Variant report

Variant	nsv932521
Chromosome Location	chrX:32947000-33798879
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	ARID3A	chrX:33144820-33145008	HepG2	liver:	n/a	n/a
2	ARID3A	chrX:33354955-33355155	HepG2	liver:	n/a	n/a
3	ATF1	chrX:32999573-32999712	K562	blood:	n/a	n/a
4	BACH1	chrX:33610540-33610740	K562	blood:	n/a	n/a
5	BACH1	chrX:33270668-33270839	H1-hESC	embryonic stem cell:	n/a	chrX:33270743-33270757
6	BACH1	chrX:33744440-33744569	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chrX:33664054-33664235	K562	blood:	n/a	n/a
8	BACH1	chrX:33147409-33147431	K562	blood:	n/a	n/a
9	BATF	chrX:33740068-33740318	GM12878	blood:	n/a	chrX:33740236-33740247
10	BATF	chrX:33740096-33740342	GM12878	blood:	n/a	chrX:33740236-33740247
11	BCLAF1	chrX:33452754-33452967	GM12878	blood:	n/a	n/a
12	BHLHE40	chrX:33128028-33128289	HepG2	liver:	n/a	n/a
13	BRCA1	chrX:33316811-33316859	GM12878	blood:	n/a	n/a
14	BRCA1	chrX:33165997-33166016	Hela-S3	cervix:	n/a	n/a
15	CEBPB	chrX:33059019-33059203	IMR90	lung:	n/a	chrX:33059141-33059154 chrX:33059141-33059152
16	CEBPB	chrX:33151542-33151711	A549	lung:	n/a	n/a
17	CEBPB	chrX:33743990-33744283	H1-hESC	embryonic stem cell:	n/a	chrX:33744150-33744163
18	CEBPB	chrX:33197332-33197603	IMR90	lung:	n/a	n/a
19	CEBPB	chrX:33434697-33434802	H1-hESC	embryonic stem cell:	n/a	chrX:33434723-33434734
20	CEBPB	chrX:33160497-33160849	Hela-S3	cervix:	n/a	chrX:33160655-33160666 chrX:33160655-33160668 chrX:33160657-33160666 chrX:33160655-33160668 chrX:33160657-33160666 chrX:33160657-33160666
21	CEBPB	chrX:33514138-33514397	IMR90	lung:	n/a	chrX:33514225-33514238
22	CEBPB	chrX:33325990-33326608	Hela-S3	cervix:	n/a	chrX:33326405-33326416 chrX:33326459-33326472
23	CEBPB	chrX:33398144-33398242	HepG2	liver:	n/a	n/a
24	CEBPB	chrX:33091405-33091686	IMR90	lung:	n/a	n/a
25	CEBPB	chrX:33016930-33017250	Hela-S3	cervix:	n/a	n/a
26	CEBPB	chrX:33719403-33719716	A549	lung:	n/a	chrX:33719560-33719573 chrX:33719562-33719573 chrX:33719560-33719573
27	CEBPB	chrX:33016964-33017159	K562	blood:	n/a	n/a
28	CEBPB	chrX:33016954-33017272	HepG2	liver:	n/a	n/a
29	CEBPB	chrX:33031602-33031889	A549	lung:	n/a	chrX:33031740-33031749 chrX:33031740-33031749 chrX:33031740-33031749 chrX:33031738-33031749 chrX:33031738-33031751 chrX:33031740-33031749
30	CEBPB	chrX:33326028-33326570	IMR90	lung:	n/a	chrX:33326405-33326416 chrX:33326459-33326472
31	CEBPB	chrX:33719408-33719679	IMR90	lung:	n/a	chrX:33719560-33719573 chrX:33719562-33719573 chrX:33719560-33719573
32	CEBPB	chrX:33059014-33059214	A549	lung:	n/a	chrX:33059201-33059212 chrX:33059199-33059212 chrX:33059201-33059212 chrX:33059141-33059154 chrX:33059141-33059152
33	CEBPB	chrX:33160520-33160820	HepG2	liver:	n/a	chrX:33160655-33160666 chrX:33160655-33160668 chrX:33160657-33160666 chrX:33160655-33160668 chrX:33160657-33160666 chrX:33160657-33160666
34	CEBPB	chrX:32949288-32949498	HepG2	liver:	n/a	chrX:32949415-32949426 chrX:32949416-32949425
35	CEBPB	chrX:33006711-33006813	HepG2	liver:	n/a	chrX:33006751-33006764 chrX:33006751-33006762 chrX:33006753-33006764
36	CEBPB	chrX:33777155-33777651	HepG2	liver:	n/a	chrX:33777513-33777524
37	CEBPB	chrX:33721377-33721664	IMR90	lung:	n/a	n/a
38	CEBPB	chrX:33171534-33171732	H1-hESC	embryonic stem cell:	n/a	chrX:33171615-33171624 chrX:33171613-33171626 chrX:33171615-33171624 chrX:33171615-33171624
39	CEBPB	chrX:33031569-33031923	IMR90	lung:	n/a	chrX:33031740-33031749 chrX:33031740-33031749 chrX:33031740-33031749 chrX:33031738-33031749 chrX:33031738-33031751 chrX:33031740-33031749
40	CEBPB	chrX:33016950-33017279	A549	lung:	n/a	n/a
41	CEBPB	chrX:33433500-33433781	IMR90	lung:	n/a	chrX:33433607-33433618
42	CEBPB	chrX:33313671-33313922	IMR90	lung:	n/a	chrX:33313803-33313814 chrX:33313803-33313816
43	CEBPB	chrX:33151479-33151834	Hela-S3	cervix:	n/a	chrX:33151746-33151758
44	CEBPB	chrX:33223111-33223603	IMR90	lung:	n/a	chrX:33223299-33223312
45	CEBPB	chrX:33160475-33160841	IMR90	lung:	n/a	chrX:33160655-33160666 chrX:33160655-33160668 chrX:33160657-33160666 chrX:33160655-33160668 chrX:33160657-33160666 chrX:33160657-33160666
46	CEBPB	chrX:33694044-33694259	HepG2	liver:	n/a	chrX:33694166-33694175 chrX:33694164-33694177 chrX:33694165-33694176 chrX:33694166-33694175 chrX:33694164-33694175 chrX:33694166-33694175 chrX:33694164-33694175 chrX:33694164-33694177 chrX:33694166-33694175 chrX:33694164-33694177
47	CEBPB	chrX:33089575-33089851	IMR90	lung:	n/a	n/a
48	CEBPB	chrX:33721446-33721650	HepG2	liver:	n/a	n/a
49	CEBPB	chrX:33031577-33031810	K562	blood:	n/a	chrX:33031740-33031749 chrX:33031740-33031749 chrX:33031740-33031749 chrX:33031738-33031749 chrX:33031738-33031751 chrX:33031740-33031749
50	CEBPB	chrX:33572587-33572703	IMR90	lung:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:33146493-33146543	Hela-S3	cervix:	n/a
2	chrX:33357661-33357711	IMR90	lung:	fetal
3	chrX:33038967-33039017	LNCaP	prostate:	n/a
4	chrX:33744453-33744503	SK-N-SH_RA	brain:	n/a
5	chrX:33231137-33231187	ovcar-3	ovarian:	n/a
6	chrX:33146609-33146659	IMR90	lung:	fetal
7	chrX:33357661-33357711	HUVEC	blood vessel:	n/a
8	chrX:33146609-33146659	GM12891	blood:	n/a
9	chrX:33229714-33229764	NT2-D1	testis:	n/a
10	chrX:33357782-33357832	HCPEpiC	choroid plexus:	n/a
11	chrX:33357554-33357604	AG09319	gingival:	n/a
12	chrX:33231153-33231203	NH-A	brain:	n/a
13	chrX:33229689-33229739	NHDF-neo	bronchial:	n/a
14	chrX:33146493-33146543	NB4	blood:	n/a
15	chrX:33357661-33357711	AG04449	skin:	fetal
16	chrX:33231137-33231187	BE2_C	brain:	n/a
17	chrX:33038967-33039017	HCPEpiC	choroid plexus:	n/a
18	chrX:33744708-33744758	Hela-S3	cervix:	n/a
19	chrX:33357661-33357711	Hela-S3	cervix:	n/a
20	chrX:33745255-33745305	SAEC	small airway:	n/a
21	chrX:33231137-33231187	K562	blood:	n/a
22	chrX:33231153-33231203	PANC-1	pancreas:	n/a
23	chrX:33740873-33740923	GM06990	blood:	n/a
24	chrX:33147978-33148028	HPAEpiC	pulmonary alveolar:	n/a
25	chrX:33357554-33357604	PrEC	prostate:	n/a
26	chrX:33229454-33229504	NH-A	brain:	n/a
27	chrX:33146500-33146550	SK-N-MC	brain:	n/a
28	chrX:33744176-33744226	CMK	blood:	n/a
29	chrX:33231153-33231203	Hela-S3	cervix:	n/a
30	chrX:33745255-33745305	AG10803	skin:	n/a
31	chrX:33744947-33744997	MCF10A-Er-Src	breast:	n/a
32	chrX:33229689-33229739	T-47D	breast:	n/a
33	chrX:33357661-33357711	Jurkat	blood:	n/a
34	chrX:33744453-33744503	NHBE	bronchial:	n/a
35	chrX:33231153-33231203	U87	brain:	n/a
36	chrX:33745255-33745305	NHDF-neo	bronchial:	n/a
37	chrX:33744947-33744997	ovcar-3	ovarian:	n/a
38	chrX:33744176-33744226	HRCEpiC	kidney:	n/a
39	chrX:33357661-33357711	BE2_C	brain:	n/a
40	chrX:33229689-33229739	U87	brain:	n/a
41	chrX:33229454-33229504	K562	blood:	n/a
42	chrX:33357554-33357604	T-47D	breast:	n/a
43	chrX:33038967-33039017	HRE	kidney:	n/a
44	chrX:33229714-33229764	RPTEC	kidney:	n/a
45	chrX:33146500-33146550	AG10803	skin:	n/a
46	chrX:33740873-33740923	HUVEC	blood vessel:	n/a
47	chrX:33745255-33745305	NB4	blood:	n/a
48	chrX:33229689-33229739	GM12892	blood:	n/a
49	chrX:33231153-33231203	H1-hESC	embryonic stem cell:	embryo
50	chrX:33357782-33357832	PrEC	prostate:	n/a

No.	Distal block	Cell Line	Cell type
1	chrX:33452653..33453196-chrX:34293832..34294482,2	MCF-7	breast:
2	chrX:33499948..33502690-chrX:33506546..33509415,2	MCF-7	breast:
3	chrX:33499948..33502690-chrX:33506546..33509415,2	MCF-7	breast:
4	chrX:33486541..33489225-chrX:33492922..33495773,2	K562	blood:
5	chrX:32978971..32981642-chrX:32988787..32991251,2	K562	blood:
6	chrX:33452418..33453265-chrX:34318700..34319352,3	MCF-7	breast:
7	chrX:33452365..33452921-chrX:34318750..34319664,2	MCF-7	breast:
8	chrX:32978971..32981642-chrX:32988787..32991251,2	K562	blood:
9	chrX:33486541..33489225-chrX:33492922..33495773,2	K562	blood:
10	chrX:32548603..32550280-chrX:33354588..33355586,5	MCF-7	breast:
11	chr8:79502951..79504471-chrX:33134966..33136486,2	MCF-7	breast:
12	chr1:188146014..188146534-chrX:33134463..33134983,2	MCF-7	breast:
13	chrX:32796881..32797760-chrX:33354782..33355607,2	MCF-7	breast:
14	chrX:33452739..33453279-chrX:34057594..34058160,2	MCF-7	breast:
15	chrX:32501410..32501936-chrX:33355099..33355614,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM47B-1	chrX:33760234-33760251	NONHSAT136607
2	lnc-FAM47B-1	chrX:33744625-33744752	XLOC_007947
3	lnc-FAM47B-3	chrX:33781653-33781753	NONHSAT136604
4	lnc-FAM47A-3	chrX:33177312-33177714	NONHSAT136602
5	lnc-FAM47B-4	chrX:33429061-33430290	NONHSAT136603
6	lnc-FAM47B-1	chrX:33744575-33744752	NONHSAT136606
7	lnc-FAM47A-3	chrX:33146180-33146544	NONHSAT136601
8	lnc-FAM47A-3	chrX:33038303-33038317	NONHSAT136601
9	lnc-FAM47A-3	chrX:33229399-33229549	NONHSAT136602
10	lnc-FAM47B-3	chrX:33654546-33654673	NONHSAT136604
11	lnc-FAM47B-3	chrX:33781653-33781753	NONHSAT136605
12	lnc-FAM47B-1	chrX:33760235-33760251	XLOC_007947
13	lnc-FAM47B-1	chrX:33744624-33744752	NONHSAT136607
14	lnc-FAM47B-3	chrX:33670156-33670172	NONHSAT136605

Variant related genes	Relation type
ENSG00000233928	TF binding region
ENSG00000215310	TF binding region
DMD	TF binding region
TBCAP1	TF binding region
ENSG00000233928	CpG island
ENSG00000215310	CpG island
DMD	CpG island
TBCAP1	CpG island
ENSG00000171033	chromatin interactions
SLC25A30	miRNA target sites

Extended variants
information (count: 5344 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:5344 , 50 per page) page: 1 2 3 4 5 6 7 ... 107

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs189228464	chrX:32949240-32949241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs57258080	chrX:32949386-32949387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs147517193	chrX:32949434-32949435	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181545882	chrX:32949460-32949461	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs550972438	chrX:32949463-32949464	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs111549245	chrX:32949484-32949485	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs569595873	chrX:32949592-32949593	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs370448345	chrX:32949607-32949608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186524966	chrX:32949643-32949644	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs191110468	chrX:32949696-32949697	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs138389924	chrX:32949718-32949719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs6631682	chrX:32949724-32949725	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182240688	chrX:32949759-32949760	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs185985407	chrX:32949992-32949993	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs190854967	chrX:32950039-32950040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs183224119	chrX:32950057-32950058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs186982803	chrX:32950068-32950069	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs5928120	chrX:32950092-32950093	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139667409	chrX:32950141-32950142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs202139662	chrX:32950143-32950144	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs578256009	chrX:32950144-32950145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545574660	chrX:32950177-32950178	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs563918768	chrX:32950347-32950348	Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs190646351	chrX:32950351-32950352	Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575789415	chrX:32950472-32950473	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs543105863	chrX:32950475-32950476	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149776112	chrX:32950503-32950504	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs12390385	chrX:32950534-32950535	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs182810398	chrX:32950569-32950570	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs187278336	chrX:32950586-32950587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs374342871	chrX:32950623-32950624	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs368317357	chrX:32950836-32950837	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs16990767	chrX:32950888-32950889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs200448160	chrX:32950948-32950949	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs144096115	chrX:32951191-32951192	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs67953460	chrX:32951292-32951293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs398101947	chrX:32951298-32951299	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201508442	chrX:32951301-32951302	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs146499008	chrX:32951303-32951304	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs12559400	chrX:32951382-32951383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs72626057	chrX:32951498-32951499	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs151175899	chrX:32951629-32951630	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs193115495	chrX:32951734-32951735	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs369396468	chrX:32951832-32951833	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs185531381	chrX:32951847-32951848	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs371204917	chrX:32951938-32951939	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs187766190	chrX:32951953-32951954	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs372838294	chrX:32951991-32951992	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs5927113	chrX:32952019-32952020	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs192685818	chrX:32952039-32952040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
abnormal development	18461090	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Breast cancer	21858162	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Cancer	20164919	CNVD
Premature ovarian failure	20952765	CNVD
Ovarian cancer	19835627	CNVD
Cerebellar hypoplasia	21569638	CNVD
X-linked lissencephaly	21569638	CNVD
Thyroid cancer	19087340	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Developmental delay	21147756	CNVD
Mental retardation	17406619	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Cancer	20164920	CNVD
Gastric cancer	17229543	CNVD
Type 2 diabetes	21760887	CNVD
Cardiomyopathy	22138850	CNVD
Muscular dystrophy	21149563	CNVD
Skeletal myopathy	22138850	CNVD
Autism	21484199	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute lymphoblastic leukemia	19039135	CNVD
Duchenne-like muscular dystrophy	22138850	CNVD
Muscular dystrophy	22138850	CNVD
Disease	22090376	CNVD
Colorectal cancer	21645411	CNVD
Ornithine transcarbamylase deficiency	21467225	CNVD
Myxofibrosarcoma	16751306	CNVD
Alcoholism	21790672	CNVD
Chronic granulomatous disease	22383943	CNVD
lymphocytic leukemia	21291569	CNVD
Breast cancer	21611746	CNVD
Duchenne and Becker muscular dystrophies	18663755	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1217 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:32949200-32950200	Weak transcription	HSMMtube	muscle
2	chrX:32950200-32950400	Enhancers	HSMMtube	muscle
3	chrX:32950400-32966000	Weak transcription	HSMMtube	muscle
4	chrX:32951600-32952000	Enhancers	ES-I3 Cell Line	embryonic stem cell
5	chrX:32951600-32952200	Enhancers	Fetal Heart	heart
6	chrX:32952200-32955400	Weak transcription	Fetal Heart	heart
7	chrX:32952400-32953200	Enhancers	Left Ventricle	heart
8	chrX:32955400-32956600	Enhancers	Fetal Heart	heart
9	chrX:32955600-32955800	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chrX:32955800-32957600	Weak transcription	Skeletal Muscle Female	skeletal muscle
11	chrX:32957600-32957800	Enhancers	Skeletal Muscle Female	skeletal muscle
12	chrX:32957800-32958200	Weak transcription	Skeletal Muscle Female	skeletal muscle
13	chrX:32958200-32958600	Enhancers	Skeletal Muscle Female	skeletal muscle
14	chrX:32960800-32961200	Enhancers	Muscle Satellite Cultured Cells	--
15	chrX:32964800-32965400	Enhancers	iPS-15b Cell Line	embryonic stem cell
16	chrX:32964800-32966600	Enhancers	ES-I3 Cell Line	embryonic stem cell
17	chrX:32964800-32966600	Enhancers	iPS-18 Cell Line	embryonic stem cell
18	chrX:32965400-32965800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chrX:32965400-32965800	Enhancers	Brain Hippocampus Middle	brain
20	chrX:32965800-32966600	Enhancers	iPS-15b Cell Line	embryonic stem cell
21	chrX:32966000-32966400	Enhancers	ES-WA7 Cell Line	embryonic stem cell
22	chrX:32966000-32966600	Enhancers	HSMMtube	muscle
23	chrX:32966200-32966400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
24	chrX:32966200-32966600	Enhancers	Rectal Smooth Muscle	rectum
25	chrX:32966400-32966800	Enhancers	Fetal Heart	heart
26	chrX:32966600-33005200	Weak transcription	HSMMtube	muscle
27	chrX:32972400-32973200	Enhancers	Skeletal Muscle Female	skeletal muscle
28	chrX:32973200-32973800	Weak transcription	Skeletal Muscle Female	skeletal muscle
29	chrX:32973800-32974000	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
30	chrX:32974000-32975200	Weak transcription	Skeletal Muscle Female	skeletal muscle
31	chrX:32977800-32978600	Enhancers	Right Ventricle	heart
32	chrX:32978800-32979200	Enhancers	ES-WA7 Cell Line	embryonic stem cell
33	chrX:32984400-32986000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chrX:32984600-32985000	Enhancers	Breast Myoepithelial Primary Cells	Breast
35	chrX:32984800-32985200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chrX:32984800-32985200	Enhancers	Brain Angular Gyrus	brain
37	chrX:32984800-32985200	Enhancers	Brain Anterior Caudate	brain
38	chrX:32984800-32985200	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chrX:32984800-32985200	Enhancers	Skeletal Muscle Female	skeletal muscle
40	chrX:32984800-32985600	Enhancers	Brain Hippocampus Middle	brain
41	chrX:32985000-32985400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
42	chrX:32985000-32985400	Enhancers	Brain Inferior Temporal Lobe	brain
43	chrX:32993600-32994000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
44	chrX:32993800-32994200	Enhancers	Brain Substantia Nigra	brain
45	chrX:33001600-33001800	Enhancers	Fetal Heart	heart
46	chrX:33003200-33003600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
47	chrX:33003600-33004200	Enhancers	Fetal Heart	heart
48	chrX:33003800-33004000	Enhancers	HUES48 Cell Line	embryonic stem cell
49	chrX:33003800-33004000	Enhancers	iPS-18 Cell Line	embryonic stem cell
50	chrX:33003800-33004000	Enhancers	Right Ventricle	heart

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