Variant report

Variant	nsv916254
Chromosome Location	chr13:87856806-88107725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:800)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:800 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:87926603-87926746	HepG2	liver:	n/a	n/a
2	ATF1	chr13:87903804-87903961	K562	blood:	n/a	n/a
3	BACH1	chr13:88082864-88082918	K562	blood:	n/a	n/a
4	BHLHE40	chr13:88096440-88096715	GM12878	blood:	n/a	n/a
5	BRCA1	chr13:87911751-87912117	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr13:88094207-88094561	HepG2	liver:	n/a	chr13:88094372-88094383
7	CEBPB	chr13:87983347-87983899	ECC-1	luminal epithelium:	n/a	n/a
8	CEBPB	chr13:87880991-87881211	HepG2	liver:	n/a	n/a
9	CEBPB	chr13:87881000-87881207	A549	lung:	n/a	n/a
10	CEBPB	chr13:87908933-87909138	HepG2	liver:	n/a	chr13:87909081-87909092
11	CEBPB	chr13:88078861-88079143	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:87983468-87983781	MCF-7	breast:	n/a	n/a
13	CEBPB	chr13:87983437-87983881	ECC-1	luminal epithelium:	n/a	n/a
14	CEBPB	chr13:87983437-87983890	MCF-7	breast:	n/a	n/a
15	CEBPB	chr13:88094236-88094497	K562	blood:	n/a	chr13:88094372-88094383
16	CEBPB	chr13:87904726-87904869	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:87983487-87983786	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:87999921-87999953	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr13:87983456-87983815	Hela-S3	cervix:	n/a	n/a
20	CHD2	chr13:87911858-87912006	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr13:87911769-87911864	H1-hESC	embryonic stem cell:	n/a	n/a
22	CTCF	chr13:87932520-87932670	MCF-7	breast:	n/a	chr13:87932586-87932602 chr13:87932585-87932603 chr13:87932587-87932608
23	CTCF	chr13:87887560-87887710	HAc	cerebellar:	n/a	n/a
24	CTCF	chr13:87926554-87926737	NHEK	skin:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
25	CTCF	chr13:87911860-87912010	NB4	blood:	n/a	n/a
26	CTCF	chr13:87911820-87911970	HCM	heart:	n/a	n/a
27	CTCF	chr13:87926520-87926670	HA-sp	spinal cord:	n/a	n/a
28	CTCF	chr13:87911840-87911990	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr13:87972937-87972965	GM10266	blood:	n/a	n/a
30	CTCF	chr13:87926615-87926756	GM20000	blood:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
31	CTCF	chr13:87911840-87911990	AoAF	blood vessel:	n/a	n/a
32	CTCF	chr13:88018772-88018811	GM20000	blood:	n/a	n/a
33	CTCF	chr13:88057250-88057450	GM12878	blood:	n/a	n/a
34	CTCF	chr13:87887460-87887610	HBMEC	blood vessel:	n/a	n/a
35	CTCF	chr13:87911780-87911930	HPAF	blood vessel:	n/a	n/a
36	CTCF	chr13:87932500-87932650	HCT-116	colon:	n/a	chr13:87932586-87932602 chr13:87932585-87932603 chr13:87932587-87932608
37	CTCF	chr13:87926520-87926670	NHDF-neo	bronchial:	n/a	n/a
38	CTCF	chr13:87932540-87932690	HBMEC	blood vessel:	n/a	chr13:87932586-87932602 chr13:87932585-87932603 chr13:87932587-87932608
39	CTCF	chr13:87911760-87911910	HVMF	connective:	n/a	n/a
40	CTCF	chr13:87926555-87926734	A549	lung:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
41	CTCF	chr13:87926580-87926730	HepG2	liver:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
42	CTCF	chr13:87911840-87911990	HepG2	liver:	n/a	n/a
43	CTCF	chr13:87926461-87926775	A549	lung:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
44	CTCF	chr13:87911830-87911952	HepG2	liver:	n/a	n/a
45	CTCF	chr13:87985320-87985470	GM12866	blood:	n/a	n/a
46	CTCF	chr13:87926465-87926894	HepG2	liver:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
47	CTCF	chr13:87911760-87911910	HAc	cerebellar:	n/a	n/a
48	CTCF	chr13:87926500-87926650	HVMF	connective:	n/a	n/a
49	CTCF	chr13:88020044-88020116	GM20000	blood:	n/a	n/a
50	CTCF	chr13:87911800-87911995	NHEK	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:88078884-88078934	AG10803	skin:	n/a
2	chr13:88078884-88078934	AG04449	skin:	fetal
3	chr13:88078884-88078934	H1-hESC	embryonic stem cell:	embryo
4	chr13:88078884-88078934	ECC-1	luminal epithelium:	n/a
5	chr13:88078884-88078934	HRPEpiC	eye:	n/a
6	chr13:88078884-88078934	HEEpiC	esophagus:	n/a
7	chr13:88078884-88078934	HRCEpiC	kidney:	n/a
8	chr13:88078884-88078934	AG09309	skin:	n/a
9	chr13:88078884-88078934	BE2_C	brain:	n/a
10	chr13:88078884-88078934	HRE	kidney:	n/a
11	chr13:88078884-88078934	HL-60	blood:	n/a
12	chr13:88078884-88078934	NT2-D1	testis:	n/a
13	chr13:88078884-88078934	HUVEC	blood vessel:	n/a
14	chr13:88078884-88078934	GM06990	blood:	n/a
15	chr13:88078884-88078934	A549	lung:	n/a
16	chr13:88078884-88078934	PFSK-1	brain:	n/a
17	chr13:88078884-88078934	SK-N-SH_RA	brain:	n/a
18	chr13:88078884-88078934	HCPEpiC	choroid plexus:	n/a
19	chr13:88078884-88078934	GM12891	blood:	n/a
20	chr13:88078884-88078934	HPAEpiC	pulmonary alveolar:	n/a
21	chr13:88078884-88078934	HNPCEpiC	eye:	n/a
22	chr13:88078884-88078934	HCT-116	colon:	n/a
23	chr13:88078884-88078934	SAEC	small airway:	n/a
24	chr13:88078884-88078934	HMEC	breast:	n/a
25	chr13:88078884-88078934	NHBE	bronchial:	n/a
26	chr13:88078884-88078934	AoSMC	blood vessel:	n/a
27	chr13:88078884-88078934	HCM	heart:	n/a
28	chr13:88078884-88078934	Jurkat	blood:	n/a
29	chr13:88078884-88078934	RPTEC	kidney:	n/a
30	chr13:88078884-88078934	GM12878	blood:	n/a
31	chr13:88078884-88078934	ProgFib	skin:	n/a
32	chr13:88078884-88078934	SKMC	muscle:	n/a
33	chr13:88078884-88078934	T-47D	breast:	n/a
34	chr13:88078884-88078934	SK-N-SH	brain:	n/a
35	chr13:88078884-88078934	NH-A	brain:	n/a
36	chr13:88078884-88078934	Hela-S3	cervix:	n/a
37	chr13:88078884-88078934	IMR90	lung:	fetal
38	chr13:88078884-88078934	U87	brain:	n/a
39	chr13:88078884-88078934	CMK	blood:	n/a
40	chr13:88078884-88078934	GM12892	blood:	n/a
41	chr13:88078884-88078934	NHDF-neo	bronchial:	n/a
42	chr13:88078884-88078934	Caco-2	colon:	n/a
43	chr13:88078884-88078934	K562	blood:	n/a
44	chr13:88078884-88078934	HAEpiC	amniotic membrane:	n/a
45	chr13:88078884-88078934	NB4	blood:	n/a
46	chr13:88078884-88078934	AG04450	lung:	fetal
47	chr13:88078884-88078934	LNCaP	prostate:	n/a
48	chr13:88078884-88078934	HEK293	kidney:	embryo
49	chr13:88078884-88078934	ovcar-3	ovarian:	n/a
50	chr13:88078884-88078934	AG09319	gingival:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:87944988..87946530-chr13:87947239..87950149,2	MCF-7	breast:
2	chr13:87911563..87912249-chr13:88321695..88322217,2	MCF-7	breast:
3	chr13:86659949..86660780-chr13:87926156..87926672,2	MCF-7	breast:
4	chr13:87522311..87523294-chr13:87926162..87927045,5	MCF-7	breast:
5	chr13:87863872..87866433-chr13:87868902..87871110,2	MCF-7	breast:
6	chr13:87863872..87866433-chr13:87868902..87871110,2	MCF-7	breast:
7	chr13:86660097..86660644-chr13:87926317..87926878,2	MCF-7	breast:
8	chr13:88107156..88107790-chr5:66024900..66025639,2	MCF-7	breast:
9	chr13:87219147..87219853-chr13:87926507..87927098,2	MCF-7	breast:
10	chr13:87944988..87946530-chr13:87947239..87950149,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-9	chr13:88079469-88079802	ENSG00000228824.2
2	lnc-SLITRK6-9	chr13:88097266-88097385	ENSG00000232636.2
3	lnc-SLITRK5-14	chr13:87992526-87992762	NONHSAT034584
4	lnc-SLITRK5-14	chr13:87992541-87992680	NONHSAT034585
5	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000228824.2
6	lnc-SLITRK6-9	chr13:88099351-88099490	ENSG00000232636.2
7	lnc-SLITRK6-9	chr13:88079455-88079802	ENSG00000232636.2
8	lnc-SLITRK6-9	chr13:88096242-88097385	XLOC_010683
9	lnc-SLITRK6-9	chr13:88099351-88099488	XLOC_010683
10	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000232636.2
11	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824.2
12	lnc-SLITRK5-14	chr13:87992158-87992228	NONHSAT034584
13	lnc-SLITRK6-8	chr13:88079469-88079802	XLOC_010682
14	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824
15	lnc-SLITRK6-8	chr13:88080353-88080528	XLOC_010682
16	lnc-SLITRK6-9	chr13:88096247-88097385	ENSG00000228824
17	lnc-SLITRK5-14	chr13:87991120-87991699	NONHSAT034584
18	lnc-SLITRK5-14	chr13:87995599-87995765	NONHSAT034585

No data

Variant related genes	Relation type
LIN28AP2	TF binding region
ENSG00000232636	TF binding region
UBBP5	TF binding region
LIN28AP2	CpG island
ENSG00000232636	CpG island
UBBP5	CpG island
DENR	miRNA target sites
WARS2	miRNA target sites

Extended variants
information (count: 5010 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:5010 , 50 per page) page: 1 2 3 4 5 6 7 ... 101

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192347376	chr13:87856824-87856825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs563194603	chr13:87856858-87856859	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs74103295	chr13:87856919-87856920	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs527978246	chr13:87856926-87856927	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs74103296	chr13:87856971-87856972	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs183311865	chr13:87856990-87856991	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs574232914	chr13:87856996-87856997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs528106423	chr13:87857039-87857040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs144255068	chr13:87857044-87857045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59046442	chr13:87857054-87857055	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs538809890	chr13:87857055-87857056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs74103297	chr13:87857057-87857058	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs569397626	chr13:87857066-87857067	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs116422339	chr13:87857098-87857099	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187522529	chr13:87857116-87857117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs539056659	chr13:87857120-87857121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542272129	chr13:87857154-87857155	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs559270563	chr13:87857166-87857167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191642873	chr13:87857192-87857193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs573158263	chr13:87857320-87857321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs531853689	chr13:87857445-87857446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs147800043	chr13:87857528-87857529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148860588	chr13:87857543-87857544	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs184313059	chr13:87857547-87857548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs73560696	chr13:87857565-87857566	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs545361982	chr13:87857684-87857685	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs186779860	chr13:87857710-87857711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs73560700	chr13:87857777-87857778	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs542689080	chr13:87857799-87857800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs560833562	chr13:87857824-87857825	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs142614830	chr13:87857825-87857826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs546199243	chr13:87857839-87857840	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564581454	chr13:87857856-87857857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs74927905	chr13:87857857-87857858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192435088	chr13:87857867-87857868	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs150991011	chr13:87857901-87857902	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185630536	chr13:87857937-87857938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs34339051	chr13:87857960-87857961	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs4511400	chr13:87858082-87858083	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs548635799	chr13:87858083-87858084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs115339187	chr13:87858087-87858088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs4553471	chr13:87858107-87858108	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs528068428	chr13:87858110-87858111	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs190248722	chr13:87858116-87858117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs577357180	chr13:87858117-87858118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535882606	chr13:87858208-87858209	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs538911091	chr13:87858218-87858219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557006880	chr13:87858230-87858231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140875081	chr13:87858257-87858258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs547757155	chr13:87858262-87858263	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
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
Myelofibrosis	22110671	CNVD
Gastric adenocarcinoma	19115996	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Mental retardation	17847001	CNVD
Medulloblastoma	19270706	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-small cell lung cancer	16651412	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD

Chromatin state (count:114 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87848400-87859400	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chr13:87854400-87858400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:87858400-87858600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:87858600-87860000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chr13:87859200-87861000	Weak transcription	Pancreas	Pancrea
6	chr13:87859400-87860200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chr13:87859600-87860000	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chr13:87859800-87860400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr13:87859800-87860400	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr13:87860000-87860400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chr13:87860400-87863600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
12	chr13:87860400-87875600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr13:87861000-87861200	ZNF genes & repeats	Pancreas	Pancrea
14	chr13:87863600-87864000	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr13:87869000-87869600	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr13:87869400-87869600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:87869600-87870600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr13:87869800-87871200	Weak transcription	HUES48 Cell Line	embryonic stem cell
19	chr13:87870200-87870400	Enhancers	HUES64 Cell Line	embryonic stem cell
20	chr13:87870400-87870800	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr13:87870400-87871400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr13:87870600-87871600	Enhancers	ES-I3 Cell Line	embryonic stem cell
23	chr13:87870800-87871200	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chr13:87871200-87871400	Enhancers	HUES6 Cell Line	embryonic stem cell
25	chr13:87871200-87871600	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chr13:87871200-87871800	Enhancers	HUES48 Cell Line	embryonic stem cell
27	chr13:87871200-87871800	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chr13:87871400-87871800	Genic enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:87871400-87871800	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chr13:87871800-87872600	Weak transcription	HUES6 Cell Line	embryonic stem cell
31	chr13:87875600-87876800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
32	chr13:87875600-87878200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chr13:87876800-87880200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:87880200-87881600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:87881600-87883600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chr13:87883600-87886000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
37	chr13:87886000-87907600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:87886400-87888400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr13:87886600-87887800	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr13:87887000-87888000	Enhancers	NH-A	brain
41	chr13:87887000-87888200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chr13:87887200-87887400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr13:87887400-87887800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
44	chr13:87894000-87894400	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr13:87894400-87896400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
46	chr13:87896200-87897200	Enhancers	Primary hematopoietic stem cells	blood
47	chr13:87896400-87896800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chr13:87896400-87897000	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr13:87896400-87897000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
50	chr13:87896400-87897400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--

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