Variant report

Variant	nsv531771
Chromosome Location	chrX:31683623-32129067
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:871)
CpG islands
(count:61)
Chromatin interactive
region (count:49)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:871 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:32011739-32012041	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:31907685-31907977	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:31890048-31890539	K562	blood:	n/a	n/a
4	ARID3A	chrX:31840662-31840756	K562	blood:	n/a	n/a
5	ARID3A	chrX:31825327-31825587	HepG2	liver:	n/a	n/a
6	ATF1	chrX:31720398-31720650	K562	blood:	n/a	n/a
7	ATF1	chrX:31865924-31866215	K562	blood:	n/a	n/a
8	ATF1	chrX:31880836-31881481	K562	blood:	n/a	n/a
9	ATF1	chrX:31856622-31856958	K562	blood:	n/a	n/a
10	ATF1	chrX:31854667-31854914	K562	blood:	n/a	n/a
11	BACH1	chrX:31890171-31890286	K562	blood:	n/a	n/a
12	BACH1	chrX:31783135-31783137	K562	blood:	n/a	n/a
13	BCL3	chrX:31737849-31738258	GM12878	blood:	n/a	n/a
14	BCL3	chrX:31737905-31738230	GM12878	blood:	n/a	n/a
15	BCL3	chrX:31766561-31766945	GM12878	blood:	n/a	n/a
16	BCL3	chrX:31766645-31766852	GM12878	blood:	n/a	n/a
17	BHLHE40	chrX:31890114-31890531	K562	blood:	n/a	n/a
18	BHLHE40	chrX:31887576-31887844	K562	blood:	n/a	n/a
19	BHLHE40	chrX:31795023-31795206	K562	blood:	n/a	n/a
20	BRCA1	chrX:31716811-31716827	Hela-S3	cervix:	n/a	n/a
21	CBX3	chrX:31890091-31890537	K562	blood:	n/a	n/a
22	CBX3	chrX:31880787-31881579	K562	blood:	n/a	n/a
23	CBX3	chrX:31880911-31881222	K562	blood:	n/a	n/a
24	CCNT2	chrX:31890215-31890561	K562	blood:	n/a	chrX:31890266-31890286
25	CCNT2	chrX:31865917-31866562	K562	blood:	n/a	n/a
26	CCNT2	chrX:31880965-31881256	K562	blood:	n/a	n/a
27	CEBPB	chrX:32062152-32062464	HepG2	liver:	n/a	n/a
28	CEBPB	chrX:31739458-31739663	IMR90	lung:	n/a	chrX:31739596-31739607
29	CEBPB	chrX:31739446-31739711	H1-hESC	embryonic stem cell:	n/a	chrX:31739596-31739607
30	CEBPB	chrX:31688381-31688643	HepG2	liver:	n/a	chrX:31688510-31688521
31	CEBPB	chrX:31745355-31745547	A549	lung:	n/a	n/a
32	CEBPB	chrX:31720394-31720668	IMR90	lung:	n/a	n/a
33	CEBPB	chrX:31949303-31949614	HepG2	liver:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
34	CEBPB	chrX:31967146-31967428	IMR90	lung:	n/a	chrX:31967281-31967292
35	CEBPB	chrX:31949328-31949638	K562	blood:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
36	CEBPB	chrX:31890217-31890462	K562	blood:	n/a	n/a
37	CEBPB	chrX:31949361-31949579	H1-hESC	embryonic stem cell:	n/a	chrX:31949465-31949474 chrX:31949465-31949476 chrX:31949465-31949474 chrX:31949463-31949474 chrX:31949465-31949474 chrX:31949465-31949474
38	CEBPB	chrX:31999045-31999149	HepG2	liver:	n/a	n/a
39	CEBPB	chrX:31999833-32000139	A549	lung:	n/a	n/a
40	CEBPB	chrX:31826556-31826776	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chrX:31880697-31881227	K562	blood:	n/a	n/a
42	CEBPB	chrX:31739551-31739655	A549	lung:	n/a	chrX:31739596-31739607
43	CEBPB	chrX:31854765-31854950	K562	blood:	n/a	chrX:31854795-31854812
44	CEBPB	chrX:31869466-31869539	K562	blood:	n/a	n/a
45	CEBPB	chrX:31839455-31839711	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chrX:31902669-31903009	K562	blood:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
47	CEBPB	chrX:31839449-31839744	K562	blood:	n/a	n/a
48	CEBPB	chrX:31984740-31984870	IMR90	lung:	n/a	chrX:31984853-31984866
49	CEBPB	chrX:31902675-31902993	IMR90	lung:	n/a	chrX:31902832-31902843 chrX:31902849-31902860
50	CEBPB	chrX:31999832-32000168	IMR90	lung:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:31889692-31889742	NHBE	bronchial:	n/a
2	chrX:31889692-31889742	HEEpiC	esophagus:	n/a
3	chrX:31889692-31889742	U87	brain:	n/a
4	chrX:31889692-31889742	K562	blood:	n/a
5	chrX:31889692-31889742	Caco-2	colon:	n/a
6	chrX:31889692-31889742	BE2_C	brain:	n/a
7	chrX:31889692-31889742	PANC-1	pancreas:	n/a
8	chrX:31889692-31889742	HIPEpiC	eye:	n/a
9	chrX:31889692-31889742	HUVEC	blood vessel:	n/a
10	chrX:31889692-31889742	H1-hESC	embryonic stem cell:	embryo
11	chrX:31889692-31889742	CMK	blood:	n/a
12	chrX:31889692-31889742	AoSMC	blood vessel:	n/a
13	chrX:31889692-31889742	Hepatocyte	liver:	n/a
14	chrX:31889692-31889742	HRCEpiC	kidney:	n/a
15	chrX:31889692-31889742	HCM	heart:	n/a
16	chrX:31889692-31889742	MCF10A-Er-Src	breast:	n/a
17	chrX:31889692-31889742	HL-60	blood:	n/a
18	chrX:31889692-31889742	NHDF-neo	bronchial:	n/a
19	chrX:31889692-31889742	ECC-1	luminal epithelium:	n/a
20	chrX:31889692-31889742	ovcar-3	ovarian:	n/a
21	chrX:31889692-31889742	ProgFib	skin:	n/a
22	chrX:31889692-31889742	AG09319	gingival:	n/a
23	chrX:31889692-31889742	GM19239	blood:	n/a
24	chrX:31889692-31889742	GM06990	blood:	n/a
25	chrX:31889692-31889742	AG04449	skin:	fetal
26	chrX:31889692-31889742	AG09309	skin:	n/a
27	chrX:31889692-31889742	MCF-7	breast:	n/a
28	chrX:31889692-31889742	PrEC	prostate:	n/a
29	chrX:31889692-31889742	HAEpiC	amniotic membrane:	n/a
30	chrX:31889692-31889742	HEK293	kidney:	embryo
31	chrX:31889692-31889742	GM12892	blood:	n/a
32	chrX:31889692-31889742	HCPEpiC	choroid plexus:	n/a
33	chrX:31889692-31889742	NH-A	brain:	n/a
34	chrX:31889692-31889742	HNPCEpiC	eye:	n/a
35	chrX:31889692-31889742	GM12878	blood:	n/a
36	chrX:31889692-31889742	SK-N-SH	brain:	n/a
37	chrX:31889692-31889742	RPTEC	kidney:	n/a
38	chrX:31889692-31889742	Hela-S3	cervix:	n/a
39	chrX:31889692-31889742	BJ	skin:	n/a
40	chrX:31889692-31889742	SK-N-MC	brain:	n/a
41	chrX:31889692-31889742	IMR90	lung:	fetal
42	chrX:31889692-31889742	HCT-116	colon:	n/a
43	chrX:31889692-31889742	SAEC	small airway:	n/a
44	chrX:31889692-31889742	A549	lung:	n/a
45	chrX:31889692-31889742	NB4	blood:	n/a
46	chrX:31889692-31889742	T-47D	breast:	n/a
47	chrX:31889692-31889742	AG10803	skin:	n/a
48	chrX:31889692-31889742	HepG2	liver:	n/a
49	chrX:31889692-31889742	Jurkat	blood:	n/a
50	chrX:31889692-31889742	PFSK-1	brain:	n/a

(count:49 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
2	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
3	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
4	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
5	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
6	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
7	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
8	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
9	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
10	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
11	chrX:31868974..31872940-chrX:31881104..31882648,3	K562	blood:
12	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
13	chrX:31879318..31881738-chrX:37568667..37570898,2	K562	blood:
14	chrX:31853042..31856013-chrX:31864412..31867304,2	K562	blood:
15	chrX:31764661..31766806-chrX:31768758..31770911,2	K562	blood:
16	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
17	chrX:31787499..31789422-chrX:31789424..31791064,2	MCF-7	breast:
18	chrX:31742627..31744241-chrX:31749463..31751678,2	K562	blood:
19	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
20	chrX:31867261..31868765-chrX:31875575..31877377,2	K562	blood:
21	chrX:32029033..32031986-chrX:32032389..32035161,2	K562	blood:
22	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
23	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
24	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:
25	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
26	chrX:31854870..31857269-chrX:31880560..31882604,2	K562	blood:
27	chrX:31854748..31856516-chrX:31874032..31875743,2	K562	blood:
28	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
29	chrX:31979563..31982546-chrX:31984260..31985779,2	K562	blood:
30	chrX:31778356..31781336-chrX:31781568..31784358,2	K562	blood:
31	chrX:31823192..31826077-chrX:31864519..31866883,2	K562	blood:
32	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
33	chrX:31879109..31884748-chrX:31886200..31892011,14	K562	blood:
34	chrX:31880368..31882445-chrX:37544523..37546582,2	K562	blood:
35	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
36	chrX:31679912..31681425-chrX:31683220..31684967,2	K562	blood:
37	chrX:31849555..31852205-chrX:31866739..31868743,2	K562	blood:
38	chrX:31894185..31896623-chrX:31899263..31901435,2	K562	blood:
39	chrX:31868973..31870576-chrX:31872637..31874406,2	K562	blood:
40	chrX:31789896..31793490-chrX:31804091..31807456,3	K562	blood:
41	chrX:31856957..31858886-chrX:31860711..31862555,2	K562	blood:
42	chrX:31870056..31872825-chrX:31875477..31878792,4	K562	blood:
43	chrX:31979563..31982546-chrX:31984260..31985779,2	K562	blood:
44	chrX:31788924..31791704-chrX:31792640..31795936,3	K562	blood:
45	chrX:31871691..31874644-chrX:31876183..31879556,5	K562	blood:
46	chrX:31693950..31696881-chrX:31751543..31754151,2	K562	blood:
47	chrX:31846736..31849689-chrX:31851521..31853181,2	K562	blood:
48	chr7:72992366..72994261-chrX:31778080..31779580,2	MCF-7	breast:
49	chrX:31860758..31862494-chrX:31865169..31867353,2	K562	blood:

No data

Variant related genes	Relation type
DMD	TF binding region
RNA5SP501	TF binding region
DMD	CpG island
RNA5SP501	CpG island
ENSG00000047597	chromatin interactions
ENSG00000198947	chromatin interactions
ENSG00000106638	chromatin interactions

Extended variants
information (count: 3548 )
Associated
traits (count: 62 )

Variant overlapped rSNPs/rCNVs (count:3548 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs193082070	chrX:31688004-31688005	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs145627324	chrX:31688174-31688175	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs5927798	chrX:31688198-31688199	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs185863249	chrX:31688238-31688239	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs7056326	chrX:31688370-31688371	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs189325566	chrX:31688501-31688502	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs112443696	chrX:31688532-31688533	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs376038592	chrX:31688586-31688587	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs180698246	chrX:31688716-31688717	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs6527110	chrX:31688917-31688918	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs62589460	chrX:31689916-31689917	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
12	rs183442758	chrX:31689917-31689918	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
13	rs186303019	chrX:31690160-31690161	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
14	rs371078489	chrX:31690198-31690199	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
15	rs73617096	chrX:31690255-31690256	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs5972430	chrX:31690354-31690355	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs73455992	chrX:31690365-31690366	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs149911463	chrX:31690505-31690506	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs73455993	chrX:31690515-31690516	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs369466499	chrX:31690739-31690740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs182167170	chrX:31690787-31690788	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs5971587	chrX:31690979-31690980	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs186898123	chrX:31691073-31691074	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs73214034	chrX:31691096-31691097	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs191111856	chrX:31691240-31691241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs183428569	chrX:31691514-31691515	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374228977	chrX:31691575-31691576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs529692081	chrX:31691590-31691591	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs374365650	chrX:31691694-31691695	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542389738	chrX:31691745-31691746	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs188363021	chrX:31691771-31691772	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs193012335	chrX:31692089-31692090	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs147748118	chrX:31692292-31692293	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs149229541	chrX:31692318-31692319	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10521975	chrX:31692329-31692330	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs377254522	chrX:31692401-31692402	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs371605435	chrX:31692471-31692472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs185196837	chrX:31692487-31692488	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs376167469	chrX:31692489-31692490	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs151307551	chrX:31692592-31692593	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs111909978	chrX:31692607-31692608	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs5927800	chrX:31692719-31692720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs5971588	chrX:31692789-31692790	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs5972431	chrX:31692796-31692797	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs141220501	chrX:31692948-31692949	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs192584090	chrX:31693016-31693017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs183582880	chrX:31693021-31693022	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs533385394	chrX:31693242-31693243	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs188320592	chrX:31693279-31693280	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs547831062	chrX:31693316-31693317	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:62)

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
Non-syndromic sensorineural hearing loss	18451855	CNVD
Autism	20531469	CNVD
Breast cancer	21611746	CNVD

Chromatin state (count:353 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:31688000-31689000	Enhancers	HUVEC	blood vessel
2	chrX:31689600-31690600	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chrX:31690600-31692400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
4	chrX:31692200-31693000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chrX:31692200-31693400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chrX:31692200-31693400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chrX:31692400-31693000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chrX:31698200-31698600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
9	chrX:31720200-31720800	Enhancers	ES-I3 Cell Line	embryonic stem cell
10	chrX:31720200-31720800	Enhancers	HUES6 Cell Line	embryonic stem cell
11	chrX:31724800-31726800	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chrX:31725000-31725600	Enhancers	Fetal Heart	heart
13	chrX:31725200-31725800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
14	chrX:31725200-31726200	Enhancers	Muscle Satellite Cultured Cells	--
15	chrX:31726000-31726600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chrX:31733800-31734400	ZNF genes & repeats	Liver	Liver
17	chrX:31734400-31754400	Weak transcription	Liver	Liver
18	chrX:31735400-31736400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chrX:31735400-31736600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chrX:31736400-31737400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
21	chrX:31736600-31736800	Enhancers	HUES48 Cell Line	embryonic stem cell
22	chrX:31736600-31749800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chrX:31739000-31747000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chrX:31741600-31742200	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chrX:31745200-31747000	Weak transcription	Stomach Smooth Muscle	stomach
26	chrX:31745200-31748600	Weak transcription	K562	blood
27	chrX:31745600-31745800	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
28	chrX:31745800-31748200	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chrX:31746200-31748400	Weak transcription	Duodenum Smooth Muscle	Duodenum
30	chrX:31746200-31748800	Weak transcription	Aorta	Aorta
31	chrX:31747000-31747600	Strong transcription	Stomach Smooth Muscle	stomach
32	chrX:31747000-31747800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
33	chrX:31747600-31749200	Weak transcription	Stomach Smooth Muscle	stomach
34	chrX:31747800-31749400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chrX:31749800-31750200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
36	chrX:31754200-31754600	Enhancers	Hela-S3	cervix
37	chrX:31754400-31754600	Enhancers	Liver	Liver
38	chrX:31763200-31763400	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chrX:31765000-31765400	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chrX:31765200-31765800	Enhancers	Brain Inferior Temporal Lobe	brain
41	chrX:31765400-31766400	Enhancers	Fetal Brain Male	brain
42	chrX:31765400-31767000	Enhancers	ES-I3 Cell Line	embryonic stem cell
43	chrX:31765600-31766400	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chrX:31765800-31766800	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chrX:31766400-31770800	Weak transcription	Fetal Brain Male	brain
46	chrX:31766800-31770800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
47	chrX:31769400-31770400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
48	chrX:31770200-31770800	Enhancers	HUES6 Cell Line	embryonic stem cell
49	chrX:31770200-31771000	Enhancers	Fetal Brain Female	brain
50	chrX:31770200-31771200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived

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