Variant report

Variant	esv2752740
Chromosome Location	chrX:124453577-124831349
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1433)
CpG islands
(count:427)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1433 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:124538307-124538911	K562	blood:	n/a	n/a
2	ARID3A	chrX:124573126-124573585	K562	blood:	n/a	n/a
3	ARID3A	chrX:124531456-124531570	K562	blood:	n/a	n/a
4	ARID3A	chrX:124532661-124533213	K562	blood:	n/a	n/a
5	ARID3A	chrX:124554665-124555085	K562	blood:	n/a	n/a
6	ARID3A	chrX:124626306-124626498	K562	blood:	n/a	n/a
7	ARID3A	chrX:124474326-124474710	K562	blood:	n/a	n/a
8	ATF1	chrX:124538361-124538958	K562	blood:	n/a	n/a
9	ATF1	chrX:124761916-124762116	K562	blood:	n/a	n/a
10	ATF1	chrX:124573169-124573627	K562	blood:	n/a	n/a
11	ATF1	chrX:124532639-124533180	K562	blood:	n/a	n/a
12	ATF1	chrX:124474355-124474773	K562	blood:	n/a	n/a
13	ATF2	chrX:124518028-124518309	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chrX:124522436-124522750	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF3	chrX:124474469-124474815	K562	blood:	n/a	n/a
16	ATF3	chrX:124538540-124538897	K562	blood:	n/a	n/a
17	BACH1	chrX:124556855-124557190	K562	blood:	n/a	n/a
18	BACH1	chrX:124528806-124529170	H1-hESC	embryonic stem cell:	n/a	chrX:124529112-124529126
19	BACH1	chrX:124588583-124588653	K562	blood:	n/a	n/a
20	BACH1	chrX:124453515-124453820	H1-hESC	embryonic stem cell:	n/a	chrX:124453702-124453716
21	BHLHE40	chrX:124538398-124539158	K562	blood:	n/a	n/a
22	BHLHE40	chrX:124578540-124578671	K562	blood:	n/a	n/a
23	BHLHE40	chrX:124626340-124626679	K562	blood:	n/a	n/a
24	BHLHE40	chrX:124573193-124573598	K562	blood:	n/a	n/a
25	BHLHE40	chrX:124474562-124474804	K562	blood:	n/a	n/a
26	BHLHE40	chrX:124532546-124533299	K562	blood:	n/a	n/a
27	CBX3	chrX:124627041-124627573	K562	blood:	n/a	n/a
28	CBX3	chrX:124600831-124601147	K562	blood:	n/a	n/a
29	CBX3	chrX:124538353-124539092	K562	blood:	n/a	n/a
30	CBX3	chrX:124478381-124478739	K562	blood:	n/a	n/a
31	CBX3	chrX:124573100-124573598	K562	blood:	n/a	n/a
32	CBX3	chrX:124671456-124671735	K562	blood:	n/a	n/a
33	CBX3	chrX:124532623-124533385	K562	blood:	n/a	n/a
34	CBX3	chrX:124620762-124621042	K562	blood:	n/a	n/a
35	CBX3	chrX:124492670-124493002	K562	blood:	n/a	n/a
36	CBX3	chrX:124626264-124626739	K562	blood:	n/a	n/a
37	CBX3	chrX:124472731-124473134	K562	blood:	n/a	n/a
38	CBX3	chrX:124578433-124579025	K562	blood:	n/a	n/a
39	CBX3	chrX:124474300-124474679	K562	blood:	n/a	n/a
40	CBX3	chrX:124572965-124573696	K562	blood:	n/a	n/a
41	CCNT2	chrX:124474308-124474654	K562	blood:	n/a	n/a
42	CCNT2	chrX:124756950-124757249	K562	blood:	n/a	n/a
43	CCNT2	chrX:124573160-124573684	K562	blood:	n/a	n/a
44	CCNT2	chrX:124538266-124539057	K562	blood:	n/a	n/a
45	CCNT2	chrX:124532708-124533182	K562	blood:	n/a	n/a
46	CEBPB	chrX:124560505-124560734	K562	blood:	n/a	chrX:124560568-124560585
47	CEBPB	chrX:124513944-124514183	K562	blood:	n/a	n/a
48	CEBPB	chrX:124578745-124578775	K562	blood:	n/a	n/a
49	CEBPB	chrX:124668764-124669112	IMR90	lung:	n/a	chrX:124668933-124668942 chrX:124668931-124668944 chrX:124668933-124668944
50	CEBPB	chrX:124464017-124464308	A549	lung:	n/a	chrX:124464168-124464181

(count:427 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:124454138-124454188	MCF-7	breast:	n/a
2	chrX:124454351-124454401	SK-N-MC	brain:	n/a
3	chrX:124456912-124456962	HMEC	breast:	n/a
4	chrX:124456912-124456962	MCF10A-Er-Src	breast:	n/a
5	chrX:124454138-124454188	HepG2	liver:	n/a
6	chrX:124456912-124456962	CMK	blood:	n/a
7	chrX:124453915-124453965	AG04449	skin:	fetal
8	chrX:124454052-124454102	NHDF-neo	bronchial:	n/a
9	chrX:124454052-124454102	AG04450	lung:	fetal
10	chrX:124453998-124454048	HNPCEpiC	eye:	n/a
11	chrX:124454138-124454188	AoSMC	blood vessel:	n/a
12	chrX:124454351-124454401	RPTEC	kidney:	n/a
13	chrX:124456912-124456962	HRE	kidney:	n/a
14	chrX:124454052-124454102	HCM	heart:	n/a
15	chrX:124453998-124454048	SK-N-MC	brain:	n/a
16	chrX:124453915-124453965	H1-hESC	embryonic stem cell:	embryo
17	chrX:124454052-124454102	HCT-116	colon:	n/a
18	chrX:124456912-124456962	GM12892	blood:	n/a
19	chrX:124453998-124454048	PrEC	prostate:	n/a
20	chrX:124453998-124454048	HCF	heart:	n/a
21	chrX:124454351-124454401	PrEC	prostate:	n/a
22	chrX:124453998-124454048	HMEC	breast:	n/a
23	chrX:124453915-124453965	HepG2	liver:	n/a
24	chrX:124454052-124454102	HUVEC	blood vessel:	n/a
25	chrX:124456912-124456962	SK-N-SH_RA	brain:	n/a
26	chrX:124453998-124454048	RPTEC	kidney:	n/a
27	chrX:124453998-124454048	LNCaP	prostate:	n/a
28	chrX:124454351-124454401	GM19239	blood:	n/a
29	chrX:124453915-124453965	GM12891	blood:	n/a
30	chrX:124453701-124453751	IMR90	lung:	fetal
31	chrX:124456912-124456962	PrEC	prostate:	n/a
32	chrX:124454138-124454188	Hepatocyte	liver:	n/a
33	chrX:124454138-124454188	HRPEpiC	eye:	n/a
34	chrX:124454138-124454188	GM19239	blood:	n/a
35	chrX:124453701-124453751	CMK	blood:	n/a
36	chrX:124453701-124453751	NT2-D1	testis:	n/a
37	chrX:124454052-124454102	U87	brain:	n/a
38	chrX:124453998-124454048	GM12892	blood:	n/a
39	chrX:124453701-124453751	Caco-2	colon:	n/a
40	chrX:124456912-124456962	AG04450	lung:	fetal
41	chrX:124454052-124454102	HMEC	breast:	n/a
42	chrX:124453701-124453751	HCT-116	colon:	n/a
43	chrX:124454052-124454102	GM12891	blood:	n/a
44	chrX:124456912-124456962	K562	blood:	n/a
45	chrX:124454138-124454188	NH-A	brain:	n/a
46	chrX:124453998-124454048	NT2-D1	testis:	n/a
47	chrX:124453915-124453965	HCPEpiC	choroid plexus:	n/a
48	chrX:124453998-124454048	NHDF-neo	bronchial:	n/a
49	chrX:124454052-124454102	HIPEpiC	eye:	n/a
50	chrX:124456912-124456962	LNCaP	prostate:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:124286744..124288828-chrX:124531482..124534155,2	K562	blood:
2	chrX:124459379..124462723-chrX:124463443..124466506,3	K562	blood:
3	chrX:124533854..124536452-chrX:124549847..124552321,2	K562	blood:
4	chrX:124586860..124588579-chrX:124611029..124613342,2	K562	blood:
5	chrX:124546882..124550088-chrX:124553422..124556329,3	K562	blood:
6	chr11:6563760..6564675-chrX:124504983..124505570,2	MCF-7	breast:
7	chrX:124463472..124465349-chrX:124537906..124540191,2	K562	blood:
8	chrX:124586860..124588579-chrX:124611029..124613342,2	K562	blood:
9	chrX:124463472..124465349-chrX:124537906..124540191,2	K562	blood:
10	chrX:124575740..124578658-chrX:124582031..124584324,2	K562	blood:
11	chrX:124625185..124626777-chrX:124629793..124632444,2	K562	blood:
12	chr10:10353343..10355322-chrX:124498843..124501284,2	MCF-7	breast:
13	chrX:124465526..124467210-chrX:124549514..124551961,2	K562	blood:
14	chrX:124531548..124534899-chrX:124536638..124539362,3	K562	blood:
15	chrX:124283216..124285131-chrX:124486668..124488289,2	K562	blood:
16	chrX:124538796..124541138-chrX:124542342..124545219,4	K562	blood:
17	chrX:124575740..124578658-chrX:124582031..124584324,2	K562	blood:
18	chrX:124533854..124536452-chrX:124549847..124552321,2	K562	blood:
19	chrX:124538796..124540373-chrX:124542342..124545024,2	K562	blood:
20	chrX:124546882..124550088-chrX:124553422..124556329,3	K562	blood:
21	chrX:124531548..124534899-chrX:124536638..124539362,3	K562	blood:
22	chrX:124538796..124541138-chrX:124542342..124545219,4	K562	blood:
23	chrX:124465526..124467210-chrX:124549514..124551961,2	K562	blood:
24	chrX:124625185..124626777-chrX:124629793..124632444,2	K562	blood:
25	chrX:124538796..124540373-chrX:124542342..124545024,2	K562	blood:

(count:2 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STAG2-2	chrX:124453629-124456969	XLOC_008063
2	lnc-STAG2-2	chrX:124457549-124459062	XLOC_008063

No data

Variant related genes	Relation type
ENSG00000213489	TF binding region
ENSG00000222518	TF binding region
ENSG00000213489	CpG island
ENSG00000222518	CpG island
ENSG00000213489	chromatin interactions

Extended variants
information (count: 1638 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:1638 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs3135230	chrX:124453577-124453578	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs190942375	chrX:124453578-124453579	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs180954129	chrX:124453596-124453597	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs185184695	chrX:124453607-124453608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73634597	chrX:124453619-124453620	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs139976641	chrX:124453733-124453734	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
7	rs73634598	chrX:124453876-124453877	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
8	rs183086858	chrX:124453897-124453898	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
9	rs187970855	chrX:124453965-124453966	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
10	rs375899922	chrX:124454083-124454084	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
11	rs113566377	chrX:124454094-124454095	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
12	rs149706721	chrX:124454187-124454188	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
13	rs145576211	chrX:124454311-124454312	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
14	rs192053192	chrX:124454391-124454392	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
15	rs183368644	chrX:124454400-124454401	Weak transcription ZNF genes & repeats	lncRNA	n/a	Overlapped CNVs	n/a
16	rs187836576	chrX:124454423-124454424	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
17	rs148419853	chrX:124454472-124454473	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
18	rs192356374	chrX:124454575-124454576	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
19	rs533141129	chrX:124454650-124454651	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
20	rs5976601	chrX:124454682-124454683	Weak transcription	lncRNA	n/a	Overlapped CNVs	n/a
21	rs186469713	chrX:124454805-124454806	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
22	rs191257614	chrX:124454876-124454877	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
23	rs185035240	chrX:124454978-124454979	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
24	rs189499649	chrX:124455170-124455171	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
25	rs367608564	chrX:124455259-124455260	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
26	rs370930316	chrX:124455307-124455308	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
27	rs182081365	chrX:124455321-124455322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
28	rs374579224	chrX:124455508-124455509	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
29	rs3135231	chrX:124455511-124455512	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
30	rs145777792	chrX:124455537-124455538	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
31	rs185066247	chrX:124455543-124455544	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
32	rs189534278	chrX:124455544-124455545	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
33	rs368215567	chrX:124455559-124455560	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
34	rs371219803	chrX:124455568-124455569	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
35	rs373947133	chrX:124455571-124455572	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
36	rs368158488	chrX:124455574-124455575	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
37	rs181806419	chrX:124455646-124455647	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
38	rs3135232	chrX:124455666-124455667	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs3135233	chrX:124455688-124455689	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs113331732	chrX:124455729-124455730	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs3135234	chrX:124455732-124455733	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs112184465	chrX:124455748-124455749	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
43	rs112537380	chrX:124455751-124455752	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
44	rs3135235	chrX:124455755-124455756	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
45	rs111226613	chrX:124455814-124455815	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
46	rs3135236	chrX:124455824-124455825	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
47	rs55827109	chrX:124455873-124455874	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
48	rs56129157	chrX:124455919-124455920	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
49	rs28720955	chrX:124455964-124455965	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs6637308	chrX:124456018-124456019	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
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
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
lymphocytic leukemia	21291569	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Astrocytoma	22246337	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Breast cancer	21364760	CNVD
Bladder cancer	24270882	CNVD
Breast cancer	17603634	CNVD
Melanoma	20877625	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Alcoholism	21790672	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD

Chromatin state (count:226 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:124453200-124454800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
2	chrX:124454000-124454400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
3	chrX:124464000-124464200	Bivalent/Poised TSS	Fetal Kidney	kidney
4	chrX:124467600-124471000	Weak transcription	K562	blood
5	chrX:124471000-124471800	Enhancers	K562	blood
6	chrX:124472600-124473000	Weak transcription	K562	blood
7	chrX:124473400-124473800	Weak transcription	K562	blood
8	chrX:124474000-124474800	Enhancers	K562	blood
9	chrX:124477800-124479800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chrX:124493200-124493400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
11	chrX:124503400-124504400	Enhancers	HUES6 Cell Line	embryonic stem cell
12	chrX:124503400-124504600	Enhancers	ES-I3 Cell Line	embryonic stem cell
13	chrX:124504200-124504600	Enhancers	iPS-15b Cell Line	embryonic stem cell
14	chrX:124512000-124512600	Enhancers	ES-I3 Cell Line	embryonic stem cell
15	chrX:124512000-124512600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
16	chrX:124512000-124512600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
17	chrX:124512000-124512800	Enhancers	HUES6 Cell Line	embryonic stem cell
18	chrX:124512400-124512800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
19	chrX:124512600-124519600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
20	chrX:124512800-124522000	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
21	chrX:124513800-124516200	Weak transcription	HUES6 Cell Line	embryonic stem cell
22	chrX:124514000-124514200	Enhancers	H9 Cell Line	embryonic stem cell
23	chrX:124514200-124518800	Weak transcription	H9 Cell Line	embryonic stem cell
24	chrX:124514600-124519400	Weak transcription	Right Atrium	heart
25	chrX:124515200-124518600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chrX:124515800-124516800	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chrX:124516000-124516200	Enhancers	H1 Cell Line	embryonic stem cell
28	chrX:124516000-124516800	Enhancers	HUES64 Cell Line	embryonic stem cell
29	chrX:124516200-124516400	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chrX:124516200-124518800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chrX:124516400-124516600	Enhancers	HUES48 Cell Line	embryonic stem cell
32	chrX:124516400-124518800	Weak transcription	HUES6 Cell Line	embryonic stem cell
33	chrX:124516600-124518200	Weak transcription	HUES48 Cell Line	embryonic stem cell
34	chrX:124516800-124518800	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chrX:124516800-124518800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
36	chrX:124517200-124518800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
37	chrX:124518200-124520400	Strong transcription	HUES48 Cell Line	embryonic stem cell
38	chrX:124518600-124520800	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
39	chrX:124518800-124519200	Genic enhancers	HUES6 Cell Line	embryonic stem cell
40	chrX:124518800-124519200	Genic enhancers	iPS-15b Cell Line	embryonic stem cell
41	chrX:124518800-124519200	ZNF genes & repeats	iPS-18 Cell Line	embryonic stem cell
42	chrX:124518800-124520800	Strong transcription	HUES64 Cell Line	embryonic stem cell
43	chrX:124518800-124521200	Strong transcription	iPS-20b Cell Line	embryonic stem cell
44	chrX:124518800-124521400	Strong transcription	H1 Cell Line	embryonic stem cell
45	chrX:124518800-124521400	Strong transcription	H9 Cell Line	embryonic stem cell
46	chrX:124519200-124520600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chrX:124519200-124521000	Strong transcription	HUES6 Cell Line	embryonic stem cell
48	chrX:124519200-124521800	Strong transcription	iPS-18 Cell Line	embryonic stem cell
49	chrX:124519400-124521800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
50	chrX:124519600-124520600	Strong transcription	ES-I3 Cell Line	embryonic stem cell

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