Variant report

Variant	nsv948484
Chromosome Location	chrX:6057749-6401143
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:6243610-6243868	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chrX:6229269-6229469	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chrX:6143762-6143781	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chrX:6102924-6103158	GM12878	blood:	n/a	n/a
5	BATF	chrX:6384038-6384307	GM12878	blood:	n/a	chrX:6384168-6384179 chrX:6384169-6384179
6	BCL11A	chrX:6102943-6103270	GM12878	blood:	n/a	chrX:6103065-6103074
7	CCNT2	chrX:6312899-6313115	K562	blood:	n/a	n/a
8	CEBPB	chrX:6294030-6294216	A549	lung:	n/a	n/a
9	CEBPB	chrX:6146621-6146954	H1-hESC	embryonic stem cell:	n/a	chrX:6146721-6146734
10	CEBPB	chrX:6392183-6392377	IMR90	lung:	n/a	n/a
11	CEBPB	chrX:6177506-6177590	K562	blood:	n/a	n/a
12	CEBPB	chrX:6196250-6196493	IMR90	lung:	n/a	n/a
13	CEBPB	chrX:6128365-6128540	H1-hESC	embryonic stem cell:	n/a	chrX:6128465-6128476
14	CEBPB	chrX:6138341-6138695	IMR90	lung:	n/a	chrX:6138520-6138529 chrX:6138495-6138506 chrX:6138520-6138531 chrX:6138520-6138529 chrX:6138520-6138529 chrX:6138518-6138531 chrX:6138518-6138531 chrX:6138520-6138529 chrX:6138518-6138529
15	CEBPB	chrX:6177455-6177729	IMR90	lung:	n/a	n/a
16	CEBPB	chrX:6108447-6108656	HepG2	liver:	n/a	chrX:6108474-6108487 chrX:6108611-6108622
17	CEBPB	chrX:6090544-6090693	A549	lung:	n/a	chrX:6090604-6090615 chrX:6090553-6090564 chrX:6090604-6090617
18	CEBPB	chrX:6138401-6138691	A549	lung:	n/a	chrX:6138520-6138529 chrX:6138495-6138506 chrX:6138520-6138531 chrX:6138520-6138529 chrX:6138520-6138529 chrX:6138518-6138531 chrX:6138518-6138531 chrX:6138520-6138529 chrX:6138518-6138529
19	CEBPB	chrX:6232280-6232583	IMR90	lung:	n/a	chrX:6232438-6232449
20	CEBPB	chrX:6295507-6295722	Hela-S3	cervix:	n/a	n/a
21	CEBPB	chrX:6088585-6088643	A549	lung:	n/a	n/a
22	CEBPB	chrX:6128357-6128557	HepG2	liver:	n/a	chrX:6128465-6128476
23	CEBPB	chrX:6196285-6196484	HepG2	liver:	n/a	n/a
24	CEBPB	chrX:6196312-6196512	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chrX:6384648-6384957	IMR90	lung:	n/a	chrX:6384810-6384823
26	CEBPB	chrX:6196213-6196522	A549	lung:	n/a	n/a
27	CEBPB	chrX:6232394-6232537	HepG2	liver:	n/a	chrX:6232438-6232449
28	CEBPB	chrX:6090505-6090705	HepG2	liver:	n/a	chrX:6090604-6090615 chrX:6090553-6090564 chrX:6090604-6090617
29	CEBPB	chrX:6138377-6138688	HepG2	liver:	n/a	chrX:6138520-6138529 chrX:6138495-6138506 chrX:6138520-6138531 chrX:6138520-6138529 chrX:6138520-6138529 chrX:6138518-6138531 chrX:6138518-6138531 chrX:6138520-6138529 chrX:6138518-6138529
30	CEBPB	chrX:6124249-6124452	HepG2	liver:	n/a	n/a
31	CHD1	chrX:6143495-6144129	H1-hESC	embryonic stem cell:	n/a	n/a
32	CHD1	chrX:6146143-6146272	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD1	chrX:6145610-6145849	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD1	chrX:6145172-6145237	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chrX:6217947-6218079	GM12878	blood:	n/a	n/a
36	CHD2	chrX:6291664-6291747	K562	blood:	n/a	n/a
37	CHD2	chrX:6143836-6144261	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chrX:6103011-6103142	GM12878	blood:	n/a	n/a
39	CHD2	chrX:6146792-6147044	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chrX:6144019-6144865	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTCF	chrX:6210686-6210933	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chrX:6210720-6210870	NHEK	skin:	n/a	n/a
43	CTCF	chrX:6289460-6289610	GM12878	blood:	n/a	chrX:6289585-6289606 chrX:6289586-6289595
44	CTCF	chrX:6107287-6107297	Medullo	brain:	n/a	n/a
45	CTCF	chrX:6167785-6167834	LNCaP	prostate:	n/a	n/a
46	CTCF	chrX:6210760-6210910	GM12868	blood:	n/a	n/a
47	CTCF	chrX:6143920-6144070	HA-sp	spinal cord:	n/a	chrX:6143992-6144010
48	CTCF	chrX:6139589-6139613	LNCaP	prostate:	n/a	n/a
49	CTCF	chrX:6068376-6068447	Lung_OC	lung:	n/a	n/a
50	CTCF	chrX:6255452-6255535	Pancreas_OC	pancreas:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:6144121-6144171	SK-N-SH_RA	brain:	n/a
2	chrX:6146809-6146859	MCF-7	breast:	n/a
3	chrX:6145771-6145821	HEEpiC	esophagus:	n/a
4	chrX:6144121-6144171	SK-N-SH_RA	brain:	n/a
5	chrX:6146809-6146859	MCF-7	breast:	n/a
6	chrX:6145771-6145821	HEEpiC	esophagus:	n/a
7	chrX:6144633-6144683	HIPEpiC	eye:	n/a
8	chrX:6146656-6146706	ProgFib	skin:	n/a
9	chrX:6146900-6146950	NHDF-neo	bronchial:	n/a
10	chrX:6146760-6146810	HCM	heart:	n/a
11	chrX:6147159-6147209	SK-N-MC	brain:	n/a
12	chrX:6146608-6146658	HCF	heart:	n/a
13	chrX:6144121-6144171	GM12892	blood:	n/a
14	chrX:6147113-6147163	RPTEC	kidney:	n/a
15	chrX:6146608-6146658	SK-N-SH	brain:	n/a
16	chrX:6145346-6145396	HRCEpiC	kidney:	n/a
17	chrX:6144633-6144683	AoSMC	blood vessel:	n/a
18	chrX:6147159-6147209	LNCaP	prostate:	n/a
19	chrX:6146780-6146830	HCT-116	colon:	n/a
20	chrX:6147159-6147209	SK-N-SH	brain:	n/a
21	chrX:6146780-6146830	A549	lung:	n/a
22	chrX:6147159-6147209	ovcar-3	ovarian:	n/a
23	chrX:6144633-6144683	AG09309	skin:	n/a
24	chrX:6144633-6144683	K562	blood:	n/a
25	chrX:6146809-6146859	BJ	skin:	n/a
26	chrX:6145771-6145821	Hepatocyte	liver:	n/a
27	chrX:6147159-6147209	PFSK-1	brain:	n/a
28	chrX:6146608-6146658	HRE	kidney:	n/a
29	chrX:6147113-6147163	GM12891	blood:	n/a
30	chrX:6147299-6147349	GM12878	blood:	n/a
31	chrX:6146608-6146658	HRPEpiC	eye:	n/a
32	chrX:6146656-6146706	HAEpiC	amniotic membrane:	n/a
33	chrX:6145096-6145146	HEK293	kidney:	embryo
34	chrX:6144121-6144171	PANC-1	pancreas:	n/a
35	chrX:6145096-6145146	HCT-116	colon:	n/a
36	chrX:6147113-6147163	AG04450	lung:	fetal
37	chrX:6145557-6145607	HUVEC	blood vessel:	n/a
38	chrX:6146656-6146706	HUVEC	blood vessel:	n/a
39	chrX:6146656-6146706	LNCaP	prostate:	n/a
40	chrX:6144633-6144683	HMEC	breast:	n/a
41	chrX:6144121-6144171	HRCEpiC	kidney:	n/a
42	chrX:6145346-6145396	HEEpiC	esophagus:	n/a
43	chrX:6145557-6145607	NHBE	bronchial:	n/a
44	chrX:6145771-6145821	HRCEpiC	kidney:	n/a
45	chrX:6146760-6146810	ECC-1	luminal epithelium:	n/a
46	chrX:6145730-6145780	Jurkat	blood:	n/a
47	chrX:6146656-6146706	HNPCEpiC	eye:	n/a
48	chrX:6145346-6145396	MCF10A-Er-Src	breast:	n/a
49	chrX:6146656-6146706	CMK	blood:	n/a
50	chrX:6145771-6145821	GM12878	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:5939484..5940010-chrX:6281086..6281665,2	MCF-7	breast:
2	chrX:6377159..6378777-chrX:6382094..6385043,2	MCF-7	breast:
3	chrX:6172159..6173803-chrX:6174746..6177645,2	MCF-7	breast:
4	chrX:6172159..6173803-chrX:6174746..6177645,2	MCF-7	breast:
5	chrX:6377159..6378777-chrX:6382094..6385043,2	MCF-7	breast:
6	chrX:6093280..6095044-chrX:6096673..6099508,2	K562	blood:
7	chr7:87849338..87850062-chrX:6327052..6327572,2	NB4	blood:
8	chrX:6093280..6095044-chrX:6096673..6099508,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STS-5	chrX:6194587-6194683	NONHSAT136166
2	lnc-STS-5	chrX:6193676-6193984	NONHSAT136166

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

Variant related genes	Relation type
MIR4770	TF binding region
ENSG00000237730	TF binding region
ENSG00000229818	TF binding region
ENSG00000225962	TF binding region
NLGN4X	TF binding region
MIR4770	CpG island
ENSG00000237730	CpG island
ENSG00000229818	CpG island
ENSG00000225962	CpG island
NLGN4X	CpG island
ENSG00000075142	chromatin interactions

Extended variants
information (count: 3212 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:3212 , 50 per page) page: 1 2 3 4 5 6 7 ... 65

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1997480	chrX:6057749-6057750	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149795230	chrX:6057767-6057768	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs73444289	chrX:6057823-6057824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs370161993	chrX:6057854-6057855	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs149079373	chrX:6057878-6057879	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs371092495	chrX:6057964-6057965	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs142150322	chrX:6058024-6058025	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375664923	chrX:6058039-6058040	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192869325	chrX:6058119-6058120	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs183728607	chrX:6058192-6058193	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs151199364	chrX:6058193-6058194	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs553987972	chrX:6058230-6058231	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs141395282	chrX:6058363-6058364	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs147010884	chrX:6058402-6058403	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs62588032	chrX:6058405-6058406	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs141995820	chrX:6058424-6058425	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs112096033	chrX:6058499-6058500	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs386823716	chrX:6058508-6058509	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs5916314	chrX:6058512-6058513	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs374332032	chrX:6058516-6058517	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs200252745	chrX:6058520-6058521	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs57413369	chrX:6058533-6058534	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56324418	chrX:6058537-6058538	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs187861895	chrX:6058554-6058555	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs368702686	chrX:6058754-6058755	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs36080808	chrX:6058786-6058787	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs60538091	chrX:6058797-6058798	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs56298059	chrX:6058871-6058872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs150108801	chrX:6059005-6059006	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs138428581	chrX:6059027-6059028	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs192913737	chrX:6059060-6059061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs561179840	chrX:6059405-6059406	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs149275926	chrX:6059414-6059415	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs374198986	chrX:6059428-6059429	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs10126716	chrX:6059593-6059594	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs183485846	chrX:6059752-6059753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs367895605	chrX:6059819-6059820	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs372159947	chrX:6060300-6060301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs138418585	chrX:6060344-6060345	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs188114205	chrX:6060388-6060389	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs374116653	chrX:6060509-6060510	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs191462273	chrX:6060650-6060651	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs113986746	chrX:6060741-6060742	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs146164681	chrX:6060773-6060774	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs57946422	chrX:6060782-6060783	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1921938	chrX:6060914-6060915	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs184617464	chrX:6061067-6061068	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs190778081	chrX:6061160-6061161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs181524816	chrX:6061203-6061204	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs185374177	chrX:6061214-6061215	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Autism	20643418	CNVD
Autism	23710042	CNVD
Schizophrenia	23710042	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
early-passage human iPS cells	21368824	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

Chromatin state (count:922 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:6048600-6069000	Strong transcription	Dnd41	blood
2	chrX:6049600-6060800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
3	chrX:6049800-6067000	Weak transcription	Fetal Brain Female	brain
4	chrX:6050400-6072200	Weak transcription	Brain Germinal Matrix	brain
5	chrX:6054800-6080000	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chrX:6055000-6067000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chrX:6055000-6077800	Weak transcription	Ovary	ovary
8	chrX:6055200-6069000	Weak transcription	H9 Cell Line	embryonic stem cell
9	chrX:6055400-6065400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
10	chrX:6055400-6068600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chrX:6055400-6069000	Weak transcription	H1 Cell Line	embryonic stem cell
12	chrX:6055600-6059000	Weak transcription	Fetal Thymus	thymus
13	chrX:6055600-6066800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chrX:6055600-6077600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
15	chrX:6055800-6065200	Weak transcription	HUES48 Cell Line	embryonic stem cell
16	chrX:6056000-6058200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
17	chrX:6057200-6059200	Strong transcription	HUES6 Cell Line	embryonic stem cell
18	chrX:6057400-6058400	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
19	chrX:6058200-6058800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chrX:6058200-6059400	Strong transcription	iPS-18 Cell Line	embryonic stem cell
21	chrX:6058400-6064200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
22	chrX:6059000-6059400	Strong transcription	Fetal Thymus	thymus
23	chrX:6059200-6067000	Weak transcription	HUES6 Cell Line	embryonic stem cell
24	chrX:6059400-6062800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chrX:6059400-6065000	Weak transcription	Fetal Thymus	thymus
26	chrX:6062400-6064400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
27	chrX:6062800-6064600	Strong transcription	iPS-18 Cell Line	embryonic stem cell
28	chrX:6064200-6064600	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
29	chrX:6064600-6066400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
30	chrX:6064600-6067000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
31	chrX:6065000-6067800	Strong transcription	Fetal Thymus	thymus
32	chrX:6065200-6066000	Strong transcription	HUES48 Cell Line	embryonic stem cell
33	chrX:6065400-6069600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
34	chrX:6065600-6066000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
35	chrX:6066000-6067200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chrX:6066000-6069000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
37	chrX:6066400-6068400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
38	chrX:6066800-6068400	Enhancers	Cortex derived primary cultured neurospheres	brain
39	chrX:6067000-6067200	Enhancers	Fetal Brain Female	brain
40	chrX:6067000-6067400	Strong transcription	HUES6 Cell Line	embryonic stem cell
41	chrX:6067000-6068200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chrX:6067000-6070000	Strong transcription	iPS-18 Cell Line	embryonic stem cell
43	chrX:6067200-6067600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chrX:6067200-6069800	Strong transcription	HUES48 Cell Line	embryonic stem cell
45	chrX:6067200-6071000	Weak transcription	Fetal Brain Female	brain
46	chrX:6067400-6067800	Enhancers	Brain Angular Gyrus	brain
47	chrX:6067400-6067800	Enhancers	Brain Anterior Caudate	brain
48	chrX:6067400-6068000	Enhancers	Brain Hippocampus Middle	brain
49	chrX:6067400-6068200	Weak transcription	HUES6 Cell Line	embryonic stem cell
50	chrX:6067600-6067800	Genic enhancers	ES-I3 Cell Line	embryonic stem cell

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