Variant report

Variant	nsv498037
Chromosome Location	chrX:75586665-76291236
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1729)
CpG islands
(count:1041)
Chromatin interactive
region (count:10)
LncRNA
region (count:31)
Mature miRNA
region (count: 2)
miRNA target
sites (count:0)

(count:1729 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chrX:76192463-76192772	GM12878	blood:	n/a	n/a
2	ATF2	chrX:76152081-76152335	GM12878	blood:	n/a	n/a
3	ATF2	chrX:76151955-76152368	GM12878	blood:	n/a	n/a
4	BACH1	chrX:75654787-75655105	H1-hESC	embryonic stem cell:	n/a	chrX:75654921-75654935
5	BACH1	chrX:76235036-76235745	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chrX:76197900-76198349	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chrX:76036215-76036417	K562	blood:	n/a	n/a
8	BATF	chrX:76224411-76224630	GM12878	blood:	n/a	chrX:76224553-76224564
9	BATF	chrX:75877918-75878160	GM12878	blood:	n/a	n/a
10	BATF	chrX:76271981-76272136	GM12878	blood:	n/a	n/a
11	BHLHE40	chrX:76180553-76180590	GM12878	blood:	n/a	n/a
12	BHLHE40	chrX:76235184-76235740	HepG2	liver:	n/a	chrX:76235605-76235621
13	BHLHE40	chrX:75901969-75901984	GM12878	blood:	n/a	n/a
14	CBX3	chrX:75775702-75775978	K562	blood:	n/a	n/a
15	CEBPB	chrX:76138649-76139025	IMR90	lung:	n/a	chrX:76138949-76138960 chrX:76138681-76138694
16	CEBPB	chrX:76033570-76033859	IMR90	lung:	n/a	n/a
17	CEBPB	chrX:75759852-75760100	IMR90	lung:	n/a	n/a
18	CEBPB	chrX:76138558-76139038	HepG2	liver:	n/a	chrX:76138949-76138960 chrX:76138681-76138694
19	CEBPB	chrX:76023032-76023642	A549	lung:	n/a	chrX:76023327-76023338
20	CEBPB	chrX:75593054-75593315	IMR90	lung:	n/a	n/a
21	CEBPB	chrX:76273946-76274569	IMR90	lung:	n/a	n/a
22	CEBPB	chrX:76137583-76137870	IMR90	lung:	n/a	n/a
23	CEBPB	chrX:76023166-76023512	A549	lung:	n/a	chrX:76023327-76023338
24	CEBPB	chrX:76142556-76142906	Hela-S3	cervix:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
25	CEBPB	chrX:76035776-76036091	IMR90	lung:	n/a	n/a
26	CEBPB	chrX:76023128-76023501	MCF-7	breast:	n/a	chrX:76023327-76023338
27	CEBPB	chrX:75682115-75682328	K562	blood:	n/a	n/a
28	CEBPB	chrX:75682076-75682373	IMR90	lung:	n/a	n/a
29	CEBPB	chrX:76142546-76142909	HepG2	liver:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
30	CEBPB	chrX:76127054-76127370	HepG2	liver:	n/a	chrX:76127191-76127202
31	CEBPB	chrX:75682119-75682359	A549	lung:	n/a	n/a
32	CEBPB	chrX:76138554-76139001	Hela-S3	cervix:	n/a	chrX:76138949-76138960 chrX:76138681-76138694
33	CEBPB	chrX:76127072-76127335	A549	lung:	n/a	chrX:76127191-76127202
34	CEBPB	chrX:76142525-76142852	A549	lung:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
35	CEBPB	chrX:76127037-76127262	IMR90	lung:	n/a	chrX:76127191-76127202
36	CEBPB	chrX:76142547-76142899	MCF-7	breast:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
37	CEBPB	chrX:76273931-76274298	HepG2	liver:	n/a	n/a
38	CEBPB	chrX:76023272-76023447	HepG2	liver:	n/a	chrX:76023327-76023338
39	CEBPB	chrX:76142548-76142909	IMR90	lung:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
40	CEBPB	chrX:76021280-76021416	K562	blood:	n/a	n/a
41	CEBPB	chrX:76137616-76137816	A549	lung:	n/a	n/a
42	CEBPB	chrX:76041045-76041306	IMR90	lung:	n/a	n/a
43	CEBPB	chrX:76127068-76127235	K562	blood:	n/a	chrX:76127191-76127202
44	CEBPB	chrX:76142635-76142827	MCF-7	breast:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
45	CEBPB	chrX:76207616-76207796	HepG2	liver:	n/a	chrX:76207770-76207781
46	CEBPB	chrX:76137566-76137851	HepG2	liver:	n/a	n/a
47	CEBPB	chrX:76023246-76023372	K562	blood:	n/a	chrX:76023327-76023338
48	CEBPB	chrX:76142571-76142896	A549	lung:	n/a	chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731 chrX:76142722-76142731
49	CEBPB	chrX:76023101-76023544	A549	lung:	n/a	chrX:76023327-76023338
50	CEBPB	chrX:76041127-76041312	K562	blood:	n/a	n/a

(count:1041 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:75648455-75648505	HCPEpiC	choroid plexus:	n/a
2	chrX:75649367-75649417	GM12878	blood:	n/a
3	chrX:75647595-75647645	CMK	blood:	n/a
4	chrX:75648083-75648133	Caco-2	colon:	n/a
5	chrX:75648455-75648505	HCPEpiC	choroid plexus:	n/a
6	chrX:75649367-75649417	GM12878	blood:	n/a
7	chrX:75647595-75647645	CMK	blood:	n/a
8	chrX:75648083-75648133	Caco-2	colon:	n/a
9	chrX:75648802-75648852	NT2-D1	testis:	n/a
10	chrX:75649761-75649811	AoSMC	blood vessel:	n/a
11	chrX:75649532-75649582	MCF-7	breast:	n/a
12	chrX:75648216-75648266	T-47D	breast:	n/a
13	chrX:75649761-75649811	LNCaP	prostate:	n/a
14	chrX:75647859-75647909	SK-N-SH	brain:	n/a
15	chrX:75648961-75649011	HMEC	breast:	n/a
16	chrX:75647436-75647486	HMEC	breast:	n/a
17	chrX:75647859-75647909	CMK	blood:	n/a
18	chrX:75648884-75648934	IMR90	lung:	fetal
19	chrX:75648455-75648505	HIPEpiC	eye:	n/a
20	chrX:75648455-75648505	HNPCEpiC	eye:	n/a
21	chrX:75648083-75648133	HNPCEpiC	eye:	n/a
22	chrX:75648992-75649042	SAEC	small airway:	n/a
23	chrX:75648802-75648852	GM06990	blood:	n/a
24	chrX:76198371-76198421	AG09319	gingival:	n/a
25	chrX:75648083-75648133	AG04450	lung:	fetal
26	chrX:75647859-75647909	AoSMC	blood vessel:	n/a
27	chrX:75647859-75647909	Jurkat	blood:	n/a
28	chrX:75647595-75647645	RPTEC	kidney:	n/a
29	chrX:75648992-75649042	PrEC	prostate:	n/a
30	chrX:75647436-75647486	HIPEpiC	eye:	n/a
31	chrX:76140313-76140363	T-47D	breast:	n/a
32	chrX:76198371-76198421	GM12891	blood:	n/a
33	chrX:75647436-75647486	HepG2	liver:	n/a
34	chrX:76140313-76140363	GM12878	blood:	n/a
35	chrX:75648961-75649011	HCPEpiC	choroid plexus:	n/a
36	chrX:75647595-75647645	A549	lung:	n/a
37	chrX:75649761-75649811	GM06990	blood:	n/a
38	chrX:75648216-75648266	HEEpiC	esophagus:	n/a
39	chrX:75647859-75647909	HIPEpiC	eye:	n/a
40	chrX:75648884-75648934	HMEC	breast:	n/a
41	chrX:75649761-75649811	A549	lung:	n/a
42	chrX:75649761-75649811	AG04450	lung:	fetal
43	chrX:75648083-75648133	HAEpiC	amniotic membrane:	n/a
44	chrX:75649761-75649811	HRCEpiC	kidney:	n/a
45	chrX:75649532-75649582	HCPEpiC	choroid plexus:	n/a
46	chrX:75649532-75649582	NHBE	bronchial:	n/a
47	chrX:75648961-75649011	GM12878	blood:	n/a
48	chrX:75648992-75649042	MCF10A-Er-Src	breast:	n/a
49	chrX:75648802-75648852	AG10803	skin:	n/a
50	chrX:75648083-75648133	BE2_C	brain:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:52749844..52752672-chrX:76227808..76229967,2	MCF-7	breast:
2	chrX:76278562..76281311-chrX:76283274..76285842,2	K562	blood:
3	chrX:76232252..76234019-chrX:76241315..76243739,2	K562	blood:
4	chrX:75912856..75913411-chrX:76635366..76635882,2	MCF-7	breast:
5	chr4:190533382..190535450-chrX:76020791..76023770,2	MCF-7	breast:
6	chr4:41992370..41992871-chrX:76089886..76090386,2	Hela-S3	cervix:
7	chrX:76278562..76281311-chrX:76283274..76285842,2	K562	blood:
8	chr7:77165670..77166520-chrX:75928241..75929119,2	NB4	blood:
9	chrX:76232252..76234019-chrX:76241315..76243739,2	K562	blood:
10	chrX:75499134..75500029-chrX:75674724..75676050,4	MCF-7	breast:

(count:31 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ATRX-1	chrX:75878198-75878709	NR_110401
2	lnc-ATRX-1	chrX:76227701-76227805	NR_110401
3	lnc-ATRX-1	chrX:75913366-75913486	NR_110400
4	lnc-ATRX-1	chrX:76234652-76234957	NR_110405
5	lnc-ATRX-1	chrX:76227701-76227805	NONHSAT137681
6	lnc-ATRX-2	chrX:76144092-76144196	ucscGeneNc_uc010nlv_1
7	lnc-ATRX-1	chrX:76001608-76001717	NR_110405
8	lnc-ATRX-1	chrX:76058235-76058317	NR_110403
9	lnc-ATRX-1	chrX:75878198-75878709	NR_110400
10	lnc-ATRX-1	chrX:75878198-75878709	NR_110403
11	lnc-CXorf26-6	chrX:75651475-75651742	NONHSAT137678
12	lnc-ATRX-1	chrX:75913366-75913486	NR_110403
13	lnc-ATRX-1	chrX:75878903-75879069	NR_110404
14	lnc-ATRX-1	chrX:75878903-75879069	NR_110400
15	lnc-ATRX-1	chrX:75878198-75878709	NR_110404
16	lnc-ATRX-2	chrX:75829770-75829890	ucscGeneNc_uc010nlv_1
17	lnc-ATRX-2	chrX:75794602-75795113	ucscGeneNc_uc010nlv_1
18	lnc-ATRX-1	chrX:76234652-76234957	NONHSAT137681
19	lnc-ATRX-1	chrX:75913366-75913486	NONHSAT137681
20	lnc-ATRX-1	chrX:76234652-76234957	NR_110406
21	lnc-ATRX-1	chrX:75878198-75878709	NR_110405
22	lnc-ATRX-1	chrX:76227701-76227805	NR_110406
23	lnc-ATRX-1	chrX:76234652-76234957	NR_110400
24	lnc-ATRX-1	chrX:75878903-75879069	NR_110401
25	lnc-ATRX-1	chrX:76234652-76234957	NR_110403
26	lnc-ATRX-1	chrX:75878198-75878709	NR_110406
27	lnc-ATRX-1	chrX:75878198-75878709	NONHSAT137681
28	lnc-ATRX-1	chrX:76234652-76234957	NR_110401
29	lnc-ATRX-1	chrX:76234652-76234957	NR_110404
30	lnc-MAGEE2-5	chrX:75875899-75876960	NONHSAT137680
31	lnc-ATRX-2	chrX:76151043-76151348	ucscGeneNc_uc010nlv_1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-325	chrX:76225889-76225911	MIMAT0000771
hsa-miR-384	chrX:76139710-76139729	MIMAT0001075

No data

Variant related genes	Relation type
RNA5SP509	TF binding region
MIR325	TF binding region
MAGEE1	TF binding region
ENSG00000235447	TF binding region
RNA5SP508	TF binding region
RNA5SP509	CpG island
MIR325	CpG island
MAGEE1	CpG island
ENSG00000235447	CpG island
RNA5SP508	CpG island
ENSG00000014824	chromatin interactions
NTRK3	Mature miRNA region

Extended variants
information (count: 2003 )
Associated
traits (count: 50 )

Variant overlapped rSNPs/rCNVs (count:2003 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs191416935	chrX:75586674-75586675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs6607695	chrX:75586710-75586711	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs148146782	chrX:75586837-75586838	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs182688662	chrX:75586857-75586858	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs371157567	chrX:75586866-75586867	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs186025233	chrX:75586886-75586887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191098095	chrX:75586913-75586914	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs183282658	chrX:75587001-75587002	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs142594049	chrX:75587034-75587035	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs6655650	chrX:75587055-75587056	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs187523947	chrX:75587113-75587114	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs191990682	chrX:75587131-75587132	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs182998148	chrX:75587153-75587154	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs188156602	chrX:75587240-75587241	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs192866032	chrX:75587252-75587253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs148301872	chrX:75587272-75587273	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs377082501	chrX:75587273-75587274	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs184479319	chrX:75587326-75587327	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs139389103	chrX:75587389-75587390	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs189308395	chrX:75587418-75587419	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs192521575	chrX:75587444-75587445	Weak transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs12850960	chrX:75587617-75587618	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs189295645	chrX:75587703-75587704	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs181714482	chrX:75587709-75587710	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs142994197	chrX:75587774-75587775	Active TSS ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
26	rs190620999	chrX:75643188-75643189	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs181625816	chrX:75643243-75643244	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs60876992	chrX:75643285-75643286	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs73493498	chrX:75643358-75643359	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs188633864	chrX:75643369-75643370	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs55926420	chrX:75643376-75643377	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs187411620	chrX:75645692-75645693	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs374211333	chrX:75645783-75645784	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs190247409	chrX:75645898-75645899	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs370796102	chrX:75646830-75646831	Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs6647995	chrX:75646934-75646935	Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs113646839	chrX:75647003-75647004	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs77331224	chrX:75647024-75647025	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs184362880	chrX:75647138-75647139	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs374751202	chrX:75647165-75647166	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187888559	chrX:75647185-75647186	Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs35563989	chrX:75647209-75647210	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs375170043	chrX:75647272-75647273	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
44	rs28566881	chrX:75647273-75647274	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs192388561	chrX:75647330-75647331	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs184351914	chrX:75647402-75647403	Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs6647996	chrX:75647627-75647628	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
48	rs138833005	chrX:75647636-75647637	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	CpG island	1 gene(s)	Overlapped CNVs	n/a
49	rs370433342	chrX:75647677-75647678	Enhancers Bivalent/Poised TSS Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs67821007	chrX:75647944-75647945	Active TSS Enhancers Bivalent/Poised TSS Flanking Active TSS Bivalent Enhancer	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:50)

Disease	PMID	Source
Neuroblastoma	18923191	CNVD
Burkitt''s lymphoma	20823134	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	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
Glioblastoma multiforme	22286061	CNVD
Autism	22495311	CNVD
Cancer	20581869	CNVD
Multiple myeloma	20724749	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
lymphocytic leukemia	21291569	CNVD
Follicular lymphoma	20505157	CNVD
primary effusion lymphomas	17116491	CNVD
Testicular germ cell tumor	18059402	CNVD
Testicular cancer	18059402	CNVD
Seminomas	18059402	CNVD
Glioblastoma multiforme	19960244	CNVD
Endometrial cancer	22040021	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	17387387	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Cancer	22429812	CNVD
Cancer	16751803	CNVD
Lujan-Fryns syndrom	21572526	CNVD
Opitz-Kaveggia syndrome	21572526	CNVD
Cerebellar atrophy	21569638	CNVD
X-linked sideroblastic anemia	21569638	CNVD
Mental retardation	21572526	CNVD
ATR-X Syndrome	22470819	CNVD
Breast cancer	21611746	CNVD
Breast cancer	21364760	CNVD
Premature ovarian failure	20952765	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Astrocytoma	22246337	CNVD
Mental retardation	17339581	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:620 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:75585800-75587600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chrX:75587400-75587800	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
3	chrX:75587600-75587800	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chrX:75646800-75649800	Active TSS	Brain Anterior Caudate	brain
5	chrX:75647000-75647200	Enhancers	Right Ventricle	heart
6	chrX:75647000-75647400	Enhancers	Brain Substantia Nigra	brain
7	chrX:75647200-75647400	Enhancers	Brain Angular Gyrus	brain
8	chrX:75647200-75647400	Enhancers	Brain Cingulate Gyrus	brain
9	chrX:75647200-75647600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
10	chrX:75647200-75647800	Enhancers	Dnd41	blood
11	chrX:75647200-75649000	Active TSS	Brain Hippocampus Middle	brain
12	chrX:75647200-75649400	Active TSS	Brain Inferior Temporal Lobe	brain
13	chrX:75647200-75649400	Active TSS	Stomach Smooth Muscle	stomach
14	chrX:75647400-75647600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chrX:75647400-75647600	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chrX:75647400-75647800	Enhancers	Primary B cells from cord blood	blood
17	chrX:75647400-75647800	Enhancers	Primary T helper cells fromperipheralblood	blood
18	chrX:75647400-75647800	Enhancers	HepG2	liver
19	chrX:75647400-75648000	Enhancers	Primary B cells from peripheral blood	blood
20	chrX:75647400-75648000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
21	chrX:75647400-75648000	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chrX:75647400-75648000	Enhancers	Primary T killer memory cells from peripheral blood	blood
23	chrX:75647400-75650000	Active TSS	Brain Angular Gyrus	brain
24	chrX:75647400-75650600	Active TSS	Brain Cingulate Gyrus	brain
25	chrX:75647600-75647800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
26	chrX:75647600-75647800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
27	chrX:75647600-75647800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chrX:75647600-75647800	Enhancers	Adipose Nuclei	Adipose
29	chrX:75647600-75647800	Flanking Active TSS	Skeletal Muscle Female	skeletal muscle
30	chrX:75647600-75648000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
31	chrX:75647600-75648000	Enhancers	iPS-15b Cell Line	embryonic stem cell
32	chrX:75647600-75648000	Enhancers	Primary T cells fromperipheralblood	blood
33	chrX:75647600-75648000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
34	chrX:75647600-75648000	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
35	chrX:75647600-75648000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
36	chrX:75647600-75648000	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chrX:75647600-75648000	Enhancers	GM12878-XiMat	blood
38	chrX:75647600-75648000	Enhancers	Osteobl	bone
39	chrX:75647600-75648600	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
40	chrX:75647600-75648600	Active TSS	Skeletal Muscle Male	skeletal muscle
41	chrX:75647600-75649000	Active TSS	Fetal Kidney	kidney
42	chrX:75647600-75649200	Active TSS	Brain Substantia Nigra	brain
43	chrX:75647600-75649200	Active TSS	Right Atrium	heart
44	chrX:75647600-75649200	Active TSS	A549	lung
45	chrX:75647600-75649400	Active TSS	Duodenum Smooth Muscle	Duodenum
46	chrX:75647800-75648000	Flanking Active TSS	Primary T helper 17 cells PMA-I stimulated	--
47	chrX:75647800-75648000	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
48	chrX:75647800-75648000	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
49	chrX:75647800-75648000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chrX:75647800-75648000	Active TSS	Fetal Brain Female	brain

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