Variant report

Variant	nsv880676
Chromosome Location	chr4:188439963-188503349
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	CEBPB	chr4:188492567-188492769	HepG2	liver:	n/a	chr4:188492666-188492677
2	CEBPB	chr4:188492564-188492757	K562	blood:	n/a	chr4:188492666-188492677
3	CEBPB	chr4:188440459-188440698	IMR90	lung:	n/a	n/a
4	CEBPB	chr4:188474103-188474183	K562	blood:	n/a	n/a
5	CEBPB	chr4:188479534-188479869	IMR90	lung:	n/a	n/a
6	CEBPB	chr4:188440289-188440620	HepG2	liver:	n/a	n/a
7	CTCF	chr4:188476228-188476262	GM20000	blood:	n/a	n/a
8	CTCF	chr4:188443124-188443168	Medullo	brain:	n/a	n/a
9	CTCF	chr4:188451774-188451781	H1-hESC	embryonic stem cell:	n/a	n/a
10	CTCF	chr4:188458880-188459030	HVMF	connective:	n/a	n/a
11	CTCF	chr4:188451786-188451820	H1-hESC	embryonic stem cell:	n/a	n/a
12	CTCF	chr4:188441212-188441256	LNCaP	prostate:	n/a	n/a
13	CTCF	chr4:188442915-188443011	Kidney_OC	kidney:	n/a	n/a
14	CTCF	chr4:188458860-188459010	BJ	skin:	n/a	n/a
15	CTCF	chr4:188458895-188458970	Fibrobl	skin:	n/a	n/a
16	CTCF	chr4:188475140-188475290	AG04450	lung:	n/a	n/a
17	FOS	chr4:188479536-188479878	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
18	FOS	chr4:188479576-188479879	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
19	FOS	chr4:188476455-188476656	MCF10A-Er-Src	breast:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
20	FOS	chr4:188479536-188479871	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
21	FOS	chr4:188476506-188476656	MCF10A-Er-Src	breast:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
22	FOS	chr4:188479537-188479903	MCF10A-Er-Src	breast:	n/a	chr4:188479709-188479719 chr4:188479709-188479719 chr4:188479710-188479719 chr4:188479709-188479719 chr4:188479709-188479719
23	FOSL2	chr4:188476250-188476756	A549	lung:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554
24	FOXA1	chr4:188482506-188482661	T-47D	breast:	n/a	n/a
25	FOXA2	chr4:188476383-188476791	A549	lung:	n/a	n/a
26	GATA3	chr4:188476912-188477168	SH-SY5Y	brain:	n/a	n/a
27	JUN	chr4:188475494-188475577	K562	blood:	n/a	n/a
28	JUN	chr4:188484429-188484629	K562	blood:	n/a	n/a
29	JUND	chr4:188476398-188476661	HepG2	liver:	n/a	chr4:188476547-188476554 chr4:188476546-188476554 chr4:188476546-188476555 chr4:188476545-188476554 chr4:188476544-188476555
30	JUND	chr4:188452451-188452524	H1-hESC	embryonic stem cell:	n/a	n/a
31	MAFF	chr4:188456784-188456861	HepG2	liver:	n/a	n/a
32	MAFK	chr4:188456684-188456898	HepG2	liver:	n/a	chr4:188456792-188456812 chr4:188456792-188456803
33	MAFK	chr4:188497530-188497696	HepG2	liver:	n/a	n/a
34	MAX	chr4:188479935-188480096	NB4	blood:	n/a	n/a
35	MAZ	chr4:188471769-188471776	HepG2	liver:	n/a	n/a
36	MYC	chr4:188498652-188498729	MCF10A-Er-Src	breast:	n/a	n/a
37	MYC	chr4:188495574-188495678	H1-hESC	embryonic stem cell:	n/a	n/a
38	POLR2A	chr4:188497610-188497614	MCF10A-Er-Src	breast:	n/a	n/a
39	POLR2A	chr4:188487205-188487339	ProgFib	skin:	n/a	n/a
40	POLR2A	chr4:188464133-188464254	H1-hESC	embryonic stem cell:	n/a	n/a
41	POLR2A	chr4:188472127-188472271	MCF10A-Er-Src	breast:	n/a	n/a
42	POLR2A	chr4:188473081-188473251	MCF10A-Er-Src	breast:	n/a	n/a
43	POLR2A	chr4:188483463-188483897	H1-neurons	neurons:	n/a	n/a
44	POLR2A	chr4:188476959-188477058	ProgFib	skin:	n/a	n/a
45	POLR2A	chr4:188479216-188479242	MCF10A-Er-Src	breast:	n/a	n/a
46	POLR2A	chr4:188483430-188483871	H1-neurons	neurons:	n/a	n/a
47	POLR2A	chr4:188487997-188488170	MCF10A-Er-Src	breast:	n/a	n/a
48	POLR2A	chr4:188484396-188484551	MCF10A-Er-Src	breast:	n/a	n/a
49	POLR2A	chr4:188502232-188502274	MCF10A-Er-Src	breast:	n/a	n/a
50	POLR2A	chr4:188447063-188447242	MCF10A-Er-Src	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr4:188462685-188462735	BE2_C	brain:	n/a
2	chr4:188462685-188462735	HCM	heart:	n/a
3	chr4:188462685-188462735	Hela-S3	cervix:	n/a
4	chr4:188462685-188462735	A549	lung:	n/a
5	chr4:188462685-188462735	HAEpiC	amniotic membrane:	n/a
6	chr4:188462685-188462735	RPTEC	kidney:	n/a
7	chr4:188462685-188462735	HNPCEpiC	eye:	n/a
8	chr4:188462685-188462735	AG09309	skin:	n/a
9	chr4:188462685-188462735	NH-A	brain:	n/a
10	chr4:188462685-188462735	GM12891	blood:	n/a
11	chr4:188462685-188462735	T-47D	breast:	n/a
12	chr4:188462685-188462735	HIPEpiC	eye:	n/a
13	chr4:188462685-188462735	GM12892	blood:	n/a
14	chr4:188462685-188462735	HEEpiC	esophagus:	n/a
15	chr4:188462685-188462735	AG04450	lung:	fetal
16	chr4:188462685-188462735	PFSK-1	brain:	n/a
17	chr4:188462685-188462735	BJ	skin:	n/a
18	chr4:188462685-188462735	HCT-116	colon:	n/a
19	chr4:188462685-188462735	AoSMC	blood vessel:	n/a
20	chr4:188462685-188462735	SK-N-MC	brain:	n/a
21	chr4:188462685-188462735	ovcar-3	ovarian:	n/a
22	chr4:188462685-188462735	H1-hESC	embryonic stem cell:	embryo
23	chr4:188462685-188462735	GM06990	blood:	n/a
24	chr4:188462685-188462735	Jurkat	blood:	n/a
25	chr4:188462685-188462735	IMR90	lung:	fetal
26	chr4:188462685-188462735	ProgFib	skin:	n/a
27	chr4:188462685-188462735	HL-60	blood:	n/a
28	chr4:188462685-188462735	PrEC	prostate:	n/a
29	chr4:188462685-188462735	HRPEpiC	eye:	n/a
30	chr4:188462685-188462735	MCF-7	breast:	n/a
31	chr4:188462685-188462735	Hepatocyte	liver:	n/a
32	chr4:188462685-188462735	NT2-D1	testis:	n/a
33	chr4:188462685-188462735	GM12878	blood:	n/a
34	chr4:188462685-188462735	NHDF-neo	bronchial:	n/a
35	chr4:188462685-188462735	HCPEpiC	choroid plexus:	n/a
36	chr4:188462685-188462735	HEK293	kidney:	embryo
37	chr4:188462685-188462735	MCF10A-Er-Src	breast:	n/a
38	chr4:188462685-188462735	U87	brain:	n/a
39	chr4:188462685-188462735	AG10803	skin:	n/a
40	chr4:188462685-188462735	NHBE	bronchial:	n/a
41	chr4:188462685-188462735	CMK	blood:	n/a
42	chr4:188462685-188462735	HMEC	breast:	n/a
43	chr4:188462685-188462735	HRE	kidney:	n/a
44	chr4:188462685-188462735	HRCEpiC	kidney:	n/a
45	chr4:188462685-188462735	AG04449	skin:	fetal
46	chr4:188462685-188462735	GM19239	blood:	n/a
47	chr4:188462685-188462735	HUVEC	blood vessel:	n/a
48	chr4:188462685-188462735	Caco-2	colon:	n/a
49	chr4:188462685-188462735	PANC-1	pancreas:	n/a
50	chr4:188462685-188462735	SKMC	muscle:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TRIML2-4	chr4:188454036-188454357	ENSG00000250590
2	lnc-TRIML2-4	chr4:188476215-188476298	ENSG00000250590
3	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
4	lnc-ZFP42-10	chr4:188493477-188493987	NONHSAT099705
5	lnc-TRIML2-4	chr4:188454033-188454357	NR_110436
6	lnc-TRIML2-4	chr4:188479231-188479418	ENSG00000250590
7	lnc-ZFP42-10	chr4:188501769-188501890	NONHSAT099705
8	lnc-TRIML2-4	chr4:188454032-188454357	ENSG00000250590
9	lnc-TRIML2-4	chr4:188479391-188479418	NONHSAT099704
10	lnc-TRIML2-4	chr4:188477065-188477112	ENSG00000250590
11	lnc-TRIML2-4	chr4:188476930-188477103	ENSG00000250590
12	lnc-TRIML2-4	chr4:188478901-188479074	ENSG00000250590
13	lnc-TRIML2-4	chr4:188476930-188477058	ENSG00000250590

Variant related genes	Relation type
ENSG00000251490	TF binding region
ENSG00000250590	TF binding region
ENSG00000251490	CpG island
ENSG00000250590	CpG island

Extended variants
information (count: 950 )
Associated
traits (count: 79 )

Variant overlapped rSNPs/rCNVs (count:950 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555757417	chr4:188440304-188440305	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs550213955	chr4:188440318-188440319	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs116746534	chr4:188440360-188440361	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs147160919	chr4:188440442-188440443	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs558380195	chr4:188440452-188440453	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs578182161	chr4:188440455-188440456	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs544003523	chr4:188440480-188440481	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs557772985	chr4:188440482-188440483	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs556747012	chr4:188440534-188440535	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs10024522	chr4:188440548-188440549	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs542237251	chr4:188440566-188440567	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs558958908	chr4:188440681-188440682	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs571923431	chr4:188441224-188441225	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs537221214	chr4:188441236-188441237	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs554296092	chr4:188442937-188442938	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs568347719	chr4:188442962-188442963	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs180824023	chr4:188442978-188442979	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs148630944	chr4:188443010-188443011	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs150708713	chr4:188443129-188443130	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs575674041	chr4:188443153-188443154	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs544574928	chr4:188443168-188443169	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs573022810	chr4:188451214-188451215	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs28558761	chr4:188451232-188451233	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs141139218	chr4:188451308-188451309	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs578145946	chr4:188451314-188451315	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs34008575	chr4:188451325-188451326	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs186592559	chr4:188451368-188451369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs563760043	chr4:188451400-188451401	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs529336270	chr4:188451463-188451464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs542628334	chr4:188451482-188451483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs560011360	chr4:188451506-188451507	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs150722908	chr4:188451507-188451508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs191000726	chr4:188451519-188451520	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs56181973	chr4:188451558-188451559	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs559578576	chr4:188451577-188451578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs62354908	chr4:188451604-188451605	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530998397	chr4:188451627-188451628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs550294878	chr4:188451648-188451649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs1505507	chr4:188451665-188451666	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs536263471	chr4:188451681-188451682	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs13118704	chr4:188451707-188451708	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs376641813	chr4:188451719-188451720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs182333376	chr4:188451766-188451767	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs538507738	chr4:188451799-188451800	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs538299388	chr4:188454038-188454039	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
46	rs10027327	chr4:188454090-188454091	Enhancers	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs139176125	chr4:188454112-188454113	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
48	rs184443651	chr4:188454197-188454198	Enhancers	lncRNA	n/a	Overlapped CNVs	n/a
49	rs149960286	chr4:188454203-188454204	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
50	rs558620757	chr4:188454223-188454224	Weak transcription	lncRNA	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
Autism	20808228	CNVD
Cognitive impairment	21505072	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:117 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr4:188451200-188451800	Enhancers	Fetal Muscle Trunk	muscle
2	chr4:188454000-188454200	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr4:188454200-188455200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
4	chr4:188454600-188456200	Enhancers	iPS-20b Cell Line	embryonic stem cell
5	chr4:188455000-188455800	Enhancers	HUES64 Cell Line	embryonic stem cell
6	chr4:188455000-188455800	Enhancers	iPS-18 Cell Line	embryonic stem cell
7	chr4:188455000-188456200	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr4:188455200-188456000	Enhancers	ES-I3 Cell Line	embryonic stem cell
9	chr4:188462000-188462600	Enhancers	iPS-18 Cell Line	embryonic stem cell
10	chr4:188462000-188462800	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr4:188462200-188462600	Enhancers	HUES64 Cell Line	embryonic stem cell
12	chr4:188462200-188462600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr4:188462200-188463600	Enhancers	Muscle Satellite Cultured Cells	--
14	chr4:188462400-188462600	Enhancers	HSMM	muscle
15	chr4:188462400-188462600	Enhancers	NHDF-Ad	bronchial
16	chr4:188462400-188462800	Enhancers	HSMMtube	muscle
17	chr4:188462600-188463000	Flanking Active TSS	HSMM	muscle
18	chr4:188462600-188463000	Flanking Active TSS	NHDF-Ad	bronchial
19	chr4:188462600-188463600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chr4:188462800-188463000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
21	chr4:188462800-188463200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
22	chr4:188462800-188463200	Flanking Active TSS	HSMMtube	muscle
23	chr4:188462800-188463600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr4:188463000-188463600	Enhancers	HSMM	muscle
25	chr4:188463000-188463600	Enhancers	NHDF-Ad	bronchial
26	chr4:188463200-188463600	Enhancers	HSMMtube	muscle
27	chr4:188463200-188468600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr4:188463600-188465600	Weak transcription	Muscle Satellite Cultured Cells	--
29	chr4:188463600-188465600	Weak transcription	HSMM	muscle
30	chr4:188463600-188465600	Weak transcription	HSMMtube	muscle
31	chr4:188463600-188465800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr4:188463600-188470600	Weak transcription	NHDF-Ad	bronchial
33	chr4:188465400-188465600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr4:188465600-188465800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr4:188465600-188465800	Enhancers	HSMM	muscle
36	chr4:188465600-188466000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr4:188465600-188466000	Enhancers	HSMMtube	muscle
38	chr4:188465600-188466200	Enhancers	Muscle Satellite Cultured Cells	--
39	chr4:188465600-188466200	Enhancers	HMEC	breast
40	chr4:188465600-188466200	Enhancers	NHEK	skin
41	chr4:188465800-188466200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr4:188465800-188466200	Weak transcription	HSMM	muscle
43	chr4:188465800-188468600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr4:188466000-188466200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr4:188466000-188468400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr4:188466200-188466400	Enhancers	HSMM	muscle
47	chr4:188466200-188468200	Weak transcription	HMEC	breast
48	chr4:188466200-188468400	Weak transcription	Muscle Satellite Cultured Cells	--
49	chr4:188466200-188471200	Weak transcription	NHEK	skin
50	chr4:188466200-188471400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin

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