Variant report

Variant	nsv900482
Chromosome Location	chr13:70186605-70383876
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:336)
CpG islands
(count:61)
Chromatin interactive
region (count:14)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:336 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr13:70258281-70258806	GM12878	blood:	n/a	n/a
2	BACH1	chr13:70250741-70250952	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr13:70251604-70251776	GM12878	blood:	n/a	chr13:70251694-70251705
4	BHLHE40	chr13:70251405-70251582	GM12878	blood:	n/a	n/a
5	BHLHE40	chr13:70275529-70275573	GM12878	blood:	n/a	n/a
6	BRCA1	chr13:70325178-70325338	GM12878	blood:	n/a	n/a
7	BRCA1	chr13:70212779-70212821	GM12878	blood:	n/a	n/a
8	CBX3	chr13:70351107-70351445	K562	blood:	n/a	n/a
9	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
10	CEBPB	chr13:70230999-70231245	HepG2	liver:	n/a	chr13:70231088-70231099
11	CEBPB	chr13:70300298-70300460	H1-hESC	embryonic stem cell:	n/a	n/a
12	CEBPB	chr13:70368078-70368276	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr13:70308944-70309274	HepG2	liver:	n/a	chr13:70309100-70309111 chr13:70309099-70309112
14	CEBPB	chr13:70222228-70222409	HepG2	liver:	n/a	chr13:70222250-70222261
15	CEBPB	chr13:70228603-70228905	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr13:70296495-70296604	HepG2	liver:	n/a	n/a
17	CEBPB	chr13:70228711-70228846	K562	blood:	n/a	n/a
18	CEBPB	chr13:70295769-70296068	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:70190558-70190930	Hela-S3	cervix:	n/a	n/a
20	CEBPB	chr13:70329765-70329832	H1-hESC	embryonic stem cell:	n/a	chr13:70329806-70329823
21	CEBPB	chr13:70191691-70191973	HepG2	liver:	n/a	n/a
22	CEBPB	chr13:70231021-70231199	A549	lung:	n/a	chr13:70231088-70231099
23	CTCF	chr13:70286989-70287010	GM12878	blood:	n/a	n/a
24	CTCF	chr13:70286980-70287130	K562	blood:	n/a	n/a
25	CTCF	chr13:70360719-70360758	Spleen_OC	spleen:	n/a	n/a
26	CTCF	chr13:70286933-70287133	GM12878	blood:	n/a	n/a
27	CTCF	chr13:70381758-70381815	Lung_OC	lung:	n/a	n/a
28	CTCF	chr13:70286964-70287049	K562	blood:	n/a	n/a
29	CTCF	chr13:70377800-70377950	GM12874	blood:	n/a	n/a
30	CTCF	chr13:70233240-70233390	BE2_C	brain:	n/a	n/a
31	CTCF	chr13:70248580-70248606	GM13976	blood:	n/a	n/a
32	CTCF	chr13:70289440-70289590	GM12869	blood:	n/a	n/a
33	CTCF	chr13:70286989-70287027	GM19239	blood:	n/a	n/a
34	CTCF	chr13:70356710-70356796	Kidney_OC	kidney:	n/a	n/a
35	CTCF	chr13:70219000-70219150	GM12872	blood:	n/a	n/a
36	CTCF	chr13:70341569-70341599	GM13977	blood:	n/a	n/a
37	CTCF	chr13:70311760-70311910	BE2_C	brain:	n/a	n/a
38	CTCF	chr13:70266080-70266230	HPF	lung:	n/a	n/a
39	CTCF	chr13:70258260-70258410	BE2_C	brain:	n/a	n/a
40	CTCF	chr13:70289400-70289550	GM12867	blood:	n/a	n/a
41	E2F4	chr13:70295665-70295786	MCF10A-Er-Src	breast:	n/a	n/a
42	E2F4	chr13:70257485-70257609	MCF10A-Er-Src	breast:	n/a	n/a
43	E2F4	chr13:70324263-70324404	MCF10A-Er-Src	breast:	n/a	n/a
44	E2F4	chr13:70216818-70217005	MCF10A-Er-Src	breast:	n/a	n/a
45	E2F4	chr13:70256200-70256365	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr13:70279575-70279882	MCF10A-Er-Src	breast:	n/a	n/a
47	E2F4	chr13:70282815-70282921	MCF10A-Er-Src	breast:	n/a	n/a
48	E2F4	chr13:70273676-70273680	MCF10A-Er-Src	breast:	n/a	n/a
49	E2F4	chr13:70255489-70255769	MCF10A-Er-Src	breast:	n/a	chr13:70255733-70255747
50	E2F4	chr13:70258995-70259121	MCF10A-Er-Src	breast:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:70369137-70369187	AG10803	skin:	n/a
2	chr13:70369137-70369187	BE2_C	brain:	n/a
3	chr13:70369137-70369187	HRPEpiC	eye:	n/a
4	chr13:70369137-70369187	LNCaP	prostate:	n/a
5	chr13:70369137-70369187	CMK	blood:	n/a
6	chr13:70369137-70369187	GM19239	blood:	n/a
7	chr13:70369137-70369187	HL-60	blood:	n/a
8	chr13:70369137-70369187	HepG2	liver:	n/a
9	chr13:70369137-70369187	PANC-1	pancreas:	n/a
10	chr13:70369137-70369187	HRE	kidney:	n/a
11	chr13:70369137-70369187	ECC-1	luminal epithelium:	n/a
12	chr13:70369137-70369187	MCF-7	breast:	n/a
13	chr13:70369137-70369187	NHBE	bronchial:	n/a
14	chr13:70369137-70369187	Jurkat	blood:	n/a
15	chr13:70369137-70369187	BJ	skin:	n/a
16	chr13:70369137-70369187	NH-A	brain:	n/a
17	chr13:70369137-70369187	PFSK-1	brain:	n/a
18	chr13:70369137-70369187	GM06990	blood:	n/a
19	chr13:70369137-70369187	A549	lung:	n/a
20	chr13:70369137-70369187	HCM	heart:	n/a
21	chr13:70369137-70369187	SK-N-SH_RA	brain:	n/a
22	chr13:70369137-70369187	U87	brain:	n/a
23	chr13:70369137-70369187	HRCEpiC	kidney:	n/a
24	chr13:70369137-70369187	HUVEC	blood vessel:	n/a
25	chr13:70369137-70369187	NB4	blood:	n/a
26	chr13:70369137-70369187	HEK293	kidney:	embryo
27	chr13:70369137-70369187	AG04450	lung:	fetal
28	chr13:70369137-70369187	HCPEpiC	choroid plexus:	n/a
29	chr13:70369137-70369187	SAEC	small airway:	n/a
30	chr13:70369137-70369187	AG09319	gingival:	n/a
31	chr13:70369137-70369187	SKMC	muscle:	n/a
32	chr13:70369137-70369187	HPAEpiC	pulmonary alveolar:	n/a
33	chr13:70369137-70369187	HCF	heart:	n/a
34	chr13:70369137-70369187	HEEpiC	esophagus:	n/a
35	chr13:70369137-70369187	H1-hESC	embryonic stem cell:	embryo
36	chr13:70369137-70369187	SK-N-SH	brain:	n/a
37	chr13:70369137-70369187	ovcar-3	ovarian:	n/a
38	chr13:70369137-70369187	Hela-S3	cervix:	n/a
39	chr13:70369137-70369187	HCT-116	colon:	n/a
40	chr13:70369137-70369187	NHDF-neo	bronchial:	n/a
41	chr13:70369137-70369187	Caco-2	colon:	n/a
42	chr13:70369137-70369187	IMR90	lung:	fetal
43	chr13:70369137-70369187	Hepatocyte	liver:	n/a
44	chr13:70369137-70369187	PrEC	prostate:	n/a
45	chr13:70369137-70369187	GM12891	blood:	n/a
46	chr13:70369137-70369187	NT2-D1	testis:	n/a
47	chr13:70369137-70369187	AoSMC	blood vessel:	n/a
48	chr13:70369137-70369187	GM12892	blood:	n/a
49	chr13:70369137-70369187	SK-N-MC	brain:	n/a
50	chr13:70369137-70369187	HNPCEpiC	eye:	n/a

(count:14 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
2	chr13:70249631..70251882-chr13:70253333..70255746,2	K562	blood:
3	chr13:70192216..70195164-chr13:70199916..70202276,2	MCF-7	breast:
4	chr13:70249631..70251882-chr13:70253333..70255746,2	K562	blood:
5	chr13:70281102..70281979-chr16:2731851..2732580,2	MCF-7	breast:
6	chr13:70344508..70346894-chr13:70348919..70351044,2	K562	blood:
7	chr13:70271603..70273702-chr13:70276559..70278431,2	K562	blood:
8	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
9	chr13:70343892..70346345-chr13:113863086..113865250,2	MCF-7	breast:
10	chr13:70192216..70195164-chr13:70199916..70202276,2	MCF-7	breast:
11	chr11:65198093..65198776-chr13:70273636..70274136,2	Hela-S3	cervix:
12	chr13:70378542..70380046-chr13:70380685..70382460,2	MCF-7	breast:
13	chr13:70207003..70207565-chr6:110796356..110796874,2	MCF-7	breast:
14	chr13:70271603..70273702-chr13:70276559..70278431,2	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: 2248 )
Associated
traits (count: 100 )

Variant overlapped rSNPs/rCNVs (count:2248 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2026130	chr13:70186605-70186606	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs550062045	chr13:70186688-70186689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs2026131	chr13:70186719-70186720	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs529458015	chr13:70186733-70186734	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs549148471	chr13:70186792-70186793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs577862156	chr13:70186804-70186805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs565796300	chr13:70186812-70186813	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs356938	chr13:70186816-70186817	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs533634606	chr13:70186829-70186830	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs374370307	chr13:70186874-70186875	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs537016635	chr13:70186893-70186894	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369017868	chr13:70186898-70186899	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs71116929	chr13:70186912-70186913	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs376625039	chr13:70186961-70186962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs573968765	chr13:70186963-70186964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs191032532	chr13:70186972-70186973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs12867185	chr13:70186983-70186984	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs572544796	chr13:70187000-70187001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs541178991	chr13:70187081-70187082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs183977829	chr13:70187085-70187086	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs577974742	chr13:70187099-70187100	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs78012810	chr13:70187108-70187109	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs79059607	chr13:70187109-70187110	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs397786772	chr13:70187116-70187117	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs188569862	chr13:70187144-70187145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs140823319	chr13:70187184-70187185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs576407017	chr13:70187211-70187212	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556827515	chr13:70187233-70187234	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs549210236	chr13:70187249-70187250	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs9572202	chr13:70187324-70187325	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs115319308	chr13:70187357-70187358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143081452	chr13:70187361-70187362	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1271433	chr13:70187367-70187368	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs150882857	chr13:70187396-70187397	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs12871412	chr13:70187398-70187399	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs9541993	chr13:70190006-70190007	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs575592981	chr13:70190014-70190015	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs563464505	chr13:70190026-70190027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs75552844	chr13:70190164-70190165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs369728814	chr13:70190168-70190169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571459837	chr13:70190177-70190178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs34720604	chr13:70190188-70190189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs372017873	chr13:70190215-70190216	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs115971886	chr13:70190231-70190232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs540856080	chr13:70190305-70190306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs207474002	chr13:70190348-70190349	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs142844890	chr13:70190351-70190352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs146411766	chr13:70190380-70190381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs552641890	chr13:70190398-70190399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs183735608	chr13:70190404-70190405	Weak transcription	n/a	n/a	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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:107 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:70186600-70187400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:70190000-70190200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr13:70190200-70190800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr13:70190800-70191600	Enhancers	Liver	Liver
5	chr13:70191600-70192400	Flanking Active TSS	Liver	Liver
6	chr13:70192400-70193800	Enhancers	Liver	Liver
7	chr13:70193600-70194000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr13:70193600-70194200	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr13:70195000-70197600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr13:70195200-70195400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chr13:70195800-70196600	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell
12	chr13:70196000-70197600	Weak transcription	H9 Cell Line	embryonic stem cell
13	chr13:70197000-70197800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr13:70197400-70198600	ZNF genes & repeats	HUES48 Cell Line	embryonic stem cell
15	chr13:70197600-70198000	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
16	chr13:70197600-70198400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
17	chr13:70198600-70198800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
18	chr13:70200600-70200800	Enhancers	Pancreas	Pancrea
19	chr13:70217600-70219200	Enhancers	GM12878-XiMat	blood
20	chr13:70217800-70218800	Enhancers	Liver	Liver
21	chr13:70218800-70219400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr13:70228000-70228400	Active TSS	Liver	Liver
23	chr13:70228400-70228600	Enhancers	Liver	Liver
24	chr13:70250400-70251000	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
25	chr13:70255800-70258800	Active TSS	K562	blood
26	chr13:70257800-70259600	Enhancers	Fetal Intestine Large	intestine
27	chr13:70257800-70259600	Enhancers	Fetal Intestine Small	intestine
28	chr13:70258000-70258400	Enhancers	Primary hematopoietic stem cells short term culture	blood
29	chr13:70258000-70258800	Enhancers	Primary hematopoietic stem cells	blood
30	chr13:70258000-70259000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chr13:70258000-70259600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr13:70258200-70258600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr13:70258200-70258800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr13:70258200-70259400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chr13:70258200-70259800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chr13:70258600-70259000	Active TSS	GM12878-XiMat	blood
37	chr13:70258600-70259800	Enhancers	iPS-20b Cell Line	embryonic stem cell
38	chr13:70258600-70260000	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr13:70258800-70263600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr13:70259400-70259800	Enhancers	HUES48 Cell Line	embryonic stem cell
41	chr13:70259400-70259800	Enhancers	iPS-15b Cell Line	embryonic stem cell
42	chr13:70259400-70265000	Weak transcription	HUES64 Cell Line	embryonic stem cell
43	chr13:70259600-70260800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr13:70259800-70262200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
45	chr13:70259800-70264600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
46	chr13:70259800-70264800	Weak transcription	HUES48 Cell Line	embryonic stem cell
47	chr13:70260000-70264600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
48	chr13:70260800-70261400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr13:70261400-70261800	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr13:70261800-70262600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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