Variant report

Variant	nsv595444
Chromosome Location	chr4:132937315-133045796
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	ATF1	chr4:133045191-133045611	K562	blood:	n/a	n/a
2	BATF	chr4:133045220-133045708	GM12878	blood:	n/a	n/a
3	BATF	chr4:133045184-133045712	GM12878	blood:	n/a	n/a
4	BCL11A	chr4:133045351-133045685	GM12878	blood:	n/a	n/a
5	BCL11A	chr4:133045279-133045718	GM12878	blood:	n/a	n/a
6	CEBPB	chr4:133029917-133030366	IMR90	lung:	n/a	chr4:133030246-133030263
7	CEBPB	chr4:132947841-132948176	IMR90	lung:	n/a	n/a
8	CEBPB	chr4:133037868-133038106	HepG2	liver:	n/a	chr4:133037963-133037974 chr4:133037961-133037974 chr4:133037961-133037972
9	CEBPB	chr4:132987113-132987581	IMR90	lung:	n/a	n/a
10	CEBPB	chr4:133036042-133036302	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:133029986-133030260	Hela-S3	cervix:	n/a	n/a
12	CHD2	chr4:133045389-133045630	GM12878	blood:	n/a	n/a
13	CTCF	chr4:132998080-132998230	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
14	CTCF	chr4:132998100-132998250	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
15	CTCF	chr4:133013096-133013130	GM13977	blood:	n/a	n/a
16	CTCF	chr4:132998140-132998290	HRPEpiC	eye:	n/a	chr4:132998177-132998186
17	CTCF	chr4:132980540-132980690	NHEK	skin:	n/a	n/a
18	CTCF	chr4:132998144-132998221	MCF-7	breast:	n/a	chr4:132998177-132998186
19	CTCF	chr4:132998060-132998210	HPF	lung:	n/a	chr4:132998177-132998186
20	CTCF	chr4:132998080-132998230	Caco-2	colon:	n/a	chr4:132998177-132998186
21	CTCF	chr4:132998060-132998210	NHEK	skin:	n/a	chr4:132998177-132998186
22	CTCF	chr4:132998140-132998290	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
23	CTCF	chr4:132998100-132998250	HCFaa	heart:	n/a	chr4:132998177-132998186
24	CTCF	chr4:132998140-132998290	HCM	heart:	n/a	chr4:132998177-132998186
25	CTCF	chr4:132998120-132998270	WERI-Rb-1	eye:	n/a	chr4:132998177-132998186
26	CTCF	chr4:132998080-132998230	HA-sp	spinal cord:	n/a	chr4:132998177-132998186
27	CTCF	chr4:132980220-132980370	HEEpiC	esophagus:	n/a	n/a
28	CTCF	chr4:132998100-132998250	BE2_C	brain:	n/a	chr4:132998177-132998186
29	CTCF	chr4:132998020-132998170	AG04450	lung:	n/a	n/a
30	CTCF	chr4:132998117-132998218	HepG2	liver:	n/a	chr4:132998177-132998186
31	CTCF	chr4:132998000-132998150	HCT-116	colon:	n/a	n/a
32	CTCF	chr4:132998060-132998210	AG04450	lung:	n/a	chr4:132998177-132998186
33	CTCF	chr4:132998100-132998250	HAc	cerebellar:	n/a	chr4:132998177-132998186
34	CTCF	chr4:132998116-132998223	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
35	CTCF	chr4:132998120-132998270	HBMEC	blood vessel:	n/a	chr4:132998177-132998186
36	CTCF	chr4:132998060-132998210	BE2_C	brain:	n/a	chr4:132998177-132998186
37	CTCF	chr4:132996960-132997110	AG09319	gingival:	n/a	n/a
38	CTCF	chr4:132998127-132998238	Gliobla	brain:	n/a	chr4:132998177-132998186
39	CTCF	chr4:132998060-132998210	MCF-7	breast:	n/a	chr4:132998177-132998186
40	CTCF	chr4:132998100-132998250	HPAF	blood vessel:	n/a	chr4:132998177-132998186
41	CTCF	chr4:132998120-132998270	HPF	lung:	n/a	chr4:132998177-132998186
42	CTCF	chr4:132998120-132998270	HRPEpiC	eye:	n/a	chr4:132998177-132998186
43	CTCF	chr4:132980420-132980570	HMEC	breast:	n/a	n/a
44	CTCF	chr4:132998120-132998270	AG04449	skin:	n/a	chr4:132998177-132998186
45	CTCF	chr4:132998100-132998250	HEK293	kidney:	n/a	chr4:132998177-132998186
46	CTCF	chr4:132998121-132998237	MCF-7	breast:	n/a	chr4:132998177-132998186
47	CTCF	chr4:132998160-132998310	HMEC	breast:	n/a	chr4:132998177-132998186
48	CTCF	chr4:132998080-132998230	AG04449	skin:	n/a	chr4:132998177-132998186
49	CTCF	chr4:132998100-132998250	HRE	kidney:	n/a	chr4:132998177-132998186
50	CTCF	chr4:132998000-132998150	WI-38	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132984152-132984202	U87	brain:	n/a
2	chr4:132984152-132984202	U87	brain:	n/a
3	chr4:133045178-133045228	HRCEpiC	kidney:	n/a
4	chr4:132984188-132984238	LNCaP	prostate:	n/a
5	chr4:133045158-133045208	HRE	kidney:	n/a
6	chr4:132984188-132984238	ProgFib	skin:	n/a
7	chr4:132984152-132984202	HEEpiC	esophagus:	n/a
8	chr4:133045158-133045208	NHBE	bronchial:	n/a
9	chr4:132984188-132984238	NH-A	brain:	n/a
10	chr4:132984188-132984238	NHDF-neo	bronchial:	n/a
11	chr4:133045114-133045164	SKMC	muscle:	n/a
12	chr4:133045114-133045164	NHDF-neo	bronchial:	n/a
13	chr4:133045178-133045228	AG09309	skin:	n/a
14	chr4:133045114-133045164	GM12892	blood:	n/a
15	chr4:132984152-132984202	HEK293	kidney:	embryo
16	chr4:133045158-133045208	Hela-S3	cervix:	n/a
17	chr4:133045158-133045208	HNPCEpiC	eye:	n/a
18	chr4:132984152-132984202	HCM	heart:	n/a
19	chr4:133045178-133045228	SK-N-MC	brain:	n/a
20	chr4:133045178-133045228	HRE	kidney:	n/a
21	chr4:133045158-133045208	BE2_C	brain:	n/a
22	chr4:132984152-132984202	AG09319	gingival:	n/a
23	chr4:133045178-133045228	PFSK-1	brain:	n/a
24	chr4:133045178-133045228	GM06990	blood:	n/a
25	chr4:133045158-133045208	RPTEC	kidney:	n/a
26	chr4:133045158-133045208	AG10803	skin:	n/a
27	chr4:132984152-132984202	A549	lung:	n/a
28	chr4:133045178-133045228	T-47D	breast:	n/a
29	chr4:132984188-132984238	NB4	blood:	n/a
30	chr4:133045114-133045164	HRCEpiC	kidney:	n/a
31	chr4:132984152-132984202	HNPCEpiC	eye:	n/a
32	chr4:133045178-133045228	SK-N-SH_RA	brain:	n/a
33	chr4:133045178-133045228	HepG2	liver:	n/a
34	chr4:133045114-133045164	Hela-S3	cervix:	n/a
35	chr4:132984188-132984238	NT2-D1	testis:	n/a
36	chr4:133045114-133045164	HPAEpiC	pulmonary alveolar:	n/a
37	chr4:133045178-133045228	HNPCEpiC	eye:	n/a
38	chr4:132984188-132984238	HRCEpiC	kidney:	n/a
39	chr4:133045178-133045228	BJ	skin:	n/a
40	chr4:133045114-133045164	GM06990	blood:	n/a
41	chr4:133045178-133045228	LNCaP	prostate:	n/a
42	chr4:132984152-132984202	GM06990	blood:	n/a
43	chr4:132984152-132984202	SAEC	small airway:	n/a
44	chr4:133045158-133045208	Jurkat	blood:	n/a
45	chr4:133045178-133045228	HCPEpiC	choroid plexus:	n/a
46	chr4:132984188-132984238	A549	lung:	n/a
47	chr4:133045158-133045208	PFSK-1	brain:	n/a
48	chr4:133045158-133045208	HRPEpiC	eye:	n/a
49	chr4:133045158-133045208	ovcar-3	ovarian:	n/a
50	chr4:133045158-133045208	AoSMC	blood vessel:	n/a

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

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	chr4:133045006-133045186	XLOC_004078
3	lnc-RP11-62N21.1.1-1	chr4:132949501-132949636	XLOC_004078
4	lnc-RP11-62N21.1.1-1	chr4:132949501-132949589	XLOC_004078

Variant related genes	Relation type
ENSG00000249463	TF binding region
ENSG00000251598	TF binding region
ENSG00000249463	CpG island
ENSG00000251598	CpG island
ENSG00000249463	chromatin interactions
ADCY9	miRNA target sites

Extended variants
information (count: 1753 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1753 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs72923406	chr4:132937821-132937822	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs572912594	chr4:132937831-132937832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545229908	chr4:132937840-132937841	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs565212728	chr4:132937872-132937873	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs574186446	chr4:132938328-132938329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs17547292	chr4:132938331-132938332	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs184494808	chr4:132938347-132938348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs562992962	chr4:132938393-132938394	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs368666582	chr4:132938398-132938399	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs536717124	chr4:132938404-132938405	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs575385137	chr4:132938503-132938504	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs556662079	chr4:132938506-132938507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs566875984	chr4:132938544-132938545	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs536254883	chr4:132938576-132938577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs190279485	chr4:132938632-132938633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182445926	chr4:132938668-132938669	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs573139990	chr4:132938670-132938671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs117479519	chr4:132938688-132938689	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs538970155	chr4:132938697-132938698	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs558505112	chr4:132938725-132938726	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs558749030	chr4:132938726-132938727	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs565561097	chr4:132938728-132938729	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs187351452	chr4:132938745-132938746	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs544669486	chr4:132938750-132938751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs369672090	chr4:132938779-132938780	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs180684659	chr4:132946790-132946791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs537390161	chr4:132946856-132946857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs149635778	chr4:132946873-132946874	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs535879748	chr4:132946926-132946927	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs112806403	chr4:132946956-132946957	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35524068	chr4:132946957-132946958	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs72923412	chr4:132946970-132946971	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs373162131	chr4:132946971-132946972	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs558748578	chr4:132946991-132946992	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs549747248	chr4:132947027-132947028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538290740	chr4:132947046-132947047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs554773795	chr4:132947060-132947061	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs143886125	chr4:132947084-132947085	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs373946293	chr4:132947100-132947101	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs560392310	chr4:132947114-132947115	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs553094171	chr4:132947118-132947119	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs577152978	chr4:132947153-132947154	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs185164294	chr4:132947218-132947219	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs567737347	chr4:132947264-132947265	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562717319	chr4:132947280-132947281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs531794518	chr4:132947346-132947347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs539077563	chr4:132947379-132947380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs544257295	chr4:132947484-132947485	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560862245	chr4:132947509-132947510	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs553847363	chr4:132947512-132947513	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:144 , 50 per page) page: 1 2 3

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

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