MCF10A-Er-Src	breast:	n/a
24	chr13:90053523-90053573	HCM	heart:	n/a
25	chr13:90014813-90014863	HRPEpiC	eye:	n/a
26	chr13:90045847-90045897	HPAEpiC	pulmonary alveolar:	n/a
27	chr13:90015518-90015568	AoSMC	blood vessel:	n/a
28	chr13:90015774-90015824	CMK	blood:	n/a
29	chr13:90045847-90045897	NHDF-neo	bronchial:	n/a
30	chr13:90015912-90015962	HUVEC	blood vessel:	n/a
31	chr13:90014513-90014563	HEK293	kidney:	embryo
32	chr13:90014813-90014863	SK-N-MC	brain:	n/a
33	chr13:90014813-90014863	HCM	heart:	n/a
34	chr13:90015633-90015683	A549	lung:	n/a
35	chr13:90014813-90014863	HL-60	blood:	n/a
36	chr13:90053523-90053573	PANC-1	pancreas:	n/a
37	chr13:90053523-90053573	CMK	blood:	n/a
38	chr13:90015518-90015568	HCF	heart:	n/a
39	chr13:90053523-90053573	GM12891	blood:	n/a
40	chr13:90015518-90015568	GM12892	blood:	n/a
41	chr13:90045847-90045897	HEK293	kidney:	embryo
42	chr13:90014813-90014863	AG04450	lung:	fetal
43	chr13:90014513-90014563	SAEC	small airway:	n/a
44	chr13:90015774-90015824	H1-hESC	embryonic stem cell:	embryo
45	chr13:90045847-90045897	CMK	blood:	n/a
46	chr13:90045847-90045897	Hela-S3	cervix:	n/a
47	chr13:90015633-90015683	HCM	heart:	n/a
48	chr13:90015518-90015568	BE2_C	brain:	n/a
49	chr13:90014513-90014563	AG10803	skin:	n/a
50	chr13:90015774-90015824	HepG2	liver:	n/a

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

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

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-11	chr13:90152628-90152763	XLOC_010685
2	lnc-SLITRK6-11	chr13:90129862-90130391	XLOC_010685

No data

Variant related genes	Relation type
SP3P	TF binding region
LINC01040	TF binding region
SP3P	CpG island
LINC01040	CpG island
ENSG00000225530	chromatin interactions

Extended variants
information (count: 3515 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:3515 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544648094	chr13:90014808-90014809	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs111560791	chr13:90014829-90014830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113937138	chr13:90014894-90014895	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs530005912	chr13:90014895-90014896	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs9560297	chr13:90014942-90014943	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs530291681	chr13:90014974-90014975	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs185386893	chr13:90014984-90014985	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs527962394	chr13:90015006-90015007	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs552535511	chr13:90015019-90015020	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs571019821	chr13:90015052-90015053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs537544803	chr13:90015056-90015057	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs114236835	chr13:90015062-90015063	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568078508	chr13:90015068-90015069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs535411693	chr13:90015094-90015095	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs149269620	chr13:90015111-90015112	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs190282821	chr13:90015136-90015137	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566021717	chr13:90015162-90015163	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539742357	chr13:90015174-90015175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs377580354	chr13:90015180-90015181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs576149717	chr13:90015196-90015197	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs544397812	chr13:90015234-90015235	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs138269901	chr13:90015243-90015244	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs574572873	chr13:90015261-90015262	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs117103612	chr13:90015262-90015263	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs3803211	chr13:90015292-90015293	Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528021941	chr13:90015346-90015347	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs56276451	chr13:90015378-90015379	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546426698	chr13:90015380-90015381	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs564534309	chr13:90015435-90015436	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs531899626	chr13:90015461-90015462	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs534335702	chr13:90015463-90015464	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs113063038	chr13:90015470-90015471	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568188433	chr13:90015500-90015501	Active TSS Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs2348563	chr13:90015578-90015579	Active TSS Weak transcription	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs547463965	chr13:90015601-90015602	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs9560298	chr13:90015602-90015603	Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs181539361	chr13:90015615-90015616	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs557999923	chr13:90015616-90015617	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs569775322	chr13:90015620-90015621	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs184154242	chr13:90015676-90015677	Active TSS Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
41	rs555258213	chr13:90015677-90015678	Active TSS Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
42	rs574631632	chr13:90015715-90015716	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs541914688	chr13:90015737-90015738	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs71444034	chr13:90015802-90015803	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
45	rs537240171	chr13:90015808-90015809	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a
46	rs188460743	chr13:90015840-90015841	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs371086982	chr13:90015873-90015874	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs572065846	chr13:90015888-90015889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs546195527	chr13:90015893-90015894	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs564773380	chr13:90015960-90015961	Weak transcription	CpG island	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

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
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
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
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

Chromatin state (count:216 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:90014800-90015600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:90015200-90015800	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr13:90015600-90015800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr13:90015800-90016000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr13:90015800-90017000	Weak transcription	HUES6 Cell Line	embryonic stem cell
6	chr13:90016600-90017200	Enhancers	HUES64 Cell Line	embryonic stem cell
7	chr13:90016600-90017600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr13:90016800-90017400	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:90016800-90017400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr13:90017000-90017200	Enhancers	iPS-15b Cell Line	embryonic stem cell
11	chr13:90017000-90017400	Enhancers	ES-I3 Cell Line	embryonic stem cell
12	chr13:90017000-90017400	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chr13:90017000-90017400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
14	chr13:90023400-90023800	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
15	chr13:90023800-90025400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:90027400-90028200	Enhancers	Fetal Muscle Leg	muscle
17	chr13:90027600-90028800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr13:90027600-90028800	Enhancers	HUVEC	blood vessel
19	chr13:90027600-90029000	Enhancers	Fetal Lung	lung
20	chr13:90027800-90028200	Enhancers	Adipose Nuclei	Adipose
21	chr13:90027800-90028400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr13:90027800-90028600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr13:90027800-90028600	Enhancers	Fetal Heart	heart
24	chr13:90027800-90028600	Enhancers	Fetal Stomach	stomach
25	chr13:90027800-90028800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:90027800-90028800	Enhancers	Muscle Satellite Cultured Cells	--
27	chr13:90027800-90028800	Enhancers	Stomach Mucosa	stomach
28	chr13:90028000-90028400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr13:90028000-90028400	Enhancers	Fetal Brain Male	brain
30	chr13:90028000-90028600	Enhancers	Colon Smooth Muscle	Colon
31	chr13:90028200-90028800	Enhancers	NHEK	skin
32	chr13:90028400-90032200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
33	chr13:90028400-90032600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr13:90028800-90029800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr13:90028800-90030000	Weak transcription	Stomach Mucosa	stomach
36	chr13:90028800-90032200	Weak transcription	NHEK	skin
37	chr13:90030000-90030200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr13:90030000-90030200	Enhancers	Stomach Mucosa	stomach
39	chr13:90030200-90031000	Weak transcription	Stomach Mucosa	stomach
40	chr13:90030400-90031000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr13:90030400-90032800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:90031000-90031200	Enhancers	Stomach Mucosa	stomach
43	chr13:90031000-90031800	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr13:90031200-90031600	Enhancers	Gastric	stomach
45	chr13:90031200-90032400	Weak transcription	Stomach Mucosa	stomach
46	chr13:90031600-90032600	Weak transcription	Gastric	stomach
47	chr13:90032200-90033000	Enhancers	NHEK	skin
48	chr13:90032200-90033200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr13:90032200-90033200	Enhancers	HMEC	breast
50	chr13:90032400-90032800	Enhancers	Rectal Mucosa Donor 31	rectum

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