Variant report

Variant	nsv878575
Chromosome Location	chr4:7715181-7767755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1112)
CpG islands
(count:2810)
Chromatin interactive
region (count:35)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1112 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr4:7751236-7751998	HepG2	liver:	n/a	n/a
2	ATF1	chr4:7755550-7755906	K562	blood:	n/a	n/a
3	ATF3	chr4:7754369-7754653	K562	blood:	n/a	n/a
4	BACH1	chr4:7762122-7762213	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr4:7763464-7763750	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr4:7762156-7762173	K562	blood:	n/a	n/a
7	BHLHE40	chr4:7721424-7721624	GM12878	blood:	n/a	chr4:7721428-7721444
8	BHLHE40	chr4:7754386-7754752	K562	blood:	n/a	n/a
9	BHLHE40	chr4:7741755-7741942	K562	blood:	n/a	n/a
10	BHLHE40	chr4:7745946-7746146	GM12878	blood:	n/a	n/a
11	BHLHE40	chr4:7765726-7765754	K562	blood:	n/a	n/a
12	BHLHE40	chr4:7763400-7763988	GM12878	blood:	n/a	n/a
13	BHLHE40	chr4:7767394-7767883	HepG2	liver:	n/a	n/a
14	BRCA1	chr4:7763449-7763688	HepG2	liver:	n/a	n/a
15	CBX3	chr4:7754473-7754711	K562	blood:	n/a	n/a
16	CBX3	chr4:7739564-7739783	K562	blood:	n/a	n/a
17	CCNT2	chr4:7762002-7762306	K562	blood:	n/a	n/a
18	CEBPB	chr4:7751252-7751778	A549	lung:	n/a	n/a
19	CEBPB	chr4:7751215-7751476	A549	lung:	n/a	n/a
20	CEBPB	chr4:7764010-7764217	HepG2	liver:	n/a	n/a
21	CEBPB	chr4:7745484-7745715	HepG2	liver:	n/a	n/a
22	CEBPB	chr4:7767371-7767575	HepG2	liver:	n/a	n/a
23	CEBPB	chr4:7721357-7721601	H1-hESC	embryonic stem cell:	n/a	n/a
24	CEBPB	chr4:7751204-7751378	K562	blood:	n/a	n/a
25	CEBPB	chr4:7767348-7767703	HepG2	liver:	n/a	n/a
26	CEBPB	chr4:7764100-7764196	A549	lung:	n/a	n/a
27	CEBPB	chr4:7754400-7754643	K562	blood:	n/a	n/a
28	CEBPB	chr4:7745489-7745675	Hela-S3	cervix:	n/a	n/a
29	CEBPB	chr4:7745530-7745746	IMR90	lung:	n/a	n/a
30	CEBPB	chr4:7751184-7751598	HepG2	liver:	n/a	n/a
31	CEBPB	chr4:7751196-7751615	HepG2	liver:	n/a	n/a
32	CEBPB	chr4:7751187-7751400	K562	blood:	n/a	n/a
33	CEBPB	chr4:7763494-7763692	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr4:7745373-7745789	ECC-1	luminal epithelium:	n/a	n/a
35	CEBPB	chr4:7751179-7751537	IMR90	lung:	n/a	n/a
36	CEBPB	chr4:7767340-7767720	HepG2	liver:	n/a	n/a
37	CEBPB	chr4:7767296-7767721	HepG2	liver:	n/a	n/a
38	CEBPD	chr4:7767274-7767724	HepG2	liver:	n/a	n/a
39	CHD2	chr4:7756411-7756412	K562	blood:	n/a	n/a
40	CHD2	chr4:7755553-7756153	K562	blood:	n/a	n/a
41	CHD2	chr4:7754555-7754610	K562	blood:	n/a	n/a
42	CHD2	chr4:7721401-7721673	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr4:7763527-7763660	GM12878	blood:	n/a	n/a
44	CREB1	chr4:7751262-7751705	HepG2	liver:	n/a	n/a
45	CTCF	chr4:7722380-7722530	GM12864	blood:	n/a	n/a
46	CTCF	chr4:7763520-7763670	HCFaa	heart:	n/a	n/a
47	CTCF	chr4:7721460-7721610	GM12864	blood:	n/a	chr4:7721475-7721493 chr4:7721585-7721598
48	CTCF	chr4:7723780-7723930	SK-N-SH_RA	brain:	n/a	n/a
49	CTCF	chr4:7723800-7723950	HPF	lung:	n/a	n/a
50	CTCF	chr4:7721337-7721558	T-47D	breast:	n/a	chr4:7721475-7721493

(count:2810 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:7742526-7742576	HPAEpiC	pulmonary alveolar:	n/a
2	chr4:7758332-7758382	U87	brain:	n/a
3	chr4:7742526-7742576	HCM	heart:	n/a
4	chr4:7740821-7740871	NT2-D1	testis:	n/a
5	chr4:7742526-7742576	HPAEpiC	pulmonary alveolar:	n/a
6	chr4:7758332-7758382	U87	brain:	n/a
7	chr4:7742526-7742576	HCM	heart:	n/a
8	chr4:7740821-7740871	NT2-D1	testis:	n/a
9	chr4:7750489-7750539	LNCaP	prostate:	n/a
10	chr4:7762705-7762755	A549	lung:	n/a
11	chr4:7755760-7755810	AG04450	lung:	fetal
12	chr4:7755760-7755810	BE2_C	brain:	n/a
13	chr4:7742291-7742341	HepG2	liver:	n/a
14	chr4:7720084-7720134	CMK	blood:	n/a
15	chr4:7750448-7750498	HepG2	liver:	n/a
16	chr4:7719899-7719949	Hepatocyte	liver:	n/a
17	chr4:7750448-7750498	AG09309	skin:	n/a
18	chr4:7742291-7742341	ovcar-3	ovarian:	n/a
19	chr4:7760060-7760110	SAEC	small airway:	n/a
20	chr4:7755730-7755780	Hela-S3	cervix:	n/a
21	chr4:7750480-7750530	SK-N-MC	brain:	n/a
22	chr4:7758332-7758382	A549	lung:	n/a
23	chr4:7740427-7740477	HRE	kidney:	n/a
24	chr4:7719984-7720034	SK-N-SH	brain:	n/a
25	chr4:7735312-7735362	A549	lung:	n/a
26	chr4:7762665-7762715	MCF10A-Er-Src	breast:	n/a
27	chr4:7721340-7721390	HIPEpiC	eye:	n/a
28	chr4:7755739-7755789	GM06990	blood:	n/a
29	chr4:7735312-7735362	NT2-D1	testis:	n/a
30	chr4:7719984-7720034	T-47D	breast:	n/a
31	chr4:7764996-7765046	PANC-1	pancreas:	n/a
32	chr4:7755220-7755270	AG09319	gingival:	n/a
33	chr4:7740821-7740871	HCPEpiC	choroid plexus:	n/a
34	chr4:7763618-7763668	HCM	heart:	n/a
35	chr4:7736057-7736107	BJ	skin:	n/a
36	chr4:7750448-7750498	HCPEpiC	choroid plexus:	n/a
37	chr4:7762665-7762715	HRCEpiC	kidney:	n/a
38	chr4:7765033-7765083	H1-hESC	embryonic stem cell:	embryo
39	chr4:7763618-7763668	HAEpiC	amniotic membrane:	n/a
40	chr4:7720788-7720838	PFSK-1	brain:	n/a
41	chr4:7762705-7762755	HMEC	breast:	n/a
42	chr4:7758332-7758382	PFSK-1	brain:	n/a
43	chr4:7758517-7758567	AG04449	skin:	fetal
44	chr4:7720084-7720134	HepG2	liver:	n/a
45	chr4:7762665-7762715	NH-A	brain:	n/a
46	chr4:7742526-7742576	HRPEpiC	eye:	n/a
47	chr4:7763703-7763753	GM12892	blood:	n/a
48	chr4:7765033-7765083	HEEpiC	esophagus:	n/a
49	chr4:7750480-7750530	AG09309	skin:	n/a
50	chr4:7750480-7750530	PFSK-1	brain:	n/a

(count:35 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr4:7763127..7763762-chr4:7803659..7804271,2	MCF-7	breast:
2	chr4:7738338..7740956-chr4:7755052..7757253,2	K562	blood:
3	chr4:7724746..7727084-chr4:7966375..7967893,2	K562	blood:
4	chr4:7720870..7722721-chr4:7731493..7735156,3	MCF-7	breast:
5	chr4:7765704..7768382-chr4:7782855..7784797,2	K562	blood:
6	chr4:7763518..7765099-chr4:7771981..7774242,3	K562	blood:
7	chr4:7716222..7719124-chr4:7719418..7721619,2	MCF-7	breast:
8	chr4:7735719..7739049-chr4:7756418..7759523,3	MCF-7	breast:
9	chr4:7723319..7725071-chr4:7788895..7790676,2	K562	blood:
10	chr4:7763037..7763633-chr4:7803589..7804397,3	MCF-7	breast:
11	chr4:7705546..7706171-chr4:7721058..7721957,2	MCF-7	breast:
12	chr4:7717845..7720426-chr4:7722093..7724959,2	K562	blood:
13	chr4:7762684..7766410-chr4:7766886..7769453,3	MCF-7	breast:
14	chr4:7739904..7741898-chr4:7754670..7757440,2	K562	blood:
15	chr4:7756665..7758201-chr4:7770408..7772068,2	K562	blood:
16	chr4:7760394..7761920-chr4:7766669..7769385,2	K562	blood:
17	chr4:7556325..7556952-chr4:7720957..7721491,2	MCF-7	breast:
18	chr4:7193893..7194671-chr4:7721003..7721515,2	K562	blood:
19	chr4:7733646..7736526-chr4:7759484..7762368,2	K562	blood:
20	chr4:7717845..7720426-chr4:7722093..7724959,2	K562	blood:
21	chr4:7767721..7770258-chr4:7770613..7772876,3	K562	blood:
22	chr4:7720870..7722721-chr4:7731493..7735156,3	MCF-7	breast:
23	chr4:7762684..7766410-chr4:7766886..7769453,3	MCF-7	breast:
24	chr4:7762573..7764644-chr4:7765812..7768936,3	K562	blood:
25	chr4:7524845..7525381-chr4:7721481..7722229,2	K562	blood:
26	chr4:7723652..7724312-chr4:7988958..7989693,2	MCF-7	breast:
27	chr4:7764728..7766346-chr4:7767900..7769988,2	K562	blood:
28	chr4:7717399..7719546-chr4:7720941..7723402,3	K562	blood:
29	chr4:7729339..7732092-chr4:7733830..7736554,3	K562	blood:
30	chr4:7716222..7719124-chr4:7719418..7721619,2	MCF-7	breast:
31	chr4:7717399..7719546-chr4:7720941..7723402,3	K562	blood:
32	chr4:7760394..7761920-chr4:7766669..7769385,2	K562	blood:
33	chr4:7762573..7764644-chr4:7765812..7768936,3	K562	blood:
34	chr4:7464162..7464863-chr4:7721037..7721847,3	MCF-7	breast:
35	chr4:7712590..7714716-chr4:7715275..7718510,3	MCF-7	breast:

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AFAP1	hsa-miR-1	chr4:7762945-7762966

Variant related genes	Relation type
SORCS2	TF binding region
AFAP1-AS1	TF binding region
SORCS2	CpG island
AFAP1-AS1	CpG island
ENSG00000272620	chromatin interactions
ENSG00000184985	chromatin interactions

Extended variants
information (count: 3201 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:3201 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11726260	chr4:7715181-7715182	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs546881123	chr4:7715204-7715205	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182119035	chr4:7715211-7715212	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs529105708	chr4:7715226-7715227	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs4346650	chr4:7715241-7715242	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs187181350	chr4:7715350-7715351	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs539842222	chr4:7715359-7715360	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs551843103	chr4:7715360-7715361	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190132856	chr4:7715367-7715368	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs59948730	chr4:7715393-7715394	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs373652600	chr4:7715457-7715458	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs556048714	chr4:7715466-7715467	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs368915892	chr4:7715481-7715482	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs574118256	chr4:7715489-7715490	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs538466117	chr4:7715501-7715502	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs556615870	chr4:7715533-7715534	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs139464744	chr4:7715545-7715546	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs575042063	chr4:7715547-7715548	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs567758938	chr4:7715577-7715578	Weak transcription Flanking Active TSS Enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs183157969	chr4:7715617-7715618	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs563695357	chr4:7715625-7715626	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs148484617	chr4:7715645-7715646	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs16840889	chr4:7715651-7715652	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs562029752	chr4:7715675-7715676	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs529059063	chr4:7715681-7715682	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs550843445	chr4:7715692-7715693	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs188291865	chr4:7715705-7715706	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs139301770	chr4:7715709-7715710	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs17466517	chr4:7715796-7715797	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs193301281	chr4:7715799-7715800	Strong transcription Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs534215156	chr4:7715824-7715825	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs549394688	chr4:7715825-7715826	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs145487497	chr4:7715826-7715827	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs538045792	chr4:7715827-7715828	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373684063	chr4:7715899-7715900	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs147662418	chr4:7715900-7715901	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs539096751	chr4:7715947-7715948	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs557854184	chr4:7715955-7715956	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs140687086	chr4:7715958-7715959	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs540252369	chr4:7715969-7715970	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376807483	chr4:7715970-7715971	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185522488	chr4:7715974-7715975	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs374471872	chr4:7715979-7715980	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs199911110	chr4:7715993-7715994	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs370004831	chr4:7716003-7716004	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs188902029	chr4:7716019-7716020	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs367713426	chr4:7716050-7716051	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs144636398	chr4:7716053-7716054	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs16840892	chr4:7716061-7716062	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs200959630	chr4:7716062-7716063	ZNF genes & repeats Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:55)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Melanoma	20688739	CNVD
Colorectal cancer	16272173	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	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
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
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Breast cancer	21785460	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Breast cancer	21509527	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Myelofibrosis	22110671	CNVD
Hirschsprung''s Disease	21712996	CNVD
Schizophrenia	22241247	CNVD
Autosomal-dominant microtia	18179897	CNVD
Glioma	17123091	CNVD
Colorectal cancer	20459617	CNVD
Breast cancer	17133270	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:934 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:7679800-7715600	Weak transcription	Brain Germinal Matrix	brain
2	chr4:7686200-7721000	Weak transcription	Brain Anterior Caudate	brain
3	chr4:7691600-7716200	Weak transcription	Brain Angular Gyrus	brain
4	chr4:7699400-7721200	Weak transcription	Brain Cingulate Gyrus	brain
5	chr4:7707400-7715400	Weak transcription	Skeletal Muscle Male	skeletal muscle
6	chr4:7707600-7715400	Weak transcription	Fetal Intestine Small	intestine
7	chr4:7707600-7715800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
8	chr4:7707800-7716000	Weak transcription	Ovary	ovary
9	chr4:7708000-7715800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
10	chr4:7712000-7715600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr4:7713200-7715800	Weak transcription	Brain Substantia Nigra	brain
12	chr4:7713200-7718600	Weak transcription	Brain Hippocampus Middle	brain
13	chr4:7713400-7721000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
14	chr4:7713600-7716200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
15	chr4:7714000-7715600	Strong transcription	Stomach Smooth Muscle	stomach
16	chr4:7714400-7715200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr4:7714400-7715400	Weak transcription	Fetal Stomach	stomach
18	chr4:7714600-7718000	Strong transcription	Brain Inferior Temporal Lobe	brain
19	chr4:7714600-7719000	Weak transcription	Primary neutrophils fromperipheralblood	blood
20	chr4:7715000-7715400	Weak transcription	Fetal Muscle Leg	muscle
21	chr4:7715200-7715400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
22	chr4:7715400-7715600	Flanking Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr4:7715400-7715600	Strong transcription	Fetal Intestine Small	intestine
24	chr4:7715400-7716000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
25	chr4:7715400-7716600	ZNF genes & repeats	Fetal Muscle Leg	muscle
26	chr4:7715400-7716600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
27	chr4:7715400-7717000	ZNF genes & repeats	Fetal Stomach	stomach
28	chr4:7715600-7715800	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr4:7715600-7715800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
30	chr4:7715600-7716200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr4:7715600-7716200	ZNF genes & repeats	Brain Germinal Matrix	brain
32	chr4:7715600-7716600	ZNF genes & repeats	Fetal Intestine Small	intestine
33	chr4:7715600-7716800	ZNF genes & repeats	Esophagus	oesophagus
34	chr4:7715600-7718000	Weak transcription	Stomach Smooth Muscle	stomach
35	chr4:7715800-7716400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
36	chr4:7715800-7716400	ZNF genes & repeats	Brain Substantia Nigra	brain
37	chr4:7715800-7717000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr4:7715800-7717800	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
39	chr4:7716000-7716400	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
40	chr4:7716000-7716400	ZNF genes & repeats	Ovary	ovary
41	chr4:7716000-7719800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr4:7716200-7716600	Strong transcription	Brain Germinal Matrix	brain
43	chr4:7716200-7716800	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr4:7716200-7718600	Strong transcription	Brain Angular Gyrus	brain
45	chr4:7716400-7717000	Strong transcription	Brain Substantia Nigra	brain
46	chr4:7716400-7721200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
47	chr4:7716400-7721200	Weak transcription	Ovary	ovary
48	chr4:7716600-7716800	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr4:7716600-7718600	Weak transcription	Fetal Intestine Small	intestine
50	chr4:7716600-7719800	Strong transcription	Fetal Muscle Leg	muscle

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