Variant report

Variant	nsv4547
Chromosome Location	chr4:151486280-151531479
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:598)
CpG islands
(count:1466)
Chromatin interactive
region (count:34)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:598 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:151493464-151495117	K562	blood:	n/a	chr4:151494365-151494380
2	ARID3A	chr4:151490560-151491159	K562	blood:	n/a	n/a
3	ARID3A	chr4:151515212-151515591	K562	blood:	n/a	n/a
4	ARID3A	chr4:151492014-151492424	K562	blood:	n/a	n/a
5	ATF1	chr4:151493800-151494715	K562	blood:	n/a	n/a
6	ATF1	chr4:151492025-151492343	K562	blood:	n/a	n/a
7	BACH1	chr4:151500680-151501309	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr4:151490764-151490864	K562	blood:	n/a	n/a
9	BACH1	chr4:151492080-151492355	K562	blood:	n/a	n/a
10	BACH1	chr4:151505016-151505156	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr4:151492660-151492753	K562	blood:	n/a	n/a
12	BACH1	chr4:151504252-151504748	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr4:151490262-151490900	A549	lung:	n/a	n/a
14	BHLHE40	chr4:151494259-151495050	GM12878	blood:	n/a	n/a
15	BHLHE40	chr4:151492084-151492284	K562	blood:	n/a	n/a
16	BHLHE40	chr4:151494118-151494617	K562	blood:	n/a	n/a
17	CBX3	chr4:151504429-151504764	K562	blood:	n/a	n/a
18	CBX3	chr4:151493722-151494555	K562	blood:	n/a	n/a
19	CBX3	chr4:151492013-151492371	K562	blood:	n/a	n/a
20	CBX3	chr4:151500734-151501406	K562	blood:	n/a	n/a
21	CBX3	chr4:151486126-151486541	K562	blood:	n/a	n/a
22	CBX3	chr4:151500564-151501506	K562	blood:	n/a	n/a
23	CBX3	chr4:151504007-151504347	K562	blood:	n/a	n/a
24	CBX3	chr4:151503979-151504865	K562	blood:	n/a	n/a
25	CCNT2	chr4:151493575-151494549	K562	blood:	n/a	n/a
26	CEBPB	chr4:151488248-151488580	K562	blood:	n/a	n/a
27	CEBPB	chr4:151499763-151500029	IMR90	lung:	n/a	chr4:151499898-151499909
28	CEBPB	chr4:151499759-151499997	HepG2	liver:	n/a	chr4:151499898-151499909
29	CEBPB	chr4:151490468-151490835	K562	blood:	n/a	n/a
30	CEBPB	chr4:151490468-151490842	MCF-7	breast:	n/a	n/a
31	CEBPB	chr4:151488253-151488586	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:151494165-151494543	K562	blood:	n/a	n/a
33	CEBPB	chr4:151525819-151525898	K562	blood:	n/a	n/a
34	CEBPB	chr4:151506986-151507145	H1-hESC	embryonic stem cell:	n/a	n/a
35	CEBPB	chr4:151490428-151490832	MCF-7	breast:	n/a	n/a
36	CEBPB	chr4:151488286-151488599	A549	lung:	n/a	n/a
37	CEBPB	chr4:151488369-151488569	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr4:151490509-151490883	A549	lung:	n/a	n/a
39	CEBPB	chr4:151488265-151488586	IMR90	lung:	n/a	n/a
40	CEBPB	chr4:151490436-151490816	K562	blood:	n/a	n/a
41	CEBPB	chr4:151490475-151490717	K562	blood:	n/a	n/a
42	CEBPB	chr4:151488231-151488547	K562	blood:	n/a	n/a
43	CEBPB	chr4:151490467-151490820	IMR90	lung:	n/a	n/a
44	CEBPB	chr4:151490455-151490820	A549	lung:	n/a	n/a
45	CEBPB	chr4:151503961-151504231	IMR90	lung:	n/a	n/a
46	CEBPB	chr4:151494781-151494981	K562	blood:	n/a	n/a
47	CEBPB	chr4:151488244-151488612	A549	lung:	n/a	n/a
48	CEBPB	chr4:151490337-151491237	A549	lung:	n/a	chr4:151491135-151491152
49	CEBPB	chr4:151494889-151494988	IMR90	lung:	n/a	n/a
50	CEBPB	chr4:151493978-151494539	K562	blood:	n/a	n/a

(count:1466 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:151503588-151503638	IMR90	lung:	fetal
2	chr4:151501298-151501348	HRE	kidney:	n/a
3	chr4:151503588-151503638	IMR90	lung:	fetal
4	chr4:151501298-151501348	HRE	kidney:	n/a
5	chr4:151496830-151496880	GM12891	blood:	n/a
6	chr4:151508942-151508992	HRPEpiC	eye:	n/a
7	chr4:151503588-151503638	HCM	heart:	n/a
8	chr4:151502935-151502985	PANC-1	pancreas:	n/a
9	chr4:151503501-151503551	Hepatocyte	liver:	n/a
10	chr4:151503546-151503596	AoSMC	blood vessel:	n/a
11	chr4:151504725-151504775	ECC-1	luminal epithelium:	n/a
12	chr4:151504725-151504775	ovcar-3	ovarian:	n/a
13	chr4:151496830-151496880	ECC-1	luminal epithelium:	n/a
14	chr4:151504725-151504775	Caco-2	colon:	n/a
15	chr4:151504187-151504237	HL-60	blood:	n/a
16	chr4:151504138-151504188	RPTEC	kidney:	n/a
17	chr4:151503878-151503928	BE2_C	brain:	n/a
18	chr4:151504920-151504970	Jurkat	blood:	n/a
19	chr4:151504138-151504188	HCPEpiC	choroid plexus:	n/a
20	chr4:151503227-151503277	SAEC	small airway:	n/a
21	chr4:151500631-151500681	RPTEC	kidney:	n/a
22	chr4:151503878-151503928	SK-N-SH_RA	brain:	n/a
23	chr4:151504138-151504188	H1-hESC	embryonic stem cell:	embryo
24	chr4:151501298-151501348	Hela-S3	cervix:	n/a
25	chr4:151508942-151508992	HNPCEpiC	eye:	n/a
26	chr4:151504725-151504775	BJ	skin:	n/a
27	chr4:151513084-151513134	PrEC	prostate:	n/a
28	chr4:151501035-151501085	BE2_C	brain:	n/a
29	chr4:151503546-151503596	AG04449	skin:	fetal
30	chr4:151505084-151505134	K562	blood:	n/a
31	chr4:151501298-151501348	GM19239	blood:	n/a
32	chr4:151500192-151500242	MCF10A-Er-Src	breast:	n/a
33	chr4:151503227-151503277	PFSK-1	brain:	n/a
34	chr4:151501623-151501673	HRPEpiC	eye:	n/a
35	chr4:151503546-151503596	HEEpiC	esophagus:	n/a
36	chr4:151500631-151500681	PANC-1	pancreas:	n/a
37	chr4:151503501-151503551	HepG2	liver:	n/a
38	chr4:151503546-151503596	SK-N-SH_RA	brain:	n/a
39	chr4:151503227-151503277	PANC-1	pancreas:	n/a
40	chr4:151500931-151500981	HCT-116	colon:	n/a
41	chr4:151503501-151503551	GM06990	blood:	n/a
42	chr4:151503501-151503551	HIPEpiC	eye:	n/a
43	chr4:151505467-151505517	NH-A	brain:	n/a
44	chr4:151504187-151504237	Hepatocyte	liver:	n/a
45	chr4:151500931-151500981	HRE	kidney:	n/a
46	chr4:151505467-151505517	RPTEC	kidney:	n/a
47	chr4:151500631-151500681	HL-60	blood:	n/a
48	chr4:151504725-151504775	RPTEC	kidney:	n/a
49	chr4:151504725-151504775	HEK293	kidney:	embryo
50	chr4:151501739-151501789	HCF	heart:	n/a

(count:34 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:151491074..151493388-chr4:151494822..151496544,2	K562	blood:
2	chr4:151492559..151495531-chr4:151941599..151944271,2	K562	blood:
3	chr4:151491888..151494429-chr4:151494545..151497741,3	K562	blood:
4	chr4:151520682..151522323-chr4:151526143..151528322,2	K562	blood:
5	chr4:151505572..151507998-chr4:151511625..151514449,2	K562	blood:
6	chr4:151485955..151488684-chr4:151492504..151494572,2	K562	blood:
7	chr4:151487662..151490527-chr4:151494648..151496977,2	K562	blood:
8	chr4:151487662..151490527-chr4:151494648..151496977,2	K562	blood:
9	chr4:151491888..151494429-chr4:151494545..151497741,3	K562	blood:
10	chr4:151487701..151489848-chr4:151490418..151492175,2	K562	blood:
11	chr4:151491074..151493388-chr4:151494822..151496544,2	K562	blood:
12	chr4:151494137..151496884-chr4:151503865..151506422,4	K562	blood:
13	chr4:151464421..151466490-chr4:151508442..151510981,2	K562	blood:
14	chr4:151487701..151489848-chr4:151490418..151492175,2	K562	blood:
15	chr4:151505300..151507598-chr4:151514768..151516765,2	K562	blood:
16	chr4:151505300..151507598-chr4:151514768..151516765,2	K562	blood:
17	chr4:151495333..151496884-chr4:151503356..151505383,3	K562	blood:
18	chr4:151507320..151511158-chr4:151523228..151526308,4	K562	blood:
19	chr4:151505572..151507998-chr4:151511625..151514449,2	K562	blood:
20	chr4:151469880..151472562-chr4:151490206..151492460,2	K562	blood:
21	chr4:151485955..151488684-chr4:151492504..151494572,2	K562	blood:
22	chr4:151512919..151514896-chr4:151526553..151529436,2	K562	blood:
23	chr4:151236254..151238436-chr4:151495963..151498535,2	K562	blood:
24	chr4:151507320..151511158-chr4:151523228..151526308,4	K562	blood:
25	chr4:151502315..151504673-chr4:151508348..151511565,3	K562	blood:
26	chr4:151512919..151514896-chr4:151526553..151529436,2	K562	blood:
27	chr4:151494137..151496884-chr4:151503865..151506422,4	K562	blood:
28	chr4:151495333..151496884-chr4:151503356..151505383,3	K562	blood:
29	chr4:151502315..151503833-chr4:151508348..151510402,2	K562	blood:
30	chr4:151493789..151495576-chr4:151498523..151500498,2	MCF-7	breast:
31	chr4:151495871..151498604-chr4:151499774..151501672,2	K562	blood:
32	chr4:151464361..151466235-chr4:151513578..151516173,2	K562	blood:
33	chr4:151520682..151522323-chr4:151526143..151528322,2	K562	blood:
34	chr4:151527915..151530188-chr4:151535611..151537674,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MAB21L2-1	chr4:151500756-151502697	ENSG00000249690
2	lnc-MAB21L2-1	chr4:151500241-151500507	ENSG00000249690

No data

Variant related genes	Relation type
ENSG00000249690	TF binding region
MAB21L2	TF binding region
LRBA	TF binding region
ENSG00000249690	CpG island
MAB21L2	CpG island
LRBA	CpG island
ENSG00000181541	chromatin interactions
ENSG00000249690	chromatin interactions
ENSG00000198589	chromatin interactions

Extended variants
information (count: 1479 )
Associated
traits (count: 76 )

Variant overlapped rSNPs/rCNVs (count:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs531846753	chr4:151486321-151486322	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs145870017	chr4:151486382-151486383	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs549966305	chr4:151486411-151486412	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs116277717	chr4:151486426-151486427	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs138753706	chr4:151486427-151486428	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs564298134	chr4:151486463-151486464	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs368140534	chr4:151486483-151486484	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs529404970	chr4:151486484-151486485	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs191959232	chr4:151486488-151486489	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182212699	chr4:151486551-151486552	ZNF genes & repeats Strong transcription Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs77991214	chr4:151486788-151486789	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs142796796	chr4:151486909-151486910	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs548754886	chr4:151486913-151486914	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs372164812	chr4:151486968-151486969	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs568642881	chr4:151486974-151486975	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs186013154	chr4:151487094-151487095	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs551378556	chr4:151487120-151487121	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs1504785	chr4:151487125-151487126	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs1504784	chr4:151487145-151487146	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs372387130	chr4:151487160-151487161	Weak transcription Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs375430380	chr4:151487216-151487217	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553278723	chr4:151487226-151487227	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs553752015	chr4:151487256-151487257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80124237	chr4:151487297-151487298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs573569029	chr4:151487325-151487326	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs372996198	chr4:151487475-151487476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs536090673	chr4:151487489-151487490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs555975610	chr4:151487535-151487536	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs147409111	chr4:151487569-151487570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs558931764	chr4:151487643-151487644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs544347038	chr4:151487644-151487645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs564517776	chr4:151487706-151487707	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190919555	chr4:151487765-151487766	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs182775777	chr4:151487807-151487808	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs551211767	chr4:151487912-151487913	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs570767660	chr4:151487965-151487966	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185642427	chr4:151487983-151487984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs75497336	chr4:151488026-151488027	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs190785234	chr4:151488132-151488133	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs77021436	chr4:151488133-151488134	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs571317059	chr4:151488180-151488181	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs533592977	chr4:151488248-151488249	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs9994153	chr4:151488297-151488298	Strong transcription Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs74917946	chr4:151488345-151488346	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs74985983	chr4:151488373-151488374	Strong transcription Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs556014499	chr4:151488411-151488412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs76141746	chr4:151488417-151488418	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs538341972	chr4:151488418-151488419	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs556343547	chr4:151488422-151488423	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs72736314	chr4:151488523-151488524	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:76)

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
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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Esophageal squamous carcinoma	18350619	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
Breast cancer	16272173	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
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Breast cancer	21364760	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Non-small cell lung cancer	21829676	CNVD
Breast cancer	17588203	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:1033 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:151470400-151503600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
2	chr4:151472000-151490000	Weak transcription	Rectal Smooth Muscle	rectum
3	chr4:151472000-151501400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
4	chr4:151472600-151500200	Weak transcription	Aorta	Aorta
5	chr4:151473400-151491200	Weak transcription	Ovary	ovary
6	chr4:151474200-151489600	Weak transcription	Primary T helper cells fromperipheralblood	blood
7	chr4:151474800-151486400	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
8	chr4:151475400-151486400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
9	chr4:151477200-151486400	Weak transcription	Fetal Intestine Small	intestine
10	chr4:151477200-151502400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr4:151478800-151489600	Weak transcription	A549	lung
12	chr4:151479400-151490200	Weak transcription	K562	blood
13	chr4:151479400-151500800	Weak transcription	Lung	lung
14	chr4:151479600-151501800	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chr4:151480600-151500800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
16	chr4:151481200-151500400	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr4:151482000-151491000	Weak transcription	Fetal Thymus	thymus
18	chr4:151482800-151488200	Weak transcription	Colon Smooth Muscle	Colon
19	chr4:151486000-151486600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
20	chr4:151486000-151486600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
21	chr4:151486000-151486600	Strong transcription	Primary hematopoietic stem cells	blood
22	chr4:151486000-151486600	ZNF genes & repeats	Primary hematopoietic stem cells short term culture	blood
23	chr4:151486000-151486600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr4:151486000-151486600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr4:151486000-151486600	Strong transcription	Duodenum Mucosa	Duodenum
26	chr4:151486000-151486600	ZNF genes & repeats	Dnd41	blood
27	chr4:151486000-151487000	ZNF genes & repeats	Primary B cells from peripheral blood	blood
28	chr4:151486200-151486400	ZNF genes & repeats	Fetal Intestine Large	intestine
29	chr4:151486200-151486400	Weak transcription	Sigmoid Colon	Sigmoid Colon
30	chr4:151486200-151486600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr4:151486200-151486600	ZNF genes & repeats	Primary T cells from cord blood	blood
32	chr4:151486200-151486600	ZNF genes & repeats	Primary T cells fromperipheralblood	blood
33	chr4:151486200-151486600	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
34	chr4:151486200-151487000	Strong transcription	Primary B cells from cord blood	blood
35	chr4:151486200-151490200	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr4:151486200-151490600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr4:151486400-151486600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:151486400-151486600	ZNF genes & repeats	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:151486400-151486600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr4:151486400-151486600	ZNF genes & repeats	Primary T helper naive cells fromperipheralblood	blood
41	chr4:151486400-151486600	ZNF genes & repeats	Primary Natural Killer cells fromperipheralblood	blood
42	chr4:151486400-151486600	ZNF genes & repeats	Left Ventricle	heart
43	chr4:151486400-151486600	ZNF genes & repeats	Pancreas	Pancrea
44	chr4:151486400-151487200	ZNF genes & repeats	Fetal Intestine Small	intestine
45	chr4:151486400-151487400	Strong transcription	Fetal Intestine Large	intestine
46	chr4:151486600-151486800	Weak transcription	Sigmoid Colon	Sigmoid Colon
47	chr4:151486600-151486800	Weak transcription	Dnd41	blood
48	chr4:151486600-151487000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr4:151486600-151488000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
50	chr4:151486600-151488000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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