Variant report

Variant	esv2830398
Chromosome Location	chrX:5618240-5882060
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	BHLHE40	chrX:5621079-5621094	GM12878	blood:	n/a	n/a
4	CEBPB	chrX:5746396-5746632	A549	lung:	n/a	n/a
5	CEBPB	chrX:5709779-5710239	H1-hESC	embryonic stem cell:	n/a	chrX:5709961-5709972
6	CEBPB	chrX:5877917-5878218	IMR90	lung:	n/a	chrX:5878044-5878055 chrX:5878197-5878210
7	CEBPB	chrX:5795341-5795575	HepG2	liver:	n/a	n/a
8	CEBPB	chrX:5620589-5620819	H1-hESC	embryonic stem cell:	n/a	n/a
9	CEBPB	chrX:5780421-5780588	IMR90	lung:	n/a	chrX:5780548-5780559
10	CEBPB	chrX:5709776-5710093	A549	lung:	n/a	chrX:5709961-5709972
11	CEBPB	chrX:5863862-5864169	HepG2	liver:	n/a	chrX:5864112-5864123
12	CEBPB	chrX:5709776-5710147	HepG2	liver:	n/a	chrX:5709961-5709972
13	CEBPB	chrX:5808670-5808870	A549	lung:	n/a	n/a
14	CEBPB	chrX:5709864-5710048	A549	lung:	n/a	chrX:5709961-5709972
15	CEBPB	chrX:5697562-5697873	HepG2	liver:	n/a	chrX:5697696-5697707 chrX:5697715-5697726 chrX:5697714-5697727
16	CEBPB	chrX:5640967-5641230	IMR90	lung:	n/a	chrX:5641078-5641091
17	CEBPB	chrX:5709777-5710265	K562	blood:	n/a	chrX:5709961-5709972
18	CEBPB	chrX:5709721-5710070	A549	lung:	n/a	chrX:5709961-5709972
19	CEBPB	chrX:5679616-5679895	HepG2	liver:	n/a	chrX:5679718-5679729
20	CEBPB	chrX:5875650-5875874	HepG2	liver:	n/a	chrX:5875769-5875782 chrX:5875769-5875782 chrX:5875685-5875698 chrX:5875685-5875696
21	CEBPB	chrX:5795476-5795521	A549	lung:	n/a	n/a
22	CEBPB	chrX:5620596-5620796	A549	lung:	n/a	n/a
23	CEBPB	chrX:5752033-5752271	A549	lung:	n/a	n/a
24	CEBPB	chrX:5877918-5878134	HepG2	liver:	n/a	chrX:5878044-5878055
25	CEBPB	chrX:5679614-5679886	A549	lung:	n/a	chrX:5679718-5679729
26	CEBPB	chrX:5875593-5875854	A549	lung:	n/a	chrX:5875769-5875782 chrX:5875769-5875782 chrX:5875685-5875698 chrX:5875685-5875696
27	CEBPB	chrX:5804956-5805176	H1-hESC	embryonic stem cell:	n/a	chrX:5805060-5805071
28	CEBPB	chrX:5875591-5875873	H1-hESC	embryonic stem cell:	n/a	chrX:5875769-5875782 chrX:5875769-5875782 chrX:5875685-5875698 chrX:5875685-5875696
29	CEBPB	chrX:5877874-5878198	A549	lung:	n/a	chrX:5878044-5878055
30	CEBPB	chrX:5709774-5710150	IMR90	lung:	n/a	chrX:5709961-5709972
31	CEBPB	chrX:5788423-5788656	HepG2	liver:	n/a	chrX:5788544-5788555 chrX:5788542-5788553
32	CEBPB	chrX:5697611-5697862	IMR90	lung:	n/a	chrX:5697696-5697707 chrX:5697715-5697726 chrX:5697714-5697727
33	CEBPB	chrX:5640908-5641229	HepG2	liver:	n/a	chrX:5641078-5641091
34	CEBPB	chrX:5679561-5679904	IMR90	lung:	n/a	chrX:5679718-5679729
35	CEBPB	chrX:5679665-5679886	K562	blood:	n/a	chrX:5679718-5679729
36	CEBPB	chrX:5709797-5710131	MCF-7	breast:	n/a	chrX:5709961-5709972
37	CHD2	chrX:5775455-5775459	GM12878	blood:	n/a	n/a
38	CTCF	chrX:5795380-5795620	MCF-7	breast:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
39	CTCF	chrX:5795289-5795835	A549	lung:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
40	CTCF	chrX:5835040-5835190	GM12865	blood:	n/a	chrX:5835158-5835171 chrX:5835151-5835172 chrX:5835156-5835174
41	CTCF	chrX:5795460-5795610	NB4	blood:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
42	CTCF	chrX:5823858-5823910	GM20000	blood:	n/a	n/a
43	CTCF	chrX:5801102-5801147	GM10248	blood:	n/a	n/a
44	CTCF	chrX:5864747-5864834	Medullo	brain:	n/a	n/a
45	CTCF	chrX:5835193-5835197	Kidney_OC	kidney:	n/a	n/a
46	CTCF	chrX:5795234-5795606	MCF-7	breast:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
47	CTCF	chrX:5662323-5662339	GM10248	blood:	n/a	n/a
48	CTCF	chrX:5813075-5813149	GM20000	blood:	n/a	n/a
49	CTCF	chrX:5795400-5795550	NHDF-neo	bronchial:	n/a	chrX:5795499-5795515 chrX:5795500-5795513 chrX:5795498-5795516 chrX:5795493-5795514
50	CTCF	chrX:5795420-5795570	HA-sp	spinal cord:	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:5811085-5811135	HCM	heart:	n/a
2	chrX:5821227-5821277	AG09309	skin:	n/a
3	chrX:5811085-5811135	HCM	heart:	n/a
4	chrX:5821227-5821277	AG09309	skin:	n/a
5	chrX:5821362-5821412	BE2_C	brain:	n/a
6	chrX:5821720-5821770	HCPEpiC	choroid plexus:	n/a
7	chrX:5811145-5811195	AG09319	gingival:	n/a
8	chrX:5808230-5808280	HEEpiC	esophagus:	n/a
9	chrX:5821720-5821770	PFSK-1	brain:	n/a
10	chrX:5821362-5821412	HIPEpiC	eye:	n/a
11	chrX:5809841-5809891	HL-60	blood:	n/a
12	chrX:5821720-5821770	ovcar-3	ovarian:	n/a
13	chrX:5817998-5818048	SKMC	muscle:	n/a
14	chrX:5821227-5821277	ECC-1	luminal epithelium:	n/a
15	chrX:5811145-5811195	HCT-116	colon:	n/a
16	chrX:5821227-5821277	NHDF-neo	bronchial:	n/a
17	chrX:5809841-5809891	AG04449	skin:	fetal
18	chrX:5821020-5821070	HCT-116	colon:	n/a
19	chrX:5821227-5821277	HRPEpiC	eye:	n/a
20	chrX:5817998-5818048	A549	lung:	n/a
21	chrX:5811145-5811195	ECC-1	luminal epithelium:	n/a
22	chrX:5817998-5818048	HEEpiC	esophagus:	n/a
23	chrX:5809841-5809891	T-47D	breast:	n/a
24	chrX:5815108-5815158	AG04449	skin:	fetal
25	chrX:5808230-5808280	HepG2	liver:	n/a
26	chrX:5821720-5821770	ProgFib	skin:	n/a
27	chrX:5809841-5809891	HUVEC	blood vessel:	n/a
28	chrX:5821020-5821070	RPTEC	kidney:	n/a
29	chrX:5821720-5821770	BE2_C	brain:	n/a
30	chrX:5811085-5811135	CMK	blood:	n/a
31	chrX:5821362-5821412	GM06990	blood:	n/a
32	chrX:5821362-5821412	IMR90	lung:	fetal
33	chrX:5811085-5811135	MCF-7	breast:	n/a
34	chrX:5824743-5824793	HepG2	liver:	n/a
35	chrX:5808230-5808280	HPAEpiC	pulmonary alveolar:	n/a
36	chrX:5808230-5808280	T-47D	breast:	n/a
37	chrX:5811145-5811195	HRE	kidney:	n/a
38	chrX:5808230-5808280	U87	brain:	n/a
39	chrX:5811085-5811135	MCF10A-Er-Src	breast:	n/a
40	chrX:5815108-5815158	NT2-D1	testis:	n/a
41	chrX:5809841-5809891	NH-A	brain:	n/a
42	chrX:5808230-5808280	GM06990	blood:	n/a
43	chrX:5821362-5821412	GM12878	blood:	n/a
44	chrX:5811085-5811135	A549	lung:	n/a
45	chrX:5821227-5821277	AG09319	gingival:	n/a
46	chrX:5821720-5821770	U87	brain:	n/a
47	chrX:5815108-5815158	NHBE	bronchial:	n/a
48	chrX:5809841-5809891	HCPEpiC	choroid plexus:	n/a
49	chrX:5821362-5821412	SK-N-SH_RA	brain:	n/a
50	chrX:5817998-5818048	GM19239	blood:	n/a

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

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

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: 2436 )
Associated
traits (count: 55 )

Variant overlapped rSNPs/rCNVs (count:2436 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs183951520	chrX:5625403-5625404	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs151331477	chrX:5625482-5625483	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs187139584	chrX:5625514-5625515	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs369834943	chrX:5625643-5625644	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs5916223	chrX:5625774-5625775	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs544187243	chrX:5625798-5625799	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs4826804	chrX:5625806-5625807	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs16983822	chrX:5625887-5625888	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs532818759	chrX:5625920-5625921	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs191183101	chrX:5625924-5625925	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs377730356	chrX:5625985-5625986	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs371678224	chrX:5626032-5626033	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs183686537	chrX:5626155-5626156	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs146555945	chrX:5626175-5626176	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs5022865	chrX:5626252-5626253	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs546213403	chrX:5626315-5626316	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs537248650	chrX:5626451-5626452	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs141297231	chrX:5626468-5626469	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs111993137	chrX:5626472-5626473	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs372425766	chrX:5626545-5626546	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs548374666	chrX:5626604-5626605	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs190490721	chrX:5626672-5626673	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs568173366	chrX:5626743-5626744	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs182146091	chrX:5626766-5626767	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs377555606	chrX:5626810-5626811	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs185882088	chrX:5626826-5626827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs113066975	chrX:5626840-5626841	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs112734797	chrX:5626876-5626877	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs149511731	chrX:5626880-5626881	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs189959302	chrX:5626893-5626894	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs182131133	chrX:5626963-5626964	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs185618073	chrX:5626965-5626966	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs190334341	chrX:5626971-5626972	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs6639472	chrX:5627008-5627009	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs73446424	chrX:5627118-5627119	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs9969941	chrX:5627196-5627197	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180742171	chrX:5627311-5627312	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs368878407	chrX:5627329-5627330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs185356506	chrX:5627439-5627440	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192094977	chrX:5627557-5627558	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs4568734	chrX:5627604-5627605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs183844139	chrX:5627668-5627669	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs549187096	chrX:5627752-5627753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs189210044	chrX:5627844-5627845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs369327590	chrX:5627856-5627857	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs374430486	chrX:5627941-5627942	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2054636	chrX:5627964-5627965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs371291467	chrX:5628123-5628124	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs6529851	chrX:5628129-5628130	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367871494	chrX:5628247-5628248	Weak transcription	n/a	n/a	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:347 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:5625400-5625800	Enhancers	Brain Inferior Temporal Lobe	brain
2	chrX:5625400-5625800	Enhancers	Brain Substantia Nigra	brain
3	chrX:5625400-5626000	Enhancers	Brain Hippocampus Middle	brain
4	chrX:5625400-5626400	Enhancers	Cortex derived primary cultured neurospheres	brain
5	chrX:5625800-5626200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
6	chrX:5625800-5626200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
7	chrX:5625800-5626200	Active TSS	Brain Substantia Nigra	brain
8	chrX:5625800-5626800	Enhancers	HSMM	muscle
9	chrX:5625800-5627200	Enhancers	HMEC	breast
10	chrX:5626000-5626200	Enhancers	Brain Anterior Caudate	brain
11	chrX:5626000-5626400	Enhancers	Muscle Satellite Cultured Cells	--
12	chrX:5626000-5626400	Flanking Active TSS	Brain Hippocampus Middle	brain
13	chrX:5626000-5626400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
14	chrX:5626000-5626800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chrX:5626000-5626800	Enhancers	NHDF-Ad	bronchial
16	chrX:5626000-5627000	Enhancers	HSMMtube	muscle
17	chrX:5626000-5627200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chrX:5626400-5631200	Weak transcription	Brain Hippocampus Middle	brain
19	chrX:5631200-5631600	Enhancers	Brain Hippocampus Middle	brain
20	chrX:5631600-5634000	Weak transcription	Fetal Heart	heart
21	chrX:5641200-5641400	Enhancers	HMEC	breast
22	chrX:5641400-5644400	Active TSS	Adipose Nuclei	Adipose
23	chrX:5642200-5644000	Active TSS	HMEC	breast
24	chrX:5643000-5643200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chrX:5643000-5643400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
26	chrX:5643400-5645000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chrX:5643600-5644200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chrX:5643800-5644000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
29	chrX:5643800-5644000	Enhancers	Muscle Satellite Cultured Cells	--
30	chrX:5643800-5644200	Active TSS	Rectal Mucosa Donor 29	rectum
31	chrX:5643800-5644200	Enhancers	NHDF-Ad	bronchial
32	chrX:5643800-5645200	Enhancers	Primary monocytes fromperipheralblood	blood
33	chrX:5644000-5644200	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
34	chrX:5644000-5644200	Flanking Active TSS	HMEC	breast
35	chrX:5644000-5644200	Enhancers	HSMM	muscle
36	chrX:5644000-5644400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
37	chrX:5644000-5644400	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chrX:5644000-5644400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
39	chrX:5644000-5644400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
40	chrX:5644000-5644400	Enhancers	NH-A	brain
41	chrX:5644000-5645000	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
42	chrX:5644000-5645000	Enhancers	Brain Substantia Nigra	brain
43	chrX:5644200-5644400	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
44	chrX:5644200-5644400	Active TSS	HMEC	breast
45	chrX:5644200-5644600	Active TSS	HSMM	muscle
46	chrX:5644200-5645000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chrX:5644400-5645000	Enhancers	Muscle Satellite Cultured Cells	--
48	chrX:5644400-5645200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chrX:5644400-5645400	Enhancers	HMEC	breast
50	chrX:5644600-5645000	Enhancers	HSMM	muscle

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