Variant report

Variant	nsv900844
Chromosome Location	chr13:89721607-89944833
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	BACH1	chr13:89937368-89937375	H1-hESC	embryonic stem cell:	n/a	n/a
2	BRCA1	chr13:89809033-89809039	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chr13:89788251-89788403	K562	blood:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
4	CEBPB	chr13:89734887-89735255	A549	lung:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
5	CEBPB	chr13:89816073-89816273	HepG2	liver:	n/a	chr13:89816134-89816145 chr13:89816156-89816167
6	CEBPB	chr13:89788021-89788642	Hela-S3	cervix:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
7	CEBPB	chr13:89734887-89735251	HepG2	liver:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
8	CEBPB	chr13:89811087-89811294	IMR90	lung:	n/a	n/a
9	CEBPB	chr13:89734962-89735178	K562	blood:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
10	CEBPB	chr13:89788283-89788664	HepG2	liver:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
11	CEBPB	chr13:89734904-89735256	Hela-S3	cervix:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
12	CEBPB	chr13:89734912-89735227	ECC-1	luminal epithelium:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
13	CEBPB	chr13:89751122-89751322	HepG2	liver:	n/a	chr13:89751225-89751236
14	CEBPB	chr13:89734889-89735264	ECC-1	luminal epithelium:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
15	CEBPB	chr13:89734909-89735246	H1-hESC	embryonic stem cell:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
16	CEBPB	chr13:89856691-89857129	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
17	CEBPB	chr13:89921156-89921403	HepG2	liver:	n/a	chr13:89921266-89921277
18	CEBPB	chr13:89856664-89857107	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
19	CEBPB	chr13:89893668-89893895	HepG2	liver:	n/a	n/a
20	CEBPB	chr13:89751155-89751382	Hela-S3	cervix:	n/a	chr13:89751225-89751236
21	CEBPB	chr13:89751096-89751336	IMR90	lung:	n/a	chr13:89751225-89751236
22	CEBPB	chr13:89785424-89785641	HepG2	liver:	n/a	chr13:89785500-89785517
23	CEBPB	chr13:89734894-89735243	IMR90	lung:	n/a	chr13:89735062-89735071 chr13:89735062-89735071 chr13:89735061-89735072 chr13:89735062-89735071
24	CEBPB	chr13:89751133-89751376	A549	lung:	n/a	chr13:89751225-89751236
25	CEBPB	chr13:89823580-89823834	HepG2	liver:	n/a	chr13:89823710-89823721
26	CEBPB	chr13:89870206-89870527	HepG2	liver:	n/a	chr13:89870358-89870367 chr13:89870358-89870369 chr13:89870356-89870367
27	CTCF	chr13:89767700-89767850	GM12870	blood:	n/a	n/a
28	CTCF	chr13:89767680-89767830	GM12873	blood:	n/a	n/a
29	CTCF	chr13:89767640-89767790	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr13:89941599-89941649	LNCaP	prostate:	n/a	n/a
31	CTCF	chr13:89907570-89907625	Medullo	brain:	n/a	n/a
32	CTCF	chr13:89767680-89767830	HEK293	kidney:	n/a	n/a
33	CTCF	chr13:89767740-89767890	BE2_C	brain:	n/a	n/a
34	CTCF	chr13:89767600-89767750	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr13:89785700-89785850	GM12870	blood:	n/a	n/a
36	CTCF	chr13:89767620-89767770	HMF	breast:	n/a	n/a
37	CTCF	chr13:89767640-89767790	NHEK	skin:	n/a	n/a
38	CTCF	chr13:89893140-89893290	GM12866	blood:	n/a	n/a
39	CTCF	chr13:89767580-89767730	HBMEC	blood vessel:	n/a	n/a
40	CTCF	chr13:89767720-89767870	GM12875	blood:	n/a	n/a
41	CTCF	chr13:89767565-89767911	GM12878	blood:	n/a	n/a
42	CTCF	chr13:89767660-89767810	GM12871	blood:	n/a	n/a
43	CTCF	chr13:89767700-89767850	GM06990	blood:	n/a	n/a
44	CTCF	chr13:89767640-89767790	AG09309	skin:	n/a	n/a
45	CTCF	chr13:89767700-89767850	GM12873	blood:	n/a	n/a
46	CTCF	chr13:89767660-89767810	BE2_C	brain:	n/a	n/a
47	CTCF	chr13:89767680-89767830	HFF-Myc	foreskin:	n/a	n/a
48	CTCF	chr13:89767660-89767810	HPAF	blood vessel:	n/a	n/a
49	CTCF	chr13:89767689-89767799	GM13977	blood:	n/a	n/a
50	CTCF	chr13:89758133-89758167	Lung_OC	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89815421-89815471	HCM	heart:	n/a
2	chr13:89815421-89815471	HCM	heart:	n/a
3	chr13:89815451-89815501	HIPEpiC	eye:	n/a
4	chr13:89815421-89815471	HAEpiC	amniotic membrane:	n/a
5	chr13:89815421-89815471	GM12892	blood:	n/a
6	chr13:89815451-89815501	AG04450	lung:	fetal
7	chr13:89815421-89815471	HUVEC	blood vessel:	n/a
8	chr13:89815421-89815471	HEK293	kidney:	embryo
9	chr13:89815421-89815471	SK-N-SH_RA	brain:	n/a
10	chr13:89815421-89815471	AG04449	skin:	fetal
11	chr13:89740340-89740390	SKMC	muscle:	n/a
12	chr13:89815421-89815471	NHBE	bronchial:	n/a
13	chr13:89740340-89740390	MCF10A-Er-Src	breast:	n/a
14	chr13:89740340-89740390	MCF-7	breast:	n/a
15	chr13:89815451-89815501	HUVEC	blood vessel:	n/a
16	chr13:89815451-89815501	MCF10A-Er-Src	breast:	n/a
17	chr13:89740340-89740390	NT2-D1	testis:	n/a
18	chr13:89815421-89815471	HepG2	liver:	n/a
19	chr13:89815421-89815471	IMR90	lung:	fetal
20	chr13:89815421-89815471	K562	blood:	n/a
21	chr13:89740340-89740390	SAEC	small airway:	n/a
22	chr13:89815451-89815501	K562	blood:	n/a
23	chr13:89815451-89815501	Jurkat	blood:	n/a
24	chr13:89815451-89815501	T-47D	breast:	n/a
25	chr13:89815421-89815471	HCT-116	colon:	n/a
26	chr13:89740340-89740390	SK-N-SH_RA	brain:	n/a
27	chr13:89815421-89815471	PFSK-1	brain:	n/a
28	chr13:89740340-89740390	GM12878	blood:	n/a
29	chr13:89815421-89815471	T-47D	breast:	n/a
30	chr13:89815421-89815471	GM19239	blood:	n/a
31	chr13:89740340-89740390	HCF	heart:	n/a
32	chr13:89815451-89815501	SK-N-MC	brain:	n/a
33	chr13:89815421-89815471	HL-60	blood:	n/a
34	chr13:89740340-89740390	RPTEC	kidney:	n/a
35	chr13:89815451-89815501	ProgFib	skin:	n/a
36	chr13:89740340-89740390	HL-60	blood:	n/a
37	chr13:89815451-89815501	HCT-116	colon:	n/a
38	chr13:89815421-89815471	Hepatocyte	liver:	n/a
39	chr13:89815451-89815501	AG09319	gingival:	n/a
40	chr13:89740340-89740390	GM19239	blood:	n/a
41	chr13:89740340-89740390	LNCaP	prostate:	n/a
42	chr13:89740340-89740390	Jurkat	blood:	n/a
43	chr13:89815421-89815471	BJ	skin:	n/a
44	chr13:89815451-89815501	AG09309	skin:	n/a
45	chr13:89815421-89815471	NH-A	brain:	n/a
46	chr13:89815421-89815471	ovcar-3	ovarian:	n/a
47	chr13:89740340-89740390	HRPEpiC	eye:	n/a
48	chr13:89815421-89815471	Jurkat	blood:	n/a
49	chr13:89815451-89815501	IMR90	lung:	fetal
50	chr13:89815421-89815471	HEEpiC	esophagus:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:
2	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
3	chr13:89905075..89907672-chr13:89908780..89911039,2	K562	blood:
4	chr13:89889445..89891378-chr13:89894578..89897231,2	MCF-7	breast:
5	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
2	lnc-SLITRK5-23	chr13:89943543-89943672	ucscGeneNc_uc001vlo_2
3	lnc-SLITRK6-10	chr13:89889073-89889144	ENSG00000232225.2
4	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
5	lnc-SLITRK6-10	chr13:89870489-89870549	XLOC_010684
6	lnc-SLITRK6-10	chr13:89867101-89867581	ENSG00000232225.2
7	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
8	lnc-SLITRK6-10	chr13:89889073-89889144	XLOC_010684
9	lnc-SLITRK6-10	chr13:89867101-89867581	XLOC_010684
10	lnc-SLITRK5-23	chr13:89943542-89943672	NONHSAT034627
11	lnc-SLITRK6-10	chr13:89871825-89871963	ENSG00000232225.2
12	lnc-SLITRK6-10	chr13:89868228-89868395	XLOC_010684
13	lnc-SLITRK6-10	chr13:89867150-89867581	XLOC_010684
14	lnc-SLITRK5-9	chr13:89925457-89925616	XLOC_010467
15	lnc-SLITRK6-10	chr13:89868228-89868395	ENSG00000232225.2
16	lnc-SLITRK6-25	chr13:89901072-89902354	NONHSAT034625
17	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
18	lnc-SLITRK6-10	chr13:89871826-89871963	XLOC_010684
19	lnc-SLITRK6-10	chr13:89872788-89872813	ENSG00000232225.2
20	lnc-SLITRK5-9	chr13:89931921-89932494	XLOC_010467
21	lnc-SLITRK6-10	chr13:89870489-89870548	ENSG00000232225.2
22	lnc-SLITRK6-10	chr13:89867150-89867581	ENSG00000232225.2
23	lnc-SLITRK6-10	chr13:89872788-89872813	XLOC_010684
24	lnc-SLITRK6-24	chr13:89811759-89811902	NONHSAT034620
25	lnc-SLITRK6-24	chr13:89815360-89815434	NONHSAT034620

Variant related genes	Relation type
LINC00440	TF binding region
LINC01047	TF binding region
TRIM60P13	TF binding region
LINC00440	CpG island
LINC01047	CpG island
TRIM60P13	CpG island
RTCD1	miRNA target sites
RTN4	miRNA target sites
RTKN	miRNA target sites
RTF1	miRNA target sites

Extended variants
information (count: 2319 )
Associated
traits (count: 89 )

Variant overlapped rSNPs/rCNVs (count:2319 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531526714	chr13:89730437-89730438	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549546758	chr13:89730451-89730452	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs567878094	chr13:89730458-89730459	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114370538	chr13:89730481-89730482	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs573931670	chr13:89730509-89730510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140077297	chr13:89730511-89730512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542659995	chr13:89730521-89730522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553041559	chr13:89730563-89730564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs73585492	chr13:89730589-89730590	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs190135144	chr13:89730624-89730625	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs558957905	chr13:89730632-89730633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs182636079	chr13:89730675-89730676	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs538573600	chr13:89730708-89730709	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs16952499	chr13:89730715-89730716	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs575060671	chr13:89730717-89730718	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs542448291	chr13:89730719-89730720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs553549284	chr13:89730763-89730764	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs541199017	chr13:89739877-89739878	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs553238839	chr13:89739880-89739881	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs577929211	chr13:89739902-89739903	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs186034144	chr13:89739903-89739904	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs564576363	chr13:89739933-89739934	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs543923270	chr13:89739999-89740000	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs191786832	chr13:89740009-89740010	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs138903161	chr13:89740011-89740012	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs398056680	chr13:89740019-89740020	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs540070829	chr13:89740022-89740023	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs183127324	chr13:89740048-89740049	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs562382856	chr13:89740059-89740060	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs188351022	chr13:89740069-89740070	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs7320663	chr13:89740121-89740122	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs565905478	chr13:89740176-89740177	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs533351168	chr13:89740177-89740178	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs532277000	chr13:89740181-89740182	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs551020990	chr13:89740194-89740195	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs569452717	chr13:89740199-89740200	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs145655808	chr13:89740202-89740203	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs555098492	chr13:89740208-89740209	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs567536680	chr13:89740211-89740212	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs7325941	chr13:89740245-89740246	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs553328398	chr13:89740278-89740279	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs577867905	chr13:89740294-89740295	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs545236745	chr13:89740300-89740301	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs566924832	chr13:89740304-89740305	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs558276643	chr13:89740305-89740306	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs576484787	chr13:89740306-89740307	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs191046589	chr13:89740316-89740317	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs7320386	chr13:89740323-89740324	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs531735348	chr13:89740340-89740341	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs9583657	chr13:89740366-89740367	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	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
Mental retardation	17847001	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Autism	20841430	CNVD
Wilms tumour	21544195	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89730400-89730800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr13:89739800-89740600	Active TSS	HUES6 Cell Line	embryonic stem cell
3	chr13:89740000-89740600	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr13:89749800-89750000	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr13:89749800-89750800	Enhancers	Dnd41	blood
6	chr13:89750000-89750400	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr13:89750000-89750600	Enhancers	Primary neutrophils fromperipheralblood	blood
8	chr13:89750000-89750600	Active TSS	Monocytes-CD14+_RO01746	blood
9	chr13:89750600-89750800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
10	chr13:89761800-89765400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
11	chr13:89764800-89766000	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chr13:89764800-89766800	Enhancers	HUES64 Cell Line	embryonic stem cell
13	chr13:89765400-89766600	Enhancers	iPS-18 Cell Line	embryonic stem cell
14	chr13:89765400-89767200	Enhancers	iPS-20b Cell Line	embryonic stem cell
15	chr13:89765600-89766200	Enhancers	ES-I3 Cell Line	embryonic stem cell
16	chr13:89765600-89766200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
17	chr13:89765600-89767400	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr13:89766000-89766400	Enhancers	H1 Cell Line	embryonic stem cell
19	chr13:89766000-89766400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:89766000-89766400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr13:89766000-89766400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
22	chr13:89766000-89767000	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr13:89766400-89767800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:89788800-89789200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr13:89813800-89816000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr13:89815000-89815600	Active TSS	Placenta	Placenta
27	chr13:89815200-89815800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr13:89822000-89822600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:89822200-89822600	Enhancers	Adipose Nuclei	Adipose
30	chr13:89822200-89822600	Enhancers	Fetal Heart	heart
31	chr13:89850800-89851200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr13:89850800-89851400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr13:89850800-89851400	Enhancers	HMEC	breast
34	chr13:89850800-89851400	Enhancers	NHEK	skin
35	chr13:89850800-89852400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr13:89851200-89852200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr13:89851400-89851800	Flanking Active TSS	NHEK	skin
38	chr13:89851400-89852000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr13:89851800-89852800	Enhancers	NHEK	skin
40	chr13:89852000-89852200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr13:89852200-89852800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr13:89852800-89857200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
43	chr13:89857200-89858000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr13:89858000-89858600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chr13:89858000-89858600	Enhancers	Fetal Lung	lung
46	chr13:89858200-89858600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr13:89860400-89861200	Enhancers	iPS-15b Cell Line	embryonic stem cell
48	chr13:89865800-89867600	Enhancers	Fetal Lung	lung
49	chr13:89866600-89867600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr13:89873400-89875000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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