Variant report

Variant	nsv900483
Chromosome Location	chr13:70254555-70464234
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:551)
CpG islands
(count:122)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:551 , 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	ARID3A	chr13:70431391-70431702	HepG2	liver:	n/a	n/a
2	ATF2	chr13:70258281-70258806	GM12878	blood:	n/a	n/a
3	BHLHE40	chr13:70430533-70430835	HepG2	liver:	n/a	chr13:70430691-70430700 chr13:70430688-70430701
4	BHLHE40	chr13:70275529-70275573	GM12878	blood:	n/a	n/a
5	BRCA1	chr13:70325178-70325338	GM12878	blood:	n/a	n/a
6	BRCA1	chr13:70431439-70431586	H1-hESC	embryonic stem cell:	n/a	n/a
7	CBX3	chr13:70351107-70351445	K562	blood:	n/a	n/a
8	CEBPB	chr13:70296495-70296604	HepG2	liver:	n/a	n/a
9	CEBPB	chr13:70329765-70329832	H1-hESC	embryonic stem cell:	n/a	chr13:70329806-70329823
10	CEBPB	chr13:70368078-70368276	H1-hESC	embryonic stem cell:	n/a	n/a
11	CEBPB	chr13:70308944-70309274	HepG2	liver:	n/a	chr13:70309100-70309111 chr13:70309099-70309112
12	CEBPB	chr13:70295769-70296068	Hela-S3	cervix:	n/a	n/a
13	CEBPB	chr13:70431436-70431605	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr13:70430376-70430903	Hela-S3	cervix:	n/a	chr13:70430726-70430738
15	CEBPB	chr13:70440679-70441116	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr13:70328822-70329838	HepG2	liver:	n/a	chr13:70328921-70328934 chr13:70329806-70329823 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70328859-70328868 chr13:70329607-70329618 chr13:70329607-70329616 chr13:70329605-70329618 chr13:70329607-70329616 chr13:70329607-70329618 chr13:70329605-70329616
17	CEBPB	chr13:70300298-70300460	H1-hESC	embryonic stem cell:	n/a	n/a
18	CHD2	chr13:70431490-70431624	H1-hESC	embryonic stem cell:	n/a	n/a
19	CTCF	chr13:70431720-70431870	GM12870	blood:	n/a	n/a
20	CTCF	chr13:70431500-70431650	BJ	skin:	n/a	n/a
21	CTCF	chr13:70431480-70431630	HepG2	liver:	n/a	n/a
22	CTCF	chr13:70431440-70431590	HEK293	kidney:	n/a	n/a
23	CTCF	chr13:70431409-70431668	GM13977	blood:	n/a	n/a
24	CTCF	chr13:70341569-70341599	GM13977	blood:	n/a	n/a
25	CTCF	chr13:70431444-70431662	GM10248	blood:	n/a	n/a
26	CTCF	chr13:70286964-70287049	K562	blood:	n/a	n/a
27	CTCF	chr13:70431480-70431630	HCPEpiC	choroid plexus:	n/a	n/a
28	CTCF	chr13:70431432-70431665	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr13:70431460-70431610	MCF-7	breast:	n/a	n/a
30	CTCF	chr13:70451020-70451170	Caco-2	colon:	n/a	n/a
31	CTCF	chr13:70431480-70431630	GM06990	blood:	n/a	n/a
32	CTCF	chr13:70431440-70431590	HA-sp	spinal cord:	n/a	n/a
33	CTCF	chr13:70431274-70431765	A549	lung:	n/a	n/a
34	CTCF	chr13:70377800-70377950	GM12874	blood:	n/a	n/a
35	CTCF	chr13:70258260-70258410	BE2_C	brain:	n/a	n/a
36	CTCF	chr13:70431420-70431570	HepG2	liver:	n/a	n/a
37	CTCF	chr13:70431400-70431550	RPTEC	kidney:	n/a	n/a
38	CTCF	chr13:70431480-70431630	HFF-Myc	foreskin:	n/a	n/a
39	CTCF	chr13:70431480-70431630	GM12864	blood:	n/a	n/a
40	CTCF	chr13:70431440-70431663	K562	blood:	n/a	n/a
41	CTCF	chr13:70431017-70431882	SK-N-SH	brain:	n/a	n/a
42	CTCF	chr13:70431520-70431670	BJ	skin:	n/a	n/a
43	CTCF	chr13:70431480-70431630	NHDF-neo	bronchial:	n/a	n/a
44	CTCF	chr13:70286989-70287010	GM12878	blood:	n/a	n/a
45	CTCF	chr13:70431460-70431610	AG09309	skin:	n/a	n/a
46	CTCF	chr13:70431420-70431570	GM12866	blood:	n/a	n/a
47	CTCF	chr13:70381758-70381815	Lung_OC	lung:	n/a	n/a
48	CTCF	chr13:70431480-70431630	AG09319	gingival:	n/a	n/a
49	CTCF	chr13:70431440-70431661	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr13:70431381-70431767	MCF-7	breast:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:70431522-70431572	HL-60	blood:	n/a
2	chr13:70431522-70431572	H1-hESC	embryonic stem cell:	embryo
3	chr13:70431522-70431572	Hela-S3	cervix:	n/a
4	chr13:70431522-70431572	HRE	kidney:	n/a
5	chr13:70369137-70369187	HCF	heart:	n/a
6	chr13:70431522-70431572	ovcar-3	ovarian:	n/a
7	chr13:70369137-70369187	ECC-1	luminal epithelium:	n/a
8	chr13:70369137-70369187	LNCaP	prostate:	n/a
9	chr13:70369137-70369187	PANC-1	pancreas:	n/a
10	chr13:70369137-70369187	PFSK-1	brain:	n/a
11	chr13:70431522-70431572	RPTEC	kidney:	n/a
12	chr13:70431522-70431572	NHBE	bronchial:	n/a
13	chr13:70431522-70431572	PANC-1	pancreas:	n/a
14	chr13:70369137-70369187	AG10803	skin:	n/a
15	chr13:70369137-70369187	GM12892	blood:	n/a
16	chr13:70431522-70431572	HUVEC	blood vessel:	n/a
17	chr13:70431522-70431572	HCPEpiC	choroid plexus:	n/a
18	chr13:70369137-70369187	HMEC	breast:	n/a
19	chr13:70369137-70369187	HUVEC	blood vessel:	n/a
20	chr13:70431522-70431572	Hepatocyte	liver:	n/a
21	chr13:70369137-70369187	ProgFib	skin:	n/a
22	chr13:70431522-70431572	HCM	heart:	n/a
23	chr13:70431522-70431572	K562	blood:	n/a
24	chr13:70369137-70369187	ovcar-3	ovarian:	n/a
25	chr13:70369137-70369187	IMR90	lung:	fetal
26	chr13:70431522-70431572	PFSK-1	brain:	n/a
27	chr13:70431522-70431572	HCT-116	colon:	n/a
28	chr13:70369137-70369187	SK-N-SH_RA	brain:	n/a
29	chr13:70431522-70431572	SKMC	muscle:	n/a
30	chr13:70369137-70369187	HNPCEpiC	eye:	n/a
31	chr13:70369137-70369187	HAEpiC	amniotic membrane:	n/a
32	chr13:70369137-70369187	HRPEpiC	eye:	n/a
33	chr13:70369137-70369187	GM19239	blood:	n/a
34	chr13:70431522-70431572	SK-N-SH	brain:	n/a
35	chr13:70369137-70369187	AoSMC	blood vessel:	n/a
36	chr13:70369137-70369187	HIPEpiC	eye:	n/a
37	chr13:70369137-70369187	NH-A	brain:	n/a
38	chr13:70431522-70431572	MCF10A-Er-Src	breast:	n/a
39	chr13:70431522-70431572	BE2_C	brain:	n/a
40	chr13:70431522-70431572	HRCEpiC	kidney:	n/a
41	chr13:70431522-70431572	HCF	heart:	n/a
42	chr13:70369137-70369187	Caco-2	colon:	n/a
43	chr13:70369137-70369187	HCM	heart:	n/a
44	chr13:70369137-70369187	MCF-7	breast:	n/a
45	chr13:70369137-70369187	HL-60	blood:	n/a
46	chr13:70369137-70369187	SKMC	muscle:	n/a
47	chr13:70431522-70431572	HAEpiC	amniotic membrane:	n/a
48	chr13:70431522-70431572	LNCaP	prostate:	n/a
49	chr13:70431522-70431572	HPAEpiC	pulmonary alveolar:	n/a
50	chr13:70431522-70431572	HNPCEpiC	eye:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
2	chr13:70111047..70112123-chr13:70431019..70432110,4	MCF-7	breast:
3	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
4	chr13:70281102..70281979-chr16:2731851..2732580,2	MCF-7	breast:
5	chr13:70343892..70346345-chr13:113863086..113865250,2	MCF-7	breast:
6	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:
7	chr13:70271603..70273702-chr13:70276559..70278431,2	K562	blood:
8	chr13:70444676..70447495-chr17:57919486..57921075,2	MCF-7	breast:
9	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
10	chr13:70153553..70154097-chr13:70431151..70432026,2	MCF-7	breast:
11	chr13:70139358..70139986-chr13:70431208..70431784,2	MCF-7	breast:
12	chr13:70249631..70251882-chr13:70253333..70255746,2	K562	blood:
13	chr13:70159894..70160626-chr13:70431095..70431958,2	MCF-7	breast:
14	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
15	chr11:65198093..65198776-chr13:70273636..70274136,2	Hela-S3	cervix:
16	chr13:70111760..70112275-chr13:70431222..70431945,2	K562	blood:
17	chr13:70271603..70273702-chr13:70276559..70278431,2	K562	blood:
18	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:

No data

Variant related genes	Relation type
RNY3P10	TF binding region
RNY3P10	CpG island
ENSG00000167977	chromatin interactions
ENSG00000139842	chromatin interactions

Extended variants
information (count: 2476 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2476 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181258001	chr13:70255878-70255879	Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs71415694	chr13:70255895-70255896	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs1932989	chr13:70255896-70255897	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs116279938	chr13:70255918-70255919	Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs530248052	chr13:70255965-70255966	Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs117425268	chr13:70255980-70255981	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs566475681	chr13:70255991-70255992	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs146388908	chr13:70256032-70256033	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs139134777	chr13:70256034-70256035	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs570100502	chr13:70256046-70256047	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs561052422	chr13:70256055-70256056	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs185222681	chr13:70256073-70256074	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs1932988	chr13:70256123-70256124	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs79659325	chr13:70256152-70256153	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs571820978	chr13:70256188-70256189	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs114209711	chr13:70256194-70256195	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs533774679	chr13:70256316-70256317	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs189741428	chr13:70256331-70256332	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs573296312	chr13:70256341-70256342	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545479858	chr13:70256353-70256354	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs558582502	chr13:70256400-70256401	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs575248860	chr13:70256421-70256422	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs2152778	chr13:70256464-70256465	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs2152777	chr13:70256482-70256483	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs180670935	chr13:70256498-70256499	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs35748656	chr13:70256520-70256521	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs111754425	chr13:70256569-70256570	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs2325240	chr13:70256583-70256584	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs74092440	chr13:70256593-70256594	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs555936437	chr13:70256598-70256599	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs12865145	chr13:70256600-70256601	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs531352140	chr13:70256614-70256615	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs548183632	chr13:70256622-70256623	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs186355760	chr13:70256623-70256624	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs115199664	chr13:70256624-70256625	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs547320476	chr13:70256626-70256627	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs183800026	chr13:70256633-70256634	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs374489518	chr13:70256678-70256679	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs539208056	chr13:70256690-70256691	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs12864266	chr13:70256773-70256774	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs188285627	chr13:70256854-70256855	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs12864670	chr13:70256858-70256859	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs146454184	chr13:70256903-70256904	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs373619591	chr13:70256905-70256906	Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs79181164	chr13:70256914-70256915	Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs12864567	chr13:70256957-70256958	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs552281119	chr13:70256986-70256987	Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs114195307	chr13:70257082-70257083	Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs577382727	chr13:70257097-70257098	Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs9529617	chr13:70257121-70257122	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:101)

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
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
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Prostate cancer	16461572	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Myelofibrosis	22110671	CNVD
Esophageal cancer	21851588	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:127 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70255800-70258800	Active TSS	K562	blood
2	chr13:70257800-70259600	Enhancers	Fetal Intestine Large	intestine
3	chr13:70257800-70259600	Enhancers	Fetal Intestine Small	intestine
4	chr13:70258000-70258400	Enhancers	Primary hematopoietic stem cells short term culture	blood
5	chr13:70258000-70258800	Enhancers	Primary hematopoietic stem cells	blood
6	chr13:70258000-70259000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
7	chr13:70258000-70259600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:70258200-70258600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
9	chr13:70258200-70258800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr13:70258200-70259400	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr13:70258200-70259800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr13:70258600-70259000	Active TSS	GM12878-XiMat	blood
13	chr13:70258600-70259800	Enhancers	iPS-20b Cell Line	embryonic stem cell
14	chr13:70258600-70260000	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr13:70258800-70263600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:70259400-70259800	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:70259400-70259800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr13:70259400-70265000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr13:70259600-70260800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
20	chr13:70259800-70262200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr13:70259800-70264600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
22	chr13:70259800-70264800	Weak transcription	HUES48 Cell Line	embryonic stem cell
23	chr13:70260000-70264600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr13:70260800-70261400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:70261400-70261800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
26	chr13:70261800-70262600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
27	chr13:70262200-70262800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
28	chr13:70263800-70264000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:70264600-70265400	Enhancers	iPS-18 Cell Line	embryonic stem cell
30	chr13:70264600-70265400	Enhancers	iPS-20b Cell Line	embryonic stem cell
31	chr13:70264800-70265600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chr13:70265000-70265400	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr13:70265000-70265400	Enhancers	HUES64 Cell Line	embryonic stem cell
34	chr13:70276400-70294200	Weak transcription	Hela-S3	cervix
35	chr13:70277800-70279200	Enhancers	Placenta Amnion	Placenta Amnion
36	chr13:70278600-70278800	Enhancers	Pancreatic Islets	Pancreatic Islet
37	chr13:70280400-70280600	Weak transcription	Pancreatic Islets	Pancreatic Islet
38	chr13:70280600-70281600	Enhancers	Pancreatic Islets	Pancreatic Islet
39	chr13:70288400-70293400	Weak transcription	Fetal Intestine Small	intestine
40	chr13:70293400-70295400	Enhancers	Fetal Intestine Small	intestine
41	chr13:70293400-70295600	Enhancers	Rectal Mucosa Donor 31	rectum
42	chr13:70294200-70295000	Active TSS	Rectal Mucosa Donor 29	rectum
43	chr13:70294400-70294600	Enhancers	Liver	Liver
44	chr13:70294400-70295000	Enhancers	HepG2	liver
45	chr13:70294600-70294800	Flanking Active TSS	Liver	Liver
46	chr13:70294800-70295000	Active TSS	Liver	Liver
47	chr13:70294800-70295600	Enhancers	Fetal Intestine Large	intestine
48	chr13:70295200-70295600	Enhancers	Rectal Mucosa Donor 29	rectum
49	chr13:70300000-70300400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr13:70311200-70312200	Enhancers	Pancreas	Pancrea

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