Variant report

Variant	nsv481920
Chromosome Location	chrX:32682536-32863787
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	chrX:32719536-32719540	K562	blood:	n/a	n/a
2	BACH1	chrX:32695625-32695644	K562	blood:	n/a	n/a
3	CEBPB	chrX:32772781-32773048	IMR90	lung:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906 chrX:32773000-32773017
4	CEBPB	chrX:32766919-32767531	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chrX:32772748-32773051	HepG2	liver:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906 chrX:32773000-32773017
6	CEBPB	chrX:32843903-32844119	IMR90	lung:	n/a	n/a
7	CEBPB	chrX:32831465-32831687	HepG2	liver:	n/a	n/a
8	CEBPB	chrX:32831425-32831725	IMR90	lung:	n/a	n/a
9	CEBPB	chrX:32772797-32772997	A549	lung:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906
10	CEBPB	chrX:32703017-32703217	IMR90	lung:	n/a	chrX:32703072-32703083
11	CEBPB	chrX:32702985-32703178	HepG2	liver:	n/a	chrX:32703072-32703083
12	CTCF	chrX:32691420-32691570	GM12874	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
13	CTCF	chrX:32797220-32797370	HMEC	breast:	n/a	n/a
14	CTCF	chrX:32794104-32794151	Pancreas_OC	pancreas:	n/a	n/a
15	CTCF	chrX:32691248-32691611	MCF-7	breast:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
16	CTCF	chrX:32792641-32792723	LNCaP	prostate:	n/a	n/a
17	CTCF	chrX:32797253-32797345	IMR90	lung:	n/a	n/a
18	CTCF	chrX:32792620-32792770	SAEC	small airway:	n/a	n/a
19	CTCF	chrX:32704439-32704456	GM10248	blood:	n/a	n/a
20	CTCF	chrX:32705725-32705764	Pancreas_OC	pancreas:	n/a	n/a
21	CTCF	chrX:32691420-32691570	RPTEC	kidney:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
22	CTCF	chrX:32831104-32831171	GM10266	blood:	n/a	n/a
23	CTCF	chrX:32705760-32705910	BE2_C	brain:	n/a	n/a
24	CTCF	chrX:32691420-32691570	GM12869	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
25	CTCF	chrX:32691384-32691542	SK-N-SH_RA	brain:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
26	CTCF	chrX:32691408-32691546	HepG2	liver:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
27	CTCF	chrX:32691363-32691553	HepG2	liver:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
28	CTCF	chrX:32691420-32691570	HPF	lung:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
29	CTCF	chrX:32760464-32760509	Pancreas_OC	pancreas:	n/a	n/a
30	CTCF	chrX:32831204-32831236	Spleen_OC	spleen:	n/a	n/a
31	CTCF	chrX:32691421-32691552	Hela-S3	cervix:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
32	CTCF	chrX:32691360-32691510	HEK293	kidney:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
33	CTCF	chrX:32705720-32705870	AoAF	blood vessel:	n/a	n/a
34	CTCF	chrX:32691400-32691550	GM12878	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
35	CTCF	chrX:32852154-32852263	GM20000	blood:	n/a	n/a
36	CTCF	chrX:32780790-32780863	GM20000	blood:	n/a	n/a
37	CTCF	chrX:32792704-32792717	HepG2	liver:	n/a	n/a
38	CTCF	chrX:32851301-32851413	LNCaP	prostate:	n/a	n/a
39	CTCF	chrX:32691400-32691550	HCFaa	heart:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
40	CTCF	chrX:32691387-32691561	H1-hESC	embryonic stem cell:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
41	CTCF	chrX:32838926-32839006	GM20000	blood:	n/a	n/a
42	CTCF	chrX:32770543-32770629	GM10266	blood:	n/a	n/a
43	CTCF	chrX:32691500-32691650	RPTEC	kidney:	n/a	n/a
44	CTCF	chrX:32691495-32691525	GM20000	blood:	n/a	n/a
45	CTCF	chrX:32691420-32691570	GM12875	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
46	CTCF	chrX:32691400-32691550	HRPEpiC	eye:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
47	CTCF	chrX:32707518-32707566	GM10266	blood:	n/a	n/a
48	CTCF	chrX:32797150-32797429	GM12878	blood:	n/a	chrX:32797392-32797400
49	CTCF	chrX:32688940-32688989	LNCaP	prostate:	n/a	n/a
50	CTCF	chrX:32705660-32705810	HepG2	liver:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:32830005-32830055	LNCaP	prostate:	n/a
2	chrX:32830005-32830055	HUVEC	blood vessel:	n/a
3	chrX:32830005-32830055	Caco-2	colon:	n/a
4	chrX:32830005-32830055	BE2_C	brain:	n/a
5	chrX:32830005-32830055	HL-60	blood:	n/a
6	chrX:32830005-32830055	ovcar-3	ovarian:	n/a
7	chrX:32830005-32830055	AG09319	gingival:	n/a
8	chrX:32830005-32830055	Hepatocyte	liver:	n/a
9	chrX:32830005-32830055	NB4	blood:	n/a
10	chrX:32830005-32830055	RPTEC	kidney:	n/a
11	chrX:32830005-32830055	HPAEpiC	pulmonary alveolar:	n/a
12	chrX:32830005-32830055	MCF10A-Er-Src	breast:	n/a
13	chrX:32830005-32830055	HCF	heart:	n/a
14	chrX:32830005-32830055	NH-A	brain:	n/a
15	chrX:32830005-32830055	Jurkat	blood:	n/a
16	chrX:32830005-32830055	HEEpiC	esophagus:	n/a
17	chrX:32830005-32830055	GM06990	blood:	n/a
18	chrX:32830005-32830055	SK-N-SH_RA	brain:	n/a
19	chrX:32830005-32830055	AG10803	skin:	n/a
20	chrX:32830005-32830055	T-47D	breast:	n/a
21	chrX:32830005-32830055	NHDF-neo	bronchial:	n/a
22	chrX:32830005-32830055	HepG2	liver:	n/a
23	chrX:32830005-32830055	HIPEpiC	eye:	n/a
24	chrX:32830005-32830055	BJ	skin:	n/a
25	chrX:32830005-32830055	GM12892	blood:	n/a
26	chrX:32830005-32830055	PANC-1	pancreas:	n/a
27	chrX:32830005-32830055	GM12891	blood:	n/a
28	chrX:32830005-32830055	HEK293	kidney:	embryo
29	chrX:32830005-32830055	SKMC	muscle:	n/a
30	chrX:32830005-32830055	HRE	kidney:	n/a
31	chrX:32830005-32830055	NT2-D1	testis:	n/a
32	chrX:32830005-32830055	AG04449	skin:	fetal
33	chrX:32830005-32830055	GM12878	blood:	n/a
34	chrX:32830005-32830055	HAEpiC	amniotic membrane:	n/a
35	chrX:32830005-32830055	NHBE	bronchial:	n/a
36	chrX:32830005-32830055	Hela-S3	cervix:	n/a
37	chrX:32830005-32830055	MCF-7	breast:	n/a
38	chrX:32830005-32830055	HMEC	breast:	n/a
39	chrX:32830005-32830055	HNPCEpiC	eye:	n/a
40	chrX:32830005-32830055	ProgFib	skin:	n/a
41	chrX:32830005-32830055	PrEC	prostate:	n/a
42	chrX:32830005-32830055	SK-N-SH	brain:	n/a
43	chrX:32830005-32830055	K562	blood:	n/a
44	chrX:32830005-32830055	SAEC	small airway:	n/a
45	chrX:32830005-32830055	IMR90	lung:	fetal
46	chrX:32830005-32830055	A549	lung:	n/a
47	chrX:32830005-32830055	AG09309	skin:	n/a
48	chrX:32830005-32830055	HCT-116	colon:	n/a
49	chrX:32830005-32830055	AoSMC	blood vessel:	n/a
50	chrX:32830005-32830055	HCM	heart:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:2781701..2782584-chrX:32736765..32737525,2	MCF-7	breast:
2	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
3	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
4	chrX:32548514..32549611-chrX:32691023..32691979,7	MCF-7	breast:
5	chrX:32501789..32502365-chrX:32691222..32691959,2	MCF-7	breast:
6	chrX:32796881..32797760-chrX:33354782..33355607,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GK-5	chrX:32773057-32773106	ENSG00000236828.1
2	lnc-GK-5	chrX:32774275-32774517	ENSG00000236828.1

Variant related genes	Relation type
DMD-AS3	TF binding region
DMD	TF binding region
DMD-AS3	CpG island
DMD	CpG island

Extended variants
information (count: 2714 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:2714 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187742165	chrX:32686421-32686422	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs531411496	chrX:32686507-32686508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147755861	chrX:32686519-32686520	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs201529557	chrX:32686520-32686521	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs142533105	chrX:32686579-32686580	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs16990570	chrX:32686611-32686612	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs189927350	chrX:32686619-32686620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs371996314	chrX:32686627-32686628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs182382320	chrX:32686671-32686672	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs186723820	chrX:32686750-32686751	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs5972644	chrX:32686771-32686772	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs367611480	chrX:32686807-32686808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs549165521	chrX:32686843-32686844	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs573933384	chrX:32686875-32686876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192784404	chrX:32686881-32686882	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184871890	chrX:32686889-32686890	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs188383995	chrX:32686933-32686934	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs567749887	chrX:32686949-32686950	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs148948121	chrX:32687006-32687007	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs547005798	chrX:32687031-32687032	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs371327849	chrX:32687059-32687060	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143712183	chrX:32687079-32687080	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs539724002	chrX:32687081-32687082	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs193027876	chrX:32687159-32687160	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs185645194	chrX:32687279-32687280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs189439723	chrX:32687320-32687321	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs181830642	chrX:32687322-32687323	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369331241	chrX:32687360-32687361	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs138179426	chrX:32687364-32687365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs142806340	chrX:32687368-32687369	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs144882848	chrX:32687448-32687449	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs183764692	chrX:32687516-32687517	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs73453061	chrX:32687678-32687679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs113561881	chrX:32687737-32687738	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs16990572	chrX:32687740-32687741	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs141251416	chrX:32687823-32687824	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs186346260	chrX:32687831-32687832	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191658161	chrX:32688094-32688095	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs181673915	chrX:32688097-32688098	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs573678328	chrX:32688201-32688202	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs139157657	chrX:32688339-32688340	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs371709679	chrX:32688498-32688499	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs386824658	chrX:32688525-32688526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186000300	chrX:32688530-32688531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs191159793	chrX:32688536-32688537	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs376672933	chrX:32688550-32688551	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183328785	chrX:32688599-32688600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs12849686	chrX:32688715-32688716	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs186968115	chrX:32688779-32688780	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs369890820	chrX:32688781-32688782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Cancer	16751803	CNVD
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Astrocytoma	17387387	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Metanephric adenoma	20802469	CNVD
Medulloblastoma	21979893	CNVD
Schizophrenia	23904455	CNVD
Olfactory neuroblastoma	18408657	CNVD
infertile	22614455	CNVD
Acute myeloid leukemia	20729466	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Premature ovarian failure	20952765	CNVD
Ovarian cancer	19835627	CNVD
Cerebellar hypoplasia	21569638	CNVD
X-linked lissencephaly	21569638	CNVD
Thyroid cancer	19087340	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Developmental delay	21147756	CNVD
Breast cancer	21364760	CNVD
Mental retardation	17406619	CNVD
Pancreatic cancer	17952125	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Gastric cancer	17229543	CNVD
Type 2 diabetes	21760887	CNVD
Cardiomyopathy	22138850	CNVD
Muscular dystrophy	21149563	CNVD
Skeletal myopathy	22138850	CNVD
Autism	21484199	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Duchenne-like muscular dystrophy	22138850	CNVD
Muscular dystrophy	22138850	CNVD
Disease	22090376	CNVD
Colorectal cancer	21645411	CNVD
Ornithine transcarbamylase deficiency	21467225	CNVD
Myxofibrosarcoma	16751306	CNVD
Alcoholism	21790672	CNVD
Chronic granulomatous disease	22383943	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Duchenne and Becker muscular dystrophies	18663755	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:146 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:32686400-32686600	Weak transcription	HUES6 Cell Line	embryonic stem cell
2	chrX:32686600-32688800	Enhancers	HUES6 Cell Line	embryonic stem cell
3	chrX:32687400-32688200	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chrX:32688200-32691200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chrX:32690600-32691200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
6	chrX:32691000-32692000	Enhancers	Fetal Heart	heart
7	chrX:32691200-32691800	Enhancers	ES-I3 Cell Line	embryonic stem cell
8	chrX:32691600-32691800	Enhancers	HUES6 Cell Line	embryonic stem cell
9	chrX:32692000-32692600	Weak transcription	Fetal Heart	heart
10	chrX:32692600-32692800	Enhancers	Fetal Heart	heart
11	chrX:32692800-32696000	Weak transcription	Fetal Heart	heart
12	chrX:32696000-32696600	Enhancers	Skeletal Muscle Male	skeletal muscle
13	chrX:32696000-32696800	Enhancers	Fetal Heart	heart
14	chrX:32708400-32711600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
15	chrX:32709200-32723600	Weak transcription	Left Ventricle	heart
16	chrX:32710400-32726200	Weak transcription	HSMMtube	muscle
17	chrX:32711600-32711800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chrX:32711800-32714200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
19	chrX:32713200-32718800	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chrX:32714200-32715000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
21	chrX:32714200-32716000	Weak transcription	Skeletal Muscle Male	skeletal muscle
22	chrX:32714400-32716800	Weak transcription	HSMM	muscle
23	chrX:32715000-32718600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chrX:32716000-32716600	Strong transcription	Skeletal Muscle Male	skeletal muscle
25	chrX:32716000-32721000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
26	chrX:32716600-32718200	Weak transcription	Skeletal Muscle Male	skeletal muscle
27	chrX:32723600-32723800	Enhancers	Left Ventricle	heart
28	chrX:32725000-32726400	Weak transcription	Right Atrium	heart
29	chrX:32725400-32726200	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chrX:32725400-32726200	Enhancers	iPS-18 Cell Line	embryonic stem cell
31	chrX:32725400-32727600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chrX:32725800-32726200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chrX:32726200-32727000	Enhancers	HSMMtube	muscle
34	chrX:32726200-32727600	Weak transcription	HUES48 Cell Line	embryonic stem cell
35	chrX:32726800-32727000	Enhancers	Right Atrium	heart
36	chrX:32727600-32728400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
37	chrX:32727600-32729200	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chrX:32728400-32728600	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chrX:32728600-32729000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chrX:32729000-32729400	Enhancers	ES-I3 Cell Line	embryonic stem cell
41	chrX:32739000-32739800	Enhancers	Fetal Heart	heart
42	chrX:32757200-32757400	Enhancers	Breast Myoepithelial Primary Cells	Breast
43	chrX:32757200-32760200	Weak transcription	Fetal Heart	heart
44	chrX:32757400-32763200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
45	chrX:32760200-32760400	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chrX:32760200-32760600	Enhancers	Fetal Heart	heart
47	chrX:32760400-32762400	Weak transcription	Skeletal Muscle Female	skeletal muscle
48	chrX:32760600-32762400	Weak transcription	Fetal Heart	heart
49	chrX:32760600-32768800	Weak transcription	Left Ventricle	heart
50	chrX:32762400-32764800	Enhancers	Fetal Heart	heart

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