Variant report

Variant	nsv832643
Chromosome Location	chr13:70324440-70486661
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:444)
CpG islands
(count:122)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:444 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:70485011-70485172	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:70431391-70431702	HepG2	liver:	n/a	n/a
3	BHLHE40	chr13:70430533-70430835	HepG2	liver:	n/a	chr13:70430691-70430700 chr13:70430688-70430701
4	BRCA1	chr13:70325178-70325338	GM12878	blood:	n/a	n/a
5	BRCA1	chr13:70431439-70431586	H1-hESC	embryonic stem cell:	n/a	n/a
6	CBX3	chr13:70351107-70351445	K562	blood:	n/a	n/a
7	CEBPB	chr13:70483573-70483710	H1-hESC	embryonic stem cell:	n/a	chr13:70483610-70483621 chr13:70483611-70483622
8	CEBPB	chr13:70440679-70441116	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr13:70483441-70483636	HepG2	liver:	n/a	chr13:70483610-70483621 chr13:70483611-70483622
10	CEBPB	chr13:70368078-70368276	H1-hESC	embryonic stem cell:	n/a	n/a
11	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
12	CEBPB	chr13:70430376-70430903	Hela-S3	cervix:	n/a	chr13:70430726-70430738
13	CEBPB	chr13:70431436-70431605	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr13:70329765-70329832	H1-hESC	embryonic stem cell:	n/a	chr13:70329806-70329823
15	CHD2	chr13:70431490-70431624	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr13:70431440-70431590	GM12872	blood:	n/a	n/a
17	CTCF	chr13:70431720-70431870	GM12870	blood:	n/a	n/a
18	CTCF	chr13:70431520-70431670	HEEpiC	esophagus:	n/a	n/a
19	CTCF	chr13:70431460-70431610	GM12872	blood:	n/a	n/a
20	CTCF	chr13:70431460-70431610	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr13:70431520-70431670	HA-sp	spinal cord:	n/a	n/a
22	CTCF	chr13:70431461-70431554	ProgFib	skin:	n/a	n/a
23	CTCF	chr13:70431460-70431610	HRE	kidney:	n/a	n/a
24	CTCF	chr13:70431500-70431650	Hela-S3	cervix:	n/a	n/a
25	CTCF	chr13:70431400-70431550	RPTEC	kidney:	n/a	n/a
26	CTCF	chr13:70431380-70431530	BE2_C	brain:	n/a	n/a
27	CTCF	chr13:70431440-70431590	GM06990	blood:	n/a	n/a
28	CTCF	chr13:70431480-70431630	WI-38	lung:	n/a	n/a
29	CTCF	chr13:70431417-70431706	Medullo	brain:	n/a	n/a
30	CTCF	chr13:70432156-70432241	GM20000	blood:	n/a	n/a
31	CTCF	chr13:70431480-70431630	Caco-2	colon:	n/a	n/a
32	CTCF	chr13:70431460-70431610	AG09309	skin:	n/a	n/a
33	CTCF	chr13:70432200-70432350	HPF	lung:	n/a	n/a
34	CTCF	chr13:70431473-70431707	Lung_OC	lung:	n/a	n/a
35	CTCF	chr13:70432181-70432274	ProgFib	skin:	n/a	n/a
36	CTCF	chr13:70431520-70431670	HCM	heart:	n/a	n/a
37	CTCF	chr13:70431500-70431650	GM12869	blood:	n/a	n/a
38	CTCF	chr13:70431325-70431773	HepG2	liver:	n/a	n/a
39	CTCF	chr13:70431500-70431650	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr13:70432276-70432278	Fibrobl	skin:	n/a	n/a
41	CTCF	chr13:70431460-70431610	GM12864	blood:	n/a	n/a
42	CTCF	chr13:70431440-70431664	GM10266	blood:	n/a	n/a
43	CTCF	chr13:70431414-70431682	GM12878	blood:	n/a	n/a
44	CTCF	chr13:70431402-70431635	HepG2	liver:	n/a	n/a
45	CTCF	chr13:70431466-70431637	LNCaP	prostate:	n/a	n/a
46	CTCF	chr13:70431313-70431687	T-47D	breast:	n/a	n/a
47	CTCF	chr13:70431381-70431767	MCF-7	breast:	n/a	n/a
48	CTCF	chr13:70476001-70476020	Fibrobl	skin:	n/a	n/a
49	CTCF	chr13:70431440-70431590	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr13:70431440-70431590	GM12873	blood:	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	K562	blood:	n/a
2	chr13:70431522-70431572	SK-N-SH_RA	brain:	n/a
3	chr13:70431522-70431572	IMR90	lung:	fetal
4	chr13:70431522-70431572	AG04450	lung:	fetal
5	chr13:70369137-70369187	HCF	heart:	n/a
6	chr13:70369137-70369187	GM19239	blood:	n/a
7	chr13:70369137-70369187	GM12892	blood:	n/a
8	chr13:70431522-70431572	HRPEpiC	eye:	n/a
9	chr13:70431522-70431572	HEK293	kidney:	embryo
10	chr13:70431522-70431572	HCPEpiC	choroid plexus:	n/a
11	chr13:70431522-70431572	GM06990	blood:	n/a
12	chr13:70369137-70369187	HCPEpiC	choroid plexus:	n/a
13	chr13:70369137-70369187	MCF10A-Er-Src	breast:	n/a
14	chr13:70431522-70431572	AG10803	skin:	n/a
15	chr13:70369137-70369187	NHDF-neo	bronchial:	n/a
16	chr13:70369137-70369187	AG09319	gingival:	n/a
17	chr13:70431522-70431572	HL-60	blood:	n/a
18	chr13:70369137-70369187	PANC-1	pancreas:	n/a
19	chr13:70369137-70369187	SK-N-SH_RA	brain:	n/a
20	chr13:70431522-70431572	HAEpiC	amniotic membrane:	n/a
21	chr13:70369137-70369187	RPTEC	kidney:	n/a
22	chr13:70369137-70369187	SAEC	small airway:	n/a
23	chr13:70369137-70369187	GM12878	blood:	n/a
24	chr13:70369137-70369187	HPAEpiC	pulmonary alveolar:	n/a
25	chr13:70369137-70369187	CMK	blood:	n/a
26	chr13:70431522-70431572	HMEC	breast:	n/a
27	chr13:70369137-70369187	IMR90	lung:	fetal
28	chr13:70431522-70431572	PrEC	prostate:	n/a
29	chr13:70369137-70369187	AG04450	lung:	fetal
30	chr13:70369137-70369187	HEK293	kidney:	embryo
31	chr13:70431522-70431572	GM19239	blood:	n/a
32	chr13:70369137-70369187	ECC-1	luminal epithelium:	n/a
33	chr13:70431522-70431572	AG09309	skin:	n/a
34	chr13:70431522-70431572	T-47D	breast:	n/a
35	chr13:70431522-70431572	Hela-S3	cervix:	n/a
36	chr13:70431522-70431572	PFSK-1	brain:	n/a
37	chr13:70369137-70369187	SK-N-MC	brain:	n/a
38	chr13:70431522-70431572	HEEpiC	esophagus:	n/a
39	chr13:70431522-70431572	NHBE	bronchial:	n/a
40	chr13:70431522-70431572	LNCaP	prostate:	n/a
41	chr13:70431522-70431572	NHDF-neo	bronchial:	n/a
42	chr13:70369137-70369187	T-47D	breast:	n/a
43	chr13:70369137-70369187	H1-hESC	embryonic stem cell:	embryo
44	chr13:70369137-70369187	NB4	blood:	n/a
45	chr13:70369137-70369187	MCF-7	breast:	n/a
46	chr13:70431522-70431572	H1-hESC	embryonic stem cell:	embryo
47	chr13:70369137-70369187	GM12891	blood:	n/a
48	chr13:70369137-70369187	HAEpiC	amniotic membrane:	n/a
49	chr13:70431522-70431572	MCF10A-Er-Src	breast:	n/a
50	chr13:70431522-70431572	MCF-7	breast:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:
2	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
3	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
4	chr13:70111760..70112275-chr13:70431222..70431945,2	K562	blood:
5	chr13:70159894..70160626-chr13:70431095..70431958,2	MCF-7	breast:
6	chr13:70343892..70346345-chr13:113863086..113865250,2	MCF-7	breast:
7	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
8	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
9	chr13:70444676..70447495-chr17:57919486..57921075,2	MCF-7	breast:
10	chr13:70111047..70112123-chr13:70431019..70432110,4	MCF-7	breast:
11	chr13:70456586..70458210-chr13:70462433..70464245,2	K562	blood:
12	chr13:70153553..70154097-chr13:70431151..70432026,2	MCF-7	breast:
13	chr13:70139358..70139986-chr13:70431208..70431784,2	MCF-7	breast:

No data

Variant related genes	Relation type
PSMC1P13	TF binding region
RNY3P10	TF binding region
PSMC1P13	CpG island
RNY3P10	CpG island
ENSG00000139842	chromatin interactions

Extended variants
information (count: 1336 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:1336 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200821332	chr13:70333236-70333237	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs12585046	chr13:70333237-70333238	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs74090445	chr13:70333248-70333249	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs564583427	chr13:70333271-70333272	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371694980	chr13:70333318-70333319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs546013925	chr13:70333378-70333379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs147743831	chr13:70333391-70333392	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs375043213	chr13:70343804-70343805	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs377466112	chr13:70343816-70343817	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs57740128	chr13:70343888-70343889	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs148361092	chr13:70343909-70343910	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs141497514	chr13:70343955-70343956	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182691867	chr13:70344056-70344057	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs534254629	chr13:70344068-70344069	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs113633162	chr13:70344079-70344080	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs577188421	chr13:70344083-70344084	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs546230424	chr13:70344150-70344151	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs370090600	chr13:70344151-70344152	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs150907396	chr13:70344179-70344180	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs541653412	chr13:70344240-70344241	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs185545186	chr13:70344251-70344252	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs9572269	chr13:70344259-70344260	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs139392850	chr13:70344267-70344268	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs142378365	chr13:70344296-70344297	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145949114	chr13:70344297-70344298	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs59525008	chr13:70344317-70344318	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs9646064	chr13:70344335-70344336	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs535584112	chr13:70344355-70344356	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs548357771	chr13:70344356-70344357	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs78322122	chr13:70344436-70344437	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs536960687	chr13:70344440-70344441	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs550860542	chr13:70344441-70344442	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs577126462	chr13:70344445-70344446	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs66985863	chr13:70344458-70344459	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs377199180	chr13:70344481-70344482	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs189908809	chr13:70344485-70344486	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs112617712	chr13:70344489-70344490	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs373787673	chr13:70344494-70344495	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs139805957	chr13:70344501-70344502	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573525913	chr13:70344502-70344503	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs143315520	chr13:70344542-70344543	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs561833279	chr13:70344543-70344544	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540822211	chr13:70344566-70344567	Enhancers ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs541282353	chr13:70344651-70344652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371835393	chr13:70344684-70344685	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs182700738	chr13:70344694-70344695	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs549508519	chr13:70344760-70344761	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs114192966	chr13:70344772-70344773	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs78554593	chr13:70344774-70344775	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs12864499	chr13:70344801-70344802	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:100)

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
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:78 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70333200-70333400	Enhancers	Esophagus	oesophagus
2	chr13:70343800-70344400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
3	chr13:70343800-70344600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr13:70343800-70344600	ZNF genes & repeats	Liver	Liver
5	chr13:70367600-70368200	Enhancers	HUES48 Cell Line	embryonic stem cell
6	chr13:70367800-70368200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
7	chr13:70367800-70368600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:70367800-70368600	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:70367800-70368600	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr13:70367800-70368800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:70368000-70368200	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr13:70368000-70368600	Enhancers	H1 Cell Line	embryonic stem cell
13	chr13:70368000-70368600	Enhancers	H9 Cell Line	embryonic stem cell
14	chr13:70368000-70368600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr13:70368000-70368600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr13:70368000-70368600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr13:70368000-70368800	Enhancers	iPS-15b Cell Line	embryonic stem cell
18	chr13:70368200-70368600	Flanking Active TSS	HUES48 Cell Line	embryonic stem cell
19	chr13:70368200-70368600	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chr13:70368200-70369000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
21	chr13:70368600-70368800	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chr13:70368600-70369000	Enhancers	HUES48 Cell Line	embryonic stem cell
23	chr13:70368600-70370400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr13:70370400-70371000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr13:70377400-70383200	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr13:70383000-70383600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr13:70383200-70383600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
28	chr13:70383600-70383800	Flanking Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr13:70383800-70384000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr13:70393200-70395000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:70394200-70394600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr13:70399800-70400200	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr13:70399800-70400400	Enhancers	iPS-20b Cell Line	embryonic stem cell
34	chr13:70399800-70400600	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr13:70400000-70400600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr13:70400000-70400800	Enhancers	iPS-18 Cell Line	embryonic stem cell
37	chr13:70400200-70402200	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chr13:70402000-70403600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr13:70402200-70403200	Enhancers	iPS-15b Cell Line	embryonic stem cell
40	chr13:70402200-70403400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chr13:70402600-70403200	Enhancers	Adipose Nuclei	Adipose
42	chr13:70402600-70403200	Enhancers	Placenta Amnion	Placenta Amnion
43	chr13:70402800-70403000	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr13:70402800-70403200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
45	chr13:70426000-70430400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr13:70428600-70430200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr13:70430200-70430600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
48	chr13:70430200-70430600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr13:70430200-70431200	Enhancers	Fetal Intestine Small	intestine
50	chr13:70430200-70431400	Enhancers	HUES48 Cell Line	embryonic stem cell

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