Variant report

Variant	nsv1044254
Chromosome Location	chr13:80419496-80457686
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:124)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:124 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr13:80443562-80443857	HepG2	liver:	n/a	n/a
2	ATF2	chr13:80444337-80444666	H1-hESC	embryonic stem cell:	n/a	n/a
3	ATF2	chr13:80444144-80444641	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr13:80448946-80448964	GM12878	blood:	n/a	n/a
5	CEBPB	chr13:80425720-80426023	IMR90	lung:	n/a	n/a
6	CEBPB	chr13:80424040-80424234	HepG2	liver:	n/a	chr13:80424152-80424163
7	CEBPB	chr13:80455023-80455273	HepG2	liver:	n/a	n/a
8	CEBPB	chr13:80455002-80455242	IMR90	lung:	n/a	n/a
9	CHD2	chr13:80436136-80436162	GM12878	blood:	n/a	n/a
10	CTCF	chr13:80449200-80449350	HEK293	kidney:	n/a	n/a
11	CTCF	chr13:80439340-80439490	BE2_C	brain:	n/a	chr13:80439422-80439431
12	CTCF	chr13:80449180-80449330	HCFaa	heart:	n/a	n/a
13	CTCF	chr13:80449280-80449430	HBMEC	blood vessel:	n/a	n/a
14	CTCF	chr13:80449240-80449390	NHEK	skin:	n/a	n/a
15	CTCF	chr13:80449320-80449470	NHEK	skin:	n/a	n/a
16	CTCF	chr13:80449180-80449330	HMEC	breast:	n/a	n/a
17	CTCF	chr13:80449220-80449370	HMEC	breast:	n/a	n/a
18	CTCF	chr13:80449240-80449390	AG09309	skin:	n/a	n/a
19	CTCF	chr13:80449200-80449350	HMF	breast:	n/a	n/a
20	CTCF	chr13:80439280-80439430	HCPEpiC	choroid plexus:	n/a	n/a
21	CTCF	chr13:80449220-80449370	AG10803	skin:	n/a	n/a
22	CTCF	chr13:80449240-80449390	HBMEC	blood vessel:	n/a	n/a
23	CTCF	chr13:80449320-80449470	BE2_C	brain:	n/a	n/a
24	CTCF	chr13:80422320-80422470	GM12866	blood:	n/a	n/a
25	CTCF	chr13:80436703-80436774	Lung_OC	lung:	n/a	n/a
26	CTCF	chr13:80449220-80449370	HEEpiC	esophagus:	n/a	n/a
27	CTCF	chr13:80449200-80449350	HAc	cerebellar:	n/a	n/a
28	CTCF	chr13:80449420-80449570	AG10803	skin:	n/a	n/a
29	CTCF	chr13:80449240-80449390	AG10803	skin:	n/a	n/a
30	CTCF	chr13:80449200-80449350	HVMF	connective:	n/a	n/a
31	CTCF	chr13:80449320-80449470	HMF	breast:	n/a	n/a
32	CTCF	chr13:80449240-80449390	AG04449	skin:	n/a	n/a
33	CTCF	chr13:80449260-80449410	HCPEpiC	choroid plexus:	n/a	n/a
34	EP300	chr13:80448896-80449108	SK-N-SH_RA	brain:	n/a	chr13:80448972-80448981
35	EP300	chr13:80443414-80443827	HepG2	liver:	n/a	n/a
36	EP300	chr13:80443522-80443784	HepG2	liver:	n/a	n/a
37	FOS	chr13:80448881-80449080	MCF10A-Er-Src	breast:	n/a	chr13:80448972-80448979 chr13:80448972-80448980 chr13:80448971-80448982 chr13:80448972-80448980 chr13:80448973-80448984
38	FOS	chr13:80448725-80449118	MCF10A-Er-Src	breast:	n/a	chr13:80448972-80448979 chr13:80448972-80448980 chr13:80448971-80448982 chr13:80448972-80448980 chr13:80448973-80448984
39	FOS	chr13:80448788-80449160	MCF10A-Er-Src	breast:	n/a	chr13:80448972-80448979 chr13:80448972-80448980 chr13:80448971-80448982 chr13:80448972-80448980 chr13:80448973-80448984
40	FOS	chr13:80444939-80445133	HUVEC	blood vessel:	n/a	n/a
41	FOS	chr13:80425450-80425733	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr13:80448787-80449136	MCF10A-Er-Src	breast:	n/a	chr13:80448972-80448979 chr13:80448972-80448980 chr13:80448971-80448982 chr13:80448972-80448980 chr13:80448973-80448984
43	FOS	chr13:80425450-80425746	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr13:80425494-80425739	MCF10A-Er-Src	breast:	n/a	n/a
45	FOXA1	chr13:80443289-80443840	HepG2	liver:	n/a	n/a
46	FOXA1	chr13:80443318-80443715	HepG2	liver:	n/a	n/a
47	FOXA1	chr13:80443383-80443758	T-47D	breast:	n/a	n/a
48	FOXA1	chr13:80443325-80443765	HepG2	liver:	n/a	n/a
49	FOXA1	chr13:80443357-80443850	HepG2	liver:	n/a	n/a
50	FOXA2	chr13:80443436-80443772	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr13:80443435-80443485	GM12891	blood:	n/a
2	chr13:80443435-80443485	HepG2	liver:	n/a
3	chr13:80443435-80443485	HCPEpiC	choroid plexus:	n/a
4	chr13:80443435-80443485	AG09319	gingival:	n/a
5	chr13:80443435-80443485	ovcar-3	ovarian:	n/a
6	chr13:80443435-80443485	K562	blood:	n/a
7	chr13:80443435-80443485	T-47D	breast:	n/a
8	chr13:80443435-80443485	HRPEpiC	eye:	n/a
9	chr13:80443435-80443485	NB4	blood:	n/a
10	chr13:80443435-80443485	NT2-D1	testis:	n/a
11	chr13:80443435-80443485	SAEC	small airway:	n/a
12	chr13:80443435-80443485	HRE	kidney:	n/a
13	chr13:80443435-80443485	GM19239	blood:	n/a
14	chr13:80443435-80443485	HCT-116	colon:	n/a
15	chr13:80443435-80443485	SK-N-SH	brain:	n/a
16	chr13:80443435-80443485	Jurkat	blood:	n/a
17	chr13:80443435-80443485	HEK293	kidney:	embryo
18	chr13:80443435-80443485	BJ	skin:	n/a
19	chr13:80443435-80443485	GM06990	blood:	n/a
20	chr13:80443435-80443485	HCF	heart:	n/a
21	chr13:80443435-80443485	HMEC	breast:	n/a
22	chr13:80443435-80443485	RPTEC	kidney:	n/a
23	chr13:80443435-80443485	CMK	blood:	n/a
24	chr13:80443435-80443485	Caco-2	colon:	n/a
25	chr13:80443435-80443485	PANC-1	pancreas:	n/a
26	chr13:80443435-80443485	SKMC	muscle:	n/a
27	chr13:80443435-80443485	HEEpiC	esophagus:	n/a
28	chr13:80443435-80443485	AG09309	skin:	n/a
29	chr13:80443435-80443485	H1-hESC	embryonic stem cell:	embryo
30	chr13:80443435-80443485	PFSK-1	brain:	n/a
31	chr13:80443435-80443485	HIPEpiC	eye:	n/a
32	chr13:80443435-80443485	A549	lung:	n/a
33	chr13:80443435-80443485	SK-N-MC	brain:	n/a
34	chr13:80443435-80443485	BE2_C	brain:	n/a
35	chr13:80443435-80443485	HNPCEpiC	eye:	n/a
36	chr13:80443435-80443485	HL-60	blood:	n/a
37	chr13:80443435-80443485	LNCaP	prostate:	n/a
38	chr13:80443435-80443485	Hepatocyte	liver:	n/a
39	chr13:80443435-80443485	HRCEpiC	kidney:	n/a
40	chr13:80443435-80443485	NHBE	bronchial:	n/a
41	chr13:80443435-80443485	MCF-7	breast:	n/a
42	chr13:80443435-80443485	NH-A	brain:	n/a
43	chr13:80443435-80443485	AG04450	lung:	fetal
44	chr13:80443435-80443485	HCM	heart:	n/a
45	chr13:80443435-80443485	Hela-S3	cervix:	n/a
46	chr13:80443435-80443485	GM12878	blood:	n/a
47	chr13:80443435-80443485	IMR90	lung:	fetal
48	chr13:80443435-80443485	SK-N-SH_RA	brain:	n/a
49	chr13:80443435-80443485	HAEpiC	amniotic membrane:	n/a
50	chr13:80443435-80443485	HUVEC	blood vessel:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr13:80450535..80451035-chr9:135645081..135646052,2	NB4	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NDFIP2-6	chr13:80446751-80446831	XLOC_010450
2	lnc-NDFIP2-7	chr13:80446719-80446831	NONHSAT034499
3	lnc-NDFIP2-7	chr13:80446721-80446831	NONHSAT034500
4	lnc-NDFIP2-6	chr13:80446721-80446831	XLOC_010450

No data

Variant related genes	Relation type
LINC00382	TF binding region
LINC00382	CpG island
ENSG00000224992	chromatin interactions
KHSRP	miRNA target sites

Extended variants
information (count: 1404 )
Associated
traits (count: 94 )

Variant overlapped rSNPs/rCNVs (count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571221080	chr13:80419556-80419557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs559132700	chr13:80419557-80419558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9601274	chr13:80419565-80419566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs538638984	chr13:80419632-80419633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs148307571	chr13:80419713-80419714	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs372365898	chr13:80419738-80419739	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs4619276	chr13:80419750-80419751	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs575487454	chr13:80419786-80419787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs529150006	chr13:80419800-80419801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs542518616	chr13:80419801-80419802	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs562143853	chr13:80419803-80419804	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs7990168	chr13:80419808-80419809	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs551047574	chr13:80419809-80419810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs571039820	chr13:80419815-80419816	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs527418217	chr13:80419832-80419833	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs547936948	chr13:80419850-80419851	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs183407752	chr13:80419865-80419866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs536904342	chr13:80419876-80419877	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188490965	chr13:80419887-80419888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570055548	chr13:80419910-80419911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs191782188	chr13:80419921-80419922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs559071119	chr13:80419962-80419963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs543025909	chr13:80420001-80420002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs572717733	chr13:80420009-80420010	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs184046813	chr13:80420033-80420034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534821115	chr13:80420034-80420035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs4283117	chr13:80420039-80420040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs573803364	chr13:80420070-80420071	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs542506220	chr13:80420084-80420085	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562478677	chr13:80420101-80420102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575611505	chr13:80420147-80420148	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs7990447	chr13:80420164-80420165	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs188339248	chr13:80420184-80420185	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs527340179	chr13:80420198-80420199	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs547178423	chr13:80420199-80420200	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561529514	chr13:80420210-80420211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs75292597	chr13:80420211-80420212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368942372	chr13:80420236-80420237	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs577611878	chr13:80420264-80420265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs75233435	chr13:80420284-80420285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs138346833	chr13:80420315-80420316	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs570388616	chr13:80420415-80420416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs552403643	chr13:80420436-80420437	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs569055340	chr13:80420471-80420472	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552567431	chr13:80420483-80420484	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs559319695	chr13:80420489-80420490	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs565946337	chr13:80420521-80420522	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs535117235	chr13:80420560-80420561	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs554808432	chr13:80420561-80420562	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs573766156	chr13:80420571-80420572	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:94)

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
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
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	21098271	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Prostate cancer	18632612	CNVD
Colorectal cancer	21586687	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Developmental delay	21147756	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
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21858162	CNVD
Metanephric adenoma	20802469	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Gastric cancer	17908304	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Liposarcoma	21253554	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
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal cancer	21851588	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prostate cancer	21965145	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	19490664	CNVD
Neurodevelopmental disorder	22521361	CNVD
Cancer	21220470	CNVD
Cancer	21183584	CNVD
Omodysplasia	19481194	CNVD
Breast cancer	22032731	CNVD
Breast cancer	21364760	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Cancer	17160897	CNVD
Mantle cell lymphoma	19690137	CNVD
Rhabdomyosarcoma	17210683	CNVD
Schizophrenia	19197363	CNVD
Ovarian clear cell carcinoma	21343371	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr13:80414400-80424000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr13:80420400-80420800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chr13:80420400-80420800	Enhancers	Fetal Intestine Small	intestine
4	chr13:80420400-80422600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr13:80420400-80422800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
6	chr13:80420600-80423600	Enhancers	Cortex derived primary cultured neurospheres	brain
7	chr13:80420800-80422000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr13:80421800-80422400	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chr13:80421800-80422400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chr13:80421800-80422600	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr13:80421800-80422600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr13:80421800-80422600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
13	chr13:80422000-80422400	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr13:80422000-80422400	Enhancers	Primary neutrophils fromperipheralblood	blood
15	chr13:80422000-80422600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr13:80422000-80422600	Enhancers	HUES48 Cell Line	embryonic stem cell
17	chr13:80422200-80422600	Enhancers	H1 Cell Line	embryonic stem cell
18	chr13:80422200-80422600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
19	chr13:80422200-80422800	Enhancers	Breast Myoepithelial Primary Cells	Breast
20	chr13:80422400-80423600	Weak transcription	HUES6 Cell Line	embryonic stem cell
21	chr13:80422400-80427200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
22	chr13:80422400-80427400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
23	chr13:80422600-80423800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
24	chr13:80422600-80425000	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
25	chr13:80422600-80425200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
26	chr13:80422600-80426000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr13:80422800-80427200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
28	chr13:80422800-80427400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
29	chr13:80423200-80424400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
30	chr13:80423400-80424000	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
31	chr13:80423400-80424200	Enhancers	Fetal Heart	heart
32	chr13:80423600-80423800	Enhancers	HUES6 Cell Line	embryonic stem cell
33	chr13:80423600-80427400	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr13:80424000-80424200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr13:80424000-80424200	Enhancers	iPS-18 Cell Line	embryonic stem cell
36	chr13:80424600-80425400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr13:80424600-80426200	Enhancers	NHEK	skin
38	chr13:80425000-80425800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr13:80425000-80426200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chr13:80425200-80425800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr13:80425400-80443200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
42	chr13:80425600-80426000	Enhancers	HMEC	breast
43	chr13:80425600-80426200	Enhancers	Gastric	stomach
44	chr13:80426000-80426200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
45	chr13:80426200-80426800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chr13:80427200-80427800	Enhancers	ES-I3 Cell Line	embryonic stem cell
47	chr13:80427200-80428600	Enhancers	Breast Myoepithelial Primary Cells	Breast
48	chr13:80427400-80427800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr13:80427400-80427800	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr13:80427400-80427800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain

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