Variant report

Variant	nsv829879
Chromosome Location	chr4:21418568-21611002
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:21509115-21509312	HepG2	liver:	n/a	n/a
2	BCL11A	chr4:21545162-21545418	H1-hESC	embryonic stem cell:	n/a	n/a
3	BRCA1	chr4:21471169-21471375	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr4:21514045-21514352	H1-hESC	embryonic stem cell:	n/a	n/a
5	CCNT2	chr4:21473772-21473970	K562	blood:	n/a	n/a
6	CEBPB	chr4:21432358-21432663	H1-hESC	embryonic stem cell:	n/a	chr4:21432515-21432524 chr4:21432513-21432526 chr4:21432515-21432524 chr4:21432514-21432525 chr4:21432513-21432526 chr4:21432515-21432524
7	CEBPB	chr4:21427707-21427907	K562	blood:	n/a	chr4:21427718-21427729
8	CEBPB	chr4:21575694-21575733	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chr4:21528872-21529203	IMR90	lung:	n/a	chr4:21529040-21529051
10	CEBPB	chr4:21528920-21529206	A549	lung:	n/a	chr4:21529040-21529051
11	CEBPB	chr4:21449371-21449658	Hela-S3	cervix:	n/a	chr4:21449511-21449522
12	CEBPB	chr4:21432340-21432662	HepG2	liver:	n/a	chr4:21432515-21432524 chr4:21432513-21432526 chr4:21432515-21432524 chr4:21432514-21432525 chr4:21432513-21432526 chr4:21432515-21432524
13	CEBPB	chr4:21599831-21600217	HepG2	liver:	n/a	chr4:21600032-21600043
14	CEBPB	chr4:21492405-21492654	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr4:21610496-21610650	H1-hESC	embryonic stem cell:	n/a	n/a
16	CEBPB	chr4:21449350-21449652	H1-hESC	embryonic stem cell:	n/a	chr4:21449511-21449522
17	CEBPB	chr4:21449344-21449649	HepG2	liver:	n/a	chr4:21449511-21449522
18	CEBPB	chr4:21537623-21538010	H1-hESC	embryonic stem cell:	n/a	chr4:21537870-21537881
19	CEBPB	chr4:21599919-21600143	IMR90	lung:	n/a	chr4:21600032-21600043
20	CEBPB	chr4:21528873-21529208	HepG2	liver:	n/a	chr4:21529040-21529051
21	CEBPB	chr4:21436283-21436393	H1-hESC	embryonic stem cell:	n/a	n/a
22	CEBPB	chr4:21427556-21427932	HepG2	liver:	n/a	chr4:21427718-21427729
23	CEBPB	chr4:21432334-21432679	IMR90	lung:	n/a	chr4:21432515-21432524 chr4:21432513-21432526 chr4:21432515-21432524 chr4:21432514-21432525 chr4:21432513-21432526 chr4:21432515-21432524
24	CEBPB	chr4:21427566-21427787	A549	lung:	n/a	chr4:21427718-21427729
25	CEBPB	chr4:21578881-21579034	HepG2	liver:	n/a	chr4:21578923-21578934 chr4:21578925-21578936 chr4:21578923-21578936
26	CHD2	chr4:21571464-21571495	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr4:21537184-21537224	GM12878	blood:	n/a	n/a
28	CTCF	chr4:21509200-21509350	AG09319	gingival:	n/a	chr4:21509245-21509252 chr4:21509243-21509264 chr4:21509242-21509258 chr4:21509285-21509293
29	CTCF	chr4:21514054-21514323	Medullo	brain:	n/a	n/a
30	CTCF	chr4:21471166-21471391	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chr4:21514120-21514270	HMF	breast:	n/a	n/a
32	CTCF	chr4:21509180-21509330	HA-sp	spinal cord:	n/a	chr4:21509245-21509252 chr4:21509243-21509264 chr4:21509242-21509258 chr4:21509285-21509293
33	CTCF	chr4:21509220-21509370	AG04450	lung:	n/a	chr4:21509245-21509252 chr4:21509243-21509264 chr4:21509242-21509258 chr4:21509285-21509293
34	CTCF	chr4:21509220-21509370	Caco-2	colon:	n/a	chr4:21509245-21509252 chr4:21509243-21509264 chr4:21509242-21509258 chr4:21509285-21509293
35	CTCF	chr4:21471165-21471377	MCF-7	breast:	n/a	n/a
36	CTCF	chr4:21514159-21514248	NHEK	skin:	n/a	n/a
37	CTCF	chr4:21471200-21471350	BJ	skin:	n/a	n/a
38	CTCF	chr4:21509120-21509270	GM12871	blood:	n/a	chr4:21509245-21509252 chr4:21509243-21509264 chr4:21509242-21509258
39	CTCF	chr4:21514091-21514173	Spleen_OC	spleen:	n/a	n/a
40	CTCF	chr4:21509120-21509270	WERI-Rb-1	eye:	n/a	chr4:21509245-21509252 chr4:21509243-21509264 chr4:21509242-21509258
41	CTCF	chr4:21514020-21514170	HVMF	connective:	n/a	n/a
42	CTCF	chr4:21471220-21471283	ProgFib	skin:	n/a	n/a
43	CTCF	chr4:21514080-21514230	HMEC	breast:	n/a	n/a
44	CTCF	chr4:21514060-21514210	RPTEC	kidney:	n/a	n/a
45	CTCF	chr4:21471160-21471310	HUVEC	blood vessel:	n/a	n/a
46	CTCF	chr4:21514020-21514170	HFF	foreskin:	n/a	n/a
47	CTCF	chr4:21509140-21509290	HA-sp	spinal cord:	n/a	chr4:21509245-21509252 chr4:21509243-21509264 chr4:21509242-21509258
48	CTCF	chr4:21471220-21471370	GM12875	blood:	n/a	n/a
49	CTCF	chr4:21514036-21514271	T-47D	breast:	n/a	n/a
50	CTCF	chr4:21514080-21514230	AoAF	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:21470137-21470187	AG10803	skin:	n/a
2	chr4:21470137-21470187	HPAEpiC	pulmonary alveolar:	n/a
3	chr4:21470137-21470187	AG09309	skin:	n/a
4	chr4:21546029-21546079	Caco-2	colon:	n/a
5	chr4:21546545-21546595	SK-N-SH	brain:	n/a
6	chr4:21546545-21546595	A549	lung:	n/a
7	chr4:21546545-21546595	RPTEC	kidney:	n/a
8	chr4:21470137-21470187	MCF-7	breast:	n/a
9	chr4:21546029-21546079	ovcar-3	ovarian:	n/a
10	chr4:21546029-21546079	Jurkat	blood:	n/a
11	chr4:21546029-21546079	PANC-1	pancreas:	n/a
12	chr4:21470137-21470187	AG04450	lung:	fetal
13	chr4:21546029-21546079	HCM	heart:	n/a
14	chr4:21546029-21546079	Hepatocyte	liver:	n/a
15	chr4:21470137-21470187	HUVEC	blood vessel:	n/a
16	chr4:21546545-21546595	NT2-D1	testis:	n/a
17	chr4:21546029-21546079	HIPEpiC	eye:	n/a
18	chr4:21546029-21546079	HRPEpiC	eye:	n/a
19	chr4:21470137-21470187	NH-A	brain:	n/a
20	chr4:21546545-21546595	SKMC	muscle:	n/a
21	chr4:21546029-21546079	HNPCEpiC	eye:	n/a
22	chr4:21470137-21470187	IMR90	lung:	fetal
23	chr4:21470137-21470187	NB4	blood:	n/a
24	chr4:21470137-21470187	ProgFib	skin:	n/a
25	chr4:21470137-21470187	RPTEC	kidney:	n/a
26	chr4:21470137-21470187	Caco-2	colon:	n/a
27	chr4:21546029-21546079	NHBE	bronchial:	n/a
28	chr4:21470137-21470187	LNCaP	prostate:	n/a
29	chr4:21546545-21546595	PFSK-1	brain:	n/a
30	chr4:21546545-21546595	Jurkat	blood:	n/a
31	chr4:21546545-21546595	HPAEpiC	pulmonary alveolar:	n/a
32	chr4:21546029-21546079	SK-N-SH	brain:	n/a
33	chr4:21546029-21546079	AG10803	skin:	n/a
34	chr4:21470137-21470187	MCF10A-Er-Src	breast:	n/a
35	chr4:21470137-21470187	SK-N-MC	brain:	n/a
36	chr4:21546029-21546079	BJ	skin:	n/a
37	chr4:21546545-21546595	SK-N-SH_RA	brain:	n/a
38	chr4:21546545-21546595	HRPEpiC	eye:	n/a
39	chr4:21470137-21470187	AoSMC	blood vessel:	n/a
40	chr4:21546029-21546079	HUVEC	blood vessel:	n/a
41	chr4:21546545-21546595	AoSMC	blood vessel:	n/a
42	chr4:21470137-21470187	HRCEpiC	kidney:	n/a
43	chr4:21546545-21546595	HUVEC	blood vessel:	n/a
44	chr4:21546545-21546595	K562	blood:	n/a
45	chr4:21546545-21546595	HAEpiC	amniotic membrane:	n/a
46	chr4:21546029-21546079	MCF10A-Er-Src	breast:	n/a
47	chr4:21546545-21546595	LNCaP	prostate:	n/a
48	chr4:21470137-21470187	GM06990	blood:	n/a
49	chr4:21470137-21470187	HepG2	liver:	n/a
50	chr4:21546545-21546595	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr4:21510988..21512730-chr4:21514428..21516962,2	K562	blood:
2	chr4:21186540..21187139-chr4:21470730..21471606,2	MCF-7	breast:
3	chr4:21513660..21514733-chr4:21769803..21771071,4	MCF-7	breast:
4	chr4:21497861..21500462-chr4:21501332..21503199,2	K562	blood:
5	chr4:21513582..21515656-chr4:21764630..21766290,2	MCF-7	breast:
6	chr4:21186139..21187069-chr4:21470759..21471732,3	MCF-7	breast:
7	chr4:21510988..21512730-chr4:21514428..21516962,2	K562	blood:
8	chr4:21508722..21509309-chr4:21767490..21768052,2	MCF-7	breast:
9	chr4:20774692..20775734-chr4:21470776..21471557,3	MCF-7	breast:
10	chr4:21513432..21514751-chr4:21767040..21768803,10	MCF-7	breast:
11	chr4:21513547..21514492-chr4:21769669..21770605,6	MCF-7	breast:
12	chr4:21497861..21500462-chr4:21501332..21503199,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PACRGL-3	chr4:21583719-21583748	ENSG00000250092.2
2	lnc-PACRGL-3	chr4:21583841-21583998	ENSG00000250092.2
3	lnc-PACRGL-3	chr4:21610433-21610568	ENSG00000250092.2
4	lnc-GPR125-6	chr4:21454062-21463909	ucscGeneNc_uc003gqj_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-7978	chr4:21466361-21466381	MIMAT0031181

Variant related genes	Relation type
KCNIP4	TF binding region
ENSG00000250092	TF binding region
KCNIP4	CpG island
ENSG00000250092	CpG island

Extended variants
information (count: 5881 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5881 , 50 per page) page: 1 2 3 4 5 6 7 ... 118

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs147261233	chr4:21424405-21424406	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
2	rs2322963	chr4:21424434-21424435	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
3	rs543095731	chr4:21424464-21424465	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
4	rs16871062	chr4:21424478-21424479	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
5	rs191757652	chr4:21424501-21424502	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
6	rs545227812	chr4:21424511-21424512	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
7	rs148745310	chr4:21424512-21424513	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
8	rs556340540	chr4:21424559-21424560	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
9	rs575645176	chr4:21424561-21424562	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
10	rs566817956	chr4:21424593-21424594	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
11	rs28695982	chr4:21424598-21424599	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs188893258	chr4:21424608-21424609	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs75627440	chr4:21424612-21424613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs4257640	chr4:21424616-21424617	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs559840276	chr4:21424619-21424620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs533265807	chr4:21424657-21424658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551977350	chr4:21424662-21424663	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs569897763	chr4:21424670-21424671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs537360598	chr4:21424691-21424692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs549234650	chr4:21424705-21424706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs79849807	chr4:21424733-21424734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs534569656	chr4:21424734-21424735	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs527572562	chr4:21424759-21424760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs142390455	chr4:21424800-21424801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs58134719	chr4:21439049-21439050	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs138217334	chr4:21439066-21439067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs369418541	chr4:21439070-21439071	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs533877356	chr4:21439078-21439079	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs571440813	chr4:21439102-21439103	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs538943445	chr4:21439104-21439105	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs559143991	chr4:21439137-21439138	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs111495182	chr4:21439138-21439139	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142924505	chr4:21439156-21439157	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs115660590	chr4:21439174-21439175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs146127664	chr4:21439179-21439180	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs542125141	chr4:21439199-21439200	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs190516526	chr4:21439465-21439466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs531213986	chr4:21439474-21439475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs530466009	chr4:21439503-21439504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs552271708	chr4:21439504-21439505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs62295488	chr4:21439505-21439506	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs577913355	chr4:21439508-21439509	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs550187018	chr4:21439517-21439518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs58599895	chr4:21439547-21439548	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs373502735	chr4:21439599-21439600	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs545189373	chr4:21439621-21439622	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs551018271	chr4:21439648-21439649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs557197289	chr4:21439659-21439660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs539341228	chr4:21439686-21439687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs563875220	chr4:21439690-21439691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Breast cancer	17603634	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	17533364	CNVD
Oral squamous cell carcinoma	17134496	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Cancer	21637783	CNVD
Melanoma	21693616	CNVD
Squamous cell cancer	21044232	CNVD
Colorectal cancer	20709793	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Non-small cell lung cancer	21044232	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	17387387	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Cervical cancer	21062161	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Glioblastoma multiforme	21080181	CNVD
Chordoma	21602918	CNVD
HIV/AIDS	22032296	CNVD
Neuroblastoma	18923191	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Cancer	21183584	CNVD
Small bowel adenocarcinoma	21586687	CNVD
Gastric cancer	21586687	CNVD
Breast cancer	17133270	CNVD
lymphocytic leukemia	21291569	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21829676	CNVD
Melanoma	22183965	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Olfactory neuroblastoma	18408657	CNVD
Burkitt''s lymphoma	20823134	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	22522925	CNVD
Breast cancer	22737080	CNVD
Pancreatic cancer	17952125	CNVD
Cancer	22183965	CNVD
Gastric cancer	16891809	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:296 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:21424400-21424600	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
2	chr4:21424600-21424800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chr4:21439000-21439200	Enhancers	Ovary	ovary
4	chr4:21439400-21449400	Weak transcription	Ovary	ovary
5	chr4:21441600-21442000	Enhancers	Pancreatic Islets	Pancreatic Islet
6	chr4:21448400-21465600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr4:21448600-21449800	Enhancers	NHEK	skin
8	chr4:21448800-21449800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr4:21448800-21449800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr4:21448800-21449800	Enhancers	HMEC	breast
11	chr4:21449800-21454000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr4:21450600-21450800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr4:21450800-21455200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr4:21451600-21455200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chr4:21452200-21453600	Enhancers	NH-A	brain
16	chr4:21452200-21455200	Enhancers	HMEC	breast
17	chr4:21452200-21456200	Enhancers	NHEK	skin
18	chr4:21452400-21453400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chr4:21452400-21456200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
20	chr4:21452600-21453000	Enhancers	HSMMtube	muscle
21	chr4:21452600-21453400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
22	chr4:21453400-21455800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr4:21454000-21455800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr4:21455200-21455400	Bivalent Enhancer	HMEC	breast
25	chr4:21455200-21455600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:21455800-21456000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr4:21456600-21456800	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr4:21467400-21467800	Enhancers	Pancreas	Pancrea
29	chr4:21468800-21469800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
30	chr4:21468800-21470000	Enhancers	NHEK	skin
31	chr4:21468800-21470200	Enhancers	HMEC	breast
32	chr4:21469000-21469200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr4:21469000-21469200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr4:21469200-21470000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr4:21469600-21471600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr4:21469800-21470200	Enhancers	Brain Cingulate Gyrus	brain
37	chr4:21469800-21471400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:21470000-21470200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
39	chr4:21470000-21470400	Active TSS	Brain Hippocampus Middle	brain
40	chr4:21470000-21470400	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr4:21470200-21470800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr4:21470200-21471600	Weak transcription	HMEC	breast
43	chr4:21470400-21470600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
44	chr4:21470400-21470600	Enhancers	Brain Hippocampus Middle	brain
45	chr4:21470600-21471600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
46	chr4:21470800-21471000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr4:21470800-21471600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
48	chr4:21470800-21472800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
49	chr4:21470800-21472800	Enhancers	Brain Germinal Matrix	brain
50	chr4:21471000-21472000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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