Variant report

Variant	esv3395599
Chromosome Location	chrX:5373033-5729174
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:780)
CpG islands
(count:122)
Chromatin interactive
region (count:6)
LncRNA
region (count:19)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:780 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chrX:5564670-5565328	GM12878	blood:	n/a	n/a
2	ATF2	chrX:5564791-5565415	GM12878	blood:	n/a	n/a
3	BACH1	chrX:5550544-5550555	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chrX:5392218-5392765	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chrX:5564825-5565221	GM12878	blood:	n/a	n/a
6	BATF	chrX:5592172-5592376	GM12878	blood:	n/a	n/a
7	BATF	chrX:5568977-5569303	GM12878	blood:	n/a	n/a
8	BCL11A	chrX:5564857-5565196	GM12878	blood:	n/a	chrX:5565045-5565054
9	BCL11A	chrX:5564808-5565237	GM12878	blood:	n/a	chrX:5565045-5565054
10	BCL11A	chrX:5568957-5569317	GM12878	blood:	n/a	n/a
11	BCL3	chrX:5644229-5644536	GM12878	blood:	n/a	n/a
12	BCL3	chrX:5564824-5565164	GM12878	blood:	n/a	chrX:5565045-5565054
13	BCLAF1	chrX:5564765-5565287	GM12878	blood:	n/a	chrX:5565045-5565054
14	BHLHE40	chrX:5621079-5621094	GM12878	blood:	n/a	n/a
15	BHLHE40	chrX:5564826-5565261	GM12878	blood:	n/a	n/a
16	BHLHE40	chrX:5569068-5569288	GM12878	blood:	n/a	n/a
17	CEBPB	chrX:5679614-5679886	A549	lung:	n/a	chrX:5679718-5679729
18	CEBPB	chrX:5679616-5679895	HepG2	liver:	n/a	chrX:5679718-5679729
19	CEBPB	chrX:5564703-5565425	GM12878	blood:	n/a	n/a
20	CEBPB	chrX:5564886-5565217	GM12878	blood:	n/a	n/a
21	CEBPB	chrX:5709864-5710048	A549	lung:	n/a	chrX:5709961-5709972
22	CEBPB	chrX:5551067-5551363	IMR90	lung:	n/a	chrX:5551200-5551211
23	CEBPB	chrX:5544187-5544312	A549	lung:	n/a	n/a
24	CEBPB	chrX:5551036-5551341	HepG2	liver:	n/a	chrX:5551200-5551211
25	CEBPB	chrX:5709779-5710239	H1-hESC	embryonic stem cell:	n/a	chrX:5709961-5709972
26	CEBPB	chrX:5640967-5641230	IMR90	lung:	n/a	chrX:5641078-5641091
27	CEBPB	chrX:5697562-5697873	HepG2	liver:	n/a	chrX:5697696-5697707 chrX:5697715-5697726 chrX:5697714-5697727
28	CEBPB	chrX:5697611-5697862	IMR90	lung:	n/a	chrX:5697696-5697707 chrX:5697715-5697726 chrX:5697714-5697727
29	CEBPB	chrX:5551099-5551345	A549	lung:	n/a	chrX:5551200-5551211
30	CEBPB	chrX:5454428-5454711	IMR90	lung:	n/a	n/a
31	CEBPB	chrX:5709774-5710150	IMR90	lung:	n/a	chrX:5709961-5709972
32	CEBPB	chrX:5640908-5641229	HepG2	liver:	n/a	chrX:5641078-5641091
33	CEBPB	chrX:5709776-5710147	HepG2	liver:	n/a	chrX:5709961-5709972
34	CEBPB	chrX:5679561-5679904	IMR90	lung:	n/a	chrX:5679718-5679729
35	CEBPB	chrX:5598094-5598370	HepG2	liver:	n/a	chrX:5598203-5598214
36	CEBPB	chrX:5679665-5679886	K562	blood:	n/a	chrX:5679718-5679729
37	CEBPB	chrX:5709776-5710093	A549	lung:	n/a	chrX:5709961-5709972
38	CEBPB	chrX:5620589-5620819	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chrX:5620596-5620796	A549	lung:	n/a	n/a
40	CEBPB	chrX:5552356-5552464	A549	lung:	n/a	n/a
41	CEBPB	chrX:5709721-5710070	A549	lung:	n/a	chrX:5709961-5709972
42	CEBPB	chrX:5709797-5710131	MCF-7	breast:	n/a	chrX:5709961-5709972
43	CEBPB	chrX:5597514-5597683	A549	lung:	n/a	n/a
44	CEBPB	chrX:5709777-5710265	K562	blood:	n/a	chrX:5709961-5709972
45	CHD1	chrX:5567466-5567690	H1-hESC	embryonic stem cell:	n/a	n/a
46	CHD2	chrX:5563029-5563044	H1-hESC	embryonic stem cell:	n/a	n/a
47	CHD2	chrX:5564832-5565292	GM12878	blood:	n/a	n/a
48	CHD2	chrX:5566901-5567469	H1-hESC	embryonic stem cell:	n/a	n/a
49	CREB1	chrX:5564753-5565281	GM12878	blood:	n/a	n/a
50	CREB1	chrX:5564573-5565400	GM12878	blood:	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	GM19239	blood:	n/a
2	chrX:5470075-5470125	HCM	heart:	n/a
3	chrX:5470290-5470340	LNCaP	prostate:	n/a
4	chrX:5470075-5470125	LNCaP	prostate:	n/a
5	chrX:5470075-5470125	NHBE	bronchial:	n/a
6	chrX:5470075-5470125	HPAEpiC	pulmonary alveolar:	n/a
7	chrX:5470290-5470340	HCM	heart:	n/a
8	chrX:5470075-5470125	NH-A	brain:	n/a
9	chrX:5470075-5470125	ECC-1	luminal epithelium:	n/a
10	chrX:5470290-5470340	PrEC	prostate:	n/a
11	chrX:5470290-5470340	NT2-D1	testis:	n/a
12	chrX:5470075-5470125	PFSK-1	brain:	n/a
13	chrX:5470075-5470125	HCPEpiC	choroid plexus:	n/a
14	chrX:5470075-5470125	ovcar-3	ovarian:	n/a
15	chrX:5470290-5470340	PANC-1	pancreas:	n/a
16	chrX:5470290-5470340	ProgFib	skin:	n/a
17	chrX:5470290-5470340	GM12892	blood:	n/a
18	chrX:5470290-5470340	HL-60	blood:	n/a
19	chrX:5470075-5470125	A549	lung:	n/a
20	chrX:5470290-5470340	AG04450	lung:	fetal
21	chrX:5470075-5470125	HCF	heart:	n/a
22	chrX:5470290-5470340	HEEpiC	esophagus:	n/a
23	chrX:5470290-5470340	H1-hESC	embryonic stem cell:	embryo
24	chrX:5470075-5470125	PANC-1	pancreas:	n/a
25	chrX:5470075-5470125	HUVEC	blood vessel:	n/a
26	chrX:5470290-5470340	SKMC	muscle:	n/a
27	chrX:5470075-5470125	SAEC	small airway:	n/a
28	chrX:5470075-5470125	SKMC	muscle:	n/a
29	chrX:5470075-5470125	GM12892	blood:	n/a
30	chrX:5470075-5470125	HL-60	blood:	n/a
31	chrX:5470075-5470125	HIPEpiC	eye:	n/a
32	chrX:5470075-5470125	BE2_C	brain:	n/a
33	chrX:5470290-5470340	GM12891	blood:	n/a
34	chrX:5470290-5470340	T-47D	breast:	n/a
35	chrX:5470075-5470125	Jurkat	blood:	n/a
36	chrX:5470075-5470125	HEK293	kidney:	embryo
37	chrX:5470290-5470340	GM19239	blood:	n/a
38	chrX:5470290-5470340	HCT-116	colon:	n/a
39	chrX:5470075-5470125	GM12891	blood:	n/a
40	chrX:5470075-5470125	ProgFib	skin:	n/a
41	chrX:5470075-5470125	GM12878	blood:	n/a
42	chrX:5470290-5470340	NHBE	bronchial:	n/a
43	chrX:5470075-5470125	HMEC	breast:	n/a
44	chrX:5470075-5470125	HepG2	liver:	n/a
45	chrX:5470290-5470340	GM06990	blood:	n/a
46	chrX:5470290-5470340	NHDF-neo	bronchial:	n/a
47	chrX:5470075-5470125	PrEC	prostate:	n/a
48	chrX:5470290-5470340	MCF-7	breast:	n/a
49	chrX:5470290-5470340	Jurkat	blood:	n/a
50	chrX:5470290-5470340	BE2_C	brain:	n/a

(count:6 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:5464584..5467087-chrX:5468527..5471240,2	K562	blood:
2	chrX:5364801..5367777-chrX:5395940..5398619,2	MCF-7	breast:
3	chrX:5376030..5377037-chrX:5795005..5796053,5	MCF-7	breast:
4	chr4:8147667..8148302-chrX:5458311..5459167,2	MCF-7	breast:
5	chrX:5464584..5467087-chrX:5468527..5471240,2	K562	blood:
6	chrX:5642806..5644817-chrX:5646712..5648581,2	MCF-7	breast:

(count:19 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLGN4X-1	chrX:5589125-5589240	ENSG00000236120
2	lnc-NLGN4X-2	chrX:5654071-5654121	NONHSAT136160
3	lnc-NLGN4X-1	chrX:5587447-5587647	ENSG00000236120
4	lnc-NLGN4X-1	chrX:5587447-5587560	ENSG00000236120
5	lnc-NLGN4X-1	chrX:5643971-5643998	ENSG00000236120
6	lnc-NLGN4X-2	chrX:5597447-5597647	NONHSAT136158
7	lnc-NLGN4X-2	chrX:5581462-5581744	NONHSAT136158
8	lnc-NLGN4X-1	chrX:5644071-5644121	ENSG00000236120
9	lnc-NLGN4X-2	chrX:5653971-5654346	NONHSAT136158
10	lnc-NLGN4X-2	chrX:5597447-5597647	NONHSAT136159
11	lnc-NLGN4X-2	chrX:5599125-5599240	NONHSAT136159
12	lnc-NLGN4X-1	chrX:5571464-5571744	ENSG00000236120
13	lnc-NLGN4X-2	chrX:5653971-5653998	NONHSAT136159
14	lnc-NLGN4X-2	chrX:5647215-5647913	l_3885_chrX:5647214-5654414_placenta
15	lnc-NLGN4X-2	chrX:5581462-5581744	NONHSAT136159
16	lnc-NLGN4X-1	chrX:5571462-5571744	ENSG00000236120
17	lnc-NLGN4X-2	chrX:5581464-5581744	NONHSAT136160
18	lnc-NLGN4X-2	chrX:5597447-5597560	NONHSAT136160
19	lnc-NLGN4X-2	chrX:5653971-5654414	l_3885_chrX:5647214-5654414_placenta

No data

Variant related genes	Relation type
ENSG00000236120	TF binding region
ENSG00000236120	CpG island
ENSG00000236120	chromatin interactions

Extended variants
information (count: 1637 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:1637 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192160632	chrX:5380623-5380624	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs34956588	chrX:5381517-5381518	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs147882263	chrX:5381578-5381579	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs140474468	chrX:5381585-5381586	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371122492	chrX:5392571-5392572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs72114248	chrX:5397914-5397915	Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs398121933	chrX:5397917-5397918	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs139648821	chrX:5397925-5397926	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs180678938	chrX:5397939-5397940	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs185766090	chrX:5397998-5397999	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs112901330	chrX:5398049-5398050	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs73189795	chrX:5398058-5398059	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs181690126	chrX:5398143-5398144	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs4320676	chrX:5398231-5398232	Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs4320675	chrX:5398312-5398313	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs4265331	chrX:5398389-5398390	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs186036664	chrX:5398396-5398397	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs79771400	chrX:5398407-5398408	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs5916073	chrX:5398478-5398479	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs192483286	chrX:5398495-5398496	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs183875889	chrX:5398510-5398511	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs528788892	chrX:5398520-5398521	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs4523411	chrX:5398550-5398551	Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs4336748	chrX:5398558-5398559	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs368512317	chrX:5398592-5398593	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs62582075	chrX:5398678-5398679	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs200804835	chrX:5398679-5398680	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs546911191	chrX:5398708-5398709	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs5916074	chrX:5398727-5398728	Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs182085782	chrX:5398728-5398729	Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs187085745	chrX:5398780-5398781	Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs367634084	chrX:5398919-5398920	Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs181023428	chrX:5433840-5433841	Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs367826260	chrX:5433861-5433862	Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs185052866	chrX:5433870-5433871	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs146827889	chrX:5433981-5433982	Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs190303972	chrX:5434006-5434007	Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs539650414	chrX:5434048-5434049	Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs77528706	chrX:5434165-5434166	Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs182527490	chrX:5434191-5434192	Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs57296017	chrX:5450400-5450401	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
42	rs536253719	chrX:5450423-5450424	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs372569089	chrX:5450501-5450502	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs28594186	chrX:5450508-5450509	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs185583533	chrX:5450518-5450519	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs28663174	chrX:5450525-5450526	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs200630924	chrX:5450555-5450556	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs58312976	chrX:5450565-5450566	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs370087460	chrX:5450579-5450580	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs191116508	chrX:5450681-5450682	ZNF genes & repeats Bivalent/Poised TSS Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:52)

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
Mental retardation	20486941	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:246 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:5380600-5380800	Enhancers	H9 Cell Line	embryonic stem cell
2	chrX:5381400-5381600	Enhancers	H9 Cell Line	embryonic stem cell
3	chrX:5392400-5392600	Enhancers	Pancreatic Islets	Pancreatic Islet
4	chrX:5397800-5399000	Active TSS	ES-I3 Cell Line	embryonic stem cell
5	chrX:5398400-5399000	Active TSS	HUES6 Cell Line	embryonic stem cell
6	chrX:5433800-5434200	Active TSS	Hela-S3	cervix
7	chrX:5450400-5450800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
8	chrX:5450400-5450800	Bivalent Enhancer	Fetal Brain Male	brain
9	chrX:5450400-5451000	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
10	chrX:5454600-5454800	Enhancers	Fetal Brain Male	brain
11	chrX:5458200-5459800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chrX:5459200-5459800	Enhancers	iPS-18 Cell Line	embryonic stem cell
13	chrX:5460000-5460400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
14	chrX:5467000-5468200	Enhancers	Fetal Stomach	stomach
15	chrX:5467200-5467400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chrX:5467400-5467800	Enhancers	Cortex derived primary cultured neurospheres	brain
17	chrX:5467400-5467800	Flanking Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
18	chrX:5467800-5468200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chrX:5468200-5468600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
20	chrX:5468200-5468600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
21	chrX:5492200-5493000	Enhancers	Fetal Stomach	stomach
22	chrX:5492800-5493200	Enhancers	Fetal Brain Male	brain
23	chrX:5494200-5494600	Enhancers	iPS-18 Cell Line	embryonic stem cell
24	chrX:5509800-5510000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chrX:5510000-5511800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
26	chrX:5510800-5511200	Enhancers	H9 Cell Line	embryonic stem cell
27	chrX:5513400-5513600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chrX:5535000-5536200	Enhancers	Brain Substantia Nigra	brain
29	chrX:5536200-5536400	Weak transcription	Brain Substantia Nigra	brain
30	chrX:5536400-5536800	Enhancers	Brain Substantia Nigra	brain
31	chrX:5545000-5546200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chrX:5545000-5546200	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chrX:5545000-5546400	Enhancers	iPS-18 Cell Line	embryonic stem cell
34	chrX:5545200-5546200	Enhancers	iPS-15b Cell Line	embryonic stem cell
35	chrX:5545400-5546000	Enhancers	HUES6 Cell Line	embryonic stem cell
36	chrX:5545800-5546200	Enhancers	H9 Cell Line	embryonic stem cell
37	chrX:5546000-5550000	Weak transcription	HUES6 Cell Line	embryonic stem cell
38	chrX:5546200-5550000	Weak transcription	HUES48 Cell Line	embryonic stem cell
39	chrX:5546200-5562000	Weak transcription	H9 Cell Line	embryonic stem cell
40	chrX:5546400-5550000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
41	chrX:5550000-5550400	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chrX:5550000-5550400	Enhancers	iPS-18 Cell Line	embryonic stem cell
43	chrX:5550000-5550600	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chrX:5550400-5552000	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chrX:5552000-5556800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chrX:5556800-5558000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
47	chrX:5557600-5558800	Enhancers	Fetal Brain Male	brain
48	chrX:5558000-5562800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chrX:5560800-5561200	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chrX:5562000-5562400	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell

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