Variant report

Variant	esv3378326
Chromosome Location	chr13:92445514-92816367
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:92598892-92598945	HepG2	liver:	n/a	n/a
2	ARID3A	chr13:92706389-92707091	HepG2	liver:	n/a	n/a
3	ARID3A	chr13:92727057-92727252	HepG2	liver:	n/a	n/a
4	ATF1	chr13:92470400-92470441	K562	blood:	n/a	n/a
5	ATF1	chr13:92463548-92463576	K562	blood:	n/a	n/a
6	ATF1	chr13:92468954-92469236	K562	blood:	n/a	n/a
7	ATF1	chr13:92450496-92450693	K562	blood:	n/a	n/a
8	ATF1	chr13:92462880-92462901	K562	blood:	n/a	n/a
9	ATF1	chr13:92461246-92461251	K562	blood:	n/a	n/a
10	ATF1	chr13:92471938-92472009	K562	blood:	n/a	n/a
11	ATF1	chr13:92460655-92460924	K562	blood:	n/a	n/a
12	ATF1	chr13:92469517-92469882	K562	blood:	n/a	n/a
13	ATF2	chr13:92556757-92557259	GM12878	blood:	n/a	n/a
14	BACH1	chr13:92599023-92599082	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr13:92457657-92457845	K562	blood:	n/a	n/a
16	BATF	chr13:92556870-92557182	GM12878	blood:	n/a	n/a
17	BHLHE40	chr13:92470981-92471020	K562	blood:	n/a	n/a
18	BHLHE40	chr13:92706676-92707043	HepG2	liver:	n/a	n/a
19	BHLHE40	chr13:92538406-92538598	GM12878	blood:	n/a	n/a
20	BRCA1	chr13:92537783-92537791	GM12878	blood:	n/a	n/a
21	BRCA1	chr13:92749581-92749765	Hela-S3	cervix:	n/a	n/a
22	BRCA1	chr13:92556588-92556667	GM12878	blood:	n/a	n/a
23	BRCA1	chr13:92598894-92599094	H1-hESC	embryonic stem cell:	n/a	n/a
24	CCNT2	chr13:92470402-92470455	K562	blood:	n/a	n/a
25	CEBPB	chr13:92789866-92790156	ECC-1	luminal epithelium:	n/a	chr13:92789934-92789945
26	CEBPB	chr13:92596730-92596763	HepG2	liver:	n/a	n/a
27	CEBPB	chr13:92789803-92790084	A549	lung:	n/a	chr13:92789934-92789945
28	CEBPB	chr13:92541962-92542286	A549	lung:	n/a	chr13:92542094-92542105
29	CEBPB	chr13:92541972-92542463	Hela-S3	cervix:	n/a	chr13:92542094-92542105
30	CEBPB	chr13:92774842-92775127	ECC-1	luminal epithelium:	n/a	chr13:92774900-92774917 chr13:92774920-92774929 chr13:92774918-92774929 chr13:92774903-92774912 chr13:92774919-92774930 chr13:92774903-92774912 chr13:92774902-92774913 chr13:92774903-92774912
31	CEBPB	chr13:92571793-92572025	HepG2	liver:	n/a	chr13:92571908-92571919 chr13:92571908-92571921
32	CEBPB	chr13:92774824-92775081	A549	lung:	n/a	chr13:92774900-92774917 chr13:92774920-92774929 chr13:92774918-92774929 chr13:92774903-92774912 chr13:92774919-92774930 chr13:92774903-92774912 chr13:92774902-92774913 chr13:92774903-92774912
33	CEBPB	chr13:92594074-92594349	HepG2	liver:	n/a	chr13:92594096-92594108 chr13:92594215-92594226
34	CEBPB	chr13:92789779-92790132	HepG2	liver:	n/a	chr13:92789934-92789945
35	CEBPB	chr13:92751439-92751782	HepG2	liver:	n/a	chr13:92751617-92751628 chr13:92751616-92751629 chr13:92751616-92751627
36	CEBPB	chr13:92789848-92790073	ECC-1	luminal epithelium:	n/a	chr13:92789934-92789945
37	CEBPB	chr13:92452755-92453125	K562	blood:	n/a	chr13:92452945-92452954 chr13:92452945-92452954 chr13:92452943-92452954 chr13:92452945-92452954 chr13:92452945-92452954 chr13:92452943-92452956
38	CEBPB	chr13:92789780-92790090	IMR90	lung:	n/a	chr13:92789934-92789945
39	CEBPB	chr13:92706703-92707067	HepG2	liver:	n/a	n/a
40	CEBPB	chr13:92452831-92452989	H1-hESC	embryonic stem cell:	n/a	chr13:92452945-92452954 chr13:92452945-92452954 chr13:92452943-92452954 chr13:92452945-92452954 chr13:92452945-92452954 chr13:92452943-92452956
41	CEBPB	chr13:92764626-92764973	HepG2	liver:	n/a	chr13:92764787-92764798 chr13:92764787-92764800 chr13:92764787-92764800 chr13:92764789-92764800 chr13:92764787-92764800
42	CEBPB	chr13:92700852-92701110	HepG2	liver:	n/a	chr13:92700942-92700953 chr13:92700942-92700955
43	CEBPB	chr13:92795350-92795619	HepG2	liver:	n/a	chr13:92795526-92795539
44	CEBPB	chr13:92774725-92775096	IMR90	lung:	n/a	chr13:92774900-92774917 chr13:92774920-92774929 chr13:92774918-92774929 chr13:92774903-92774912 chr13:92774919-92774930 chr13:92774903-92774912 chr13:92774902-92774913 chr13:92774903-92774912
45	CEBPB	chr13:92808890-92809080	A549	lung:	n/a	chr13:92808950-92808961
46	CEBPB	chr13:92541920-92542294	IMR90	lung:	n/a	chr13:92542094-92542105
47	CEBPB	chr13:92706727-92707008	HepG2	liver:	n/a	n/a
48	CEBPB	chr13:92764704-92764936	H1-hESC	embryonic stem cell:	n/a	chr13:92764787-92764798 chr13:92764787-92764800 chr13:92764787-92764800 chr13:92764789-92764800 chr13:92764787-92764800
49	CEBPB	chr13:92639843-92640081	HepG2	liver:	n/a	chr13:92639879-92639892 chr13:92639966-92639977
50	CEBPB	chr13:92789872-92790007	HepG2	liver:	n/a	chr13:92789934-92789945

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:92601293-92601343	GM12892	blood:	n/a
2	chr13:92601293-92601343	SK-N-MC	brain:	n/a
3	chr13:92601293-92601343	H1-hESC	embryonic stem cell:	embryo
4	chr13:92601293-92601343	HEK293	kidney:	embryo
5	chr13:92601293-92601343	PFSK-1	brain:	n/a
6	chr13:92601293-92601343	ovcar-3	ovarian:	n/a
7	chr13:92601293-92601343	Hela-S3	cervix:	n/a
8	chr13:92601293-92601343	SAEC	small airway:	n/a
9	chr13:92601293-92601343	SK-N-SH	brain:	n/a
10	chr13:92601293-92601343	HL-60	blood:	n/a
11	chr13:92601293-92601343	PANC-1	pancreas:	n/a
12	chr13:92601293-92601343	AoSMC	blood vessel:	n/a
13	chr13:92601293-92601343	HAEpiC	amniotic membrane:	n/a
14	chr13:92601293-92601343	GM12878	blood:	n/a
15	chr13:92601293-92601343	HNPCEpiC	eye:	n/a
16	chr13:92601293-92601343	AG09319	gingival:	n/a
17	chr13:92601293-92601343	HCM	heart:	n/a
18	chr13:92601293-92601343	AG04450	lung:	fetal
19	chr13:92601293-92601343	MCF-7	breast:	n/a
20	chr13:92601293-92601343	IMR90	lung:	fetal
21	chr13:92601293-92601343	CMK	blood:	n/a
22	chr13:92601293-92601343	Caco-2	colon:	n/a
23	chr13:92601293-92601343	HUVEC	blood vessel:	n/a
24	chr13:92601293-92601343	PrEC	prostate:	n/a
25	chr13:92601293-92601343	AG09309	skin:	n/a
26	chr13:92601293-92601343	AG04449	skin:	fetal
27	chr13:92601293-92601343	ProgFib	skin:	n/a
28	chr13:92601293-92601343	ECC-1	luminal epithelium:	n/a
29	chr13:92601293-92601343	SKMC	muscle:	n/a
30	chr13:92601293-92601343	T-47D	breast:	n/a
31	chr13:92601293-92601343	GM19239	blood:	n/a
32	chr13:92601293-92601343	NHBE	bronchial:	n/a
33	chr13:92601293-92601343	HepG2	liver:	n/a
34	chr13:92601293-92601343	NT2-D1	testis:	n/a
35	chr13:92601293-92601343	HPAEpiC	pulmonary alveolar:	n/a
36	chr13:92601293-92601343	NB4	blood:	n/a
37	chr13:92601293-92601343	HCF	heart:	n/a
38	chr13:92601293-92601343	A549	lung:	n/a
39	chr13:92601293-92601343	Hepatocyte	liver:	n/a
40	chr13:92601293-92601343	BJ	skin:	n/a
41	chr13:92601293-92601343	K562	blood:	n/a
42	chr13:92601293-92601343	HCT-116	colon:	n/a
43	chr13:92601293-92601343	U87	brain:	n/a
44	chr13:92601293-92601343	NH-A	brain:	n/a
45	chr13:92601293-92601343	AG10803	skin:	n/a
46	chr13:92601293-92601343	RPTEC	kidney:	n/a
47	chr13:92601293-92601343	HRCEpiC	kidney:	n/a
48	chr13:92601293-92601343	HIPEpiC	eye:	n/a
49	chr13:92601293-92601343	SK-N-SH_RA	brain:	n/a
50	chr13:92601293-92601343	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr13:92464505..92466650-chr13:92470454..92472788,2	K562	blood:
2	chr13:92598658..92599490-chr13:92726652..92727595,3	MCF-7	breast:
3	chr13:92696291..92699011-chr13:92703757..92705620,2	K562	blood:
4	chr13:92447696..92448196-chr14:81686779..81687651,2	NB4	blood:
5	chr13:92598658..92599490-chr13:92726652..92727595,3	MCF-7	breast:
6	chr13:92598605..92599754-chr13:92795676..92796694,3	MCF-7	breast:
7	chr13:92013065..92015045-chr13:92455620..92457213,2	K562	blood:
8	chr13:92468912..92469761-chr13:92598813..92599378,2	MCF-7	breast:
9	chr13:92602210..92602711-chr5:139088387..139089016,2	MCF-7	breast:
10	chr13:91998535..92001268-chr13:92468179..92469811,2	K562	blood:
11	chr13:92696291..92699011-chr13:92703757..92705620,2	K562	blood:
12	chr13:92338961..92341299-chr13:92468919..92471382,2	K562	blood:
13	chr13:92598605..92599754-chr13:92795676..92796694,3	MCF-7	breast:
14	chr13:92468912..92469761-chr13:92598813..92599378,2	MCF-7	breast:
15	chr13:92464505..92466650-chr13:92470454..92472788,2	K562	blood:
16	chr13:92448522..92450690-chr15:34895323..34897374,2	K562	blood:
17	chr13:92425245..92427379-chr13:92459575..92462429,2	K562	blood:
18	chr13:92598450..92599301-chr13:92827714..92828302,2	MCF-7	breast:
19	chr13:92009180..92011434-chr13:92452798..92454691,2	K562	blood:
20	chr13:91999497..92001290-chr13:92470942..92473538,2	K562	blood:
21	chr13:92777089..92778054-chr2:189460184..189460902,2	MCF-7	breast:
22	chr13:92022295..92024727-chr13:92447599..92449200,2	K562	blood:
23	chr13:92008413..92010506-chr13:92466310..92469194,2	K562	blood:
24	chr13:92291902..92294855-chr13:92469701..92472559,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPC6-3	chr13:92506911-92506952	NONHSAT034698
2	lnc-GPC6-3	chr13:92508013-92508180	NONHSAT034698
3	lnc-GPC6-4	chr13:92483240-92483466	l_901_chr13:92483239-92484579_testes
4	lnc-GPC6-4	chr13:92484168-92484579	l_901_chr13:92483239-92484579_testes

Variant related genes	Relation type
RNU4ATAC3P	TF binding region
RNU4ATAC3P	CpG island
ENSG00000165417	chromatin interactions
ENSG00000215417	chromatin interactions

Extended variants
information (count: 4287 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:4287 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528624950	chr13:92446648-92446649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs551569118	chr13:92446664-92446665	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs36011642	chr13:92446698-92446699	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369271005	chr13:92446725-92446726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs1332090	chr13:92446741-92446742	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs386773352	chr13:92446769-92446770	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs2352030	chr13:92446770-92446771	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs58932811	chr13:92446780-92446781	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs536497176	chr13:92446794-92446795	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs555383583	chr13:92446796-92446797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543224062	chr13:92447003-92447004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs549306238	chr13:92447042-92447043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs186707783	chr13:92447149-92447150	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs9301753	chr13:92447151-92447152	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs117776547	chr13:92447181-92447182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs559731052	chr13:92447219-92447220	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs528453127	chr13:92447239-92447240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs35403380	chr13:92447250-92447251	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571497886	chr13:92447300-92447301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs149315594	chr13:92447302-92447303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs535906355	chr13:92447304-92447305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs565391672	chr13:92447388-92447389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs9301754	chr13:92447390-92447391	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs551197742	chr13:92447428-92447429	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs567851880	chr13:92447477-92447478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs530461724	chr13:92447522-92447523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs570698424	chr13:92447530-92447531	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs546959337	chr13:92447531-92447532	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs75607780	chr13:92447563-92447564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs556695817	chr13:92447584-92447585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs386773353	chr13:92447667-92447668	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1854976	chr13:92447669-92447670	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs370237335	chr13:92447714-92447715	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs571014610	chr13:92447736-92447737	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs536746887	chr13:92447744-92447745	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs556776460	chr13:92447752-92447753	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs142566603	chr13:92447770-92447771	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs536576051	chr13:92447777-92447778	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs191321304	chr13:92447798-92447799	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs144692298	chr13:92447804-92447805	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs545426996	chr13:92447872-92447873	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs565229456	chr13:92447898-92447899	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575852672	chr13:92447908-92447909	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs1854977	chr13:92447936-92447937	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs76414556	chr13:92447941-92447942	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs530256293	chr13:92447961-92447962	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs572632521	chr13:92447996-92447997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs547137785	chr13:92448028-92448029	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs2990003	chr13:92448093-92448094	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs564330177	chr13:92448167-92448168	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
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
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Ovarian cancer	22174824	CNVD
Myoepithelioma	18604193	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	18632612	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Melanoma	18172304	CNVD
Prostate cancer	16573809	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Basal cell lymphoma	17053054	CNVD
Metanephric adenoma	20802469	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21364760	CNVD
Medulloblastoma	19270706	CNVD
Myelofibrosis	22110671	CNVD
coloboma	21285886	CNVD
Cancer	20164920	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Acute myeloid leukemia	19651601	CNVD
Effusion lymphoma	18079361	CNVD
Developmental delay	21147756	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Osteosarcoma	21215367	CNVD
Melanoma	20877625	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:272 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:92446600-92446800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:92447000-92448200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr13:92447200-92450000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr13:92448200-92448600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
5	chr13:92448600-92450000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr13:92450000-92450200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
7	chr13:92450000-92450200	Enhancers	Fetal Heart	heart
8	chr13:92450200-92454000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr13:92452000-92452800	Weak transcription	Fetal Heart	heart
10	chr13:92452600-92453000	Enhancers	Fetal Lung	lung
11	chr13:92452600-92454000	Enhancers	Rectal Smooth Muscle	rectum
12	chr13:92452800-92453600	Enhancers	Fetal Heart	heart
13	chr13:92453000-92453800	Weak transcription	Fetal Lung	lung
14	chr13:92453400-92454200	Enhancers	Fetal Brain Male	brain
15	chr13:92453600-92456200	Weak transcription	Fetal Heart	heart
16	chr13:92453800-92454200	Enhancers	Fetal Lung	lung
17	chr13:92454000-92456400	Weak transcription	Rectal Smooth Muscle	rectum
18	chr13:92454200-92456600	Weak transcription	Fetal Lung	lung
19	chr13:92456200-92458000	Enhancers	Fetal Heart	heart
20	chr13:92456400-92457400	Enhancers	Rectal Smooth Muscle	rectum
21	chr13:92456600-92458000	Enhancers	Fetal Lung	lung
22	chr13:92456800-92457000	Enhancers	Placenta Amnion	Placenta Amnion
23	chr13:92457200-92457400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr13:92457200-92457400	Enhancers	H9 Cell Line	embryonic stem cell
25	chr13:92457400-92460600	Weak transcription	Rectal Smooth Muscle	rectum
26	chr13:92457400-92465600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:92457600-92457800	Enhancers	Placenta Amnion	Placenta Amnion
28	chr13:92458000-92463800	Weak transcription	Fetal Heart	heart
29	chr13:92458000-92464000	Weak transcription	Fetal Lung	lung
30	chr13:92458400-92459600	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chr13:92458400-92459800	Enhancers	HUES64 Cell Line	embryonic stem cell
32	chr13:92458800-92459000	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chr13:92458800-92459200	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chr13:92459000-92463600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
35	chr13:92459200-92465000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
36	chr13:92459600-92463200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
37	chr13:92459800-92461600	Weak transcription	HUES64 Cell Line	embryonic stem cell
38	chr13:92460600-92461000	Enhancers	HUES48 Cell Line	embryonic stem cell
39	chr13:92460600-92461600	Enhancers	Rectal Smooth Muscle	rectum
40	chr13:92461000-92463400	Weak transcription	HUES48 Cell Line	embryonic stem cell
41	chr13:92461200-92461800	Enhancers	Colon Smooth Muscle	Colon
42	chr13:92461600-92461800	Enhancers	HUES64 Cell Line	embryonic stem cell
43	chr13:92461600-92462000	Enhancers	iPS-15b Cell Line	embryonic stem cell
44	chr13:92461600-92464800	Weak transcription	Rectal Smooth Muscle	rectum
45	chr13:92461800-92462400	Weak transcription	HUES64 Cell Line	embryonic stem cell
46	chr13:92461800-92463800	Weak transcription	Colon Smooth Muscle	Colon
47	chr13:92462000-92462400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr13:92462400-92463800	Enhancers	HUES64 Cell Line	embryonic stem cell
49	chr13:92462400-92464400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr13:92463200-92464000	Enhancers	iPS-18 Cell Line	embryonic stem cell

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