Variant report

Variant	nsv900779
Chromosome Location	chr13:87443524-87658986
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:87638730-87639049	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:87522825-87522873	K562	blood:	n/a	n/a
3	ATF1	chr13:87535053-87535541	K562	blood:	n/a	n/a
4	ATF1	chr13:87561569-87561897	K562	blood:	n/a	n/a
5	ATF1	chr13:87534480-87534795	K562	blood:	n/a	n/a
6	ATF2	chr13:87534270-87534796	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr13:87534377-87534846	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr13:87533625-87533952	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr13:87599091-87599291	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr13:87650294-87650417	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr13:87533665-87533941	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr13:87597888-87598181	Hela-S3	cervix:	n/a	n/a
13	CCNT2	chr13:87535109-87535399	K562	blood:	n/a	n/a
14	CEBPB	chr13:87623791-87624024	HepG2	liver:	n/a	chr13:87623853-87623864
15	CEBPB	chr13:87464946-87465050	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr13:87535123-87535452	K562	blood:	n/a	chr13:87535277-87535288
17	CEBPB	chr13:87528428-87528706	HepG2	liver:	n/a	n/a
18	CEBPB	chr13:87469814-87470097	HepG2	liver:	n/a	chr13:87469948-87469959
19	CEBPB	chr13:87525573-87525763	HepG2	liver:	n/a	chr13:87525610-87525621
20	CEBPB	chr13:87546429-87546598	H1-hESC	embryonic stem cell:	n/a	chr13:87546483-87546494 chr13:87546515-87546526
21	CEBPB	chr13:87599037-87599123	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr13:87546354-87546670	Hela-S3	cervix:	n/a	chr13:87546483-87546494 chr13:87546515-87546526
23	CEBPB	chr13:87569830-87570107	HepG2	liver:	n/a	chr13:87569929-87569940
24	CEBPB	chr13:87597731-87598317	Hela-S3	cervix:	n/a	n/a
25	CEBPB	chr13:87535120-87535586	HepG2	liver:	n/a	chr13:87535277-87535288
26	CEBPB	chr13:87533644-87534006	H1-hESC	embryonic stem cell:	n/a	n/a
27	CEBPB	chr13:87596830-87597421	H1-hESC	embryonic stem cell:	n/a	chr13:87597373-87597386 chr13:87596913-87596922 chr13:87596913-87596922 chr13:87597375-87597386 chr13:87596908-87596925 chr13:87596913-87596922 chr13:87596911-87596922 chr13:87597375-87597386 chr13:87597373-87597386 chr13:87596913-87596922
28	CEBPB	chr13:87534327-87534679	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr13:87535059-87535367	K562	blood:	n/a	chr13:87535277-87535288
30	CEBPB	chr13:87464869-87465069	IMR90	lung:	n/a	n/a
31	CEBPB	chr13:87509486-87509874	IMR90	lung:	n/a	n/a
32	CEBPB	chr13:87623746-87623959	A549	lung:	n/a	chr13:87623853-87623864
33	CEBPB	chr13:87575160-87575465	MCF-7	breast:	n/a	n/a
34	CEBPB	chr13:87558087-87558399	IMR90	lung:	n/a	chr13:87558216-87558229 chr13:87558218-87558229 chr13:87558218-87558227 chr13:87558218-87558227 chr13:87558218-87558227 chr13:87558218-87558227
35	CEBPB	chr13:87475314-87475565	A549	lung:	n/a	chr13:87475414-87475425
36	CEBPB	chr13:87593817-87594091	HepG2	liver:	n/a	n/a
37	CEBPB	chr13:87596748-87597517	IMR90	lung:	n/a	chr13:87597373-87597386 chr13:87596913-87596922 chr13:87596913-87596922 chr13:87597375-87597386 chr13:87596908-87596925 chr13:87596913-87596922 chr13:87596911-87596922 chr13:87597375-87597386 chr13:87597373-87597386 chr13:87596913-87596922
38	CEBPB	chr13:87482236-87482598	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr13:87596795-87597091	A549	lung:	n/a	chr13:87596913-87596922 chr13:87596913-87596922 chr13:87596908-87596925 chr13:87596913-87596922 chr13:87596911-87596922 chr13:87596913-87596922
40	CEBPB	chr13:87596743-87597505	HepG2	liver:	n/a	chr13:87597373-87597386 chr13:87596913-87596922 chr13:87596913-87596922 chr13:87597375-87597386 chr13:87596908-87596925 chr13:87596913-87596922 chr13:87596911-87596922 chr13:87597375-87597386 chr13:87597373-87597386 chr13:87596913-87596922
41	CEBPB	chr13:87593860-87594049	A549	lung:	n/a	n/a
42	CEBPB	chr13:87623720-87624000	IMR90	lung:	n/a	chr13:87623853-87623864
43	CEBPB	chr13:87575260-87575510	MCF-7	breast:	n/a	n/a
44	CEBPB	chr13:87475251-87475602	IMR90	lung:	n/a	chr13:87475414-87475425
45	CEBPB	chr13:87641387-87641668	H1-hESC	embryonic stem cell:	n/a	chr13:87641504-87641515
46	CEBPB	chr13:87596780-87597505	Hela-S3	cervix:	n/a	chr13:87597373-87597386 chr13:87596913-87596922 chr13:87596913-87596922 chr13:87597375-87597386 chr13:87596908-87596925 chr13:87596913-87596922 chr13:87596911-87596922 chr13:87597375-87597386 chr13:87597373-87597386 chr13:87596913-87596922
47	CEBPB	chr13:87641137-87641643	HepG2	liver:	n/a	chr13:87641148-87641161 chr13:87641504-87641515 chr13:87641219-87641232 chr13:87641148-87641161
48	CEBPB	chr13:87546337-87546663	HepG2	liver:	n/a	chr13:87546483-87546494 chr13:87546515-87546526
49	CEBPB	chr13:87475265-87475574	HepG2	liver:	n/a	chr13:87475414-87475425
50	CHD1	chr13:87534405-87534566	H1-hESC	embryonic stem cell:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:87444696-87444746	IMR90	lung:	fetal
2	chr13:87444712-87444762	HIPEpiC	eye:	n/a
3	chr13:87444696-87444746	PANC-1	pancreas:	n/a
4	chr13:87444712-87444762	Hepatocyte	liver:	n/a
5	chr13:87444696-87444746	HCM	heart:	n/a
6	chr13:87444712-87444762	NHDF-neo	bronchial:	n/a
7	chr13:87444696-87444746	CMK	blood:	n/a
8	chr13:87444712-87444762	HEEpiC	esophagus:	n/a
9	chr13:87444696-87444746	HNPCEpiC	eye:	n/a
10	chr13:87444712-87444762	NH-A	brain:	n/a
11	chr13:87444712-87444762	SK-N-MC	brain:	n/a
12	chr13:87444696-87444746	MCF-7	breast:	n/a
13	chr13:87444696-87444746	PFSK-1	brain:	n/a
14	chr13:87444696-87444746	MCF10A-Er-Src	breast:	n/a
15	chr13:87444712-87444762	BJ	skin:	n/a
16	chr13:87444712-87444762	PFSK-1	brain:	n/a
17	chr13:87444712-87444762	SK-N-SH	brain:	n/a
18	chr13:87444712-87444762	SAEC	small airway:	n/a
19	chr13:87444712-87444762	T-47D	breast:	n/a
20	chr13:87444696-87444746	HIPEpiC	eye:	n/a
21	chr13:87444712-87444762	AG04449	skin:	fetal
22	chr13:87444696-87444746	SAEC	small airway:	n/a
23	chr13:87444712-87444762	GM19239	blood:	n/a
24	chr13:87444696-87444746	NHDF-neo	bronchial:	n/a
25	chr13:87444696-87444746	HRPEpiC	eye:	n/a
26	chr13:87444696-87444746	ovcar-3	ovarian:	n/a
27	chr13:87444712-87444762	HL-60	blood:	n/a
28	chr13:87444712-87444762	PrEC	prostate:	n/a
29	chr13:87444696-87444746	NH-A	brain:	n/a
30	chr13:87444712-87444762	HCF	heart:	n/a
31	chr13:87444696-87444746	GM12892	blood:	n/a
32	chr13:87444712-87444762	AG09319	gingival:	n/a
33	chr13:87444712-87444762	SK-N-SH_RA	brain:	n/a
34	chr13:87444696-87444746	HL-60	blood:	n/a
35	chr13:87444712-87444762	ProgFib	skin:	n/a
36	chr13:87444712-87444762	HMEC	breast:	n/a
37	chr13:87444696-87444746	HRCEpiC	kidney:	n/a
38	chr13:87444712-87444762	MCF-7	breast:	n/a
39	chr13:87444696-87444746	NB4	blood:	n/a
40	chr13:87444696-87444746	ProgFib	skin:	n/a
41	chr13:87444696-87444746	PrEC	prostate:	n/a
42	chr13:87444712-87444762	Jurkat	blood:	n/a
43	chr13:87444696-87444746	HEEpiC	esophagus:	n/a
44	chr13:87444696-87444746	HCT-116	colon:	n/a
45	chr13:87444696-87444746	AoSMC	blood vessel:	n/a
46	chr13:87444712-87444762	HCPEpiC	choroid plexus:	n/a
47	chr13:87444712-87444762	GM06990	blood:	n/a
48	chr13:87444712-87444762	AG10803	skin:	n/a
49	chr13:87444696-87444746	T-47D	breast:	n/a
50	chr13:87444696-87444746	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr13:87522311..87523294-chr13:87926162..87927045,5	MCF-7	breast:
2	chr13:87530439..87532752-chr13:87534404..87536619,2	K562	blood:
3	chr13:87465454..87468131-chr13:87475693..87478573,2	MCF-7	breast:
4	chr13:87530439..87532752-chr13:87534404..87536619,2	K562	blood:
5	chr13:87465454..87468131-chr13:87475693..87478573,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK5-6	chr13:87588831-87589062	XLOC_010461
2	lnc-SLITRK5-6	chr13:87564173-87564236	XLOC_010461
3	lnc-SLITRK5-6	chr13:87588831-87589271	ENSG00000233528.3
4	lnc-SLITRK5-6	chr13:87564173-87564236	ENSG00000233528.3

Variant related genes	Relation type
LINC00430	TF binding region
LINC00430	CpG island

Extended variants
information (count: 4800 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:4800 , 50 per page) page: 1 2 3 4 5 6 7 ... 96

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7988039	chr13:87443524-87443525	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181204123	chr13:87443535-87443536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148808950	chr13:87443566-87443567	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs9556104	chr13:87443582-87443583	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs185057960	chr13:87443589-87443590	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs76154368	chr13:87443591-87443592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs74101927	chr13:87443609-87443610	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs528857365	chr13:87443627-87443628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs547475315	chr13:87443660-87443661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74101928	chr13:87443673-87443674	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs191181613	chr13:87443682-87443683	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35783088	chr13:87443691-87443692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372238412	chr13:87443726-87443727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs551726382	chr13:87443755-87443756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561003103	chr13:87443757-87443758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs375299439	chr13:87443763-87443764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs537376576	chr13:87443798-87443799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs528478433	chr13:87443806-87443807	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs115364282	chr13:87443818-87443819	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs142504037	chr13:87443877-87443878	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs370074679	chr13:87443907-87443908	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs546633330	chr13:87443965-87443966	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs542676190	chr13:87443978-87443979	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs558019347	chr13:87444031-87444032	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs553170361	chr13:87444044-87444045	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183802480	chr13:87444134-87444135	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs571546103	chr13:87444155-87444156	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532462363	chr13:87444274-87444275	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs555657198	chr13:87444288-87444289	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs573582771	chr13:87444340-87444341	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187582162	chr13:87444349-87444350	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs192033028	chr13:87444355-87444356	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs182913112	chr13:87444357-87444358	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs187526719	chr13:87444365-87444366	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs530976287	chr13:87444396-87444397	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs549275445	chr13:87444420-87444421	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs536422625	chr13:87444519-87444520	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs554706889	chr13:87444586-87444587	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs567574905	chr13:87444593-87444594	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs535096144	chr13:87450260-87450261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs138934025	chr13:87450263-87450264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs572235385	chr13:87450265-87450266	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs367565673	chr13:87450292-87450293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186528863	chr13:87450293-87450294	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs567693047	chr13:87450325-87450326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs34680510	chr13:87450340-87450341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs149436778	chr13:87450344-87450345	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201544169	chr13:87450384-87450385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs397801726	chr13:87450393-87450394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs147131468	chr13:87450399-87450400	Enhancers	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
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	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
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Osteosarcoma	21215367	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:276 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:87441200-87444400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
2	chr13:87443800-87444400	Active TSS	ES-I3 Cell Line	embryonic stem cell
3	chr13:87444000-87444400	Active TSS	iPS-15b Cell Line	embryonic stem cell
4	chr13:87444400-87444600	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr13:87444400-87444600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr13:87450200-87450600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:87450200-87450600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
8	chr13:87452600-87453200	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:87455200-87455600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr13:87456600-87478400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
11	chr13:87462200-87463400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
12	chr13:87462200-87463400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
13	chr13:87462400-87462800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chr13:87462400-87463200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr13:87462800-87463000	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:87463000-87463200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr13:87465400-87465800	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chr13:87465600-87466000	Enhancers	H9 Cell Line	embryonic stem cell
19	chr13:87465600-87466000	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr13:87474600-87474800	Enhancers	Liver	Liver
21	chr13:87475000-87477200	Weak transcription	Liver	Liver
22	chr13:87477200-87478400	Enhancers	Liver	Liver
23	chr13:87478400-87478600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr13:87478600-87480000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
25	chr13:87479000-87479600	Active TSS	Brain Inferior Temporal Lobe	brain
26	chr13:87479400-87479600	Enhancers	iPS-18 Cell Line	embryonic stem cell
27	chr13:87479400-87479800	Enhancers	Brain Cingulate Gyrus	brain
28	chr13:87482000-87482800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:87482200-87482400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr13:87482200-87482600	Enhancers	ES-I3 Cell Line	embryonic stem cell
31	chr13:87482200-87482800	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr13:87482400-87482600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
33	chr13:87482400-87483800	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chr13:87488400-87490400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
35	chr13:87488600-87489000	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr13:87489000-87492400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
37	chr13:87490400-87490600	Enhancers	Gastric	stomach
38	chr13:87490600-87491000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr13:87490600-87491000	Flanking Active TSS	Gastric	stomach
40	chr13:87490600-87491800	Enhancers	Pancreas	Pancrea
41	chr13:87490600-87492000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr13:87491000-87491400	Enhancers	Placenta Amnion	Placenta Amnion
43	chr13:87491400-87498400	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr13:87492400-87492800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr13:87498200-87499200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr13:87498200-87499200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr13:87498200-87499800	Enhancers	HMEC	breast
48	chr13:87498400-87499000	Enhancers	Placenta Amnion	Placenta Amnion
49	chr13:87508600-87509000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr13:87508800-87509800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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