Variant report

Variant	nsv879989
Chromosome Location	chr4:132773067-133001527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:423)
CpG islands
(count:856)
Chromatin interactive
region (count:3)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:423 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr4:132857911-132858250	GM12878	blood:	n/a	n/a
2	BATF	chr4:132857922-132858212	GM12878	blood:	n/a	n/a
3	BATF	chr4:132800260-132800528	GM12878	blood:	n/a	chr4:132800367-132800378
4	BATF	chr4:132800279-132800515	GM12878	blood:	n/a	chr4:132800367-132800378
5	BATF	chr4:132838254-132838466	GM12878	blood:	n/a	n/a
6	BATF	chr4:132850740-132850958	GM12878	blood:	n/a	n/a
7	BCL11A	chr4:132888375-132888594	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:132800227-132800577	GM12878	blood:	n/a	n/a
9	BCL11A	chr4:132888535-132888793	GM12878	blood:	n/a	n/a
10	CEBPB	chr4:132947841-132948176	IMR90	lung:	n/a	n/a
11	CEBPB	chr4:132865127-132865413	Hela-S3	cervix:	n/a	chr4:132865138-132865150
12	CEBPB	chr4:132933791-132934099	IMR90	lung:	n/a	chr4:132933900-132933911
13	CEBPB	chr4:132922726-132923101	IMR90	lung:	n/a	n/a
14	CEBPB	chr4:132911685-132911991	IMR90	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
15	CEBPB	chr4:132933770-132934069	HepG2	liver:	n/a	chr4:132933900-132933911
16	CEBPB	chr4:132911736-132911961	HepG2	liver:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
17	CEBPB	chr4:132790795-132790862	HepG2	liver:	n/a	chr4:132790812-132790829 chr4:132790815-132790826
18	CEBPB	chr4:132911717-132911917	A549	lung:	n/a	chr4:132911802-132911813 chr4:132911802-132911815
19	CEBPB	chr4:132866543-132866744	HepG2	liver:	n/a	chr4:132866623-132866634 chr4:132866624-132866635 chr4:132866623-132866636 chr4:132866623-132866636
20	CEBPB	chr4:132987113-132987581	IMR90	lung:	n/a	n/a
21	CTCF	chr4:132998060-132998210	MCF-7	breast:	n/a	chr4:132998177-132998186
22	CTCF	chr4:132896412-132896440	Fibrobl	skin:	n/a	n/a
23	CTCF	chr4:132998060-132998210	BE2_C	brain:	n/a	chr4:132998177-132998186
24	CTCF	chr4:132998080-132998230	HA-sp	spinal cord:	n/a	chr4:132998177-132998186
25	CTCF	chr4:132998060-132998210	AG04450	lung:	n/a	chr4:132998177-132998186
26	CTCF	chr4:132998080-132998230	HCPEpiC	choroid plexus:	n/a	chr4:132998177-132998186
27	CTCF	chr4:132998080-132998230	HepG2	liver:	n/a	chr4:132998177-132998186
28	CTCF	chr4:132998140-132998290	HUVEC	blood vessel:	n/a	chr4:132998177-132998186
29	CTCF	chr4:132998080-132998230	Caco-2	colon:	n/a	chr4:132998177-132998186
30	CTCF	chr4:132998000-132998150	HCT-116	colon:	n/a	n/a
31	CTCF	chr4:132959616-132959722	GM13976	blood:	n/a	n/a
32	CTCF	chr4:132897911-132898096	GM12891	blood:	n/a	n/a
33	CTCF	chr4:132998160-132998310	RPTEC	kidney:	n/a	chr4:132998177-132998186
34	CTCF	chr4:132998020-132998170	AG04450	lung:	n/a	n/a
35	CTCF	chr4:132998100-132998250	HVMF	connective:	n/a	chr4:132998177-132998186
36	CTCF	chr4:132998100-132998250	HPAF	blood vessel:	n/a	chr4:132998177-132998186
37	CTCF	chr4:132924740-132924890	HAc	cerebellar:	n/a	n/a
38	CTCF	chr4:132998160-132998310	HMEC	breast:	n/a	chr4:132998177-132998186
39	CTCF	chr4:132873943-132873981	Pancreas_OC	pancreas:	n/a	n/a
40	CTCF	chr4:132998120-132998270	WERI-Rb-1	eye:	n/a	chr4:132998177-132998186
41	CTCF	chr4:132906019-132906077	LNCaP	prostate:	n/a	n/a
42	CTCF	chr4:132998144-132998221	MCF-7	breast:	n/a	chr4:132998177-132998186
43	CTCF	chr4:132983529-132983535	GM13976	blood:	n/a	n/a
44	CTCF	chr4:132985140-132985290	HPAF	blood vessel:	n/a	n/a
45	CTCF	chr4:132900873-132900899	Medullo	brain:	n/a	n/a
46	CTCF	chr4:132998100-132998250	HCFaa	heart:	n/a	chr4:132998177-132998186
47	CTCF	chr4:132998100-132998250	BE2_C	brain:	n/a	chr4:132998177-132998186
48	CTCF	chr4:132998120-132998270	AG04449	skin:	n/a	chr4:132998177-132998186
49	CTCF	chr4:132998220-132998370	HCT-116	colon:	n/a	n/a
50	CTCF	chr4:132998140-132998290	HRPEpiC	eye:	n/a	chr4:132998177-132998186

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132897018-132897068	Caco-2	colon:	n/a
2	chr4:132899028-132899078	SAEC	small airway:	n/a
3	chr4:132897018-132897068	Caco-2	colon:	n/a
4	chr4:132899028-132899078	SAEC	small airway:	n/a
5	chr4:132896266-132896316	SK-N-SH_RA	brain:	n/a
6	chr4:132899460-132899510	AG10803	skin:	n/a
7	chr4:132899064-132899114	BE2_C	brain:	n/a
8	chr4:132984152-132984202	SKMC	muscle:	n/a
9	chr4:132899028-132899078	SKMC	muscle:	n/a
10	chr4:132899064-132899114	SK-N-MC	brain:	n/a
11	chr4:132896736-132896786	HEEpiC	esophagus:	n/a
12	chr4:132898592-132898642	HMEC	breast:	n/a
13	chr4:132897691-132897741	HRCEpiC	kidney:	n/a
14	chr4:132898790-132898840	NH-A	brain:	n/a
15	chr4:132899028-132899078	NB4	blood:	n/a
16	chr4:132896266-132896316	AG10803	skin:	n/a
17	chr4:132896374-132896424	HPAEpiC	pulmonary alveolar:	n/a
18	chr4:132896579-132896629	HIPEpiC	eye:	n/a
19	chr4:132896405-132896455	HPAEpiC	pulmonary alveolar:	n/a
20	chr4:132899028-132899078	SK-N-MC	brain:	n/a
21	chr4:132899028-132899078	NH-A	brain:	n/a
22	chr4:132896579-132896629	HUVEC	blood vessel:	n/a
23	chr4:132896374-132896424	H1-hESC	embryonic stem cell:	embryo
24	chr4:132899460-132899510	AoSMC	blood vessel:	n/a
25	chr4:132896374-132896424	HIPEpiC	eye:	n/a
26	chr4:132896405-132896455	HNPCEpiC	eye:	n/a
27	chr4:132984188-132984238	MCF-7	breast:	n/a
28	chr4:132897691-132897741	SK-N-SH	brain:	n/a
29	chr4:132897018-132897068	HRCEpiC	kidney:	n/a
30	chr4:132897691-132897741	ProgFib	skin:	n/a
31	chr4:132896579-132896629	AG09309	skin:	n/a
32	chr4:132897018-132897068	NHBE	bronchial:	n/a
33	chr4:132897018-132897068	HepG2	liver:	n/a
34	chr4:132896374-132896424	ECC-1	luminal epithelium:	n/a
35	chr4:132896374-132896424	AG04449	skin:	fetal
36	chr4:132896266-132896316	SK-N-SH	brain:	n/a
37	chr4:132896405-132896455	MCF-7	breast:	n/a
38	chr4:132899460-132899510	K562	blood:	n/a
39	chr4:132896736-132896786	NHDF-neo	bronchial:	n/a
40	chr4:132897018-132897068	ProgFib	skin:	n/a
41	chr4:132896266-132896316	SAEC	small airway:	n/a
42	chr4:132899028-132899078	ECC-1	luminal epithelium:	n/a
43	chr4:132897691-132897741	Hela-S3	cervix:	n/a
44	chr4:132899460-132899510	GM06990	blood:	n/a
45	chr4:132984188-132984238	PANC-1	pancreas:	n/a
46	chr4:132899028-132899078	ProgFib	skin:	n/a
47	chr4:132896405-132896455	NHDF-neo	bronchial:	n/a
48	chr4:132984188-132984238	SAEC	small airway:	n/a
49	chr4:132896405-132896455	K562	blood:	n/a
50	chr4:132896736-132896786	GM12878	blood:	n/a

(count:3 , 50 per page) page: 1

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

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-16	chr4:132834360-132834427	NONHSAT098318
2	lnc-PCDH10-16	chr4:132833286-132833387	NONHSAT098318
3	lnc-PCDH10-12	chr4:132914719-132914974	l_2731_chr4:132914718-132932069_testes
4	lnc-RP11-62N21.1.1-1	chr4:132949501-132949589	XLOC_004078
5	lnc-RP11-62N21.1.1-1	chr4:132949501-132949636	XLOC_004078
6	lnc-PCDH10-16	chr4:132835557-132837346	NONHSAT098318
7	lnc-RP11-62N21.1.1-2	chr4:132897078-132897107	ENSG00000251555
8	lnc-PCDH10-12	chr4:132931815-132932069	l_2731_chr4:132914718-132932069_testes
9	lnc-RP11-62N21.1.1-1	chr4:132948330-132948587	XLOC_004078
10	lnc-RP11-62N21.1.1-1	chr4:132925965-132926229	XLOC_004078
11	lnc-RP11-62N21.1.1-2	chr4:132851186-132851466	ENSG00000251555
12	lnc-RP11-62N21.1.1-2	chr4:132854661-132854803	ENSG00000251555

No data

Variant related genes	Relation type
ENSG00000251555	TF binding region
ENSG00000249463	TF binding region
RPL7AP28	TF binding region
ENSG00000251555	CpG island
ENSG00000249463	CpG island
RPL7AP28	CpG island
ENSG00000185220	chromatin interactions
ADCY9	miRNA target sites

Extended variants
information (count: 2311 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:2311 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3961470	chr4:132782162-132782163	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs171208	chr4:132782202-132782203	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs60008863	chr4:132782222-132782223	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs187073937	chr4:132782260-132782261	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs189748683	chr4:132782281-132782282	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs200871693	chr4:132782320-132782321	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs367888177	chr4:132782323-132782324	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs564311313	chr4:132782324-132782325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs62305991	chr4:132783050-132783051	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555587728	chr4:132783065-132783066	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs688164	chr4:132783068-132783069	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs572235546	chr4:132783109-132783110	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs562288770	chr4:132783214-132783215	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs62305992	chr4:132783246-132783247	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs62305993	chr4:132783285-132783286	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs633149	chr4:132783294-132783295	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs558239296	chr4:132783305-132783306	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs62305994	chr4:132783324-132783325	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs577909444	chr4:132783331-132783332	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs543430218	chr4:132783336-132783337	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs551899778	chr4:132792833-132792834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs3977689	chr4:132792863-132792864	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs2863853	chr4:132792903-132792904	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs2863854	chr4:132792924-132792925	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs571346294	chr4:132792936-132792937	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs569425138	chr4:132792949-132792950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs538075013	chr4:132792953-132792954	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs2863855	chr4:132792954-132792955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs370310627	chr4:132792961-132792962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs184662153	chr4:132792962-132792963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs567233737	chr4:132792973-132792974	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs536374106	chr4:132792982-132792983	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs552690438	chr4:132793009-132793010	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs572545431	chr4:132793011-132793012	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs2863856	chr4:132793027-132793028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs544863771	chr4:132793038-132793039	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs570350	chr4:132793135-132793136	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs553628661	chr4:132793143-132793144	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190291469	chr4:132793147-132793148	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs200336248	chr4:132793155-132793156	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2902592	chr4:132793158-132793159	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2863857	chr4:132793162-132793163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs544093257	chr4:132793178-132793179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs544850278	chr4:132793179-132793180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs561172630	chr4:132793194-132793195	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs530117641	chr4:132793204-132793205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs201394262	chr4:132793210-132793211	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs182512317	chr4:132793226-132793227	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs560479609	chr4:132793240-132793241	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs114178609	chr4:132793259-132793260	Enhancers	n/a	n/a	Overlapped CNVs	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:191 , 50 per page) page: 1 2 3 4

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

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