Variant report

Variant	esv1811738
Chromosome Location	chr4:132699078-132903485
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:347)
CpG islands
(count:732)
Chromatin interactive
region (count:0)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:347 , 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	BATF	chr4:132800279-132800515	GM12878	blood:	n/a	chr4:132800367-132800378
2	BATF	chr4:132756090-132756314	GM12878	blood:	n/a	n/a
3	BATF	chr4:132838254-132838466	GM12878	blood:	n/a	n/a
4	BATF	chr4:132725694-132726042	GM12878	blood:	n/a	n/a
5	BATF	chr4:132725785-132726083	GM12878	blood:	n/a	n/a
6	BATF	chr4:132740151-132740463	GM12878	blood:	n/a	n/a
7	BATF	chr4:132850740-132850958	GM12878	blood:	n/a	n/a
8	BATF	chr4:132857922-132858212	GM12878	blood:	n/a	n/a
9	BATF	chr4:132857911-132858250	GM12878	blood:	n/a	n/a
10	BATF	chr4:132800260-132800528	GM12878	blood:	n/a	chr4:132800367-132800378
11	BATF	chr4:132758324-132758797	GM12878	blood:	n/a	n/a
12	BATF	chr4:132758273-132758804	GM12878	blood:	n/a	n/a
13	BATF	chr4:132755814-132756305	GM12878	blood:	n/a	n/a
14	BCL11A	chr4:132888535-132888793	GM12878	blood:	n/a	n/a
15	BCL11A	chr4:132740261-132740436	GM12878	blood:	n/a	n/a
16	BCL11A	chr4:132756052-132756295	GM12878	blood:	n/a	n/a
17	BCL11A	chr4:132888375-132888594	GM12878	blood:	n/a	n/a
18	BCL11A	chr4:132753934-132754118	GM12878	blood:	n/a	n/a
19	BCL11A	chr4:132800227-132800577	GM12878	blood:	n/a	n/a
20	BCL11A	chr4:132758346-132758733	GM12878	blood:	n/a	n/a
21	BCL11A	chr4:132755806-132756342	GM12878	blood:	n/a	n/a
22	BCL11A	chr4:132725879-132726110	GM12878	blood:	n/a	n/a
23	CEBPB	chr4:132790795-132790862	HepG2	liver:	n/a	chr4:132790812-132790829 chr4:132790815-132790826
24	CEBPB	chr4:132866543-132866744	HepG2	liver:	n/a	chr4:132866623-132866634 chr4:132866624-132866635 chr4:132866623-132866636 chr4:132866623-132866636
25	CEBPB	chr4:132865127-132865413	Hela-S3	cervix:	n/a	chr4:132865138-132865150
26	CTCF	chr4:132898878-132899014	GM12891	blood:	n/a	chr4:132898934-132898947
27	CTCF	chr4:132896412-132896440	Fibrobl	skin:	n/a	n/a
28	CTCF	chr4:132760059-132760096	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:132808642-132808705	GM10266	blood:	n/a	n/a
30	CTCF	chr4:132718032-132718149	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr4:132740304-132740504	GM12878	blood:	n/a	n/a
32	CTCF	chr4:132896451-132896473	Fibrobl	skin:	n/a	chr4:132896458-132896471
33	CTCF	chr4:132727749-132727809	Medullo	brain:	n/a	n/a
34	CTCF	chr4:132852639-132852671	Spleen_OC	spleen:	n/a	n/a
35	CTCF	chr4:132740334-132740417	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:132897911-132898096	GM12891	blood:	n/a	n/a
37	CTCF	chr4:132727228-132727256	Kidney_OC	kidney:	n/a	n/a
38	CTCF	chr4:132740319-132740349	GM13977	blood:	n/a	n/a
39	CTCF	chr4:132740295-132740442	MCF-7	breast:	n/a	n/a
40	CTCF	chr4:132759940-132760090	HepG2	liver:	n/a	n/a
41	CTCF	chr4:132740180-132740330	GM12878	blood:	n/a	n/a
42	CTCF	chr4:132781362-132781400	Lung_OC	lung:	n/a	n/a
43	CTCF	chr4:132759920-132760070	WERI-Rb-1	eye:	n/a	n/a
44	CTCF	chr4:132896396-132896551	GM12891	blood:	n/a	chr4:132896458-132896471
45	CTCF	chr4:132873943-132873981	Pancreas_OC	pancreas:	n/a	n/a
46	CTCF	chr4:132740317-132740436	MCF-7	breast:	n/a	n/a
47	CTCF	chr4:132740334-132740412	Gliobla	brain:	n/a	n/a
48	CTCF	chr4:132849965-132850041	GM20000	blood:	n/a	n/a
49	CTCF	chr4:132740200-132740350	BE2_C	brain:	n/a	n/a
50	CTCF	chr4:132759902-132759937	GM20000	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132896405-132896455	AG04450	lung:	fetal
2	chr4:132897691-132897741	HCPEpiC	choroid plexus:	n/a
3	chr4:132896736-132896786	AG04450	lung:	fetal
4	chr4:132899028-132899078	HEEpiC	esophagus:	n/a
5	chr4:132897018-132897068	SK-N-MC	brain:	n/a
6	chr4:132896266-132896316	HRPEpiC	eye:	n/a
7	chr4:132897691-132897741	NHDF-neo	bronchial:	n/a
8	chr4:132899028-132899078	GM06990	blood:	n/a
9	chr4:132896405-132896455	HRE	kidney:	n/a
10	chr4:132899460-132899510	HIPEpiC	eye:	n/a
11	chr4:132896266-132896316	GM12878	blood:	n/a
12	chr4:132896736-132896786	HUVEC	blood vessel:	n/a
13	chr4:132898592-132898642	Hela-S3	cervix:	n/a
14	chr4:132897018-132897068	ECC-1	luminal epithelium:	n/a
15	chr4:132898592-132898642	AG09319	gingival:	n/a
16	chr4:132896405-132896455	HRPEpiC	eye:	n/a
17	chr4:132897018-132897068	A549	lung:	n/a
18	chr4:132896374-132896424	HRPEpiC	eye:	n/a
19	chr4:132897018-132897068	MCF-7	breast:	n/a
20	chr4:132896405-132896455	HCT-116	colon:	n/a
21	chr4:132896266-132896316	AoSMC	blood vessel:	n/a
22	chr4:132896736-132896786	RPTEC	kidney:	n/a
23	chr4:132898790-132898840	ovcar-3	ovarian:	n/a
24	chr4:132896266-132896316	U87	brain:	n/a
25	chr4:132898790-132898840	HMEC	breast:	n/a
26	chr4:132896736-132896786	SAEC	small airway:	n/a
27	chr4:132899028-132899078	RPTEC	kidney:	n/a
28	chr4:132899460-132899510	MCF10A-Er-Src	breast:	n/a
29	chr4:132896736-132896786	LNCaP	prostate:	n/a
30	chr4:132896405-132896455	GM19239	blood:	n/a
31	chr4:132896405-132896455	HCF	heart:	n/a
32	chr4:132896405-132896455	HL-60	blood:	n/a
33	chr4:132898790-132898840	LNCaP	prostate:	n/a
34	chr4:132898592-132898642	GM19239	blood:	n/a
35	chr4:132899028-132899078	HepG2	liver:	n/a
36	chr4:132896374-132896424	HCM	heart:	n/a
37	chr4:132896405-132896455	PFSK-1	brain:	n/a
38	chr4:132899064-132899114	K562	blood:	n/a
39	chr4:132896374-132896424	HIPEpiC	eye:	n/a
40	chr4:132899460-132899510	HEEpiC	esophagus:	n/a
41	chr4:132899064-132899114	T-47D	breast:	n/a
42	chr4:132898790-132898840	PFSK-1	brain:	n/a
43	chr4:132899028-132899078	MCF-7	breast:	n/a
44	chr4:132899064-132899114	SK-N-SH	brain:	n/a
45	chr4:132897691-132897741	PFSK-1	brain:	n/a
46	chr4:132896579-132896629	NT2-D1	testis:	n/a
47	chr4:132899460-132899510	T-47D	breast:	n/a
48	chr4:132899028-132899078	HCM	heart:	n/a
49	chr4:132896266-132896316	HCPEpiC	choroid plexus:	n/a
50	chr4:132899064-132899114	AG09309	skin:	n/a

No data

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-2	chr4:132854661-132854803	ENSG00000251555
2	lnc-PCDH10-16	chr4:132833286-132833387	NONHSAT098318
3	lnc-RP11-62N21.1.1-2	chr4:132851186-132851466	ENSG00000251555
4	lnc-PCDH10-16	chr4:132834360-132834427	NONHSAT098318
5	lnc-PCDH10-16	chr4:132749772-132750082	NONHSAT098318
6	lnc-RP11-62N21.1.1-2	chr4:132897078-132897107	ENSG00000251555
7	lnc-PCDH10-16	chr4:132835557-132837346	NONHSAT098318
8	lnc-PCDH10-4	chr4:132712365-132712637	XLOC_003690
9	lnc-PCDH10-16	chr4:132751665-132751738	NONHSAT098318

No data

Variant related genes	Relation type
ENSG00000251555	TF binding region
RPL7AP28	TF binding region
ENSG00000251555	CpG island
RPL7AP28	CpG island

Extended variants
information (count: 1279 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1279 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542382557	chr4:132712384-132712385	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs562584375	chr4:132712433-132712434	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs573739851	chr4:132712478-132712479	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs62305945	chr4:132712481-132712482	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs145441244	chr4:132712495-132712496	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs559544902	chr4:132712501-132712502	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs3961517	chr4:132712560-132712561	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs573351537	chr4:132712576-132712577	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs3876901	chr4:132712590-132712591	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs201528870	chr4:132712599-132712600	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs3978006	chr4:132712600-132712601	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs35693514	chr4:132712615-132712616	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs62305946	chr4:132712625-132712626	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs575975597	chr4:132730820-132730821	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185432415	chr4:132730947-132730948	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs541600595	chr4:132730960-132730961	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs187602822	chr4:132730966-132730967	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs62307084	chr4:132730989-132730990	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs62307085	chr4:132731003-132731004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs78948879	chr4:132731020-132731021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs78336964	chr4:132731021-132731022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs75236848	chr4:132731078-132731079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs572413494	chr4:132731103-132731104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs78916377	chr4:132731138-132731139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs75525133	chr4:132731144-132731145	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs541535448	chr4:132731157-132731158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76366700	chr4:132731168-132731169	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs192879098	chr4:132731178-132731179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533372514	chr4:132731182-132731183	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs75062322	chr4:132731188-132731189	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs111498453	chr4:132731192-132731193	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs1913005	chr4:132731194-132731195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs79633684	chr4:132731198-132731199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs190746661	chr4:132731204-132731205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs57683592	chr4:132731210-132731211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs75191120	chr4:132731253-132731254	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs111579313	chr4:132731255-132731256	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs377568339	chr4:132731256-132731257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs561265	chr4:132731258-132731259	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs561988	chr4:132731285-132731286	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs562014	chr4:132731292-132731293	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs671613	chr4:132731305-132731306	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs1826286	chr4:132731318-132731319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs200587349	chr4:132731323-132731324	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs543877838	chr4:132731327-132731328	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563970102	chr4:132731340-132731341	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs62307086	chr4:132731351-132731352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs529643948	chr4:132731405-132731406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs62307087	chr4:132731413-132731414	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs549584713	chr4:132731414-132731415	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:82)

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
small cell lung cancer	20016488	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Autism	19492091	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:116 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132730800-132732600	Enhancers	Dnd41	blood
2	chr4:132731000-132732000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr4:132731200-132731800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr4:132731400-132732000	Enhancers	HMEC	breast
5	chr4:132731600-132732600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr4:132743000-132743600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr4:132743200-132743400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr4:132746000-132746200	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:132746800-132747000	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chr4:132749800-132750200	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chr4:132750200-132750600	Weak transcription	Skeletal Muscle Female	skeletal muscle
12	chr4:132750600-132751000	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr4:132755400-132756600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
14	chr4:132769200-132770200	Enhancers	Dnd41	blood
15	chr4:132792800-132793400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr4:132799600-132800800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr4:132799600-132800800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chr4:132809400-132810200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
19	chr4:132821800-132822400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr4:132857800-132858200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:132860200-132860600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
22	chr4:132868200-132869000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr4:132869000-132871000	Weak transcription	Pancreatic Islets	Pancreatic Islet
24	chr4:132872200-132872800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr4:132888200-132888400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr4:132888200-132889600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
27	chr4:132895400-132895600	Enhancers	HUVEC	blood vessel
28	chr4:132895400-132895800	Enhancers	GM12878-XiMat	blood
29	chr4:132895400-132897200	Active TSS	Pancreatic Islets	Pancreatic Islet
30	chr4:132895600-132896000	Active TSS	HUVEC	blood vessel
31	chr4:132895800-132896000	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr4:132895800-132896000	Enhancers	Placenta	Placenta
33	chr4:132895800-132896400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
34	chr4:132895800-132897800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
35	chr4:132896000-132896200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chr4:132896000-132896200	Flanking Active TSS	Placenta	Placenta
37	chr4:132896000-132896200	Flanking Active TSS	HUVEC	blood vessel
38	chr4:132896000-132896400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
39	chr4:132896000-132896400	Active TSS	Fetal Intestine Large	intestine
40	chr4:132896000-132896600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
41	chr4:132896000-132896600	Active TSS	Fetal Intestine Small	intestine
42	chr4:132896000-132896800	Active TSS	Duodenum Mucosa	Duodenum
43	chr4:132896000-132896800	Active TSS	NHEK	skin
44	chr4:132896000-132897000	Active TSS	Primary B cells from cord blood	blood
45	chr4:132896000-132897000	Active TSS	NHDF-Ad	bronchial
46	chr4:132896000-132897200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr4:132896000-132897200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr4:132896000-132897400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chr4:132896000-132897400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
50	chr4:132896000-132897400	Active TSS	Duodenum Smooth Muscle	Duodenum

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