Variant report

Variant	nsv541779
Chromosome Location	chr13:55159674-55459161
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:501)
CpG islands
(count:368)
Chromatin interactive
region (count:13)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:501 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr13:55211507-55211887	HepG2	liver:	n/a	chr13:55211690-55211701
6	CEBPB	chr13:55187469-55187719	A549	lung:	n/a	chr13:55187618-55187631 chr13:55187618-55187629
7	CEBPB	chr13:55286181-55286506	IMR90	lung:	n/a	n/a
8	CEBPB	chr13:55232297-55232476	K562	blood:	n/a	chr13:55232380-55232391 chr13:55232380-55232393 chr13:55232380-55232393 chr13:55232382-55232393
9	CEBPB	chr13:55211593-55211722	HepG2	liver:	n/a	chr13:55211690-55211701
10	CEBPB	chr13:55232236-55232497	HepG2	liver:	n/a	chr13:55232380-55232391 chr13:55232380-55232393 chr13:55232380-55232393 chr13:55232382-55232393
11	CEBPB	chr13:55170702-55170894	K562	blood:	n/a	chr13:55170850-55170861
12	CEBPB	chr13:55187469-55187752	H1-hESC	embryonic stem cell:	n/a	chr13:55187618-55187631 chr13:55187618-55187629
13	CEBPB	chr13:55202631-55202891	HepG2	liver:	n/a	chr13:55202731-55202742
14	CEBPB	chr13:55189067-55189270	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr13:55202575-55202863	A549	lung:	n/a	chr13:55202731-55202742
16	CEBPB	chr13:55211492-55211994	MCF-7	breast:	n/a	chr13:55211690-55211701
17	CEBPB	chr13:55170692-55170975	H1-hESC	embryonic stem cell:	n/a	chr13:55170850-55170861
18	CEBPB	chr13:55262924-55263177	HepG2	liver:	n/a	n/a
19	CEBPB	chr13:55312589-55312727	H1-hESC	embryonic stem cell:	n/a	chr13:55312652-55312665
20	CEBPB	chr13:55211544-55211859	ECC-1	luminal epithelium:	n/a	chr13:55211690-55211701
21	CEBPB	chr13:55170698-55170985	HepG2	liver:	n/a	chr13:55170850-55170861
22	CEBPB	chr13:55286252-55286511	A549	lung:	n/a	n/a
23	CEBPB	chr13:55211565-55211841	Hela-S3	cervix:	n/a	chr13:55211690-55211701
24	CEBPB	chr13:55211524-55211825	ECC-1	luminal epithelium:	n/a	chr13:55211690-55211701
25	CEBPB	chr13:55211527-55211897	MCF-7	breast:	n/a	chr13:55211690-55211701
26	CEBPB	chr13:55211507-55211875	H1-hESC	embryonic stem cell:	n/a	chr13:55211690-55211701
27	CEBPB	chr13:55218359-55218620	HepG2	liver:	n/a	chr13:55218503-55218516 chr13:55218503-55218514
28	CEBPB	chr13:55187442-55187803	HepG2	liver:	n/a	chr13:55187618-55187631 chr13:55187618-55187629
29	CEBPB	chr13:55170698-55170995	IMR90	lung:	n/a	chr13:55170850-55170861
30	CHD2	chr13:55200786-55200839	GM12878	blood:	n/a	n/a
31	CTCF	chr13:55307900-55308050	HepG2	liver:	n/a	n/a
32	CTCF	chr13:55292483-55292541	GM20000	blood:	n/a	n/a
33	CTCF	chr13:55211600-55211750	NHEK	skin:	n/a	n/a
34	CTCF	chr13:55396444-55396546	Medullo	brain:	n/a	n/a
35	CTCF	chr13:55307788-55308164	MCF-7	breast:	n/a	n/a
36	CTCF	chr13:55288560-55288599	LNCaP	prostate:	n/a	n/a
37	CTCF	chr13:55307780-55307930	BE2_C	brain:	n/a	n/a
38	CTCF	chr13:55211680-55211830	HRE	kidney:	n/a	n/a
39	CTCF	chr13:55307840-55307990	HEK293	kidney:	n/a	n/a
40	CTCF	chr13:55359233-55359313	Kidney_OC	kidney:	n/a	n/a
41	CTCF	chr13:55307900-55308050	MCF-7	breast:	n/a	n/a
42	CTCF	chr13:55456540-55456690	GM12873	blood:	n/a	n/a
43	CTCF	chr13:55307921-55307993	HepG2	liver:	n/a	n/a
44	CTCF	chr13:55403091-55403172	GM10248	blood:	n/a	n/a
45	CTCF	chr13:55211620-55211770	Caco-2	colon:	n/a	n/a
46	CTCF	chr13:55307758-55308090	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr13:55162460-55162610	AG09309	skin:	n/a	n/a
48	CTCF	chr13:55361132-55361233	GM10248	blood:	n/a	n/a
49	CTCF	chr13:55307900-55308050	Caco-2	colon:	n/a	n/a
50	CTCF	chr13:55217128-55217182	MCF-7	breast:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:55211764-55211814	NH-A	brain:	n/a
2	chr13:55373912-55373962	HEEpiC	esophagus:	n/a
3	chr13:55211764-55211814	NH-A	brain:	n/a
4	chr13:55373912-55373962	HEEpiC	esophagus:	n/a
5	chr13:55211764-55211814	AG09319	gingival:	n/a
6	chr13:55211764-55211814	HEK293	kidney:	embryo
7	chr13:55373388-55373438	ECC-1	luminal epithelium:	n/a
8	chr13:55419681-55419731	Jurkat	blood:	n/a
9	chr13:55211764-55211814	HRE	kidney:	n/a
10	chr13:55419681-55419731	U87	brain:	n/a
11	chr13:55408596-55408646	ECC-1	luminal epithelium:	n/a
12	chr13:55408596-55408646	HCF	heart:	n/a
13	chr13:55373388-55373438	AoSMC	blood vessel:	n/a
14	chr13:55211764-55211814	SK-N-SH	brain:	n/a
15	chr13:55449282-55449332	AG09309	skin:	n/a
16	chr13:55408596-55408646	NB4	blood:	n/a
17	chr13:55408596-55408646	GM12892	blood:	n/a
18	chr13:55373912-55373962	MCF10A-Er-Src	breast:	n/a
19	chr13:55449282-55449332	NT2-D1	testis:	n/a
20	chr13:55408596-55408646	NH-A	brain:	n/a
21	chr13:55419681-55419731	NHBE	bronchial:	n/a
22	chr13:55408596-55408646	AG10803	skin:	n/a
23	chr13:55408596-55408646	K562	blood:	n/a
24	chr13:55419681-55419731	LNCaP	prostate:	n/a
25	chr13:55449282-55449332	GM06990	blood:	n/a
26	chr13:55211764-55211814	HEEpiC	esophagus:	n/a
27	chr13:55449282-55449332	GM19239	blood:	n/a
28	chr13:55449282-55449332	Hela-S3	cervix:	n/a
29	chr13:55373912-55373962	RPTEC	kidney:	n/a
30	chr13:55373388-55373438	A549	lung:	n/a
31	chr13:55373912-55373962	HMEC	breast:	n/a
32	chr13:55419681-55419731	NB4	blood:	n/a
33	chr13:55373388-55373438	PFSK-1	brain:	n/a
34	chr13:55419681-55419731	HEEpiC	esophagus:	n/a
35	chr13:55449282-55449332	HEEpiC	esophagus:	n/a
36	chr13:55408596-55408646	CMK	blood:	n/a
37	chr13:55408596-55408646	HRPEpiC	eye:	n/a
38	chr13:55419681-55419731	Hepatocyte	liver:	n/a
39	chr13:55373912-55373962	ECC-1	luminal epithelium:	n/a
40	chr13:55408596-55408646	BE2_C	brain:	n/a
41	chr13:55408596-55408646	HCT-116	colon:	n/a
42	chr13:55373912-55373962	NHBE	bronchial:	n/a
43	chr13:55449282-55449332	IMR90	lung:	fetal
44	chr13:55449282-55449332	A549	lung:	n/a
45	chr13:55373912-55373962	HCT-116	colon:	n/a
46	chr13:55373912-55373962	PFSK-1	brain:	n/a
47	chr13:55449282-55449332	PrEC	prostate:	n/a
48	chr13:55373912-55373962	AG04449	skin:	fetal
49	chr13:55449282-55449332	BJ	skin:	n/a
50	chr13:55408596-55408646	Jurkat	blood:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:55225858..55228081-chr13:55229883..55232107,2	MCF-7	breast:
2	chr13:55225858..55228081-chr13:55229883..55232107,2	MCF-7	breast:
3	chr13:55321697..55323262-chr13:55324790..55327522,2	K562	blood:
4	chr13:55372674..55374590-chr7:122830546..122833222,2	MCF-7	breast:
5	chr13:55165909..55168648-chr13:55172019..55174969,2	MCF-7	breast:
6	chr13:55165909..55168648-chr13:55172019..55174969,2	MCF-7	breast:
7	chr1:114505901..114506720-chr13:55199515..55200372,2	MCF-7	breast:
8	chr13:55199830..55202056-chr13:55206437..55209228,2	MCF-7	breast:
9	chr13:55145225..55147281-chr13:55171713..55173554,2	MCF-7	breast:
10	chr13:55321697..55323262-chr13:55324790..55327522,2	K562	blood:
11	chr13:55286253..55286882-chr13:55307575..55308197,2	MCF-7	breast:
12	chr13:55199830..55202056-chr13:55206437..55209228,2	MCF-7	breast:
13	chr13:55286253..55286882-chr13:55307575..55308197,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OLFM4-12	chr13:55359420-55359736	NONHSAT034035
2	lnc-OLFM4-5	chr13:55260674-55260848	XLOC_010400
3	lnc-OLFM4-5	chr13:55264457-55264577	XLOC_010400
4	lnc-OLFM4-12	chr13:55361374-55361452	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: 5236 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:5236 , 50 per page) page: 1 2 3 4 5 6 7 ... 105

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs145164952	chr13:55159674-55159675	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531890380	chr13:55159676-55159677	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs117726561	chr13:55159677-55159678	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs139001516	chr13:55159701-55159702	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149408454	chr13:55159736-55159737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs144779154	chr13:55159803-55159804	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs567115775	chr13:55159815-55159816	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs535827452	chr13:55159843-55159844	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs532583699	chr13:55159844-55159845	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs181573834	chr13:55159852-55159853	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs148228055	chr13:55159865-55159866	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs80030908	chr13:55159898-55159899	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186330311	chr13:55159905-55159906	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191230370	chr13:55159913-55159914	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs141204044	chr13:55159920-55159921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs147363652	chr13:55159926-55159927	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533619424	chr13:55159955-55159956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs182907172	chr13:55159996-55159997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113790171	chr13:55160002-55160003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs543041929	chr13:55160047-55160048	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs562912527	chr13:55160055-55160056	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs576567927	chr13:55160097-55160098	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs545489401	chr13:55160156-55160157	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534563403	chr13:55160165-55160166	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs373088292	chr13:55160192-55160193	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs565306319	chr13:55160249-55160250	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs7994187	chr13:55160268-55160269	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs547706835	chr13:55160270-55160271	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561221749	chr13:55160301-55160302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs530371524	chr13:55160304-55160305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9527228	chr13:55160307-55160308	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187257117	chr13:55160330-55160331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs538327390	chr13:55160337-55160338	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs9536770	chr13:55160401-55160402	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs34562600	chr13:55160469-55160470	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201355128	chr13:55160479-55160480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs9536771	chr13:55160480-55160481	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs534796515	chr13:55160493-55160494	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs554516745	chr13:55160495-55160496	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs9527229	chr13:55160504-55160505	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
41	rs139455903	chr13:55160507-55160508	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs569965866	chr13:55160508-55160509	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556553069	chr13:55160509-55160510	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs576524537	chr13:55160567-55160568	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs545135162	chr13:55160574-55160575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565362706	chr13:55160576-55160577	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572473468	chr13:55160580-55160581	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs541609388	chr13:55160605-55160606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539001645	chr13:55160712-55160713	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs561186162	chr13:55160748-55160749	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

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

Chromatin state (count:294 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:55146000-55167000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr13:55146800-55160000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr13:55149400-55160400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr13:55157200-55160400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr13:55158200-55159800	Weak transcription	H1 Cell Line	embryonic stem cell
6	chr13:55158200-55159800	Weak transcription	HUES64 Cell Line	embryonic stem cell
7	chr13:55158200-55160200	Weak transcription	HUES48 Cell Line	embryonic stem cell
8	chr13:55158200-55160600	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr13:55158600-55160800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:55159600-55161400	Enhancers	ES-I3 Cell Line	embryonic stem cell
11	chr13:55159800-55161200	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr13:55160200-55161200	Enhancers	HUES48 Cell Line	embryonic stem cell
13	chr13:55160400-55161000	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr13:55160400-55161200	Enhancers	iPS-15b Cell Line	embryonic stem cell
15	chr13:55160600-55161200	Enhancers	HUES6 Cell Line	embryonic stem cell
16	chr13:55160800-55161200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
17	chr13:55161000-55173200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
18	chr13:55161200-55166800	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr13:55161200-55168200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:55161200-55171200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
21	chr13:55161200-55171400	Weak transcription	HUES64 Cell Line	embryonic stem cell
22	chr13:55164200-55164400	Enhancers	Aorta	Aorta
23	chr13:55164400-55167400	Weak transcription	Pancreas	Pancrea
24	chr13:55166800-55168000	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
25	chr13:55167000-55167400	Strong transcription	ES-UCSF4 Cell Line	embryonic stem cell
26	chr13:55167200-55168000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr13:55167200-55168000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
28	chr13:55167400-55168000	ZNF genes & repeats	Pancreas	Pancrea
29	chr13:55167400-55169800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr13:55167600-55168200	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
31	chr13:55168000-55168600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr13:55168200-55168400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
33	chr13:55168400-55174800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:55169200-55172200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chr13:55171200-55172400	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr13:55171400-55172400	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr13:55171600-55172200	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chr13:55171800-55172400	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr13:55172000-55172400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr13:55172200-55172400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
41	chr13:55172200-55173400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
42	chr13:55172400-55172800	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr13:55172400-55173400	Weak transcription	HUES48 Cell Line	embryonic stem cell
44	chr13:55172400-55173400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
45	chr13:55172800-55173800	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr13:55173200-55173800	Enhancers	iPS-20b Cell Line	embryonic stem cell
47	chr13:55173400-55173600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chr13:55173400-55173800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chr13:55173400-55174000	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr13:55174800-55175000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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