Variant report

Variant	nsv1018100
Chromosome Location	chr5:119749898-119802014
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:941)
CpG islands
(count:1102)
Chromatin interactive
region (count:13)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:941 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr5:119793643-119794138	K562	blood:	n/a	n/a
2	ATF2	chr5:119793456-119794141	GM12878	blood:	n/a	n/a
3	ATF2	chr5:119793413-119794075	GM12878	blood:	n/a	n/a
4	ATF3	chr5:119793575-119793776	GM12878	blood:	n/a	n/a
5	ATF3	chr5:119793581-119793842	K562	blood:	n/a	n/a
6	ATF3	chr5:119793531-119793905	GM12878	blood:	n/a	n/a
7	ATF3	chr5:119793562-119793757	K562	blood:	n/a	n/a
8	ATF3	chr5:119799801-119800020	K562	blood:	n/a	n/a
9	BATF	chr5:119793497-119794263	GM12878	blood:	n/a	n/a
10	BATF	chr5:119793535-119793841	GM12878	blood:	n/a	n/a
11	BCL11A	chr5:119793538-119794246	GM12878	blood:	n/a	n/a
12	BCL11A	chr5:119793578-119794002	GM12878	blood:	n/a	n/a
13	BCLAF1	chr5:119793512-119793944	GM12878	blood:	n/a	n/a
14	BHLHE40	chr5:119793468-119794222	K562	blood:	n/a	n/a
15	BHLHE40	chr5:119793446-119794136	GM12878	blood:	n/a	n/a
16	BHLHE40	chr5:119800557-119800862	K562	blood:	n/a	n/a
17	BHLHE40	chr5:119799728-119800086	K562	blood:	n/a	chr5:119799917-119799933
18	BHLHE40	chr5:119793451-119794227	HepG2	liver:	n/a	n/a
19	CBX3	chr5:119793992-119794270	K562	blood:	n/a	n/a
20	CBX3	chr5:119766312-119766599	K562	blood:	n/a	n/a
21	CBX3	chr5:119766328-119766517	K562	blood:	n/a	n/a
22	CCNT2	chr5:119799743-119800201	K562	blood:	n/a	n/a
23	CCNT2	chr5:119800844-119801044	K562	blood:	n/a	n/a
24	CCNT2	chr5:119801326-119801526	K562	blood:	n/a	chr5:119801482-119801491
25	CEBPB	chr5:119793870-119793873	K562	blood:	n/a	n/a
26	CEBPB	chr5:119781713-119782170	Hela-S3	cervix:	n/a	n/a
27	CEBPB	chr5:119751624-119752006	ECC-1	luminal epithelium:	n/a	n/a
28	CEBPB	chr5:119751652-119752056	ECC-1	luminal epithelium:	n/a	n/a
29	CEBPB	chr5:119751681-119751991	A549	lung:	n/a	n/a
30	CEBPB	chr5:119751648-119752032	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr5:119751752-119751990	H1-hESC	embryonic stem cell:	n/a	n/a
32	CEBPB	chr5:119789893-119790365	IMR90	lung:	n/a	chr5:119789975-119789988 chr5:119789977-119789988 chr5:119789975-119789988
33	CEBPB	chr5:119801582-119802014	K562	blood:	n/a	n/a
34	CEBPB	chr5:119793540-119794182	GM12878	blood:	n/a	n/a
35	CEBPB	chr5:119751710-119751957	IMR90	lung:	n/a	n/a
36	CEBPB	chr5:119790034-119790418	ECC-1	luminal epithelium:	n/a	n/a
37	CEBPB	chr5:119781622-119782289	IMR90	lung:	n/a	n/a
38	CEBPB	chr5:119801541-119802055	IMR90	lung:	n/a	n/a
39	CHD1	chr5:119800370-119800816	H1-hESC	embryonic stem cell:	n/a	chr5:119800453-119800460
40	CHD2	chr5:119799841-119799863	K562	blood:	n/a	n/a
41	CHD2	chr5:119793657-119794009	GM12878	blood:	n/a	n/a
42	CREB1	chr5:119799653-119800125	H1-hESC	embryonic stem cell:	n/a	n/a
43	CREB1	chr5:119793527-119794038	GM12878	blood:	n/a	n/a
44	CREB1	chr5:119793551-119794058	GM12878	blood:	n/a	n/a
45	CREB1	chr5:119799699-119800166	K562	blood:	n/a	n/a
46	CTBP2	chr5:119799721-119801638	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr5:119794040-119794190	GM12872	blood:	n/a	n/a
48	CTCF	chr5:119793870-119794291	GM19238	blood:	n/a	n/a
49	CTCF	chr5:119794060-119794210	MCF-7	breast:	n/a	n/a
50	CTCF	chr5:119799803-119800127	LNCaP	prostate:	n/a	chr5:119799930-119799943

(count:1102 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:119799531-119799581	LNCaP	prostate:	n/a
2	chr5:119799822-119799872	GM12878	blood:	n/a
3	chr5:119800143-119800193	SKMC	muscle:	n/a
4	chr5:119801643-119801693	HRPEpiC	eye:	n/a
5	chr5:119799531-119799581	LNCaP	prostate:	n/a
6	chr5:119799822-119799872	GM12878	blood:	n/a
7	chr5:119800143-119800193	SKMC	muscle:	n/a
8	chr5:119801643-119801693	HRPEpiC	eye:	n/a
9	chr5:119799384-119799434	PANC-1	pancreas:	n/a
10	chr5:119800742-119800792	HMEC	breast:	n/a
11	chr5:119800403-119800453	SAEC	small airway:	n/a
12	chr5:119800742-119800792	A549	lung:	n/a
13	chr5:119800972-119801022	SK-N-SH	brain:	n/a
14	chr5:119801643-119801693	HMEC	breast:	n/a
15	chr5:119801643-119801693	SK-N-SH	brain:	n/a
16	chr5:119799384-119799434	ECC-1	luminal epithelium:	n/a
17	chr5:119800234-119800284	NHBE	bronchial:	n/a
18	chr5:119799864-119799914	HRE	kidney:	n/a
19	chr5:119799822-119799872	AG10803	skin:	n/a
20	chr5:119799864-119799914	MCF-7	breast:	n/a
21	chr5:119800742-119800792	HepG2	liver:	n/a
22	chr5:119801431-119801481	HRPEpiC	eye:	n/a
23	chr5:119801142-119801192	CMK	blood:	n/a
24	chr5:119799822-119799872	HNPCEpiC	eye:	n/a
25	chr5:119799384-119799434	GM12891	blood:	n/a
26	chr5:119801431-119801481	NT2-D1	testis:	n/a
27	chr5:119800143-119800193	HRCEpiC	kidney:	n/a
28	chr5:119801643-119801693	HNPCEpiC	eye:	n/a
29	chr5:119800234-119800284	HUVEC	blood vessel:	n/a
30	chr5:119782696-119782746	HIPEpiC	eye:	n/a
31	chr5:119800972-119801022	HRCEpiC	kidney:	n/a
32	chr5:119800143-119800193	HCF	heart:	n/a
33	chr5:119799862-119799912	NHBE	bronchial:	n/a
34	chr5:119800742-119800792	NB4	blood:	n/a
35	chr5:119799832-119799882	GM12892	blood:	n/a
36	chr5:119800687-119800737	HepG2	liver:	n/a
37	chr5:119801643-119801693	T-47D	breast:	n/a
38	chr5:119800143-119800193	NHBE	bronchial:	n/a
39	chr5:119799862-119799912	MCF-7	breast:	n/a
40	chr5:119799531-119799581	SK-N-MC	brain:	n/a
41	chr5:119801142-119801192	RPTEC	kidney:	n/a
42	chr5:119799384-119799434	HL-60	blood:	n/a
43	chr5:119799220-119799270	GM19239	blood:	n/a
44	chr5:119801643-119801693	HCM	heart:	n/a
45	chr5:119782696-119782746	Jurkat	blood:	n/a
46	chr5:119799531-119799581	K562	blood:	n/a
47	chr5:119800742-119800792	AG09319	gingival:	n/a
48	chr5:119800143-119800193	Hela-S3	cervix:	n/a
49	chr5:119801193-119801243	HIPEpiC	eye:	n/a
50	chr5:119799822-119799872	HCT-116	colon:	n/a

(count:13 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr5:119801561..119803830-chr5:119805628..119808715,3	K562	blood:
2	chr5:119278619..119279545-chr5:119793318..119794660,3	MCF-7	breast:
3	chr5:119795709..119798645-chr5:119801095..119805087,3	K562	blood:
4	chr5:119785992..119787497-chr5:119792334..119794755,2	K562	blood:
5	chr5:119775909..119777540-chr5:119783720..119785397,2	K562	blood:
6	chr5:119769254..119771036-chr5:119773578..119776402,2	K562	blood:
7	chr5:119769254..119771036-chr5:119773578..119776402,2	K562	blood:
8	chr5:119784118..119786225-chr5:119788090..119789969,2	K562	blood:
9	chr5:119784118..119786225-chr5:119788090..119789969,2	K562	blood:
10	chr5:119792597..119795401-chr5:119799043..119801706,2	K562	blood:
11	chr5:119775909..119777540-chr5:119783720..119785397,2	K562	blood:
12	chr5:119785992..119787497-chr5:119792334..119794755,2	K562	blood:
13	chr5:119721254..119725042-chr5:119751252..119754462,3	K562	blood:

No data

Variant related genes	Relation type
PRR16	TF binding region
PRR16	CpG island
ENSG00000184838	chromatin interactions

Extended variants
information (count: 2204 )
Associated
traits (count: 73 )

Variant overlapped rSNPs/rCNVs (count:2204 , 50 per page) page: 1 2 3 4 5 6 7 ... 45

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571422719	chr5:119749904-119749905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191032825	chr5:119749968-119749969	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs554215402	chr5:119749993-119749994	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs573982936	chr5:119749996-119749997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542995900	chr5:119749999-119750000	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs183053838	chr5:119750042-119750043	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs149106738	chr5:119750102-119750103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs187391638	chr5:119750103-119750104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs190317923	chr5:119750148-119750149	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs115004680	chr5:119750175-119750176	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs540804933	chr5:119750213-119750214	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs561030705	chr5:119750227-119750228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs551212407	chr5:119750237-119750238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182844997	chr5:119750351-119750352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs143211088	chr5:119750362-119750363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs531850654	chr5:119750378-119750379	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs551579930	chr5:119750415-119750416	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571775056	chr5:119750432-119750433	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs534385065	chr5:119750465-119750466	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs571201603	chr5:119750479-119750480	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs536683917	chr5:119750498-119750499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs188165641	chr5:119750521-119750522	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536647682	chr5:119750611-119750612	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192449925	chr5:119750624-119750625	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs35179152	chr5:119750674-119750675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs576430233	chr5:119750697-119750698	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538965780	chr5:119750701-119750702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112406535	chr5:119750727-119750728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs79859274	chr5:119750748-119750749	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs35490570	chr5:119750749-119750750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs558877620	chr5:119750795-119750796	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs13435959	chr5:119750850-119750851	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs140049753	chr5:119750860-119750861	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs560823608	chr5:119750865-119750866	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184426852	chr5:119750884-119750885	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs145243332	chr5:119750898-119750899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs556829378	chr5:119750962-119750963	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs137920120	chr5:119751073-119751074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs551690067	chr5:119751096-119751097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs72784199	chr5:119751170-119751171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs557257518	chr5:119751205-119751206	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs77904796	chr5:119751264-119751265	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs527923932	chr5:119751291-119751292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs547921183	chr5:119751317-119751318	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs558373230	chr5:119751320-119751321	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs567672963	chr5:119751342-119751343	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs536718588	chr5:119751370-119751371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550279311	chr5:119751381-119751382	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs375043002	chr5:119751401-119751402	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs11955854	chr5:119751428-119751429	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:73)

Disease	PMID	Source
Metanephric adenoma	20802469	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Cancer	16751803	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21858162	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Lung cancer	18438408	CNVD
Bipolar disorder	18458673	CNVD
Thyroid cancer	19087340	CNVD
Breast cancer	21785460	CNVD
Squamous cell cancer	20885788	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	22521361	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	17133270	CNVD
Acute myeloid leukemia	20729466	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164920	CNVD
Myelodysplastic syndrome	21251322	CNVD
Colorectal cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Multiple myeloma	17550852	CNVD
Ovarian cancer	21720365	CNVD
Salivary gland tumor	18059337	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Renal cell carcinoma	19377443	CNVD
Prostate cancer	16461572	CNVD
Myelofibrosis	22110671	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Glaucoma	21310917	CNVD
Glioblastoma multiforme	22286061	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18194544	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Prostate cancer	22341455	CNVD

Chromatin state (count:809 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:119742000-119775000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr5:119751200-119752000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr5:119751600-119754800	Weak transcription	Primary hematopoietic stem cells	blood
4	chr5:119752000-119752400	Enhancers	HSMM	muscle
5	chr5:119752200-119755600	Enhancers	Muscle Satellite Cultured Cells	--
6	chr5:119752400-119754200	Weak transcription	HSMM	muscle
7	chr5:119753600-119755000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
8	chr5:119753800-119755000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr5:119753800-119755600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chr5:119754000-119754400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
11	chr5:119754200-119755600	Enhancers	HSMM	muscle
12	chr5:119754400-119755200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
13	chr5:119754400-119755200	Enhancers	Osteobl	bone
14	chr5:119754400-119755600	Enhancers	HSMMtube	muscle
15	chr5:119754800-119755200	Enhancers	Primary hematopoietic stem cells	blood
16	chr5:119755000-119755400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr5:119755000-119755600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr5:119755000-119755600	Enhancers	Dnd41	blood
19	chr5:119755400-119755600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
20	chr5:119755600-119757600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
21	chr5:119761800-119762000	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr5:119762600-119763000	Active TSS	ES-I3 Cell Line	embryonic stem cell
23	chr5:119763000-119763600	Active TSS	K562	blood
24	chr5:119766800-119775600	Weak transcription	Psoas Muscle	Psoas
25	chr5:119767600-119768400	ZNF genes & repeats	HSMMtube	muscle
26	chr5:119767800-119768600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
27	chr5:119767800-119770200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
28	chr5:119768200-119770800	Enhancers	Skeletal Muscle Male	skeletal muscle
29	chr5:119768400-119768600	Enhancers	HSMMtube	muscle
30	chr5:119768400-119769200	Enhancers	HSMM	muscle
31	chr5:119768400-119770200	Enhancers	Skeletal Muscle Female	skeletal muscle
32	chr5:119768600-119769000	Weak transcription	HSMMtube	muscle
33	chr5:119769000-119769200	Enhancers	HSMMtube	muscle
34	chr5:119769200-119769800	Weak transcription	HSMMtube	muscle
35	chr5:119769200-119780800	Weak transcription	HSMM	muscle
36	chr5:119769800-119770000	Enhancers	HSMMtube	muscle
37	chr5:119769800-119772200	Enhancers	Fetal Heart	heart
38	chr5:119770000-119772000	Weak transcription	HSMMtube	muscle
39	chr5:119770200-119771400	Weak transcription	Skeletal Muscle Female	skeletal muscle
40	chr5:119770200-119772600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr5:119770800-119771200	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr5:119770800-119771600	Enhancers	Muscle Satellite Cultured Cells	--
43	chr5:119771000-119771400	Enhancers	Aorta	Aorta
44	chr5:119771200-119772200	Enhancers	Skeletal Muscle Male	skeletal muscle
45	chr5:119771400-119772200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr5:119771600-119772000	Weak transcription	Muscle Satellite Cultured Cells	--
47	chr5:119771800-119772000	Enhancers	Aorta	Aorta
48	chr5:119772000-119772200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr5:119772000-119772600	Enhancers	HSMMtube	muscle
50	chr5:119772000-119773800	Enhancers	Muscle Satellite Cultured Cells	--

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