Variant report

Variant	esv2752328
Chromosome Location	chrX:5058980-5587394
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1039)
CpG islands
(count:122)
Chromatin interactive
region (count:12)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1039 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chrX:5224661-5225054	K562	blood:	n/a	n/a
2	ATF2	chrX:5564670-5565328	GM12878	blood:	n/a	n/a
3	ATF2	chrX:5564791-5565415	GM12878	blood:	n/a	n/a
4	BACH1	chrX:5392218-5392765	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chrX:5550544-5550555	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chrX:5160840-5160851	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chrX:5568977-5569303	GM12878	blood:	n/a	n/a
8	BATF	chrX:5564825-5565221	GM12878	blood:	n/a	n/a
9	BATF	chrX:5081052-5081344	GM12878	blood:	n/a	n/a
10	BCL11A	chrX:5081140-5081333	GM12878	blood:	n/a	n/a
11	BCL11A	chrX:5564808-5565237	GM12878	blood:	n/a	chrX:5565045-5565054
12	BCL11A	chrX:5568957-5569317	GM12878	blood:	n/a	n/a
13	BCL11A	chrX:5564857-5565196	GM12878	blood:	n/a	chrX:5565045-5565054
14	BCL11A	chrX:5081123-5081345	GM12878	blood:	n/a	n/a
15	BCL3	chrX:5564824-5565164	GM12878	blood:	n/a	chrX:5565045-5565054
16	BCLAF1	chrX:5564765-5565287	GM12878	blood:	n/a	chrX:5565045-5565054
17	BHLHE40	chrX:5569068-5569288	GM12878	blood:	n/a	n/a
18	BHLHE40	chrX:5564826-5565261	GM12878	blood:	n/a	n/a
19	BHLHE40	chrX:5081840-5081882	GM12878	blood:	n/a	n/a
20	CEBPB	chrX:5317432-5317770	A549	lung:	n/a	n/a
21	CEBPB	chrX:5342911-5343207	IMR90	lung:	n/a	n/a
22	CEBPB	chrX:5154862-5155091	A549	lung:	n/a	chrX:5154947-5154960
23	CEBPB	chrX:5076753-5077021	A549	lung:	n/a	n/a
24	CEBPB	chrX:5317360-5317866	MCF-7	breast:	n/a	n/a
25	CEBPB	chrX:5226681-5226987	IMR90	lung:	n/a	chrX:5226804-5226815
26	CEBPB	chrX:5317393-5317826	MCF-7	breast:	n/a	n/a
27	CEBPB	chrX:5329967-5330167	Hela-S3	cervix:	n/a	chrX:5330019-5330030 chrX:5330018-5330031
28	CEBPB	chrX:5564886-5565217	GM12878	blood:	n/a	n/a
29	CEBPB	chrX:5224730-5225018	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chrX:5076860-5076975	H1-hESC	embryonic stem cell:	n/a	n/a
31	CEBPB	chrX:5320583-5320829	MCF-7	breast:	n/a	n/a
32	CEBPB	chrX:5083744-5083950	HepG2	liver:	n/a	n/a
33	CEBPB	chrX:5075215-5075556	A549	lung:	n/a	n/a
34	CEBPB	chrX:5255286-5255523	Hela-S3	cervix:	n/a	chrX:5255425-5255434 chrX:5255425-5255434 chrX:5255425-5255434 chrX:5255423-5255436
35	CEBPB	chrX:5075241-5075519	IMR90	lung:	n/a	n/a
36	CEBPB	chrX:5329921-5330178	A549	lung:	n/a	chrX:5330019-5330030 chrX:5330018-5330031
37	CEBPB	chrX:5342905-5343208	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chrX:5255264-5255539	A549	lung:	n/a	chrX:5255425-5255434 chrX:5255425-5255434 chrX:5255425-5255434 chrX:5255423-5255436
39	CEBPB	chrX:5552356-5552464	A549	lung:	n/a	n/a
40	CEBPB	chrX:5226719-5226930	HepG2	liver:	n/a	chrX:5226804-5226815
41	CEBPB	chrX:5329904-5330106	HepG2	liver:	n/a	chrX:5330019-5330030 chrX:5330018-5330031
42	CEBPB	chrX:5129631-5129855	HepG2	liver:	n/a	chrX:5129788-5129801
43	CEBPB	chrX:5317485-5317713	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chrX:5357805-5358046	IMR90	lung:	n/a	chrX:5357936-5357947
45	CEBPB	chrX:5308142-5308437	HepG2	liver:	n/a	chrX:5308312-5308323 chrX:5308292-5308303
46	CEBPB	chrX:5255262-5255595	IMR90	lung:	n/a	chrX:5255425-5255434 chrX:5255425-5255434 chrX:5255425-5255434 chrX:5255423-5255436
47	CEBPB	chrX:5308227-5308367	IMR90	lung:	n/a	chrX:5308312-5308323 chrX:5308292-5308303
48	CEBPB	chrX:5308178-5308378	H1-hESC	embryonic stem cell:	n/a	chrX:5308312-5308323 chrX:5308292-5308303
49	CEBPB	chrX:5342927-5343127	HepG2	liver:	n/a	n/a
50	CEBPB	chrX:5317433-5317774	HepG2	liver:	n/a	n/a

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:5470075-5470125	ProgFib	skin:	n/a
2	chrX:5470075-5470125	LNCaP	prostate:	n/a
3	chrX:5470290-5470340	LNCaP	prostate:	n/a
4	chrX:5470290-5470340	PFSK-1	brain:	n/a
5	chrX:5470075-5470125	GM19239	blood:	n/a
6	chrX:5470290-5470340	PrEC	prostate:	n/a
7	chrX:5470075-5470125	ECC-1	luminal epithelium:	n/a
8	chrX:5470290-5470340	SK-N-SH_RA	brain:	n/a
9	chrX:5470290-5470340	AG04450	lung:	fetal
10	chrX:5470075-5470125	HepG2	liver:	n/a
11	chrX:5470075-5470125	HMEC	breast:	n/a
12	chrX:5470290-5470340	AG09319	gingival:	n/a
13	chrX:5470290-5470340	Hela-S3	cervix:	n/a
14	chrX:5470290-5470340	K562	blood:	n/a
15	chrX:5470290-5470340	PANC-1	pancreas:	n/a
16	chrX:5470075-5470125	AG04449	skin:	fetal
17	chrX:5470290-5470340	HCF	heart:	n/a
18	chrX:5470290-5470340	HepG2	liver:	n/a
19	chrX:5470075-5470125	IMR90	lung:	fetal
20	chrX:5470290-5470340	CMK	blood:	n/a
21	chrX:5470290-5470340	GM12891	blood:	n/a
22	chrX:5470290-5470340	RPTEC	kidney:	n/a
23	chrX:5470290-5470340	HL-60	blood:	n/a
24	chrX:5470290-5470340	BE2_C	brain:	n/a
25	chrX:5470075-5470125	HEEpiC	esophagus:	n/a
26	chrX:5470075-5470125	Hela-S3	cervix:	n/a
27	chrX:5470075-5470125	K562	blood:	n/a
28	chrX:5470290-5470340	SK-N-SH	brain:	n/a
29	chrX:5470075-5470125	GM06990	blood:	n/a
30	chrX:5470290-5470340	HCT-116	colon:	n/a
31	chrX:5470075-5470125	HL-60	blood:	n/a
32	chrX:5470290-5470340	SKMC	muscle:	n/a
33	chrX:5470290-5470340	HIPEpiC	eye:	n/a
34	chrX:5470075-5470125	MCF10A-Er-Src	breast:	n/a
35	chrX:5470075-5470125	Caco-2	colon:	n/a
36	chrX:5470075-5470125	NT2-D1	testis:	n/a
37	chrX:5470075-5470125	HPAEpiC	pulmonary alveolar:	n/a
38	chrX:5470290-5470340	HRE	kidney:	n/a
39	chrX:5470290-5470340	NHDF-neo	bronchial:	n/a
40	chrX:5470290-5470340	HUVEC	blood vessel:	n/a
41	chrX:5470290-5470340	ProgFib	skin:	n/a
42	chrX:5470075-5470125	PrEC	prostate:	n/a
43	chrX:5470290-5470340	AoSMC	blood vessel:	n/a
44	chrX:5470290-5470340	GM12878	blood:	n/a
45	chrX:5470290-5470340	MCF-7	breast:	n/a
46	chrX:5470290-5470340	SAEC	small airway:	n/a
47	chrX:5470075-5470125	ovcar-3	ovarian:	n/a
48	chrX:5470075-5470125	SK-N-MC	brain:	n/a
49	chrX:5470075-5470125	HRCEpiC	kidney:	n/a
50	chrX:5470290-5470340	HPAEpiC	pulmonary alveolar:	n/a

(count:12 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:5376030..5377037-chrX:5795005..5796053,5	MCF-7	breast:
2	chrX:5364801..5367777-chrX:5395940..5398619,2	MCF-7	breast:
3	chrX:5464584..5467087-chrX:5468527..5471240,2	K562	blood:
4	chrX:5464584..5467087-chrX:5468527..5471240,2	K562	blood:
5	chr8:43094720..43095220-chrX:5115604..5116140,2	MCF-7	breast:
6	chr4:8147667..8148302-chrX:5458311..5459167,2	MCF-7	breast:
7	chrX:5092554..5094353-chrX:5104934..5106634,2	MCF-7	breast:
8	chr9:29610453..29611027-chrX:5299764..5300614,2	MCF-7	breast:
9	chrX:5364801..5367777-chrX:5395940..5398619,2	MCF-7	breast:
10	chr11:74408478..74408979-chrX:5168701..5169217,2	Hela-S3	cervix:
11	chrX:5092554..5094353-chrX:5104934..5106634,2	MCF-7	breast:
12	chrX:5054174..5056224-chrX:5056341..5059009,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLGN4X-1	chrX:5571464-5571744	ENSG00000236120
2	lnc-CXorf28-10	chrX:5087553-5088686	NONHSAT136153
3	lnc-NLGN4X-2	chrX:5581462-5581744	NONHSAT136158
4	lnc-NLGN4X-2	chrX:5581464-5581744	NONHSAT136160
5	lnc-NLGN4X-2	chrX:5581462-5581744	NONHSAT136159
6	lnc-NLGN4X-3	chrX:5086959-5087480	NONHSAT136152
7	lnc-NLGN4X-1	chrX:5571462-5571744	ENSG00000236120

No data

Variant related genes	Relation type
ENSG00000201660	TF binding region
MTND6P12	TF binding region
ENSG00000238193	TF binding region
ENSG00000226313	TF binding region
ENSG00000201660	CpG island
MTND6P12	CpG island
ENSG00000238193	CpG island
ENSG00000226313	CpG island
ENSG00000054938	chromatin interactions

Extended variants
information (count: 1890 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:1890 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs181869338	chrX:5062666-5062667	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs10218069	chrX:5062836-5062837	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs558430971	chrX:5062951-5062952	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs5915987	chrX:5063029-5063030	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs111562737	chrX:5063152-5063153	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186945264	chrX:5063185-5063186	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs5915988	chrX:5063228-5063229	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs5915989	chrX:5063260-5063261	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs192051267	chrX:5063309-5063310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs199559514	chrX:5063353-5063354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs112089233	chrX:5063355-5063356	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs35532109	chrX:5063361-5063362	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs199689000	chrX:5063362-5063363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs367652120	chrX:5063367-5063368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs200784192	chrX:5063390-5063391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs199584893	chrX:5063397-5063398	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs77507402	chrX:5063398-5063399	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs5915992	chrX:5063402-5063403	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs112440926	chrX:5063416-5063417	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs186117439	chrX:5063458-5063459	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs16997018	chrX:5063464-5063465	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113721242	chrX:5063474-5063475	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs535631270	chrX:5063515-5063516	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs374780509	chrX:5063575-5063576	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs143148409	chrX:5063591-5063592	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs5915993	chrX:5063596-5063597	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs5915500	chrX:5063607-5063608	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs189794359	chrX:5063633-5063634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs5915994	chrX:5063643-5063644	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs113683884	chrX:5063715-5063716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182055852	chrX:5063798-5063799	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs371576117	chrX:5063801-5063802	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs1463540	chrX:5063828-5063829	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs143473039	chrX:5063961-5063962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs145868062	chrX:5063967-5063968	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs138765332	chrX:5064027-5064028	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs187050195	chrX:5064048-5064049	Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs191386727	chrX:5064071-5064072	Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs183636402	chrX:5064093-5064094	Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs1463539	chrX:5064112-5064113	Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs1463538	chrX:5064115-5064116	Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs148158028	chrX:5064277-5064278	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs11459149	chrX:5064299-5064300	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs397936236	chrX:5064318-5064319	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs188584410	chrX:5064319-5064320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs202169075	chrX:5064332-5064333	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200590322	chrX:5064339-5064340	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs5961635	chrX:5073000-5073001	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs190207795	chrX:5073015-5073016	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs181042575	chrX:5073040-5073041	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
short stature	22470819	CNVD
turner syndrome	20877625	CNVD
Kallmann Syndrome 1	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
Alcoholism	21790672	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Mental retardation	20486941	CNVD

Chromatin state (count:293 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:5062600-5062800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
2	chrX:5062800-5063800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
3	chrX:5063800-5064200	Enhancers	iPS-18 Cell Line	embryonic stem cell
4	chrX:5063800-5064400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
5	chrX:5063800-5064400	Enhancers	HUES6 Cell Line	embryonic stem cell
6	chrX:5073000-5073200	Enhancers	HUES6 Cell Line	embryonic stem cell
7	chrX:5073000-5073200	Enhancers	iPS-18 Cell Line	embryonic stem cell
8	chrX:5073000-5073800	Enhancers	HUES64 Cell Line	embryonic stem cell
9	chrX:5073200-5073400	Enhancers	iPS-20b Cell Line	embryonic stem cell
10	chrX:5073200-5073800	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
11	chrX:5073200-5073800	Flanking Active TSS	HUES6 Cell Line	embryonic stem cell
12	chrX:5073200-5073800	Flanking Active TSS	iPS-18 Cell Line	embryonic stem cell
13	chrX:5073200-5074000	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chrX:5073200-5074000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
15	chrX:5073200-5074000	Enhancers	HUES48 Cell Line	embryonic stem cell
16	chrX:5073200-5074000	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chrX:5073200-5074800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
18	chrX:5073200-5075400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chrX:5073400-5073800	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
20	chrX:5073800-5074000	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chrX:5073800-5074000	Enhancers	iPS-20b Cell Line	embryonic stem cell
22	chrX:5073800-5075000	Enhancers	iPS-18 Cell Line	embryonic stem cell
23	chrX:5074000-5082000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
24	chrX:5081600-5082400	Enhancers	HUES48 Cell Line	embryonic stem cell
25	chrX:5081600-5082400	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chrX:5081600-5082600	Enhancers	iPS-15b Cell Line	embryonic stem cell
27	chrX:5081600-5082600	Enhancers	iPS-18 Cell Line	embryonic stem cell
28	chrX:5082000-5082200	Enhancers	ES-I3 Cell Line	embryonic stem cell
29	chrX:5091600-5092200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chrX:5094600-5095000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
31	chrX:5094600-5095000	Active TSS	Breast Myoepithelial Primary Cells	Breast
32	chrX:5095200-5095400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
33	chrX:5097200-5098000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
34	chrX:5097200-5098000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chrX:5098000-5098800	Flanking Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chrX:5098000-5098800	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
37	chrX:5098200-5098600	Enhancers	iPS-18 Cell Line	embryonic stem cell
38	chrX:5098200-5098600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
39	chrX:5098200-5098800	Enhancers	ES-I3 Cell Line	embryonic stem cell
40	chrX:5098800-5099000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chrX:5098800-5099200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chrX:5137200-5137800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
43	chrX:5140600-5141000	Enhancers	iPS-18 Cell Line	embryonic stem cell
44	chrX:5140600-5141800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
45	chrX:5154000-5154200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chrX:5154000-5154600	Enhancers	iPS-15b Cell Line	embryonic stem cell
47	chrX:5154000-5154600	Enhancers	iPS-18 Cell Line	embryonic stem cell
48	chrX:5154200-5154600	Enhancers	H9 Cell Line	embryonic stem cell
49	chrX:5154600-5157600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
50	chrX:5154600-5157600	Weak transcription	iPS-18 Cell Line	embryonic stem cell

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