Variant report

Variant	nsv1048599
Chromosome Location	chr13:55143426-55476042
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:560)
CpG islands
(count:489)
Chromatin interactive
region (count:18)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:560 , 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	chr13:55456488-55456688	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr13:55231858-55231995	GM12878	blood:	n/a	chr13:55231951-55231962
3	BATF	chr13:55231840-55232014	GM12878	blood:	n/a	chr13:55231951-55231962
4	BRCA1	chr13:55418582-55418666	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr13:55211527-55211897	MCF-7	breast:	n/a	chr13:55211690-55211701
6	CEBPB	chr13:55187469-55187719	A549	lung:	n/a	chr13:55187618-55187631 chr13:55187618-55187629
7	CEBPB	chr13:55232297-55232476	K562	blood:	n/a	chr13:55232380-55232391 chr13:55232380-55232393 chr13:55232380-55232393 chr13:55232382-55232393
8	CEBPB	chr13:55232236-55232497	HepG2	liver:	n/a	chr13:55232380-55232391 chr13:55232380-55232393 chr13:55232380-55232393 chr13:55232382-55232393
9	CEBPB	chr13:55187442-55187803	HepG2	liver:	n/a	chr13:55187618-55187631 chr13:55187618-55187629
10	CEBPB	chr13:55286181-55286506	IMR90	lung:	n/a	n/a
11	CEBPB	chr13:55202575-55202863	A549	lung:	n/a	chr13:55202731-55202742
12	CEBPB	chr13:55211524-55211825	ECC-1	luminal epithelium:	n/a	chr13:55211690-55211701
13	CEBPB	chr13:55211565-55211841	Hela-S3	cervix:	n/a	chr13:55211690-55211701
14	CEBPB	chr13:55189067-55189270	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr13:55218359-55218620	HepG2	liver:	n/a	chr13:55218503-55218516 chr13:55218503-55218514
16	CEBPB	chr13:55262924-55263177	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:55202631-55202891	HepG2	liver:	n/a	chr13:55202731-55202742
18	CEBPB	chr13:55211507-55211875	H1-hESC	embryonic stem cell:	n/a	chr13:55211690-55211701
19	CEBPB	chr13:55312589-55312727	H1-hESC	embryonic stem cell:	n/a	chr13:55312652-55312665
20	CEBPB	chr13:55211507-55211887	HepG2	liver:	n/a	chr13:55211690-55211701
21	CEBPB	chr13:55211544-55211859	ECC-1	luminal epithelium:	n/a	chr13:55211690-55211701
22	CEBPB	chr13:55170692-55170975	H1-hESC	embryonic stem cell:	n/a	chr13:55170850-55170861
23	CEBPB	chr13:55170698-55170985	HepG2	liver:	n/a	chr13:55170850-55170861
24	CEBPB	chr13:55211593-55211722	HepG2	liver:	n/a	chr13:55211690-55211701
25	CEBPB	chr13:55187469-55187752	H1-hESC	embryonic stem cell:	n/a	chr13:55187618-55187631 chr13:55187618-55187629
26	CEBPB	chr13:55170702-55170894	K562	blood:	n/a	chr13:55170850-55170861
27	CEBPB	chr13:55170698-55170995	IMR90	lung:	n/a	chr13:55170850-55170861
28	CEBPB	chr13:55286252-55286511	A549	lung:	n/a	n/a
29	CEBPB	chr13:55211492-55211994	MCF-7	breast:	n/a	chr13:55211690-55211701
30	CHD2	chr13:55200786-55200839	GM12878	blood:	n/a	n/a
31	CTCF	chr13:55307820-55307970	MCF-7	breast:	n/a	n/a
32	CTCF	chr13:55307919-55307996	Hela-S3	cervix:	n/a	n/a
33	CTCF	chr13:55162460-55162610	AG09309	skin:	n/a	n/a
34	CTCF	chr13:55307960-55308110	NHEK	skin:	n/a	n/a
35	CTCF	chr13:55211680-55211830	HRE	kidney:	n/a	n/a
36	CTCF	chr13:55307840-55307990	HEK293	kidney:	n/a	n/a
37	CTCF	chr13:55147412-55147601	H1-hESC	embryonic stem cell:	n/a	n/a
38	CTCF	chr13:55442428-55442495	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr13:55147388-55147631	MCF-7	breast:	n/a	n/a
40	CTCF	chr13:55211620-55211770	Caco-2	colon:	n/a	n/a
41	CTCF	chr13:55307860-55308010	WERI-Rb-1	eye:	n/a	n/a
42	CTCF	chr13:55147434-55147637	H1-hESC	embryonic stem cell:	n/a	n/a
43	CTCF	chr13:55211600-55211750	NHEK	skin:	n/a	n/a
44	CTCF	chr13:55396444-55396546	Medullo	brain:	n/a	n/a
45	CTCF	chr13:55307913-55308014	Medullo	brain:	n/a	n/a
46	CTCF	chr13:55147395-55147611	MCF-7	breast:	n/a	n/a
47	CTCF	chr13:55211620-55211770	HAc	cerebellar:	n/a	n/a
48	CTCF	chr13:55244455-55244482	Lung_OC	lung:	n/a	n/a
49	CTCF	chr13:55307758-55308090	H1-hESC	embryonic stem cell:	n/a	n/a
50	CTCF	chr13:55307770-55308078	H1-hESC	embryonic stem cell:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:55419681-55419731	MCF-7	breast:	n/a
2	chr13:55419681-55419731	MCF-7	breast:	n/a
3	chr13:55475951-55476001	HRPEpiC	eye:	n/a
4	chr13:55373912-55373962	SKMC	muscle:	n/a
5	chr13:55373388-55373438	HepG2	liver:	n/a
6	chr13:55373912-55373962	HEEpiC	esophagus:	n/a
7	chr13:55373388-55373438	SKMC	muscle:	n/a
8	chr13:55211764-55211814	ovcar-3	ovarian:	n/a
9	chr13:55211764-55211814	PANC-1	pancreas:	n/a
10	chr13:55475951-55476001	HEK293	kidney:	embryo
11	chr13:55373912-55373962	AG10803	skin:	n/a
12	chr13:55373912-55373962	Caco-2	colon:	n/a
13	chr13:55475951-55476001	HL-60	blood:	n/a
14	chr13:55211764-55211814	GM12891	blood:	n/a
15	chr13:55146537-55146587	NHBE	bronchial:	n/a
16	chr13:55373912-55373962	GM12878	blood:	n/a
17	chr13:55373912-55373962	AG04449	skin:	fetal
18	chr13:55146537-55146587	MCF10A-Er-Src	breast:	n/a
19	chr13:55211764-55211814	NHBE	bronchial:	n/a
20	chr13:55475951-55476001	HRE	kidney:	n/a
21	chr13:55146537-55146587	SKMC	muscle:	n/a
22	chr13:55408596-55408646	IMR90	lung:	fetal
23	chr13:55146537-55146587	T-47D	breast:	n/a
24	chr13:55408596-55408646	HCPEpiC	choroid plexus:	n/a
25	chr13:55475951-55476001	NT2-D1	testis:	n/a
26	chr13:55373912-55373962	SK-N-SH_RA	brain:	n/a
27	chr13:55475951-55476001	GM12891	blood:	n/a
28	chr13:55449282-55449332	LNCaP	prostate:	n/a
29	chr13:55146537-55146587	RPTEC	kidney:	n/a
30	chr13:55211764-55211814	HEK293	kidney:	embryo
31	chr13:55146537-55146587	ovcar-3	ovarian:	n/a
32	chr13:55449282-55449332	NH-A	brain:	n/a
33	chr13:55475951-55476001	AG04450	lung:	fetal
34	chr13:55449282-55449332	NT2-D1	testis:	n/a
35	chr13:55449282-55449332	HAEpiC	amniotic membrane:	n/a
36	chr13:55408596-55408646	AoSMC	blood vessel:	n/a
37	chr13:55373912-55373962	LNCaP	prostate:	n/a
38	chr13:55373388-55373438	CMK	blood:	n/a
39	chr13:55449282-55449332	ProgFib	skin:	n/a
40	chr13:55419681-55419731	HPAEpiC	pulmonary alveolar:	n/a
41	chr13:55408596-55408646	SK-N-MC	brain:	n/a
42	chr13:55373388-55373438	A549	lung:	n/a
43	chr13:55146537-55146587	PFSK-1	brain:	n/a
44	chr13:55211764-55211814	Hela-S3	cervix:	n/a
45	chr13:55211764-55211814	GM19239	blood:	n/a
46	chr13:55449282-55449332	RPTEC	kidney:	n/a
47	chr13:55449282-55449332	HEEpiC	esophagus:	n/a
48	chr13:55408596-55408646	HCF	heart:	n/a
49	chr13:55419681-55419731	HepG2	liver:	n/a
50	chr13:55373388-55373438	MCF10A-Er-Src	breast:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:55321697..55323262-chr13:55324790..55327522,2	K562	blood:
2	chr13:55165909..55168648-chr13:55172019..55174969,2	MCF-7	breast:
3	chr13:55165909..55168648-chr13:55172019..55174969,2	MCF-7	breast:
4	chr13:55372674..55374590-chr7:122830546..122833222,2	MCF-7	breast:
5	chr13:55145343..55147455-chr16:12696633..12698151,2	MCF-7	breast:
6	chr13:55225858..55228081-chr13:55229883..55232107,2	MCF-7	breast:
7	chr13:55147191..55149509-chr13:55154393..55156642,2	MCF-7	breast:
8	chr13:55286253..55286882-chr13:55307575..55308197,2	MCF-7	breast:
9	chr13:55139502..55142309-chr13:55146026..55147750,2	MCF-7	breast:
10	chr13:55199830..55202056-chr13:55206437..55209228,2	MCF-7	breast:
11	chr13:55286253..55286882-chr13:55307575..55308197,2	MCF-7	breast:
12	chr13:55145225..55147281-chr13:55171713..55173554,2	MCF-7	breast:
13	chr13:55147191..55149509-chr13:55154393..55156642,2	MCF-7	breast:
14	chr13:55199830..55202056-chr13:55206437..55209228,2	MCF-7	breast:
15	chr13:55145225..55147281-chr13:55171713..55173554,2	MCF-7	breast:
16	chr13:55225858..55228081-chr13:55229883..55232107,2	MCF-7	breast:
17	chr13:55321697..55323262-chr13:55324790..55327522,2	K562	blood:
18	chr1:114505901..114506720-chr13:55199515..55200372,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-5	chr13:55264457-55264577	XLOC_010400
2	lnc-OLFM4-5	chr13:55260674-55260848	XLOC_010400
3	lnc-OLFM4-12	chr13:55361374-55361452	NONHSAT034035
4	lnc-OLFM4-12	chr13:55359420-55359736	NONHSAT034035

No data

Variant related genes	Relation type
ENSG00000266699	TF binding region
ENSG00000266699	CpG island
ENSG00000163349	chromatin interactions
THADA	miRNA target sites
MTMR1	miRNA target sites

Extended variants
information (count: 6106 )
Associated
traits (count: 116 )

Variant overlapped rSNPs/rCNVs (count:6106 , 50 per page) page: 1 2 3 4 5 6 7 ... 123

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs577660088	chr13:55144818-55144819	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs558323267	chr13:55144853-55144854	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs190167515	chr13:55144893-55144894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs370517116	chr13:55144910-55144911	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs560295904	chr13:55144934-55144935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs375031241	chr13:55144955-55144956	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs181096567	chr13:55144958-55144959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376556653	chr13:55144997-55144998	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs185981599	chr13:55145051-55145052	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs143157351	chr13:55145065-55145066	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs370368727	chr13:55145109-55145110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35269597	chr13:55145121-55145122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113050351	chr13:55145122-55145123	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs544816381	chr13:55145198-55145199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs564695026	chr13:55145209-55145210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs527484438	chr13:55145238-55145239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs372327951	chr13:55145257-55145258	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs549272521	chr13:55145262-55145263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs567236500	chr13:55145295-55145296	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs562754468	chr13:55145297-55145298	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs190432514	chr13:55145351-55145352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs553256085	chr13:55145375-55145376	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs141236178	chr13:55145377-55145378	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs569199071	chr13:55145387-55145388	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75150860	chr13:55145392-55145393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs557974371	chr13:55145470-55145471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs9316734	chr13:55145475-55145476	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs9536764	chr13:55145502-55145503	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs61950868	chr13:55145512-55145513	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs147484362	chr13:55145528-55145529	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs542996297	chr13:55145563-55145564	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs201367206	chr13:55145578-55145579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs71439529	chr13:55145615-55145616	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138370147	chr13:55145621-55145622	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs9597008	chr13:55145682-55145683	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs545040148	chr13:55145692-55145693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs564657905	chr13:55145701-55145702	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs184063119	chr13:55145727-55145728	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs111527704	chr13:55145747-55145748	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560797597	chr13:55145776-55145777	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs529994607	chr13:55145779-55145780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs191786310	chr13:55145810-55145811	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs35090937	chr13:55145891-55145892	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs549819364	chr13:55145974-55145975	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs569186107	chr13:55146047-55146048	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs535657380	chr13:55146057-55146058	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs182879394	chr13:55146108-55146109	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs546691920	chr13:55146115-55146116	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs573160193	chr13:55146132-55146133	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs143852423	chr13:55146151-55146152	Active TSS Flanking Active TSS Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:116)

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
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	16774939	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17133270	CNVD
Myoepithelioma	18604193	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prostate cancer	16573809	CNVD
Prostate cancer	18632612	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	19242612	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	17245344	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Retinoblastoma	19183342	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Developmental delay	21147756	CNVD
Melanoma	18172304	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	17053054	CNVD
Multiple myeloma	19135901	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Prostate cancer	16461572	CNVD
Merkel cell carcinoma	19020549	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Breast cancer	21858162	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	17237825	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
Glioblastoma multiforme	21922591	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	17908304	CNVD
Breast cancer	18852474	CNVD
Myelofibrosis	22110671	CNVD
craniofacial dysmorphism	21918468	CNVD
Glioblastoma multiforme	22286061	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
Urothelial carcinoma	21177765	CNVD
early-passage human iPS cells	21368824	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Esophageal squamous carcinoma	17470683	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:364 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:55144800-55146200	Enhancers	iPS-15b Cell Line	embryonic stem cell
2	chr13:55145800-55146000	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chr13:55145800-55146000	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr13:55146000-55146400	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
5	chr13:55146000-55146400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
6	chr13:55146000-55146600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chr13:55146000-55146600	Active TSS	iPS-20b Cell Line	embryonic stem cell
8	chr13:55146000-55147400	Active TSS	ES-I3 Cell Line	embryonic stem cell
9	chr13:55146000-55167000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:55146200-55146400	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
11	chr13:55146200-55146800	Active TSS	H1 Cell Line	embryonic stem cell
12	chr13:55146200-55146800	Active TSS	HUES64 Cell Line	embryonic stem cell
13	chr13:55146400-55146800	Active TSS	H9 Cell Line	embryonic stem cell
14	chr13:55146400-55146800	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr13:55146400-55146800	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr13:55146400-55146800	Active TSS	iPS-15b Cell Line	embryonic stem cell
17	chr13:55146400-55146800	Active TSS	iPS-18 Cell Line	embryonic stem cell
18	chr13:55146400-55146800	Active TSS	Placenta	Placenta
19	chr13:55146400-55147200	Active TSS	HUES6 Cell Line	embryonic stem cell
20	chr13:55146600-55148800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr13:55146800-55147600	Weak transcription	HUES48 Cell Line	embryonic stem cell
22	chr13:55146800-55147600	Weak transcription	HUES64 Cell Line	embryonic stem cell
23	chr13:55146800-55149400	Enhancers	iPS-15b Cell Line	embryonic stem cell
24	chr13:55146800-55155800	Weak transcription	H1 Cell Line	embryonic stem cell
25	chr13:55146800-55160000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr13:55147200-55147400	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
27	chr13:55147200-55147600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr13:55147400-55147800	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
29	chr13:55147400-55148200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr13:55147600-55148000	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chr13:55147600-55148000	Flanking Active TSS	HUES64 Cell Line	embryonic stem cell
32	chr13:55147800-55148000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr13:55148000-55148400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr13:55148000-55155800	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chr13:55148000-55159600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr13:55148200-55155600	Weak transcription	HUES6 Cell Line	embryonic stem cell
37	chr13:55148400-55148800	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr13:55148800-55149400	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chr13:55148800-55149400	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr13:55149400-55155600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr13:55149400-55156400	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chr13:55149400-55160400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
43	chr13:55155600-55156200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr13:55155600-55158200	Strong transcription	HUES6 Cell Line	embryonic stem cell
45	chr13:55155800-55156200	Strong transcription	H1 Cell Line	embryonic stem cell
46	chr13:55155800-55158200	Strong transcription	HUES48 Cell Line	embryonic stem cell
47	chr13:55156000-55156400	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr13:55156200-55156600	ZNF genes & repeats	Placenta	Placenta
49	chr13:55156200-55157200	Weak transcription	H1 Cell Line	embryonic stem cell
50	chr13:55156200-55158600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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