Variant report

Variant	nsv916714
Chromosome Location	chrX:64178342-64589821
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1162)
CpG islands
(count:1162)
Chromatin interactive
region (count:8)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:64196286-64196660	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:64416252-64416374	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:64414475-64414787	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:64416696-64417137	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:64313546-64313855	HepG2	liver:	n/a	n/a
6	ARID3A	chrX:64415577-64415931	HepG2	liver:	n/a	n/a
7	ARID3A	chrX:64254539-64254883	HepG2	liver:	n/a	n/a
8	ARID3A	chrX:64460959-64461631	HepG2	liver:	n/a	n/a
9	ATF2	chrX:64520272-64520693	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chrX:64254554-64254813	K562	blood:	n/a	n/a
11	BACH1	chrX:64255167-64255425	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chrX:64416839-64417155	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chrX:64254403-64254878	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chrX:64254337-64254736	K562	blood:	n/a	n/a
15	BHLHE40	chrX:64554722-64554914	K562	blood:	n/a	n/a
16	BHLHE40	chrX:64416852-64417205	HepG2	liver:	n/a	n/a
17	BHLHE40	chrX:64237067-64237141	GM12878	blood:	n/a	n/a
18	BHLHE40	chrX:64254449-64254813	K562	blood:	n/a	chrX:64254761-64254777
19	BHLHE40	chrX:64255359-64255559	K562	blood:	n/a	n/a
20	CCNT2	chrX:64254483-64255200	K562	blood:	n/a	chrX:64255081-64255090 chrX:64254622-64254631
21	CEBPB	chrX:64461880-64461987	A549	lung:	n/a	n/a
22	CEBPB	chrX:64214194-64214641	HepG2	liver:	n/a	chrX:64214490-64214501 chrX:64214492-64214503
23	CEBPB	chrX:64433916-64434183	K562	blood:	n/a	n/a
24	CEBPB	chrX:64459120-64459415	HepG2	liver:	n/a	chrX:64459263-64459274
25	CEBPB	chrX:64460992-64462135	HepG2	liver:	n/a	n/a
26	CEBPB	chrX:64214441-64214570	A549	lung:	n/a	chrX:64214490-64214501 chrX:64214492-64214503
27	CEBPB	chrX:64459246-64459344	IMR90	lung:	n/a	chrX:64459263-64459274
28	CEBPB	chrX:64523837-64524062	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:64313588-64313868	HepG2	liver:	n/a	chrX:64313747-64313758
30	CEBPB	chrX:64424947-64425160	IMR90	lung:	n/a	n/a
31	CEBPB	chrX:64523684-64523978	HepG2	liver:	n/a	chrX:64523739-64523750
32	CEBPB	chrX:64313652-64313841	HepG2	liver:	n/a	chrX:64313747-64313758
33	CEBPB	chrX:64383864-64384064	HepG2	liver:	n/a	n/a
34	CEBPB	chrX:64491299-64491461	H1-hESC	embryonic stem cell:	n/a	chrX:64491358-64491369
35	CEBPB	chrX:64256692-64256925	HepG2	liver:	n/a	chrX:64256817-64256828
36	CEBPB	chrX:64313557-64313919	HepG2	liver:	n/a	chrX:64313747-64313758
37	CEBPB	chrX:64416977-64417229	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPD	chrX:64460934-64461157	HepG2	liver:	n/a	n/a
39	CHD1	chrX:64255124-64255207	H1-hESC	embryonic stem cell:	n/a	chrX:64255184-64255191
40	CHD1	chrX:64255482-64255489	H1-hESC	embryonic stem cell:	n/a	n/a
41	CHD2	chrX:64318802-64318980	HepG2	liver:	n/a	n/a
42	CHD2	chrX:64195471-64195875	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chrX:64254432-64255122	HepG2	liver:	n/a	n/a
44	CHD2	chrX:64416878-64417156	HepG2	liver:	n/a	chrX:64417139-64417146 chrX:64417013-64417020
45	CHD2	chrX:64254443-64255168	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chrX:64416836-64417145	H1-hESC	embryonic stem cell:	n/a	chrX:64417013-64417020
47	CHD2	chrX:64195481-64195681	HepG2	liver:	n/a	n/a
48	CHD2	chrX:64254439-64254685	K562	blood:	n/a	n/a
49	CREB1	chrX:64254463-64254934	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chrX:64416951-64417138	A549	lung:	n/a	n/a

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:64258522-64258572	RPTEC	kidney:	n/a
2	chrX:64196642-64196692	HEEpiC	esophagus:	n/a
3	chrX:64196495-64196545	SK-N-SH_RA	brain:	n/a
4	chrX:64258522-64258572	RPTEC	kidney:	n/a
5	chrX:64196642-64196692	HEEpiC	esophagus:	n/a
6	chrX:64196495-64196545	SK-N-SH_RA	brain:	n/a
7	chrX:64254409-64254459	HEEpiC	esophagus:	n/a
8	chrX:64196688-64196738	NT2-D1	testis:	n/a
9	chrX:64255215-64255265	LNCaP	prostate:	n/a
10	chrX:64196367-64196417	SK-N-SH	brain:	n/a
11	chrX:64254615-64254665	NT2-D1	testis:	n/a
12	chrX:64196367-64196417	IMR90	lung:	fetal
13	chrX:64258522-64258572	K562	blood:	n/a
14	chrX:64254240-64254290	Jurkat	blood:	n/a
15	chrX:64254409-64254459	MCF-7	breast:	n/a
16	chrX:64254409-64254459	AG09309	skin:	n/a
17	chrX:64196343-64196393	HEEpiC	esophagus:	n/a
18	chrX:64196343-64196393	GM12878	blood:	n/a
19	chrX:64254961-64255011	HepG2	liver:	n/a
20	chrX:64196343-64196393	HAEpiC	amniotic membrane:	n/a
21	chrX:64195554-64195604	T-47D	breast:	n/a
22	chrX:64252337-64252387	GM12892	blood:	n/a
23	chrX:64254240-64254290	BJ	skin:	n/a
24	chrX:64255215-64255265	HL-60	blood:	n/a
25	chrX:64254240-64254290	SK-N-SH_RA	brain:	n/a
26	chrX:64196688-64196738	HNPCEpiC	eye:	n/a
27	chrX:64255215-64255265	SK-N-SH	brain:	n/a
28	chrX:64196751-64196801	BJ	skin:	n/a
29	chrX:64254961-64255011	BJ	skin:	n/a
30	chrX:64255552-64255602	SK-N-MC	brain:	n/a
31	chrX:64196367-64196417	BE2_C	brain:	n/a
32	chrX:64254961-64255011	HNPCEpiC	eye:	n/a
33	chrX:64196688-64196738	HRPEpiC	eye:	n/a
34	chrX:64196688-64196738	HEEpiC	esophagus:	n/a
35	chrX:64254961-64255011	AG04450	lung:	fetal
36	chrX:64196429-64196479	PFSK-1	brain:	n/a
37	chrX:64196642-64196692	SK-N-SH	brain:	n/a
38	chrX:64254667-64254717	HAEpiC	amniotic membrane:	n/a
39	chrX:64254615-64254665	SK-N-SH	brain:	n/a
40	chrX:64196429-64196479	SK-N-SH	brain:	n/a
41	chrX:64196751-64196801	NB4	blood:	n/a
42	chrX:64196278-64196328	SK-N-SH	brain:	n/a
43	chrX:64258522-64258572	SKMC	muscle:	n/a
44	chrX:64254615-64254665	ovcar-3	ovarian:	n/a
45	chrX:64255552-64255602	SK-N-SH	brain:	n/a
46	chrX:64196343-64196393	SK-N-SH	brain:	n/a
47	chrX:64255552-64255602	HCF	heart:	n/a
48	chrX:64196278-64196328	ECC-1	luminal epithelium:	n/a
49	chrX:64254667-64254717	HMEC	breast:	n/a
50	chrX:64196343-64196393	LNCaP	prostate:	n/a

(count:8 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:64250483..64252430-chrX:64253204..64254797,2	K562	blood:
2	chrX:63149790..63150339-chrX:64416655..64417486,2	MCF-7	breast:
3	chrX:64257340..64260132-chrX:64261723..64264244,2	K562	blood:
4	chrX:64254509..64258840-chrX:64260564..64264244,4	K562	blood:
5	chrX:64257340..64260132-chrX:64261723..64264244,2	K562	blood:
6	chrX:64254063..64256043-chrX:64262099..64265105,3	K562	blood:
7	chrX:64192783..64194290-chrX:64194685..64197450,2	K562	blood:
8	chrX:64114357..64115134-chrX:64416597..64417121,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZC3H12B-2	chrX:64295724-64295792	XLOC_008000
2	lnc-ZC3H12B-3	chrX:64254714-64255149	XLOC_007999
3	lnc-ZC4H2-1	chrX:64407010-64407145	NONHSAT137330
4	lnc-ZC3H12B-2	chrX:64311000-64311672	XLOC_008000
5	lnc-ZC4H2-1	chrX:64406389-64406425	NONHSAT137330
6	lnc-ZC3H12B-1	chrX:64586534-64586642	XLOC_008001
7	lnc-LAS1L-4	chrX:64550687-64551113	NONHSAT137333
8	lnc-ZC3H12B-8	chrX:64490793-64491321	NONHSAT137332
9	lnc-ZC3H12B-1	chrX:64588709-64588866	XLOC_008001
10	lnc-ZC3H12B-8	chrX:64491555-64491807	NONHSAT137332
11	lnc-ZC3H12B-2	chrX:64333544-64333726	XLOC_008000
12	lnc-ZC3H12B-3	chrX:64271342-64272117	XLOC_007999
13	lnc-LAS1L-4	chrX:64547868-64548401	NONHSAT137333
14	lnc-ZC3H12B-1	chrX:64588724-64588878	XLOC_008001
15	lnc-ZC4H2-1	chrX:64404898-64406086	NONHSAT137330
16	lnc-ZC3H12B-2	chrX:64295733-64295792	XLOC_008000
17	lnc-ZC3H12B-8	chrX:64492134-64492899	NONHSAT137332
18	lnc-ZC3H12B-2	chrX:64295361-64295550	XLOC_008000

No data

Variant related genes	Relation type
CCT4P2	TF binding region
ENSG00000237963	TF binding region
MORF4L1P5	TF binding region
ENSG00000237971	TF binding region
ENSG00000222596	TF binding region
ZC4H2	TF binding region
CCT4P2	CpG island
ENSG00000237963	CpG island
MORF4L1P5	CpG island
ENSG00000237971	CpG island
ENSG00000222596	CpG island
ZC4H2	CpG island
ENSG00000126970	chromatin interactions
USP25	miRNA target sites
UBL3	miRNA target sites
UBN2	miRNA target sites
USP3	miRNA target sites

Extended variants
information (count: 2416 )
Associated
traits (count: 40 )

Variant overlapped rSNPs/rCNVs (count:2416 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs188352461	chrX:64179670-64179671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs193035285	chrX:64179833-64179834	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs73512577	chrX:64179873-64179874	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs141678146	chrX:64179927-64179928	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185626596	chrX:64179975-64179976	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190532342	chrX:64180023-64180024	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs180982059	chrX:64180026-64180027	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs183730575	chrX:64180113-64180114	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs5964889	chrX:64180115-64180116	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
10	rs200355569	chrX:64180192-64180193	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs559620898	chrX:64180281-64180282	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs188840822	chrX:64180515-64180516	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs149630357	chrX:64180548-64180549	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs143395875	chrX:64180825-64180826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs375550131	chrX:64180937-64180938	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs181274386	chrX:64180983-64180984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs566409944	chrX:64181020-64181021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs186314746	chrX:64181037-64181038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs191618857	chrX:64181057-64181058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs181660927	chrX:64181102-64181103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs187300484	chrX:64181181-64181182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190801546	chrX:64181195-64181196	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs372613642	chrX:64181298-64181299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182306272	chrX:64181327-64181328	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs374766032	chrX:64181383-64181384	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs186616862	chrX:64181441-64181442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs199498661	chrX:64181517-64181518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs144713066	chrX:64181525-64181526	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs138513693	chrX:64181649-64181650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs190281338	chrX:64181825-64181826	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs183002968	chrX:64181887-64181888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs375661297	chrX:64181925-64181926	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs188138237	chrX:64182020-64182021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs72623472	chrX:64182037-64182038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs146192765	chrX:64182228-64182229	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs192952067	chrX:64182304-64182305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs185206285	chrX:64182340-64182341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs12014990	chrX:64182388-64182389	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs188036107	chrX:64182504-64182505	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539822391	chrX:64182848-64182849	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs192495650	chrX:64182972-64182973	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183966162	chrX:64182986-64182987	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs188300159	chrX:64182994-64182995	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs150559070	chrX:64183014-64183015	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs180703131	chrX:64183028-64183029	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs530775822	chrX:64183348-64183349	ZNF genes & repeats Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs199782941	chrX:64183444-64183445	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
48	rs184837288	chrX:64183503-64183504	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs189731938	chrX:64183642-64183643	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs73512581	chrX:64183647-64183648	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:40)

Disease	PMID	Source
Intellectual disability	23615299	CNVD
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	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
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Wilms tumour	17204608	CNVD
craniofacial dysmorphism	21918468	CNVD
Astrocytoma	22246337	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
turner syndrome	20570968	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1086 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:64179600-64180600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
2	chrX:64179800-64180600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chrX:64180600-64187000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chrX:64182600-64183400	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
5	chrX:64182800-64185600	ZNF genes & repeats	Dnd41	blood
6	chrX:64183400-64184200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
7	chrX:64183600-64195200	Weak transcription	Duodenum Smooth Muscle	Duodenum
8	chrX:64184200-64184400	ZNF genes & repeats	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
9	chrX:64184200-64184600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chrX:64184200-64185000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chrX:64184400-64184600	ZNF genes & repeats	Primary hematopoietic stem cells	blood
12	chrX:64184400-64194800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chrX:64184600-64191400	Weak transcription	Primary hematopoietic stem cells	blood
14	chrX:64184600-64191400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chrX:64184800-64185000	Enhancers	Primary T helper naive cells from peripheral blood	blood
16	chrX:64184800-64190600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chrX:64185000-64191200	Weak transcription	Fetal Lung	lung
18	chrX:64185000-64191800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
19	chrX:64185000-64194400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chrX:64185600-64185800	Enhancers	Left Ventricle	heart
21	chrX:64185600-64191600	Weak transcription	Dnd41	blood
22	chrX:64185800-64186400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chrX:64185800-64186400	Enhancers	iPS-20b Cell Line	embryonic stem cell
24	chrX:64186000-64186400	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chrX:64186400-64191600	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chrX:64187000-64187200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
27	chrX:64187600-64195200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
28	chrX:64188200-64188400	ZNF genes & repeats	H9 Derived Neuron Cultured Cells	ES cell derived
29	chrX:64188400-64194600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
30	chrX:64188800-64189000	Enhancers	HSMMtube	muscle
31	chrX:64189000-64189600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
32	chrX:64189000-64195000	Weak transcription	HSMMtube	muscle
33	chrX:64189800-64190000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
34	chrX:64189800-64190400	Weak transcription	Ovary	ovary
35	chrX:64189800-64191600	Weak transcription	H1 Cell Line	embryonic stem cell
36	chrX:64189800-64195000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chrX:64190000-64191400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chrX:64190200-64194800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
39	chrX:64190400-64191800	Strong transcription	Ovary	ovary
40	chrX:64190600-64192400	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
41	chrX:64190600-64192600	ZNF genes & repeats	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chrX:64191400-64192400	ZNF genes & repeats	Primary hematopoietic stem cells	blood
43	chrX:64191400-64192400	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Male	--
44	chrX:64191600-64191800	Strong transcription	H1 Cell Line	embryonic stem cell
45	chrX:64191600-64192400	Strong transcription	Dnd41	blood
46	chrX:64191600-64193000	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
47	chrX:64191800-64192000	Weak transcription	H1 Cell Line	embryonic stem cell
48	chrX:64191800-64192200	ZNF genes & repeats	Liver	Liver
49	chrX:64191800-64192400	ZNF genes & repeats	Fetal Kidney	kidney
50	chrX:64191800-64193000	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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