Variant report

Variant	nsv532878
Chromosome Location	chrX:73603325-74057587
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3669)
CpG islands
(count:2564)
Chromatin interactive
region (count:97)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:3)

(count:3669 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chrX:73707407-73707514	K562	blood:	n/a	n/a
2	ARID3A	chrX:73834485-73834685	HepG2	liver:	n/a	n/a
3	ARID3A	chrX:73770150-73770547	HepG2	liver:	n/a	n/a
4	ARID3A	chrX:73770172-73770531	K562	blood:	n/a	n/a
5	ATF1	chrX:73834371-73834819	K562	blood:	n/a	chrX:73834727-73834741
6	ATF2	chrX:74019859-74020329	GM12878	blood:	n/a	n/a
7	ATF2	chrX:73998820-73999413	GM12878	blood:	n/a	n/a
8	ATF2	chrX:73834299-73834842	GM12878	blood:	n/a	chrX:73834727-73834741
9	ATF2	chrX:73834263-73834991	GM12878	blood:	n/a	chrX:73834727-73834741
10	ATF2	chrX:74019768-74020420	GM12878	blood:	n/a	n/a
11	ATF2	chrX:73834555-73834816	H1-hESC	embryonic stem cell:	n/a	chrX:73834727-73834741
12	ATF2	chrX:74000732-74002129	GM12878	blood:	n/a	n/a
13	ATF2	chrX:74001160-74002022	GM12878	blood:	n/a	n/a
14	ATF3	chrX:73770190-73770412	K562	blood:	n/a	n/a
15	BACH1	chrX:73841908-73842042	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chrX:73640340-73640380	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chrX:73766377-73766905	K562	blood:	n/a	n/a
18	BACH1	chrX:73809618-73809637	K562	blood:	n/a	n/a
19	BACH1	chrX:73755901-73756522	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chrX:73998998-73999483	GM12878	blood:	n/a	n/a
21	BATF	chrX:74001737-74001961	GM12878	blood:	n/a	n/a
22	BATF	chrX:73628187-73628495	GM12878	blood:	n/a	chrX:73628313-73628324
23	BATF	chrX:73834582-73834912	GM12878	blood:	n/a	n/a
24	BATF	chrX:73754311-73754649	GM12878	blood:	n/a	n/a
25	BATF	chrX:73798029-73798302	GM12878	blood:	n/a	chrX:73798180-73798191
26	BATF	chrX:73726362-73726692	GM12878	blood:	n/a	n/a
27	BATF	chrX:73770248-73770465	GM12878	blood:	n/a	n/a
28	BATF	chrX:73730183-73730580	GM12878	blood:	n/a	n/a
29	BATF	chrX:73754245-73754716	GM12878	blood:	n/a	n/a
30	BATF	chrX:74019940-74020209	GM12878	blood:	n/a	n/a
31	BATF	chrX:73730275-73730499	GM12878	blood:	n/a	n/a
32	BCL11A	chrX:73726336-73726595	GM12878	blood:	n/a	chrX:73726578-73726585 chrX:73726503-73726512
33	BCL3	chrX:73726319-73726725	GM12878	blood:	n/a	chrX:73726578-73726585 chrX:73726503-73726512
34	BCL3	chrX:73834234-73834763	GM12878	blood:	n/a	chrX:73834291-73834304 chrX:73834465-73834474 chrX:73834292-73834305 chrX:73834294-73834303
35	BCL3	chrX:73754321-73754667	GM12878	blood:	n/a	n/a
36	BCL3	chrX:73766186-73767295	GM12878	blood:	n/a	n/a
37	BCL3	chrX:73766255-73767222	GM12878	blood:	n/a	n/a
38	BCL3	chrX:73765676-73766174	GM12878	blood:	n/a	n/a
39	BCL3	chrX:74019853-74020309	GM12878	blood:	n/a	n/a
40	BCL3	chrX:74001247-74001835	GM12878	blood:	n/a	n/a
41	BCL3	chrX:73765703-73766169	GM12878	blood:	n/a	n/a
42	BCL3	chrX:74001094-74001956	GM12878	blood:	n/a	n/a
43	BCLAF1	chrX:73834185-73834844	GM12878	blood:	n/a	chrX:73834291-73834304 chrX:73834465-73834474 chrX:73834292-73834305 chrX:73834294-73834303
44	BCLAF1	chrX:73834220-73834902	GM12878	blood:	n/a	chrX:73834291-73834304 chrX:73834465-73834474 chrX:73834292-73834305 chrX:73834294-73834303
45	BCLAF1	chrX:73770109-73770486	GM12878	blood:	n/a	n/a
46	BCLAF1	chrX:73770059-73770472	GM12878	blood:	n/a	n/a
47	BHLHE40	chrX:74001257-74001749	GM12878	blood:	n/a	n/a
48	BHLHE40	chrX:73770030-73770495	GM12878	blood:	n/a	n/a
49	BHLHE40	chrX:73770092-73770464	K562	blood:	n/a	n/a
50	BHLHE40	chrX:73834198-73834843	GM12878	blood:	n/a	chrX:73834291-73834307

(count:2564 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chrX:73833865-73833915	HCPEpiC	choroid plexus:	n/a
2	chrX:73834683-73834733	AG10803	skin:	n/a
3	chrX:73833865-73833915	HCPEpiC	choroid plexus:	n/a
4	chrX:73834683-73834733	AG10803	skin:	n/a
5	chrX:73641615-73641665	NHBE	bronchial:	n/a
6	chrX:73640648-73640698	GM12878	blood:	n/a
7	chrX:73834707-73834757	HEEpiC	esophagus:	n/a
8	chrX:73644754-73644804	HEEpiC	esophagus:	n/a
9	chrX:73754570-73754620	RPTEC	kidney:	n/a
10	chrX:73756802-73756852	NH-A	brain:	n/a
11	chrX:73639809-73639859	NB4	blood:	n/a
12	chrX:73755969-73756019	SAEC	small airway:	n/a
13	chrX:73834332-73834382	T-47D	breast:	n/a
14	chrX:73638176-73638226	HCM	heart:	n/a
15	chrX:73752397-73752447	A549	lung:	n/a
16	chrX:73834821-73834871	K562	blood:	n/a
17	chrX:73646094-73646144	LNCaP	prostate:	n/a
18	chrX:73756189-73756239	NHBE	bronchial:	n/a
19	chrX:73836760-73836810	AoSMC	blood vessel:	n/a
20	chrX:73640043-73640093	Jurkat	blood:	n/a
21	chrX:73755969-73756019	IMR90	lung:	fetal
22	chrX:73642885-73642935	HRCEpiC	kidney:	n/a
23	chrX:73755969-73756019	HepG2	liver:	n/a
24	chrX:73834821-73834871	NH-A	brain:	n/a
25	chrX:73834821-73834871	AoSMC	blood vessel:	n/a
26	chrX:73834596-73834646	AG09309	skin:	n/a
27	chrX:73639809-73639859	NHDF-neo	bronchial:	n/a
28	chrX:73641073-73641123	GM12892	blood:	n/a
29	chrX:73641615-73641665	HEEpiC	esophagus:	n/a
30	chrX:73835412-73835462	ECC-1	luminal epithelium:	n/a
31	chrX:73642385-73642435	ovcar-3	ovarian:	n/a
32	chrX:73646094-73646144	Hepatocyte	liver:	n/a
33	chrX:73756723-73756773	AG09319	gingival:	n/a
34	chrX:73756698-73756748	NT2-D1	testis:	n/a
35	chrX:73834821-73834871	LNCaP	prostate:	n/a
36	chrX:73641955-73642005	HL-60	blood:	n/a
37	chrX:73646094-73646144	AG10803	skin:	n/a
38	chrX:73646094-73646144	HPAEpiC	pulmonary alveolar:	n/a
39	chrX:73644754-73644804	Hela-S3	cervix:	n/a
40	chrX:73641370-73641420	GM12892	blood:	n/a
41	chrX:73642734-73642784	HNPCEpiC	eye:	n/a
42	chrX:73834332-73834382	NT2-D1	testis:	n/a
43	chrX:73759065-73759115	PFSK-1	brain:	n/a
44	chrX:73641370-73641420	GM06990	blood:	n/a
45	chrX:73752397-73752447	ECC-1	luminal epithelium:	n/a
46	chrX:73642618-73642668	AoSMC	blood vessel:	n/a
47	chrX:73642618-73642668	NHDF-neo	bronchial:	n/a
48	chrX:73641615-73641665	NB4	blood:	n/a
49	chrX:73759065-73759115	K562	blood:	n/a
50	chrX:73646094-73646144	RPTEC	kidney:	n/a

(count:97 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chrX:73509039..73511824-chrX:73830797..73833330,2	K562	blood:
2	chrX:73812034..73814010-chrX:73814336..73817265,3	K562	blood:
3	chrX:73712436..73713291-chrX:73769831..73770334,2	MCF-7	breast:
4	chrX:73820035..73821678-chrX:73823192..73825276,2	MCF-7	breast:
5	chr11:18656070..18656623-chrX:73834052..73834881,2	Hela-S3	cervix:
6	chrX:73832009..73834528-chrX:73853194..73854894,2	MCF-7	breast:
7	chr12:109123745..109124693-chrX:73833479..73834373,2	Hela-S3	cervix:
8	chrX:73603244..73604146-chrX:73678258..73678803,3	MCF-7	breast:
9	chrX:73813372..73815041-chrX:73832585..73834357,2	MCF-7	breast:
10	chrX:73603018..73603600-chrX:73640981..73641874,2	MCF-7	breast:
11	chrX:73603244..73604146-chrX:73678258..73678803,3	MCF-7	breast:
12	chrX:73812034..73814010-chrX:73814336..73817265,3	K562	blood:
13	chrX:73644493..73646727-chrX:73670364..73672571,2	MCF-7	breast:
14	chrX:73834701..73838034-chrX:73840299..73843007,3	K562	blood:
15	chrX:73657745..73659270-chrX:73663065..73665992,2	MCF-7	breast:
16	chrX:73641524..73644343-chrX:73668070..73670153,2	MCF-7	breast:
17	chrX:73685296..73685826-chrX:73770265..73770777,2	MCF-7	breast:
18	chrX:73626645..73629607-chrX:73634521..73637156,2	MCF-7	breast:
19	chrX:73834701..73838034-chrX:73840299..73843007,3	K562	blood:
20	chrX:73646237..73648099-chrX:73653565..73655855,2	MCF-7	breast:
21	chr11:133695379..133696248-chrX:73926195..73926774,2	MCF-7	breast:
22	chrX:73639270..73641033-chrX:73663295..73665992,2	MCF-7	breast:
23	chrX:73654355..73656096-chrX:73661337..73663117,2	MCF-7	breast:
24	chrX:73565416..73566092-chrX:73769898..73770502,2	MCF-7	breast:
25	chrX:73654355..73656096-chrX:73661337..73663117,2	MCF-7	breast:
26	chrX:73756226..73758881-chrX:73826636..73828230,2	K562	blood:
27	chrX:73603198..73603899-chrX:73754929..73756065,4	MCF-7	breast:
28	chrX:73756226..73758881-chrX:73826636..73828230,2	K562	blood:
29	chrX:73634535..73636449-chrX:73644492..73646504,2	MCF-7	breast:
30	chrX:73639270..73641033-chrX:73663295..73665992,2	MCF-7	breast:
31	chrX:73741222..73743061-chrX:73743344..73746337,2	MCF-7	breast:
32	chrX:73755843..73757713-chrX:73759270..73760848,2	MCF-7	breast:
33	chrX:73811615..73813140-chrX:73814881..73817415,2	MCF-7	breast:
34	chr1:149857366..149858274-chrX:73833636..73834515,2	Hela-S3	cervix:
35	chrX:73819960..73822642-chrX:73832307..73835331,3	MCF-7	breast:
36	chrX:73756326..73757264-chrX:73769833..73770772,2	MCF-7	breast:
37	chrX:73712799..73713370-chrX:73770239..73770806,2	MCF-7	breast:
38	chr1:51425433..51426414-chrX:73833678..73834486,2	Hela-S3	cervix:
39	chr5:39074053..39075125-chrX:73833706..73834858,3	Hela-S3	cervix:
40	chrX:73741685..73745108-chrX:73747636..73750354,3	K562	blood:
41	chrX:73640488..73644070-chrX:73647813..73650987,3	MCF-7	breast:
42	chrX:73871841..73874318-chrX:73882022..73884094,2	K562	blood:
43	chrX:73741685..73745108-chrX:73747636..73750354,3	K562	blood:
44	chr5:176730265..176731166-chrX:73832459..73832999,2	Hela-S3	cervix:
45	chrX:73602581..73603332-chrX:73678366..73679146,2	MCF-7	breast:
46	chrX:73755843..73757713-chrX:73759270..73760848,2	MCF-7	breast:
47	chrX:73663502..73665376-chrX:73668807..73671667,2	K562	blood:
48	chrX:73641312..73645233-chrX:73652537..73656511,3	MCF-7	breast:
49	chrX:73809458..73813064-chrX:73832812..73834574,3	MCF-7	breast:
50	chrX:73737329..73740159-chrX:73740814..73742890,3	MCF-7	breast:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RLIM-1	chrX:73635238-73635396	XLOC_008188
2	lnc-SLC16A2-1	chrX:73610527-73610822	NONHSAT137637
3	lnc-RLIM-1	chrX:73640141-73640357	XLOC_008188
4	lnc-RLIM-1	chrX:73633219-73633224	XLOC_008188
5	lnc-RLIM-6	chrX:73673458-73673691	NONHSAT137639

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	SLC16A2	hsa-miR-17-5p	chrX:73752625-73752648
2	RLIM	hsa-miR-15b-5p	chrX:73806001-73805995
3	RLIM	hsa-miR-10a-5p	chrX:73809144-73809138

Variant related genes	Relation type
PRKRIRP1	TF binding region
ENSG00000271589	TF binding region
KIAA2022	TF binding region
RN7SL790P	TF binding region
RPS7P14	TF binding region
SLC16A2	TF binding region
RLIM	TF binding region
HNRNPA1P25	TF binding region
RN7SL641P	TF binding region
PABPC1P3	TF binding region
RNU6-330P	TF binding region
PRKRIRP1	CpG island
ENSG00000271589	CpG island
KIAA2022	CpG island
RN7SL790P	CpG island
RPS7P14	CpG island
SLC16A2	CpG island
RLIM	CpG island
HNRNPA1P25	CpG island
RN7SL641P	CpG island
PABPC1P3	CpG island
RNU6-330P	CpG island
ENSG00000110880	chromatin interactions
ENSG00000184678	chromatin interactions
ENSG00000164327	chromatin interactions
ENSG00000213695	chromatin interactions
ENSG00000130475	chromatin interactions
ENSG00000170955	chromatin interactions
ENSG00000147100	chromatin interactions
ENSG00000179119	chromatin interactions
ENSG00000264531	chromatin interactions
ENSG00000172586	chromatin interactions
ENSG00000185104	chromatin interactions
ENSG00000169230	chromatin interactions
ENSG00000131263	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000169228	chromatin interactions
ANKRD52	miRNA target sites
PYGO2	miRNA target sites
OTUD1	miRNA target sites

Extended variants
information (count: 3098 )
Associated
traits (count: 52 )

Variant overlapped rSNPs/rCNVs (count:3098 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs148491566	chrX:73603333-73603334	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs373764067	chrX:73603660-73603661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs367596421	chrX:73603678-73603679	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1748318	chrX:73603855-73603856	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs147627974	chrX:73603927-73603928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs140459313	chrX:73603931-73603932	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs189786225	chrX:73603954-73603955	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs683443	chrX:73603987-73603988	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs376809140	chrX:73608923-73608924	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs115770700	chrX:73608924-73608925	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs186135976	chrX:73608941-73608942	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs145903007	chrX:73609104-73609105	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs192251294	chrX:73609159-73609160	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs184038223	chrX:73609231-73609232	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs188576173	chrX:73609324-73609325	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs573615627	chrX:73609372-73609373	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs143474854	chrX:73610544-73610545	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs185631088	chrX:73610705-73610706	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs188794658	chrX:73610816-73610817	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs190071542	chrX:73619839-73619840	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs143912451	chrX:73619844-73619845	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs191646516	chrX:73622688-73622689	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs150381577	chrX:73623872-73623873	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs191453635	chrX:73623873-73623874	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs184724639	chrX:73624024-73624025	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs111724343	chrX:73625865-73625866	Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs76373767	chrX:73625977-73625978	Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs556717846	chrX:73626016-73626017	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs542606323	chrX:73626036-73626037	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186278542	chrX:73626121-73626122	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs142858569	chrX:73626129-73626130	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs146080030	chrX:73626378-73626379	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs557351	chrX:73626402-73626403	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs141400136	chrX:73626479-73626480	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs529588819	chrX:73626593-73626594	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs547803373	chrX:73626673-73626674	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs12853970	chrX:73626827-73626828	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs12852422	chrX:73626837-73626838	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs12851858	chrX:73626843-73626844	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs12851859	chrX:73626847-73626848	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs12834119	chrX:73627922-73627923	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs557647	chrX:73628430-73628431	Inactive region	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs140877900	chrX:73628440-73628441	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs187506099	chrX:73633371-73633372	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs368625228	chrX:73633382-73633383	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs192745859	chrX:73633501-73633502	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs183672600	chrX:73633720-73633721	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs187769064	chrX:73633745-73633746	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs192693772	chrX:73633786-73633787	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs148507356	chrX:73633796-73633797	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:52)

Disease	PMID	Source
Intellectual disability	23615299	CNVD
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
Mental retardation	20877625	CNVD
brachycephaly	20877625	CNVD
epicanthic folds	20877625	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	19602461	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ovarian cancer	21781307	CNVD
Premature ovarian failure	20952765	CNVD
Intellectual disability	21811512	CNVD

Chromatin state (count:2548 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chrX:73602400-73603400	Enhancers	HUES6 Cell Line	embryonic stem cell
2	chrX:73602400-73603600	Enhancers	ES-I3 Cell Line	embryonic stem cell
3	chrX:73602400-73604000	Enhancers	iPS-15b Cell Line	embryonic stem cell
4	chrX:73602800-73603600	Enhancers	HMEC	breast
5	chrX:73608800-73609400	Enhancers	Osteobl	bone
6	chrX:73625800-73626600	Enhancers	HSMMtube	muscle
7	chrX:73638000-73638800	Enhancers	HMEC	breast
8	chrX:73638200-73638400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chrX:73638400-73639000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chrX:73638800-73639200	Weak transcription	HMEC	breast
11	chrX:73638800-73639400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
12	chrX:73638800-73643200	Active TSS	ES-I3 Cell Line	embryonic stem cell
13	chrX:73639000-73639200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chrX:73639000-73639400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chrX:73639200-73639400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chrX:73639200-73639400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
17	chrX:73639200-73639400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
18	chrX:73639200-73639400	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
19	chrX:73639200-73639400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
20	chrX:73639200-73639400	Bivalent Enhancer	Stomach Smooth Muscle	stomach
21	chrX:73639200-73639400	Enhancers	HMEC	breast
22	chrX:73639200-73639400	Enhancers	NH-A	brain
23	chrX:73639200-73639400	Enhancers	NHEK	skin
24	chrX:73639200-73639600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chrX:73639200-73639600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
26	chrX:73639200-73639800	Bivalent/Poised TSS	Breast Myoepithelial Primary Cells	Breast
27	chrX:73639200-73640000	Bivalent/Poised TSS	iPS-20b Cell Line	embryonic stem cell
28	chrX:73639200-73643000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chrX:73639200-73643000	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
30	chrX:73639200-73643000	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chrX:73639400-73639600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
32	chrX:73639400-73639600	Flanking Bivalent TSS/Enh	H9 Cell Line	embryonic stem cell
33	chrX:73639400-73639600	Flanking Bivalent TSS/Enh	HUES64 Cell Line	embryonic stem cell
34	chrX:73639400-73639600	Flanking Active TSS	iPS-15b Cell Line	embryonic stem cell
35	chrX:73639400-73639600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
36	chrX:73639400-73639600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
37	chrX:73639400-73639600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chrX:73639400-73639600	Bivalent/Poised TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chrX:73639400-73639600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
40	chrX:73639400-73639600	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
41	chrX:73639400-73639600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
42	chrX:73639400-73639600	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chrX:73639400-73639600	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chrX:73639400-73639600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chrX:73639400-73639600	Bivalent Enhancer	Adipose Nuclei	Adipose
46	chrX:73639400-73639600	Active TSS	Brain Anterior Caudate	brain
47	chrX:73639400-73639600	Enhancers	Brain Hippocampus Middle	brain
48	chrX:73639400-73639600	Enhancers	Duodenum Mucosa	Duodenum
49	chrX:73639400-73639600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chrX:73639400-73639600	Enhancers	Fetal Brain Male	brain

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