Variant report

Variant	nsv1043448
Chromosome Location	chr13:87835419-88140970
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:865)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:25)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:865 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

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	chr13:87881000-87881207	A549	lung:	n/a	n/a
7	CEBPB	chr13:88094207-88094561	HepG2	liver:	n/a	chr13:88094372-88094383
8	CEBPB	chr13:88094236-88094497	K562	blood:	n/a	chr13:88094372-88094383
9	CEBPB	chr13:87983437-87983881	ECC-1	luminal epithelium:	n/a	n/a
10	CEBPB	chr13:87983456-87983815	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr13:88107751-88107960	HepG2	liver:	n/a	chr13:88107869-88107880
12	CEBPB	chr13:87983437-87983890	MCF-7	breast:	n/a	n/a
13	CEBPB	chr13:87880991-87881211	HepG2	liver:	n/a	n/a
14	CEBPB	chr13:87983468-87983781	MCF-7	breast:	n/a	n/a
15	CEBPB	chr13:87999921-87999953	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr13:87983347-87983899	ECC-1	luminal epithelium:	n/a	n/a
17	CEBPB	chr13:87983487-87983786	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:87908933-87909138	HepG2	liver:	n/a	chr13:87909081-87909092
19	CEBPB	chr13:88078861-88079143	H1-hESC	embryonic stem cell:	n/a	n/a
20	CEBPB	chr13:87904726-87904869	HepG2	liver:	n/a	n/a
21	CHD2	chr13:87911769-87911864	H1-hESC	embryonic stem cell:	n/a	n/a
22	CHD2	chr13:87911858-87912006	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr13:87926600-87926750	NHEK	skin:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
24	CTCF	chr13:87926640-87926790	GM12867	blood:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
25	CTCF	chr13:87911840-87911990	HBMEC	blood vessel:	n/a	n/a
26	CTCF	chr13:87926559-87926781	LNCaP	prostate:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
27	CTCF	chr13:87926528-87926784	HUVEC	blood vessel:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
28	CTCF	chr13:87926571-87926750	K562	blood:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
29	CTCF	chr13:87926520-87926670	GM12872	blood:	n/a	n/a
30	CTCF	chr13:87911880-87912030	NHLF	lung:	n/a	n/a
31	CTCF	chr13:87911700-87911850	WI-38	lung:	n/a	n/a
32	CTCF	chr13:87926620-87926770	NB4	blood:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
33	CTCF	chr13:87932520-87932670	MCF-7	breast:	n/a	chr13:87932586-87932602 chr13:87932585-87932603 chr13:87932587-87932608
34	CTCF	chr13:87926562-87926775	Pancreas_OC	pancreas:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
35	CTCF	chr13:87926540-87926690	GM12864	blood:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
36	CTCF	chr13:87926580-87926730	HCPEpiC	choroid plexus:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
37	CTCF	chr13:87887460-87887610	HCPEpiC	choroid plexus:	n/a	n/a
38	CTCF	chr13:87911840-87911990	HMF	breast:	n/a	n/a
39	CTCF	chr13:87926600-87926750	HEEpiC	esophagus:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
40	CTCF	chr13:87932520-87932670	NB4	blood:	n/a	chr13:87932586-87932602 chr13:87932585-87932603 chr13:87932587-87932608
41	CTCF	chr13:87932500-87932650	HCT-116	colon:	n/a	chr13:87932586-87932602 chr13:87932585-87932603 chr13:87932587-87932608
42	CTCF	chr13:87911750-87912095	HepG2	liver:	n/a	n/a
43	CTCF	chr13:87911820-87911970	HRE	kidney:	n/a	n/a
44	CTCF	chr13:87911800-87911950	AG04450	lung:	n/a	n/a
45	CTCF	chr13:87926580-87926730	HEK293	kidney:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
46	CTCF	chr13:87932480-87932630	HL-60	blood:	n/a	chr13:87932586-87932602 chr13:87932585-87932603 chr13:87932587-87932608
47	CTCF	chr13:87887420-87887570	HA-sp	spinal cord:	n/a	n/a
48	CTCF	chr13:87926533-87926825	ECC-1	luminal epithelium:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
49	CTCF	chr13:87926560-87926710	HUVEC	blood vessel:	n/a	chr13:87926662-87926672 chr13:87926661-87926674
50	CTCF	chr13:88050400-88050550	HAc	cerebellar:	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	AG04449	skin:	fetal
2	chr13:88078884-88078934	AG10803	skin:	n/a
3	chr13:88078884-88078934	RPTEC	kidney:	n/a
4	chr13:88078884-88078934	HMEC	breast:	n/a
5	chr13:88078884-88078934	HIPEpiC	eye:	n/a
6	chr13:88078884-88078934	IMR90	lung:	fetal
7	chr13:88078884-88078934	SK-N-SH_RA	brain:	n/a
8	chr13:88078884-88078934	HL-60	blood:	n/a
9	chr13:88078884-88078934	BJ	skin:	n/a
10	chr13:88078884-88078934	HRE	kidney:	n/a
11	chr13:88078884-88078934	ProgFib	skin:	n/a
12	chr13:88078884-88078934	HCM	heart:	n/a
13	chr13:88078884-88078934	ECC-1	luminal epithelium:	n/a
14	chr13:88078884-88078934	AG09309	skin:	n/a
15	chr13:88078884-88078934	GM19239	blood:	n/a
16	chr13:88078884-88078934	GM12891	blood:	n/a
17	chr13:88078884-88078934	U87	brain:	n/a
18	chr13:88078884-88078934	PFSK-1	brain:	n/a
19	chr13:88078884-88078934	LNCaP	prostate:	n/a
20	chr13:88078884-88078934	Hela-S3	cervix:	n/a
21	chr13:88078884-88078934	HEEpiC	esophagus:	n/a
22	chr13:88078884-88078934	T-47D	breast:	n/a
23	chr13:88078884-88078934	SK-N-MC	brain:	n/a
24	chr13:88078884-88078934	H1-hESC	embryonic stem cell:	embryo
25	chr13:88078884-88078934	AoSMC	blood vessel:	n/a
26	chr13:88078884-88078934	PANC-1	pancreas:	n/a
27	chr13:88078884-88078934	HUVEC	blood vessel:	n/a
28	chr13:88078884-88078934	SK-N-SH	brain:	n/a
29	chr13:88078884-88078934	NB4	blood:	n/a
30	chr13:88078884-88078934	HRPEpiC	eye:	n/a
31	chr13:88078884-88078934	GM06990	blood:	n/a
32	chr13:88078884-88078934	MCF-7	breast:	n/a
33	chr13:88078884-88078934	MCF10A-Er-Src	breast:	n/a
34	chr13:88078884-88078934	CMK	blood:	n/a
35	chr13:88078884-88078934	AG09319	gingival:	n/a
36	chr13:88078884-88078934	GM12892	blood:	n/a
37	chr13:88078884-88078934	HepG2	liver:	n/a
38	chr13:88078884-88078934	K562	blood:	n/a
39	chr13:88078884-88078934	Hepatocyte	liver:	n/a
40	chr13:88078884-88078934	HAEpiC	amniotic membrane:	n/a
41	chr13:88078884-88078934	BE2_C	brain:	n/a
42	chr13:88078884-88078934	HCF	heart:	n/a
43	chr13:88078884-88078934	NT2-D1	testis:	n/a
44	chr13:88078884-88078934	Jurkat	blood:	n/a
45	chr13:88078884-88078934	NHDF-neo	bronchial:	n/a
46	chr13:88078884-88078934	SAEC	small airway:	n/a
47	chr13:88078884-88078934	Caco-2	colon:	n/a
48	chr13:88078884-88078934	A549	lung:	n/a
49	chr13:88078884-88078934	HNPCEpiC	eye:	n/a
50	chr13:88078884-88078934	SKMC	muscle:	n/a

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

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

(count:25 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-9	chr13:88079455-88079802	ENSG00000232636.2
2	lnc-SLITRK6-9	chr13:88125695-88125808	XLOC_010683
3	lnc-SLITRK5-14	chr13:87992158-87992228	NONHSAT034584
4	lnc-SLITRK6-9	chr13:88113179-88113224	ENSG00000228824.2
5	lnc-SLITRK6-9	chr13:88096242-88097385	XLOC_010683
6	lnc-SLITRK6-9	chr13:88099351-88099488	XLOC_010683
7	lnc-SLITRK6-9	chr13:88079469-88079802	ENSG00000228824.2
8	lnc-SLITRK6-9	chr13:88099351-88099490	ENSG00000232636.2
9	lnc-SLITRK6-9	chr13:88113179-88113224	ENSG00000228824
10	lnc-SLITRK5-17	chr13:87842458-87842506	NONHSAT034582
11	lnc-SLITRK5-14	chr13:87992526-87992762	NONHSAT034584
12	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000232636.2
13	lnc-SLITRK5-17	chr13:87840003-87840983	NONHSAT034582
14	lnc-SLITRK5-14	chr13:87992541-87992680	NONHSAT034585
15	lnc-SLITRK6-9	chr13:88096247-88097385	ENSG00000228824
16	lnc-SLITRK6-8	chr13:88079469-88079802	XLOC_010682
17	lnc-SLITRK6-9	chr13:88113179-88113224	XLOC_010683
18	lnc-SLITRK5-14	chr13:87995599-87995765	NONHSAT034585
19	lnc-SLITRK6-9	chr13:88097266-88097385	ENSG00000232636.2
20	lnc-SLITRK6-9	chr13:88080353-88080410	ENSG00000228824.2
21	lnc-SLITRK5-14	chr13:87991120-87991699	NONHSAT034584
22	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824.2
23	lnc-SLITRK6-9	chr13:88099351-88099488	ENSG00000228824
24	lnc-SLITRK6-8	chr13:88080353-88080528	XLOC_010682
25	lnc-SLITRK6-9	chr13:88125695-88125808	ENSG00000228824

No data

Variant related genes	Relation type
ENSG00000232636	TF binding region
MIR4500HG	TF binding region
LIN28AP2	TF binding region
UBBP5	TF binding region
ENSG00000232636	CpG island
MIR4500HG	CpG island
LIN28AP2	CpG island
UBBP5	CpG island
WARS2	miRNA target sites
SCD	miRNA target sites
DENR	miRNA target sites
MIB1	miRNA target sites

Extended variants
information (count: 6134 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:6134 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555564064	chr13:87835435-87835436	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs574107422	chr13:87835446-87835447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs367697076	chr13:87835483-87835484	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs200826261	chr13:87835520-87835521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs10691317	chr13:87835521-87835522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs10689154	chr13:87835522-87835523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200809477	chr13:87835523-87835524	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201606767	chr13:87835524-87835525	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs555521833	chr13:87835538-87835539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs534680568	chr13:87835558-87835559	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs146519275	chr13:87835623-87835624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573441494	chr13:87835635-87835636	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs183299407	chr13:87835642-87835643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs557673898	chr13:87835661-87835662	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs575821165	chr13:87835673-87835674	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs543638735	chr13:87835678-87835679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs187558796	chr13:87835721-87835722	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs529007645	chr13:87835728-87835729	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540638282	chr13:87835798-87835799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs74103212	chr13:87835808-87835809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs533622207	chr13:87835816-87835817	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs141153249	chr13:87835833-87835834	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs577183801	chr13:87835856-87835857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs191454687	chr13:87835860-87835861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs59565413	chr13:87835869-87835870	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs58772527	chr13:87835870-87835871	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs142442244	chr13:87835871-87835872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs373545996	chr13:87835872-87835873	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs567617932	chr13:87835877-87835878	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs116815414	chr13:87835886-87835887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs56009892	chr13:87835896-87835897	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs143234547	chr13:87835900-87835901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs571302565	chr13:87835939-87835940	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538684449	chr13:87836018-87836019	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564657568	chr13:87836036-87836037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184621607	chr13:87836087-87836088	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148306197	chr13:87836093-87836094	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs140489866	chr13:87836107-87836108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs150433098	chr13:87836118-87836119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs559538339	chr13:87836273-87836274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs532873803	chr13:87836287-87836288	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs545049939	chr13:87836303-87836304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs72636483	chr13:87836343-87836344	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs531250371	chr13:87836423-87836424	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549269675	chr13:87836433-87836434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567848861	chr13:87836486-87836487	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs562264745	chr13:87836527-87836528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368351804	chr13:87836546-87836547	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs547058386	chr13:87836553-87836554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs138454439	chr13:87836567-87836568	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:168 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87834000-87836600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr13:87836600-87837000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr13:87837800-87838400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chr13:87838000-87839000	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr13:87838000-87839800	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:87838200-87838400	Enhancers	ES-I3 Cell Line	embryonic stem cell
7	chr13:87838400-87838800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:87838400-87839000	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:87838400-87839400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr13:87838400-87839800	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
11	chr13:87838400-87839800	Enhancers	iPS-18 Cell Line	embryonic stem cell
12	chr13:87838400-87840200	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr13:87838800-87840600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:87839000-87839600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chr13:87839000-87839800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
16	chr13:87839400-87840200	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chr13:87839600-87839800	Enhancers	iPS-20b Cell Line	embryonic stem cell
18	chr13:87839800-87840800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr13:87839800-87842400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr13:87839800-87842600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
21	chr13:87840200-87841200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr13:87840600-87845200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:87840800-87844200	Active TSS	HUES6 Cell Line	embryonic stem cell
24	chr13:87841200-87844800	Active TSS	ES-I3 Cell Line	embryonic stem cell
25	chr13:87842400-87843800	Active TSS	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:87842400-87844200	Active TSS	iPS-18 Cell Line	embryonic stem cell
27	chr13:87842600-87842800	Flanking Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr13:87842600-87843600	Active TSS	H9 Cell Line	embryonic stem cell
29	chr13:87842800-87843000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
30	chr13:87842800-87843200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
31	chr13:87843000-87843400	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
32	chr13:87843200-87843400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr13:87844200-87844600	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
34	chr13:87844200-87845200	Enhancers	iPS-18 Cell Line	embryonic stem cell
35	chr13:87844400-87844800	Enhancers	HUES48 Cell Line	embryonic stem cell
36	chr13:87844600-87845000	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr13:87844800-87845800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
38	chr13:87845200-87845800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:87845800-87846000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
40	chr13:87845800-87848400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr13:87847400-87847800	Active TSS	Liver	Liver
42	chr13:87847800-87848200	Bivalent/Poised TSS	Liver	Liver
43	chr13:87847800-87848400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
44	chr13:87848400-87852200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr13:87848400-87859400	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chr13:87849800-87850200	Enhancers	iPS-18 Cell Line	embryonic stem cell
47	chr13:87850400-87851000	Enhancers	Fetal Heart	heart
48	chr13:87852200-87852400	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr13:87852400-87853200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr13:87853200-87853800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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