Variant report

Variant	esv2760881
Chromosome Location	chr4:188207893-188245051
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:83)
CpG islands
(count:184)
Chromatin interactive
region (count:2)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:83 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	CEBPB	chr4:188234147-188234350	IMR90	lung:	n/a	n/a
2	CEBPB	chr4:188223685-188224011	IMR90	lung:	n/a	n/a
3	CEBPB	chr4:188213364-188213403	K562	blood:	n/a	n/a
4	CTCF	chr4:188243984-188244028	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chr4:188241480-188241630	HBMEC	blood vessel:	n/a	n/a
6	CTCF	chr4:188243900-188244050	HepG2	liver:	n/a	n/a
7	CTCF	chr4:188230709-188230813	NHEK	skin:	n/a	n/a
8	CTCF	chr4:188228291-188228408	NHEK	skin:	n/a	n/a
9	CTCF	chr4:188229160-188229310	HEEpiC	esophagus:	n/a	n/a
10	CTCF	chr4:188230727-188230815	ProgFib	skin:	n/a	n/a
11	CTCF	chr4:188230711-188230796	Gliobla	brain:	n/a	n/a
12	CTCF	chr4:188228280-188228430	HEEpiC	esophagus:	n/a	n/a
13	CTCF	chr4:188228280-188228430	HMEC	breast:	n/a	n/a
14	CTCF	chr4:188243900-188244050	BE2_C	brain:	n/a	n/a
15	CTCF	chr4:188230720-188230870	AG10803	skin:	n/a	n/a
16	CTCF	chr4:188230700-188230850	AG04449	skin:	n/a	n/a
17	CTCF	chr4:188228292-188228390	Fibrobl	skin:	n/a	n/a
18	E2F4	chr4:188210966-188211166	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F4	chr4:188209892-188210218	MCF10A-Er-Src	breast:	n/a	n/a
20	E2F4	chr4:188216123-188216574	MCF10A-Er-Src	breast:	n/a	n/a
21	E2F4	chr4:188208953-188209159	MCF10A-Er-Src	breast:	n/a	n/a
22	ESR1	chr4:188210332-188210592	T-47D	breast:	n/a	n/a
23	FOS	chr4:188240035-188240194	MCF10A-Er-Src	breast:	n/a	n/a
24	FOS	chr4:188230811-188231011	MCF10A-Er-Src	breast:	n/a	n/a
25	FOS	chr4:188215943-188216421	MCF10A-Er-Src	breast:	n/a	chr4:188215975-188215984
26	FOS	chr4:188216038-188216390	MCF10A-Er-Src	breast:	n/a	n/a
27	FOS	chr4:188240003-188240203	MCF10A-Er-Src	breast:	n/a	n/a
28	FOS	chr4:188230726-188230921	MCF10A-Er-Src	breast:	n/a	n/a
29	FOS	chr4:188228368-188228512	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chr4:188239885-188240193	MCF10A-Er-Src	breast:	n/a	n/a
31	FOS	chr4:188230743-188230969	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chr4:188226960-188227128	MCF10A-Er-Src	breast:	n/a	chr4:188227077-188227084 chr4:188227076-188227084 chr4:188227076-188227085 chr4:188227075-188227084
33	FOS	chr4:188216011-188216399	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chr4:188230726-188231129	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr4:188216032-188216379	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr4:188227007-188227153	MCF10A-Er-Src	breast:	n/a	chr4:188227077-188227084 chr4:188227076-188227084 chr4:188227076-188227085 chr4:188227075-188227084
37	FOS	chr4:188228345-188228500	MCF10A-Er-Src	breast:	n/a	n/a
38	FOXA1	chr4:188216137-188216264	T-47D	breast:	n/a	n/a
39	FOXA1	chr4:188215551-188215709	T-47D	breast:	n/a	n/a
40	FOXA1	chr4:188229964-188230240	T-47D	breast:	n/a	n/a
41	GATA3	chr4:188229793-188230344	T-47D	breast:	n/a	n/a
42	GATA3	chr4:188242833-188243286	SK-N-SH	brain:	n/a	chr4:188243147-188243157 chr4:188243147-188243154 chr4:188243147-188243154 chr4:188243147-188243154
43	GATA3	chr4:188229973-188230353	T-47D	breast:	n/a	n/a
44	GATA3	chr4:188215994-188216363	MCF-7	breast:	n/a	n/a
45	GATA3	chr4:188207750-188208068	SK-N-SH	brain:	n/a	n/a
46	IRF1	chr4:188221454-188221460	K562	blood:	n/a	n/a
47	JUN	chr4:188215831-188216085	HepG2	liver:	n/a	chr4:188215975-188215984 chr4:188215974-188215987
48	JUN	chr4:188240037-188240056	HepG2	liver:	n/a	n/a
49	JUND	chr4:188239920-188240223	HepG2	liver:	n/a	chr4:188240045-188240056
50	JUND	chr4:188229859-188230337	T-47D	breast:	n/a	n/a

(count:184 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188208070-188208120	HRE	kidney:	n/a
2	chr4:188208070-188208120	HRE	kidney:	n/a
3	chr4:188223108-188223158	Hela-S3	cervix:	n/a
4	chr4:188208070-188208120	Hela-S3	cervix:	n/a
5	chr4:188230390-188230440	GM19239	blood:	n/a
6	chr4:188230390-188230440	HMEC	breast:	n/a
7	chr4:188223108-188223158	NB4	blood:	n/a
8	chr4:188208070-188208120	RPTEC	kidney:	n/a
9	chr4:188230390-188230440	HL-60	blood:	n/a
10	chr4:188230390-188230440	SK-N-SH	brain:	n/a
11	chr4:188230390-188230440	Hela-S3	cervix:	n/a
12	chr4:188223108-188223158	MCF-7	breast:	n/a
13	chr4:188230390-188230440	IMR90	lung:	fetal
14	chr4:188230390-188230440	HepG2	liver:	n/a
15	chr4:188208070-188208120	HL-60	blood:	n/a
16	chr4:188223108-188223158	HCM	heart:	n/a
17	chr4:188230390-188230440	ovcar-3	ovarian:	n/a
18	chr4:188223108-188223158	Jurkat	blood:	n/a
19	chr4:188208070-188208120	GM19239	blood:	n/a
20	chr4:188223108-188223158	RPTEC	kidney:	n/a
21	chr4:188223108-188223158	ECC-1	luminal epithelium:	n/a
22	chr4:188208070-188208120	BE2_C	brain:	n/a
23	chr4:188230390-188230440	RPTEC	kidney:	n/a
24	chr4:188223108-188223158	NT2-D1	testis:	n/a
25	chr4:188230390-188230440	AG04450	lung:	fetal
26	chr4:188230390-188230440	HRPEpiC	eye:	n/a
27	chr4:188223108-188223158	AG10803	skin:	n/a
28	chr4:188208070-188208120	Caco-2	colon:	n/a
29	chr4:188223108-188223158	HEK293	kidney:	embryo
30	chr4:188208070-188208120	SKMC	muscle:	n/a
31	chr4:188223108-188223158	HUVEC	blood vessel:	n/a
32	chr4:188223108-188223158	HIPEpiC	eye:	n/a
33	chr4:188208070-188208120	HAEpiC	amniotic membrane:	n/a
34	chr4:188230390-188230440	AG09309	skin:	n/a
35	chr4:188230390-188230440	BJ	skin:	n/a
36	chr4:188230390-188230440	AG09319	gingival:	n/a
37	chr4:188230390-188230440	SK-N-MC	brain:	n/a
38	chr4:188223108-188223158	Hepatocyte	liver:	n/a
39	chr4:188230390-188230440	SK-N-SH_RA	brain:	n/a
40	chr4:188230390-188230440	H1-hESC	embryonic stem cell:	embryo
41	chr4:188208070-188208120	SAEC	small airway:	n/a
42	chr4:188208070-188208120	PrEC	prostate:	n/a
43	chr4:188208070-188208120	HEEpiC	esophagus:	n/a
44	chr4:188208070-188208120	HCF	heart:	n/a
45	chr4:188230390-188230440	ECC-1	luminal epithelium:	n/a
46	chr4:188223108-188223158	IMR90	lung:	fetal
47	chr4:188223108-188223158	HNPCEpiC	eye:	n/a
48	chr4:188208070-188208120	Hepatocyte	liver:	n/a
49	chr4:188223108-188223158	SK-N-SH_RA	brain:	n/a
50	chr4:188208070-188208120	SK-N-MC	brain:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:
2	chr4:188218935..188220617-chr4:188223273..188225640,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAT1-3	chr4:188230336-188230836	XLOC_004217
2	lnc-ZFP42-13	chr4:188228509-188228694	NONHSAT099691
3	lnc-FAT1-3	chr4:188228260-188228423	XLOC_004217
4	lnc-ZFP42-13	chr4:188237423-188237596	NONHSAT099691
5	lnc-FAT1-3	chr4:188225792-188226855	XLOC_004217
6	lnc-FAT1-3	chr4:188225237-188225621	XLOC_004217

No data

Variant related genes	Relation type
ENSG00000250658	TF binding region
ENSG00000250658	CpG island

Extended variants
information (count: 1505 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:1505 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs114638781	chr4:188207904-188207905	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs193040017	chr4:188207935-188207936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs531639050	chr4:188207998-188207999	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185635727	chr4:188208010-188208011	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs141357996	chr4:188208070-188208071	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs530189286	chr4:188208075-188208076	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs188874575	chr4:188208079-188208080	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146946253	chr4:188208109-188208110	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs372205291	chr4:188208120-188208121	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs573216331	chr4:188208189-188208190	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558953836	chr4:188208212-188208213	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs569401453	chr4:188208222-188208223	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs56391716	chr4:188208238-188208239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs540405453	chr4:188208263-188208264	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs538537874	chr4:188208264-188208265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs554828955	chr4:188208287-188208288	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574672519	chr4:188208302-188208303	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141706998	chr4:188208350-188208351	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs10024204	chr4:188208354-188208355	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs576579715	chr4:188208448-188208449	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs545435382	chr4:188208457-188208458	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs192364420	chr4:188208468-188208469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs529297819	chr4:188208499-188208500	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs112047524	chr4:188208532-188208533	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs550760779	chr4:188208539-188208540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542131430	chr4:188208542-188208543	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538972706	chr4:188208551-188208552	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs78541177	chr4:188208573-188208574	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs183764611	chr4:188208597-188208598	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs547652464	chr4:188208672-188208673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs566968573	chr4:188208674-188208675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112425625	chr4:188208698-188208699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188143595	chr4:188208699-188208700	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs569247488	chr4:188208718-188208719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs373345501	chr4:188208796-188208797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs181297540	chr4:188208800-188208801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs115447274	chr4:188208836-188208837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs559618820	chr4:188208871-188208872	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs9998520	chr4:188208906-188208907	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs534125510	chr4:188208988-188208989	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs147721644	chr4:188208999-188209000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs189007560	chr4:188209012-188209013	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs576489803	chr4:188209044-188209045	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs539536257	chr4:188209113-188209114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs181703840	chr4:188209151-188209152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs575969032	chr4:188209163-188209164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533485093	chr4:188209164-188209165	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs9998820	chr4:188209182-188209183	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs561954174	chr4:188209220-188209221	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs36006072	chr4:188209226-188209227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:79)

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
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
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
Breast cancer	16608533	CNVD
Wilms tumour	21544195	CNVD
Lung cancer	18438408	CNVD
Cancer	22429812	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital anomalies of the kidney and urinary tract	20505237	CNVD
Testicular germ cell tumor	18059402	CNVD
Ovarian cancer	22174824	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	21785460	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	17952124	CNVD
Breast cancer	21633010	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Cancer	20581869	CNVD
Hepatocellular carcinoma	16750200	CNVD
abnormal development	18461090	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16774939	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Basal cell lymphoma	17053054	CNVD
Facioscapulohumeral muscular dystrophy	21829175	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	20844748	CNVD
Autism	18414403	CNVD
Urothelial carcinoma	21177765	CNVD
Cancer	20164920	CNVD
Cancer	20164919	CNVD
Breast cancer	20409316	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	21399695	CNVD
Developmental delay	22127048	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cervical cancer	21063398	CNVD
Oral cancer	21386901	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Autism	20808228	CNVD

Chromatin state (count:149 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188205000-188210200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
2	chr4:188205000-188210200	Weak transcription	Muscle Satellite Cultured Cells	--
3	chr4:188205000-188210400	Weak transcription	Osteobl	bone
4	chr4:188207400-188208600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr4:188207600-188208000	Enhancers	Placenta Amnion	Placenta Amnion
6	chr4:188207600-188208200	Enhancers	NHLF	lung
7	chr4:188207600-188208400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr4:188207600-188208400	Enhancers	Fetal Kidney	kidney
9	chr4:188207600-188208400	Enhancers	Fetal Lung	lung
10	chr4:188207800-188208000	Enhancers	Ovary	ovary
11	chr4:188207800-188209600	Weak transcription	Fetal Intestine Large	intestine
12	chr4:188208200-188210400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
13	chr4:188208600-188210200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr4:188209600-188211000	Enhancers	Fetal Intestine Large	intestine
15	chr4:188210200-188210400	Enhancers	Muscle Satellite Cultured Cells	--
16	chr4:188210200-188210600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr4:188210200-188211000	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
18	chr4:188210200-188211000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr4:188210200-188211000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr4:188210400-188210600	Flanking Active TSS	Muscle Satellite Cultured Cells	--
21	chr4:188210400-188210600	Enhancers	Osteobl	bone
22	chr4:188210400-188210800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
23	chr4:188210400-188211000	Enhancers	NHEK	skin
24	chr4:188210600-188210800	Enhancers	Muscle Satellite Cultured Cells	--
25	chr4:188210600-188212200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr4:188210800-188211000	Flanking Active TSS	Muscle Satellite Cultured Cells	--
27	chr4:188210800-188216200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr4:188211000-188211600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr4:188211000-188215400	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
30	chr4:188211000-188215600	Weak transcription	NHEK	skin
31	chr4:188211600-188216000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr4:188212200-188212600	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
33	chr4:188212600-188217200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr4:188215200-188216400	Enhancers	Fetal Lung	lung
35	chr4:188215400-188215600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
36	chr4:188215400-188215600	Enhancers	Fetal Stomach	stomach
37	chr4:188215400-188216600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr4:188215600-188216200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr4:188215600-188216600	Enhancers	NHEK	skin
40	chr4:188216000-188216400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr4:188216200-188216400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
42	chr4:188216200-188216400	Enhancers	Fetal Stomach	stomach
43	chr4:188216200-188216600	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr4:188216200-188216600	Enhancers	HMEC	breast
45	chr4:188216200-188216800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
46	chr4:188216400-188223000	Weak transcription	Fetal Lung	lung
47	chr4:188216800-188217400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr4:188217200-188217400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr4:188217200-188217800	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
50	chr4:188217200-188217800	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell

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