Variant report

Variant	nsv1039160
Chromosome Location	chr15:30734745-30981033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2459)
CpG islands
(count:1404)
Chromatin interactive
region (count:7)
LncRNA
region (count:38)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2459 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:30941065-30941323	HepG2	liver:	n/a	chr15:30941184-30941200 chr15:30941198-30941214
2	ARID3A	chr15:30917819-30918297	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:30917841-30918381	K562	blood:	n/a	n/a
4	ATF1	chr15:30942408-30942747	K562	blood:	n/a	n/a
5	ATF1	chr15:30917774-30918461	K562	blood:	n/a	n/a
6	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
7	ATF2	chr15:30917694-30918103	GM12878	blood:	n/a	n/a
8	ATF2	chr15:30917709-30918426	GM12878	blood:	n/a	n/a
9	ATF2	chr15:30917808-30918347	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr15:30918103-30918425	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF3	chr15:30917703-30918445	A549	lung:	n/a	n/a
12	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
13	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
14	BATF	chr15:30832413-30833670	GM12878	blood:	n/a	chr15:30833063-30833074
15	BATF	chr15:30763776-30764872	GM12878	blood:	n/a	n/a
16	BATF	chr15:30765290-30765504	GM12878	blood:	n/a	n/a
17	BATF	chr15:30793879-30794120	GM12878	blood:	n/a	n/a
18	BATF	chr15:30793866-30794121	GM12878	blood:	n/a	n/a
19	BATF	chr15:30871690-30872015	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
20	BATF	chr15:30871617-30871985	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
21	BATF	chr15:30763589-30764924	GM12878	blood:	n/a	n/a
22	BATF	chr15:30765283-30765578	GM12878	blood:	n/a	n/a
23	BATF	chr15:30858799-30859444	GM12878	blood:	n/a	n/a
24	BATF	chr15:30763002-30763213	GM12878	blood:	n/a	n/a
25	BATF	chr15:30880957-30881265	GM12878	blood:	n/a	n/a
26	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
27	BATF	chr15:30917720-30918566	GM12878	blood:	n/a	n/a
28	BATF	chr15:30832414-30833216	GM12878	blood:	n/a	chr15:30833063-30833074
29	BATF	chr15:30829434-30829723	GM12878	blood:	n/a	n/a
30	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
31	BATF	chr15:30881037-30881316	GM12878	blood:	n/a	n/a
32	BCL11A	chr15:30880980-30881263	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:30871637-30871932	GM12878	blood:	n/a	chr15:30871825-30871834 chr15:30871780-30871789
34	BCL11A	chr15:30793856-30794157	GM12878	blood:	n/a	n/a
35	BCL11A	chr15:30763771-30764696	GM12878	blood:	n/a	n/a
36	BCL11A	chr15:30763746-30764847	GM12878	blood:	n/a	n/a
37	BCL11A	chr15:30942112-30942840	GM12878	blood:	n/a	n/a
38	BCL11A	chr15:30832618-30833226	GM12878	blood:	n/a	n/a
39	BCL11A	chr15:30871697-30871948	GM12878	blood:	n/a	chr15:30871825-30871834 chr15:30871780-30871789
40	BCL11A	chr15:30858936-30859213	GM12878	blood:	n/a	n/a
41	BCL11A	chr15:30859004-30859344	GM12878	blood:	n/a	chr15:30859230-30859243
42	BCL11A	chr15:30765257-30765493	GM12878	blood:	n/a	n/a
43	BCL11A	chr15:30917933-30918639	GM12878	blood:	n/a	chr15:30918103-30918112 chr15:30918531-30918544
44	BCL11A	chr15:30832593-30833514	GM12878	blood:	n/a	n/a
45	BCL11A	chr15:30918059-30918429	GM12878	blood:	n/a	chr15:30918103-30918112
46	BCL3	chr15:30917699-30918306	A549	lung:	n/a	chr15:30918103-30918112
47	BCL3	chr15:30917685-30918459	A549	lung:	n/a	chr15:30918103-30918112
48	BCLAF1	chr15:30917705-30918445	GM12878	blood:	n/a	chr15:30918103-30918112
49	BCLAF1	chr15:30942082-30942772	GM12878	blood:	n/a	n/a
50	BCLAF1	chr15:30917749-30918426	GM12878	blood:	n/a	chr15:30918103-30918112

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30919014-30919064	HEEpiC	esophagus:	n/a
2	chr15:30919014-30919064	HEEpiC	esophagus:	n/a
3	chr15:30896060-30896110	HRCEpiC	kidney:	n/a
4	chr15:30896216-30896266	Hela-S3	cervix:	n/a
5	chr15:30763199-30763249	K562	blood:	n/a
6	chr15:30865200-30865250	HUVEC	blood vessel:	n/a
7	chr15:30865200-30865250	SK-N-SH	brain:	n/a
8	chr15:30917991-30918041	AG09319	gingival:	n/a
9	chr15:30865200-30865250	NB4	blood:	n/a
10	chr15:30896060-30896110	HCT-116	colon:	n/a
11	chr15:30896216-30896266	GM19239	blood:	n/a
12	chr15:30918595-30918645	K562	blood:	n/a
13	chr15:30918065-30918115	HPAEpiC	pulmonary alveolar:	n/a
14	chr15:30844060-30844110	T-47D	breast:	n/a
15	chr15:30917918-30917968	AG04450	lung:	fetal
16	chr15:30763199-30763249	LNCaP	prostate:	n/a
17	chr15:30816232-30816282	U87	brain:	n/a
18	chr15:30918339-30918389	LNCaP	prostate:	n/a
19	chr15:30917991-30918041	HNPCEpiC	eye:	n/a
20	chr15:30919020-30919070	Hela-S3	cervix:	n/a
21	chr15:30866091-30866141	MCF10A-Er-Src	breast:	n/a
22	chr15:30865200-30865250	ECC-1	luminal epithelium:	n/a
23	chr15:30918339-30918389	PFSK-1	brain:	n/a
24	chr15:30896216-30896266	HRE	kidney:	n/a
25	chr15:30930499-30930549	HCT-116	colon:	n/a
26	chr15:30918339-30918389	AG04450	lung:	fetal
27	chr15:30844060-30844110	SK-N-SH_RA	brain:	n/a
28	chr15:30763487-30763537	HCF	heart:	n/a
29	chr15:30919014-30919064	U87	brain:	n/a
30	chr15:30896216-30896266	NH-A	brain:	n/a
31	chr15:30917958-30918008	HUVEC	blood vessel:	n/a
32	chr15:30918065-30918115	GM06990	blood:	n/a
33	chr15:30896060-30896110	NH-A	brain:	n/a
34	chr15:30917958-30918008	HEK293	kidney:	embryo
35	chr15:30844060-30844110	HIPEpiC	eye:	n/a
36	chr15:30918339-30918389	NHBE	bronchial:	n/a
37	chr15:30861172-30861222	IMR90	lung:	fetal
38	chr15:30917958-30918008	ECC-1	luminal epithelium:	n/a
39	chr15:30918339-30918389	GM19239	blood:	n/a
40	chr15:30918328-30918378	GM06990	blood:	n/a
41	chr15:30919014-30919064	HPAEpiC	pulmonary alveolar:	n/a
42	chr15:30919014-30919064	NHDF-neo	bronchial:	n/a
43	chr15:30896060-30896110	BE2_C	brain:	n/a
44	chr15:30917918-30917968	NB4	blood:	n/a
45	chr15:30918595-30918645	GM12878	blood:	n/a
46	chr15:30918595-30918645	HRCEpiC	kidney:	n/a
47	chr15:30816232-30816282	HUVEC	blood vessel:	n/a
48	chr15:30917991-30918041	HRCEpiC	kidney:	n/a
49	chr15:30918313-30918363	U87	brain:	n/a
50	chr15:30917918-30917968	NHDF-neo	bronchial:	n/a

(count:7 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:30917826..30919798-chr15:32905900..32908033,2	K562	blood:
2	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
3	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
4	chr15:30957691..30960365-chr15:30968745..30971745,3	K562	blood:
5	chr15:30957691..30960365-chr15:30969306..30971745,2	K562	blood:
6	chr15:30918095..30918834-chr2:231728599..231729465,2	Hela-S3	cervix:
7	chr15:30916698..30918883-chr15:32905767..32907284,2	MCF-7	breast:

(count:38 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT041366
2	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041366
3	lnc-AC026150.9.1-3	chr15:30780166-30782516	ENSG00000270055.1
4	lnc-CHRNA7-2	chr15:30892305-30892911	NONHSAT041366
5	lnc-AC026150.9.1-4	chr15:30749372-30751192	ucscGeneNc_uc001zhb_2
6	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041368
7	lnc-AC026150.9.1-1	chr15:30838015-30838172	ENSG00000260693.1
8	lnc-ARHGAP11B-1	chr15:30939871-30939917	NONHSAT041382
9	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT140224
10	lnc-CHRNA7-2	chr15:30865088-30865219	NONHSAT041367
11	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT041368
12	lnc-ARHGAP11B-1	chr15:30916697-30916815	NONHSAT041376
13	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041367
14	lnc-GOLGA8H-1	chr15:30909161-30909952	ENSG00000269930.1
15	lnc-RP11-382B18.2.1-1	chr15:30917254-30917976	ENSG00000247728
16	lnc-RP11-382B18.2.1-1	chr15:30917254-30917976	ENSG00000247728.2
17	lnc-GOLGA8H-2	chr15:30941000-30941732	ENSG00000269974.1
18	lnc-AC026150.9.1-1	chr15:30836768-30836863	ENSG00000260693.1
19	lnc-ARHGAP11B-1	chr15:30938335-30938498	NONHSAT041382
20	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT140224
21	lnc-AC026150.9.1-1	chr15:30832296-30832742	ENSG00000260693.1
22	lnc-ARHGAP11B-1	chr15:30916926-30917019	NONHSAT041376
23	lnc-ARHGAP11B-1	chr15:30917557-30918469	NONHSAT041376
24	lnc-RP11-382B18.2.1-1	chr15:30909201-30909447	ENSG00000247728.2
25	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT140224
26	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT041368
27	lnc-ARHGAP11B-1	chr15:30950920-30951047	NONHSAT041384
28	lnc-CHRNA7-2	chr15:30864758-30864774	NONHSAT041366
29	lnc-CHRNA7-2	chr15:30878081-30878127	NONHSAT041368
30	lnc-CHRNA7-2	chr15:30892305-30892850	NONHSAT140224
31	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT041366
32	lnc-RP11-382B18.2.1-1	chr15:30857143-30857384	ENSG00000247728
33	lnc-CHRNA7-2	chr15:30892305-30892900	NONHSAT041368
34	lnc-CHRNA7-3	chr15:30852855-30853133	NONHSAT041364
35	lnc-CHRNA7-2	chr15:30888863-30889187	NONHSAT041367
36	lnc-ARHGAP11B-2	chr15:30904916-30905194	NONHSAT041372
37	lnc-CHRNA7-2	chr15:30875097-30875160	NONHSAT041368
38	lnc-RP11-382B18.2.1-3	chr15:30899898-30900396	ENSG00000270016.1

No data

Variant related genes	Relation type
ENSG00000270016	TF binding region
ENSG00000221593	TF binding region
ENSG00000207430	TF binding region
ULK4P2	TF binding region
RN7SL628P	TF binding region
GOLGA8H	TF binding region
ARHGAP11B	TF binding region
ENSG00000269930	TF binding region
ENSG00000269974	TF binding region
ENSG00000247728	TF binding region
ENSG00000270055	TF binding region
ENSG00000206846	TF binding region
ENSG00000260693	TF binding region
RN7SL796P	TF binding region
DNM1P50	TF binding region
ENSG00000260784	TF binding region
ENSG00000252602	TF binding region
ENSG00000215302	TF binding region
ENSG00000221358	TF binding region
GOLGA8Q	TF binding region
ENSG00000270016	CpG island
ENSG00000221593	CpG island
ENSG00000207430	CpG island
ULK4P2	CpG island
RN7SL628P	CpG island
GOLGA8H	CpG island
ARHGAP11B	CpG island
ENSG00000269930	CpG island
ENSG00000269974	CpG island
ENSG00000247728	CpG island
ENSG00000270055	CpG island
ENSG00000206846	CpG island
ENSG00000260693	CpG island
RN7SL796P	CpG island
DNM1P50	CpG island
ENSG00000260784	CpG island
ENSG00000252602	CpG island
ENSG00000215302	CpG island
ENSG00000221358	CpG island
GOLGA8Q	CpG island
ENSG00000262728	chromatin interactions
ENSG00000244952	chromatin interactions
ENSG00000135916	chromatin interactions
ENSG00000198826	chromatin interactions
TGFB2	miRNA target sites
PRKAB2	miRNA target sites

Extended variants
information (count: 4085 )
Associated
traits (count: 141 )

Variant overlapped rSNPs/rCNVs (count:4085 , 50 per page) page: 1 2 3 4 5 6 7 ... 82

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs200198562	chr15:30749441-30749442	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs56101817	chr15:30749810-30749811	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs3852664	chr15:30749829-30749830	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs200738538	chr15:30749928-30749929	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs373828359	chr15:30750040-30750041	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs201422473	chr15:30750295-30750296	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs533270928	chr15:30750324-30750325	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs546878718	chr15:30750329-30750330	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs566700239	chr15:30750352-30750353	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs62017467	chr15:30750359-30750360	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs535288867	chr15:30750360-30750361	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs548692261	chr15:30750362-30750363	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs568447240	chr15:30750368-30750369	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs537118586	chr15:30750379-30750380	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs375994513	chr15:30750695-30750696	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs201015015	chr15:30750771-30750772	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs200417119	chr15:30750960-30750961	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
18	rs62017468	chr15:30750971-30750972	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
19	rs62017469	chr15:30751148-30751149	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
20	rs2912154	chr15:30760478-30760479	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs290148	chr15:30762807-30762808	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs377643842	chr15:30762863-30762864	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs185674680	chr15:30762930-30762931	Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs373659073	chr15:30762999-30763000	Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs376855991	chr15:30763048-30763049	Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs548926676	chr15:30763207-30763208	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs568986466	chr15:30763210-30763211	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs371560824	chr15:30763253-30763254	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs537157425	chr15:30763421-30763422	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs550651025	chr15:30763423-30763424	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs570555466	chr15:30763438-30763439	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs539423762	chr15:30763453-30763454	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs553661585	chr15:30763454-30763455	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573471868	chr15:30763578-30763579	Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62017486	chr15:30764188-30764189	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs62017487	chr15:30764234-30764235	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs2943114	chr15:30764334-30764335	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62017489	chr15:30764594-30764595	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs62017490	chr15:30764609-30764610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536120241	chr15:30764996-30764997	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs555688194	chr15:30765146-30765147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs190094787	chr15:30765157-30765158	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs62017491	chr15:30765455-30765456	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs71239677	chr15:30766786-30766787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372494140	chr15:30766853-30766854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs4780013	chr15:30767231-30767232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs368103000	chr15:30767263-30767264	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs368699787	chr15:30767264-30767265	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs575868587	chr15:30767302-30767303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs536650596	chr15:30767333-30767334	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:141)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Prader-willi syndrome	21504564	CNVD
The inv dup or idic syndrome	19019226	CNVD
Prader-willi syndrome	21233802	CNVD
Angelman syndrome	16617304	CNVD
Angelman syndrome	20970697	CNVD
Autism	22958593	CNVD
Prader-willi syndrome	16617304	CNVD
Prader-willi syndrome	18923514	CNVD
Prader-willi syndrome	20970697	CNVD
Angelman syndrome	16183798	CNVD
Angelman syndrome	18923514	CNVD
Prader-willi syndrome	22241247	CNVD
Epilepsy	20970697	CNVD
Autism	20970697	CNVD
Autism	19935738	CNVD
Autism	22930557	CNVD
Autism	19966786	CNVD
Autism	18923514	CNVD
Autism	18925931	CNVD
Autism	18835857	CNVD
Prader-willi syndrome	18835857	CNVD
Prader-willi syndrome	22152151	CNVD
Autism	22241247	CNVD
15q-syndrome	21725066	CNVD
Prader-willi syndrome	21503198	CNVD
Autism	21956041	CNVD
Prader-willi syndrome	16760730	CNVD
Prader-willi syndrome	22470819	CNVD
prenatal diagnosis	20453657	CNVD
Prader-willi syndrome	17867985	CNVD
Angelman syndrome	21072004	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Prader-willi syndrome	18781185	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Prostate cancer	18632612	CNVD
Angelman syndrome	18787571	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Abnormal corpus callosum	21572526	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Epilepsy	22499536	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Bipolar disorder	19114987	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Mental retardation	19951919	CNVD
Mental retardation	21956041	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Autism	21269290	CNVD
Intellectual disability	21269290	CNVD
Schizophrenia	21269290	CNVD
Colorectal cancer	21128281	CNVD
Epilepsy	19289393	CNVD
Epilepsy	20643615	CNVD
Mental retardation	19289393	CNVD
Mental retardation	20152051	CNVD
Schizophrenia	19289393	CNVD
dysmorphic features	19289393	CNVD
idiopathic epilepsies	19341504	CNVD
idiopathic generalized epilepsy	19592580	CNVD
idiopathic generalized epilepsy	19136953	CNVD
Autism	22094647	CNVD
Developmental delay	19898479	CNVD
Mental retardation	18278044	CNVD
Mental retardation	19898479	CNVD
Prader-willi syndrome	18854863	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Epilepsy	20502679	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Intellectual disability	21811512	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1185 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30762800-30763200	Active TSS	Fetal Thymus	thymus
2	chr15:30762800-30763600	Active TSS	Psoas Muscle	Psoas
3	chr15:30762800-30763600	Active TSS	Thymus	Thymus
4	chr15:30763000-30763600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
5	chr15:30763000-30763600	Active TSS	Cortex derived primary cultured neurospheres	brain
6	chr15:30763000-30763600	Active TSS	Right Ventricle	heart
7	chr15:30763000-30763600	Active TSS	NHLF	lung
8	chr15:30763000-30763600	Active TSS	Osteobl	bone
9	chr15:30763200-30763600	Active TSS	H1 Cell Line	embryonic stem cell
10	chr15:30763200-30763600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr15:30763200-30763600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr15:30763200-30763600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr15:30763200-30763600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
14	chr15:30763200-30763600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
15	chr15:30763200-30763600	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr15:30763200-30763600	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr15:30763200-30763600	Active TSS	HUES64 Cell Line	embryonic stem cell
18	chr15:30763200-30763600	Active TSS	IMR90 fetal lung fibroblasts Cell Line	lung
19	chr15:30763200-30763600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr15:30763200-30763600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr15:30763200-30763600	Active TSS	Breast Myoepithelial Primary Cells	Breast
22	chr15:30763200-30763600	Active TSS	Primary hematopoietic stem cells short term culture	blood
23	chr15:30763200-30763600	Active TSS	Primary T helper naive cells fromperipheralblood	blood
24	chr15:30763200-30763600	Active TSS	Primary T helper cells fromperipheralblood	blood
25	chr15:30763200-30763600	Active TSS	Primary T regulatory cells fromperipheralblood	blood
26	chr15:30763200-30763600	Active TSS	Primary T killer naive cells fromperipheralblood	blood
27	chr15:30763200-30763600	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
28	chr15:30763200-30763600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr15:30763200-30763600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:30763200-30763600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
31	chr15:30763200-30763600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:30763200-30763600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
33	chr15:30763200-30763600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr15:30763200-30763600	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr15:30763200-30763600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
36	chr15:30763200-30763600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr15:30763200-30763600	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
38	chr15:30763200-30763600	Active TSS	Colonic Mucosa	Colon
39	chr15:30763200-30763600	Active TSS	Esophagus	oesophagus
40	chr15:30763200-30763600	Active TSS	Fetal Brain Female	brain
41	chr15:30763200-30763600	Active TSS	Left Ventricle	heart
42	chr15:30763200-30763600	Active TSS	Lung	lung
43	chr15:30763200-30763600	Active TSS	Ovary	ovary
44	chr15:30763200-30763600	Active TSS	Pancreas	Pancrea
45	chr15:30763200-30763600	Active TSS	Right Atrium	heart
46	chr15:30763200-30763600	Active TSS	Skeletal Muscle Male	skeletal muscle
47	chr15:30763200-30763600	Active TSS	Skeletal Muscle Female	skeletal muscle
48	chr15:30763200-30763600	Active TSS	Stomach Smooth Muscle	stomach
49	chr15:30763200-30763600	Active TSS	Dnd41	blood
50	chr15:30763200-30763600	Active TSS	HSMM	muscle

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