Variant report

Variant	nsv880000
Chromosome Location	chr4:132932856-133022641
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:181)
CpG islands
(count:122)
Chromatin interactive
region (count:5)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:181 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:132947841-132948176	IMR90	lung:	n/a	n/a
2	CEBPB	chr4:132933770-132934069	HepG2	liver:	n/a	chr4:132933900-132933911
3	CEBPB	chr4:132987113-132987581	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:132933791-132934099	IMR90	lung:	n/a	chr4:132933900-132933911
5	CTCF	chr4:132998100-132998250	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
6	CTCF	chr4:132998100-132998250	HEK293	kidney:	n/a	chr4:132998177-132998186
7	CTCF	chr4:132980220-132980370	HEEpiC	esophagus:	n/a	n/a
8	CTCF	chr4:132998127-132998238	Gliobla	brain:	n/a	chr4:132998177-132998186
9	CTCF	chr4:132998120-132998270	MCF-7	breast:	n/a	chr4:132998177-132998186
10	CTCF	chr4:132998135-132998244	Medullo	brain:	n/a	chr4:132998177-132998186
11	CTCF	chr4:132998121-132998237	MCF-7	breast:	n/a	chr4:132998177-132998186
12	CTCF	chr4:132998144-132998221	MCF-7	breast:	n/a	chr4:132998177-132998186
13	CTCF	chr4:132985080-132985230	BE2_C	brain:	n/a	n/a
14	CTCF	chr4:132998160-132998310	A549	lung:	n/a	chr4:132998177-132998186
15	CTCF	chr4:132998060-132998210	NHEK	skin:	n/a	chr4:132998177-132998186
16	CTCF	chr4:132983529-132983535	GM13976	blood:	n/a	n/a
17	CTCF	chr4:132998060-132998210	BE2_C	brain:	n/a	chr4:132998177-132998186
18	CTCF	chr4:132998220-132998370	HCT-116	colon:	n/a	n/a
19	CTCF	chr4:132998080-132998230	Caco-2	colon:	n/a	chr4:132998177-132998186
20	CTCF	chr4:132998180-132998330	AG04450	lung:	n/a	n/a
21	CTCF	chr4:132998080-132998230	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
22	CTCF	chr4:132997960-132998366	MCF-7	breast:	n/a	chr4:132998177-132998186
23	CTCF	chr4:132998100-132998250	HPAF	blood vessel:	n/a	chr4:132998177-132998186
24	CTCF	chr4:132996960-132997110	AG09319	gingival:	n/a	n/a
25	CTCF	chr4:132998100-132998250	BE2_C	brain:	n/a	chr4:132998177-132998186
26	CTCF	chr4:132980540-132980690	NHEK	skin:	n/a	n/a
27	CTCF	chr4:132998020-132998170	AG04450	lung:	n/a	n/a
28	CTCF	chr4:132998060-132998210	HPF	lung:	n/a	chr4:132998177-132998186
29	CTCF	chr4:132959616-132959722	GM13976	blood:	n/a	n/a
30	CTCF	chr4:132998060-132998210	AG04450	lung:	n/a	chr4:132998177-132998186
31	CTCF	chr4:132998060-132998210	MCF-7	breast:	n/a	chr4:132998177-132998186
32	CTCF	chr4:132998117-132998218	HepG2	liver:	n/a	chr4:132998177-132998186
33	CTCF	chr4:132998000-132998150	WI-38	lung:	n/a	n/a
34	CTCF	chr4:132980420-132980570	HMEC	breast:	n/a	n/a
35	CTCF	chr4:132998116-132998223	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
36	CTCF	chr4:132998120-132998270	AG04449	skin:	n/a	chr4:132998177-132998186
37	CTCF	chr4:132998140-132998290	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
38	CTCF	chr4:132998140-132998290	HMF	breast:	n/a	chr4:132998177-132998186
39	CTCF	chr4:132998080-132998230	HepG2	liver:	n/a	chr4:132998177-132998186
40	CTCF	chr4:132998000-132998150	HCT-116	colon:	n/a	n/a
41	CTCF	chr4:133013920-133014070	HMEC	breast:	n/a	n/a
42	CTCF	chr4:132998160-132998310	HMEC	breast:	n/a	chr4:132998177-132998186
43	CTCF	chr4:132955042-132955089	GM13977	blood:	n/a	n/a
44	CTCF	chr4:132998120-132998270	WERI-Rb-1	eye:	n/a	chr4:132998177-132998186
45	CTCF	chr4:132998084-132998217	HepG2	liver:	n/a	chr4:132998177-132998186
46	CTCF	chr4:132998120-132998270	HBMEC	blood vessel:	n/a	chr4:132998177-132998186
47	CTCF	chr4:132985140-132985290	HPAF	blood vessel:	n/a	n/a
48	CTCF	chr4:132998100-132998250	HRE	kidney:	n/a	chr4:132998177-132998186
49	CTCF	chr4:132980520-132980670	HMEC	breast:	n/a	n/a
50	CTCF	chr4:132998140-132998290	HRPEpiC	eye:	n/a	chr4:132998177-132998186

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132984152-132984202	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:132984188-132984238	HUVEC	blood vessel:	n/a
3	chr4:132984188-132984238	Jurkat	blood:	n/a
4	chr4:132984188-132984238	AG04450	lung:	fetal
5	chr4:132984188-132984238	HEEpiC	esophagus:	n/a
6	chr4:132984188-132984238	ovcar-3	ovarian:	n/a
7	chr4:132984188-132984238	PANC-1	pancreas:	n/a
8	chr4:132984188-132984238	BE2_C	brain:	n/a
9	chr4:132984152-132984202	HCF	heart:	n/a
10	chr4:132984188-132984238	SK-N-SH_RA	brain:	n/a
11	chr4:132984188-132984238	AG04449	skin:	fetal
12	chr4:132984152-132984202	NH-A	brain:	n/a
13	chr4:132984152-132984202	PANC-1	pancreas:	n/a
14	chr4:132984152-132984202	SK-N-SH_RA	brain:	n/a
15	chr4:132984152-132984202	HNPCEpiC	eye:	n/a
16	chr4:132984152-132984202	HRCEpiC	kidney:	n/a
17	chr4:132984152-132984202	H1-hESC	embryonic stem cell:	embryo
18	chr4:132984188-132984238	MCF-7	breast:	n/a
19	chr4:132984152-132984202	NB4	blood:	n/a
20	chr4:132984188-132984238	Hela-S3	cervix:	n/a
21	chr4:132984152-132984202	PrEC	prostate:	n/a
22	chr4:132984152-132984202	Hepatocyte	liver:	n/a
23	chr4:132984188-132984238	A549	lung:	n/a
24	chr4:132984152-132984202	ProgFib	skin:	n/a
25	chr4:132984152-132984202	AG09319	gingival:	n/a
26	chr4:132984188-132984238	HIPEpiC	eye:	n/a
27	chr4:132984188-132984238	BJ	skin:	n/a
28	chr4:132984188-132984238	HEK293	kidney:	embryo
29	chr4:132984152-132984202	GM19239	blood:	n/a
30	chr4:132984188-132984238	GM12892	blood:	n/a
31	chr4:132984188-132984238	HRPEpiC	eye:	n/a
32	chr4:132984152-132984202	BE2_C	brain:	n/a
33	chr4:132984188-132984238	Caco-2	colon:	n/a
34	chr4:132984152-132984202	HRE	kidney:	n/a
35	chr4:132984188-132984238	NHBE	bronchial:	n/a
36	chr4:132984188-132984238	HNPCEpiC	eye:	n/a
37	chr4:132984188-132984238	HL-60	blood:	n/a
38	chr4:132984188-132984238	NH-A	brain:	n/a
39	chr4:132984188-132984238	HMEC	breast:	n/a
40	chr4:132984188-132984238	NT2-D1	testis:	n/a
41	chr4:132984152-132984202	MCF-7	breast:	n/a
42	chr4:132984152-132984202	Caco-2	colon:	n/a
43	chr4:132984188-132984238	CMK	blood:	n/a
44	chr4:132984188-132984238	HRE	kidney:	n/a
45	chr4:132984152-132984202	MCF10A-Er-Src	breast:	n/a
46	chr4:132984188-132984238	H1-hESC	embryonic stem cell:	embryo
47	chr4:132984152-132984202	CMK	blood:	n/a
48	chr4:132984188-132984238	GM19239	blood:	n/a
49	chr4:132984188-132984238	HCPEpiC	choroid plexus:	n/a
50	chr4:132984152-132984202	HMEC	breast:	n/a

(count:5 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr21:46369779..46370335-chr4:133015624..133016125,2	MCF-7	breast:
2	chr4:132949068..132951871-chr4:133002686..133005668,2	K562	blood:
3	chr11:46257959..46258806-chr4:132939267..132939767,2	NB4	blood:
4	chr4:133016619..133019412-chr4:133020673..133022375,2	K562	blood:
5	chr4:133016619..133019412-chr4:133020673..133022375,2	K562	blood:

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

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

No data

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

Extended variants
information (count: 1317 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1317 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs35581614	chr4:132935425-132935426	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs397878324	chr4:132935435-132935436	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs117020021	chr4:132935442-132935443	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs540716315	chr4:132935445-132935446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570712072	chr4:132935460-132935461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs533108912	chr4:132935478-132935479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs13121011	chr4:132935517-132935518	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs13148496	chr4:132935625-132935626	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs529054528	chr4:132935666-132935667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140898459	chr4:132935689-132935690	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs12505153	chr4:132935692-132935693	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs35575106	chr4:132935735-132935736	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs535018310	chr4:132935741-132935742	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs397879009	chr4:132935744-132935745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs201269634	chr4:132935745-132935746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs112624760	chr4:132935759-132935760	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs35958903	chr4:132935760-132935761	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs397879732	chr4:132935772-132935773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538634746	chr4:132935849-132935850	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs144818609	chr4:132935859-132935860	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558625969	chr4:132935914-132935915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs571896619	chr4:132935915-132935916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs183001386	chr4:132935961-132935962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs75345135	chr4:132935990-132935991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs574238413	chr4:132935992-132935993	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs561703296	chr4:132936001-132936002	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs540798675	chr4:132936068-132936069	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs150305975	chr4:132936163-132936164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs369951238	chr4:132936164-132936165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs557533927	chr4:132936185-132936186	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs555498343	chr4:132936186-132936187	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs578253522	chr4:132936193-132936194	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs572074977	chr4:132936244-132936245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs202223921	chr4:132936258-132936259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs547539194	chr4:132936309-132936310	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs577586323	chr4:132936350-132936351	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs569395659	chr4:132936354-132936355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188608158	chr4:132936385-132936386	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs77501281	chr4:132936386-132936387	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs193254526	chr4:132936427-132936428	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs548814969	chr4:132936436-132936437	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs559777564	chr4:132936456-132936457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs528615558	chr4:132936477-132936478	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs140433949	chr4:132936532-132936533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs571523718	chr4:132936543-132936544	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs537447618	chr4:132936585-132936586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs143613702	chr4:132936590-132936591	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs568005995	chr4:132936606-132936607	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs536818690	chr4:132936613-132936614	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs185045313	chr4:132936664-132936665	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:80 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132935400-132937200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr4:132937800-132938000	Enhancers	Fetal Intestine Large	intestine
3	chr4:132938200-132938800	Enhancers	Fetal Intestine Small	intestine
4	chr4:132938600-132938800	Enhancers	Fetal Intestine Large	intestine
5	chr4:132946600-132948000	Enhancers	Fetal Brain Male	brain
6	chr4:132946600-132948600	Enhancers	Fetal Intestine Large	intestine
7	chr4:132946600-132948600	Enhancers	Fetal Intestine Small	intestine
8	chr4:132947200-132947600	Enhancers	Dnd41	blood
9	chr4:132947200-132947800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr4:132947400-132947800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr4:132947400-132947800	Enhancers	Brain Germinal Matrix	brain
12	chr4:132947400-132948000	Enhancers	Fetal Brain Female	brain
13	chr4:132947400-132948200	Enhancers	Fetal Lung	lung
14	chr4:132947400-132948600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr4:132947600-132948000	Enhancers	NHEK	skin
16	chr4:132947600-132948200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr4:132977600-132977800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
18	chr4:132977800-132979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:132978200-132978600	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr4:132979000-132980400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chr4:132979200-132979600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr4:132979200-132979800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:132979200-132980400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
24	chr4:132979600-132980000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr4:132979800-132980200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chr4:132979800-132983000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr4:132980000-132980200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr4:132980200-132980600	Enhancers	NHEK	skin
29	chr4:132980200-132980800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
30	chr4:132980400-132983200	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr4:132980400-132983200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
32	chr4:132980600-132980800	Enhancers	HMEC	breast
33	chr4:132983000-132984400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
34	chr4:132983200-132984600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chr4:132983200-132985200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
36	chr4:132984000-132984400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr4:132984000-132984400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr4:132984400-132987600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:132984800-132985400	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr4:132984800-132986000	Enhancers	HUVEC	blood vessel
41	chr4:132985000-132985400	Enhancers	Primary hematopoietic stem cells	blood
42	chr4:132985000-132985800	Enhancers	Pancreatic Islets	Pancreatic Islet
43	chr4:132985800-132987200	Weak transcription	Pancreatic Islets	Pancreatic Islet
44	chr4:132986000-132987200	Weak transcription	HUVEC	blood vessel
45	chr4:132986400-132986800	Enhancers	NHDF-Ad	bronchial
46	chr4:132986400-132988200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr4:132987000-132987800	Enhancers	Muscle Satellite Cultured Cells	--
48	chr4:132987200-132987600	Enhancers	HUVEC	blood vessel
49	chr4:132987200-132988400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr4:132987400-132987600	Enhancers	Pancreatic Islets	Pancreatic Islet

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