Variant report

Variant	nsv832672
Chromosome Location	chr13:87994963-88167897
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:283)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:21)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:88082864-88082918	K562	blood:	n/a	n/a
2	BHLHE40	chr13:88096440-88096715	GM12878	blood:	n/a	n/a
3	CEBPB	chr13:88166206-88166451	HepG2	liver:	n/a	chr13:88166294-88166307 chr13:88166294-88166305 chr13:88166296-88166307
4	CEBPB	chr13:87999921-87999953	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr13:88107751-88107960	HepG2	liver:	n/a	chr13:88107869-88107880
6	CEBPB	chr13:88094207-88094561	HepG2	liver:	n/a	chr13:88094372-88094383
7	CEBPB	chr13:88078861-88079143	H1-hESC	embryonic stem cell:	n/a	n/a
8	CEBPB	chr13:88094236-88094497	K562	blood:	n/a	chr13:88094372-88094383
9	CTCF	chr13:88009128-88009197	GM20000	blood:	n/a	n/a
10	CTCF	chr13:88048420-88048570	GM12867	blood:	n/a	n/a
11	CTCF	chr13:88050408-88050589	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr13:88020044-88020116	GM20000	blood:	n/a	n/a
13	CTCF	chr13:88050400-88050550	WERI-Rb-1	eye:	n/a	n/a
14	CTCF	chr13:88050360-88050510	RPTEC	kidney:	n/a	n/a
15	CTCF	chr13:88057280-88057430	RPTEC	kidney:	n/a	n/a
16	CTCF	chr13:88033720-88033870	NB4	blood:	n/a	n/a
17	CTCF	chr13:88050356-88050608	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr13:88050469-88050532	Medullo	brain:	n/a	n/a
19	CTCF	chr13:88050400-88050550	HAc	cerebellar:	n/a	n/a
20	CTCF	chr13:88008420-88008570	HEK293	kidney:	n/a	n/a
21	CTCF	chr13:88050400-88050550	RPTEC	kidney:	n/a	n/a
22	CTCF	chr13:88057250-88057450	GM12878	blood:	n/a	n/a
23	CTCF	chr13:88050456-88050519	Hela-S3	cervix:	n/a	n/a
24	CTCF	chr13:88018772-88018811	GM20000	blood:	n/a	n/a
25	CTCF	chr13:88112920-88113070	GM06990	blood:	n/a	n/a
26	CTCF	chr13:88050482-88050517	HepG2	liver:	n/a	n/a
27	CTCF	chr13:88151800-88151950	GM06990	blood:	n/a	n/a
28	CTCF	chr13:88050460-88050610	HBMEC	blood vessel:	n/a	n/a
29	E2F4	chr13:88151541-88151638	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr13:88022788-88022988	MCF10A-Er-Src	breast:	n/a	n/a
31	E2F4	chr13:88060491-88060691	MCF10A-Er-Src	breast:	n/a	n/a
32	E2F4	chr13:88107539-88107633	MCF10A-Er-Src	breast:	n/a	n/a
33	E2F4	chr13:88125345-88125541	MCF10A-Er-Src	breast:	n/a	n/a
34	E2F4	chr13:88007944-88008057	MCF10A-Er-Src	breast:	n/a	n/a
35	E2F4	chr13:88127724-88128291	MCF10A-Er-Src	breast:	n/a	n/a
36	E2F4	chr13:88092929-88093361	MCF10A-Er-Src	breast:	n/a	n/a
37	EBF1	chr13:88096403-88096631	GM12878	blood:	n/a	n/a
38	ELK1	chr13:88158985-88158999	Hela-S3	cervix:	n/a	n/a
39	EP300	chr13:88044835-88044852	GM12878	blood:	n/a	n/a
40	FOS	chr13:88007912-88007927	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr13:88008622-88008830	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr13:88008647-88008814	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr13:88008683-88008921	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr13:88008718-88008802	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr13:88007806-88008064	MCF10A-Er-Src	breast:	n/a	chr13:88008043-88008052
46	FOS	chr13:88111704-88112020	MCF10A-Er-Src	breast:	n/a	chr13:88111884-88111891 chr13:88111882-88111891 chr13:88111882-88111892 chr13:88111882-88111892
47	FOS	chr13:88012435-88012632	MCF10A-Er-Src	breast:	n/a	n/a
48	FOS	chr13:88151099-88151178	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr13:88111705-88112189	MCF10A-Er-Src	breast:	n/a	chr13:88111884-88111891 chr13:88111882-88111891 chr13:88111882-88111892 chr13:88111882-88111892
50	FOS	chr13:88007937-88008047	MCF10A-Er-Src	breast:	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	H1-hESC	embryonic stem cell:	embryo
2	chr13:88078884-88078934	HCF	heart:	n/a
3	chr13:88078884-88078934	Caco-2	colon:	n/a
4	chr13:88078884-88078934	RPTEC	kidney:	n/a
5	chr13:88078884-88078934	HEEpiC	esophagus:	n/a
6	chr13:88078884-88078934	HNPCEpiC	eye:	n/a
7	chr13:88078884-88078934	SKMC	muscle:	n/a
8	chr13:88078884-88078934	HCM	heart:	n/a
9	chr13:88078884-88078934	HRCEpiC	kidney:	n/a
10	chr13:88078884-88078934	Jurkat	blood:	n/a
11	chr13:88078884-88078934	Hepatocyte	liver:	n/a
12	chr13:88078884-88078934	AoSMC	blood vessel:	n/a
13	chr13:88078884-88078934	PANC-1	pancreas:	n/a
14	chr13:88078884-88078934	BJ	skin:	n/a
15	chr13:88078884-88078934	SAEC	small airway:	n/a
16	chr13:88078884-88078934	HRE	kidney:	n/a
17	chr13:88078884-88078934	U87	brain:	n/a
18	chr13:88078884-88078934	PrEC	prostate:	n/a
19	chr13:88078884-88078934	Hela-S3	cervix:	n/a
20	chr13:88078884-88078934	HCT-116	colon:	n/a
21	chr13:88078884-88078934	AG09309	skin:	n/a
22	chr13:88078884-88078934	SK-N-MC	brain:	n/a
23	chr13:88078884-88078934	HRPEpiC	eye:	n/a
24	chr13:88078884-88078934	GM19239	blood:	n/a
25	chr13:88078884-88078934	NB4	blood:	n/a
26	chr13:88078884-88078934	GM12892	blood:	n/a
27	chr13:88078884-88078934	NH-A	brain:	n/a
28	chr13:88078884-88078934	HAEpiC	amniotic membrane:	n/a
29	chr13:88078884-88078934	SK-N-SH	brain:	n/a
30	chr13:88078884-88078934	HEK293	kidney:	embryo
31	chr13:88078884-88078934	HUVEC	blood vessel:	n/a
32	chr13:88078884-88078934	GM12878	blood:	n/a
33	chr13:88078884-88078934	NHBE	bronchial:	n/a
34	chr13:88078884-88078934	HIPEpiC	eye:	n/a
35	chr13:88078884-88078934	GM06990	blood:	n/a
36	chr13:88078884-88078934	NHDF-neo	bronchial:	n/a
37	chr13:88078884-88078934	A549	lung:	n/a
38	chr13:88078884-88078934	HCPEpiC	choroid plexus:	n/a
39	chr13:88078884-88078934	K562	blood:	n/a
40	chr13:88078884-88078934	PFSK-1	brain:	n/a
41	chr13:88078884-88078934	SK-N-SH_RA	brain:	n/a
42	chr13:88078884-88078934	HL-60	blood:	n/a
43	chr13:88078884-88078934	HMEC	breast:	n/a
44	chr13:88078884-88078934	ProgFib	skin:	n/a
45	chr13:88078884-88078934	ovcar-3	ovarian:	n/a
46	chr13:88078884-88078934	BE2_C	brain:	n/a
47	chr13:88078884-88078934	AG04450	lung:	fetal
48	chr13:88078884-88078934	HPAEpiC	pulmonary alveolar:	n/a
49	chr13:88078884-88078934	AG09319	gingival:	n/a
50	chr13:88078884-88078934	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:88107156..88107790-chr5:66024900..66025639,2	MCF-7	breast:

(count:21 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-9	chr13:88099351-88099490	ENSG00000232636.2
2	lnc-SLITRK5-14	chr13:87995599-87995765	NONHSAT034585
3	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824
4	lnc-SLITRK6-9	chr13:88125695-88125808	ENSG00000228824
5	lnc-SLITRK6-9	chr13:88097266-88097385	ENSG00000232636.2
6	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000228824.2
7	lnc-SLITRK6-9	chr13:88163621-88163725	ENSG00000228824
8	lnc-SLITRK6-8	chr13:88079469-88079802	XLOC_010682
9	lnc-SLITRK6-9	chr13:88113179-88113224	XLOC_010683
10	lnc-SLITRK6-9	chr13:88079469-88079802	ENSG00000228824.2
11	lnc-SLITRK6-9	chr13:88113179-88113224	ENSG00000228824.2
12	lnc-SLITRK6-9	chr13:88163621-88163725	XLOC_010683
13	lnc-SLITRK6-8	chr13:88080353-88080528	XLOC_010682
14	lnc-SLITRK6-9	chr13:88113179-88113224	ENSG00000228824
15	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824.2
16	lnc-SLITRK6-9	chr13:88079455-88079802	ENSG00000232636.2
17	lnc-SLITRK6-9	chr13:88096242-88097385	XLOC_010683
18	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000232636.2
19	lnc-SLITRK6-9	chr13:88125695-88125808	XLOC_010683
20	lnc-SLITRK6-9	chr13:88099351-88099488	XLOC_010683
21	lnc-SLITRK6-9	chr13:88096247-88097385	ENSG00000228824

No data

Variant related genes	Relation type
ENSG00000232636	TF binding region
MIR4500HG	TF binding region
LIN28AP2	TF binding region
ENSG00000232636	CpG island
MIR4500HG	CpG island
LIN28AP2	CpG island
MIB1	miRNA target sites
DPF2	miRNA target sites
DENR	miRNA target sites
WARS2	miRNA target sites
SCD	miRNA target sites

Extended variants
information (count: 2432 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2432 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs185134857	chr13:87994964-87994965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs374436889	chr13:87995013-87995014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147826308	chr13:87995021-87995022	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs190811276	chr13:87995078-87995079	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs537961639	chr13:87995180-87995181	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs565159371	chr13:87995204-87995205	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs183448221	chr13:87995206-87995207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs574466739	chr13:87995212-87995213	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186717072	chr13:87995220-87995221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs556204204	chr13:87995223-87995224	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs115280824	chr13:87995255-87995256	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs73563761	chr13:87995271-87995272	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs72638078	chr13:87995346-87995347	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs564720859	chr13:87995361-87995362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531668749	chr13:87995441-87995442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs140352114	chr13:87995457-87995458	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs150382005	chr13:87995467-87995468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs550707279	chr13:87995487-87995488	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs374474643	chr13:87995489-87995490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs569784927	chr13:87995499-87995500	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs9556681	chr13:87995522-87995523	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs566608320	chr13:87995528-87995529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145157527	chr13:87995541-87995542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs529716906	chr13:87995558-87995559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191670418	chr13:87995581-87995582	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183457249	chr13:87995591-87995592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs569127279	chr13:87995625-87995626	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
28	rs546945270	chr13:87995626-87995627	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
29	rs375824984	chr13:87995628-87995629	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
30	rs548074064	chr13:87995630-87995631	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
31	rs369304550	chr13:87995638-87995639	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
32	rs568206244	chr13:87995665-87995666	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
33	rs188163504	chr13:87995666-87995667	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
34	rs9516826	chr13:87995701-87995702	Weak transcription	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs572618567	chr13:87995703-87995704	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
36	rs533629559	chr13:87995706-87995707	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
37	rs558198076	chr13:87995713-87995714	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
38	rs576213986	chr13:87995753-87995754	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
39	rs543650306	chr13:87995759-87995760	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
40	rs561844109	chr13:87995769-87995770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs9516827	chr13:87995798-87995799	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs138863949	chr13:87995847-87995848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570127740	chr13:87995856-87995857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533196911	chr13:87995866-87995867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs546379416	chr13:87995898-87995899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs191842065	chr13:87995904-87995905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs7332906	chr13:87995905-87995906	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs34128761	chr13:87995907-87995908	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs182247092	chr13:87995908-87995909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs186897655	chr13:87995943-87995944	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-small cell lung cancer	16651412	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:42 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87982200-87998600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:87993800-88005800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr13:87996200-87996800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr13:87996400-87996800	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chr13:87996400-87997000	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:87996600-87997000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
7	chr13:87996600-87997000	Enhancers	HMEC	breast
8	chr13:87996600-87997200	Enhancers	NHEK	skin
9	chr13:87996800-88005600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr13:87997200-87997800	Weak transcription	NHEK	skin
11	chr13:87997800-87998000	Enhancers	NHEK	skin
12	chr13:87998600-87999000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr13:87999000-88012600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:88005600-88006200	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chr13:88008600-88009000	Enhancers	NHEK	skin
16	chr13:88010800-88011400	Enhancers	Fetal Brain Female	brain
17	chr13:88012600-88013800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chr13:88013800-88014400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chr13:88014400-88015200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:88015200-88025000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:88020600-88021200	Active TSS	Hela-S3	cervix
22	chr13:88025000-88026200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:88026200-88038800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
24	chr13:88038400-88039200	Enhancers	Breast Myoepithelial Primary Cells	Breast
25	chr13:88056200-88056800	Enhancers	Liver	Liver
26	chr13:88059400-88060000	ZNF genes & repeats	Primary T helper memory cells from peripheral blood 1	blood
27	chr13:88060000-88062000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
28	chr13:88078400-88079600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr13:88078800-88080000	Enhancers	HUES48 Cell Line	embryonic stem cell
30	chr13:88079000-88079400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
31	chr13:88079000-88079400	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr13:88079000-88079800	Enhancers	HUES64 Cell Line	embryonic stem cell
33	chr13:88079000-88081000	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr13:88079200-88080000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chr13:88110800-88111400	Enhancers	HUVEC	blood vessel
36	chr13:88111400-88111800	Flanking Active TSS	HUVEC	blood vessel
37	chr13:88111800-88113200	Enhancers	HUVEC	blood vessel
38	chr13:88114000-88114400	Enhancers	iPS-20b Cell Line	embryonic stem cell
39	chr13:88162400-88162800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:88166800-88167400	Enhancers	iPS-20b Cell Line	embryonic stem cell
41	chr13:88167000-88167200	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr13:88167000-88167400	Enhancers	iPS-15b Cell Line	embryonic stem cell

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