Variant report

Variant	nsv481919
Chromosome Location	chrX:32627779-32864894
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:32702985-32703178	HepG2	liver:	n/a	chrX:32703072-32703083
4	CEBPB	chrX:32766919-32767531	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chrX:32831465-32831687	HepG2	liver:	n/a	n/a
6	CEBPB	chrX:32665303-32665641	HepG2	liver:	n/a	n/a
7	CEBPB	chrX:32772797-32772997	A549	lung:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906
8	CEBPB	chrX:32656576-32656845	IMR90	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
9	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
10	CEBPB	chrX:32656679-32656865	A549	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
11	CEBPB	chrX:32703017-32703217	IMR90	lung:	n/a	chrX:32703072-32703083
12	CEBPB	chrX:32831425-32831725	IMR90	lung:	n/a	n/a
13	CEBPB	chrX:32843903-32844119	IMR90	lung:	n/a	n/a
14	CEBPB	chrX:32627620-32627925	IMR90	lung:	n/a	n/a
15	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
16	CTCF	chrX:32688940-32688989	LNCaP	prostate:	n/a	n/a
17	CTCF	chrX:32704439-32704456	GM10248	blood:	n/a	n/a
18	CTCF	chrX:32691380-32691530	HCM	heart:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
19	CTCF	chrX:32691440-32691590	HRPEpiC	eye:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
20	CTCF	chrX:32691440-32691590	HPF	lung:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
21	CTCF	chrX:32641709-32641787	GM13976	blood:	n/a	n/a
22	CTCF	chrX:32691408-32691546	HepG2	liver:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
23	CTCF	chrX:32691114-32691796	SK-N-SH	brain:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
24	CTCF	chrX:32691480-32691630	GM06990	blood:	n/a	chrX:32691480-32691496
25	CTCF	chrX:32705760-32705910	NHEK	skin:	n/a	n/a
26	CTCF	chrX:32792641-32792723	LNCaP	prostate:	n/a	n/a
27	CTCF	chrX:32691360-32691510	Hela-S3	cervix:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
28	CTCF	chrX:32691391-32691584	GM12878	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
29	CTCF	chrX:32691420-32691570	SK-N-SH_RA	brain:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
30	CTCF	chrX:32705640-32705790	HEK293	kidney:	n/a	n/a
31	CTCF	chrX:32649523-32649567	GM10248	blood:	n/a	n/a
32	CTCF	chrX:32691420-32691570	HCPEpiC	choroid plexus:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
33	CTCF	chrX:32691280-32691430	HMF	breast:	n/a	n/a
34	CTCF	chrX:32797253-32797345	IMR90	lung:	n/a	n/a
35	CTCF	chrX:32759672-32759724	Pancreas_OC	pancreas:	n/a	n/a
36	CTCF	chrX:32691400-32691550	HMEC	breast:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
37	CTCF	chrX:32691400-32691550	HCFaa	heart:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
38	CTCF	chrX:32691405-32691542	Kidney_OC	kidney:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
39	CTCF	chrX:32705580-32705730	Caco-2	colon:	n/a	n/a
40	CTCF	chrX:32691500-32691650	RPTEC	kidney:	n/a	n/a
41	CTCF	chrX:32705700-32705850	BE2_C	brain:	n/a	n/a
42	CTCF	chrX:32691380-32691530	GM12873	blood:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
43	CTCF	chrX:32797220-32797370	HMEC	breast:	n/a	n/a
44	CTCF	chrX:32757629-32757691	LNCaP	prostate:	n/a	n/a
45	CTCF	chrX:32738407-32738465	GM10248	blood:	n/a	n/a
46	CTCF	chrX:32691440-32691590	SK-N-SH_RA	brain:	n/a	chrX:32691479-32691497 chrX:32691474-32691495 chrX:32691480-32691496
47	CTCF	chrX:32831104-32831171	GM10266	blood:	n/a	n/a
48	CTCF	chrX:32655624-32655643	Medullo	brain:	n/a	n/a
49	CTCF	chrX:32838926-32839006	GM20000	blood:	n/a	n/a
50	CTCF	chrX:32691760-32691910	HMEC	breast:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:32830005-32830055	SAEC	small airway:	n/a
2	chrX:32830005-32830055	A549	lung:	n/a
3	chrX:32830005-32830055	GM19239	blood:	n/a
4	chrX:32830005-32830055	SK-N-SH_RA	brain:	n/a
5	chrX:32830005-32830055	AG09319	gingival:	n/a
6	chrX:32830005-32830055	NHDF-neo	bronchial:	n/a
7	chrX:32830005-32830055	T-47D	breast:	n/a
8	chrX:32830005-32830055	HCT-116	colon:	n/a
9	chrX:32830005-32830055	AG04449	skin:	fetal
10	chrX:32830005-32830055	HMEC	breast:	n/a
11	chrX:32830005-32830055	NH-A	brain:	n/a
12	chrX:32830005-32830055	NHBE	bronchial:	n/a
13	chrX:32830005-32830055	Hepatocyte	liver:	n/a
14	chrX:32830005-32830055	HNPCEpiC	eye:	n/a
15	chrX:32830005-32830055	BJ	skin:	n/a
16	chrX:32830005-32830055	HIPEpiC	eye:	n/a
17	chrX:32830005-32830055	U87	brain:	n/a
18	chrX:32830005-32830055	NT2-D1	testis:	n/a
19	chrX:32830005-32830055	ECC-1	luminal epithelium:	n/a
20	chrX:32830005-32830055	HAEpiC	amniotic membrane:	n/a
21	chrX:32830005-32830055	ProgFib	skin:	n/a
22	chrX:32830005-32830055	SK-N-MC	brain:	n/a
23	chrX:32830005-32830055	IMR90	lung:	fetal
24	chrX:32830005-32830055	HCPEpiC	choroid plexus:	n/a
25	chrX:32830005-32830055	GM12892	blood:	n/a
26	chrX:32830005-32830055	GM12878	blood:	n/a
27	chrX:32830005-32830055	AG04450	lung:	fetal
28	chrX:32830005-32830055	PrEC	prostate:	n/a
29	chrX:32830005-32830055	RPTEC	kidney:	n/a
30	chrX:32830005-32830055	MCF-7	breast:	n/a
31	chrX:32830005-32830055	Hela-S3	cervix:	n/a
32	chrX:32830005-32830055	CMK	blood:	n/a
33	chrX:32830005-32830055	PFSK-1	brain:	n/a
34	chrX:32830005-32830055	HepG2	liver:	n/a
35	chrX:32830005-32830055	ovcar-3	ovarian:	n/a
36	chrX:32830005-32830055	SK-N-SH	brain:	n/a
37	chrX:32830005-32830055	GM12891	blood:	n/a
38	chrX:32830005-32830055	HEK293	kidney:	embryo
39	chrX:32830005-32830055	Jurkat	blood:	n/a
40	chrX:32830005-32830055	LNCaP	prostate:	n/a
41	chrX:32830005-32830055	PANC-1	pancreas:	n/a
42	chrX:32830005-32830055	SKMC	muscle:	n/a
43	chrX:32830005-32830055	H1-hESC	embryonic stem cell:	embryo
44	chrX:32830005-32830055	HCF	heart:	n/a
45	chrX:32830005-32830055	BE2_C	brain:	n/a
46	chrX:32830005-32830055	HUVEC	blood vessel:	n/a
47	chrX:32830005-32830055	HPAEpiC	pulmonary alveolar:	n/a
48	chrX:32830005-32830055	K562	blood:	n/a
49	chrX:32830005-32830055	HRCEpiC	kidney:	n/a
50	chrX:32830005-32830055	HRE	kidney:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:2781701..2782584-chrX:32736765..32737525,2	MCF-7	breast:
2	chrX:32655856..32658575-chrX:32677287..32679370,2	K562	blood:
3	chrX:32501789..32502365-chrX:32691222..32691959,2	MCF-7	breast:
4	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
5	chrX:32655856..32658575-chrX:32677287..32679370,2	K562	blood:
6	chr1:185868339..185869318-chrX:32631259..32632008,2	MCF-7	breast:
7	chrX:32796881..32797760-chrX:33354782..33355607,2	MCF-7	breast:
8	chrX:32548514..32549611-chrX:32691023..32691979,7	MCF-7	breast:
9	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548f-3p	chrX:32659607-32659625	MIMAT0005895_4

Variant related genes	Relation type
MIR548F5	TF binding region
DMD	TF binding region
DMD-AS3	TF binding region
MIR548F5	CpG island
DMD	CpG island
DMD-AS3	CpG island

Extended variants
information (count: 3627 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:3627 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs141316736	chrX:32627924-32627925	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs576258851	chrX:32628023-32628024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs5928046	chrX:32628032-32628033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs5928047	chrX:32628049-32628050	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs12385244	chrX:32628206-32628207	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs529134463	chrX:32628237-32628238	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs182863883	chrX:32628298-32628299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs5928048	chrX:32628324-32628325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147165434	chrX:32628334-32628335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs186506185	chrX:32628350-32628351	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs191847581	chrX:32628354-32628355	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs183998216	chrX:32628472-32628473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs572597281	chrX:32628478-32628479	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144186263	chrX:32628489-32628490	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs147778816	chrX:32628495-32628496	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs187695041	chrX:32628528-32628529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533577967	chrX:32628640-32628641	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs558109359	chrX:32628644-32628645	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372593372	chrX:32628686-32628687	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs532900923	chrX:32628689-32628690	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs551093921	chrX:32628691-32628692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs569682021	chrX:32628725-32628726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148829938	chrX:32628736-32628737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs116065387	chrX:32628823-32628824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs699457	chrX:32628882-32628883	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs115668192	chrX:32628975-32628976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs577090129	chrX:32629025-32629026	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs182684928	chrX:32629032-32629033	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs140527155	chrX:32629040-32629041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs145846801	chrX:32629064-32629065	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs138310033	chrX:32629101-32629102	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs141317213	chrX:32629211-32629212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs186868718	chrX:32629246-32629247	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs16990505	chrX:32629256-32629257	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs17243652	chrX:32629283-32629284	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs201949471	chrX:32629319-32629320	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200234428	chrX:32629320-32629321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201565492	chrX:32629321-32629322	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs397707509	chrX:32629331-32629332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192120274	chrX:32629332-32629333	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs149352277	chrX:32629390-32629391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs544144720	chrX:32629506-32629507	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs114256600	chrX:32629513-32629514	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs808515	chrX:32629522-32629523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs141729402	chrX:32629538-32629539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs368385309	chrX:32629551-32629552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs184210592	chrX:32629561-32629562	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs147201552	chrX:32629643-32629644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs11796029	chrX:32629696-32629697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575632503	chrX:32629800-32629801	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

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	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:190 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:32584000-32661400	Weak transcription	HSMMtube	muscle
2	chrX:32625200-32632000	Weak transcription	Psoas Muscle	Psoas
3	chrX:32627600-32627800	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chrX:32627800-32628000	Weak transcription	Skeletal Muscle Male	skeletal muscle
5	chrX:32627800-32635400	Weak transcription	Skeletal Muscle Female	skeletal muscle
6	chrX:32628000-32628200	Enhancers	Skeletal Muscle Male	skeletal muscle
7	chrX:32628200-32633000	Weak transcription	Skeletal Muscle Male	skeletal muscle
8	chrX:32632000-32632200	Enhancers	Psoas Muscle	Psoas
9	chrX:32633000-32633400	Enhancers	Skeletal Muscle Male	skeletal muscle
10	chrX:32635400-32635600	Enhancers	Skeletal Muscle Female	skeletal muscle
11	chrX:32640800-32641400	Enhancers	HUES48 Cell Line	embryonic stem cell
12	chrX:32647800-32648200	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chrX:32648200-32650400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chrX:32650400-32650600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
15	chrX:32650600-32653000	Weak transcription	HUES6 Cell Line	embryonic stem cell
16	chrX:32651400-32662800	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chrX:32651600-32655600	Weak transcription	Aorta	Aorta
18	chrX:32651800-32652800	Enhancers	Skeletal Muscle Female	skeletal muscle
19	chrX:32652600-32664200	Weak transcription	Ovary	ovary
20	chrX:32659000-32659200	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chrX:32659000-32659400	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chrX:32659400-32662000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
23	chrX:32660600-32663800	Weak transcription	Fetal Muscle Leg	muscle
24	chrX:32661800-32662000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
25	chrX:32662000-32663200	Enhancers	iPS-15b Cell Line	embryonic stem cell
26	chrX:32662000-32663400	Enhancers	ES-I3 Cell Line	embryonic stem cell
27	chrX:32662200-32662600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chrX:32662200-32663200	Enhancers	HUES48 Cell Line	embryonic stem cell
29	chrX:32662200-32663200	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chrX:32662400-32663200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
31	chrX:32662600-32663200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chrX:32663200-32664000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
33	chrX:32663200-32664000	Weak transcription	HUES6 Cell Line	embryonic stem cell
34	chrX:32664000-32664400	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chrX:32664000-32666000	Enhancers	HepG2	liver
36	chrX:32664200-32664400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chrX:32664200-32664800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
38	chrX:32664200-32665400	Enhancers	Ovary	ovary
39	chrX:32674200-32674400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
40	chrX:32674400-32674600	Weak transcription	HUES6 Cell Line	embryonic stem cell
41	chrX:32686400-32686600	Weak transcription	HUES6 Cell Line	embryonic stem cell
42	chrX:32686600-32688800	Enhancers	HUES6 Cell Line	embryonic stem cell
43	chrX:32687400-32688200	Enhancers	ES-I3 Cell Line	embryonic stem cell
44	chrX:32688200-32691200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chrX:32690600-32691200	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
46	chrX:32691000-32692000	Enhancers	Fetal Heart	heart
47	chrX:32691200-32691800	Enhancers	ES-I3 Cell Line	embryonic stem cell
48	chrX:32691600-32691800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chrX:32692000-32692600	Weak transcription	Fetal Heart	heart
50	chrX:32692600-32692800	Enhancers	Fetal Heart	heart

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