Variant report

Variant	esv2422345
Chromosome Location	chrX:6279519-6709757
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:6650200-6650576	GM12878	blood:	n/a	n/a
2	ATF2	chrX:6656510-6657531	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:6656848-6657191	GM12878	blood:	n/a	n/a
6	BATF	chrX:6656817-6657350	GM12878	blood:	n/a	n/a
7	BATF	chrX:6384038-6384307	GM12878	blood:	n/a	chrX:6384168-6384179 chrX:6384169-6384179
8	BCL11A	chrX:6656657-6657479	GM12878	blood:	n/a	n/a
9	BCL11A	chrX:6656822-6657366	GM12878	blood:	n/a	n/a
10	BCL3	chrX:6676642-6677002	GM12878	blood:	n/a	n/a
11	BCL3	chrX:6656849-6657373	GM12878	blood:	n/a	n/a
12	BCL3	chrX:6656968-6657313	GM12878	blood:	n/a	n/a
13	BCLAF1	chrX:6656899-6657442	GM12878	blood:	n/a	n/a
14	BCLAF1	chrX:6650178-6650508	GM12878	blood:	n/a	n/a
15	BCLAF1	chrX:6656774-6657546	GM12878	blood:	n/a	n/a
16	BHLHE40	chrX:6666733-6666965	GM12878	blood:	n/a	n/a
17	BHLHE40	chrX:6650232-6650482	GM12878	blood:	n/a	n/a
18	BHLHE40	chrX:6656602-6657589	GM12878	blood:	n/a	n/a
19	BRCA1	chrX:6656940-6657436	GM12878	blood:	n/a	n/a
20	CCNT2	chrX:6312899-6313115	K562	blood:	n/a	n/a
21	CEBPB	chrX:6475740-6476115	HepG2	liver:	n/a	chrX:6475939-6475950
22	CEBPB	chrX:6471293-6471471	A549	lung:	n/a	chrX:6471422-6471433
23	CEBPB	chrX:6524963-6525194	IMR90	lung:	n/a	chrX:6525062-6525075
24	CEBPB	chrX:6670740-6670985	A549	lung:	n/a	chrX:6670833-6670844 chrX:6670846-6670857 chrX:6670832-6670845
25	CEBPB	chrX:6392183-6392377	IMR90	lung:	n/a	n/a
26	CEBPB	chrX:6670704-6670919	Hela-S3	cervix:	n/a	chrX:6670833-6670844 chrX:6670846-6670857 chrX:6670832-6670845
27	CEBPB	chrX:6670723-6670987	IMR90	lung:	n/a	chrX:6670833-6670844 chrX:6670846-6670857 chrX:6670832-6670845
28	CEBPB	chrX:6648377-6648623	IMR90	lung:	n/a	chrX:6648460-6648469 chrX:6648460-6648471
29	CEBPB	chrX:6656583-6657408	GM12878	blood:	n/a	n/a
30	CEBPB	chrX:6646306-6646609	IMR90	lung:	n/a	chrX:6646447-6646456 chrX:6646447-6646458 chrX:6646447-6646456 chrX:6646447-6646456 chrX:6646445-6646456 chrX:6646447-6646456
31	CEBPB	chrX:6524895-6525228	A549	lung:	n/a	chrX:6525062-6525075
32	CEBPB	chrX:6636411-6636698	HepG2	liver:	n/a	chrX:6636549-6636560
33	CEBPB	chrX:6555739-6556013	IMR90	lung:	n/a	chrX:6555877-6555888
34	CEBPB	chrX:6670703-6670928	HepG2	liver:	n/a	chrX:6670833-6670844 chrX:6670846-6670857 chrX:6670832-6670845
35	CEBPB	chrX:6294030-6294216	A549	lung:	n/a	n/a
36	CEBPB	chrX:6674442-6674623	A549	lung:	n/a	n/a
37	CEBPB	chrX:6555794-6556010	HepG2	liver:	n/a	chrX:6555877-6555888
38	CEBPB	chrX:6471282-6471527	K562	blood:	n/a	chrX:6471422-6471433
39	CEBPB	chrX:6636401-6636732	IMR90	lung:	n/a	chrX:6636549-6636560
40	CEBPB	chrX:6584701-6584981	IMR90	lung:	n/a	n/a
41	CEBPB	chrX:6471389-6471556	HepG2	liver:	n/a	chrX:6471422-6471433
42	CEBPB	chrX:6295507-6295722	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chrX:6584778-6584931	A549	lung:	n/a	n/a
44	CEBPB	chrX:6475811-6475996	HepG2	liver:	n/a	chrX:6475939-6475950
45	CEBPB	chrX:6484827-6485100	IMR90	lung:	n/a	n/a
46	CEBPB	chrX:6636479-6636630	K562	blood:	n/a	chrX:6636549-6636560
47	CEBPB	chrX:6636405-6636717	A549	lung:	n/a	chrX:6636549-6636560
48	CEBPB	chrX:6471257-6471479	IMR90	lung:	n/a	chrX:6471422-6471433
49	CEBPB	chrX:6384648-6384957	IMR90	lung:	n/a	chrX:6384810-6384823
50	CEBPB	chrX:6648360-6648619	HepG2	liver:	n/a	chrX:6648460-6648469 chrX:6648460-6648471

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:6452751-6452801	SAEC	small airway:	n/a
2	chrX:6452751-6452801	SAEC	small airway:	n/a
3	chrX:6453787-6453837	K562	blood:	n/a
4	chrX:6451812-6451862	MCF-7	breast:	n/a
5	chrX:6453787-6453837	HL-60	blood:	n/a
6	chrX:6453041-6453091	AG04450	lung:	fetal
7	chrX:6453787-6453837	PrEC	prostate:	n/a
8	chrX:6453041-6453091	NH-A	brain:	n/a
9	chrX:6453041-6453091	ovcar-3	ovarian:	n/a
10	chrX:6453041-6453091	Hepatocyte	liver:	n/a
11	chrX:6453041-6453091	CMK	blood:	n/a
12	chrX:6452751-6452801	SK-N-SH	brain:	n/a
13	chrX:6453787-6453837	Hepatocyte	liver:	n/a
14	chrX:6453787-6453837	SKMC	muscle:	n/a
15	chrX:6451812-6451862	Caco-2	colon:	n/a
16	chrX:6452751-6452801	HMEC	breast:	n/a
17	chrX:6452751-6452801	HCPEpiC	choroid plexus:	n/a
18	chrX:6451812-6451862	HNPCEpiC	eye:	n/a
19	chrX:6451812-6451862	BE2_C	brain:	n/a
20	chrX:6453041-6453091	HCM	heart:	n/a
21	chrX:6453041-6453091	H1-hESC	embryonic stem cell:	embryo
22	chrX:6452751-6452801	HPAEpiC	pulmonary alveolar:	n/a
23	chrX:6453787-6453837	HEK293	kidney:	embryo
24	chrX:6451812-6451862	H1-hESC	embryonic stem cell:	embryo
25	chrX:6452751-6452801	HRE	kidney:	n/a
26	chrX:6451812-6451862	GM12892	blood:	n/a
27	chrX:6453041-6453091	RPTEC	kidney:	n/a
28	chrX:6452751-6452801	AG10803	skin:	n/a
29	chrX:6451812-6451862	HL-60	blood:	n/a
30	chrX:6452751-6452801	ProgFib	skin:	n/a
31	chrX:6451812-6451862	HepG2	liver:	n/a
32	chrX:6453041-6453091	BJ	skin:	n/a
33	chrX:6453787-6453837	HNPCEpiC	eye:	n/a
34	chrX:6453041-6453091	HUVEC	blood vessel:	n/a
35	chrX:6453787-6453837	HEEpiC	esophagus:	n/a
36	chrX:6452751-6452801	K562	blood:	n/a
37	chrX:6453787-6453837	GM19239	blood:	n/a
38	chrX:6453787-6453837	HepG2	liver:	n/a
39	chrX:6451812-6451862	Hepatocyte	liver:	n/a
40	chrX:6453787-6453837	MCF-7	breast:	n/a
41	chrX:6453041-6453091	SK-N-SH_RA	brain:	n/a
42	chrX:6451812-6451862	MCF10A-Er-Src	breast:	n/a
43	chrX:6451812-6451862	NH-A	brain:	n/a
44	chrX:6453041-6453091	Caco-2	colon:	n/a
45	chrX:6453041-6453091	AG09309	skin:	n/a
46	chrX:6453041-6453091	SK-N-SH	brain:	n/a
47	chrX:6453787-6453837	NH-A	brain:	n/a
48	chrX:6451812-6451862	HIPEpiC	eye:	n/a
49	chrX:6453041-6453091	PFSK-1	brain:	n/a
50	chrX:6453041-6453091	AG04449	skin:	fetal

No.	Distal block	Cell Line	Cell type
1	chr7:87849338..87850062-chrX:6327052..6327572,2	NB4	blood:
2	chrX:6611316..6614128-chrX:6615657..6618460,2	MCF-7	breast:
3	chrX:6611316..6614128-chrX:6615657..6618460,2	MCF-7	breast:
4	chrX:6705927..6707578-chrX:6712936..6714694,2	K562	blood:
5	chrX:6377159..6378777-chrX:6382094..6385043,2	MCF-7	breast:
6	chrX:5939484..5940010-chrX:6281086..6281665,2	MCF-7	breast:
7	chrX:6377159..6378777-chrX:6382094..6385043,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HDHD1-1	chrX:6687405-6687709	XLOC_008109
2	lnc-HDHD1-1	chrX:6701362-6701527	XLOC_008109
3	lnc-VCX3A-2	chrX:6634384-6634507	NONHSAT136173
4	lnc-HDHD1-1	chrX:6685657-6685752	XLOC_008109
5	lnc-VCX3A-2	chrX:6649458-6649585	NONHSAT136173
6	lnc-VCX3A-2	chrX:6595906-6596170	NONHSAT136173
7	lnc-HDHD1-1	chrX:6687394-6687709	XLOC_008109

miRNA name	Chromosome Location	mirBase accession
hsa-miR-4770	chrX:6301948-6301965	MIMAT0019924

Variant related genes	Relation type
ENSG00000237730	TF binding region
ENSG00000231217	TF binding region
ENSG00000225962	TF binding region
MIR4770	TF binding region
VCX3A	TF binding region
ENSG00000229818	TF binding region
ENSG00000237730	CpG island
ENSG00000231217	CpG island
ENSG00000225962	CpG island
MIR4770	CpG island
VCX3A	CpG island
ENSG00000229818	CpG island
ENSG00000075142	chromatin interactions
MTSS1L	miRNA target sites
MTSS1	miRNA target sites
CLOCK	miRNA target sites

Extended variants
information (count: 3570 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3570 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs564691481	chrX:6280460-6280461	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs192190396	chrX:6280471-6280472	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183861755	chrX:6280670-6280671	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs146493499	chrX:6280684-6280685	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs372164108	chrX:6280923-6280924	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs141099271	chrX:6280990-6280991	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188485952	chrX:6281003-6281004	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs111739952	chrX:6281111-6281112	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs34069612	chrX:6281463-6281464	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs531887634	chrX:6281498-6281499	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs184310908	chrX:6281537-6281538	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs189493336	chrX:6281561-6281562	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs200360310	chrX:6281577-6281578	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs146762309	chrX:6281704-6281705	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs181923778	chrX:6281710-6281711	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs187562193	chrX:6281739-6281740	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs113152117	chrX:6281764-6281765	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs181539207	chrX:6281941-6281942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs375717279	chrX:6281971-6281972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs201211213	chrX:6281975-6281976	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs67556214	chrX:6281976-6281977	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs386416540	chrX:6281979-6281980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56303896	chrX:6281982-6281983	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs12394112	chrX:6282015-6282016	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs555504396	chrX:6282043-6282044	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs376922225	chrX:6282082-6282083	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs374268013	chrX:6282083-6282084	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs370472192	chrX:6282104-6282105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs186191290	chrX:6282144-6282145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs60397837	chrX:6282145-6282146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs12836153	chrX:6282146-6282147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs112373625	chrX:6282210-6282211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs58157104	chrX:6282211-6282212	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs145901057	chrX:6282218-6282219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs397751184	chrX:6282227-6282228	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183437699	chrX:6282256-6282257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs373495844	chrX:6282270-6282271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201759799	chrX:6282271-6282272	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs59815146	chrX:6282272-6282273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs36017798	chrX:6282274-6282275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs58202375	chrX:6282300-6282301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs199676639	chrX:6282305-6282306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs185797315	chrX:6282389-6282390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200211157	chrX:6282446-6282447	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs6529942	chrX:6282504-6282505	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs191049723	chrX:6282541-6282542	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs183741616	chrX:6282746-6282747	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs550218514	chrX:6282830-6282831	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs200544854	chrX:6282886-6282887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187822323	chrX:6282922-6282923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

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	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	21293372	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

Chromatin state (count:530 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:6280400-6281200	Enhancers	H1 Cell Line	embryonic stem cell
2	chrX:6280400-6281400	Enhancers	HUES48 Cell Line	embryonic stem cell
3	chrX:6280400-6281400	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chrX:6280400-6281800	Enhancers	H9 Cell Line	embryonic stem cell
5	chrX:6280600-6281400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
6	chrX:6280600-6281400	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chrX:6281800-6301200	Weak transcription	H9 Cell Line	embryonic stem cell
8	chrX:6283600-6283800	Enhancers	HUES48 Cell Line	embryonic stem cell
9	chrX:6291200-6291600	Enhancers	Fetal Intestine Small	intestine
10	chrX:6291200-6291800	Enhancers	Fetal Intestine Large	intestine
11	chrX:6291200-6291800	Enhancers	Small Intestine	intestine
12	chrX:6292800-6293400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chrX:6293400-6293600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
14	chrX:6293600-6294200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
15	chrX:6294200-6294400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chrX:6294400-6294800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chrX:6294400-6300600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
18	chrX:6294800-6296000	Enhancers	Dnd41	blood
19	chrX:6296000-6300600	Weak transcription	Dnd41	blood
20	chrX:6298600-6300400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
21	chrX:6299200-6301200	Enhancers	Fetal Intestine Large	intestine
22	chrX:6299400-6302400	Enhancers	Fetal Thymus	thymus
23	chrX:6299800-6301200	Enhancers	Liver	Liver
24	chrX:6300400-6301800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chrX:6300600-6301000	Enhancers	Dnd41	blood
26	chrX:6300600-6301200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chrX:6300600-6301200	Enhancers	Pancreas	Pancrea
28	chrX:6300600-6301400	Enhancers	Fetal Intestine Small	intestine
29	chrX:6300600-6303200	Enhancers	HUES64 Cell Line	embryonic stem cell
30	chrX:6300800-6303200	Enhancers	HUES48 Cell Line	embryonic stem cell
31	chrX:6300800-6303200	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chrX:6301000-6302200	Enhancers	iPS-20b Cell Line	embryonic stem cell
33	chrX:6301000-6303000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
34	chrX:6301200-6301600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
35	chrX:6301200-6302400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
36	chrX:6301200-6302600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chrX:6301200-6303000	Enhancers	H9 Cell Line	embryonic stem cell
38	chrX:6301200-6303000	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chrX:6301400-6301600	Enhancers	H1 Cell Line	embryonic stem cell
40	chrX:6301400-6301600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
41	chrX:6301400-6302200	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
42	chrX:6301400-6302600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
43	chrX:6301400-6303000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
44	chrX:6301400-6303200	Enhancers	Cortex derived primary cultured neurospheres	brain
45	chrX:6301600-6302600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
46	chrX:6301600-6302800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
47	chrX:6301600-6309600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chrX:6301800-6302200	Flanking Active TSS	ES-I3 Cell Line	embryonic stem cell
49	chrX:6301800-6302200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
50	chrX:6302000-6302800	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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