Variant report

Variant	esv3485324
Chromosome Location	chrX:124701343-125429067
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	ATF1	chrX:124891761-124892546	K562	blood:	n/a	n/a
2	ATF1	chrX:124761916-124762116	K562	blood:	n/a	n/a
3	ATF3	chrX:124892173-124892545	K562	blood:	n/a	n/a
4	BACH1	chrX:124901075-124901139	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chrX:125304750-125305056	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chrX:125405987-125406002	K562	blood:	n/a	n/a
7	BACH1	chrX:125079593-125079639	K562	blood:	n/a	n/a
8	BHLHE40	chrX:124892017-124892207	K562	blood:	n/a	n/a
9	CCNT2	chrX:124756950-124757249	K562	blood:	n/a	n/a
10	CEBPB	chrX:124712576-124712833	HepG2	liver:	n/a	n/a
11	CEBPB	chrX:124912986-124913253	K562	blood:	n/a	n/a
12	CEBPB	chrX:124994237-124994521	HepG2	liver:	n/a	chrX:124994386-124994403 chrX:124994329-124994342 chrX:124994389-124994400
13	CEBPB	chrX:124934292-124934492	IMR90	lung:	n/a	chrX:124934437-124934450
14	CEBPB	chrX:124806434-124806689	HepG2	liver:	n/a	chrX:124806558-124806567 chrX:124806556-124806569 chrX:124806558-124806569 chrX:124806556-124806569 chrX:124806558-124806567 chrX:124806558-124806567 chrX:124806556-124806567 chrX:124806558-124806567
15	CEBPB	chrX:124858967-124859217	IMR90	lung:	n/a	n/a
16	CEBPB	chrX:124712550-124712749	K562	blood:	n/a	n/a
17	CEBPB	chrX:124892983-124893065	K562	blood:	n/a	n/a
18	CEBPB	chrX:125060309-125060669	HepG2	liver:	n/a	chrX:125060481-125060494 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060481-125060492 chrX:125060483-125060492 chrX:125060481-125060494
19	CEBPB	chrX:125060299-125060676	IMR90	lung:	n/a	chrX:125060481-125060494 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060481-125060492 chrX:125060483-125060492 chrX:125060481-125060494
20	CEBPB	chrX:124789251-124789454	IMR90	lung:	n/a	chrX:124789333-124789342 chrX:124789333-124789344 chrX:124789333-124789342 chrX:124789333-124789342 chrX:124789331-124789344 chrX:124789333-124789342
21	CEBPB	chrX:124900305-124900417	K562	blood:	n/a	n/a
22	CEBPB	chrX:125305366-125305609	HepG2	liver:	n/a	chrX:125305485-125305496
23	CEBPB	chrX:124789183-124789325	K562	blood:	n/a	n/a
24	CEBPB	chrX:125311539-125311678	IMR90	lung:	n/a	n/a
25	CEBPB	chrX:124840823-124841023	HepG2	liver:	n/a	chrX:124840918-124840929
26	CEBPB	chrX:124912939-124913278	IMR90	lung:	n/a	n/a
27	CEBPB	chrX:124994273-124994500	IMR90	lung:	n/a	chrX:124994386-124994403 chrX:124994329-124994342 chrX:124994389-124994400
28	CEBPB	chrX:124806471-124806712	IMR90	lung:	n/a	chrX:124806558-124806567 chrX:124806556-124806569 chrX:124806558-124806569 chrX:124806556-124806569 chrX:124806558-124806567 chrX:124806558-124806567 chrX:124806556-124806567 chrX:124806558-124806567
29	CEBPB	chrX:124726439-124726653	HepG2	liver:	n/a	chrX:124726566-124726577
30	CEBPB	chrX:124810412-124810640	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chrX:124913043-124913259	A549	lung:	n/a	n/a
32	CEBPB	chrX:125074776-125074974	HepG2	liver:	n/a	chrX:125074925-125074936
33	CEBPB	chrX:124800402-124800705	IMR90	lung:	n/a	n/a
34	CEBPB	chrX:125089679-125089894	A549	lung:	n/a	chrX:125089828-125089841 chrX:125089828-125089841
35	CEBPB	chrX:125060310-125060666	A549	lung:	n/a	chrX:125060481-125060494 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060481-125060492 chrX:125060483-125060492 chrX:125060481-125060494
36	CEBPB	chrX:125060275-125060678	K562	blood:	n/a	chrX:125060481-125060494 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060481-125060492 chrX:125060483-125060492 chrX:125060481-125060494
37	CEBPB	chrX:125060347-125060638	Hela-S3	cervix:	n/a	chrX:125060481-125060494 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060481-125060492 chrX:125060483-125060492 chrX:125060481-125060494
38	CEBPB	chrX:124994279-124994510	K562	blood:	n/a	chrX:124994386-124994403 chrX:124994329-124994342 chrX:124994389-124994400
39	CEBPB	chrX:125060313-125060652	H1-hESC	embryonic stem cell:	n/a	chrX:125060481-125060494 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060483-125060492 chrX:125060481-125060492 chrX:125060483-125060492 chrX:125060481-125060494
40	CEBPB	chrX:124891937-124892174	K562	blood:	n/a	n/a
41	CEBPD	chrX:124864996-124865287	K562	blood:	n/a	n/a
42	CEBPD	chrX:124891848-124892325	K562	blood:	n/a	n/a
43	CEBPD	chrX:124915771-124916094	K562	blood:	n/a	n/a
44	CEBPD	chrX:124756936-124757364	K562	blood:	n/a	n/a
45	CREB1	chrX:124761876-124762119	K562	blood:	n/a	n/a
46	CREB1	chrX:125299970-125300391	H1-hESC	embryonic stem cell:	n/a	n/a
47	CREB1	chrX:125299958-125300400	H1-hESC	embryonic stem cell:	n/a	n/a
48	CTCF	chrX:124780266-124780507	A549	lung:	n/a	n/a
49	CTCF	chrX:125392252-125392271	GM20000	blood:	n/a	n/a
50	CTCF	chrX:125372822-125372874	GM10266	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:125299033-125299083	AG09309	skin:	n/a
2	chrX:125299033-125299083	HNPCEpiC	eye:	n/a
3	chrX:125300360-125300410	AG09319	gingival:	n/a
4	chrX:125300078-125300128	U87	brain:	n/a
5	chrX:125299403-125299453	MCF-7	breast:	n/a
6	chrX:125300035-125300085	T-47D	breast:	n/a
7	chrX:125301098-125301148	AG04449	skin:	fetal
8	chrX:125300360-125300410	CMK	blood:	n/a
9	chrX:125295590-125295640	GM12891	blood:	n/a
10	chrX:125299484-125299534	AG09309	skin:	n/a
11	chrX:125300082-125300132	HCT-116	colon:	n/a
12	chrX:125298533-125298583	NH-A	brain:	n/a
13	chrX:125300481-125300531	AG04449	skin:	fetal
14	chrX:125299033-125299083	HRE	kidney:	n/a
15	chrX:125300035-125300085	HPAEpiC	pulmonary alveolar:	n/a
16	chrX:125300481-125300531	A549	lung:	n/a
17	chrX:125298533-125298583	NHDF-neo	bronchial:	n/a
18	chrX:125300035-125300085	GM06990	blood:	n/a
19	chrX:125300481-125300531	HEK293	kidney:	embryo
20	chrX:125298533-125298583	BE2_C	brain:	n/a
21	chrX:125301098-125301148	IMR90	lung:	fetal
22	chrX:125300084-125300134	CMK	blood:	n/a
23	chrX:125295590-125295640	SAEC	small airway:	n/a
24	chrX:125300078-125300128	ProgFib	skin:	n/a
25	chrX:125300360-125300410	Jurkat	blood:	n/a
26	chrX:125300360-125300410	PrEC	prostate:	n/a
27	chrX:125300360-125300410	NT2-D1	testis:	n/a
28	chrX:125300082-125300132	CMK	blood:	n/a
29	chrX:125298533-125298583	HCM	heart:	n/a
30	chrX:125300481-125300531	T-47D	breast:	n/a
31	chrX:125300481-125300531	MCF10A-Er-Src	breast:	n/a
32	chrX:125300481-125300531	AoSMC	blood vessel:	n/a
33	chrX:125300111-125300161	NT2-D1	testis:	n/a
34	chrX:125300035-125300085	HUVEC	blood vessel:	n/a
35	chrX:125300082-125300132	Caco-2	colon:	n/a
36	chrX:125300084-125300134	HCF	heart:	n/a
37	chrX:125300082-125300132	AoSMC	blood vessel:	n/a
38	chrX:125298533-125298583	GM06990	blood:	n/a
39	chrX:125300082-125300132	PANC-1	pancreas:	n/a
40	chrX:125299484-125299534	HL-60	blood:	n/a
41	chrX:125298533-125298583	HL-60	blood:	n/a
42	chrX:125298533-125298583	SKMC	muscle:	n/a
43	chrX:125300111-125300161	LNCaP	prostate:	n/a
44	chrX:125300360-125300410	IMR90	lung:	fetal
45	chrX:125300111-125300161	Jurkat	blood:	n/a
46	chrX:125300360-125300410	HL-60	blood:	n/a
47	chrX:125299033-125299083	HUVEC	blood vessel:	n/a
48	chrX:125300082-125300132	HCPEpiC	choroid plexus:	n/a
49	chrX:125300481-125300531	AG09309	skin:	n/a
50	chrX:125299403-125299453	A549	lung:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:125080869..125082413-chrX:125088835..125090618,2	K562	blood:
2	chrX:125132320..125133131-chrX:126172183..126172720,2	MCF-7	breast:
3	chrX:124901242..124902978-chrX:124903402..124905989,2	K562	blood:
4	chrX:125132457..125133034-chrX:125274768..125275708,2	MCF-7	breast:
5	chrX:125080869..125082413-chrX:125088835..125090618,2	K562	blood:
6	chr1:224376992..224377644-chrX:125292998..125293831,2	MCF-7	breast:
7	chrX:124876251..124879157-chrX:124890337..124893306,2	K562	blood:
8	chrX:125132457..125133034-chrX:125274768..125275708,2	MCF-7	breast:
9	chrX:124901242..124902978-chrX:124903402..124905989,2	K562	blood:
10	chrX:124876251..124879157-chrX:124890337..124893306,2	K562	blood:
11	chrX:125182687..125184775-chrX:125212188..125214503,2	K562	blood:
12	chrX:125295904..125297728-chrX:125298952..125301710,2	MCF-7	breast:
13	chrX:125182687..125184775-chrX:125212188..125214503,2	K562	blood:
14	chr17:41399050..41402495-chrX:125205303..125206823,5	K562	blood:
15	chr6:26020538..26022385-chrX:125032838..125034358,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CXorf64-7	chrX:125071578-125071812	NONHSAT138476
2	lnc-CXorf64-7	chrX:125076866-125077226	NONHSAT138476
3	lnc-DCAF12L2-1	chrX:125138428-125140100	NONHSAT138477
4	lnc-CXorf64-7	chrX:125071426-125071468	NONHSAT138476

Variant related genes	Relation type
ENSG00000237208	TF binding region
DCAF12L2	TF binding region
ENSG00000222518	TF binding region
ENSG00000237208	CpG island
DCAF12L2	CpG island
ENSG00000222518	CpG island
ENSG00000196176	chromatin interactions
ENSG00000198366	chromatin interactions
ENSG00000198354	chromatin interactions

Extended variants
information (count: 1285 )
Associated
traits (count: 49 )

Variant overlapped rSNPs/rCNVs (count:1285 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs5932298	chrX:124701804-124701805	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs177006	chrX:124701807-124701808	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs177005	chrX:124701833-124701834	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs144169113	chrX:124701856-124701857	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs185926961	chrX:124701870-124701871	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs190039321	chrX:124701948-124701949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs177004	chrX:124701962-124701963	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs568321896	chrX:124701970-124701971	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs534190092	chrX:124702066-124702067	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs546159379	chrX:124702164-124702165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs112774732	chrX:124702242-124702243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181209432	chrX:124702256-124702257	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs141280457	chrX:124702312-124702313	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs34641871	chrX:124702321-124702322	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs192697776	chrX:124738472-124738473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs185399006	chrX:124738479-124738480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs28397012	chrX:124738619-124738620	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs373064251	chrX:124738785-124738786	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs201986111	chrX:124738797-124738798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs571755133	chrX:124738837-124738838	Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138114176	chrX:124739086-124739087	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs149537746	chrX:124739103-124739104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs189929480	chrX:124739126-124739127	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs5976807	chrX:124739164-124739165	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs193270123	chrX:124739261-124739262	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs184522578	chrX:124739365-124739366	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs370835936	chrX:124739487-124739488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs188188588	chrX:124739645-124739646	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs180998011	chrX:124739748-124739749	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs185065326	chrX:124739780-124739781	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs10560328	chrX:124739797-124739798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2858277	chrX:124748810-124748811	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs188132932	chrX:124748891-124748892	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs137965535	chrX:124748894-124748895	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs190083587	chrX:124748928-124748929	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs28835387	chrX:124749013-124749014	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs187313399	chrX:124749208-124749209	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs192563242	chrX:124749251-124749252	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs373757598	chrX:124749319-124749320	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs371569066	chrX:124749356-124749357	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs185441843	chrX:124749413-124749414	Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs551137730	chrX:124749514-124749515	Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs2819540	chrX:124749542-124749543	Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs368731210	chrX:124756366-124756367	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs371086276	chrX:124756402-124756403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192865828	chrX:124756457-124756458	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs185296459	chrX:124756460-124756461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374295832	chrX:124756479-124756480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190095017	chrX:124756491-124756492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs202207482	chrX:124756497-124756498	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:49)

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	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:241 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:124701800-124702400	Enhancers	K562	blood
2	chrX:124738200-124739800	Enhancers	Liver	Liver
3	chrX:124748800-124749400	Active TSS	K562	blood
4	chrX:124748800-124749600	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chrX:124756200-124756600	Enhancers	K562	blood
6	chrX:124756600-124757400	Weak transcription	K562	blood
7	chrX:124757400-124757600	Enhancers	K562	blood
8	chrX:124761800-124762600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
9	chrX:124761800-124763200	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
10	chrX:124762200-124762600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
11	chrX:124762200-124762600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
12	chrX:124762400-124762800	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
13	chrX:124762600-124762800	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chrX:124807600-124809000	Enhancers	Liver	Liver
15	chrX:124809000-124809400	Flanking Active TSS	Liver	Liver
16	chrX:124809400-124810000	Enhancers	Liver	Liver
17	chrX:124814800-124817200	Enhancers	Primary B cells from peripheral blood	blood
18	chrX:124815800-124816400	Enhancers	GM12878-XiMat	blood
19	chrX:124819600-124820000	Enhancers	ES-I3 Cell Line	embryonic stem cell
20	chrX:124843400-124844600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
21	chrX:124844200-124846200	Enhancers	Liver	Liver
22	chrX:124844600-124844800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chrX:124844800-124848000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chrX:124846200-124847600	Weak transcription	Liver	Liver
25	chrX:124847600-124848200	Enhancers	Liver	Liver
26	chrX:124848000-124848200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chrX:124880000-124880600	Enhancers	ES-I3 Cell Line	embryonic stem cell
28	chrX:124891600-124892800	Active TSS	K562	blood
29	chrX:124891800-124892600	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chrX:124891800-124892800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
31	chrX:124892000-124892600	Active TSS	Adipose Nuclei	Adipose
32	chrX:124903200-124904000	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chrX:124903600-124904000	Enhancers	HUES6 Cell Line	embryonic stem cell
34	chrX:124904000-124911200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
35	chrX:124904000-124911600	Weak transcription	HUES6 Cell Line	embryonic stem cell
36	chrX:124909000-124913400	Enhancers	iPS-15b Cell Line	embryonic stem cell
37	chrX:124911000-124913800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chrX:124911200-124913400	Enhancers	ES-I3 Cell Line	embryonic stem cell
39	chrX:124911600-124911800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chrX:124911600-124913400	Enhancers	HUES6 Cell Line	embryonic stem cell
41	chrX:124911800-124915200	Weak transcription	HUES64 Cell Line	embryonic stem cell
42	chrX:124913000-124913200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chrX:124913200-124920400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
44	chrX:124913400-124914400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
45	chrX:124913400-124914600	Weak transcription	HUES6 Cell Line	embryonic stem cell
46	chrX:124913400-124914600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chrX:124913800-124914200	Weak transcription	HUES48 Cell Line	embryonic stem cell
48	chrX:124914200-124916800	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chrX:124914400-124916000	Enhancers	ES-I3 Cell Line	embryonic stem cell
50	chrX:124914600-124917000	Enhancers	HUES6 Cell Line	embryonic stem cell

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