Variant report

Variant	nsv1045010
Chromosome Location	chr15:30643084-30981033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2968)
CpG islands
(count:1771)
Chromatin interactive
region (count:7)
LncRNA
region (count:47)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2968 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:30917841-30918381	K562	blood:	n/a	n/a
2	ARID3A	chr15:30917819-30918297	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:30941065-30941323	HepG2	liver:	n/a	chr15:30941184-30941200 chr15:30941198-30941214
4	ATF1	chr15:30942408-30942747	K562	blood:	n/a	n/a
5	ATF1	chr15:30917774-30918461	K562	blood:	n/a	n/a
6	ATF2	chr15:30917808-30918347	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:30918103-30918425	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:30917694-30918103	GM12878	blood:	n/a	n/a
9	ATF2	chr15:30917709-30918426	GM12878	blood:	n/a	n/a
10	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
11	ATF3	chr15:30917703-30918445	A549	lung:	n/a	n/a
12	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
13	BATF	chr15:30716939-30717383	GM12878	blood:	n/a	n/a
14	BATF	chr15:30717393-30718193	GM12878	blood:	n/a	n/a
15	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
16	BATF	chr15:30793866-30794121	GM12878	blood:	n/a	n/a
17	BATF	chr15:30678631-30678956	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
18	BATF	chr15:30881037-30881316	GM12878	blood:	n/a	n/a
19	BATF	chr15:30832413-30833670	GM12878	blood:	n/a	chr15:30833063-30833074
20	BATF	chr15:30720885-30721174	GM12878	blood:	n/a	n/a
21	BATF	chr15:30880957-30881265	GM12878	blood:	n/a	n/a
22	BATF	chr15:30678661-30679029	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
23	BATF	chr15:30763002-30763213	GM12878	blood:	n/a	n/a
24	BATF	chr15:30691171-30691739	GM12878	blood:	n/a	n/a
25	BATF	chr15:30763589-30764924	GM12878	blood:	n/a	n/a
26	BATF	chr15:30765290-30765504	GM12878	blood:	n/a	n/a
27	BATF	chr15:30832414-30833216	GM12878	blood:	n/a	chr15:30833063-30833074
28	BATF	chr15:30763776-30764872	GM12878	blood:	n/a	n/a
29	BATF	chr15:30858799-30859444	GM12878	blood:	n/a	n/a
30	BATF	chr15:30871617-30871985	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
31	BATF	chr15:30871690-30872015	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
32	BATF	chr15:30829434-30829723	GM12878	blood:	n/a	n/a
33	BATF	chr15:30765283-30765578	GM12878	blood:	n/a	n/a
34	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
35	BATF	chr15:30793879-30794120	GM12878	blood:	n/a	n/a
36	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
37	BATF	chr15:30917720-30918566	GM12878	blood:	n/a	n/a
38	BATF	chr15:30717407-30718307	GM12878	blood:	n/a	n/a
39	BCL11A	chr15:30678698-30678949	GM12878	blood:	n/a	chr15:30678847-30678856 chr15:30678892-30678901
40	BCL11A	chr15:30871697-30871948	GM12878	blood:	n/a	chr15:30871825-30871834 chr15:30871780-30871789
41	BCL11A	chr15:30871637-30871932	GM12878	blood:	n/a	chr15:30871825-30871834 chr15:30871780-30871789
42	BCL11A	chr15:30763746-30764847	GM12878	blood:	n/a	n/a
43	BCL11A	chr15:30793856-30794157	GM12878	blood:	n/a	n/a
44	BCL11A	chr15:30832618-30833226	GM12878	blood:	n/a	n/a
45	BCL11A	chr15:30859004-30859344	GM12878	blood:	n/a	chr15:30859230-30859243
46	BCL11A	chr15:30763771-30764696	GM12878	blood:	n/a	n/a
47	BCL11A	chr15:30858936-30859213	GM12878	blood:	n/a	n/a
48	BCL11A	chr15:30880980-30881263	GM12878	blood:	n/a	n/a
49	BCL11A	chr15:30717383-30717989	GM12878	blood:	n/a	n/a
50	BCL11A	chr15:30678714-30679009	GM12878	blood:	n/a	chr15:30678847-30678856 chr15:30678892-30678901

(count:1771 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30685198-30685248	AG04449	skin:	fetal
2	chr15:30918328-30918378	HMEC	breast:	n/a
3	chr15:30685198-30685248	AG04449	skin:	fetal
4	chr15:30918328-30918378	HMEC	breast:	n/a
5	chr15:30918313-30918363	NHBE	bronchial:	n/a
6	chr15:30699977-30700027	AG10803	skin:	n/a
7	chr15:30920627-30920677	AG09319	gingival:	n/a
8	chr15:30763484-30763534	HNPCEpiC	eye:	n/a
9	chr15:30763199-30763249	Jurkat	blood:	n/a
10	chr15:30866091-30866141	PFSK-1	brain:	n/a
11	chr15:30763484-30763534	RPTEC	kidney:	n/a
12	chr15:30918328-30918378	PFSK-1	brain:	n/a
13	chr15:30919020-30919070	HMEC	breast:	n/a
14	chr15:30844060-30844110	HEEpiC	esophagus:	n/a
15	chr15:30917991-30918041	HepG2	liver:	n/a
16	chr15:30700112-30700162	IMR90	lung:	fetal
17	chr15:30866091-30866141	HEK293	kidney:	embryo
18	chr15:30919020-30919070	AG04449	skin:	fetal
19	chr15:30763487-30763537	AG09319	gingival:	n/a
20	chr15:30865200-30865250	SK-N-SH	brain:	n/a
21	chr15:30685198-30685248	NT2-D1	testis:	n/a
22	chr15:30896216-30896266	AoSMC	blood vessel:	n/a
23	chr15:30918328-30918378	GM06990	blood:	n/a
24	chr15:30918595-30918645	GM06990	blood:	n/a
25	chr15:30919020-30919070	PANC-1	pancreas:	n/a
26	chr15:30654880-30654930	HCPEpiC	choroid plexus:	n/a
27	chr15:30844060-30844110	ECC-1	luminal epithelium:	n/a
28	chr15:30896216-30896266	BJ	skin:	n/a
29	chr15:30763199-30763249	HRE	kidney:	n/a
30	chr15:30763199-30763249	HL-60	blood:	n/a
31	chr15:30865191-30865241	HEEpiC	esophagus:	n/a
32	chr15:30918313-30918363	SKMC	muscle:	n/a
33	chr15:30918339-30918389	HEEpiC	esophagus:	n/a
34	chr15:30918328-30918378	ECC-1	luminal epithelium:	n/a
35	chr15:30685198-30685248	HUVEC	blood vessel:	n/a
36	chr15:30866091-30866141	SK-N-SH_RA	brain:	n/a
37	chr15:30918595-30918645	HPAEpiC	pulmonary alveolar:	n/a
38	chr15:30918313-30918363	GM12892	blood:	n/a
39	chr15:30816232-30816282	SK-N-SH	brain:	n/a
40	chr15:30918065-30918115	MCF10A-Er-Src	breast:	n/a
41	chr15:30917991-30918041	K562	blood:	n/a
42	chr15:30918595-30918645	AG09309	skin:	n/a
43	chr15:30930499-30930549	AG09319	gingival:	n/a
44	chr15:30666736-30666786	HCT-116	colon:	n/a
45	chr15:30654880-30654930	Caco-2	colon:	n/a
46	chr15:30844060-30844110	NHDF-neo	bronchial:	n/a
47	chr15:30918328-30918378	BJ	skin:	n/a
48	chr15:30917991-30918041	ovcar-3	ovarian:	n/a
49	chr15:30865191-30865241	AG09319	gingival:	n/a
50	chr15:30763199-30763249	K562	blood:	n/a

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

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

(count:47 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041368
2	lnc-RP11-382B18.2.1-2	chr15:30673906-30674079	NONHSAT041347
3	lnc-AC026150.9.1-1	chr15:30836768-30836863	ENSG00000260693.1
4	lnc-GOLGA8H-1	chr15:30909161-30909952	ENSG00000269930.1
5	lnc-AC026150.9.1-5	chr15:30702037-30703662	NONHSAT041356
6	lnc-RP11-382B18.2.1-1	chr15:30917254-30917976	ENSG00000247728.2
7	lnc-CHRNA7-2	chr15:30888863-30889187	NONHSAT041367
8	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041367
9	lnc-RP11-382B18.2.1-3	chr15:30899898-30900396	ENSG00000270016.1
10	lnc-AC026150.9.1-1	chr15:30838015-30838172	ENSG00000260693.1
11	lnc-CHRNA7-3	chr15:30852855-30853133	NONHSAT041364
12	lnc-ARHGAP11B-1	chr15:30917557-30918469	NONHSAT041376
13	lnc-CHRNA7-2	chr15:30892305-30892850	NONHSAT140224
14	lnc-RP11-382B18.2.1-2	chr15:30675247-30675585	NONHSAT041348
15	lnc-CHRNA7-2	chr15:30864758-30864774	NONHSAT041366
16	lnc-CHRNA7-2	chr15:30875097-30875160	NONHSAT041368
17	lnc-RP11-382B18.2.1-2	chr15:30672556-30672602	NONHSAT041347
18	lnc-AC026150.9.1-3	chr15:30780166-30782516	ENSG00000270055.1
19	lnc-RP11-382B18.2.1-2	chr15:30679066-30679190	NONHSAT041348
20	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT140224
21	lnc-ARHGAP11B-2	chr15:30904916-30905194	NONHSAT041372
22	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT140224
23	lnc-RP11-382B18.2.1-2	chr15:30675522-30675585	NONHSAT041347
24	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT041366
25	lnc-CHRNA7-2	chr15:30878081-30878127	NONHSAT041368
26	lnc-RP11-382B18.2.1-1	chr15:30909201-30909447	ENSG00000247728.2
27	lnc-ARHGAP11B-1	chr15:30950920-30951047	NONHSAT041384
28	lnc-ARHGAP11B-1	chr15:30939871-30939917	NONHSAT041382
29	lnc-CHRFAM7A-2	chr15:30649969-30650976	ENSG00000270173.1
30	lnc-CHRNA7-2	chr15:30865172-30865219	NONHSAT041368
31	lnc-RP11-382B18.2.1-1	chr15:30857143-30857384	ENSG00000247728
32	lnc-CHRNA7-2	chr15:30892305-30892911	NONHSAT041366
33	lnc-ARHGAP11B-1	chr15:30916926-30917019	NONHSAT041376
34	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT140224
35	lnc-ARHGAP11B-1	chr15:30938335-30938498	NONHSAT041382
36	lnc-CHRNA7-2	chr15:30865088-30865219	NONHSAT041367
37	lnc-ARHGAP11B-1	chr15:30916697-30916815	NONHSAT041376
38	lnc-CHRNA7-2	chr15:30892305-30892900	NONHSAT041368
39	lnc-AC026150.9.1-1	chr15:30832296-30832742	ENSG00000260693.1
40	lnc-RP11-382B18.2.1-1	chr15:30917254-30917976	ENSG00000247728
41	lnc-AC026150.9.1-4	chr15:30749372-30751192	ucscGeneNc_uc001zhb_2
42	lnc-CHRNA7-2	chr15:30871491-30871615	NONHSAT041366
43	lnc-CHRFAM7A-3	chr15:30697514-30697792	NONHSAT041354
44	lnc-GOLGA8H-2	chr15:30941000-30941732	ENSG00000269974.1
45	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT041368
46	lnc-RP11-382B18.2.1-2	chr15:30679087-30679190	NONHSAT041347
47	lnc-CHRNA7-2	chr15:30888863-30888941	NONHSAT041366

No data

Variant related genes	Relation type
ENSG00000270016	TF binding region
ENSG00000221723	TF binding region
ENSG00000221593	TF binding region
ENSG00000207430	TF binding region
RN7SL196P	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
ENSG00000238519	TF binding region
ENSG00000260693	TF binding region
GOLGA8R	TF binding region
RN7SL796P	TF binding region
DNM1P50	TF binding region
ENSG00000238783	TF binding region
ENSG00000263070	TF binding region
ENSG00000260784	TF binding region
ENSG00000270173	TF binding region
ENSG00000252602	TF binding region
ENSG00000271333	TF binding region
ENSG00000215302	TF binding region
ENSG00000221358	TF binding region
GOLGA8Q	TF binding region
CHRFAM7A	TF binding region
ENSG00000270016	CpG island
ENSG00000221723	CpG island
ENSG00000221593	CpG island
ENSG00000207430	CpG island
RN7SL196P	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
ENSG00000238519	CpG island
ENSG00000260693	CpG island
GOLGA8R	CpG island
RN7SL796P	CpG island
DNM1P50	CpG island
ENSG00000238783	CpG island
ENSG00000263070	CpG island
ENSG00000260784	CpG island
ENSG00000270173	CpG island
ENSG00000252602	CpG island
ENSG00000271333	CpG island
ENSG00000215302	CpG island
ENSG00000221358	CpG island
GOLGA8Q	CpG island
CHRFAM7A	CpG island
ENSG00000244952	chromatin interactions
ENSG00000198826	chromatin interactions
ENSG00000262728	chromatin interactions
ENSG00000135916	chromatin interactions
TGFB2	miRNA target sites
PRKAB2	miRNA target sites

Extended variants
information (count: 4611 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:4611 , 50 per page) page: 1 2 3 4 5 6 7 ... 93

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566151821	chr15:30649999-30650000	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs535211618	chr15:30650038-30650039	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs554292389	chr15:30650075-30650076	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs567795045	chr15:30650081-30650082	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs536685695	chr15:30650082-30650083	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
6	rs556556633	chr15:30650133-30650134	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
7	rs576748147	chr15:30650134-30650135	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
8	rs202180935	chr15:30650321-30650322	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs564541884	chr15:30650458-30650459	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs370532030	chr15:30650474-30650475	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs200419153	chr15:30650507-30650508	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs545784415	chr15:30650747-30650748	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs553190005	chr15:30650853-30650854	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs572991845	chr15:30650873-30650874	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs539408244	chr15:30653448-30653449	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs377742720	chr15:30653903-30653904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs201193172	chr15:30653904-30653905	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112808378	chr15:30653921-30653922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs75948040	chr15:30653922-30653923	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs542078948	chr15:30653956-30653957	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs112633028	chr15:30653973-30653974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs113285763	chr15:30654120-30654121	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs200433111	chr15:30654670-30654671	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs201668516	chr15:30654736-30654737	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs555614573	chr15:30654835-30654836	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs201471858	chr15:30654961-30654962	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs575481986	chr15:30655048-30655049	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs543936587	chr15:30655053-30655054	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs563794028	chr15:30655059-30655060	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs577216154	chr15:30655067-30655068	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs546157421	chr15:30655069-30655070	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs559830735	chr15:30655102-30655103	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs147722464	chr15:30655141-30655142	Weak transcription	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs528776758	chr15:30655144-30655145	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs548447468	chr15:30655170-30655171	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561951640	chr15:30655194-30655195	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs530972248	chr15:30655201-30655202	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550440990	chr15:30655247-30655248	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs199628706	chr15:30655267-30655268	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs185887798	chr15:30655274-30655275	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs570521278	chr15:30655283-30655284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs149179555	chr15:30655284-30655285	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539088058	chr15:30655291-30655292	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs546557580	chr15:30655309-30655310	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566440237	chr15:30655362-30655363	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs570300787	chr15:30655433-30655434	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs535769595	chr15:30655511-30655512	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs555653289	chr15:30655516-30655517	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs140458770	chr15:30655518-30655519	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs575551005	chr15:30655528-30655529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:146)

Disease	PMID	Source
Ovarian cancer	21720365	CNVD
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
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	18496225	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
small cell lung cancer	20016488	CNVD
Epilepsy	20502679	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Intellectual disability	21811512	CNVD
Glioma	20126413	CNVD

Chromatin state (count:1237 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30653800-30661000	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr15:30654000-30664400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
3	chr15:30654200-30668200	Weak transcription	Aorta	Aorta
4	chr15:30655000-30659600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
5	chr15:30658800-30659000	Enhancers	Brain Angular Gyrus	brain
6	chr15:30659600-30659800	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
7	chr15:30667000-30669400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr15:30668000-30668200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
9	chr15:30668000-30668200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr15:30668200-30668400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
11	chr15:30668200-30668400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
12	chr15:30668200-30668400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
13	chr15:30668200-30668400	Enhancers	Aorta	Aorta
14	chr15:30668200-30668400	ZNF genes & repeats	Fetal Kidney	kidney
15	chr15:30668200-30668400	Active TSS	Fetal Lung	lung
16	chr15:30668200-30668400	Enhancers	Gastric	stomach
17	chr15:30668200-30668400	ZNF genes & repeats	Pancreas	Pancrea
18	chr15:30668200-30668400	Enhancers	Spleen	Spleen
19	chr15:30685000-30685400	Active TSS	H1 Cell Line	embryonic stem cell
20	chr15:30685000-30685400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr15:30685000-30685400	Active TSS	HUES6 Cell Line	embryonic stem cell
22	chr15:30685000-30685400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
23	chr15:30685000-30685400	Active TSS	Primary neutrophils fromperipheralblood	blood
24	chr15:30685000-30685400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
25	chr15:30685000-30685400	Active TSS	Pancreas	Pancrea
26	chr15:30685000-30685400	Active TSS	Right Atrium	heart
27	chr15:30697800-30699800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr15:30698400-30699800	Weak transcription	Fetal Stomach	stomach
29	chr15:30698400-30712800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
30	chr15:30698800-30701200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
31	chr15:30698800-30701200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr15:30698800-30701200	Weak transcription	Placenta	Placenta
33	chr15:30699000-30701400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
34	chr15:30699000-30701400	Weak transcription	Liver	Liver
35	chr15:30699000-30701400	Weak transcription	Duodenum Smooth Muscle	Duodenum
36	chr15:30699000-30701400	Weak transcription	Ovary	ovary
37	chr15:30699000-30701400	Weak transcription	Rectal Mucosa Donor 29	rectum
38	chr15:30699000-30701400	Weak transcription	Spleen	Spleen
39	chr15:30699600-30700000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
40	chr15:30699800-30700400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr15:30699800-30700400	Strong transcription	Fetal Stomach	stomach
42	chr15:30700000-30700200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
43	chr15:30700000-30700200	Enhancers	Brain Angular Gyrus	brain
44	chr15:30700000-30700200	ZNF genes & repeats	Esophagus	oesophagus
45	chr15:30700000-30700200	Enhancers	Pancreas	Pancrea
46	chr15:30700000-30700400	Enhancers	H1 Cell Line	embryonic stem cell
47	chr15:30700200-30700400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
48	chr15:30700400-30701800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
49	chr15:30700400-30701800	Weak transcription	Fetal Stomach	stomach
50	chr15:30712800-30713200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--

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