Variant report

Variant	nsv491895
Chromosome Location	chrX:32519833-32950412
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	ARID3A	chrX:32549077-32549283	HepG2	liver:	n/a	n/a
3	ATF2	chrX:32533045-32533465	GM12878	blood:	n/a	n/a
4	BACH1	chrX:32695625-32695644	K562	blood:	n/a	n/a
5	BATF	chrX:32533082-32533395	GM12878	blood:	n/a	chrX:32533220-32533230 chrX:32533219-32533230
6	BATF	chrX:32552003-32552326	GM12878	blood:	n/a	n/a
7	BATF	chrX:32533103-32533341	GM12878	blood:	n/a	chrX:32533220-32533230 chrX:32533219-32533230
8	BATF	chrX:32552060-32552305	GM12878	blood:	n/a	n/a
9	BCL11A	chrX:32533073-32533391	GM12878	blood:	n/a	chrX:32533223-32533232 chrX:32533222-32533231
10	BCL11A	chrX:32552025-32552248	GM12878	blood:	n/a	n/a
11	BHLHE40	chrX:32533196-32533287	GM12878	blood:	n/a	n/a
12	BRCA1	chrX:32924311-32924335	GM12878	blood:	n/a	n/a
13	CEBPB	chrX:32766919-32767531	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chrX:32949269-32949597	IMR90	lung:	n/a	chrX:32949502-32949513 chrX:32949415-32949426 chrX:32949500-32949513 chrX:32949416-32949425
15	CEBPB	chrX:32936731-32936967	A549	lung:	n/a	n/a
16	CEBPB	chrX:32772797-32772997	A549	lung:	n/a	chrX:32772894-32772905 chrX:32772892-32772909 chrX:32772893-32772906 chrX:32772893-32772904 chrX:32772893-32772906
17	CEBPB	chrX:32889591-32889922	IMR90	lung:	n/a	chrX:32889745-32889758
18	CEBPB	chrX:32656576-32656845	IMR90	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
19	CEBPB	chrX:32886639-32886884	HepG2	liver:	n/a	chrX:32886759-32886770
20	CEBPB	chrX:32702985-32703178	HepG2	liver:	n/a	chrX:32703072-32703083
21	CEBPB	chrX:32831425-32831725	IMR90	lung:	n/a	n/a
22	CEBPB	chrX:32898887-32899628	IMR90	lung:	n/a	chrX:32899493-32899506 chrX:32899408-32899420 chrX:32899495-32899504 chrX:32899495-32899504 chrX:32899495-32899504
23	CEBPB	chrX:32627620-32627925	IMR90	lung:	n/a	n/a
24	CEBPB	chrX:32889603-32889915	Hela-S3	cervix:	n/a	chrX:32889745-32889758
25	CEBPB	chrX:32550343-32550726	Hela-S3	cervix:	n/a	chrX:32550449-32550460
26	CEBPB	chrX:32869772-32869902	A549	lung:	n/a	n/a
27	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
28	CEBPB	chrX:32556163-32556300	A549	lung:	n/a	n/a
29	CEBPB	chrX:32843903-32844119	IMR90	lung:	n/a	n/a
30	CEBPB	chrX:32866060-32866260	HepG2	liver:	n/a	chrX:32866223-32866234
31	CEBPB	chrX:32899394-32899507	K562	blood:	n/a	chrX:32899493-32899506 chrX:32899408-32899420 chrX:32899495-32899504 chrX:32899495-32899504 chrX:32899495-32899504
32	CEBPB	chrX:32622293-32622487	IMR90	lung:	n/a	n/a
33	CEBPB	chrX:32548912-32549270	Hela-S3	cervix:	n/a	n/a
34	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
35	CEBPB	chrX:32831465-32831687	HepG2	liver:	n/a	n/a
36	CEBPB	chrX:32936661-32936954	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:32703017-32703217	IMR90	lung:	n/a	chrX:32703072-32703083
38	CEBPB	chrX:32665303-32665641	HepG2	liver:	n/a	n/a
39	CEBPB	chrX:32656679-32656865	A549	lung:	n/a	chrX:32656758-32656769 chrX:32656750-32656762 chrX:32656705-32656718
40	CEBPB	chrX:32600924-32601258	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chrX:32895778-32896050	ECC-1	luminal epithelium:	n/a	n/a
42	CEBPB	chrX:32949288-32949498	HepG2	liver:	n/a	chrX:32949415-32949426 chrX:32949416-32949425
43	CEBPB	chrX:32865997-32866399	Hela-S3	cervix:	n/a	chrX:32866223-32866234
44	CHD2	chrX:32924317-32924414	K562	blood:	n/a	n/a
45	CTCF	chrX:32916838-32916881	H1-hESC	embryonic stem cell:	n/a	n/a
46	CTCF	chrX:32549020-32549170	WERI-Rb-1	eye:	n/a	chrX:32549115-32549123 chrX:32549112-32549133 chrX:32549110-32549128 chrX:32549111-32549127
47	CTCF	chrX:32548944-32549331	K562	blood:	n/a	chrX:32549115-32549123 chrX:32549112-32549133 chrX:32549110-32549128 chrX:32549111-32549127
48	CTCF	chrX:32549080-32549230	GM06990	blood:	n/a	chrX:32549115-32549123 chrX:32549112-32549133 chrX:32549110-32549128 chrX:32549111-32549127
49	CTCF	chrX:32691340-32691490	AG09319	gingival:	n/a	n/a
50	CTCF	chrX:32792620-32792770	SAEC	small airway:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:32830005-32830055	MCF-7	breast:	n/a
2	chrX:32886461-32886511	AG09319	gingival:	n/a
3	chrX:32886461-32886511	IMR90	lung:	fetal
4	chrX:32830005-32830055	PrEC	prostate:	n/a
5	chrX:32830005-32830055	ovcar-3	ovarian:	n/a
6	chrX:32830005-32830055	GM12891	blood:	n/a
7	chrX:32830005-32830055	BE2_C	brain:	n/a
8	chrX:32886526-32886576	MCF-7	breast:	n/a
9	chrX:32886461-32886511	LNCaP	prostate:	n/a
10	chrX:32830005-32830055	AoSMC	blood vessel:	n/a
11	chrX:32830005-32830055	AG10803	skin:	n/a
12	chrX:32886461-32886511	SK-N-MC	brain:	n/a
13	chrX:32886526-32886576	MCF10A-Er-Src	breast:	n/a
14	chrX:32886461-32886511	T-47D	breast:	n/a
15	chrX:32886461-32886511	CMK	blood:	n/a
16	chrX:32830005-32830055	ECC-1	luminal epithelium:	n/a
17	chrX:32886526-32886576	HRPEpiC	eye:	n/a
18	chrX:32886526-32886576	HPAEpiC	pulmonary alveolar:	n/a
19	chrX:32830005-32830055	HCM	heart:	n/a
20	chrX:32830005-32830055	GM06990	blood:	n/a
21	chrX:32886526-32886576	SK-N-SH	brain:	n/a
22	chrX:32886461-32886511	HCF	heart:	n/a
23	chrX:32830005-32830055	NHBE	bronchial:	n/a
24	chrX:32886526-32886576	AG04449	skin:	fetal
25	chrX:32886526-32886576	HCF	heart:	n/a
26	chrX:32830005-32830055	IMR90	lung:	fetal
27	chrX:32830005-32830055	BJ	skin:	n/a
28	chrX:32886526-32886576	PrEC	prostate:	n/a
29	chrX:32830005-32830055	Jurkat	blood:	n/a
30	chrX:32830005-32830055	MCF10A-Er-Src	breast:	n/a
31	chrX:32830005-32830055	HCT-116	colon:	n/a
32	chrX:32830005-32830055	HMEC	breast:	n/a
33	chrX:32886526-32886576	AoSMC	blood vessel:	n/a
34	chrX:32886461-32886511	NHBE	bronchial:	n/a
35	chrX:32886461-32886511	MCF-7	breast:	n/a
36	chrX:32886526-32886576	GM12878	blood:	n/a
37	chrX:32830005-32830055	AG04450	lung:	fetal
38	chrX:32886461-32886511	ECC-1	luminal epithelium:	n/a
39	chrX:32886526-32886576	HL-60	blood:	n/a
40	chrX:32886461-32886511	SAEC	small airway:	n/a
41	chrX:32830005-32830055	T-47D	breast:	n/a
42	chrX:32886461-32886511	AG10803	skin:	n/a
43	chrX:32886461-32886511	NT2-D1	testis:	n/a
44	chrX:32886461-32886511	PFSK-1	brain:	n/a
45	chrX:32886461-32886511	SK-N-SH	brain:	n/a
46	chrX:32886526-32886576	BE2_C	brain:	n/a
47	chrX:32886526-32886576	GM12892	blood:	n/a
48	chrX:32886526-32886576	NHDF-neo	bronchial:	n/a
49	chrX:32830005-32830055	HL-60	blood:	n/a
50	chrX:32830005-32830055	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chrX:32655856..32658575-chrX:32677287..32679370,2	K562	blood:
2	chrX:32606529..32609056-chrX:32614717..32616684,2	MCF-7	breast:
3	chrX:32796881..32797760-chrX:33354782..33355607,2	MCF-7	breast:
4	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
5	chrX:32548514..32549611-chrX:32691023..32691979,7	MCF-7	breast:
6	chrX:32548514..32549611-chrX:32691023..32691979,7	MCF-7	breast:
7	chrX:32730300..32733184-chrX:32737729..32739420,3	K562	blood:
8	chrX:32614664..32616473-chrX:32617936..32619637,2	K562	blood:
9	chr7:145238372..145239192-chrX:32945954..32946528,2	MCF-7	breast:
10	chrX:32614664..32616473-chrX:32617936..32619637,2	K562	blood:
11	chrX:32548603..32550280-chrX:33354588..33355586,5	MCF-7	breast:
12	chr17:2781701..2782584-chrX:32736765..32737525,2	MCF-7	breast:
13	chrX:32606529..32609056-chrX:32614717..32616684,2	MCF-7	breast:
14	chr14:62163002..62163505-chrX:32541852..32542352,2	Hela-S3	cervix:
15	chrX:32501789..32502365-chrX:32691222..32691959,2	MCF-7	breast:
16	chrX:32655856..32658575-chrX:32677287..32679370,2	K562	blood:
17	chr1:185868339..185869318-chrX:32631259..32632008,2	MCF-7	breast:

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

miRNA name	Chromosome Location	mirBase accession
hsa-miR-548f-3p	chrX:32659607-32659625	MIMAT0005895_4
hsa-miR-3915	chrX:32601828-32601849	MIMAT0018189

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	DMD	hsa-miR-31-5p	chrX:32535896-32535916
2	DMD	hsa-miR-155-5p	chrX:32534996-32535018

Variant related genes	Relation type
MIR548F5	TF binding region
DMD-AS3	TF binding region
DMD	TF binding region
MIR3915	TF binding region
ENSG00000238969	TF binding region
MIR548F5	CpG island
DMD-AS3	CpG island
DMD	CpG island
MIR3915	CpG island
ENSG00000238969	CpG island

Extended variants
information (count: 7363 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:7363 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs371594190	chrX:32519856-32519857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs373821159	chrX:32519858-32519859	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs183120304	chrX:32519861-32519862	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372330460	chrX:32519862-32519863	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs398123885	chrX:32519870-32519871	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs398123884	chrX:32519871-32519872	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs398123886	chrX:32519872-32519873	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs376648723	chrX:32519885-32519886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142006072	chrX:32519900-32519901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs1800260	chrX:32519901-32519902	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs150692967	chrX:32519906-32519907	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs398123883	chrX:32519920-32519921	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs369659071	chrX:32519921-32519922	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs128626244	chrX:32519935-32519936	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs267606770	chrX:32519938-32519939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs128626243	chrX:32519944-32519945	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201366610	chrX:32519950-32519951	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs398123882	chrX:32519955-32519956	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs372490563	chrX:32519956-32519957	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs377050013	chrX:32519967-32519968	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs369384547	chrX:32519974-32519975	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs200635632	chrX:32519996-32519997	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs6631594	chrX:32519999-32520000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs554295315	chrX:32520111-32520112	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs188722153	chrX:32520121-32520122	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs113653591	chrX:32520138-32520139	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs72468685	chrX:32520141-32520142	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs72468686	chrX:32520142-32520143	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs72468687	chrX:32520144-32520145	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs2473457	chrX:32520168-32520169	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs368099332	chrX:32520194-32520195	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375551991	chrX:32520229-32520230	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs191146390	chrX:32520263-32520264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs112608737	chrX:32520301-32520302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs182573760	chrX:32520306-32520307	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs368408048	chrX:32520316-32520317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs572997872	chrX:32520330-32520331	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188437755	chrX:32520347-32520348	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs540421987	chrX:32520439-32520440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs191636749	chrX:32520504-32520505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs6631595	chrX:32520522-32520523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs112014765	chrX:32520555-32520556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs564887936	chrX:32520598-32520599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529003503	chrX:32520607-32520608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs375396590	chrX:32520637-32520638	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs201590856	chrX:32520749-32520750	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187413725	chrX:32520770-32520771	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs145557597	chrX:32520799-32520800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs192564199	chrX:32520811-32520812	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367667824	chrX:32520836-32520837	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
Duchenne and Becker muscular dystrophies	18663755	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:32509400-32520200	Weak transcription	Skeletal Muscle Female	skeletal muscle
2	chrX:32519800-32520200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chrX:32520200-32523400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chrX:32523400-32523600	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin03	Skin
5	chrX:32523600-32524200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
6	chrX:32524200-32525200	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
7	chrX:32525200-32525400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
8	chrX:32527800-32529200	Enhancers	Fetal Heart	heart
9	chrX:32542600-32543000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
10	chrX:32542600-32543800	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chrX:32542800-32543200	Active TSS	Brain Inferior Temporal Lobe	brain
12	chrX:32542800-32544200	Enhancers	Brain Hippocampus Middle	brain
13	chrX:32543000-32543200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
14	chrX:32543000-32546400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
15	chrX:32543200-32543600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chrX:32543200-32543800	Enhancers	Brain Substantia Nigra	brain
17	chrX:32543200-32544200	Enhancers	Brain Inferior Temporal Lobe	brain
18	chrX:32543400-32543600	Enhancers	Brain Angular Gyrus	brain
19	chrX:32543400-32543800	Enhancers	Brain Anterior Caudate	brain
20	chrX:32543600-32549200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
21	chrX:32546000-32546800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chrX:32546000-32546800	Enhancers	HUES6 Cell Line	embryonic stem cell
23	chrX:32546400-32546800	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chrX:32546800-32551200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
25	chrX:32546800-32552000	Weak transcription	HUES6 Cell Line	embryonic stem cell
26	chrX:32546800-32556000	Weak transcription	HUES48 Cell Line	embryonic stem cell
27	chrX:32548800-32549400	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chrX:32549000-32549400	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
29	chrX:32549000-32549400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chrX:32549000-32549400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
31	chrX:32549000-32549400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chrX:32549000-32549400	Active TSS	Fetal Kidney	kidney
33	chrX:32549000-32549400	Active TSS	Ovary	ovary
34	chrX:32549200-32549400	Enhancers	HUES64 Cell Line	embryonic stem cell
35	chrX:32549200-32549400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
36	chrX:32549200-32549400	Enhancers	Fetal Brain Male	brain
37	chrX:32549200-32549400	Active TSS	Fetal Intestine Small	intestine
38	chrX:32549200-32549600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
39	chrX:32549200-32549600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
40	chrX:32549200-32549600	Enhancers	Primary T cells from cord blood	blood
41	chrX:32549200-32549600	Active TSS	Brain Substantia Nigra	brain
42	chrX:32549200-32549600	Active TSS	Duodenum Smooth Muscle	Duodenum
43	chrX:32549200-32550800	Enhancers	Muscle Satellite Cultured Cells	--
44	chrX:32549400-32549800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chrX:32549400-32549800	Enhancers	Brain Angular Gyrus	brain
46	chrX:32549400-32550800	Enhancers	HUVEC	blood vessel
47	chrX:32549400-32554000	Weak transcription	Fetal Intestine Small	intestine
48	chrX:32549600-32549800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
49	chrX:32549600-32551600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
50	chrX:32551200-32552600	Enhancers	ES-I3 Cell Line	embryonic stem cell

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