Variant report

Variant	esv2756769
Chromosome Location	chrX:6389443-6866338
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	ATF2	chrX:6656510-6657531	GM12878	blood:	n/a	n/a
2	ATF2	chrX:6650200-6650576	GM12878	blood:	n/a	n/a
3	ATF2	chrX:6656521-6657470	GM12878	blood:	n/a	n/a
4	BACH1	chrX:6696430-6696950	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chrX:6656817-6657350	GM12878	blood:	n/a	n/a
6	BATF	chrX:6656848-6657191	GM12878	blood:	n/a	n/a
7	BATF	chrX:6728802-6729064	GM12878	blood:	n/a	chrX:6728956-6728967 chrX:6728967-6728978
8	BCL11A	chrX:6656822-6657366	GM12878	blood:	n/a	n/a
9	BCL11A	chrX:6656657-6657479	GM12878	blood:	n/a	n/a
10	BCL3	chrX:6656849-6657373	GM12878	blood:	n/a	n/a
11	BCL3	chrX:6656968-6657313	GM12878	blood:	n/a	n/a
12	BCL3	chrX:6676642-6677002	GM12878	blood:	n/a	n/a
13	BCLAF1	chrX:6656774-6657546	GM12878	blood:	n/a	n/a
14	BCLAF1	chrX:6650178-6650508	GM12878	blood:	n/a	n/a
15	BCLAF1	chrX:6656899-6657442	GM12878	blood:	n/a	n/a
16	BHLHE40	chrX:6650232-6650482	GM12878	blood:	n/a	n/a
17	BHLHE40	chrX:6656602-6657589	GM12878	blood:	n/a	n/a
18	BHLHE40	chrX:6666733-6666965	GM12878	blood:	n/a	n/a
19	BRCA1	chrX:6656940-6657436	GM12878	blood:	n/a	n/a
20	CEBPB	chrX:6864590-6864775	H1-hESC	embryonic stem cell:	n/a	chrX:6864625-6864636
21	CEBPB	chrX:6864462-6864800	IMR90	lung:	n/a	chrX:6864625-6864636
22	CEBPB	chrX:6524963-6525194	IMR90	lung:	n/a	chrX:6525062-6525075
23	CEBPB	chrX:6711263-6711518	A549	lung:	n/a	n/a
24	CEBPB	chrX:6484827-6485100	IMR90	lung:	n/a	n/a
25	CEBPB	chrX:6754933-6755256	IMR90	lung:	n/a	chrX:6755093-6755102 chrX:6755091-6755102 chrX:6755091-6755104 chrX:6755093-6755102 chrX:6755093-6755102 chrX:6755091-6755104 chrX:6755093-6755102 chrX:6755091-6755102 chrX:6755091-6755104 chrX:6755092-6755103
26	CEBPB	chrX:6674442-6674623	A549	lung:	n/a	n/a
27	CEBPB	chrX:6648377-6648623	IMR90	lung:	n/a	chrX:6648460-6648469 chrX:6648460-6648471
28	CEBPB	chrX:6721678-6722020	HepG2	liver:	n/a	chrX:6721863-6721876 chrX:6721865-6721874 chrX:6721865-6721876 chrX:6721863-6721874
29	CEBPB	chrX:6725414-6725647	IMR90	lung:	n/a	n/a
30	CEBPB	chrX:6773608-6773867	HepG2	liver:	n/a	chrX:6773744-6773755
31	CEBPB	chrX:6475811-6475996	HepG2	liver:	n/a	chrX:6475939-6475950
32	CEBPB	chrX:6646348-6646551	HepG2	liver:	n/a	chrX:6646447-6646456 chrX:6646447-6646458 chrX:6646447-6646456 chrX:6646447-6646456 chrX:6646445-6646456 chrX:6646447-6646456
33	CEBPB	chrX:6471293-6471471	A549	lung:	n/a	chrX:6471422-6471433
34	CEBPB	chrX:6471389-6471556	HepG2	liver:	n/a	chrX:6471422-6471433
35	CEBPB	chrX:6471257-6471479	IMR90	lung:	n/a	chrX:6471422-6471433
36	CEBPB	chrX:6721720-6721981	IMR90	lung:	n/a	chrX:6721863-6721876 chrX:6721865-6721874 chrX:6721865-6721876 chrX:6721863-6721874
37	CEBPB	chrX:6475740-6476115	HepG2	liver:	n/a	chrX:6475939-6475950
38	CEBPB	chrX:6656583-6657408	GM12878	blood:	n/a	n/a
39	CEBPB	chrX:6721723-6721938	A549	lung:	n/a	chrX:6721863-6721876 chrX:6721865-6721874 chrX:6721865-6721876 chrX:6721863-6721874
40	CEBPB	chrX:6754983-6755217	HepG2	liver:	n/a	chrX:6755093-6755102 chrX:6755091-6755102 chrX:6755091-6755104 chrX:6755093-6755102 chrX:6755093-6755102 chrX:6755091-6755104 chrX:6755093-6755102 chrX:6755091-6755102 chrX:6755091-6755104 chrX:6755092-6755103
41	CEBPB	chrX:6555739-6556013	IMR90	lung:	n/a	chrX:6555877-6555888
42	CEBPB	chrX:6670740-6670985	A549	lung:	n/a	chrX:6670833-6670844 chrX:6670846-6670857 chrX:6670832-6670845
43	CEBPB	chrX:6584701-6584981	IMR90	lung:	n/a	n/a
44	CEBPB	chrX:6670704-6670919	Hela-S3	cervix:	n/a	chrX:6670833-6670844 chrX:6670846-6670857 chrX:6670832-6670845
45	CEBPB	chrX:6670723-6670987	IMR90	lung:	n/a	chrX:6670833-6670844 chrX:6670846-6670857 chrX:6670832-6670845
46	CEBPB	chrX:6636479-6636630	K562	blood:	n/a	chrX:6636549-6636560
47	CEBPB	chrX:6774375-6774597	IMR90	lung:	n/a	chrX:6774454-6774465
48	CEBPB	chrX:6636405-6636717	A549	lung:	n/a	chrX:6636549-6636560
49	CEBPB	chrX:6779440-6779724	HepG2	liver:	n/a	chrX:6779538-6779549 chrX:6779537-6779550 chrX:6779537-6779550 chrX:6779537-6779548 chrX:6779537-6779550
50	CEBPB	chrX:6754961-6755241	A549	lung:	n/a	chrX:6755093-6755102 chrX:6755091-6755102 chrX:6755091-6755104 chrX:6755093-6755102 chrX:6755093-6755102 chrX:6755091-6755104 chrX:6755093-6755102 chrX:6755091-6755102 chrX:6755091-6755104 chrX:6755092-6755103

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:6453041-6453091	AG10803	skin:	n/a
2	chrX:6453041-6453091	AG10803	skin:	n/a
3	chrX:6451812-6451862	AoSMC	blood vessel:	n/a
4	chrX:6451812-6451862	PANC-1	pancreas:	n/a
5	chrX:6453041-6453091	NHBE	bronchial:	n/a
6	chrX:6453787-6453837	IMR90	lung:	fetal
7	chrX:6453787-6453837	RPTEC	kidney:	n/a
8	chrX:6453787-6453837	SK-N-MC	brain:	n/a
9	chrX:6453041-6453091	ovcar-3	ovarian:	n/a
10	chrX:6452751-6452801	Jurkat	blood:	n/a
11	chrX:6452751-6452801	ovcar-3	ovarian:	n/a
12	chrX:6453787-6453837	PrEC	prostate:	n/a
13	chrX:6452751-6452801	GM12892	blood:	n/a
14	chrX:6453041-6453091	SK-N-SH_RA	brain:	n/a
15	chrX:6453041-6453091	NT2-D1	testis:	n/a
16	chrX:6453041-6453091	Hela-S3	cervix:	n/a
17	chrX:6451812-6451862	IMR90	lung:	fetal
18	chrX:6453787-6453837	HEK293	kidney:	embryo
19	chrX:6453787-6453837	ovcar-3	ovarian:	n/a
20	chrX:6453787-6453837	Jurkat	blood:	n/a
21	chrX:6451812-6451862	SK-N-MC	brain:	n/a
22	chrX:6453787-6453837	HepG2	liver:	n/a
23	chrX:6453041-6453091	HCT-116	colon:	n/a
24	chrX:6453787-6453837	HRCEpiC	kidney:	n/a
25	chrX:6451812-6451862	HEK293	kidney:	embryo
26	chrX:6453787-6453837	ECC-1	luminal epithelium:	n/a
27	chrX:6451812-6451862	HRCEpiC	kidney:	n/a
28	chrX:6453041-6453091	GM12891	blood:	n/a
29	chrX:6453787-6453837	HCT-116	colon:	n/a
30	chrX:6452751-6452801	HMEC	breast:	n/a
31	chrX:6453787-6453837	SKMC	muscle:	n/a
32	chrX:6451812-6451862	AG04449	skin:	fetal
33	chrX:6451812-6451862	MCF10A-Er-Src	breast:	n/a
34	chrX:6451812-6451862	HCT-116	colon:	n/a
35	chrX:6451812-6451862	HCPEpiC	choroid plexus:	n/a
36	chrX:6451812-6451862	NHDF-neo	bronchial:	n/a
37	chrX:6453787-6453837	HPAEpiC	pulmonary alveolar:	n/a
38	chrX:6451812-6451862	A549	lung:	n/a
39	chrX:6452751-6452801	BE2_C	brain:	n/a
40	chrX:6451812-6451862	LNCaP	prostate:	n/a
41	chrX:6453041-6453091	AG09309	skin:	n/a
42	chrX:6451812-6451862	HNPCEpiC	eye:	n/a
43	chrX:6452751-6452801	LNCaP	prostate:	n/a
44	chrX:6452751-6452801	K562	blood:	n/a
45	chrX:6453787-6453837	Caco-2	colon:	n/a
46	chrX:6453787-6453837	BJ	skin:	n/a
47	chrX:6453787-6453837	AG04449	skin:	fetal
48	chrX:6453787-6453837	HIPEpiC	eye:	n/a
49	chrX:6453041-6453091	NB4	blood:	n/a
50	chrX:6451812-6451862	AG09309	skin:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:6727253..6730128-chrX:6730834..6733404,2	K562	blood:
2	chrX:6829596..6832442-chrX:6832521..6834622,2	MCF-7	breast:
3	chrX:6727253..6730128-chrX:6730834..6733404,2	K562	blood:
4	chrX:6611316..6614128-chrX:6615657..6618460,2	MCF-7	breast:
5	chrX:6714475..6716736-chrX:6719216..6721082,2	K562	blood:
6	chrX:6829596..6832442-chrX:6832521..6834622,2	MCF-7	breast:
7	chrX:6705927..6707578-chrX:6712936..6714694,2	K562	blood:
8	chrX:6611316..6614128-chrX:6615657..6618460,2	MCF-7	breast:
9	chrX:6714475..6716736-chrX:6719216..6721082,2	K562	blood:
10	chrX:6705927..6707578-chrX:6712936..6714694,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STS-4	chrX:6846023-6846564	NONHSAT136176
2	lnc-STS-4	chrX:6771241-6771518	NONHSAT136176
3	lnc-VCX3A-2	chrX:6595906-6596170	NONHSAT136173
4	lnc-VCX3A-2	chrX:6649458-6649585	NONHSAT136173
5	lnc-VCX3A-2	chrX:6634384-6634507	NONHSAT136173
6	lnc-STS-4	chrX:6827243-6827839	NONHSAT136176
7	lnc-HDHD1-1	chrX:6685657-6685752	XLOC_008109
8	lnc-STS-4	chrX:6842800-6843288	NONHSAT136176
9	lnc-HDHD1-1	chrX:6687394-6687709	XLOC_008109
10	lnc-HDHD1-1	chrX:6701362-6701527	XLOC_008109
11	lnc-HDHD1-1	chrX:6687405-6687709	XLOC_008109

Variant related genes	Relation type
ENSG00000231217	TF binding region
VCX3A	TF binding region
ENSG00000231217	CpG island
VCX3A	CpG island
MTSS1	miRNA target sites
CLOCK	miRNA target sites
MTSS1L	miRNA target sites

Extended variants
information (count: 4471 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:4471 , 50 per page) page: 1 2 3 4 5 6 7 ... 90

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs535536511	chrX:6390031-6390032	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs191862270	chrX:6390071-6390072	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs184100141	chrX:6390134-6390135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs147007527	chrX:6390145-6390146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs114529603	chrX:6390151-6390152	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs187891150	chrX:6390225-6390226	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs575529194	chrX:6390362-6390363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs201811567	chrX:6390819-6390820	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs370810354	chrX:6390832-6390833	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs185610139	chrX:6390866-6390867	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs111066068	chrX:6390997-6390998	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs111213504	chrX:6391019-6391020	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs62643591	chrX:6391026-6391027	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs111213505	chrX:6391190-6391191	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs111162488	chrX:6391201-6391202	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs200523220	chrX:6391336-6391337	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs188496634	chrX:6391361-6391362	ZNF genes & repeats Bivalent/Poised TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs201327507	chrX:6391491-6391492	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs375859719	chrX:6391502-6391503	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs73459027	chrX:6391514-6391515	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs369605310	chrX:6415608-6415609	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs192934569	chrX:6415618-6415619	Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs144852253	chrX:6415632-6415633	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs572155865	chrX:6415644-6415645	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs147953516	chrX:6415649-6415650	Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs148998891	chrX:6415680-6415681	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs377207153	chrX:6415888-6415889	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs73627079	chrX:6415895-6415896	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs5916406	chrX:6416009-6416010	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs371363116	chrX:6418405-6418406	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs115969985	chrX:6418440-6418441	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs181447875	chrX:6418455-6418456	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs185193090	chrX:6418470-6418471	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs202017612	chrX:6418490-6418491	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs558287253	chrX:6418558-6418559	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs372426268	chrX:6418559-6418560	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs189747913	chrX:6418715-6418716	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs375930625	chrX:6418718-6418719	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs572158637	chrX:6418719-6418720	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs149131952	chrX:6418797-6418798	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs182414008	chrX:6418993-6418994	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs549083942	chrX:6419176-6419177	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs534682087	chrX:6419187-6419188	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs554390131	chrX:6419222-6419223	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs73459061	chrX:6419267-6419268	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs5962033	chrX:6419354-6419355	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140585095	chrX:6419383-6419384	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs371035422	chrX:6423466-6423467	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs184151965	chrX:6423483-6423484	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145291213	chrX:6423484-6423485	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:67)

Disease	PMID	Source
turner syndrome	20877625	CNVD
Kallmann Syndrome 1	22470819	CNVD
short stature	22470819	CNVD
Oro-facial digital syndrome	19023858	CNVD
Oro-facial digital syndrome	21572526	CNVD
Aicardi syndrome	21572526	CNVD
Vermis hypoplasia	21569638	CNVD
Opitz syndrome	21569638	CNVD
Opitz syndrome	21572526	CNVD
Oro-facial digital syndrome	21569638	CNVD
Abnormal corpus callosum	21572526	CNVD
T-cell lymphomas	19863542	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Seminomas	18059402	CNVD
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	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
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
Mental retardation	17406619	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Lung cancer	18438408	CNVD
Multiple myeloma	20724749	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Breast cancer	21785460	CNVD
XY gonadal dysgenesis	20685758	CNVD
Breast cancer	21364760	CNVD
Mental retardation	20486941	CNVD
Abnormal phenotypes	21355048	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	21549014	CNVD
Mental retardation	21549014	CNVD
Microphthalmia	21572526	CNVD
Steroid sulfatase deficiency	21549014	CNVD
Attention deficit hyperactivity disorder	21355048	CNVD
Ichthyosis	21355048	CNVD
Mental retardation	21355048	CNVD
Immune disease	21076436	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Developmental delay	21147756	CNVD
Epilepsy	22083797	CNVD
Bladder cancer	21909424	CNVD
Mental retardation	20877625	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:643 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:6390000-6390600	Weak transcription	Fetal Kidney	kidney
2	chrX:6390800-6391400	Bivalent/Poised TSS	Fetal Lung	lung
3	chrX:6390800-6391600	ZNF genes & repeats	Fetal Kidney	kidney
4	chrX:6415600-6416000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chrX:6415600-6416200	Enhancers	H9 Cell Line	embryonic stem cell
6	chrX:6415600-6416200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chrX:6418400-6419400	Enhancers	Liver	Liver
8	chrX:6423400-6424400	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chrX:6423800-6424200	Enhancers	H1 Cell Line	embryonic stem cell
10	chrX:6423800-6424400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
11	chrX:6423800-6424400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chrX:6424000-6424600	Enhancers	HUES6 Cell Line	embryonic stem cell
13	chrX:6430200-6431400	Enhancers	Fetal Brain Male	brain
14	chrX:6444200-6445600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
15	chrX:6458400-6460200	Enhancers	Dnd41	blood
16	chrX:6459200-6460000	Enhancers	Primary T cells from cord blood	blood
17	chrX:6463600-6464000	Enhancers	Fetal Thymus	thymus
18	chrX:6475000-6476600	Enhancers	Liver	Liver
19	chrX:6479000-6486000	Weak transcription	H9 Cell Line	embryonic stem cell
20	chrX:6482400-6482600	Enhancers	Placenta	Placenta
21	chrX:6482600-6484800	Weak transcription	Placenta	Placenta
22	chrX:6483800-6484200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
23	chrX:6484800-6486600	Enhancers	Placenta	Placenta
24	chrX:6486000-6486600	Enhancers	H9 Cell Line	embryonic stem cell
25	chrX:6494600-6499000	Weak transcription	H9 Cell Line	embryonic stem cell
26	chrX:6499400-6499600	Enhancers	H9 Cell Line	embryonic stem cell
27	chrX:6506800-6508600	Enhancers	Dnd41	blood
28	chrX:6517000-6517800	Enhancers	Liver	Liver
29	chrX:6525200-6525400	Enhancers	H9 Cell Line	embryonic stem cell
30	chrX:6525400-6529600	Weak transcription	H9 Cell Line	embryonic stem cell
31	chrX:6526200-6526600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chrX:6532000-6532800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
33	chrX:6532000-6532800	Enhancers	Fetal Brain Male	brain
34	chrX:6532000-6533600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chrX:6532200-6533200	Enhancers	Fetal Brain Female	brain
36	chrX:6548000-6548600	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chrX:6548000-6548600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chrX:6548000-6548800	Enhancers	Fetal Thymus	thymus
39	chrX:6560800-6561400	Enhancers	Dnd41	blood
40	chrX:6564400-6564800	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
41	chrX:6564600-6567000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chrX:6573000-6573200	Enhancers	H9 Cell Line	embryonic stem cell
43	chrX:6573200-6574800	Weak transcription	H9 Cell Line	embryonic stem cell
44	chrX:6573600-6575600	Enhancers	HUES48 Cell Line	embryonic stem cell
45	chrX:6574400-6575600	Enhancers	iPS-18 Cell Line	embryonic stem cell
46	chrX:6575600-6576400	Weak transcription	H9 Cell Line	embryonic stem cell
47	chrX:6576000-6576400	ZNF genes & repeats	H1 Cell Line	embryonic stem cell
48	chrX:6576000-6576600	ZNF genes & repeats	HUES64 Cell Line	embryonic stem cell
49	chrX:6577000-6583600	Weak transcription	H9 Cell Line	embryonic stem cell
50	chrX:6577800-6580000	Enhancers	NHEK	skin

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