Variant report

Variant	nsv832675
Chromosome Location	chr13:89772410-89926955
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:220)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:220 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BRCA1	chr13:89809033-89809039	Hela-S3	cervix:	n/a	n/a
2	CEBPB	chr13:89921156-89921403	HepG2	liver:	n/a	chr13:89921266-89921277
3	CEBPB	chr13:89823580-89823834	HepG2	liver:	n/a	chr13:89823710-89823721
4	CEBPB	chr13:89785424-89785641	HepG2	liver:	n/a	chr13:89785500-89785517
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	chr13:89788251-89788403	K562	blood:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
8	CEBPB	chr13:89856691-89857129	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
9	CEBPB	chr13:89870206-89870527	HepG2	liver:	n/a	chr13:89870358-89870367 chr13:89870358-89870369 chr13:89870356-89870367
10	CEBPB	chr13:89788283-89788664	HepG2	liver:	n/a	chr13:89788370-89788381 chr13:89788372-89788383 chr13:89788370-89788383 chr13:89788372-89788381
11	CEBPB	chr13:89893668-89893895	HepG2	liver:	n/a	n/a
12	CEBPB	chr13:89856664-89857107	ECC-1	luminal epithelium:	n/a	chr13:89856807-89856824
13	CEBPB	chr13:89811087-89811294	IMR90	lung:	n/a	n/a
14	CTCF	chr13:89920420-89920570	HPF	lung:	n/a	n/a
15	CTCF	chr13:89893140-89893290	GM12866	blood:	n/a	n/a
16	CTCF	chr13:89778340-89778490	HL-60	blood:	n/a	n/a
17	CTCF	chr13:89785700-89785850	GM12870	blood:	n/a	n/a
18	CTCF	chr13:89907570-89907625	Medullo	brain:	n/a	n/a
19	CTCF	chr13:89873440-89873590	WERI-Rb-1	eye:	n/a	n/a
20	CUX1	chr13:89793933-89794023	GM12878	blood:	n/a	n/a
21	E2F4	chr13:89879725-89880049	MCF10A-Er-Src	breast:	n/a	n/a
22	E2F4	chr13:89858454-89858750	MCF10A-Er-Src	breast:	n/a	n/a
23	E2F4	chr13:89797098-89797372	MCF10A-Er-Src	breast:	n/a	n/a
24	E2F4	chr13:89884837-89884998	MCF10A-Er-Src	breast:	n/a	n/a
25	E2F4	chr13:89886058-89886204	MCF10A-Er-Src	breast:	n/a	n/a
26	E2F4	chr13:89856319-89856519	MCF10A-Er-Src	breast:	n/a	n/a
27	E2F4	chr13:89782665-89782781	MCF10A-Er-Src	breast:	n/a	n/a
28	E2F4	chr13:89862284-89862740	MCF10A-Er-Src	breast:	n/a	n/a
29	E2F4	chr13:89918486-89918648	MCF10A-Er-Src	breast:	n/a	n/a
30	E2F4	chr13:89800879-89801240	MCF10A-Er-Src	breast:	n/a	n/a
31	EBF1	chr13:89789874-89789897	GM12878	blood:	n/a	n/a
32	EBF1	chr13:89788671-89788801	GM12878	blood:	n/a	chr13:89788774-89788785
33	EBF1	chr13:89789130-89789467	GM12878	blood:	n/a	chr13:89789322-89789333
34	EP300	chr13:89922037-89922308	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr13:89911319-89911555	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr13:89834322-89834358	Hela-S3	cervix:	n/a	n/a
37	EP300	chr13:89922061-89922361	SK-N-SH_RA	brain:	n/a	n/a
38	EP300	chr13:89856582-89857113	ECC-1	luminal epithelium:	n/a	chr13:89856961-89856971
39	EP300	chr13:89856527-89857222	ECC-1	luminal epithelium:	n/a	chr13:89856961-89856971
40	FOS	chr13:89891662-89892177	MCF10A-Er-Src	breast:	n/a	chr13:89891888-89891900
41	FOS	chr13:89891634-89892178	MCF10A-Er-Src	breast:	n/a	chr13:89891888-89891900
42	FOS	chr13:89879704-89880017	MCF10A-Er-Src	breast:	n/a	n/a
43	FOS	chr13:89797902-89798134	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr13:89879522-89879998	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr13:89918944-89918974	MCF10A-Er-Src	breast:	n/a	n/a
46	FOS	chr13:89797882-89798173	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr13:89919910-89920581	MCF10A-Er-Src	breast:	n/a	chr13:89920146-89920154 chr13:89920147-89920154 chr13:89920145-89920155 chr13:89920145-89920155 chr13:89920146-89920154 chr13:89920145-89920155 chr13:89920145-89920155
48	FOS	chr13:89851357-89851651	MCF10A-Er-Src	breast:	n/a	n/a
49	FOS	chr13:89775750-89775896	MCF10A-Er-Src	breast:	n/a	chr13:89775858-89775867 chr13:89775858-89775865
50	FOS	chr13:89775704-89776015	MCF10A-Er-Src	breast:	n/a	chr13:89775858-89775867 chr13:89775858-89775865

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:89815451-89815501	BJ	skin:	n/a
2	chr13:89815421-89815471	T-47D	breast:	n/a
3	chr13:89815451-89815501	HNPCEpiC	eye:	n/a
4	chr13:89815421-89815471	SK-N-MC	brain:	n/a
5	chr13:89815421-89815471	PFSK-1	brain:	n/a
6	chr13:89815421-89815471	H1-hESC	embryonic stem cell:	embryo
7	chr13:89815421-89815471	HNPCEpiC	eye:	n/a
8	chr13:89815451-89815501	H1-hESC	embryonic stem cell:	embryo
9	chr13:89815451-89815501	HEEpiC	esophagus:	n/a
10	chr13:89815451-89815501	AG09319	gingival:	n/a
11	chr13:89815421-89815471	LNCaP	prostate:	n/a
12	chr13:89815421-89815471	BJ	skin:	n/a
13	chr13:89815451-89815501	LNCaP	prostate:	n/a
14	chr13:89815421-89815471	HEK293	kidney:	embryo
15	chr13:89815451-89815501	PANC-1	pancreas:	n/a
16	chr13:89815421-89815471	CMK	blood:	n/a
17	chr13:89815451-89815501	AG09309	skin:	n/a
18	chr13:89815451-89815501	BE2_C	brain:	n/a
19	chr13:89815421-89815471	HCM	heart:	n/a
20	chr13:89815421-89815471	U87	brain:	n/a
21	chr13:89815451-89815501	SK-N-MC	brain:	n/a
22	chr13:89815421-89815471	HEEpiC	esophagus:	n/a
23	chr13:89815451-89815501	PFSK-1	brain:	n/a
24	chr13:89815451-89815501	GM19239	blood:	n/a
25	chr13:89815421-89815471	AG04449	skin:	fetal
26	chr13:89815421-89815471	MCF10A-Er-Src	breast:	n/a
27	chr13:89815451-89815501	SAEC	small airway:	n/a
28	chr13:89815451-89815501	ProgFib	skin:	n/a
29	chr13:89815451-89815501	SK-N-SH_RA	brain:	n/a
30	chr13:89815421-89815471	Hepatocyte	liver:	n/a
31	chr13:89815451-89815501	SKMC	muscle:	n/a
32	chr13:89815421-89815471	HCF	heart:	n/a
33	chr13:89815451-89815501	HCF	heart:	n/a
34	chr13:89815451-89815501	HMEC	breast:	n/a
35	chr13:89815451-89815501	HCT-116	colon:	n/a
36	chr13:89815451-89815501	HRPEpiC	eye:	n/a
37	chr13:89815451-89815501	HPAEpiC	pulmonary alveolar:	n/a
38	chr13:89815451-89815501	Hepatocyte	liver:	n/a
39	chr13:89815421-89815471	A549	lung:	n/a
40	chr13:89815451-89815501	HIPEpiC	eye:	n/a
41	chr13:89815451-89815501	GM12891	blood:	n/a
42	chr13:89815421-89815471	PANC-1	pancreas:	n/a
43	chr13:89815421-89815471	HAEpiC	amniotic membrane:	n/a
44	chr13:89815451-89815501	AG10803	skin:	n/a
45	chr13:89815451-89815501	ovcar-3	ovarian:	n/a
46	chr13:89815421-89815471	NT2-D1	testis:	n/a
47	chr13:89815451-89815501	HepG2	liver:	n/a
48	chr13:89815421-89815471	ProgFib	skin:	n/a
49	chr13:89815451-89815501	A549	lung:	n/a
50	chr13:89815451-89815501	HCM	heart:	n/a

(count:5 , 50 per page) page: 1

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

(count:22 , 50 per page) page: 1

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

No data

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
RTKN	miRNA target sites
RTF1	miRNA target sites
RTN4	miRNA target sites
RTCD1	miRNA target sites

Extended variants
information (count: 1865 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1865 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538988214	chr13:89788815-89788816	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs568769008	chr13:89788863-89788864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs534239563	chr13:89788878-89788879	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141955414	chr13:89788891-89788892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs147319598	chr13:89788925-89788926	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs34844165	chr13:89788940-89788941	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs73589073	chr13:89788961-89788962	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs145016418	chr13:89788964-89788965	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34366982	chr13:89788976-89788977	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs71212960	chr13:89788979-89788980	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs34498546	chr13:89788981-89788982	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs9583658	chr13:89788982-89788983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs528360613	chr13:89788997-89788998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs552903885	chr13:89789006-89789007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs554758439	chr13:89789056-89789057	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs551619931	chr13:89789066-89789067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs564787021	chr13:89789111-89789112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs562973685	chr13:89789190-89789191	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2253547	chr13:89811760-89811761	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs186389	chr13:89811772-89811773	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs187053224	chr13:89811817-89811818	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs138016542	chr13:89811848-89811849	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs527375145	chr13:89813809-89813810	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs314386	chr13:89813913-89813914	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs570545603	chr13:89813918-89813919	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs117092295	chr13:89813929-89813930	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs314387	chr13:89813937-89813938	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs78664868	chr13:89813944-89813945	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs535789977	chr13:89813964-89813965	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs553929307	chr13:89813996-89813997	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs566916133	chr13:89814002-89814003	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs572101060	chr13:89814018-89814019	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs539628613	chr13:89814044-89814045	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs558747622	chr13:89814047-89814048	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs149834899	chr13:89814156-89814157	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs141003416	chr13:89814165-89814166	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs68014328	chr13:89814167-89814168	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs548703948	chr13:89814168-89814169	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs398117699	chr13:89814171-89814172	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs535932508	chr13:89814217-89814218	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs184375588	chr13:89814218-89814219	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs532511436	chr13:89814232-89814233	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs574780840	chr13:89814281-89814282	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs141993785	chr13:89814298-89814299	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs376403981	chr13:89814299-89814300	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs377134884	chr13:89814308-89814309	Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs552697830	chr13:89814318-89814319	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181269360	chr13:89814321-89814322	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs182605	chr13:89814343-89814344	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs370024595	chr13:89814370-89814371	Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

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
Autism	20841430	CNVD
Wilms tumour	21544195	CNVD

Chromatin state (count:48 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:89788800-89789200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr13:89813800-89816000	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
3	chr13:89815000-89815600	Active TSS	Placenta	Placenta
4	chr13:89815200-89815800	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
5	chr13:89822000-89822600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr13:89822200-89822600	Enhancers	Adipose Nuclei	Adipose
7	chr13:89822200-89822600	Enhancers	Fetal Heart	heart
8	chr13:89850800-89851200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr13:89850800-89851400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr13:89850800-89851400	Enhancers	HMEC	breast
11	chr13:89850800-89851400	Enhancers	NHEK	skin
12	chr13:89850800-89852400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr13:89851200-89852200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr13:89851400-89851800	Flanking Active TSS	NHEK	skin
15	chr13:89851400-89852000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr13:89851800-89852800	Enhancers	NHEK	skin
17	chr13:89852000-89852200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr13:89852200-89852800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr13:89852800-89857200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr13:89857200-89858000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr13:89858000-89858600	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chr13:89858000-89858600	Enhancers	Fetal Lung	lung
23	chr13:89858200-89858600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr13:89860400-89861200	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr13:89865800-89867600	Enhancers	Fetal Lung	lung
26	chr13:89866600-89867600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
27	chr13:89873400-89875000	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr13:89875000-89890600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr13:89879600-89880000	Enhancers	Muscle Satellite Cultured Cells	--
30	chr13:89885000-89902400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
31	chr13:89890600-89892200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr13:89890800-89891800	Enhancers	HMEC	breast
33	chr13:89890800-89891800	Enhancers	NHEK	skin
34	chr13:89895400-89896000	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr13:89898200-89898600	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr13:89898200-89898600	Enhancers	Stomach Mucosa	stomach
37	chr13:89898600-89899600	Weak transcription	Stomach Mucosa	stomach
38	chr13:89899600-89899800	Enhancers	Stomach Mucosa	stomach
39	chr13:89908000-89909000	Enhancers	Fetal Heart	heart
40	chr13:89919800-89920400	Enhancers	Placenta Amnion	Placenta Amnion
41	chr13:89920000-89920400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr13:89920000-89920400	Enhancers	HMEC	breast
43	chr13:89920200-89920400	Enhancers	Muscle Satellite Cultured Cells	--
44	chr13:89920200-89920600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr13:89920200-89920600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr13:89920600-89921600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr13:89921800-89922200	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr13:89922200-89922400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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