Variant report

Variant	nsv949393
Chromosome Location	chrX:5637763-5883977
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:5876562-5876924	H1-hESC	embryonic stem cell:	n/a	chrX:5876751-5876765
2	BCL3	chrX:5644229-5644536	GM12878	blood:	n/a	n/a
3	CEBPB	chrX:5709777-5710265	K562	blood:	n/a	chrX:5709961-5709972
4	CEBPB	chrX:5709779-5710239	H1-hESC	embryonic stem cell:	n/a	chrX:5709961-5709972
5	CEBPB	chrX:5795476-5795521	A549	lung:	n/a	n/a
6	CEBPB	chrX:5697562-5697873	HepG2	liver:	n/a	chrX:5697696-5697707 chrX:5697715-5697726 chrX:5697714-5697727
7	CEBPB	chrX:5780421-5780588	IMR90	lung:	n/a	chrX:5780548-5780559
8	CEBPB	chrX:5788423-5788656	HepG2	liver:	n/a	chrX:5788544-5788555 chrX:5788542-5788553
9	CEBPB	chrX:5875593-5875854	A549	lung:	n/a	chrX:5875769-5875782 chrX:5875769-5875782 chrX:5875685-5875698 chrX:5875685-5875696
10	CEBPB	chrX:5709776-5710093	A549	lung:	n/a	chrX:5709961-5709972
11	CEBPB	chrX:5877918-5878134	HepG2	liver:	n/a	chrX:5878044-5878055
12	CEBPB	chrX:5863862-5864169	HepG2	liver:	n/a	chrX:5864112-5864123
13	CEBPB	chrX:5746396-5746632	A549	lung:	n/a	n/a
14	CEBPB	chrX:5808670-5808870	A549	lung:	n/a	n/a
15	CEBPB	chrX:5697611-5697862	IMR90	lung:	n/a	chrX:5697696-5697707 chrX:5697715-5697726 chrX:5697714-5697727
16	CEBPB	chrX:5679665-5679886	K562	blood:	n/a	chrX:5679718-5679729
17	CEBPB	chrX:5709776-5710147	HepG2	liver:	n/a	chrX:5709961-5709972
18	CEBPB	chrX:5679614-5679886	A549	lung:	n/a	chrX:5679718-5679729
19	CEBPB	chrX:5640908-5641229	HepG2	liver:	n/a	chrX:5641078-5641091
20	CEBPB	chrX:5875650-5875874	HepG2	liver:	n/a	chrX:5875769-5875782 chrX:5875769-5875782 chrX:5875685-5875698 chrX:5875685-5875696
21	CEBPB	chrX:5752033-5752271	A549	lung:	n/a	n/a
22	CEBPB	chrX:5795341-5795575	HepG2	liver:	n/a	n/a
23	CEBPB	chrX:5877874-5878198	A549	lung:	n/a	chrX:5878044-5878055
24	CEBPB	chrX:5709797-5710131	MCF-7	breast:	n/a	chrX:5709961-5709972
25	CEBPB	chrX:5709864-5710048	A549	lung:	n/a	chrX:5709961-5709972
26	CEBPB	chrX:5679616-5679895	HepG2	liver:	n/a	chrX:5679718-5679729
27	CEBPB	chrX:5804956-5805176	H1-hESC	embryonic stem cell:	n/a	chrX:5805060-5805071
28	CEBPB	chrX:5640967-5641230	IMR90	lung:	n/a	chrX:5641078-5641091
29	CEBPB	chrX:5875591-5875873	H1-hESC	embryonic stem cell:	n/a	chrX:5875769-5875782 chrX:5875769-5875782 chrX:5875685-5875698 chrX:5875685-5875696
30	CEBPB	chrX:5709721-5710070	A549	lung:	n/a	chrX:5709961-5709972
31	CEBPB	chrX:5709774-5710150	IMR90	lung:	n/a	chrX:5709961-5709972
32	CEBPB	chrX:5877917-5878218	IMR90	lung:	n/a	chrX:5878044-5878055 chrX:5878197-5878210
33	CEBPB	chrX:5679561-5679904	IMR90	lung:	n/a	chrX:5679718-5679729
34	CHD2	chrX:5775455-5775459	GM12878	blood:	n/a	n/a
35	CTCF	chrX:5795460-5795610	HVMF	connective:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
36	CTCF	chrX:5795355-5795633	MCF-7	breast:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
37	CTCF	chrX:5681702-5681800	GM10266	blood:	n/a	n/a
38	CTCF	chrX:5818709-5818742	ProgFib	skin:	n/a	n/a
39	CTCF	chrX:5795440-5795590	HMEC	breast:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
40	CTCF	chrX:5849940-5850090	NHEK	skin:	n/a	n/a
41	CTCF	chrX:5795380-5795530	SAEC	small airway:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
42	CTCF	chrX:5833920-5834070	HL-60	blood:	n/a	n/a
43	CTCF	chrX:5835170-5835255	GM19240	blood:	n/a	n/a
44	CTCF	chrX:5835109-5835268	MCF-7	breast:	n/a	chrX:5835158-5835171 chrX:5835151-5835172 chrX:5835156-5835174
45	CTCF	chrX:5795289-5795835	A549	lung:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
46	CTCF	chrX:5825999-5826093	Pancreas_OC	pancreas:	n/a	n/a
47	CTCF	chrX:5795413-5795593	K562	blood:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
48	CTCF	chrX:5795393-5795597	T-47D	breast:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
49	CTCF	chrX:5795440-5795590	Caco-2	colon:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
50	CTCF	chrX:5795380-5795530	GM12878	blood:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:5824743-5824793	AG04450	lung:	fetal
2	chrX:5817998-5818048	PrEC	prostate:	n/a
3	chrX:5821720-5821770	K562	blood:	n/a
4	chrX:5811303-5811353	GM12891	blood:	n/a
5	chrX:5821227-5821277	HAEpiC	amniotic membrane:	n/a
6	chrX:5808230-5808280	NH-A	brain:	n/a
7	chrX:5821227-5821277	SKMC	muscle:	n/a
8	chrX:5821020-5821070	T-47D	breast:	n/a
9	chrX:5821720-5821770	HRE	kidney:	n/a
10	chrX:5815108-5815158	PFSK-1	brain:	n/a
11	chrX:5821020-5821070	SKMC	muscle:	n/a
12	chrX:5821362-5821412	SKMC	muscle:	n/a
13	chrX:5821020-5821070	A549	lung:	n/a
14	chrX:5811303-5811353	PrEC	prostate:	n/a
15	chrX:5815108-5815158	AG10803	skin:	n/a
16	chrX:5808230-5808280	NHBE	bronchial:	n/a
17	chrX:5821020-5821070	AG09319	gingival:	n/a
18	chrX:5809841-5809891	Hela-S3	cervix:	n/a
19	chrX:5821227-5821277	NHDF-neo	bronchial:	n/a
20	chrX:5821720-5821770	HL-60	blood:	n/a
21	chrX:5821362-5821412	AG09309	skin:	n/a
22	chrX:5821227-5821277	PrEC	prostate:	n/a
23	chrX:5821362-5821412	Jurkat	blood:	n/a
24	chrX:5811145-5811195	HRE	kidney:	n/a
25	chrX:5821362-5821412	BE2_C	brain:	n/a
26	chrX:5824743-5824793	K562	blood:	n/a
27	chrX:5811145-5811195	Caco-2	colon:	n/a
28	chrX:5809841-5809891	T-47D	breast:	n/a
29	chrX:5824743-5824793	ovcar-3	ovarian:	n/a
30	chrX:5817998-5818048	AG09309	skin:	n/a
31	chrX:5821362-5821412	IMR90	lung:	fetal
32	chrX:5824743-5824793	HepG2	liver:	n/a
33	chrX:5821227-5821277	BJ	skin:	n/a
34	chrX:5821720-5821770	HEK293	kidney:	embryo
35	chrX:5808230-5808280	HL-60	blood:	n/a
36	chrX:5821720-5821770	HAEpiC	amniotic membrane:	n/a
37	chrX:5811085-5811135	AG04449	skin:	fetal
38	chrX:5821227-5821277	HL-60	blood:	n/a
39	chrX:5811303-5811353	GM12878	blood:	n/a
40	chrX:5824743-5824793	Hela-S3	cervix:	n/a
41	chrX:5821720-5821770	AG09319	gingival:	n/a
42	chrX:5824743-5824793	HCT-116	colon:	n/a
43	chrX:5821227-5821277	AG04449	skin:	fetal
44	chrX:5821362-5821412	AG09319	gingival:	n/a
45	chrX:5811085-5811135	ProgFib	skin:	n/a
46	chrX:5815108-5815158	U87	brain:	n/a
47	chrX:5821362-5821412	AG04449	skin:	fetal
48	chrX:5817998-5818048	GM12878	blood:	n/a
49	chrX:5821362-5821412	A549	lung:	n/a
50	chrX:5809841-5809891	CMK	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:5746877..5749431-chrX:5755613..5757245,2	MCF-7	breast:
2	chrX:5746877..5749431-chrX:5755613..5757245,2	MCF-7	breast:
3	chrX:3880371..3881142-chrX:5795232..5795927,2	MCF-7	breast:
4	chrX:5376030..5377037-chrX:5795005..5796053,5	MCF-7	breast:
5	chrX:5642806..5644817-chrX:5646712..5648581,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NLGN4X-1	chrX:5644071-5644121	ENSG00000236120
2	lnc-NLGN4X-2	chrX:5653971-5653998	NONHSAT136159
3	lnc-VCX3A-5	chrX:5808101-5809458	NONHSAT136161
4	lnc-NLGN4X-2	chrX:5653971-5654414	l_3885_chrX:5647214-5654414_placenta
5	lnc-NLGN4X-1	chrX:5643971-5643998	ENSG00000236120
6	lnc-NLGN4X-2	chrX:5653971-5654346	NONHSAT136158
7	lnc-NLGN4X-2	chrX:5647215-5647913	l_3885_chrX:5647214-5654414_placenta
8	lnc-NLGN4X-2	chrX:5654071-5654121	NONHSAT136160

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	NLGN4X	hsa-miR-26b-5p	chrX:5808325-5808346

Variant related genes	Relation type
NLGN4X	TF binding region
ENSG00000236120	TF binding region
NLGN4X	CpG island
ENSG00000236120	CpG island
ENSG00000236120	chromatin interactions

Extended variants
information (count: 2298 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2298 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs184030673	chrX:5641263-5641264	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs375697394	chrX:5641353-5641354	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs11387253	chrX:5641356-5641357	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs397768622	chrX:5641362-5641363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs371810440	chrX:5641363-5641364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs374683112	chrX:5641364-5641365	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs188919193	chrX:5641448-5641449	Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs12012227	chrX:5641548-5641549	Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs191752882	chrX:5641648-5641649	Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs182960955	chrX:5641896-5641897	Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs554446646	chrX:5642100-5642101	Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs186882687	chrX:5642234-5642235	Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs149967226	chrX:5642408-5642409	Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs12013439	chrX:5642484-5642485	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs140802446	chrX:5642503-5642504	Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs191734763	chrX:5642556-5642557	Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs182060836	chrX:5642560-5642561	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs576349190	chrX:5642792-5642793	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs186648006	chrX:5642797-5642798	Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs545078860	chrX:5642821-5642822	Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs192494195	chrX:5642909-5642910	Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs185616998	chrX:5642948-5642949	Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs56104555	chrX:5643135-5643136	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs146699612	chrX:5643173-5643174	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs376786343	chrX:5643210-5643211	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs148859124	chrX:5643311-5643312	Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs143752205	chrX:5643321-5643322	Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs190492050	chrX:5643378-5643379	Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs373836362	chrX:5643477-5643478	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs193048398	chrX:5643502-5643503	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs79164557	chrX:5643569-5643570	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs373234756	chrX:5643574-5643575	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs377136752	chrX:5643578-5643579	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs370430346	chrX:5643582-5643583	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs200406426	chrX:5643583-5643584	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs567718128	chrX:5643586-5643587	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs199839631	chrX:5643590-5643591	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs67846091	chrX:5643594-5643595	Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
39	rs538892136	chrX:5643610-5643611	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs6638544	chrX:5643624-5643625	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs377728008	chrX:5643657-5643658	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs141093024	chrX:5643732-5643733	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs146907116	chrX:5643812-5643813	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs138986488	chrX:5643854-5643855	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs184584894	chrX:5643877-5643878	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs368685979	chrX:5643968-5643969	Weak transcription Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs188515161	chrX:5644029-5644030	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs181287158	chrX:5644144-5644145	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs5916233	chrX:5644408-5644409	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs147474894	chrX:5644443-5644444	Enhancers Weak transcription Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:55)

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
Pancreatic cancer	17952125	CNVD
Autism	20643418	CNVD
Autism	23710042	CNVD
Schizophrenia	23710042	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Abnormal phenotypes	21355048	CNVD

Chromatin state (count:329 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:5641200-5641400	Enhancers	HMEC	breast
2	chrX:5641400-5644400	Active TSS	Adipose Nuclei	Adipose
3	chrX:5642200-5644000	Active TSS	HMEC	breast
4	chrX:5643000-5643200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chrX:5643000-5643400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
6	chrX:5643400-5645000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chrX:5643600-5644200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chrX:5643800-5644000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chrX:5643800-5644000	Enhancers	Muscle Satellite Cultured Cells	--
10	chrX:5643800-5644200	Active TSS	Rectal Mucosa Donor 29	rectum
11	chrX:5643800-5644200	Enhancers	NHDF-Ad	bronchial
12	chrX:5643800-5645200	Enhancers	Primary monocytes fromperipheralblood	blood
13	chrX:5644000-5644200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chrX:5644000-5644200	Flanking Active TSS	HMEC	breast
15	chrX:5644000-5644200	Enhancers	HSMM	muscle
16	chrX:5644000-5644400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chrX:5644000-5644400	Enhancers	HUES48 Cell Line	embryonic stem cell
18	chrX:5644000-5644400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chrX:5644000-5644400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
20	chrX:5644000-5644400	Enhancers	NH-A	brain
21	chrX:5644000-5645000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
22	chrX:5644000-5645000	Enhancers	Brain Substantia Nigra	brain
23	chrX:5644200-5644400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
24	chrX:5644200-5644400	Active TSS	HMEC	breast
25	chrX:5644200-5644600	Active TSS	HSMM	muscle
26	chrX:5644200-5645000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chrX:5644400-5645000	Enhancers	Muscle Satellite Cultured Cells	--
28	chrX:5644400-5645200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chrX:5644400-5645400	Enhancers	HMEC	breast
30	chrX:5644600-5645000	Enhancers	HSMM	muscle
31	chrX:5645000-5645200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chrX:5645000-5646600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chrX:5645400-5645800	Weak transcription	HMEC	breast
34	chrX:5645800-5649400	Enhancers	HMEC	breast
35	chrX:5646600-5647800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chrX:5647800-5648800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chrX:5651200-5651600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
38	chrX:5665000-5665400	Enhancers	Brain Germinal Matrix	brain
39	chrX:5666600-5667000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chrX:5666800-5667200	Enhancers	Fetal Stomach	stomach
41	chrX:5672600-5673800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chrX:5673800-5679200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chrX:5679400-5679600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
44	chrX:5689200-5690400	Enhancers	Primary monocytes fromperipheralblood	blood
45	chrX:5690400-5692000	Weak transcription	Primary monocytes fromperipheralblood	blood
46	chrX:5692000-5695200	Enhancers	Primary monocytes fromperipheralblood	blood
47	chrX:5693000-5694000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chrX:5693000-5694800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
49	chrX:5693200-5694800	Enhancers	Primary hematopoietic stem cells	blood
50	chrX:5693400-5694800	Enhancers	Primary neutrophils fromperipheralblood	blood

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