Variant report

Variant	nsv834520
Chromosome Location	chr2:211101265-211257068
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	ARID3A	chr2:211113387-211113738	HepG2	liver:	n/a	chr2:211113389-211113405 chr2:211113390-211113406
2	BHLHE40	chr2:211117672-211117742	GM12878	blood:	n/a	n/a
3	BRCA1	chr2:211228548-211228557	HepG2	liver:	n/a	n/a
4	CEBPB	chr2:211153819-211154128	IMR90	lung:	n/a	n/a
5	CEBPB	chr2:211126127-211126519	MCF-7	breast:	n/a	n/a
6	CEBPB	chr2:211123715-211123833	H1-hESC	embryonic stem cell:	n/a	chr2:211123742-211123753
7	CEBPB	chr2:211178085-211178214	A549	lung:	n/a	chr2:211178132-211178141 chr2:211178130-211178141
8	CEBPB	chr2:211126182-211126488	HepG2	liver:	n/a	n/a
9	CEBPB	chr2:211178099-211178158	Hela-S3	cervix:	n/a	chr2:211178132-211178141 chr2:211178130-211178141
10	CEBPB	chr2:211153833-211154120	HepG2	liver:	n/a	n/a
11	CEBPB	chr2:211177490-211177820	HepG2	liver:	n/a	chr2:211177640-211177649 chr2:211177640-211177651 chr2:211177638-211177649 chr2:211177638-211177651
12	CEBPB	chr2:211123613-211123956	HepG2	liver:	n/a	chr2:211123742-211123753
13	CEBPB	chr2:211177522-211177741	IMR90	lung:	n/a	chr2:211177640-211177649 chr2:211177640-211177651 chr2:211177638-211177649 chr2:211177638-211177651
14	CEBPB	chr2:211123634-211123928	A549	lung:	n/a	chr2:211123742-211123753
15	CEBPB	chr2:211153891-211154063	H1-hESC	embryonic stem cell:	n/a	n/a
16	CTCF	chr2:211228040-211228190	GM12874	blood:	n/a	n/a
17	CTCF	chr2:211113508-211113661	GM12878	blood:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
18	CTCF	chr2:211113270-211113869	HCT-116	colon:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
19	CTCF	chr2:211113479-211113644	LNCaP	prostate:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
20	CTCF	chr2:211113455-211113686	SK-N-SH_RA	brain:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
21	CTCF	chr2:211228060-211228210	GM12878	blood:	n/a	n/a
22	CTCF	chr2:211228060-211228210	GM12866	blood:	n/a	n/a
23	CTCF	chr2:211228400-211228550	HEEpiC	esophagus:	n/a	n/a
24	CTCF	chr2:211228073-211228203	Gliobla	brain:	n/a	n/a
25	CTCF	chr2:211228056-211228244	MCF-7	breast:	n/a	n/a
26	CTCF	chr2:211228040-211228190	SK-N-SH_RA	brain:	n/a	n/a
27	CTCF	chr2:211113500-211113650	NHEK	skin:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
28	CTCF	chr2:211113463-211113647	LNCaP	prostate:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
29	CTCF	chr2:211221780-211221930	HRPEpiC	eye:	n/a	n/a
30	CTCF	chr2:211104634-211104723	ProgFib	skin:	n/a	n/a
31	CTCF	chr2:211228100-211228250	GM12872	blood:	n/a	n/a
32	CTCF	chr2:211228060-211228210	GM12874	blood:	n/a	n/a
33	CTCF	chr2:211104626-211104727	MCF-7	breast:	n/a	n/a
34	CTCF	chr2:211113479-211113676	A549	lung:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
35	CTCF	chr2:211228280-211228430	HEK293	kidney:	n/a	n/a
36	CTCF	chr2:211228061-211228245	Hela-S3	cervix:	n/a	n/a
37	CTCF	chr2:211221800-211221950	BE2_C	brain:	n/a	n/a
38	CTCF	chr2:211113540-211113690	HMEC	breast:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
39	CTCF	chr2:211228052-211228250	LNCaP	prostate:	n/a	n/a
40	CTCF	chr2:211221793-211221914	MCF-7	breast:	n/a	n/a
41	CTCF	chr2:211113420-211113570	HEEpiC	esophagus:	n/a	n/a
42	CTCF	chr2:211221796-211221879	GM19238	blood:	n/a	n/a
43	CTCF	chr2:211113480-211113630	HCFaa	heart:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
44	CTCF	chr2:211113520-211113670	SAEC	small airway:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
45	CTCF	chr2:211113400-211113550	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr2:211113460-211113610	AG10803	skin:	n/a	chr2:211113555-211113573 chr2:211113557-211113578 chr2:211113556-211113572
47	CTCF	chr2:211228040-211228190	GM12875	blood:	n/a	n/a
48	CTCF	chr2:211228060-211228210	WERI-Rb-1	eye:	n/a	n/a
49	CTCF	chr2:211204986-211205017	GM10248	blood:	n/a	n/a
50	CTCF	chr2:211221760-211221910	Hela-S3	cervix:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:211179902-211179952	BE2_C	brain:	n/a
2	chr2:211168547-211168597	AoSMC	blood vessel:	n/a
3	chr2:211179902-211179952	PANC-1	pancreas:	n/a
4	chr2:211179560-211179610	HEEpiC	esophagus:	n/a
5	chr2:211155085-211155135	HCM	heart:	n/a
6	chr2:211180001-211180051	HPAEpiC	pulmonary alveolar:	n/a
7	chr2:211179959-211180009	Jurkat	blood:	n/a
8	chr2:211180001-211180051	MCF-7	breast:	n/a
9	chr2:211179902-211179952	HEEpiC	esophagus:	n/a
10	chr2:211168547-211168597	ovcar-3	ovarian:	n/a
11	chr2:211155085-211155135	NT2-D1	testis:	n/a
12	chr2:211180001-211180051	A549	lung:	n/a
13	chr2:211180386-211180436	Hela-S3	cervix:	n/a
14	chr2:211180386-211180436	NHBE	bronchial:	n/a
15	chr2:211179959-211180009	HIPEpiC	eye:	n/a
16	chr2:211169638-211169688	MCF-7	breast:	n/a
17	chr2:211179560-211179610	IMR90	lung:	fetal
18	chr2:211179560-211179610	AG10803	skin:	n/a
19	chr2:211155085-211155135	NH-A	brain:	n/a
20	chr2:211169638-211169688	HCM	heart:	n/a
21	chr2:211155085-211155135	NB4	blood:	n/a
22	chr2:211168547-211168597	AG04449	skin:	fetal
23	chr2:211179560-211179610	K562	blood:	n/a
24	chr2:211179902-211179952	PFSK-1	brain:	n/a
25	chr2:211179902-211179952	HPAEpiC	pulmonary alveolar:	n/a
26	chr2:211169638-211169688	AG09309	skin:	n/a
27	chr2:211179707-211179757	HIPEpiC	eye:	n/a
28	chr2:211179902-211179952	HRCEpiC	kidney:	n/a
29	chr2:211179707-211179757	H1-hESC	embryonic stem cell:	embryo
30	chr2:211180386-211180436	HL-60	blood:	n/a
31	chr2:211179959-211180009	HEK293	kidney:	embryo
32	chr2:211179959-211180009	HCT-116	colon:	n/a
33	chr2:211179902-211179952	HCT-116	colon:	n/a
34	chr2:211179560-211179610	AG09319	gingival:	n/a
35	chr2:211168547-211168597	HCM	heart:	n/a
36	chr2:211179560-211179610	PrEC	prostate:	n/a
37	chr2:211180386-211180436	GM19239	blood:	n/a
38	chr2:211179707-211179757	SK-N-SH_RA	brain:	n/a
39	chr2:211179959-211180009	Caco-2	colon:	n/a
40	chr2:211180386-211180436	HCF	heart:	n/a
41	chr2:211179959-211180009	HL-60	blood:	n/a
42	chr2:211179902-211179952	SK-N-MC	brain:	n/a
43	chr2:211179707-211179757	HNPCEpiC	eye:	n/a
44	chr2:211155085-211155135	HRE	kidney:	n/a
45	chr2:211179902-211179952	BJ	skin:	n/a
46	chr2:211180386-211180436	CMK	blood:	n/a
47	chr2:211179959-211180009	ProgFib	skin:	n/a
48	chr2:211155085-211155135	Jurkat	blood:	n/a
49	chr2:211179707-211179757	GM12891	blood:	n/a
50	chr2:211179959-211180009	HNPCEpiC	eye:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:211128325..211129018-chr2:211137774..211138284,2	MCF-7	breast:
2	chr2:211173735..211175248-chr2:211176739..211178731,2	MCF-7	breast:
3	chr2:211173735..211175248-chr2:211176739..211178731,2	MCF-7	breast:
4	chr2:211106656..211109050-chr2:211112844..211114921,2	K562	blood:
5	chr2:211106656..211109050-chr2:211112844..211114921,2	K562	blood:
6	chr2:211113028..211114042-chr2:211263878..211264898,6	MCF-7	breast:
7	chr2:211227904..211228774-chr2:211263806..211264757,2	MCF-7	breast:
8	chr2:211128325..211129018-chr2:211137774..211138284,2	MCF-7	breast:
9	chr2:211112989..211113918-chr2:211900038..211900547,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CPS1-1	chr2:211189490-211189558	ENSG00000234281.1
2	lnc-CPS1-2	chr2:211190540-211192675	ucscGeneNc_uc002vef_1
3	lnc-CPS1-1	chr2:211189483-211189558	ENSG00000234281.1

Variant related genes	Relation type
ENSG00000199203	TF binding region
MYL1	TF binding region
ENSG00000234281	TF binding region
ENSG00000199203	CpG island
MYL1	CpG island
ENSG00000234281	CpG island

Extended variants
information (count: 3008 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:3008 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs144873655	chr2:211113842-211113843	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs529336037	chr2:211113864-211113865	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs551242629	chr2:211113958-211113959	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs547699619	chr2:211113972-211113973	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191154841	chr2:211114062-211114063	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs535996163	chr2:211114064-211114065	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs547562511	chr2:211114067-211114068	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs572720503	chr2:211114073-211114074	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372750229	chr2:211114134-211114135	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs60099944	chr2:211114162-211114163	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs201002621	chr2:211114164-211114165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs13393103	chr2:211114165-211114166	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
13	rs201137837	chr2:211114166-211114167	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs540394805	chr2:211114177-211114178	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs71043983	chr2:211114178-211114179	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs182158256	chr2:211114198-211114199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558535049	chr2:211114206-211114207	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575182364	chr2:211114237-211114238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs28496757	chr2:211114250-211114251	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs560791194	chr2:211114298-211114299	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs139596401	chr2:211114306-211114307	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs542783665	chr2:211114316-211114317	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs559819981	chr2:211114353-211114354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs540625686	chr2:211114359-211114360	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545388573	chr2:211114384-211114385	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs565574536	chr2:211114420-211114421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs149869821	chr2:211114439-211114440	Enhancers	n/a	n/a	Overlapped CNVs	mRNA abundance
28	rs111268256	chr2:211114460-211114461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs144905996	chr2:211114478-211114479	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs567885805	chr2:211114592-211114593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs370919922	chr2:211114627-211114628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs530336235	chr2:211114648-211114649	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs142214354	chr2:211114674-211114675	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs566568289	chr2:211114723-211114724	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs560282682	chr2:211114792-211114793	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs538213150	chr2:211114967-211114968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs558179253	chr2:211114984-211114985	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs188875098	chr2:211115008-211115009	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs34236096	chr2:211115030-211115031	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs537784214	chr2:211115117-211115118	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs554323013	chr2:211115119-211115120	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs574520598	chr2:211115163-211115164	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs540438287	chr2:211115205-211115206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs146770176	chr2:211115221-211115222	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs140328885	chr2:211115263-211115264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs545063873	chr2:211115320-211115321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs569631395	chr2:211115330-211115331	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs565312265	chr2:211115395-211115396	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs531207912	chr2:211115420-211115421	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs193247855	chr2:211115449-211115450	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Medulloblastoma	21979893	CNVD
Ependymoma	16718352	CNVD
Melanoma	18172304	CNVD
Cancer	16751803	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	17603634	CNVD
Testicular germ cell tumor	18059402	CNVD
Breast cancer	16272173	CNVD
Ewing''s sarcoma	17952124	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Liposarcoma	21253554	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Autism	16446308	CNVD
Autism	19401682	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
small cell lung cancer	20016488	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Urothelial carcinoma	21177765	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Cervical cancer	21062161	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Non-small cell lung cancer	21829676	CNVD
Autism	20808228	CNVD
Renal cell carcinoma	18765545	CNVD
Ovarian cancer	19193619	CNVD
Non-small cell lung cancer	18676828	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Chordoma	18071362	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	18923514	CNVD
Schizophrenia	22241247	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Urothelial cell carcinoma	18451213	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:217 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:211113800-211115600	Enhancers	Fetal Heart	heart
2	chr2:211117600-211118000	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chr2:211117600-211118000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chr2:211117600-211118000	Enhancers	iPS-18 Cell Line	embryonic stem cell
5	chr2:211117600-211118000	Enhancers	iPS-20b Cell Line	embryonic stem cell
6	chr2:211117600-211118000	Active TSS	Skeletal Muscle Female	skeletal muscle
7	chr2:211118000-211118200	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
8	chr2:211118200-211119000	Enhancers	Fetal Lung	lung
9	chr2:211128800-211129000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr2:211147400-211152000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
11	chr2:211147600-211150000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr2:211150000-211150200	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
13	chr2:211150200-211150800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
14	chr2:211150400-211150600	Enhancers	Fetal Muscle Leg	muscle
15	chr2:211150600-211152000	Weak transcription	Fetal Muscle Leg	muscle
16	chr2:211151800-211152200	Enhancers	HSMMtube	muscle
17	chr2:211152000-211152600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
18	chr2:211152000-211152600	Enhancers	Fetal Muscle Leg	muscle
19	chr2:211152000-211152600	Enhancers	Skeletal Muscle Female	skeletal muscle
20	chr2:211152000-211152800	Enhancers	Skeletal Muscle Male	skeletal muscle
21	chr2:211152000-211153200	Enhancers	HSMM	muscle
22	chr2:211152200-211152600	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chr2:211152200-211152800	Flanking Active TSS	HSMMtube	muscle
24	chr2:211152600-211156600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr2:211152600-211160000	Weak transcription	Fetal Muscle Trunk	muscle
26	chr2:211152600-211163000	Weak transcription	Fetal Muscle Leg	muscle
27	chr2:211152800-211156600	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr2:211152800-211166400	Weak transcription	HSMMtube	muscle
29	chr2:211156600-211156800	Genic enhancers	Skeletal Muscle Female	skeletal muscle
30	chr2:211156600-211163000	Strong transcription	Skeletal Muscle Male	skeletal muscle
31	chr2:211156800-211157600	Strong transcription	Skeletal Muscle Female	skeletal muscle
32	chr2:211157600-211158000	Weak transcription	Skeletal Muscle Female	skeletal muscle
33	chr2:211158000-211158400	Strong transcription	Skeletal Muscle Female	skeletal muscle
34	chr2:211158400-211159200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
35	chr2:211159200-211160200	Strong transcription	Skeletal Muscle Female	skeletal muscle
36	chr2:211160000-211160400	Enhancers	Fetal Muscle Trunk	muscle
37	chr2:211160200-211161600	Genic enhancers	Skeletal Muscle Female	skeletal muscle
38	chr2:211160400-211164600	Weak transcription	Fetal Muscle Trunk	muscle
39	chr2:211161200-211161400	Enhancers	Psoas Muscle	Psoas
40	chr2:211161400-211164400	Weak transcription	Psoas Muscle	Psoas
41	chr2:211161600-211163000	Strong transcription	Skeletal Muscle Female	skeletal muscle
42	chr2:211162800-211163200	Active TSS	Breast Myoepithelial Primary Cells	Breast
43	chr2:211163000-211163200	Active TSS	Fetal Muscle Leg	muscle
44	chr2:211163000-211163200	Enhancers	Pancreas	Pancrea
45	chr2:211163000-211163400	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
46	chr2:211163000-211163400	Transcr. at gene 5' and 3'	Skeletal Muscle Female	skeletal muscle
47	chr2:211163200-211163400	Transcr. at gene 5' and 3'	Fetal Muscle Leg	muscle
48	chr2:211163400-211167400	Active TSS	Fetal Muscle Leg	muscle
49	chr2:211163400-211168600	Active TSS	Skeletal Muscle Male	skeletal muscle
50	chr2:211163400-211168800	Active TSS	Skeletal Muscle Female	skeletal muscle

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