Variant report

Variant	nsv522266
Chromosome Location	chrX:31502157-31554545
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	BACH1	chrX:31517260-31517602	H1-hESC	embryonic stem cell:	n/a	n/a
2	CEBPB	chrX:31529159-31529352	Hela-S3	cervix:	n/a	n/a
3	CEBPB	chrX:31524549-31524822	H1-hESC	embryonic stem cell:	n/a	n/a
4	CHD1	chrX:31519110-31519142	H1-hESC	embryonic stem cell:	n/a	n/a
5	CTCF	chrX:31525123-31525215	GM10248	blood:	n/a	n/a
6	CTCF	chrX:31523373-31523454	GM10248	blood:	n/a	n/a
7	CTCF	chrX:31515024-31515083	GM20000	blood:	n/a	n/a
8	CTCF	chrX:31523167-31523229	LNCaP	prostate:	n/a	n/a
9	CTCF	chrX:31516558-31516608	Pancreas_OC	pancreas:	n/a	n/a
10	CTCF	chrX:31508080-31508158	GM20000	blood:	n/a	n/a
11	CTCF	chrX:31505574-31505632	GM10248	blood:	n/a	n/a
12	CTCF	chrX:31504543-31504615	Pancreas_OC	pancreas:	n/a	n/a
13	CTCF	chrX:31526464-31526537	LNCaP	prostate:	n/a	n/a
14	CTCF	chrX:31540242-31540297	ProgFib	skin:	n/a	n/a
15	E2F4	chrX:31514322-31515011	MCF10A-Er-Src	breast:	n/a	n/a
16	EP300	chrX:31526262-31526894	SK-N-SH_RA	brain:	n/a	n/a
17	EP300	chrX:31526038-31527132	SK-N-SH	brain:	n/a	chrX:31526898-31526912
18	EP300	chrX:31525978-31526028	GM12878	blood:	n/a	n/a
19	EP300	chrX:31525003-31525432	SK-N-SH_RA	brain:	n/a	n/a
20	EP300	chrX:31517281-31517610	Hela-S3	cervix:	n/a	n/a
21	EP300	chrX:31514797-31515132	SK-N-SH_RA	brain:	n/a	n/a
22	EP300	chrX:31526275-31526906	SK-N-SH_RA	brain:	n/a	n/a
23	EP300	chrX:31525091-31525426	SK-N-SH_RA	brain:	n/a	n/a
24	EP300	chrX:31526301-31527061	SK-N-SH	brain:	n/a	chrX:31526898-31526912
25	EP300	chrX:31526237-31526994	SK-N-SH	brain:	n/a	chrX:31526898-31526912
26	EP300	chrX:31514799-31515235	SK-N-SH_RA	brain:	n/a	n/a
27	FAM48A	chrX:31548213-31548401	GM12878	blood:	n/a	n/a
28	FOS	chrX:31515287-31515575	MCF10A-Er-Src	breast:	n/a	chrX:31515412-31515421 chrX:31515416-31515423 chrX:31515414-31515425 chrX:31515411-31515422
29	FOS	chrX:31502741-31503059	MCF10A-Er-Src	breast:	n/a	n/a
30	FOS	chrX:31529143-31529456	MCF10A-Er-Src	breast:	n/a	chrX:31529303-31529311 chrX:31529299-31529310 chrX:31529301-31529312 chrX:31529303-31529312 chrX:31529301-31529308 chrX:31529301-31529313 chrX:31529304-31529311
31	FOS	chrX:31502720-31503043	MCF10A-Er-Src	breast:	n/a	n/a
32	FOS	chrX:31517336-31517536	MCF10A-Er-Src	breast:	n/a	chrX:31517523-31517533 chrX:31517522-31517534 chrX:31517524-31517532 chrX:31517523-31517533
33	FOS	chrX:31502728-31503039	MCF10A-Er-Src	breast:	n/a	n/a
34	FOS	chrX:31517136-31517674	HUVEC	blood vessel:	n/a	chrX:31517523-31517533 chrX:31517522-31517534 chrX:31517524-31517532 chrX:31517523-31517533
35	FOS	chrX:31517272-31517374	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chrX:31517286-31517486	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chrX:31529254-31529348	MCF10A-Er-Src	breast:	n/a	chrX:31529303-31529311 chrX:31529299-31529310 chrX:31529301-31529312 chrX:31529303-31529312 chrX:31529301-31529308 chrX:31529301-31529313 chrX:31529304-31529311
38	FOS	chrX:31529141-31529454	MCF10A-Er-Src	breast:	n/a	chrX:31529303-31529311 chrX:31529299-31529310 chrX:31529301-31529312 chrX:31529303-31529312 chrX:31529301-31529308 chrX:31529301-31529313 chrX:31529304-31529311
39	FOS	chrX:31515005-31515581	HUVEC	blood vessel:	n/a	chrX:31515412-31515421 chrX:31515416-31515423 chrX:31515414-31515425 chrX:31515411-31515422
40	FOS	chrX:31515251-31515575	MCF10A-Er-Src	breast:	n/a	chrX:31515412-31515421 chrX:31515416-31515423 chrX:31515414-31515425 chrX:31515411-31515422
41	FOS	chrX:31529141-31529370	HUVEC	blood vessel:	n/a	chrX:31529303-31529311 chrX:31529299-31529310 chrX:31529301-31529312 chrX:31529303-31529312 chrX:31529301-31529308 chrX:31529301-31529313 chrX:31529304-31529311
42	FOS	chrX:31529232-31529342	MCF10A-Er-Src	breast:	n/a	chrX:31529303-31529311 chrX:31529299-31529310 chrX:31529301-31529312 chrX:31529303-31529312 chrX:31529301-31529308 chrX:31529301-31529313 chrX:31529304-31529311
43	FOS	chrX:31515233-31515571	MCF10A-Er-Src	breast:	n/a	chrX:31515412-31515421 chrX:31515416-31515423 chrX:31515414-31515425 chrX:31515411-31515422
44	FOS	chrX:31515233-31515588	MCF10A-Er-Src	breast:	n/a	chrX:31515412-31515421 chrX:31515416-31515423 chrX:31515414-31515425 chrX:31515411-31515422
45	FOSL2	chrX:31515256-31515642	SK-N-SH	brain:	n/a	chrX:31515412-31515421 chrX:31515416-31515423 chrX:31515414-31515425
46	FOSL2	chrX:31525076-31525420	SK-N-SH	brain:	n/a	n/a
47	FOSL2	chrX:31517156-31517655	SK-N-SH	brain:	n/a	chrX:31517523-31517533 chrX:31517522-31517534 chrX:31517524-31517532 chrX:31517523-31517533
48	FOXA2	chrX:31548667-31548956	A549	lung:	n/a	n/a
49	GABPA	chrX:31549057-31549149	Hela-S3	cervix:	n/a	n/a
50	GATA2	chrX:31542196-31542883	SH-SY5Y	brain:	n/a	chrX:31542748-31542765 chrX:31542759-31542769

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31526531-31526581	SAEC	small airway:	n/a
2	chrX:31526745-31526795	HRCEpiC	kidney:	n/a
3	chrX:31526745-31526795	GM12891	blood:	n/a
4	chrX:31526745-31526795	SAEC	small airway:	n/a
5	chrX:31526745-31526795	MCF10A-Er-Src	breast:	n/a
6	chrX:31526745-31526795	HEEpiC	esophagus:	n/a
7	chrX:31526531-31526581	AG09319	gingival:	n/a
8	chrX:31526531-31526581	AG09309	skin:	n/a
9	chrX:31526745-31526795	HMEC	breast:	n/a
10	chrX:31526531-31526581	NB4	blood:	n/a
11	chrX:31526531-31526581	Hepatocyte	liver:	n/a
12	chrX:31526745-31526795	NT2-D1	testis:	n/a
13	chrX:31526531-31526581	NH-A	brain:	n/a
14	chrX:31526745-31526795	H1-hESC	embryonic stem cell:	embryo
15	chrX:31526745-31526795	ovcar-3	ovarian:	n/a
16	chrX:31526531-31526581	GM06990	blood:	n/a
17	chrX:31526745-31526795	HCM	heart:	n/a
18	chrX:31526531-31526581	GM12891	blood:	n/a
19	chrX:31526531-31526581	BJ	skin:	n/a
20	chrX:31526531-31526581	HRPEpiC	eye:	n/a
21	chrX:31526531-31526581	GM19239	blood:	n/a
22	chrX:31526745-31526795	Hela-S3	cervix:	n/a
23	chrX:31526531-31526581	AoSMC	blood vessel:	n/a
24	chrX:31526531-31526581	HepG2	liver:	n/a
25	chrX:31526531-31526581	MCF10A-Er-Src	breast:	n/a
26	chrX:31526745-31526795	HAEpiC	amniotic membrane:	n/a
27	chrX:31526531-31526581	HRE	kidney:	n/a
28	chrX:31526745-31526795	NH-A	brain:	n/a
29	chrX:31526531-31526581	GM12878	blood:	n/a
30	chrX:31526531-31526581	IMR90	lung:	fetal
31	chrX:31526531-31526581	ProgFib	skin:	n/a
32	chrX:31526531-31526581	Hela-S3	cervix:	n/a
33	chrX:31526531-31526581	HIPEpiC	eye:	n/a
34	chrX:31526531-31526581	T-47D	breast:	n/a
35	chrX:31526745-31526795	HUVEC	blood vessel:	n/a
36	chrX:31526745-31526795	GM12878	blood:	n/a
37	chrX:31526531-31526581	NT2-D1	testis:	n/a
38	chrX:31526531-31526581	HCF	heart:	n/a
39	chrX:31526531-31526581	A549	lung:	n/a
40	chrX:31526531-31526581	PANC-1	pancreas:	n/a
41	chrX:31526531-31526581	ovcar-3	ovarian:	n/a
42	chrX:31526745-31526795	CMK	blood:	n/a
43	chrX:31526745-31526795	HCPEpiC	choroid plexus:	n/a
44	chrX:31526745-31526795	NHBE	bronchial:	n/a
45	chrX:31526531-31526581	HCM	heart:	n/a
46	chrX:31526745-31526795	HEK293	kidney:	embryo
47	chrX:31526745-31526795	AG09319	gingival:	n/a
48	chrX:31526531-31526581	Jurkat	blood:	n/a
49	chrX:31526745-31526795	HCF	heart:	n/a
50	chrX:31526531-31526581	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chrX:31479350..31481011-chrX:31523171..31525113,2	K562	blood:

Variant related genes	Relation type
DMD	TF binding region
DMD	CpG island

Extended variants
information (count: 677 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:677 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6653851	chrX:31502157-31502158	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs140395331	chrX:31502217-31502218	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs150388689	chrX:31502245-31502246	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs372016049	chrX:31502335-31502336	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs73212373	chrX:31502615-31502616	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141037897	chrX:31502621-31502622	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs67178585	chrX:31502738-31502739	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371763288	chrX:31503084-31503085	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs57007006	chrX:31503272-31503273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs182335647	chrX:31503334-31503335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs369842456	chrX:31503477-31503478	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs185989588	chrX:31503565-31503566	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs113861248	chrX:31503572-31503573	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs144442784	chrX:31503701-31503702	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs7058993	chrX:31503781-31503782	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373093299	chrX:31503834-31503835	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141569548	chrX:31503905-31503906	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs191235606	chrX:31504067-31504068	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs557430880	chrX:31504143-31504144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs183086061	chrX:31504307-31504308	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs188517740	chrX:31504361-31504362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs553489662	chrX:31504609-31504610	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs12687479	chrX:31504693-31504694	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs192288218	chrX:31504910-31504911	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377360946	chrX:31505033-31505034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183292911	chrX:31505034-31505035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs188065240	chrX:31505095-31505096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs9698860	chrX:31505137-31505138	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs145580130	chrX:31505187-31505188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs147263338	chrX:31505340-31505341	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs575687627	chrX:31505363-31505364	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs373319668	chrX:31505441-31505442	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs111304001	chrX:31505507-31505508	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs207478223	chrX:31505585-31505586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs184291077	chrX:31505953-31505954	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs201581978	chrX:31506011-31506012	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs200085252	chrX:31506013-31506014	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201228866	chrX:31506022-31506023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs192860931	chrX:31506023-31506024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs377379071	chrX:31506092-31506093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs184840353	chrX:31506158-31506159	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs111400545	chrX:31506218-31506219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs17338604	chrX:31506284-31506285	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs377163471	chrX:31506494-31506495	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs148518743	chrX:31506511-31506512	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs142668245	chrX:31506536-31506537	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190184296	chrX:31506540-31506541	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs201411543	chrX:31506571-31506572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs376101454	chrX:31506576-31506577	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs146523563	chrX:31506661-31506662	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Duchenne and Becker muscular dystrophies	18663755	CNVD

Chromatin state (count:171 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31493400-31506400	Weak transcription	HSMMtube	muscle
2	chrX:31501400-31503000	Enhancers	Muscle Satellite Cultured Cells	--
3	chrX:31501600-31502800	Enhancers	HUVEC	blood vessel
4	chrX:31501800-31502200	Enhancers	HSMM	muscle
5	chrX:31501800-31503000	Enhancers	NHEK	skin
6	chrX:31501800-31503200	Enhancers	HMEC	breast
7	chrX:31502000-31502600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chrX:31502000-31503200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chrX:31503000-31504600	Weak transcription	Muscle Satellite Cultured Cells	--
10	chrX:31504600-31504800	Enhancers	Muscle Satellite Cultured Cells	--
11	chrX:31506400-31507200	Enhancers	HSMMtube	muscle
12	chrX:31507200-31515600	Weak transcription	HSMMtube	muscle
13	chrX:31507400-31507600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chrX:31513000-31526000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chrX:31513400-31515800	Weak transcription	Liver	Liver
16	chrX:31514200-31516600	Weak transcription	Skeletal Muscle Female	skeletal muscle
17	chrX:31514800-31515200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chrX:31514800-31515200	Enhancers	NHLF	lung
19	chrX:31514800-31516200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
20	chrX:31514800-31519400	Enhancers	HUVEC	blood vessel
21	chrX:31515000-31515200	Enhancers	Colon Smooth Muscle	Colon
22	chrX:31515000-31515400	Enhancers	Brain Anterior Caudate	brain
23	chrX:31515000-31515800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chrX:31515000-31515800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chrX:31515000-31515800	Enhancers	Hela-S3	cervix
26	chrX:31515000-31516000	Enhancers	HMEC	breast
27	chrX:31515000-31516200	Enhancers	Muscle Satellite Cultured Cells	--
28	chrX:31515200-31515400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
29	chrX:31515200-31515400	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chrX:31515200-31515400	Enhancers	Osteobl	bone
31	chrX:31515200-31515600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
32	chrX:31515200-31515800	Enhancers	NH-A	brain
33	chrX:31515200-31519000	Weak transcription	Colon Smooth Muscle	Colon
34	chrX:31515400-31515800	Enhancers	ES-I3 Cell Line	embryonic stem cell
35	chrX:31515600-31515800	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chrX:31515600-31515800	Enhancers	HSMMtube	muscle
37	chrX:31515600-31516800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
38	chrX:31515800-31516200	Enhancers	iPS-15b Cell Line	embryonic stem cell
39	chrX:31515800-31516800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chrX:31515800-31517000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
41	chrX:31515800-31517000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chrX:31515800-31517000	Weak transcription	Hela-S3	cervix
43	chrX:31516000-31517000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chrX:31516000-31517000	Weak transcription	HMEC	breast
45	chrX:31516200-31516600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chrX:31516200-31516600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chrX:31516200-31516600	Weak transcription	Muscle Satellite Cultured Cells	--
48	chrX:31516600-31517400	Enhancers	iPS-15b Cell Line	embryonic stem cell
49	chrX:31516600-31517400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chrX:31516600-31518000	Enhancers	Muscle Satellite Cultured Cells	--

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