Variant report

Variant	nsv900245
Chromosome Location	chr13:61873379-62057698
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:1468)
Chromatin interactive
region (count:11)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:584 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr13:62051827-62052095	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr13:61989073-61989080	H1-hESC	embryonic stem cell:	n/a	n/a
3	BHLHE40	chr13:61965785-61965997	GM12878	blood:	n/a	n/a
4	CEBPB	chr13:61991399-61991696	MCF-7	breast:	n/a	chr13:61991520-61991533 chr13:61991521-61991532 chr13:61991520-61991531 chr13:61991520-61991533
5	CEBPB	chr13:61950913-61951154	A549	lung:	n/a	chr13:61950975-61950986 chr13:61950975-61950988
6	CEBPB	chr13:61950860-61951119	HepG2	liver:	n/a	chr13:61950975-61950986 chr13:61950975-61950988
7	CEBPB	chr13:61983510-61983698	HepG2	liver:	n/a	chr13:61983629-61983640
8	CEBPB	chr13:61950835-61951165	IMR90	lung:	n/a	chr13:61950975-61950986 chr13:61950975-61950988
9	CEBPB	chr13:61988936-61989251	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr13:61991381-61991687	HepG2	liver:	n/a	chr13:61991520-61991533 chr13:61991521-61991532 chr13:61991520-61991531 chr13:61991520-61991533
11	CHD2	chr13:61988785-61988924	H1-hESC	embryonic stem cell:	n/a	n/a
12	CHD2	chr13:61989233-61989545	H1-hESC	embryonic stem cell:	n/a	n/a
13	CTBP2	chr13:61989057-61989987	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr13:61984940-61985090	AG09309	skin:	n/a	n/a
15	CTCF	chr13:61984920-61985070	AG04449	skin:	n/a	n/a
16	CTCF	chr13:62040508-62040732	MCF-7	breast:	n/a	n/a
17	CTCF	chr13:61984841-61985192	IMR90	lung:	n/a	n/a
18	CTCF	chr13:62040520-62040670	GM12865	blood:	n/a	n/a
19	CTCF	chr13:61984820-61984970	NHLF	lung:	n/a	n/a
20	CTCF	chr13:62040580-62040730	RPTEC	kidney:	n/a	n/a
21	CTCF	chr13:62040580-62040730	GM12866	blood:	n/a	n/a
22	CTCF	chr13:62040420-62040570	A549	lung:	n/a	n/a
23	CTCF	chr13:62040528-62040724	MCF-7	breast:	n/a	n/a
24	CTCF	chr13:61984960-61985110	HEK293	kidney:	n/a	n/a
25	CTCF	chr13:61984960-61985110	HPF	lung:	n/a	n/a
26	CTCF	chr13:62040540-62040690	NHEK	skin:	n/a	n/a
27	CTCF	chr13:62040480-62040630	HRPEpiC	eye:	n/a	n/a
28	CTCF	chr13:61918105-61918150	K562	blood:	n/a	n/a
29	CTCF	chr13:61984960-61985110	GM12872	blood:	n/a	n/a
30	CTCF	chr13:61984960-61985110	MCF-7	breast:	n/a	n/a
31	CTCF	chr13:61984918-61985144	LNCaP	prostate:	n/a	n/a
32	CTCF	chr13:61984980-61985130	HCM	heart:	n/a	n/a
33	CTCF	chr13:61984960-61985110	HCFaa	heart:	n/a	n/a
34	CTCF	chr13:62009500-62009650	HAc	cerebellar:	n/a	n/a
35	CTCF	chr13:61984860-61985010	GM12801	blood:	n/a	n/a
36	CTCF	chr13:61984940-61985090	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr13:61985320-61985470	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr13:61913666-61913760	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr13:61984920-61985070	BE2_C	brain:	n/a	n/a
40	CTCF	chr13:61985360-61985510	HPF	lung:	n/a	n/a
41	CTCF	chr13:62009664-62009804	HepG2	liver:	n/a	n/a
42	CTCF	chr13:61890837-61891003	GM12878	blood:	n/a	n/a
43	CTCF	chr13:62040580-62040730	HRPEpiC	eye:	n/a	n/a
44	CTCF	chr13:61984900-61985050	HCT-116	colon:	n/a	n/a
45	CTCF	chr13:61913640-61913790	HRE	kidney:	n/a	n/a
46	CTCF	chr13:61984940-61985090	AG09319	gingival:	n/a	n/a
47	CTCF	chr13:61984940-61985090	GM12865	blood:	n/a	n/a
48	CTCF	chr13:61984877-61985144	ECC-1	luminal epithelium:	n/a	n/a
49	CTCF	chr13:61984960-61985110	GM12871	blood:	n/a	n/a
50	CTCF	chr13:61984951-61985104	Kidney_OC	kidney:	n/a	n/a

(count:1468 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:61913482-61913532	H1-hESC	embryonic stem cell:	embryo
2	chr13:61989701-61989751	PANC-1	pancreas:	n/a
3	chr13:61989203-61989253	HepG2	liver:	n/a
4	chr13:61913482-61913532	ovcar-3	ovarian:	n/a
5	chr13:61913482-61913532	H1-hESC	embryonic stem cell:	embryo
6	chr13:61989701-61989751	PANC-1	pancreas:	n/a
7	chr13:61989203-61989253	HepG2	liver:	n/a
8	chr13:61913482-61913532	ovcar-3	ovarian:	n/a
9	chr13:61989037-61989087	T-47D	breast:	n/a
10	chr13:61989817-61989867	HNPCEpiC	eye:	n/a
11	chr13:61989037-61989087	GM06990	blood:	n/a
12	chr13:61989701-61989751	HCF	heart:	n/a
13	chr13:61989737-61989787	HMEC	breast:	n/a
14	chr13:61990025-61990075	MCF-7	breast:	n/a
15	chr13:62002989-62003039	NT2-D1	testis:	n/a
16	chr13:61989770-61989820	HUVEC	blood vessel:	n/a
17	chr13:61988802-61988852	AoSMC	blood vessel:	n/a
18	chr13:61989726-61989776	BE2_C	brain:	n/a
19	chr13:61989770-61989820	ECC-1	luminal epithelium:	n/a
20	chr13:61932410-61932460	NH-A	brain:	n/a
21	chr13:61989597-61989647	ProgFib	skin:	n/a
22	chr13:61990025-61990075	AG10803	skin:	n/a
23	chr13:61988802-61988852	GM12892	blood:	n/a
24	chr13:62002615-62002665	NHDF-neo	bronchial:	n/a
25	chr13:61989724-61989774	GM19239	blood:	n/a
26	chr13:61913395-61913445	HCF	heart:	n/a
27	chr13:61989859-61989909	PFSK-1	brain:	n/a
28	chr13:61990741-61990791	SKMC	muscle:	n/a
29	chr13:61989475-61989525	HCPEpiC	choroid plexus:	n/a
30	chr13:61989817-61989867	NT2-D1	testis:	n/a
31	chr13:61995249-61995299	HPAEpiC	pulmonary alveolar:	n/a
32	chr13:61990025-61990075	HCPEpiC	choroid plexus:	n/a
33	chr13:61913395-61913445	Caco-2	colon:	n/a
34	chr13:61995249-61995299	Hela-S3	cervix:	n/a
35	chr13:61990741-61990791	AG10803	skin:	n/a
36	chr13:61913482-61913532	HepG2	liver:	n/a
37	chr13:61989726-61989776	MCF-7	breast:	n/a
38	chr13:61989475-61989525	GM12891	blood:	n/a
39	chr13:61989701-61989751	GM12891	blood:	n/a
40	chr13:61913482-61913532	NB4	blood:	n/a
41	chr13:61989037-61989087	SK-N-SH	brain:	n/a
42	chr13:61989859-61989909	HNPCEpiC	eye:	n/a
43	chr13:61989817-61989867	T-47D	breast:	n/a
44	chr13:61989037-61989087	H1-hESC	embryonic stem cell:	embryo
45	chr13:61989203-61989253	A549	lung:	n/a
46	chr13:61932410-61932460	HepG2	liver:	n/a
47	chr13:61990025-61990075	NHBE	bronchial:	n/a
48	chr13:61989737-61989787	GM06990	blood:	n/a
49	chr13:61989597-61989647	Hepatocyte	liver:	n/a
50	chr13:61989701-61989751	Jurkat	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:61860028..61861070-chr13:61984556..61985605,8	MCF-7	breast:
2	chr13:61954466..61956080-chr13:61958714..61961634,2	K562	blood:
3	chr13:61200948..61201884-chr13:61984819..61985392,2	K562	blood:
4	chr13:61980884..61982584-chr13:61984499..61986608,2	K562	blood:
5	chr13:61954466..61956080-chr13:61958714..61961634,2	K562	blood:
6	chr13:61980884..61982584-chr13:61984499..61986608,2	K562	blood:
7	chr13:61985804..61987884-chr13:62010090..62011843,2	K562	blood:
8	chr13:61984597..61985106-chr13:62259471..62259973,2	MCF-7	breast:
9	chr13:62018252..62020987-chr19:47730290..47733067,2	MCF-7	breast:
10	chr13:61985804..61987884-chr13:62010090..62011843,2	K562	blood:
11	chr13:61200993..61201900-chr13:61984142..61985108,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH20-11	chr13:61998853-61999119	NONHSAT034128
2	lnc-PCDH20-11	chr13:62001626-62002220	NONHSAT034128

No data

Variant related genes	Relation type
PCDH20	TF binding region
PCDH20	CpG island
ENSG00000105327	chromatin interactions

Extended variants
information (count: 2556 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2556 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541574800	chr13:61890206-61890207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs549175727	chr13:61890218-61890219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560949570	chr13:61890317-61890318	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs377760073	chr13:61890364-61890365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371249824	chr13:61890371-61890372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs528463664	chr13:61890379-61890380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs546295799	chr13:61890420-61890421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs182130444	chr13:61890521-61890522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs539281161	chr13:61890602-61890603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs368366054	chr13:61890631-61890632	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs551572276	chr13:61890695-61890696	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs77277623	chr13:61890704-61890705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs186563673	chr13:61890707-61890708	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs553054151	chr13:61890819-61890820	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs375777949	chr13:61890823-61890824	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs113972662	chr13:61890868-61890869	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs191343099	chr13:61890881-61890882	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs555457445	chr13:61890944-61890945	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs200623894	chr13:61890999-61891000	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs573727733	chr13:61891042-61891043	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs377636019	chr13:61891088-61891089	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534593468	chr13:61891134-61891135	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553739908	chr13:61891141-61891142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs578181208	chr13:61891162-61891163	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs149411003	chr13:61891175-61891176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs143702369	chr13:61891189-61891190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs575700910	chr13:61891210-61891211	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9634701	chr13:61891233-61891234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561037943	chr13:61891248-61891249	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs184718883	chr13:61891279-61891280	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540209256	chr13:61891335-61891336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373204727	chr13:61891351-61891352	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs564904862	chr13:61891374-61891375	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs561636097	chr13:61891377-61891378	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs533271311	chr13:61891388-61891389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9539110	chr13:61891419-61891420	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs569838933	chr13:61891500-61891501	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs530617653	chr13:61891504-61891505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs189581731	chr13:61891516-61891517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs148118136	chr13:61891525-61891526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs567356984	chr13:61891544-61891545	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs534632561	chr13:61891557-61891558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534605315	chr13:61891597-61891598	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs141827441	chr13:61891602-61891603	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs146061546	chr13:61891675-61891676	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368144984	chr13:61891681-61891682	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199839920	chr13:61891703-61891704	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9570554	chr13:61891714-61891715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200438863	chr13:61891730-61891731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs141562843	chr13:61891731-61891732	Weak transcription	n/a	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
small cell lung cancer	20016488	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
Lung cancer	18438408	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
Esophageal squamous carcinoma	20200074	CNVD
Myelofibrosis	22110671	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Bipolar disorder	19214233	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:398 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:61890200-61890800	Enhancers	HUES64 Cell Line	embryonic stem cell
2	chr13:61890800-61891000	ZNF genes & repeats	Pancreas	Pancrea
3	chr13:61890800-61891200	Enhancers	H1 Cell Line	embryonic stem cell
4	chr13:61890800-61891200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr13:61890800-61891400	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr13:61891000-61892200	Weak transcription	Pancreas	Pancrea
7	chr13:61893400-61897800	Weak transcription	Pancreas	Pancrea
8	chr13:61897800-61898000	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
9	chr13:61897800-61898000	ZNF genes & repeats	Pancreas	Pancrea
10	chr13:61911800-61913000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr13:61913000-61913400	Strong transcription	iPS DF 19.11 Cell Line	embryonic stem cell
12	chr13:61913000-61913600	Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chr13:61913000-61913800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
14	chr13:61913200-61913600	Active TSS	HUES6 Cell Line	embryonic stem cell
15	chr13:61913400-61913600	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr13:61913600-61916000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr13:61916000-61916200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr13:61916000-61916200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr13:61916000-61916400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr13:61916200-61916600	Enhancers	H9 Cell Line	embryonic stem cell
21	chr13:61931200-61933400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chr13:61931800-61933400	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr13:61932000-61933800	Enhancers	HUES48 Cell Line	embryonic stem cell
24	chr13:61932400-61933400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:61932600-61933000	Enhancers	ES-I3 Cell Line	embryonic stem cell
26	chr13:61932600-61933000	Enhancers	H1 Cell Line	embryonic stem cell
27	chr13:61932600-61933000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr13:61932600-61933000	Enhancers	HUES6 Cell Line	embryonic stem cell
29	chr13:61932600-61933000	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr13:61932600-61933200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
31	chr13:61932600-61933400	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr13:61932600-61933400	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr13:61933400-61935000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr13:61933800-61935000	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr13:61935000-61935200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr13:61935200-61935400	Enhancers	HUES48 Cell Line	embryonic stem cell
37	chr13:61936600-61937000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr13:61938200-61938400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr13:61946600-61946800	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr13:61946800-61947800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
41	chr13:61947800-61948400	Enhancers	ES-I3 Cell Line	embryonic stem cell
42	chr13:61947800-61948400	Enhancers	iPS-15b Cell Line	embryonic stem cell
43	chr13:61962200-61963000	Enhancers	Brain Substantia Nigra	brain
44	chr13:61965200-61966200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr13:61966200-61969800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
46	chr13:61969800-61970000	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr13:61969800-61971000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr13:61970000-61971000	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chr13:61970000-61971000	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr13:61970200-61970800	Enhancers	ES-WA7 Cell Line	embryonic stem cell

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