Variant report

Variant	nsv1069
Chromosome Location	chr13:63305907-63644059
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:960)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:960 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:63630119-63630924	K562	blood:	n/a	n/a
2	ATF1	chr13:63618922-63619134	K562	blood:	n/a	n/a
3	BACH1	chr13:63582960-63583004	K562	blood:	n/a	n/a
4	BATF	chr13:63449339-63449575	GM12878	blood:	n/a	chr13:63449426-63449437
5	BATF	chr13:63615780-63616039	GM12878	blood:	n/a	n/a
6	BCL3	chr13:63636565-63636764	K562	blood:	n/a	n/a
7	BCL3	chr13:63629979-63630226	K562	blood:	n/a	n/a
8	BDP1	chr13:63621761-63622431	Hela-S3	cervix:	n/a	n/a
9	BHLHE40	chr13:63621363-63621647	GM12878	blood:	n/a	n/a
10	BHLHE40	chr13:63321881-63322081	HepG2	liver:	n/a	n/a
11	BRCA1	chr13:63636779-63637019	GM12878	blood:	n/a	n/a
12	BRCA1	chr13:63631196-63631347	GM12878	blood:	n/a	n/a
13	BRCA1	chr13:63621532-63621757	GM12878	blood:	n/a	n/a
14	BRCA1	chr13:63617055-63617144	GM12878	blood:	n/a	n/a
15	BRCA1	chr13:63488576-63488593	GM12878	blood:	n/a	n/a
16	CCNT2	chr13:63623533-63624047	K562	blood:	n/a	n/a
17	CCNT2	chr13:63625757-63626259	K562	blood:	n/a	n/a
18	CCNT2	chr13:63636783-63637288	K562	blood:	n/a	n/a
19	CEBPB	chr13:63345100-63345369	A549	lung:	n/a	chr13:63345274-63345285
20	CEBPB	chr13:63322272-63322576	HepG2	liver:	n/a	chr13:63322373-63322382 chr13:63322371-63322382
21	CEBPB	chr13:63615917-63616597	IMR90	lung:	n/a	n/a
22	CEBPB	chr13:63432074-63432425	IMR90	lung:	n/a	chr13:63432246-63432257
23	CEBPB	chr13:63639251-63639536	K562	blood:	n/a	n/a
24	CEBPB	chr13:63322255-63322610	IMR90	lung:	n/a	chr13:63322373-63322382 chr13:63322371-63322382
25	CEBPB	chr13:63378022-63378232	HepG2	liver:	n/a	chr13:63378135-63378148 chr13:63378136-63378147 chr13:63378134-63378151 chr13:63378135-63378148
26	CEBPB	chr13:63630292-63630980	K562	blood:	n/a	n/a
27	CEBPB	chr13:63345104-63345397	HepG2	liver:	n/a	chr13:63345274-63345285
28	CEBPB	chr13:63420304-63420618	IMR90	lung:	n/a	chr13:63420421-63420434
29	CEBPB	chr13:63630006-63631026	HepG2	liver:	n/a	chr13:63630260-63630273
30	CEBPB	chr13:63507671-63507971	IMR90	lung:	n/a	n/a
31	CEBPB	chr13:63432076-63432444	Hela-S3	cervix:	n/a	chr13:63432246-63432257
32	CEBPB	chr13:63411996-63412388	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr13:63632992-63633617	HepG2	liver:	n/a	chr13:63633575-63633588 chr13:63633467-63633478 chr13:63633463-63633480
34	CEBPB	chr13:63432068-63432403	A549	lung:	n/a	chr13:63432246-63432257
35	CEBPB	chr13:63602186-63602386	A549	lung:	n/a	n/a
36	CEBPB	chr13:63345098-63345406	Hela-S3	cervix:	n/a	chr13:63345274-63345285
37	CEBPB	chr13:63412008-63412411	IMR90	lung:	n/a	n/a
38	CEBPB	chr13:63506091-63506628	IMR90	lung:	n/a	n/a
39	CEBPB	chr13:63458384-63458584	HepG2	liver:	n/a	chr13:63458505-63458516 chr13:63458505-63458518 chr13:63458505-63458518
40	CEBPB	chr13:63623458-63623824	HepG2	liver:	n/a	chr13:63623529-63623546 chr13:63623716-63623729 chr13:63623627-63623644
41	CEBPB	chr13:63558691-63558837	A549	lung:	n/a	n/a
42	CEBPB	chr13:63342444-63342551	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr13:63432074-63432428	HepG2	liver:	n/a	chr13:63432246-63432257
44	CEBPB	chr13:63396473-63396780	HepG2	liver:	n/a	chr13:63396623-63396634 chr13:63396594-63396605 chr13:63396592-63396603 chr13:63396625-63396636 chr13:63396625-63396634 chr13:63396589-63396606
45	CEBPB	chr13:63345122-63345399	IMR90	lung:	n/a	chr13:63345274-63345285
46	CEBPB	chr13:63497473-63497639	HepG2	liver:	n/a	chr13:63497538-63497549 chr13:63497537-63497550 chr13:63497626-63497637
47	CEBPB	chr13:63634182-63634519	K562	blood:	n/a	chr13:63634337-63634348 chr13:63634337-63634350
48	CEBPB	chr13:63639071-63639547	HepG2	liver:	n/a	n/a
49	CEBPZ	chr13:63613217-63613401	HepG2	liver:	n/a	n/a
50	CEBPZ	chr13:63637441-63638445	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:63617080-63617130	PrEC	prostate:	n/a
2	chr13:63617080-63617130	HRE	kidney:	n/a
3	chr13:63617080-63617130	SK-N-MC	brain:	n/a
4	chr13:63637003-63637053	AG04450	lung:	fetal
5	chr13:63637003-63637053	SAEC	small airway:	n/a
6	chr13:63637003-63637053	MCF-7	breast:	n/a
7	chr13:63637003-63637053	HIPEpiC	eye:	n/a
8	chr13:63637003-63637053	HAEpiC	amniotic membrane:	n/a
9	chr13:63617080-63617130	ProgFib	skin:	n/a
10	chr13:63617080-63617130	NT2-D1	testis:	n/a
11	chr13:63637003-63637053	ProgFib	skin:	n/a
12	chr13:63637003-63637053	HCF	heart:	n/a
13	chr13:63617080-63617130	ECC-1	luminal epithelium:	n/a
14	chr13:63617080-63617130	GM12878	blood:	n/a
15	chr13:63617080-63617130	SK-N-SH	brain:	n/a
16	chr13:63617080-63617130	SAEC	small airway:	n/a
17	chr13:63637003-63637053	GM12892	blood:	n/a
18	chr13:63617080-63617130	PFSK-1	brain:	n/a
19	chr13:63637003-63637053	HCM	heart:	n/a
20	chr13:63637003-63637053	HEEpiC	esophagus:	n/a
21	chr13:63637003-63637053	Hela-S3	cervix:	n/a
22	chr13:63617080-63617130	GM12891	blood:	n/a
23	chr13:63637003-63637053	NB4	blood:	n/a
24	chr13:63637003-63637053	ECC-1	luminal epithelium:	n/a
25	chr13:63617080-63617130	HIPEpiC	eye:	n/a
26	chr13:63637003-63637053	Caco-2	colon:	n/a
27	chr13:63637003-63637053	ovcar-3	ovarian:	n/a
28	chr13:63637003-63637053	GM06990	blood:	n/a
29	chr13:63637003-63637053	HRPEpiC	eye:	n/a
30	chr13:63637003-63637053	GM19239	blood:	n/a
31	chr13:63637003-63637053	Jurkat	blood:	n/a
32	chr13:63637003-63637053	BE2_C	brain:	n/a
33	chr13:63617080-63617130	AG04450	lung:	fetal
34	chr13:63637003-63637053	GM12878	blood:	n/a
35	chr13:63637003-63637053	NHBE	bronchial:	n/a
36	chr13:63637003-63637053	T-47D	breast:	n/a
37	chr13:63637003-63637053	K562	blood:	n/a
38	chr13:63637003-63637053	HCT-116	colon:	n/a
39	chr13:63637003-63637053	HRE	kidney:	n/a
40	chr13:63617080-63617130	HCPEpiC	choroid plexus:	n/a
41	chr13:63637003-63637053	CMK	blood:	n/a
42	chr13:63617080-63617130	NH-A	brain:	n/a
43	chr13:63617080-63617130	NB4	blood:	n/a
44	chr13:63617080-63617130	A549	lung:	n/a
45	chr13:63617080-63617130	AG09319	gingival:	n/a
46	chr13:63617080-63617130	HRCEpiC	kidney:	n/a
47	chr13:63637003-63637053	AG04449	skin:	fetal
48	chr13:63617080-63617130	SKMC	muscle:	n/a
49	chr13:63617080-63617130	HL-60	blood:	n/a
50	chr13:63617080-63617130	AG04449	skin:	fetal

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:63305859..63307828-chr13:63368512..63371200,2	K562	blood:
2	chr10:97173416..97174286-chr13:63349578..63350296,2	MCF-7	breast:
3	chr13:63620345..63622864-chr17:21666900..21668712,2	K562	blood:
4	chr13:63619880..63624018-chr17:21665172..21668893,6	K562	blood:
5	chr13:63637281..63639152-chr20:26145559..26147940,2	K562	blood:
6	chr13:63619768..63621405-chr17:21665172..21666856,2	MCF-7	breast:
7	chr13:63637188..63639152-chr20:26145559..26148373,3	K562	blood:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-18	chr13:63315448-63316259	ucscGeneNc_uc010aeh_1
2	lnc-PCDH20-3	chr13:63306427-63306492	ENSG00000228669
3	lnc-PCDH20-3	chr13:63305993-63306328	ENSG00000228669
4	lnc-PCDH20-4	chr13:63370693-63370823	XLOC_010638
5	lnc-PCDH20-4	chr13:63368629-63368704	XLOC_010638
6	lnc-PCDH20-20	chr13:63547376-63548145	NONHSAT034156
7	lnc-PCDH20-20	chr13:63506481-63506671	NONHSAT034156
8	lnc-AL445989.1-3	chr13:63609108-63609165	NONHSAT034157
9	lnc-PCDH20-20	chr13:63462230-63462334	NONHSAT034156
10	lnc-PCDH20-20	chr13:63474519-63474543	NONHSAT034156
11	lnc-AL445989.1-3	chr13:63609109-63609165	XLOC_010410
12	lnc-PCDH20-20	chr13:63475482-63475599	NONHSAT034156
13	lnc-PCDH20-18	chr13:63311204-63311359	ucscGeneNc_uc010aeh_1
14	lnc-PCDH20-3	chr13:63306227-63306313	ENSG00000228669
15	lnc-PCDH20-4	chr13:63368629-63368706	NONHSAT034155
16	lnc-PCDH20-4	chr13:63321841-63322054	NONHSAT034155
17	lnc-PCDH20-4	chr13:63321740-63322054	XLOC_010638
18	lnc-PCDH20-18	chr13:63311883-63313757	ucscGeneNc_uc010aeh_1
19	lnc-PCDH20-20	chr13:63458505-63459173	NONHSAT034156

No data

Variant related genes	Relation type
LINC00448	TF binding region
LINC00448	CpG island
ENSG00000228669	chromatin interactions
ENSG00000095637	chromatin interactions
DNMT1	miRNA target sites

Extended variants
information (count: 4806 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:4806 , 50 per page) page: 1 2 3 4 5 6 7 ... 97

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs113975033	chr13:63306004-63306005	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs538674196	chr13:63306007-63306008	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs556919674	chr13:63306019-63306020	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs575547881	chr13:63306025-63306026	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs74083824	chr13:63306063-63306064	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs532587331	chr13:63306081-63306082	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs184108061	chr13:63306146-63306147	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs549184022	chr13:63306162-63306163	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs371996172	chr13:63306178-63306179	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs376273676	chr13:63306182-63306183	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs147907176	chr13:63306211-63306212	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs76205634	chr13:63306238-63306239	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs111568036	chr13:63306247-63306248	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs576999208	chr13:63306322-63306323	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs535035938	chr13:63306435-63306436	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs73493463	chr13:63306443-63306444	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs188456600	chr13:63306449-63306450	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs181602311	chr13:63306450-63306451	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs184213828	chr13:63306478-63306479	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs562946509	chr13:63306487-63306488	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
21	rs571440474	chr13:63306489-63306490	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs185819946	chr13:63307896-63307897	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs73493469	chr13:63307897-63307898	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs553489877	chr13:63308010-63308011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs374640726	chr13:63308014-63308015	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs532311909	chr13:63308019-63308020	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs571964163	chr13:63308025-63308026	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs138606460	chr13:63308034-63308035	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs543832808	chr13:63310054-63310055	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs116811846	chr13:63310073-63310074	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs372358195	chr13:63310094-63310095	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs559938268	chr13:63310142-63310143	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs376341659	chr13:63310203-63310204	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs369635545	chr13:63310206-63310207	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs528695836	chr13:63310214-63310215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs574280065	chr13:63310216-63310217	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs541323583	chr13:63310243-63310244	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs111328498	chr13:63311210-63311211	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs139188483	chr13:63311221-63311222	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs377636629	chr13:63311233-63311234	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs568912395	chr13:63311322-63311323	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs548560773	chr13:63311908-63311909	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs183336400	chr13:63311911-63311912	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs7994086	chr13:63311925-63311926	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs372561861	chr13:63311993-63311994	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs529876314	chr13:63312020-63312021	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs548351335	chr13:63312025-63312026	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs144783593	chr13:63312035-63312036	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs528540484	chr13:63312041-63312042	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs546594598	chr13:63312076-63312077	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

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
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	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
Squamous cell cancer	20885788	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Thyroid cancer	19087340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Prostate cancer	16573809	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	17245344	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Merkel cell carcinoma	19020549	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21858162	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Glioblastoma multiforme	21750150	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Breast cancer	17393978	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Colorectal cancer	16774939	CNVD
Adenoid cystic carcinoma	17372589	CNVD
abnormal development	18461090	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Acute myeloid leukemia	20729466	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Breast cancer	22522925	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:188 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:63321200-63321600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
2	chr13:63341800-63342000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
3	chr13:63341800-63342000	Enhancers	Gastric	stomach
4	chr13:63350200-63351000	Enhancers	Brain Hippocampus Middle	brain
5	chr13:63352800-63354200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr13:63353000-63354000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr13:63353000-63354200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chr13:63353400-63354200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr13:63353400-63354400	Enhancers	H9 Cell Line	embryonic stem cell
10	chr13:63362800-63363000	Enhancers	Adipose Nuclei	Adipose
11	chr13:63363000-63366600	Weak transcription	Adipose Nuclei	Adipose
12	chr13:63366600-63367000	Enhancers	Adipose Nuclei	Adipose
13	chr13:63373000-63373200	Enhancers	Adipose Nuclei	Adipose
14	chr13:63373200-63374000	Flanking Active TSS	Adipose Nuclei	Adipose
15	chr13:63373200-63375600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
16	chr13:63374000-63374200	Active TSS	Adipose Nuclei	Adipose
17	chr13:63375000-63375200	Enhancers	Adipose Nuclei	Adipose
18	chr13:63399800-63400200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr13:63400400-63401600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:63412000-63412200	Enhancers	Hela-S3	cervix
21	chr13:63413000-63413800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
22	chr13:63420000-63421400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr13:63420600-63421000	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
24	chr13:63427200-63428200	Enhancers	Dnd41	blood
25	chr13:63431800-63432200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
26	chr13:63431800-63432400	Enhancers	Adipose Nuclei	Adipose
27	chr13:63449000-63449800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr13:63449600-63450000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr13:63449800-63452400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr13:63450000-63452400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chr13:63452400-63452600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr13:63452400-63454200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
33	chr13:63452600-63453000	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
34	chr13:63453000-63453600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr13:63453000-63454000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
36	chr13:63453400-63453800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr13:63461000-63461200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr13:63461200-63461600	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
39	chr13:63461600-63461800	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr13:63461800-63462800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr13:63463000-63463400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr13:63466400-63466600	Active TSS	H9 Cell Line	embryonic stem cell
43	chr13:63480600-63481200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:63480600-63481400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:63482000-63485400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
46	chr13:63482200-63482400	Enhancers	NHDF-Ad	bronchial
47	chr13:63482200-63483000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
48	chr13:63482400-63482800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr13:63483000-63484200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr13:63484200-63484800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived

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