Variant report

Variant	nsv880001
Chromosome Location	chr4:132938331-133016451
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	CEBPB	chr4:132987113-132987581	IMR90	lung:	n/a	n/a
2	CEBPB	chr4:132947841-132948176	IMR90	lung:	n/a	n/a
3	CTCF	chr4:132985140-132985290	HPAF	blood vessel:	n/a	n/a
4	CTCF	chr4:132980540-132980690	NHEK	skin:	n/a	n/a
5	CTCF	chr4:132998140-132998290	HMF	breast:	n/a	chr4:132998177-132998186
6	CTCF	chr4:132998160-132998310	RPTEC	kidney:	n/a	chr4:132998177-132998186
7	CTCF	chr4:132998100-132998250	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
8	CTCF	chr4:132998000-132998150	WI-38	lung:	n/a	n/a
9	CTCF	chr4:132998060-132998210	HPF	lung:	n/a	chr4:132998177-132998186
10	CTCF	chr4:132998080-132998230	HA-sp	spinal cord:	n/a	chr4:132998177-132998186
11	CTCF	chr4:132980420-132980570	HMEC	breast:	n/a	n/a
12	CTCF	chr4:132998127-132998238	Gliobla	brain:	n/a	chr4:132998177-132998186
13	CTCF	chr4:132998140-132998290	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
14	CTCF	chr4:132998100-132998250	HAc	cerebellar:	n/a	chr4:132998177-132998186
15	CTCF	chr4:132998160-132998310	A549	lung:	n/a	chr4:132998177-132998186
16	CTCF	chr4:132998116-132998223	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
17	CTCF	chr4:132998121-132998237	MCF-7	breast:	n/a	chr4:132998177-132998186
18	CTCF	chr4:132998160-132998310	HMEC	breast:	n/a	chr4:132998177-132998186
19	CTCF	chr4:132998060-132998210	MCF-7	breast:	n/a	chr4:132998177-132998186
20	CTCF	chr4:132998080-132998230	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
21	CTCF	chr4:132998120-132998270	HBMEC	blood vessel:	n/a	chr4:132998177-132998186
22	CTCF	chr4:132998000-132998150	HCT-116	colon:	n/a	n/a
23	CTCF	chr4:132998100-132998250	HVMF	connective:	n/a	chr4:132998177-132998186
24	CTCF	chr4:132998220-132998370	HCT-116	colon:	n/a	n/a
25	CTCF	chr4:132980220-132980370	HEEpiC	esophagus:	n/a	n/a
26	CTCF	chr4:132998140-132998290	HCM	heart:	n/a	chr4:132998177-132998186
27	CTCF	chr4:132997960-132998366	MCF-7	breast:	n/a	chr4:132998177-132998186
28	CTCF	chr4:132998100-132998250	HRE	kidney:	n/a	chr4:132998177-132998186
29	CTCF	chr4:132998080-132998230	HepG2	liver:	n/a	chr4:132998177-132998186
30	CTCF	chr4:132998144-132998221	MCF-7	breast:	n/a	chr4:132998177-132998186
31	CTCF	chr4:132980520-132980670	HMEC	breast:	n/a	n/a
32	CTCF	chr4:132998060-132998210	HCT-116	colon:	n/a	chr4:132998177-132998186
33	CTCF	chr4:132998120-132998270	HPF	lung:	n/a	chr4:132998177-132998186
34	CTCF	chr4:132955042-132955089	GM13977	blood:	n/a	n/a
35	CTCF	chr4:132983529-132983535	GM13976	blood:	n/a	n/a
36	CTCF	chr4:132998120-132998270	HRPEpiC	eye:	n/a	chr4:132998177-132998186
37	CTCF	chr4:132998135-132998244	Medullo	brain:	n/a	chr4:132998177-132998186
38	CTCF	chr4:132998120-132998270	WERI-Rb-1	eye:	n/a	chr4:132998177-132998186
39	CTCF	chr4:132998020-132998170	AG04450	lung:	n/a	n/a
40	CTCF	chr4:132998080-132998230	AG04449	skin:	n/a	chr4:132998177-132998186
41	CTCF	chr4:132996960-132997110	AG09319	gingival:	n/a	n/a
42	CTCF	chr4:132998100-132998250	HEK293	kidney:	n/a	chr4:132998177-132998186
43	CTCF	chr4:132998060-132998210	BE2_C	brain:	n/a	chr4:132998177-132998186
44	CTCF	chr4:132998100-132998250	HCFaa	heart:	n/a	chr4:132998177-132998186
45	CTCF	chr4:132998117-132998218	HepG2	liver:	n/a	chr4:132998177-132998186
46	CTCF	chr4:132998040-132998190	HPAF	blood vessel:	n/a	chr4:132998177-132998186
47	CTCF	chr4:132998120-132998270	AG04449	skin:	n/a	chr4:132998177-132998186
48	CTCF	chr4:132998100-132998250	BE2_C	brain:	n/a	chr4:132998177-132998186
49	CTCF	chr4:133013920-133014070	HMEC	breast:	n/a	n/a
50	CTCF	chr4:132998180-132998330	AG04450	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132984188-132984238	MCF-7	breast:	n/a
2	chr4:132984188-132984238	MCF-7	breast:	n/a
3	chr4:132984152-132984202	Caco-2	colon:	n/a
4	chr4:132984188-132984238	T-47D	breast:	n/a
5	chr4:132984188-132984238	IMR90	lung:	fetal
6	chr4:132984152-132984202	K562	blood:	n/a
7	chr4:132984188-132984238	GM06990	blood:	n/a
8	chr4:132984188-132984238	HL-60	blood:	n/a
9	chr4:132984152-132984202	SK-N-SH	brain:	n/a
10	chr4:132984188-132984238	BE2_C	brain:	n/a
11	chr4:132984188-132984238	MCF10A-Er-Src	breast:	n/a
12	chr4:132984152-132984202	SK-N-MC	brain:	n/a
13	chr4:132984152-132984202	AG09319	gingival:	n/a
14	chr4:132984152-132984202	ProgFib	skin:	n/a
15	chr4:132984188-132984238	RPTEC	kidney:	n/a
16	chr4:132984188-132984238	A549	lung:	n/a
17	chr4:132984152-132984202	HUVEC	blood vessel:	n/a
18	chr4:132984152-132984202	MCF10A-Er-Src	breast:	n/a
19	chr4:132984188-132984238	HMEC	breast:	n/a
20	chr4:132984188-132984238	AG09319	gingival:	n/a
21	chr4:132984188-132984238	PANC-1	pancreas:	n/a
22	chr4:132984188-132984238	HUVEC	blood vessel:	n/a
23	chr4:132984188-132984238	HPAEpiC	pulmonary alveolar:	n/a
24	chr4:132984152-132984202	GM12878	blood:	n/a
25	chr4:132984152-132984202	SKMC	muscle:	n/a
26	chr4:132984152-132984202	T-47D	breast:	n/a
27	chr4:132984152-132984202	LNCaP	prostate:	n/a
28	chr4:132984188-132984238	Hela-S3	cervix:	n/a
29	chr4:132984188-132984238	LNCaP	prostate:	n/a
30	chr4:132984188-132984238	PFSK-1	brain:	n/a
31	chr4:132984188-132984238	GM19239	blood:	n/a
32	chr4:132984188-132984238	HAEpiC	amniotic membrane:	n/a
33	chr4:132984152-132984202	NT2-D1	testis:	n/a
34	chr4:132984152-132984202	PrEC	prostate:	n/a
35	chr4:132984152-132984202	PANC-1	pancreas:	n/a
36	chr4:132984152-132984202	SK-N-SH_RA	brain:	n/a
37	chr4:132984152-132984202	AoSMC	blood vessel:	n/a
38	chr4:132984152-132984202	GM12891	blood:	n/a
39	chr4:132984188-132984238	SK-N-MC	brain:	n/a
40	chr4:132984152-132984202	NHBE	bronchial:	n/a
41	chr4:132984188-132984238	PrEC	prostate:	n/a
42	chr4:132984188-132984238	HCM	heart:	n/a
43	chr4:132984188-132984238	AoSMC	blood vessel:	n/a
44	chr4:132984188-132984238	ProgFib	skin:	n/a
45	chr4:132984152-132984202	PFSK-1	brain:	n/a
46	chr4:132984152-132984202	HMEC	breast:	n/a
47	chr4:132984188-132984238	NT2-D1	testis:	n/a
48	chr4:132984188-132984238	GM12891	blood:	n/a
49	chr4:132984188-132984238	HepG2	liver:	n/a
50	chr4:132984188-132984238	BJ	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chr11:46257959..46258806-chr4:132939267..132939767,2	NB4	blood:
2	chr21:46369779..46370335-chr4:133015624..133016125,2	MCF-7	breast:
3	chr4:132949068..132951871-chr4:133002686..133005668,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-1	chr4:132949501-132949589	XLOC_004078
2	lnc-RP11-62N21.1.1-1	chr4:132948330-132948587	XLOC_004078
3	lnc-RP11-62N21.1.1-1	chr4:132949501-132949636	XLOC_004078

Variant related genes	Relation type
ENSG00000249463	TF binding region
ENSG00000249463	CpG island
ENSG00000249463	chromatin interactions
ADCY9	miRNA target sites

Extended variants
information (count: 1207 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1207 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17547292	chr4:132938331-132938332	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs184494808	chr4:132938347-132938348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs562992962	chr4:132938393-132938394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs368666582	chr4:132938398-132938399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs536717124	chr4:132938404-132938405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575385137	chr4:132938503-132938504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs556662079	chr4:132938506-132938507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs566875984	chr4:132938544-132938545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs536254883	chr4:132938576-132938577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs190279485	chr4:132938632-132938633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs182445926	chr4:132938668-132938669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs573139990	chr4:132938670-132938671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs117479519	chr4:132938688-132938689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538970155	chr4:132938697-132938698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs558505112	chr4:132938725-132938726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558749030	chr4:132938726-132938727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs565561097	chr4:132938728-132938729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs187351452	chr4:132938745-132938746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs544669486	chr4:132938750-132938751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369672090	chr4:132938779-132938780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs180684659	chr4:132946790-132946791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs537390161	chr4:132946856-132946857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs149635778	chr4:132946873-132946874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535879748	chr4:132946926-132946927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs112806403	chr4:132946956-132946957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs35524068	chr4:132946957-132946958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs72923412	chr4:132946970-132946971	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs373162131	chr4:132946971-132946972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs558748578	chr4:132946991-132946992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs549747248	chr4:132947027-132947028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs538290740	chr4:132947046-132947047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs554773795	chr4:132947060-132947061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs143886125	chr4:132947084-132947085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs373946293	chr4:132947100-132947101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560392310	chr4:132947114-132947115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs553094171	chr4:132947118-132947119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs577152978	chr4:132947153-132947154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185164294	chr4:132947218-132947219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs567737347	chr4:132947264-132947265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs562717319	chr4:132947280-132947281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs531794518	chr4:132947346-132947347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs539077563	chr4:132947379-132947380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544257295	chr4:132947484-132947485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs560862245	chr4:132947509-132947510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs553847363	chr4:132947512-132947513	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs546311477	chr4:132947535-132947536	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs568142758	chr4:132947544-132947545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs116697986	chr4:132947546-132947547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs552502523	chr4:132947588-132947589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs76976849	chr4:132947612-132947613	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

Disease	PMID	Source
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Medulloblastoma	21979893	CNVD
Neuroblastoma	18923191	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	21858162	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Breast cancer	16272173	CNVD
Colorectal cancer	19359472	CNVD
Malignant mesothelioma	18160781	CNVD
Medulloblastoma	18056178	CNVD
Multiple myeloma	17077331	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Oral squamous cell carcinoma	17134496	CNVD
4q-syndrome	17576883	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Colorectal cancer	20709793	CNVD
Muscular dystrophy	21149563	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
Liposarcoma	21253554	CNVD
Oligodendroglial tumors	17285580	CNVD
Cervical cancer	21062161	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Lung cancer	19208797	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21785460	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	21183584	CNVD
primary effusion lymphomas	17116491	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17133270	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Breast cancer	17393978	CNVD
Esophageal cancer	21851588	CNVD
Colorectal cancer	16272173	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Neuroblastoma	21899760	CNVD
Renal cell carcinoma	18194544	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hepatocellular carcinoma	16750200	CNVD
Acute myeloid leukemia	16864856	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20459617	CNVD
Lung squamous cell carcinoma	22363434	CNVD
Mental retardation	17847001	CNVD
Myelofibrosis	22110671	CNVD
Autism	18923514	CNVD
Autism	22241247	CNVD
Mental retardation	17901693	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:73 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132938200-132938800	Enhancers	Fetal Intestine Small	intestine
2	chr4:132938600-132938800	Enhancers	Fetal Intestine Large	intestine
3	chr4:132946600-132948000	Enhancers	Fetal Brain Male	brain
4	chr4:132946600-132948600	Enhancers	Fetal Intestine Large	intestine
5	chr4:132946600-132948600	Enhancers	Fetal Intestine Small	intestine
6	chr4:132947200-132947600	Enhancers	Dnd41	blood
7	chr4:132947200-132947800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr4:132947400-132947800	Enhancers	Cortex derived primary cultured neurospheres	brain
9	chr4:132947400-132947800	Enhancers	Brain Germinal Matrix	brain
10	chr4:132947400-132948000	Enhancers	Fetal Brain Female	brain
11	chr4:132947400-132948200	Enhancers	Fetal Lung	lung
12	chr4:132947400-132948600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr4:132947600-132948000	Enhancers	NHEK	skin
14	chr4:132947600-132948200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr4:132977600-132977800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr4:132977800-132979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
17	chr4:132978200-132978600	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr4:132979000-132980400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:132979200-132979600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr4:132979200-132979800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr4:132979200-132980400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
22	chr4:132979600-132980000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:132979800-132980200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr4:132979800-132983000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr4:132980000-132980200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
26	chr4:132980200-132980600	Enhancers	NHEK	skin
27	chr4:132980200-132980800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:132980400-132983200	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr4:132980400-132983200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
30	chr4:132980600-132980800	Enhancers	HMEC	breast
31	chr4:132983000-132984400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr4:132983200-132984600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
33	chr4:132983200-132985200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
34	chr4:132984000-132984400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr4:132984000-132984400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:132984400-132987600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:132984800-132985400	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr4:132984800-132986000	Enhancers	HUVEC	blood vessel
39	chr4:132985000-132985400	Enhancers	Primary hematopoietic stem cells	blood
40	chr4:132985000-132985800	Enhancers	Pancreatic Islets	Pancreatic Islet
41	chr4:132985800-132987200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr4:132986000-132987200	Weak transcription	HUVEC	blood vessel
43	chr4:132986400-132986800	Enhancers	NHDF-Ad	bronchial
44	chr4:132986400-132988200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
45	chr4:132987000-132987800	Enhancers	Muscle Satellite Cultured Cells	--
46	chr4:132987200-132987600	Enhancers	HUVEC	blood vessel
47	chr4:132987200-132988400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr4:132987400-132987600	Enhancers	Pancreatic Islets	Pancreatic Islet
49	chr4:132987600-132987800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr4:132987600-132991800	Weak transcription	HUVEC	blood vessel

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