Variant report

Variant	nsv900932
Chromosome Location	chr13:95991263-96035883
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:472)
CpG islands
(count:61)
Chromatin interactive
region (count:10)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:96033005-96033202	K562	blood:	n/a	n/a
2	ATF2	chr13:96032895-96033280	GM12878	blood:	n/a	n/a
3	BACH1	chr13:96001635-96001886	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr13:96032838-96033332	GM12878	blood:	n/a	n/a
5	BHLHE40	chr13:96032939-96033253	K562	blood:	n/a	n/a
6	BHLHE40	chr13:96012862-96013164	K562	blood:	n/a	n/a
7	BHLHE40	chr13:96035160-96035373	GM12878	blood:	n/a	n/a
8	CBX3	chr13:96032887-96033228	K562	blood:	n/a	n/a
9	CBX3	chr13:96008953-96009226	K562	blood:	n/a	n/a
10	CBX3	chr13:96015553-96015829	K562	blood:	n/a	n/a
11	CEBPB	chr13:96034720-96035000	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr13:96033058-96033095	K562	blood:	n/a	n/a
13	CEBPB	chr13:96022480-96022768	K562	blood:	n/a	chr13:96022629-96022640
14	CEBPB	chr13:96032742-96033284	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chr13:96034766-96034993	IMR90	lung:	n/a	n/a
16	CEBPB	chr13:96030860-96031124	A549	lung:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
17	CEBPB	chr13:96022569-96022728	HepG2	liver:	n/a	chr13:96022629-96022640
18	CEBPB	chr13:96004765-96005063	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr13:96030846-96031187	A549	lung:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
20	CEBPB	chr13:96030842-96031109	K562	blood:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
21	CEBPB	chr13:96030922-96031151	ECC-1	luminal epithelium:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
22	CEBPB	chr13:96030830-96031188	Hela-S3	cervix:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
23	CEBPB	chr13:96030771-96031254	A549	lung:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
24	CEBPB	chr13:96030745-96031177	ECC-1	luminal epithelium:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
25	CEBPB	chr13:96001631-96001874	K562	blood:	n/a	n/a
26	CEBPB	chr13:96022472-96022715	IMR90	lung:	n/a	chr13:96022629-96022640
27	CEBPB	chr13:96030860-96031170	IMR90	lung:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
28	CEBPB	chr13:96030962-96031041	H1-hESC	embryonic stem cell:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
29	CEBPB	chr13:96030851-96031164	HepG2	liver:	n/a	chr13:96031008-96031019 chr13:96031009-96031018 chr13:96031007-96031018
30	CHD2	chr13:96032717-96033227	Hela-S3	cervix:	n/a	n/a
31	CREB1	chr13:96032962-96033181	A549	lung:	n/a	n/a
32	CTCF	chr13:96033019-96033263	GM10266	blood:	n/a	n/a
33	CTCF	chr13:96012942-96013126	K562	blood:	n/a	n/a
34	CTCF	chr13:96033040-96033190	GM12868	blood:	n/a	n/a
35	CTCF	chr13:96033007-96033218	A549	lung:	n/a	n/a
36	CTCF	chr13:96033029-96033249	GM13976	blood:	n/a	n/a
37	CTCF	chr13:96004719-96004845	MCF-7	breast:	n/a	n/a
38	CTCF	chr13:96033060-96033210	HMF	breast:	n/a	n/a
39	CTCF	chr13:96033060-96033210	HRPEpiC	eye:	n/a	n/a
40	CTCF	chr13:96004700-96004850	HRE	kidney:	n/a	n/a
41	CTCF	chr13:96032987-96033271	GM12878	blood:	n/a	n/a
42	CTCF	chr13:96033080-96033230	MCF-7	breast:	n/a	n/a
43	CTCF	chr13:96033020-96033170	GM12866	blood:	n/a	n/a
44	CTCF	chr13:96033040-96033190	GM12878	blood:	n/a	n/a
45	CTCF	chr13:96033020-96033170	NB4	blood:	n/a	n/a
46	CTCF	chr13:96033013-96033257	GM13977	blood:	n/a	n/a
47	CTCF	chr13:96033060-96033210	AG04449	skin:	n/a	n/a
48	CTCF	chr13:96033020-96033170	GM12872	blood:	n/a	n/a
49	CTCF	chr13:96004762-96004802	HepG2	liver:	n/a	n/a
50	CTCF	chr13:96032997-96033249	Fibrobl	skin:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:96008021-96008071	Jurkat	blood:	n/a
2	chr13:96008021-96008071	AG10803	skin:	n/a
3	chr13:96008021-96008071	MCF-7	breast:	n/a
4	chr13:96008021-96008071	A549	lung:	n/a
5	chr13:96008021-96008071	GM06990	blood:	n/a
6	chr13:96008021-96008071	H1-hESC	embryonic stem cell:	embryo
7	chr13:96008021-96008071	NB4	blood:	n/a
8	chr13:96008021-96008071	ovcar-3	ovarian:	n/a
9	chr13:96008021-96008071	NHBE	bronchial:	n/a
10	chr13:96008021-96008071	HepG2	liver:	n/a
11	chr13:96008021-96008071	IMR90	lung:	fetal
12	chr13:96008021-96008071	HRCEpiC	kidney:	n/a
13	chr13:96008021-96008071	GM12891	blood:	n/a
14	chr13:96008021-96008071	Caco-2	colon:	n/a
15	chr13:96008021-96008071	MCF10A-Er-Src	breast:	n/a
16	chr13:96008021-96008071	U87	brain:	n/a
17	chr13:96008021-96008071	HCM	heart:	n/a
18	chr13:96008021-96008071	HEK293	kidney:	embryo
19	chr13:96008021-96008071	BE2_C	brain:	n/a
20	chr13:96008021-96008071	SAEC	small airway:	n/a
21	chr13:96008021-96008071	HCF	heart:	n/a
22	chr13:96008021-96008071	SK-N-SH_RA	brain:	n/a
23	chr13:96008021-96008071	SK-N-MC	brain:	n/a
24	chr13:96008021-96008071	NHDF-neo	bronchial:	n/a
25	chr13:96008021-96008071	HRE	kidney:	n/a
26	chr13:96008021-96008071	AG09319	gingival:	n/a
27	chr13:96008021-96008071	T-47D	breast:	n/a
28	chr13:96008021-96008071	AG09309	skin:	n/a
29	chr13:96008021-96008071	HRPEpiC	eye:	n/a
30	chr13:96008021-96008071	K562	blood:	n/a
31	chr13:96008021-96008071	HNPCEpiC	eye:	n/a
32	chr13:96008021-96008071	AG04450	lung:	fetal
33	chr13:96008021-96008071	GM19239	blood:	n/a
34	chr13:96008021-96008071	GM12892	blood:	n/a
35	chr13:96008021-96008071	HAEpiC	amniotic membrane:	n/a
36	chr13:96008021-96008071	HIPEpiC	eye:	n/a
37	chr13:96008021-96008071	Hela-S3	cervix:	n/a
38	chr13:96008021-96008071	AG04449	skin:	fetal
39	chr13:96008021-96008071	HL-60	blood:	n/a
40	chr13:96008021-96008071	HEEpiC	esophagus:	n/a
41	chr13:96008021-96008071	SK-N-SH	brain:	n/a
42	chr13:96008021-96008071	ProgFib	skin:	n/a
43	chr13:96008021-96008071	Hepatocyte	liver:	n/a
44	chr13:96008021-96008071	NT2-D1	testis:	n/a
45	chr13:96008021-96008071	SKMC	muscle:	n/a
46	chr13:96008021-96008071	HCPEpiC	choroid plexus:	n/a
47	chr13:96008021-96008071	CMK	blood:	n/a
48	chr13:96008021-96008071	LNCaP	prostate:	n/a
49	chr13:96008021-96008071	HUVEC	blood vessel:	n/a
50	chr13:96008021-96008071	HPAEpiC	pulmonary alveolar:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr13:95948663..95949423-chr13:96032842..96033682,2	MCF-7	breast:
2	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
3	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
4	chr13:95841692..95842231-chr13:96032699..96033435,2	MCF-7	breast:
5	chr13:95948695..95951282-chr13:96033304..96035769,2	MCF-7	breast:
6	chr13:95990065..95992069-chr13:95994982..95997042,2	K562	blood:
7	chr13:95841276..95841834-chr13:96032679..96033583,3	K562	blood:
8	chr13:96010392..96012474-chr13:96022109..96025076,2	K562	blood:
9	chr13:95843696..95844640-chr13:96032651..96033707,6	K562	blood:
10	chr13:95843719..95844609-chr13:96033049..96033649,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ABCC4-2	chr13:96003796-96003967	NONHSAT034758

No data

Variant related genes	Relation type
RNY4P27	TF binding region
RNY4P27	CpG island

Extended variants
information (count: 1616 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:1616 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs12871476	chr13:95991263-95991264	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs549820510	chr13:95991287-95991288	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs569823834	chr13:95991316-95991317	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs548903680	chr13:95991317-95991318	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs9302067	chr13:95991340-95991341	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs373328232	chr13:95991355-95991356	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs12874059	chr13:95991373-95991374	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs187717750	chr13:95991430-95991431	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs369077669	chr13:95991484-95991485	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs114560197	chr13:95991525-95991526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs191485215	chr13:95991526-95991527	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs545756275	chr13:95991551-95991552	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs557966341	chr13:95991557-95991558	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144520121	chr13:95991592-95991593	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs576620246	chr13:95991596-95991597	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs146626862	chr13:95991606-95991607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs141362775	chr13:95991611-95991612	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs149832637	chr13:95991612-95991613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs145805717	chr13:95991655-95991656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs564137923	chr13:95991691-95991692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs533083392	chr13:95991737-95991738	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549749491	chr13:95991816-95991817	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539971536	chr13:95991818-95991819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs184337762	chr13:95991886-95991887	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574929305	chr13:95991892-95991893	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs188092416	chr13:95991957-95991958	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs34896565	chr13:95991960-95991961	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs565863785	chr13:95992006-95992007	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs534494104	chr13:95992027-95992028	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs12875072	chr13:95992048-95992049	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs570990121	chr13:95992094-95992095	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs143078245	chr13:95992113-95992114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs192882508	chr13:95992119-95992120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs138663391	chr13:95992129-95992130	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs141080153	chr13:95992133-95992134	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs556013243	chr13:95992177-95992178	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs147014062	chr13:95992185-95992186	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs386773585	chr13:95992208-95992209	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs541612452	chr13:95992211-95992212	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2993603	chr13:95992217-95992218	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs71207425	chr13:95992219-95992220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs373608895	chr13:95992220-95992221	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs200718641	chr13:95992222-95992223	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs370529621	chr13:95992225-95992226	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs112641737	chr13:95992229-95992230	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs4773889	chr13:95992232-95992233	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs80066650	chr13:95992238-95992239	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs4773890	chr13:95992275-95992276	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs185332072	chr13:95992321-95992322	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs565930655	chr13:95992382-95992383	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:85)

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
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
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Rhabdomyosarcoma	17210683	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Developmental delay	21147756	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thyroid cancer	19087340	CNVD
abortions and stillbirths	19751515	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute myeloid leukemia	21251322	CNVD
Acute myeloid leukemia	19651601	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	22102821	CNVD
Burkitt''s lymphoma	20823134	CNVD

Chromatin state (count:260 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:95986600-95993800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr13:95990000-95991600	Weak transcription	Colon Smooth Muscle	Colon
3	chr13:95990400-95996200	Weak transcription	Skeletal Muscle Male	skeletal muscle
4	chr13:95991200-95993000	Enhancers	Rectal Smooth Muscle	rectum
5	chr13:95991400-95992000	Enhancers	Duodenum Smooth Muscle	Duodenum
6	chr13:95991600-95993000	Enhancers	Colon Smooth Muscle	Colon
7	chr13:95993000-95994200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr13:95993800-95994200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr13:95993800-95994200	Enhancers	Osteobl	bone
10	chr13:95996000-95996800	Enhancers	HUVEC	blood vessel
11	chr13:95996200-95996400	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr13:95999800-96000200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr13:95999800-96000200	Enhancers	Cortex derived primary cultured neurospheres	brain
14	chr13:96001200-96001800	Enhancers	Psoas Muscle	Psoas
15	chr13:96001400-96001800	Enhancers	K562	blood
16	chr13:96001600-96002000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
17	chr13:96001800-96005800	Weak transcription	K562	blood
18	chr13:96003800-96004200	Enhancers	HepG2	liver
19	chr13:96004200-96004600	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
20	chr13:96004200-96006800	Weak transcription	HepG2	liver
21	chr13:96004400-96005200	Enhancers	Hela-S3	cervix
22	chr13:96004600-96005200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
23	chr13:96005000-96005400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
24	chr13:96005200-96008000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr13:96005400-96007000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
26	chr13:96005800-96006200	Enhancers	HMEC	breast
27	chr13:96005800-96007000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
28	chr13:96005800-96007000	Enhancers	K562	blood
29	chr13:96006000-96008000	Enhancers	Cortex derived primary cultured neurospheres	brain
30	chr13:96006000-96008200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
31	chr13:96006000-96008400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
32	chr13:96006200-96007200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chr13:96006400-96009600	Enhancers	Liver	Liver
34	chr13:96006600-96007000	Enhancers	Brain Hippocampus Middle	brain
35	chr13:96006600-96007400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr13:96006600-96008000	Enhancers	Brain Anterior Caudate	brain
37	chr13:96006600-96008200	Enhancers	Stomach Mucosa	stomach
38	chr13:96006800-96007200	Enhancers	Brain Angular Gyrus	brain
39	chr13:96006800-96007400	Enhancers	Brain Inferior Temporal Lobe	brain
40	chr13:96006800-96007600	Enhancers	HepG2	liver
41	chr13:96006800-96008000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
42	chr13:96006800-96008000	Enhancers	Brain Substantia Nigra	brain
43	chr13:96006800-96008200	Enhancers	HUVEC	blood vessel
44	chr13:96006800-96008400	Enhancers	Fetal Stomach	stomach
45	chr13:96007000-96007400	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr13:96007000-96007400	Enhancers	Brain Germinal Matrix	brain
47	chr13:96007000-96007400	Flanking Active TSS	Brain Hippocampus Middle	brain
48	chr13:96007000-96007400	Enhancers	Colon Smooth Muscle	Colon
49	chr13:96007000-96007400	Enhancers	Gastric	stomach
50	chr13:96007000-96008200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin

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