Variant report

Variant	nsv879996
Chromosome Location	chr4:132880203-133005854
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:310)
CpG islands
(count:854)
Chromatin interactive
region (count:4)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:310 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BCL11A	chr4:132888375-132888594	GM12878	blood:	n/a	n/a
2	BCL11A	chr4:132888535-132888793	GM12878	blood:	n/a	n/a
3	CEBPB	chr4:132922726-132923101	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:132911685-132911991	IMR90	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
5	CEBPB	chr4:132987113-132987581	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:132911717-132911917	A549	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
7	CEBPB	chr4:132933770-132934069	HepG2	liver:	n/a	chr4:132933900-132933911
8	CEBPB	chr4:132947841-132948176	IMR90	lung:	n/a	n/a
9	CEBPB	chr4:132911736-132911961	HepG2	liver:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
10	CEBPB	chr4:132933791-132934099	IMR90	lung:	n/a	chr4:132933900-132933911
11	CTCF	chr4:132998100-132998250	HEK293	kidney:	n/a	chr4:132998177-132998186
12	CTCF	chr4:132998127-132998238	Gliobla	brain:	n/a	chr4:132998177-132998186
13	CTCF	chr4:132997960-132998366	MCF-7	breast:	n/a	chr4:132998177-132998186
14	CTCF	chr4:132998100-132998250	HPAF	blood vessel:	n/a	chr4:132998177-132998186
15	CTCF	chr4:132998100-132998250	HVMF	connective:	n/a	chr4:132998177-132998186
16	CTCF	chr4:132998120-132998270	HBMEC	blood vessel:	n/a	chr4:132998177-132998186
17	CTCF	chr4:132900873-132900899	Medullo	brain:	n/a	n/a
18	CTCF	chr4:132998060-132998210	HPF	lung:	n/a	chr4:132998177-132998186
19	CTCF	chr4:132898878-132899014	GM12891	blood:	n/a	chr4:132898934-132898947
20	CTCF	chr4:132909818-132910127	IMR90	lung:	n/a	chr4:132909997-132910018
21	CTCF	chr4:132998060-132998210	MCF-7	breast:	n/a	chr4:132998177-132998186
22	CTCF	chr4:132998080-132998230	AG04449	skin:	n/a	chr4:132998177-132998186
23	CTCF	chr4:132998100-132998250	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
24	CTCF	chr4:132998140-132998290	HMF	breast:	n/a	chr4:132998177-132998186
25	CTCF	chr4:132998100-132998250	HCFaa	heart:	n/a	chr4:132998177-132998186
26	CTCF	chr4:132998144-132998221	MCF-7	breast:	n/a	chr4:132998177-132998186
27	CTCF	chr4:132896451-132896473	Fibrobl	skin:	n/a	chr4:132896458-132896471
28	CTCF	chr4:132897911-132898096	GM12891	blood:	n/a	n/a
29	CTCF	chr4:132998140-132998290	HCM	heart:	n/a	chr4:132998177-132998186
30	CTCF	chr4:132998120-132998270	HPF	lung:	n/a	chr4:132998177-132998186
31	CTCF	chr4:132998084-132998217	HepG2	liver:	n/a	chr4:132998177-132998186
32	CTCF	chr4:132980520-132980670	HMEC	breast:	n/a	n/a
33	CTCF	chr4:132998120-132998270	WERI-Rb-1	eye:	n/a	chr4:132998177-132998186
34	CTCF	chr4:132906019-132906077	LNCaP	prostate:	n/a	n/a
35	CTCF	chr4:132998160-132998310	RPTEC	kidney:	n/a	chr4:132998177-132998186
36	CTCF	chr4:132998080-132998230	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
37	CTCF	chr4:132998160-132998310	HMEC	breast:	n/a	chr4:132998177-132998186
38	CTCF	chr4:132998060-132998210	NHEK	skin:	n/a	chr4:132998177-132998186
39	CTCF	chr4:132996960-132997110	AG09319	gingival:	n/a	n/a
40	CTCF	chr4:132998120-132998270	MCF-7	breast:	n/a	chr4:132998177-132998186
41	CTCF	chr4:132922089-132922139	LNCaP	prostate:	n/a	n/a
42	CTCF	chr4:132924740-132924890	HAc	cerebellar:	n/a	n/a
43	CTCF	chr4:132955042-132955089	GM13977	blood:	n/a	n/a
44	CTCF	chr4:132998000-132998150	WI-38	lung:	n/a	n/a
45	CTCF	chr4:132998180-132998330	AG04450	lung:	n/a	n/a
46	CTCF	chr4:132998160-132998310	A549	lung:	n/a	chr4:132998177-132998186
47	CTCF	chr4:132980220-132980370	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr4:132998120-132998270	HRPEpiC	eye:	n/a	chr4:132998177-132998186
49	CTCF	chr4:132998060-132998210	BE2_C	brain:	n/a	chr4:132998177-132998186
50	CTCF	chr4:132980540-132980690	NHEK	skin:	n/a	n/a

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132898592-132898642	MCF10A-Er-Src	breast:	n/a
2	chr4:132896579-132896629	BJ	skin:	n/a
3	chr4:132899028-132899078	HMEC	breast:	n/a
4	chr4:132896374-132896424	AG09319	gingival:	n/a
5	chr4:132896266-132896316	NHBE	bronchial:	n/a
6	chr4:132984152-132984202	GM06990	blood:	n/a
7	chr4:132896579-132896629	U87	brain:	n/a
8	chr4:132896736-132896786	AG04449	skin:	fetal
9	chr4:132898592-132898642	NHBE	bronchial:	n/a
10	chr4:132898592-132898642	HPAEpiC	pulmonary alveolar:	n/a
11	chr4:132896405-132896455	HCT-116	colon:	n/a
12	chr4:132984188-132984238	NT2-D1	testis:	n/a
13	chr4:132897691-132897741	HCM	heart:	n/a
14	chr4:132896374-132896424	Hepatocyte	liver:	n/a
15	chr4:132896579-132896629	GM12892	blood:	n/a
16	chr4:132897691-132897741	HCT-116	colon:	n/a
17	chr4:132984188-132984238	HCM	heart:	n/a
18	chr4:132896374-132896424	H1-hESC	embryonic stem cell:	embryo
19	chr4:132896266-132896316	AG10803	skin:	n/a
20	chr4:132899064-132899114	NT2-D1	testis:	n/a
21	chr4:132898790-132898840	BE2_C	brain:	n/a
22	chr4:132897018-132897068	BE2_C	brain:	n/a
23	chr4:132896266-132896316	HepG2	liver:	n/a
24	chr4:132896266-132896316	AG04450	lung:	fetal
25	chr4:132899028-132899078	LNCaP	prostate:	n/a
26	chr4:132896736-132896786	AoSMC	blood vessel:	n/a
27	chr4:132896374-132896424	MCF-7	breast:	n/a
28	chr4:132899064-132899114	Caco-2	colon:	n/a
29	chr4:132984188-132984238	SK-N-SH_RA	brain:	n/a
30	chr4:132984152-132984202	SKMC	muscle:	n/a
31	chr4:132984152-132984202	AoSMC	blood vessel:	n/a
32	chr4:132899460-132899510	HRPEpiC	eye:	n/a
33	chr4:132897018-132897068	AoSMC	blood vessel:	n/a
34	chr4:132898592-132898642	HCT-116	colon:	n/a
35	chr4:132896579-132896629	HRE	kidney:	n/a
36	chr4:132899064-132899114	HCPEpiC	choroid plexus:	n/a
37	chr4:132896736-132896786	Caco-2	colon:	n/a
38	chr4:132897691-132897741	NHBE	bronchial:	n/a
39	chr4:132896374-132896424	CMK	blood:	n/a
40	chr4:132984152-132984202	H1-hESC	embryonic stem cell:	embryo
41	chr4:132896736-132896786	GM12878	blood:	n/a
42	chr4:132896405-132896455	SKMC	muscle:	n/a
43	chr4:132899064-132899114	GM12878	blood:	n/a
44	chr4:132897691-132897741	HRCEpiC	kidney:	n/a
45	chr4:132984188-132984238	K562	blood:	n/a
46	chr4:132984152-132984202	HPAEpiC	pulmonary alveolar:	n/a
47	chr4:132896374-132896424	PFSK-1	brain:	n/a
48	chr4:132896579-132896629	GM06990	blood:	n/a
49	chr4:132899028-132899078	Hela-S3	cervix:	n/a
50	chr4:132899064-132899114	Hela-S3	cervix:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr1:249200230..249200936-chr4:132915036..132915536,2	Hela-S3	cervix:
2	chr11:46257959..46258806-chr4:132939267..132939767,2	NB4	blood:
3	chr4:132949068..132951871-chr4:133002686..133005668,2	K562	blood:
4	chr10:16933616..16934139-chr4:132930526..132931027,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-2	chr4:132897078-132897107	ENSG00000251555
2	lnc-RP11-62N21.1.1-1	chr4:132949501-132949589	XLOC_004078
3	lnc-RP11-62N21.1.1-1	chr4:132949501-132949636	XLOC_004078
4	lnc-RP11-62N21.1.1-1	chr4:132948330-132948587	XLOC_004078
5	lnc-PCDH10-12	chr4:132914719-132914974	l_2731_chr4:132914718-132932069_testes
6	lnc-RP11-62N21.1.1-1	chr4:132925965-132926229	XLOC_004078
7	lnc-PCDH10-12	chr4:132931815-132932069	l_2731_chr4:132914718-132932069_testes

No data

Variant related genes	Relation type
ENSG00000251555	TF binding region
ENSG00000249463	TF binding region
ENSG00000251555	CpG island
ENSG00000249463	CpG island
ENSG00000249463	chromatin interactions
ENSG00000185220	chromatin interactions
ADCY9	miRNA target sites

Extended variants
information (count: 2009 )
Associated
traits (count: 80 )

Variant overlapped rSNPs/rCNVs (count:2009 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs57625382	chr4:132888209-132888210	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537565669	chr4:132888217-132888218	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs191819627	chr4:132888221-132888222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs137969283	chr4:132888238-132888239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs570989466	chr4:132888243-132888244	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs28548557	chr4:132888245-132888246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs536547931	chr4:132888259-132888260	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs553294871	chr4:132888260-132888261	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs199878929	chr4:132888262-132888263	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs9985728	chr4:132888302-132888303	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs545301075	chr4:132888322-132888323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs11099168	chr4:132888330-132888331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs56406960	chr4:132888341-132888342	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs147205144	chr4:132888342-132888343	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs11099169	chr4:132888346-132888347	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs559129147	chr4:132888348-132888349	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs577630446	chr4:132888400-132888401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs9985863	chr4:132888401-132888402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs349291	chr4:132888450-132888451	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs373943451	chr4:132888467-132888468	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2661642	chr4:132888469-132888470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs199597090	chr4:132888518-132888519	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs9307671	chr4:132888546-132888547	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs202169156	chr4:132888550-132888551	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs563270451	chr4:132888555-132888556	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs9307672	chr4:132888567-132888568	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs11099170	chr4:132888579-132888580	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs59606271	chr4:132888680-132888681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs528937136	chr4:132888710-132888711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2661643	chr4:132888755-132888756	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs373621695	chr4:132888786-132888787	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs59900240	chr4:132888802-132888803	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs542927104	chr4:132888876-132888877	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs187099971	chr4:132888929-132888930	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs528407113	chr4:132888934-132888935	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs1238536	chr4:132888939-132888940	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs551251403	chr4:132888951-132888952	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs2773018	chr4:132888970-132888971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs573549496	chr4:132888973-132888974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs2902609	chr4:132888985-132888986	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs199581327	chr4:132888993-132888994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs57965851	chr4:132888994-132888995	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs78173630	chr4:132888996-132888997	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186298529	chr4:132888998-132888999	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs2773019	chr4:132889004-132889005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs370394861	chr4:132889013-132889014	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs2863920	chr4:132889026-132889027	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs571427009	chr4:132889039-132889040	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs2863921	chr4:132889042-132889043	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs2863922	chr4:132889059-132889060	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:80)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132888200-132888400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr4:132888200-132889600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
3	chr4:132895400-132895600	Enhancers	HUVEC	blood vessel
4	chr4:132895400-132895800	Enhancers	GM12878-XiMat	blood
5	chr4:132895400-132897200	Active TSS	Pancreatic Islets	Pancreatic Islet
6	chr4:132895600-132896000	Active TSS	HUVEC	blood vessel
7	chr4:132895800-132896000	Enhancers	Primary hematopoietic stem cells short term culture	blood
8	chr4:132895800-132896000	Enhancers	Placenta	Placenta
9	chr4:132895800-132896400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr4:132895800-132897800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
11	chr4:132896000-132896200	Enhancers	iPS-15b Cell Line	embryonic stem cell
12	chr4:132896000-132896200	Flanking Active TSS	Placenta	Placenta
13	chr4:132896000-132896200	Flanking Active TSS	HUVEC	blood vessel
14	chr4:132896000-132896400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
15	chr4:132896000-132896400	Active TSS	Fetal Intestine Large	intestine
16	chr4:132896000-132896600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
17	chr4:132896000-132896600	Active TSS	Fetal Intestine Small	intestine
18	chr4:132896000-132896800	Active TSS	Duodenum Mucosa	Duodenum
19	chr4:132896000-132896800	Active TSS	NHEK	skin
20	chr4:132896000-132897000	Active TSS	Primary B cells from cord blood	blood
21	chr4:132896000-132897000	Active TSS	NHDF-Ad	bronchial
22	chr4:132896000-132897200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr4:132896000-132897200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr4:132896000-132897400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
25	chr4:132896000-132897400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr4:132896000-132897400	Active TSS	Duodenum Smooth Muscle	Duodenum
27	chr4:132896000-132897400	Active TSS	Fetal Muscle Trunk	muscle
28	chr4:132896000-132897400	Active TSS	Thymus	Thymus
29	chr4:132896000-132897400	Active TSS	GM12878-XiMat	blood
30	chr4:132896000-132897600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
31	chr4:132896000-132897600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr4:132896000-132897600	Active TSS	Primary hematopoietic stem cells	blood
33	chr4:132896000-132897600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
34	chr4:132896000-132897600	Active TSS	Esophagus	oesophagus
35	chr4:132896000-132897600	Active TSS	Fetal Stomach	stomach
36	chr4:132896000-132897800	Active TSS	HUES6 Cell Line	embryonic stem cell
37	chr4:132896000-132897800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
38	chr4:132896000-132897800	ZNF genes & repeats	Fetal Thymus	thymus
39	chr4:132896000-132897800	Active TSS	Ovary	ovary
40	chr4:132896000-132897800	Active TSS	Stomach Smooth Muscle	stomach
41	chr4:132896000-132897800	Active TSS	Osteobl	bone
42	chr4:132896000-132898000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
43	chr4:132896000-132898000	Active TSS	Rectal Mucosa Donor 31	rectum
44	chr4:132896000-132898000	Active TSS	HSMM	muscle
45	chr4:132896000-132898000	Active TSS	HSMMtube	muscle
46	chr4:132896200-132896400	Bivalent Enhancer	Placenta	Placenta
47	chr4:132896200-132897000	Active TSS	Fetal Lung	lung
48	chr4:132896200-132897000	Active TSS	Monocytes-CD14+_RO01746	blood
49	chr4:132896200-132897200	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr4:132896200-132897200	Active TSS	Fetal Muscle Leg	muscle

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