Variant report

Variant	esv1812429
Chromosome Location	chr4:132757207-132930726
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:284)
CpG islands
(count:733)
Chromatin interactive
region (count:2)
LncRNA
region (count:8)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:284 , 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	BATF	chr4:132758324-132758797	GM12878	blood:	n/a	n/a
2	BATF	chr4:132857922-132858212	GM12878	blood:	n/a	n/a
3	BATF	chr4:132800279-132800515	GM12878	blood:	n/a	chr4:132800367-132800378
4	BATF	chr4:132857911-132858250	GM12878	blood:	n/a	n/a
5	BATF	chr4:132758273-132758804	GM12878	blood:	n/a	n/a
6	BATF	chr4:132850740-132850958	GM12878	blood:	n/a	n/a
7	BATF	chr4:132838254-132838466	GM12878	blood:	n/a	n/a
8	BATF	chr4:132800260-132800528	GM12878	blood:	n/a	chr4:132800367-132800378
9	BCL11A	chr4:132888535-132888793	GM12878	blood:	n/a	n/a
10	BCL11A	chr4:132758346-132758733	GM12878	blood:	n/a	n/a
11	BCL11A	chr4:132888375-132888594	GM12878	blood:	n/a	n/a
12	BCL11A	chr4:132800227-132800577	GM12878	blood:	n/a	n/a
13	CEBPB	chr4:132866543-132866744	HepG2	liver:	n/a	chr4:132866623-132866634 chr4:132866624-132866635 chr4:132866623-132866636 chr4:132866623-132866636
14	CEBPB	chr4:132911736-132911961	HepG2	liver:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
15	CEBPB	chr4:132911685-132911991	IMR90	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
16	CEBPB	chr4:132922726-132923101	IMR90	lung:	n/a	n/a
17	CEBPB	chr4:132911717-132911917	A549	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
18	CEBPB	chr4:132790795-132790862	HepG2	liver:	n/a	chr4:132790812-132790829 chr4:132790815-132790826
19	CEBPB	chr4:132865127-132865413	Hela-S3	cervix:	n/a	chr4:132865138-132865150
20	CTCF	chr4:132922089-132922139	LNCaP	prostate:	n/a	n/a
21	CTCF	chr4:132851520-132851670	AoAF	blood vessel:	n/a	n/a
22	CTCF	chr4:132873943-132873981	Pancreas_OC	pancreas:	n/a	n/a
23	CTCF	chr4:132849976-132850033	Pancreas_OC	pancreas:	n/a	n/a
24	CTCF	chr4:132760059-132760096	MCF-7	breast:	n/a	n/a
25	CTCF	chr4:132781362-132781400	Lung_OC	lung:	n/a	n/a
26	CTCF	chr4:132897963-132898042	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr4:132898878-132899014	GM12891	blood:	n/a	chr4:132898934-132898947
28	CTCF	chr4:132924740-132924890	HAc	cerebellar:	n/a	n/a
29	CTCF	chr4:132896396-132896551	GM12891	blood:	n/a	chr4:132896458-132896471
30	CTCF	chr4:132897911-132898096	GM12891	blood:	n/a	n/a
31	CTCF	chr4:132852639-132852671	Spleen_OC	spleen:	n/a	n/a
32	CTCF	chr4:132871123-132871153	GM13976	blood:	n/a	n/a
33	CTCF	chr4:132906019-132906077	LNCaP	prostate:	n/a	n/a
34	CTCF	chr4:132760063-132760163	GM10248	blood:	n/a	n/a
35	CTCF	chr4:132896412-132896440	Fibrobl	skin:	n/a	n/a
36	CTCF	chr4:132759902-132759937	GM20000	blood:	n/a	n/a
37	CTCF	chr4:132849965-132850041	GM20000	blood:	n/a	n/a
38	CTCF	chr4:132909818-132910127	IMR90	lung:	n/a	chr4:132909997-132910018
39	CTCF	chr4:132759940-132760090	HepG2	liver:	n/a	n/a
40	CTCF	chr4:132759920-132760070	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr4:132896451-132896473	Fibrobl	skin:	n/a	chr4:132896458-132896471
42	CTCF	chr4:132900873-132900899	Medullo	brain:	n/a	n/a
43	CTCF	chr4:132766280-132766430	HCM	heart:	n/a	n/a
44	CTCF	chr4:132808642-132808705	GM10266	blood:	n/a	n/a
45	E2F4	chr4:132929969-132930178	MCF10A-Er-Src	breast:	n/a	n/a
46	E2F4	chr4:132922797-132923055	MCF10A-Er-Src	breast:	n/a	n/a
47	EBF1	chr4:132897158-132897418	GM12878	blood:	n/a	n/a
48	EBF1	chr4:132880056-132880296	GM12878	blood:	n/a	n/a
49	ELF1	chr4:132896458-132897242	GM12878	blood:	n/a	n/a
50	EP300	chr4:132878292-132878550	GM12878	blood:	n/a	n/a

(count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132897018-132897068	HCT-116	colon:	n/a
2	chr4:132897018-132897068	HCT-116	colon:	n/a
3	chr4:132899460-132899510	T-47D	breast:	n/a
4	chr4:132898592-132898642	AG04449	skin:	fetal
5	chr4:132896579-132896629	HCM	heart:	n/a
6	chr4:132896736-132896786	NB4	blood:	n/a
7	chr4:132899064-132899114	SK-N-SH	brain:	n/a
8	chr4:132896266-132896316	CMK	blood:	n/a
9	chr4:132899028-132899078	AG09319	gingival:	n/a
10	chr4:132899028-132899078	SK-N-SH_RA	brain:	n/a
11	chr4:132897018-132897068	ovcar-3	ovarian:	n/a
12	chr4:132899460-132899510	NHDF-neo	bronchial:	n/a
13	chr4:132899028-132899078	HepG2	liver:	n/a
14	chr4:132899064-132899114	IMR90	lung:	fetal
15	chr4:132896266-132896316	PrEC	prostate:	n/a
16	chr4:132896736-132896786	SK-N-MC	brain:	n/a
17	chr4:132896266-132896316	HCM	heart:	n/a
18	chr4:132899460-132899510	CMK	blood:	n/a
19	chr4:132899460-132899510	HCF	heart:	n/a
20	chr4:132896405-132896455	BJ	skin:	n/a
21	chr4:132899460-132899510	H1-hESC	embryonic stem cell:	embryo
22	chr4:132897018-132897068	HPAEpiC	pulmonary alveolar:	n/a
23	chr4:132897691-132897741	HRPEpiC	eye:	n/a
24	chr4:132898592-132898642	HMEC	breast:	n/a
25	chr4:132896374-132896424	ProgFib	skin:	n/a
26	chr4:132896405-132896455	NT2-D1	testis:	n/a
27	chr4:132896579-132896629	U87	brain:	n/a
28	chr4:132896579-132896629	HL-60	blood:	n/a
29	chr4:132896736-132896786	Hela-S3	cervix:	n/a
30	chr4:132896374-132896424	HRE	kidney:	n/a
31	chr4:132897691-132897741	HEK293	kidney:	embryo
32	chr4:132897691-132897741	NB4	blood:	n/a
33	chr4:132897691-132897741	SKMC	muscle:	n/a
34	chr4:132898790-132898840	HUVEC	blood vessel:	n/a
35	chr4:132896579-132896629	PANC-1	pancreas:	n/a
36	chr4:132899028-132899078	HMEC	breast:	n/a
37	chr4:132896405-132896455	IMR90	lung:	fetal
38	chr4:132899460-132899510	HRE	kidney:	n/a
39	chr4:132899064-132899114	AG09309	skin:	n/a
40	chr4:132896579-132896629	HCF	heart:	n/a
41	chr4:132898790-132898840	HAEpiC	amniotic membrane:	n/a
42	chr4:132897691-132897741	AG04449	skin:	fetal
43	chr4:132896405-132896455	HEK293	kidney:	embryo
44	chr4:132898790-132898840	GM12892	blood:	n/a
45	chr4:132896405-132896455	HRPEpiC	eye:	n/a
46	chr4:132897691-132897741	AoSMC	blood vessel:	n/a
47	chr4:132898592-132898642	GM12878	blood:	n/a
48	chr4:132898592-132898642	SAEC	small airway:	n/a
49	chr4:132897691-132897741	HCM	heart:	n/a
50	chr4:132898592-132898642	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:249200230..249200936-chr4:132915036..132915536,2	Hela-S3	cervix:
2	chr10:16933616..16934139-chr4:132930526..132931027,2	HCT-116	colon:

(count:8 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-16	chr4:132834360-132834427	NONHSAT098318
2	lnc-RP11-62N21.1.1-1	chr4:132925965-132926229	XLOC_004078
3	lnc-RP11-62N21.1.1-2	chr4:132897078-132897107	ENSG00000251555
4	lnc-PCDH10-16	chr4:132833286-132833387	NONHSAT098318
5	lnc-PCDH10-12	chr4:132914719-132914974	l_2731_chr4:132914718-132932069_testes
6	lnc-RP11-62N21.1.1-2	chr4:132851186-132851466	ENSG00000251555
7	lnc-RP11-62N21.1.1-2	chr4:132854661-132854803	ENSG00000251555
8	lnc-PCDH10-16	chr4:132835557-132837346	NONHSAT098318

No data

Variant related genes	Relation type
ENSG00000251555	TF binding region
RPL7AP28	TF binding region
ENSG00000251555	CpG island
RPL7AP28	CpG island
ENSG00000185220	chromatin interactions
ADCY9	miRNA target sites

Extended variants
information (count: 1391 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:1391 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79166500	chr4:132769227-132769228	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs75754425	chr4:132769252-132769253	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs558129497	chr4:132769357-132769358	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs164403	chr4:132769368-132769369	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs186563900	chr4:132769372-132769373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140634744	chr4:132769379-132769380	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs191295868	chr4:132769380-132769381	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs164402	chr4:132769382-132769383	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs200813168	chr4:132769415-132769416	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs115996640	chr4:132769419-132769420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184553308	chr4:132769426-132769427	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs201984997	chr4:132769456-132769457	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs545295572	chr4:132769496-132769497	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs200617007	chr4:132769523-132769524	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs565278558	chr4:132769524-132769525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531094856	chr4:132769588-132769589	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377421545	chr4:132769638-132769639	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs138440672	chr4:132769653-132769654	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs141336777	chr4:132769706-132769707	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs549090201	chr4:132769714-132769715	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs1849321	chr4:132769744-132769745	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs534643936	chr4:132769821-132769822	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs558041707	chr4:132769838-132769839	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs571843864	chr4:132769843-132769844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs537218490	chr4:132769914-132769915	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs556890326	chr4:132769915-132769916	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs573817050	chr4:132769954-132769955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs576935711	chr4:132770032-132770033	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542736496	chr4:132770035-132770036	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs553100626	chr4:132770046-132770047	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs35494975	chr4:132770093-132770094	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs150238785	chr4:132770157-132770158	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs565192785	chr4:132770163-132770164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs531133122	chr4:132770183-132770184	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs202194497	chr4:132770184-132770185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs3961470	chr4:132782162-132782163	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs171208	chr4:132782202-132782203	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs60008863	chr4:132782222-132782223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs187073937	chr4:132782260-132782261	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs189748683	chr4:132782281-132782282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs200871693	chr4:132782320-132782321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs367888177	chr4:132782323-132782324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs564311313	chr4:132782324-132782325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs62305991	chr4:132783050-132783051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs555587728	chr4:132783065-132783066	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs688164	chr4:132783068-132783069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs572235546	chr4:132783109-132783110	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs562288770	chr4:132783214-132783215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs62305992	chr4:132783246-132783247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs62305993	chr4:132783285-132783286	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:81)

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
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	20967226	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:121 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132769200-132770200	Enhancers	Dnd41	blood
2	chr4:132792800-132793400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr4:132799600-132800800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr4:132799600-132800800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr4:132809400-132810200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
6	chr4:132821800-132822400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:132857800-132858200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr4:132860200-132860600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
9	chr4:132868200-132869000	Enhancers	Pancreatic Islets	Pancreatic Islet
10	chr4:132869000-132871000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr4:132872200-132872800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
12	chr4:132888200-132888400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
13	chr4:132888200-132889600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
14	chr4:132895400-132895600	Enhancers	HUVEC	blood vessel
15	chr4:132895400-132895800	Enhancers	GM12878-XiMat	blood
16	chr4:132895400-132897200	Active TSS	Pancreatic Islets	Pancreatic Islet
17	chr4:132895600-132896000	Active TSS	HUVEC	blood vessel
18	chr4:132895800-132896000	Enhancers	Primary hematopoietic stem cells short term culture	blood
19	chr4:132895800-132896000	Enhancers	Placenta	Placenta
20	chr4:132895800-132896400	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
21	chr4:132895800-132897800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:132896000-132896200	Enhancers	iPS-15b Cell Line	embryonic stem cell
23	chr4:132896000-132896200	Flanking Active TSS	Placenta	Placenta
24	chr4:132896000-132896200	Flanking Active TSS	HUVEC	blood vessel
25	chr4:132896000-132896400	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
26	chr4:132896000-132896400	Active TSS	Fetal Intestine Large	intestine
27	chr4:132896000-132896600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
28	chr4:132896000-132896600	Active TSS	Fetal Intestine Small	intestine
29	chr4:132896000-132896800	Active TSS	Duodenum Mucosa	Duodenum
30	chr4:132896000-132896800	Active TSS	NHEK	skin
31	chr4:132896000-132897000	Active TSS	Primary B cells from cord blood	blood
32	chr4:132896000-132897000	Active TSS	NHDF-Ad	bronchial
33	chr4:132896000-132897200	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
34	chr4:132896000-132897200	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:132896000-132897400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
36	chr4:132896000-132897400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:132896000-132897400	Active TSS	Duodenum Smooth Muscle	Duodenum
38	chr4:132896000-132897400	Active TSS	Fetal Muscle Trunk	muscle
39	chr4:132896000-132897400	Active TSS	Thymus	Thymus
40	chr4:132896000-132897400	Active TSS	GM12878-XiMat	blood
41	chr4:132896000-132897600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:132896000-132897600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
43	chr4:132896000-132897600	Active TSS	Primary hematopoietic stem cells	blood
44	chr4:132896000-132897600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
45	chr4:132896000-132897600	Active TSS	Esophagus	oesophagus
46	chr4:132896000-132897600	Active TSS	Fetal Stomach	stomach
47	chr4:132896000-132897800	Active TSS	HUES6 Cell Line	embryonic stem cell
48	chr4:132896000-132897800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr4:132896000-132897800	ZNF genes & repeats	Fetal Thymus	thymus
50	chr4:132896000-132897800	Active TSS	Ovary	ovary

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