Variant report

Variant	nsv984043
Chromosome Location	chr15:31079844-31094725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:372)
CpG islands
(count:489)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:372 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr15:31084274-31084474	HepG2	liver:	n/a	n/a
2	CHD2	chr15:31083705-31083711	H1-hESC	embryonic stem cell:	n/a	n/a
3	CTCF	chr15:31091805-31091987	GM10266	blood:	n/a	n/a
4	CTCF	chr15:31091760-31091910	HAc	cerebellar:	n/a	n/a
5	CTCF	chr15:31091795-31092071	MCF-7	breast:	n/a	n/a
6	CTCF	chr15:31091720-31091870	SAEC	small airway:	n/a	n/a
7	CTCF	chr15:31091760-31091910	HFF-Myc	foreskin:	n/a	n/a
8	CTCF	chr15:31088520-31088670	GM12864	blood:	n/a	n/a
9	CTCF	chr15:31093420-31093570	HMF	breast:	n/a	n/a
10	CTCF	chr15:31091740-31092047	A549	lung:	n/a	n/a
11	CTCF	chr15:31091720-31091870	NHEK	skin:	n/a	n/a
12	CTCF	chr15:31093500-31093650	HRE	kidney:	n/a	n/a
13	CTCF	chr15:31091744-31092048	HepG2	liver:	n/a	n/a
14	CTCF	chr15:31093374-31093809	A549	lung:	n/a	n/a
15	CTCF	chr15:31093420-31093570	HCFaa	heart:	n/a	n/a
16	CTCF	chr15:31092060-31092210	HBMEC	blood vessel:	n/a	n/a
17	CTCF	chr15:31093360-31093510	BJ	skin:	n/a	n/a
18	CTCF	chr15:31091812-31092008	GM12892	blood:	n/a	n/a
19	CTCF	chr15:31091740-31091890	GM12871	blood:	n/a	n/a
20	CTCF	chr15:31091720-31091870	HEEpiC	esophagus:	n/a	n/a
21	CTCF	chr15:31093420-31093570	HBMEC	blood vessel:	n/a	n/a
22	CTCF	chr15:31092020-31092170	GM12872	blood:	n/a	n/a
23	CTCF	chr15:31091805-31091988	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr15:31093360-31093510	NHEK	skin:	n/a	n/a
25	CTCF	chr15:31091746-31092231	A549	lung:	n/a	n/a
26	CTCF	chr15:31093400-31093550	NHEK	skin:	n/a	n/a
27	CTCF	chr15:31093420-31093570	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr15:31093420-31093570	AG09309	skin:	n/a	n/a
29	CTCF	chr15:31092020-31092170	GM12864	blood:	n/a	n/a
30	CTCF	chr15:31092040-31092190	HCT-116	colon:	n/a	n/a
31	CTCF	chr15:31086160-31086310	Caco-2	colon:	n/a	n/a
32	CTCF	chr15:31091732-31092045	H1-hESC	embryonic stem cell:	n/a	n/a
33	CTCF	chr15:31093390-31093660	Medullo	brain:	n/a	n/a
34	CTCF	chr15:31091740-31091890	HCFaa	heart:	n/a	n/a
35	CTCF	chr15:31091872-31091965	GM10248	blood:	n/a	n/a
36	CTCF	chr15:31093420-31093570	HEK293	kidney:	n/a	n/a
37	CTCF	chr15:31093380-31093530	HRE	kidney:	n/a	n/a
38	CTCF	chr15:31091720-31091870	GM12864	blood:	n/a	n/a
39	CTCF	chr15:31093400-31093550	HCPEpiC	choroid plexus:	n/a	n/a
40	CTCF	chr15:31092000-31092150	Caco-2	colon:	n/a	n/a
41	CTCF	chr15:31091823-31092031	K562	blood:	n/a	n/a
42	CTCF	chr15:31093380-31093530	HAc	cerebellar:	n/a	n/a
43	CTCF	chr15:31091846-31091974	Lung_OC	lung:	n/a	n/a
44	CTCF	chr15:31091760-31091910	GM12871	blood:	n/a	n/a
45	CTCF	chr15:31092000-31092150	HCPEpiC	choroid plexus:	n/a	n/a
46	CTCF	chr15:31091809-31091918	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr15:31093420-31093570	WERI-Rb-1	eye:	n/a	n/a
48	CTCF	chr15:31091720-31091870	GM12878	blood:	n/a	n/a
49	CTCF	chr15:31091740-31091890	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr15:31091814-31091994	NHEK	skin:	n/a	n/a

(count:489 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:31090636-31090686	PrEC	prostate:	n/a
2	chr15:31090636-31090686	PrEC	prostate:	n/a
3	chr15:31090636-31090686	NH-A	brain:	n/a
4	chr15:31088666-31088716	H1-hESC	embryonic stem cell:	embryo
5	chr15:31086755-31086805	HRCEpiC	kidney:	n/a
6	chr15:31093049-31093099	T-47D	breast:	n/a
7	chr15:31092120-31092170	NB4	blood:	n/a
8	chr15:31086755-31086805	ECC-1	luminal epithelium:	n/a
9	chr15:31093049-31093099	PFSK-1	brain:	n/a
10	chr15:31090636-31090686	CMK	blood:	n/a
11	chr15:31093040-31093090	BJ	skin:	n/a
12	chr15:31093811-31093861	GM12891	blood:	n/a
13	chr15:31093811-31093861	ProgFib	skin:	n/a
14	chr15:31093811-31093861	PrEC	prostate:	n/a
15	chr15:31090636-31090686	NT2-D1	testis:	n/a
16	chr15:31092120-31092170	HL-60	blood:	n/a
17	chr15:31086755-31086805	GM06990	blood:	n/a
18	chr15:31093049-31093099	LNCaP	prostate:	n/a
19	chr15:31093040-31093090	IMR90	lung:	fetal
20	chr15:31093040-31093090	PrEC	prostate:	n/a
21	chr15:31090636-31090686	GM06990	blood:	n/a
22	chr15:31090995-31091045	MCF10A-Er-Src	breast:	n/a
23	chr15:31093049-31093099	AG04450	lung:	fetal
24	chr15:31090995-31091045	PANC-1	pancreas:	n/a
25	chr15:31092120-31092170	HNPCEpiC	eye:	n/a
26	chr15:31093049-31093099	AG09309	skin:	n/a
27	chr15:31093049-31093099	BE2_C	brain:	n/a
28	chr15:31090636-31090686	ovcar-3	ovarian:	n/a
29	chr15:31090636-31090686	GM12892	blood:	n/a
30	chr15:31093811-31093861	HPAEpiC	pulmonary alveolar:	n/a
31	chr15:31093811-31093861	SAEC	small airway:	n/a
32	chr15:31092120-31092170	NH-A	brain:	n/a
33	chr15:31093049-31093099	Caco-2	colon:	n/a
34	chr15:31086755-31086805	HMEC	breast:	n/a
35	chr15:31086755-31086805	HCM	heart:	n/a
36	chr15:31086755-31086805	Caco-2	colon:	n/a
37	chr15:31086755-31086805	PrEC	prostate:	n/a
38	chr15:31092120-31092170	HCM	heart:	n/a
39	chr15:31093049-31093099	A549	lung:	n/a
40	chr15:31090995-31091045	Jurkat	blood:	n/a
41	chr15:31093811-31093861	HL-60	blood:	n/a
42	chr15:31093049-31093099	SK-N-MC	brain:	n/a
43	chr15:31093049-31093099	H1-hESC	embryonic stem cell:	embryo
44	chr15:31093040-31093090	K562	blood:	n/a
45	chr15:31086755-31086805	HCPEpiC	choroid plexus:	n/a
46	chr15:31090995-31091045	GM06990	blood:	n/a
47	chr15:31088666-31088716	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:31093811-31093861	HIPEpiC	eye:	n/a
49	chr15:31086755-31086805	IMR90	lung:	fetal
50	chr15:31093811-31093861	HUVEC	blood vessel:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ARHGAP11B-5	chr15:31092352-31092630	NONHSAT041399

No data

Variant related genes	Relation type
GOLGA8UP	TF binding region
ENSG00000221379	TF binding region
RN7SL82P	TF binding region
GOLGA8UP	CpG island
ENSG00000221379	CpG island
RN7SL82P	CpG island

Extended variants
information (count: 380 )
Associated
traits (count: 139 )

Variant overlapped rSNPs/rCNVs (count:380 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556728070	chr15:31080113-31080114	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs192472659	chr15:31080130-31080131	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs553258157	chr15:31080173-31080174	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs147016036	chr15:31080174-31080175	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs578126392	chr15:31080214-31080215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs535837435	chr15:31080235-31080236	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs528332592	chr15:31080240-31080241	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs138080608	chr15:31080250-31080251	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs575676668	chr15:31080275-31080276	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs115326967	chr15:31080345-31080346	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs547561305	chr15:31083408-31083409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs576729600	chr15:31083410-31083411	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139949974	chr15:31083411-31083412	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs545680872	chr15:31083412-31083413	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs568418946	chr15:31083424-31083425	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs71106629	chr15:31083426-31083427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565560347	chr15:31083456-31083457	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs572747895	chr15:31083457-31083458	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs369559024	chr15:31083480-31083481	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs549174855	chr15:31083498-31083499	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs541060456	chr15:31083499-31083500	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs74009256	chr15:31083510-31083511	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs530093980	chr15:31083516-31083517	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs192638396	chr15:31083567-31083568	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs811768	chr15:31083568-31083569	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs532160518	chr15:31083573-31083574	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs183039744	chr15:31083591-31083592	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs187325450	chr15:31083631-31083632	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs534958127	chr15:31083642-31083643	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs547833429	chr15:31083643-31083644	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs191908768	chr15:31083658-31083659	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs184714974	chr15:31083665-31083666	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs73379134	chr15:31083669-31083670	Active TSS Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs557105991	chr15:31083693-31083694	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs577044590	chr15:31083697-31083698	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs539211114	chr15:31083712-31083713	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs550055280	chr15:31083727-31083728	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs111584509	chr15:31083737-31083738	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs148530559	chr15:31083742-31083743	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs142886682	chr15:31083743-31083744	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs561099956	chr15:31083747-31083748	Active TSS Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs574509219	chr15:31083780-31083781	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs543446575	chr15:31083793-31083794	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs563420057	chr15:31083847-31083848	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs532516308	chr15:31083857-31083858	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs7178345	chr15:31083884-31083885	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs13380339	chr15:31083885-31083886	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs548485311	chr15:31083927-31083928	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567927105	chr15:31083952-31083953	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs189224657	chr15:31083957-31083958	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:139)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Intellectual disability	21811512	CNVD
Pancreatic cancer	17952125	CNVD
Glioma	20126413	CNVD

Chromatin state (count:26 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:31083400-31084200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr15:31083600-31084000	Enhancers	Placenta	Placenta
3	chr15:31083600-31084200	Active TSS	ES-I3 Cell Line	embryonic stem cell
4	chr15:31083600-31084200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
5	chr15:31084200-31084400	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:31084200-31084400	Enhancers	Pancreas	Pancrea
7	chr15:31084400-31084800	Enhancers	Fetal Stomach	stomach
8	chr15:31084400-31085400	Weak transcription	Pancreas	Pancrea
9	chr15:31084800-31085200	Weak transcription	Fetal Stomach	stomach
10	chr15:31085000-31085400	Enhancers	Muscle Satellite Cultured Cells	--
11	chr15:31085000-31085600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr15:31085200-31085800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr15:31085200-31085800	Enhancers	Fetal Stomach	stomach
14	chr15:31085400-31085800	Enhancers	Pancreas	Pancrea
15	chr15:31088200-31088400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
16	chr15:31089400-31089600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr15:31092000-31092200	Enhancers	ES-I3 Cell Line	embryonic stem cell
18	chr15:31092000-31092200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr15:31092000-31092200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:31092000-31093200	Active TSS	Pancreas	Pancrea
21	chr15:31092200-31093800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr15:31093600-31094000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:31093600-31094000	Enhancers	Brain Hippocampus Middle	brain
24	chr15:31093600-31094600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
25	chr15:31093800-31094000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:31093800-31094000	Enhancers	Pancreas	Pancrea

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