Variant report

Variant	nsv879970
Chromosome Location	chr4:132191528-132305574
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:285)
CpG islands
(count:122)
Chromatin interactive
region (count:7)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:285 , 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	ATF2	chr4:132230758-132231240	GM12878	blood:	n/a	n/a
2	BACH1	chr4:132237834-132237865	H1-hESC	embryonic stem cell:	n/a	n/a
3	BATF	chr4:132237297-132237506	GM12878	blood:	n/a	chr4:132237434-132237445
4	BATF	chr4:132230793-132231130	GM12878	blood:	n/a	chr4:132230925-132230936
5	BATF	chr4:132269461-132269747	GM12878	blood:	n/a	n/a
6	BATF	chr4:132230807-132231142	GM12878	blood:	n/a	chr4:132230925-132230936
7	BATF	chr4:132269393-132269798	GM12878	blood:	n/a	n/a
8	BCL11A	chr4:132230818-132231127	GM12878	blood:	n/a	n/a
9	CBX3	chr4:132209558-132210022	HCT-116	colon:	n/a	n/a
10	CCNT2	chr4:132205064-132205471	K562	blood:	n/a	n/a
11	CCNT2	chr4:132300478-132300751	K562	blood:	n/a	n/a
12	CEBPB	chr4:132300197-132300397	HepG2	liver:	n/a	chr4:132300269-132300282 chr4:132300270-132300281 chr4:132300256-132300267
13	CEBPB	chr4:132299279-132299529	K562	blood:	n/a	n/a
14	CEBPB	chr4:132246573-132246902	HepG2	liver:	n/a	chr4:132246745-132246756
15	CEBPB	chr4:132246621-132246930	K562	blood:	n/a	chr4:132246745-132246756
16	CEBPB	chr4:132246562-132246885	IMR90	lung:	n/a	chr4:132246745-132246756
17	CTCF	chr4:132223440-132223590	HEEpiC	esophagus:	n/a	n/a
18	CTCF	chr4:132223496-132223583	Pancreas_OC	pancreas:	n/a	n/a
19	CTCF	chr4:132223480-132223630	HMEC	breast:	n/a	n/a
20	CTCF	chr4:132218311-132218355	LNCaP	prostate:	n/a	n/a
21	CTCF	chr4:132223440-132223590	GM12865	blood:	n/a	n/a
22	CTCF	chr4:132223340-132223490	GM12873	blood:	n/a	n/a
23	CTCF	chr4:132223299-132223432	H1-hESC	embryonic stem cell:	n/a	n/a
24	CTCF	chr4:132223532-132223591	A549	lung:	n/a	n/a
25	CTCF	chr4:132297223-132297230	Kidney_OC	kidney:	n/a	n/a
26	CTCF	chr4:132223440-132223590	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr4:132223537-132223618	MCF-7	breast:	n/a	n/a
28	CTCF	chr4:132223292-132223429	MCF-7	breast:	n/a	n/a
29	CTCF	chr4:132223286-132223425	MCF-7	breast:	n/a	n/a
30	CTCF	chr4:132223437-132223641	MCF-7	breast:	n/a	n/a
31	CTCF	chr4:132300627-132300750	H1-hESC	embryonic stem cell:	n/a	n/a
32	CTCF	chr4:132223355-132223722	MCF-7	breast:	n/a	n/a
33	CTCF	chr4:132223519-132223621	MCF-7	breast:	n/a	n/a
34	CTCF	chr4:132223380-132223530	GM12865	blood:	n/a	n/a
35	CTCF	chr4:132244604-132244611	Kidney_OC	kidney:	n/a	n/a
36	CTCF	chr4:132223400-132223550	HEEpiC	esophagus:	n/a	n/a
37	CTCF	chr4:132223494-132223623	MCF-7	breast:	n/a	n/a
38	CTCF	chr4:132223400-132223550	A549	lung:	n/a	n/a
39	CTCF	chr4:132223480-132223630	A549	lung:	n/a	n/a
40	CTCF	chr4:132223414-132223593	T-47D	breast:	n/a	n/a
41	CTCF	chr4:132223456-132223610	HepG2	liver:	n/a	n/a
42	CTCF	chr4:132300624-132300790	LNCaP	prostate:	n/a	n/a
43	CTCF	chr4:132244613-132244650	Kidney_OC	kidney:	n/a	n/a
44	CTCF	chr4:132223460-132223610	BE2_C	brain:	n/a	n/a
45	CTCF	chr4:132274246-132274320	Fibrobl	skin:	n/a	n/a
46	CTCF	chr4:132223311-132223365	Kidney_OC	kidney:	n/a	n/a
47	CTCF	chr4:132223519-132223576	HepG2	liver:	n/a	n/a
48	CTCF	chr4:132223534-132223633	MCF-7	breast:	n/a	n/a
49	CTCF	chr4:132223375-132223719	GM12878	blood:	n/a	n/a
50	CTCF	chr4:132223566-132223601	LNCaP	prostate:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:132273830-132273880	NH-A	brain:	n/a
2	chr4:132300589-132300639	GM19239	blood:	n/a
3	chr4:132273830-132273880	BE2_C	brain:	n/a
4	chr4:132300589-132300639	CMK	blood:	n/a
5	chr4:132273830-132273880	Hela-S3	cervix:	n/a
6	chr4:132273830-132273880	GM12892	blood:	n/a
7	chr4:132300589-132300639	HRPEpiC	eye:	n/a
8	chr4:132300589-132300639	Hepatocyte	liver:	n/a
9	chr4:132300589-132300639	SKMC	muscle:	n/a
10	chr4:132273830-132273880	AG09309	skin:	n/a
11	chr4:132273830-132273880	CMK	blood:	n/a
12	chr4:132273830-132273880	NB4	blood:	n/a
13	chr4:132300589-132300639	NH-A	brain:	n/a
14	chr4:132300589-132300639	Hela-S3	cervix:	n/a
15	chr4:132273830-132273880	HUVEC	blood vessel:	n/a
16	chr4:132300589-132300639	H1-hESC	embryonic stem cell:	embryo
17	chr4:132273830-132273880	AG04449	skin:	fetal
18	chr4:132300589-132300639	RPTEC	kidney:	n/a
19	chr4:132273830-132273880	Jurkat	blood:	n/a
20	chr4:132273830-132273880	HEEpiC	esophagus:	n/a
21	chr4:132273830-132273880	A549	lung:	n/a
22	chr4:132300589-132300639	HepG2	liver:	n/a
23	chr4:132300589-132300639	HEK293	kidney:	embryo
24	chr4:132300589-132300639	IMR90	lung:	fetal
25	chr4:132273830-132273880	HRE	kidney:	n/a
26	chr4:132273830-132273880	HRCEpiC	kidney:	n/a
27	chr4:132273830-132273880	HNPCEpiC	eye:	n/a
28	chr4:132273830-132273880	HIPEpiC	eye:	n/a
29	chr4:132273830-132273880	GM12878	blood:	n/a
30	chr4:132300589-132300639	HMEC	breast:	n/a
31	chr4:132273830-132273880	ECC-1	luminal epithelium:	n/a
32	chr4:132300589-132300639	PANC-1	pancreas:	n/a
33	chr4:132273830-132273880	PrEC	prostate:	n/a
34	chr4:132273830-132273880	ProgFib	skin:	n/a
35	chr4:132300589-132300639	GM12892	blood:	n/a
36	chr4:132300589-132300639	T-47D	breast:	n/a
37	chr4:132273830-132273880	Caco-2	colon:	n/a
38	chr4:132300589-132300639	AG04449	skin:	fetal
39	chr4:132273830-132273880	AG09319	gingival:	n/a
40	chr4:132300589-132300639	HCT-116	colon:	n/a
41	chr4:132273830-132273880	LNCaP	prostate:	n/a
42	chr4:132273830-132273880	HCPEpiC	choroid plexus:	n/a
43	chr4:132273830-132273880	AoSMC	blood vessel:	n/a
44	chr4:132300589-132300639	U87	brain:	n/a
45	chr4:132300589-132300639	GM12878	blood:	n/a
46	chr4:132300589-132300639	A549	lung:	n/a
47	chr4:132273830-132273880	HepG2	liver:	n/a
48	chr4:132300589-132300639	SK-N-SH	brain:	n/a
49	chr4:132300589-132300639	HEEpiC	esophagus:	n/a
50	chr4:132273830-132273880	GM12891	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
2	chr4:132287444..132289970-chr4:132292320..132294677,2	K562	blood:
3	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
4	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
5	chr4:132252754..132254764-chr4:132258466..132259992,2	K562	blood:
6	chr4:132208528..132210188-chr4:132213412..132215740,2	MCF-7	breast:
7	chr4:132302079..132303796-chr4:132308673..132311556,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PCDH10-7	chr4:132300925-132301522	NONHSAT098311
2	lnc-PCDH10-7	chr4:132301168-132301496	ENSG00000250102.1

No data

Variant related genes	Relation type
ENSG00000250102	TF binding region
RNU6-224P	TF binding region
ENSG00000250102	CpG island
RNU6-224P	CpG island

Extended variants
information (count: 761 )
Associated
traits (count: 77 )

Variant overlapped rSNPs/rCNVs (count:761 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs528706985	chr4:132192800-132192801	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs563822480	chr4:132192831-132192832	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs9992958	chr4:132192859-132192860	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs549515792	chr4:132192889-132192890	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs188573720	chr4:132192931-132192932	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs531118483	chr4:132193671-132193672	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs113668342	chr4:132208424-132208425	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs569384280	chr4:132208429-132208430	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs370866780	chr4:132208430-132208431	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs538523248	chr4:132208436-132208437	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs28813973	chr4:132208478-132208479	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs74485068	chr4:132208488-132208489	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs569471692	chr4:132208547-132208548	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs553022137	chr4:132208615-132208616	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs572869839	chr4:132208674-132208675	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs544805769	chr4:132208711-132208712	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs558706323	chr4:132208762-132208763	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs575394906	chr4:132208804-132208805	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs544002394	chr4:132208805-132208806	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs560806961	chr4:132208845-132208846	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs529952142	chr4:132208859-132208860	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs148476568	chr4:132208904-132208905	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs191326904	chr4:132208933-132208934	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs548666147	chr4:132208959-132208960	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs532621549	chr4:132208961-132208962	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs552432693	chr4:132208962-132208963	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs569432680	chr4:132208988-132208989	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs59870328	chr4:132209007-132209008	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs531765390	chr4:132209034-132209035	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs374029814	chr4:132209045-132209046	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs142292182	chr4:132209077-132209078	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs568738446	chr4:132209079-132209080	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs534522205	chr4:132209139-132209140	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs546599264	chr4:132209143-132209144	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs566380777	chr4:132209172-132209173	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs578093134	chr4:132209183-132209184	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs540354993	chr4:132209199-132209200	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
38	rs28817612	chr4:132209263-132209264	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575304651	chr4:132209313-132209314	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
40	rs537612834	chr4:132209320-132209321	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
41	rs372389522	chr4:132209378-132209379	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
42	rs528951108	chr4:132209392-132209393	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
43	rs150822524	chr4:132209415-132209416	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
44	rs540169685	chr4:132209421-132209422	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
45	rs183513702	chr4:132209451-132209452	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
46	rs549000800	chr4:132209453-132209454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
47	rs577216313	chr4:132209456-132209457	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs546183757	chr4:132209470-132209471	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs562801890	chr4:132209495-132209496	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs188637833	chr4:132209517-132209518	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:77)

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
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:68 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:132208400-132210400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
2	chr4:132211600-132211800	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
3	chr4:132211600-132211800	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	HSMM	muscle
5	chr4:132211600-132211800	Enhancers	HSMMtube	muscle
6	chr4:132211600-132211800	ZNF genes & repeats	HUVEC	blood vessel
7	chr4:132211600-132211800	ZNF genes & repeats	K562	blood
8	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NH-A	brain
9	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NHEK	skin
10	chr4:132211600-132211800	Flanking Bivalent TSS/Enh	NHLF	lung
11	chr4:132211600-132211800	Enhancers	Osteobl	bone
12	chr4:132211600-132212000	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr4:132211600-132212000	ZNF genes & repeats	Primary T cells from cord blood	blood
14	chr4:132211600-132212000	ZNF genes & repeats	GM12878-XiMat	blood
15	chr4:132211600-132212000	Active TSS	HMEC	breast
16	chr4:132211800-132212000	Active TSS	HSMM	muscle
17	chr4:132211800-132212000	Bivalent/Poised TSS	NHEK	skin
18	chr4:132214600-132214800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
19	chr4:132215200-132215400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr4:132223600-132223800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr4:132223800-132224800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr4:132237000-132238600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr4:132265600-132266600	Enhancers	HUES64 Cell Line	embryonic stem cell
24	chr4:132265800-132269800	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chr4:132265800-132269800	Enhancers	iPS-18 Cell Line	embryonic stem cell
26	chr4:132266000-132266200	Enhancers	H9 Cell Line	embryonic stem cell
27	chr4:132266000-132266400	Enhancers	Cortex derived primary cultured neurospheres	brain
28	chr4:132266000-132266600	Enhancers	iPS-15b Cell Line	embryonic stem cell
29	chr4:132266000-132266800	Enhancers	H1 Cell Line	embryonic stem cell
30	chr4:132266000-132266800	Enhancers	HUES6 Cell Line	embryonic stem cell
31	chr4:132266000-132268800	Enhancers	iPS-20b Cell Line	embryonic stem cell
32	chr4:132266600-132267600	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr4:132266600-132267600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
34	chr4:132266800-132267800	Weak transcription	H1 Cell Line	embryonic stem cell
35	chr4:132266800-132267800	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chr4:132267600-132268600	Enhancers	HUES64 Cell Line	embryonic stem cell
37	chr4:132267600-132269800	Enhancers	iPS-15b Cell Line	embryonic stem cell
38	chr4:132267800-132268200	Enhancers	H9 Cell Line	embryonic stem cell
39	chr4:132267800-132268400	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chr4:132267800-132268400	Enhancers	H1 Cell Line	embryonic stem cell
41	chr4:132267800-132268400	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr4:132268400-132270800	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr4:132268600-132269000	Weak transcription	HUES64 Cell Line	embryonic stem cell
44	chr4:132268800-132270800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
45	chr4:132269000-132269200	Enhancers	HUES64 Cell Line	embryonic stem cell
46	chr4:132269000-132269800	Active TSS	GM12878-XiMat	blood
47	chr4:132269200-132270800	Weak transcription	HUES64 Cell Line	embryonic stem cell
48	chr4:132269800-132270800	Weak transcription	HUES48 Cell Line	embryonic stem cell
49	chr4:132269800-132270800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chr4:132270800-132271000	Enhancers	HUES48 Cell Line	embryonic stem cell

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