Variant report

Variant	nsv880002
Chromosome Location	chr4:132970231-133082999
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:259)
CpG islands
(count:305)
Chromatin interactive
region (count:7)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:259 , 50 per page) page: 1 2 3 4 5 6

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	chr4:133045184-133045712	GM12878	blood:	n/a	n/a
3	BATF	chr4:133045220-133045708	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	BRCA1	chr4:133046730-133046899	H1-hESC	embryonic stem cell:	n/a	n/a
7	CEBPB	chr4:133029917-133030366	IMR90	lung:	n/a	chr4:133030246-133030263
8	CEBPB	chr4:133029986-133030260	Hela-S3	cervix:	n/a	n/a
9	CEBPB	chr4:133046379-133046732	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr4:132987113-132987581	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:133037868-133038106	HepG2	liver:	n/a	chr4:133037963-133037974 chr4:133037961-133037974 chr4:133037961-133037972
12	CEBPB	chr4:133036042-133036302	IMR90	lung:	n/a	n/a
13	CHD2	chr4:133045389-133045630	GM12878	blood:	n/a	n/a
14	CTCF	chr4:132998117-132998218	HepG2	liver:	n/a	chr4:132998177-132998186
15	CTCF	chr4:132998080-132998230	HA-sp	spinal cord:	n/a	chr4:132998177-132998186
16	CTCF	chr4:132998000-132998150	WI-38	lung:	n/a	n/a
17	CTCF	chr4:132998100-132998250	HCFaa	heart:	n/a	chr4:132998177-132998186
18	CTCF	chr4:132998160-132998310	RPTEC	kidney:	n/a	chr4:132998177-132998186
19	CTCF	chr4:132983529-132983535	GM13976	blood:	n/a	n/a
20	CTCF	chr4:132998135-132998244	Medullo	brain:	n/a	chr4:132998177-132998186
21	CTCF	chr4:133053080-133053230	HepG2	liver:	n/a	n/a
22	CTCF	chr4:132998121-132998237	MCF-7	breast:	n/a	chr4:132998177-132998186
23	CTCF	chr4:132997960-132998366	MCF-7	breast:	n/a	chr4:132998177-132998186
24	CTCF	chr4:132998116-132998223	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
25	CTCF	chr4:132998180-132998330	AG04450	lung:	n/a	n/a
26	CTCF	chr4:132998120-132998270	MCF-7	breast:	n/a	chr4:132998177-132998186
27	CTCF	chr4:133054643-133054720	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr4:132998040-132998190	HPAF	blood vessel:	n/a	chr4:132998177-132998186
29	CTCF	chr4:132998060-132998210	AG04450	lung:	n/a	chr4:132998177-132998186
30	CTCF	chr4:132998120-132998270	AG04449	skin:	n/a	chr4:132998177-132998186
31	CTCF	chr4:132998160-132998310	A549	lung:	n/a	chr4:132998177-132998186
32	CTCF	chr4:132998100-132998250	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
33	CTCF	chr4:132998127-132998238	Gliobla	brain:	n/a	chr4:132998177-132998186
34	CTCF	chr4:132998140-132998290	HRPEpiC	eye:	n/a	chr4:132998177-132998186
35	CTCF	chr4:132998100-132998250	HAc	cerebellar:	n/a	chr4:132998177-132998186
36	CTCF	chr4:132998060-132998210	BE2_C	brain:	n/a	chr4:132998177-132998186
37	CTCF	chr4:133013096-133013130	GM13977	blood:	n/a	n/a
38	CTCF	chr4:132998020-132998170	AG04450	lung:	n/a	n/a
39	CTCF	chr4:132998000-132998150	HCT-116	colon:	n/a	n/a
40	CTCF	chr4:132998120-132998270	WERI-Rb-1	eye:	n/a	chr4:132998177-132998186
41	CTCF	chr4:132980520-132980670	HMEC	breast:	n/a	n/a
42	CTCF	chr4:132998084-132998217	HepG2	liver:	n/a	chr4:132998177-132998186
43	CTCF	chr4:132998080-132998230	HepG2	liver:	n/a	chr4:132998177-132998186
44	CTCF	chr4:132998060-132998210	HCT-116	colon:	n/a	chr4:132998177-132998186
45	CTCF	chr4:132998080-132998230	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
46	CTCF	chr4:132980420-132980570	HMEC	breast:	n/a	n/a
47	CTCF	chr4:132998100-132998250	HRE	kidney:	n/a	chr4:132998177-132998186
48	CTCF	chr4:132998100-132998250	HEK293	kidney:	n/a	chr4:132998177-132998186
49	CTCF	chr4:132996960-132997110	AG09319	gingival:	n/a	n/a
50	CTCF	chr4:132998100-132998250	HPAF	blood vessel:	n/a	chr4:132998177-132998186

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:133045114-133045164	GM12891	blood:	n/a
2	chr4:132984188-132984238	SKMC	muscle:	n/a
3	chr4:132984152-132984202	HMEC	breast:	n/a
4	chr4:132984188-132984238	SK-N-MC	brain:	n/a
5	chr4:133045158-133045208	Hepatocyte	liver:	n/a
6	chr4:132984188-132984238	AoSMC	blood vessel:	n/a
7	chr4:132984188-132984238	RPTEC	kidney:	n/a
8	chr4:132984152-132984202	ProgFib	skin:	n/a
9	chr4:132984152-132984202	HRPEpiC	eye:	n/a
10	chr4:132984188-132984238	BE2_C	brain:	n/a
11	chr4:133045114-133045164	BE2_C	brain:	n/a
12	chr4:133045114-133045164	HCT-116	colon:	n/a
13	chr4:133045158-133045208	HAEpiC	amniotic membrane:	n/a
14	chr4:133045158-133045208	BJ	skin:	n/a
15	chr4:133045178-133045228	LNCaP	prostate:	n/a
16	chr4:133045158-133045208	CMK	blood:	n/a
17	chr4:133045178-133045228	HRCEpiC	kidney:	n/a
18	chr4:133045178-133045228	ovcar-3	ovarian:	n/a
19	chr4:132984188-132984238	IMR90	lung:	fetal
20	chr4:133045114-133045164	SK-N-SH	brain:	n/a
21	chr4:132984152-132984202	NHDF-neo	bronchial:	n/a
22	chr4:133045158-133045208	MCF10A-Er-Src	breast:	n/a
23	chr4:132984188-132984238	LNCaP	prostate:	n/a
24	chr4:132984188-132984238	MCF10A-Er-Src	breast:	n/a
25	chr4:133045114-133045164	GM06990	blood:	n/a
26	chr4:132984188-132984238	HRCEpiC	kidney:	n/a
27	chr4:133045114-133045164	NB4	blood:	n/a
28	chr4:132984152-132984202	CMK	blood:	n/a
29	chr4:133045114-133045164	SK-N-MC	brain:	n/a
30	chr4:132984188-132984238	NB4	blood:	n/a
31	chr4:133045114-133045164	HCF	heart:	n/a
32	chr4:133045178-133045228	H1-hESC	embryonic stem cell:	embryo
33	chr4:133045158-133045208	PANC-1	pancreas:	n/a
34	chr4:132984188-132984238	HRE	kidney:	n/a
35	chr4:133045158-133045208	HRCEpiC	kidney:	n/a
36	chr4:132984188-132984238	NHBE	bronchial:	n/a
37	chr4:132984188-132984238	MCF-7	breast:	n/a
38	chr4:133045114-133045164	HRE	kidney:	n/a
39	chr4:132984152-132984202	Caco-2	colon:	n/a
40	chr4:133045114-133045164	AG04450	lung:	fetal
41	chr4:132984152-132984202	U87	brain:	n/a
42	chr4:133045114-133045164	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:132984188-132984238	HIPEpiC	eye:	n/a
44	chr4:133045178-133045228	BJ	skin:	n/a
45	chr4:133045178-133045228	CMK	blood:	n/a
46	chr4:133045178-133045228	AG10803	skin:	n/a
47	chr4:133045114-133045164	AoSMC	blood vessel:	n/a
48	chr4:132984152-132984202	GM19239	blood:	n/a
49	chr4:132984152-132984202	LNCaP	prostate:	n/a
50	chr4:133045114-133045164	AG09309	skin:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:132949068..132951871-chr4:133002686..133005668,2	K562	blood:
2	chr21:46369779..46370335-chr4:133015624..133016125,2	MCF-7	breast:
3	chr1:163041256..163042238-chr4:133048166..133048870,2	MCF-7	breast:
4	chr4:133016619..133019412-chr4:133020673..133022375,2	K562	blood:
5	chr4:133062137..133063772-chr4:133065440..133067202,2	K562	blood:
6	chr4:133016619..133019412-chr4:133020673..133022375,2	K562	blood:
7	chr4:133062137..133063772-chr4:133065440..133067202,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-1	chr4:133045006-133045186	XLOC_004078

No data

Variant related genes	Relation type
ENSG00000251598	TF binding region
ENSG00000251598	CpG island
ENSG00000117152	chromatin interactions
ENSG00000249463	chromatin interactions
ADCY9	miRNA target sites

Extended variants
information (count: 2510 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:2510 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs553698314	chr4:132977602-132977603	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs570305655	chr4:132977660-132977661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs139474190	chr4:132977704-132977705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs556325144	chr4:132977738-132977739	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183700330	chr4:132977739-132977740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs58944881	chr4:132977790-132977791	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs555460097	chr4:132977855-132977856	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs572500505	chr4:132977880-132977881	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190250580	chr4:132977891-132977892	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs564809852	chr4:132977916-132977917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs578251118	chr4:132977920-132977921	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs543627025	chr4:132977921-132977922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs115434477	chr4:132977972-132977973	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs376598395	chr4:132978077-132978078	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs531291375	chr4:132978104-132978105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs182323300	chr4:132978107-132978108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs561347179	chr4:132978113-132978114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146639188	chr4:132978116-132978117	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs63358261	chr4:132978117-132978118	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202021555	chr4:132978118-132978119	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs67715462	chr4:132978119-132978120	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs34780028	chr4:132978120-132978121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs78957665	chr4:132978121-132978122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs200781595	chr4:132978131-132978132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs201634341	chr4:132978137-132978138	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs568131369	chr4:132978138-132978139	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs80013330	chr4:132978143-132978144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs76590245	chr4:132978144-132978145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs70948171	chr4:132978161-132978162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs375186489	chr4:132978163-132978164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs369123114	chr4:132978164-132978165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4602513	chr4:132978194-132978195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs539739170	chr4:132978233-132978234	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs13125252	chr4:132978239-132978240	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs572771066	chr4:132978251-132978252	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569865784	chr4:132978255-132978256	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs541734707	chr4:132978275-132978276	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs4458468	chr4:132978286-132978287	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs13125080	chr4:132978313-132978314	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs574894996	chr4:132978319-132978320	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555874579	chr4:132978320-132978321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368631084	chr4:132978362-132978363	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs572460218	chr4:132978432-132978433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs534970814	chr4:132978437-132978438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558207045	chr4:132978522-132978523	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs187331103	chr4:132978525-132978526	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs112191182	chr4:132978532-132978533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs1961156	chr4:132978550-132978551	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs574224878	chr4:132978601-132978602	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs111703850	chr4:132978706-132978707	Weak transcription	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:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132977600-132977800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
2	chr4:132977800-132979200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr4:132978200-132978600	Enhancers	Primary hematopoietic stem cells short term culture	blood
4	chr4:132979000-132980400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
5	chr4:132979200-132979600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr4:132979200-132979800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr4:132979200-132980400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
8	chr4:132979600-132980000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr4:132979800-132980200	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr4:132979800-132983000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
11	chr4:132980000-132980200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr4:132980200-132980600	Enhancers	NHEK	skin
13	chr4:132980200-132980800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
14	chr4:132980400-132983200	Weak transcription	H1 Cell Line	embryonic stem cell
15	chr4:132980400-132983200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
16	chr4:132980600-132980800	Enhancers	HMEC	breast
17	chr4:132983000-132984400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr4:132983200-132984600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
19	chr4:132983200-132985200	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
20	chr4:132984000-132984400	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:132984000-132984400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr4:132984400-132987600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr4:132984800-132985400	Enhancers	Primary hematopoietic stem cells short term culture	blood
24	chr4:132984800-132986000	Enhancers	HUVEC	blood vessel
25	chr4:132985000-132985400	Enhancers	Primary hematopoietic stem cells	blood
26	chr4:132985000-132985800	Enhancers	Pancreatic Islets	Pancreatic Islet
27	chr4:132985800-132987200	Weak transcription	Pancreatic Islets	Pancreatic Islet
28	chr4:132986000-132987200	Weak transcription	HUVEC	blood vessel
29	chr4:132986400-132986800	Enhancers	NHDF-Ad	bronchial
30	chr4:132986400-132988200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr4:132987000-132987800	Enhancers	Muscle Satellite Cultured Cells	--
32	chr4:132987200-132987600	Enhancers	HUVEC	blood vessel
33	chr4:132987200-132988400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:132987400-132987600	Enhancers	Pancreatic Islets	Pancreatic Islet
35	chr4:132987600-132987800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
36	chr4:132987600-132991800	Weak transcription	HUVEC	blood vessel
37	chr4:132987800-132988000	Enhancers	NHDF-Ad	bronchial
38	chr4:132987800-132992400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:132987800-132993000	Weak transcription	Muscle Satellite Cultured Cells	--
40	chr4:132988200-132993000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr4:132988400-132992400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr4:132991800-132993800	Enhancers	HUVEC	blood vessel
43	chr4:132992400-132993600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr4:132992400-132993600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr4:132992400-132993600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr4:132993000-132993600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chr4:132993000-132993600	Enhancers	Muscle Satellite Cultured Cells	--
48	chr4:132993000-132993600	Enhancers	HMEC	breast
49	chr4:132993000-132993600	Enhancers	NHEK	skin
50	chr4:132993000-132993800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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