Variant report

Variant	nsv519013
Chromosome Location	chrX:57405163-57928734
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2788)
CpG islands
(count:610)
Chromatin interactive
region (count:36)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2788 , 50 per page) page: 1 2 3 4 5 6 7 ... 56

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:57618075-57618272	K562	blood:	n/a	n/a
2	ARID3A	chrX:57622601-57623204	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:57545963-57546457	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:57666501-57667488	HepG2	liver:	n/a	n/a
5	ARID3A	chrX:57617946-57618343	HepG2	liver:	n/a	n/a
6	ARID3A	chrX:57670088-57670644	HepG2	liver:	n/a	n/a
7	ARID3A	chrX:57639933-57640067	HepG2	liver:	n/a	n/a
8	ARID3A	chrX:57671687-57671877	HepG2	liver:	n/a	n/a
9	ARID3A	chrX:57621748-57622144	HepG2	liver:	n/a	n/a
10	ATF3	chrX:57474246-57474758	HCT-116	colon:	n/a	n/a
11	ATF3	chrX:57474385-57474565	HepG2	liver:	n/a	n/a
12	BACH1	chrX:57621922-57622065	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chrX:57623386-57623431	K562	blood:	n/a	n/a
14	BACH1	chrX:57609921-57610196	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chrX:57633816-57634114	H1-hESC	embryonic stem cell:	n/a	n/a
16	BATF	chrX:57406814-57407187	GM12878	blood:	n/a	chrX:57406991-57407002 chrX:57406967-57406978
17	BATF	chrX:57429923-57430134	GM12878	blood:	n/a	n/a
18	BATF	chrX:57621806-57622031	GM12878	blood:	n/a	n/a
19	BATF	chrX:57429880-57430141	GM12878	blood:	n/a	n/a
20	BATF	chrX:57406875-57407037	GM12878	blood:	n/a	chrX:57406991-57407002 chrX:57406967-57406978
21	BHLHE40	chrX:57848241-57848426	K562	blood:	n/a	n/a
22	BHLHE40	chrX:57621861-57621951	GM12878	blood:	n/a	n/a
23	BHLHE40	chrX:57619471-57619473	GM12878	blood:	n/a	n/a
24	BHLHE40	chrX:57600219-57600551	GM12878	blood:	n/a	n/a
25	BHLHE40	chrX:57848220-57848485	GM12878	blood:	n/a	n/a
26	BRCA1	chrX:57617877-57618371	Hela-S3	cervix:	n/a	n/a
27	BRCA1	chrX:57542099-57542134	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chrX:57619145-57619488	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chrX:57764318-57764638	Hela-S3	cervix:	n/a	n/a
30	CEBPB	chrX:57621117-57621476	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chrX:57670163-57670468	Hela-S3	cervix:	n/a	n/a
32	CEBPB	chrX:57670129-57670439	A549	lung:	n/a	n/a
33	CEBPB	chrX:57619235-57619656	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chrX:57622698-57623012	HepG2	liver:	n/a	chrX:57622860-57622871
35	CEBPB	chrX:57621682-57622263	Hela-S3	cervix:	n/a	n/a
36	CEBPB	chrX:57621160-57621465	IMR90	lung:	n/a	n/a
37	CEBPB	chrX:57619484-57619644	HepG2	liver:	n/a	n/a
38	CEBPB	chrX:57764034-57765026	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chrX:57472764-57473090	HepG2	liver:	n/a	chrX:57472928-57472939
40	CEBPB	chrX:57609488-57609835	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chrX:57471550-57471861	MCF-7	breast:	n/a	n/a
42	CEBPB	chrX:57480579-57480689	K562	blood:	n/a	n/a
43	CEBPB	chrX:57447995-57448240	HepG2	liver:	n/a	n/a
44	CEBPB	chrX:57621802-57622170	IMR90	lung:	n/a	n/a
45	CEBPB	chrX:57584211-57584458	IMR90	lung:	n/a	n/a
46	CEBPB	chrX:57666435-57666799	HepG2	liver:	n/a	chrX:57666602-57666613
47	CEBPB	chrX:57447975-57448299	IMR90	lung:	n/a	n/a
48	CEBPB	chrX:57472758-57473050	IMR90	lung:	n/a	chrX:57472928-57472939
49	CEBPB	chrX:57670097-57670437	HepG2	liver:	n/a	n/a
50	CEBPB	chrX:57474198-57474711	HCT-116	colon:	n/a	chrX:57474478-57474489

(count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:57618914-57618964	HAEpiC	amniotic membrane:	n/a
2	chrX:57619327-57619377	HPAEpiC	pulmonary alveolar:	n/a
3	chrX:57617470-57617520	ovcar-3	ovarian:	n/a
4	chrX:57622899-57622949	NB4	blood:	n/a
5	chrX:57618891-57618941	NHDF-neo	bronchial:	n/a
6	chrX:57618144-57618194	HRCEpiC	kidney:	n/a
7	chrX:57618891-57618941	HepG2	liver:	n/a
8	chrX:57617561-57617611	GM12878	blood:	n/a
9	chrX:57617561-57617611	HCM	heart:	n/a
10	chrX:57617561-57617611	HPAEpiC	pulmonary alveolar:	n/a
11	chrX:57618144-57618194	NB4	blood:	n/a
12	chrX:57618144-57618194	SAEC	small airway:	n/a
13	chrX:57619974-57620024	HMEC	breast:	n/a
14	chrX:57619974-57620024	HUVEC	blood vessel:	n/a
15	chrX:57618059-57618109	HRE	kidney:	n/a
16	chrX:57617561-57617611	NHDF-neo	bronchial:	n/a
17	chrX:57619974-57620024	AG09319	gingival:	n/a
18	chrX:57618144-57618194	BJ	skin:	n/a
19	chrX:57618144-57618194	Hepatocyte	liver:	n/a
20	chrX:57618059-57618109	Caco-2	colon:	n/a
21	chrX:57622899-57622949	MCF-7	breast:	n/a
22	chrX:57619327-57619377	NT2-D1	testis:	n/a
23	chrX:57616301-57616351	H1-hESC	embryonic stem cell:	embryo
24	chrX:57619974-57620024	BJ	skin:	n/a
25	chrX:57617470-57617520	NT2-D1	testis:	n/a
26	chrX:57617561-57617611	HAEpiC	amniotic membrane:	n/a
27	chrX:57618059-57618109	RPTEC	kidney:	n/a
28	chrX:57619327-57619377	IMR90	lung:	fetal
29	chrX:57619327-57619377	MCF10A-Er-Src	breast:	n/a
30	chrX:57618059-57618109	HRPEpiC	eye:	n/a
31	chrX:57622899-57622949	HRE	kidney:	n/a
32	chrX:57618914-57618964	IMR90	lung:	fetal
33	chrX:57617561-57617611	GM12892	blood:	n/a
34	chrX:57617470-57617520	PrEC	prostate:	n/a
35	chrX:57619974-57620024	HIPEpiC	eye:	n/a
36	chrX:57617470-57617520	CMK	blood:	n/a
37	chrX:57618914-57618964	HPAEpiC	pulmonary alveolar:	n/a
38	chrX:57622899-57622949	Jurkat	blood:	n/a
39	chrX:57616301-57616351	Hela-S3	cervix:	n/a
40	chrX:57618914-57618964	HNPCEpiC	eye:	n/a
41	chrX:57619974-57620024	LNCaP	prostate:	n/a
42	chrX:57617561-57617611	SKMC	muscle:	n/a
43	chrX:57618891-57618941	SK-N-SH_RA	brain:	n/a
44	chrX:57617561-57617611	HRCEpiC	kidney:	n/a
45	chrX:57617561-57617611	Jurkat	blood:	n/a
46	chrX:57618891-57618941	HCT-116	colon:	n/a
47	chrX:57616301-57616351	CMK	blood:	n/a
48	chrX:57618914-57618964	GM12892	blood:	n/a
49	chrX:57619327-57619377	HCT-116	colon:	n/a
50	chrX:57618914-57618964	BJ	skin:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chrX:57614044..57616560-chrX:57623623..57626400,2	K562	blood:
2	chrX:57312784..57314553-chrX:57460706..57462258,2	MCF-7	breast:
3	chrX:57355124..57356053-chrX:57479973..57480835,2	MCF-7	breast:
4	chrX:57847837..57849053-chrX:57955600..57956476,4	MCF-7	breast:
5	chrX:57509231..57511711-chrX:57522993..57525169,2	MCF-7	breast:
6	chrX:57309045..57309569-chrX:57555198..57555707,2	MCF-7	breast:
7	chrX:57874195..57876996-chrX:57879495..57881455,2	MCF-7	breast:
8	chrX:57682992..57684642-chrX:57687037..57689864,2	MCF-7	breast:
9	chrX:57610731..57612693-chrX:57617782..57619539,2	MCF-7	breast:
10	chrX:57705635..57707267-chrX:57707321..57710024,2	MCF-7	breast:
11	chrX:57848200..57848796-chrX:57944842..57945766,2	MCF-7	breast:
12	chrX:57599875..57600849-chrX:57955568..57956254,2	MCF-7	breast:
13	chrX:57617996..57620588-chrX:57675872..57678039,2	MCF-7	breast:
14	chrX:57601606..57603386-chrX:57604937..57607787,2	MCF-7	breast:
15	chrX:57676792..57678804-chrX:57680775..57682824,2	MCF-7	breast:
16	chrX:57618405..57619078-chrX:57936166..57936723,2	MCF-7	breast:
17	chr19:2475703..2476241-chrX:57618085..57618762,2	Hela-S3	cervix:
18	chrX:57509231..57511711-chrX:57522993..57525169,2	MCF-7	breast:
19	chrX:57308677..57309238-chrX:57480174..57481114,2	MCF-7	breast:
20	chrX:57847902..57848941-chrX:57955530..57956361,5	MCF-7	breast:
21	chrX:57616778..57619182-chrX:57669301..57671313,2	MCF-7	breast:
22	chrX:57847913..57848811-chrX:58052114..58052903,5	MCF-7	breast:
23	chrX:57614423..57616273-chrX:57616637..57619351,2	MCF-7	breast:
24	chrX:57614044..57616560-chrX:57623623..57626400,2	K562	blood:
25	chrX:57618288..57620414-chrX:57932796..57935174,2	MCF-7	breast:
26	chrX:57847901..57848958-chrX:57945372..57946185,3	MCF-7	breast:
27	chrX:57874195..57876996-chrX:57879495..57881455,2	MCF-7	breast:
28	chrX:57847862..57848818-chrX:58052130..58053088,3	MCF-7	breast:
29	chrX:57182386..57183122-chrX:57480091..57480609,2	MCF-7	breast:
30	chr3:179248693..179249390-chrX:57616388..57617183,2	MCF-7	breast:
31	chrX:57676792..57678804-chrX:57680775..57682824,2	MCF-7	breast:
32	chrX:57601606..57603386-chrX:57604937..57607787,2	MCF-7	breast:
33	chrX:56815042..56815858-chrX:57555231..57555778,2	MCF-7	breast:
34	chr7:121689235..121689772-chrX:57477123..57477731,2	MCF-7	breast:
35	chrX:57682992..57684642-chrX:57687037..57689864,2	MCF-7	breast:
36	chrX:57848736..57850264-chrX:57955258..57957705,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZXDB-3	chrX:57925278-57930797	NONHSAT137292
2	lnc-ZXDB-1	chrX:57667298-57667326	XLOC_007998
3	lnc-ZXDB-1	chrX:57680523-57680873	XLOC_007998

No data

Variant related genes	Relation type
ENSG00000227427	TF binding region
ZXDB	TF binding region
ENSG00000215174	TF binding region
FAAH2	TF binding region
MTHFD1P1	TF binding region
ENSG00000227427	CpG island
ZXDB	CpG island
ENSG00000215174	CpG island
FAAH2	CpG island
MTHFD1P1	CpG island
ENSG00000198455	chromatin interactions
ENSG00000099860	chromatin interactions
ENSG00000215174	chromatin interactions
ENSG00000165591	chromatin interactions

Extended variants
information (count: 3104 )
Associated
traits (count: 45 )

Variant overlapped rSNPs/rCNVs (count:3104 , 50 per page) page: 1 2 3 4 5 6 7 ... 63

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4826543	chrX:57405163-57405164	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs148907702	chrX:57405179-57405180	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs142771015	chrX:57405210-57405211	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs202011260	chrX:57405218-57405219	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs145167792	chrX:57405256-57405257	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs147006343	chrX:57405505-57405506	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs186145484	chrX:57405518-57405519	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs190621439	chrX:57405527-57405528	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs147652327	chrX:57405585-57405586	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs184053875	chrX:57405642-57405643	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187165695	chrX:57405706-57405707	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs142168854	chrX:57405919-57405920	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192040963	chrX:57405929-57405930	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs371178179	chrX:57405939-57405940	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs72343722	chrX:57405965-57405966	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs57962376	chrX:57405966-57405967	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201113030	chrX:57405977-57405978	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs5914998	chrX:57405978-57405979	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs12388546	chrX:57405980-57405981	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs5914999	chrX:57406001-57406002	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs202232617	chrX:57406002-57406003	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs373772089	chrX:57406007-57406008	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536993137	chrX:57406063-57406064	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs80106968	chrX:57406066-57406067	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs555300027	chrX:57406075-57406076	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs141186478	chrX:57406099-57406100	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs182963663	chrX:57406118-57406119	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs2116363	chrX:57406237-57406238	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs34967842	chrX:57406246-57406247	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs61178623	chrX:57406260-57406261	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs187428607	chrX:57406305-57406306	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs137873924	chrX:57406346-57406347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112651540	chrX:57406490-57406491	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs146151701	chrX:57406521-57406522	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs191842815	chrX:57406622-57406623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs140156824	chrX:57406670-57406671	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs182538649	chrX:57406752-57406753	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs5960961	chrX:57406814-57406815	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs368484002	chrX:57406837-57406838	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs62598827	chrX:57406840-57406841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187879528	chrX:57406910-57406911	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192304998	chrX:57406927-57406928	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs534407896	chrX:57406960-57406961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs372796481	chrX:57407054-57407055	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs144767996	chrX:57407059-57407060	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs148565499	chrX:57407060-57407061	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs374735147	chrX:57407073-57407074	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs5960962	chrX:57407197-57407198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs201566499	chrX:57407297-57407298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs369074361	chrX:57407318-57407319	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:45)

Disease	PMID	Source
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
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Acute myeloid leukemia	21251322	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	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
Thyroid cancer	19087340	CNVD
lymphocytic leukemia	21291569	CNVD
Cervical cancer	21062161	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Breast cancer	21785460	CNVD
Ovarian cancer	19835627	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21364760	CNVD
Congenital diaphragmatic hernia	21525063	CNVD

Chromatin state (count:1140 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:57389800-57405200	Weak transcription	Primary T helper cells PMA-I stimulated	--
2	chrX:57390400-57419600	Weak transcription	Primary T cells from cord blood	blood
3	chrX:57390800-57421000	Weak transcription	Primary T helper cells fromperipheralblood	blood
4	chrX:57392000-57423600	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chrX:57395200-57406000	Weak transcription	Liver	Liver
6	chrX:57400400-57408000	Weak transcription	Fetal Intestine Large	intestine
7	chrX:57404200-57408000	Weak transcription	HUES6 Cell Line	embryonic stem cell
8	chrX:57404800-57407800	Weak transcription	Duodenum Mucosa	Duodenum
9	chrX:57405000-57405800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
10	chrX:57405200-57406800	Strong transcription	Primary T helper cells PMA-I stimulated	--
11	chrX:57405600-57426400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
12	chrX:57405800-57406800	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chrX:57406000-57407800	Strong transcription	Liver	Liver
14	chrX:57406800-57408400	Weak transcription	Primary T helper cells PMA-I stimulated	--
15	chrX:57406800-57408800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chrX:57407800-57422600	Weak transcription	Liver	Liver
17	chrX:57416000-57420400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
18	chrX:57417400-57425000	Weak transcription	Pancreas	Pancrea
19	chrX:57417800-57421400	Weak transcription	Sigmoid Colon	Sigmoid Colon
20	chrX:57418200-57420600	Weak transcription	Primary T cells fromperipheralblood	blood
21	chrX:57418600-57419400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
22	chrX:57419200-57422400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
23	chrX:57419400-57420600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
24	chrX:57419600-57420200	ZNF genes & repeats	Fetal Intestine Small	intestine
25	chrX:57419600-57421600	Strong transcription	Primary T cells from cord blood	blood
26	chrX:57419600-57422200	Weak transcription	Left Ventricle	heart
27	chrX:57419800-57436800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
28	chrX:57421600-57423200	Weak transcription	Primary T cells from cord blood	blood
29	chrX:57423600-57424000	ZNF genes & repeats	ES-I3 Cell Line	embryonic stem cell
30	chrX:57424000-57429200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chrX:57426600-57426800	ZNF genes & repeats	iPS-15b Cell Line	embryonic stem cell
32	chrX:57426800-57430800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chrX:57429200-57429800	Enhancers	ES-I3 Cell Line	embryonic stem cell
34	chrX:57430800-57431000	Enhancers	HUES6 Cell Line	embryonic stem cell
35	chrX:57430800-57431200	Enhancers	iPS-15b Cell Line	embryonic stem cell
36	chrX:57432400-57434000	ZNF genes & repeats	Adipose Nuclei	Adipose
37	chrX:57432800-57433200	ZNF genes & repeats	Pancreas	Pancrea
38	chrX:57433000-57433600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
39	chrX:57433000-57433800	Enhancers	Fetal Heart	heart
40	chrX:57433600-57450000	Weak transcription	Pancreas	Pancrea
41	chrX:57436800-57437000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
42	chrX:57437400-57438000	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
43	chrX:57443000-57480800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
44	chrX:57443600-57445000	Enhancers	Dnd41	blood
45	chrX:57444000-57444600	Enhancers	HUES6 Cell Line	embryonic stem cell
46	chrX:57446400-57448800	Weak transcription	Primary T helper cells PMA-I stimulated	--
47	chrX:57448000-57450400	Enhancers	Fetal Heart	heart
48	chrX:57448000-57451800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
49	chrX:57448800-57449200	Strong transcription	Primary T helper cells PMA-I stimulated	--
50	chrX:57449200-57451200	Weak transcription	Primary T helper cells PMA-I stimulated	--

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