Variant report

Variant	nsv967797
Chromosome Location	chr4:132892272-132902984
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:56)
CpG islands
(count:734)
Chromatin interactive
region (count:0)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:56 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CTCF	chr4:132896412-132896440	Fibrobl	skin:	n/a	n/a
2	CTCF	chr4:132896451-132896473	Fibrobl	skin:	n/a	chr4:132896458-132896471
3	CTCF	chr4:132897911-132898096	GM12891	blood:	n/a	n/a
4	CTCF	chr4:132898878-132899014	GM12891	blood:	n/a	chr4:132898934-132898947
5	CTCF	chr4:132897963-132898042	H1-hESC	embryonic stem cell:	n/a	n/a
6	CTCF	chr4:132900873-132900899	Medullo	brain:	n/a	n/a
7	CTCF	chr4:132896396-132896551	GM12891	blood:	n/a	chr4:132896458-132896471
8	EBF1	chr4:132897158-132897418	GM12878	blood:	n/a	n/a
9	ELF1	chr4:132896458-132897242	GM12878	blood:	n/a	n/a
10	FOXA1	chr4:132894212-132894684	HepG2	liver:	n/a	n/a
11	FOXA2	chr4:132896442-132896838	A549	lung:	n/a	n/a
12	HEY1	chr4:132897099-132897483	HepG2	liver:	n/a	n/a
13	HEY1	chr4:132897166-132897392	K562	blood:	n/a	n/a
14	MAFK	chr4:132899695-132899930	HepG2	liver:	n/a	n/a
15	MYC	chr4:132896905-132896942	MCF-7	breast:	n/a	n/a
16	POLR2A	chr4:132896868-132897458	A549	lung:	n/a	n/a
17	POLR2A	chr4:132897145-132897323	GM12878	blood:	n/a	n/a
18	POLR2A	chr4:132897151-132897313	A549	lung:	n/a	n/a
19	POLR2A	chr4:132896804-132897564	GM12878	blood:	n/a	n/a
20	POLR2A	chr4:132896767-132897549	GM12878	blood:	n/a	n/a
21	POLR2A	chr4:132897040-132897555	GM12878	blood:	n/a	n/a
22	POLR2A	chr4:132897327-132897457	H1-hESC	embryonic stem cell:	n/a	n/a
23	POLR2A	chr4:132897202-132897308	A549	lung:	n/a	n/a
24	POLR2A	chr4:132897164-132897408	Hela-S3	cervix:	n/a	n/a
25	POLR2A	chr4:132896976-132897102	Hela-S3	cervix:	n/a	n/a
26	POLR2A	chr4:132896207-132896257	Gliobla	brain:	n/a	n/a
27	POLR2A	chr4:132897193-132897401	HepG2	liver:	n/a	n/a
28	POLR2A	chr4:132897363-132897422	A549	lung:	n/a	n/a
29	POLR2A	chr4:132896764-132897492	GM12891	blood:	n/a	n/a
30	POLR2A	chr4:132897169-132897438	HepG2	liver:	n/a	n/a
31	POLR2A	chr4:132897125-132897505	GM12892	blood:	n/a	n/a
32	POLR2A	chr4:132897048-132897393	H1-hESC	embryonic stem cell:	n/a	n/a
33	POLR2A	chr4:132897194-132897435	A549	lung:	n/a	n/a
34	POLR2A	chr4:132897147-132897391	Hela-S3	cervix:	n/a	n/a
35	POLR2A	chr4:132897199-132897314	HepG2	liver:	n/a	n/a
36	POLR2A	chr4:132896955-132897124	Hela-S3	cervix:	n/a	n/a
37	POU2F2	chr4:132897342-132897484	GM12878	blood:	n/a	n/a
38	RUNX3	chr4:132897185-132897441	GM12878	blood:	n/a	n/a
39	SETDB1	chr4:132900014-132900214	U2OS	brain:	n/a	n/a
40	STAT3	chr4:132900271-132900536	MCF10A-Er-Src	breast:	n/a	n/a
41	STAT3	chr4:132892351-132892418	MCF10A-Er-Src	breast:	n/a	n/a
42	TAF1	chr4:132897311-132897503	H1-hESC	embryonic stem cell:	n/a	n/a
43	TAF1	chr4:132896886-132897485	HepG2	liver:	n/a	n/a
44	TAF1	chr4:132897258-132897501	A549	lung:	n/a	n/a
45	TAF1	chr4:132897150-132897532	GM12878	blood:	n/a	n/a
46	TAF1	chr4:132897165-132897352	Hela-S3	cervix:	n/a	n/a
47	TAF1	chr4:132897231-132897504	H1-hESC	embryonic stem cell:	n/a	n/a
48	TAF1	chr4:132896901-132897155	HepG2	liver:	n/a	n/a
49	TCF3	chr4:132896949-132897593	GM12878	blood:	n/a	n/a
50	YY1	chr4:132897305-132897546	GM12891	blood:	n/a	n/a

(count:734 , 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	AG04450	lung:	fetal
2	chr4:132897691-132897741	T-47D	breast:	n/a
3	chr4:132897018-132897068	AG04450	lung:	fetal
4	chr4:132897691-132897741	T-47D	breast:	n/a
5	chr4:132897691-132897741	HEEpiC	esophagus:	n/a
6	chr4:132896579-132896629	HMEC	breast:	n/a
7	chr4:132896579-132896629	NHBE	bronchial:	n/a
8	chr4:132899460-132899510	GM12892	blood:	n/a
9	chr4:132896405-132896455	PFSK-1	brain:	n/a
10	chr4:132899028-132899078	Hepatocyte	liver:	n/a
11	chr4:132896736-132896786	HUVEC	blood vessel:	n/a
12	chr4:132896405-132896455	AG09319	gingival:	n/a
13	chr4:132899460-132899510	NB4	blood:	n/a
14	chr4:132899064-132899114	GM19239	blood:	n/a
15	chr4:132898592-132898642	GM06990	blood:	n/a
16	chr4:132896266-132896316	HRPEpiC	eye:	n/a
17	chr4:132896736-132896786	HL-60	blood:	n/a
18	chr4:132899460-132899510	NT2-D1	testis:	n/a
19	chr4:132899460-132899510	HRE	kidney:	n/a
20	chr4:132896266-132896316	GM19239	blood:	n/a
21	chr4:132896266-132896316	GM12892	blood:	n/a
22	chr4:132896374-132896424	AoSMC	blood vessel:	n/a
23	chr4:132897018-132897068	BJ	skin:	n/a
24	chr4:132896579-132896629	Hepatocyte	liver:	n/a
25	chr4:132896579-132896629	AG09319	gingival:	n/a
26	chr4:132897691-132897741	HCM	heart:	n/a
27	chr4:132899460-132899510	HNPCEpiC	eye:	n/a
28	chr4:132899064-132899114	Caco-2	colon:	n/a
29	chr4:132897018-132897068	SK-N-SH_RA	brain:	n/a
30	chr4:132899028-132899078	HCPEpiC	choroid plexus:	n/a
31	chr4:132897018-132897068	HEK293	kidney:	embryo
32	chr4:132896405-132896455	H1-hESC	embryonic stem cell:	embryo
33	chr4:132898790-132898840	SK-N-MC	brain:	n/a
34	chr4:132898592-132898642	BJ	skin:	n/a
35	chr4:132896405-132896455	AG10803	skin:	n/a
36	chr4:132899064-132899114	NB4	blood:	n/a
37	chr4:132896405-132896455	GM19239	blood:	n/a
38	chr4:132898790-132898840	ECC-1	luminal epithelium:	n/a
39	chr4:132899028-132899078	HCM	heart:	n/a
40	chr4:132897691-132897741	Caco-2	colon:	n/a
41	chr4:132896736-132896786	HRE	kidney:	n/a
42	chr4:132898592-132898642	HPAEpiC	pulmonary alveolar:	n/a
43	chr4:132896579-132896629	HRPEpiC	eye:	n/a
44	chr4:132898790-132898840	HUVEC	blood vessel:	n/a
45	chr4:132896266-132896316	Hela-S3	cervix:	n/a
46	chr4:132896405-132896455	Caco-2	colon:	n/a
47	chr4:132898592-132898642	Hela-S3	cervix:	n/a
48	chr4:132897018-132897068	HIPEpiC	eye:	n/a
49	chr4:132898790-132898840	SKMC	muscle:	n/a
50	chr4:132896266-132896316	AG09319	gingival:	n/a

No data

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-62N21.1.1-2	chr4:132897078-132897107	ENSG00000251555

No data

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

Extended variants
information (count: 377 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:377 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564075497	chr4:132895413-132895414	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs553548046	chr4:132895440-132895441	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs76131540	chr4:132895450-132895451	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs349300	chr4:132895451-132895452	Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs541127327	chr4:132895472-132895473	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs563925795	chr4:132895514-132895515	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs190521338	chr4:132895517-132895518	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs532999318	chr4:132895548-132895549	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs543726370	chr4:132895552-132895553	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs563603950	chr4:132895572-132895573	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs181931821	chr4:132895635-132895636	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs141152146	chr4:132895667-132895668	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs559501992	chr4:132895678-132895679	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs113829184	chr4:132895792-132895793	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs185937028	chr4:132895799-132895800	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs558669374	chr4:132895848-132895849	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190602611	chr4:132895851-132895852	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs146922631	chr4:132895899-132895900	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148010669	chr4:132895933-132895934	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs140752250	chr4:132895959-132895960	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs150150803	chr4:132895980-132895981	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs35442981	chr4:132896007-132896008	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs34878676	chr4:132896034-132896035	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs113395358	chr4:132896039-132896040	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs72914685	chr4:132896066-132896067	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs202186347	chr4:132896067-132896068	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs534410372	chr4:132896130-132896131	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs557868564	chr4:132896147-132896148	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs562749185	chr4:132896167-132896168	Active TSS Enhancers Flanking Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs577691175	chr4:132896216-132896217	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs543416197	chr4:132896246-132896247	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs563280565	chr4:132896252-132896253	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs573934688	chr4:132896253-132896254	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs34298855	chr4:132896272-132896273	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs151013564	chr4:132896292-132896293	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs186429047	chr4:132896341-132896342	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs150434868	chr4:132896347-132896348	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs531218140	chr4:132896361-132896362	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
39	rs528320670	chr4:132896381-132896382	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs115433643	chr4:132896382-132896383	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs191329552	chr4:132896398-132896399	Active TSS Flanking Active TSS Bivalent Enhancer ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs113065559	chr4:132896406-132896407	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs530925519	chr4:132896409-132896410	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs111707718	chr4:132896424-132896425	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs200299222	chr4:132896439-132896440	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs187678586	chr4:132896442-132896443	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs190721682	chr4:132896446-132896447	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs113088989	chr4:132896461-132896462	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs541096345	chr4:132896462-132896463	Active TSS ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs560977386	chr4:132896471-132896472	Active TSS ZNF genes & repeats Bivalent/Poised TSS	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:90 , 50 per page) page: 1 2

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

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