Variant report

Variant	nsv1051353
Chromosome Location	chr15:30665561-30946657
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2530)
CpG islands
(count:1710)
Chromatin interactive
region (count:3)
LncRNA
region (count:45)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2530 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

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	chr15:30917774-30918461	K562	blood:	n/a	n/a
5	ATF1	chr15:30942408-30942747	K562	blood:	n/a	n/a
6	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
7	ATF2	chr15:30917808-30918347	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:30918103-30918425	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:30917709-30918426	GM12878	blood:	n/a	n/a
10	ATF2	chr15:30917694-30918103	GM12878	blood:	n/a	n/a
11	ATF3	chr15:30917703-30918445	A549	lung:	n/a	n/a
12	BATF	chr15:30720885-30721174	GM12878	blood:	n/a	n/a
13	BATF	chr15:30691171-30691739	GM12878	blood:	n/a	n/a
14	BATF	chr15:30765290-30765504	GM12878	blood:	n/a	n/a
15	BATF	chr15:30832413-30833670	GM12878	blood:	n/a	chr15:30833063-30833074
16	BATF	chr15:30716939-30717383	GM12878	blood:	n/a	n/a
17	BATF	chr15:30717393-30718193	GM12878	blood:	n/a	n/a
18	BATF	chr15:30793879-30794120	GM12878	blood:	n/a	n/a
19	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
20	BATF	chr15:30763002-30763213	GM12878	blood:	n/a	n/a
21	BATF	chr15:30765283-30765578	GM12878	blood:	n/a	n/a
22	BATF	chr15:30832414-30833216	GM12878	blood:	n/a	chr15:30833063-30833074
23	BATF	chr15:30793866-30794121	GM12878	blood:	n/a	n/a
24	BATF	chr15:30763776-30764872	GM12878	blood:	n/a	n/a
25	BATF	chr15:30917720-30918566	GM12878	blood:	n/a	n/a
26	BATF	chr15:30763589-30764924	GM12878	blood:	n/a	n/a
27	BATF	chr15:30829434-30829723	GM12878	blood:	n/a	n/a
28	BATF	chr15:30880957-30881265	GM12878	blood:	n/a	n/a
29	BATF	chr15:30881037-30881316	GM12878	blood:	n/a	n/a
30	BATF	chr15:30678661-30679029	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
31	BATF	chr15:30858799-30859444	GM12878	blood:	n/a	n/a
32	BATF	chr15:30717407-30718307	GM12878	blood:	n/a	n/a
33	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
34	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
35	BATF	chr15:30678631-30678956	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
36	BATF	chr15:30871617-30871985	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
37	BATF	chr15:30871690-30872015	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
38	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
39	BCL11A	chr15:30858936-30859213	GM12878	blood:	n/a	n/a
40	BCL11A	chr15:30832618-30833226	GM12878	blood:	n/a	n/a
41	BCL11A	chr15:30793856-30794157	GM12878	blood:	n/a	n/a
42	BCL11A	chr15:30942112-30942840	GM12878	blood:	n/a	n/a
43	BCL11A	chr15:30717095-30717386	GM12878	blood:	n/a	n/a
44	BCL11A	chr15:30918059-30918429	GM12878	blood:	n/a	chr15:30918103-30918112
45	BCL11A	chr15:30917933-30918639	GM12878	blood:	n/a	chr15:30918103-30918112 chr15:30918531-30918544
46	BCL11A	chr15:30717394-30718057	GM12878	blood:	n/a	n/a
47	BCL11A	chr15:30763746-30764847	GM12878	blood:	n/a	n/a
48	BCL11A	chr15:30763771-30764696	GM12878	blood:	n/a	n/a
49	BCL11A	chr15:30691441-30691613	GM12878	blood:	n/a	n/a
50	BCL11A	chr15:30859004-30859344	GM12878	blood:	n/a	chr15:30859230-30859243

(count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30919014-30919064	BJ	skin:	n/a
2	chr15:30918328-30918378	HRE	kidney:	n/a
3	chr15:30919014-30919064	BJ	skin:	n/a
4	chr15:30918328-30918378	HRE	kidney:	n/a
5	chr15:30677804-30677854	HIPEpiC	eye:	n/a
6	chr15:30763199-30763249	HEK293	kidney:	embryo
7	chr15:30920627-30920677	HL-60	blood:	n/a
8	chr15:30763484-30763534	ECC-1	luminal epithelium:	n/a
9	chr15:30918339-30918389	HCM	heart:	n/a
10	chr15:30896060-30896110	ECC-1	luminal epithelium:	n/a
11	chr15:30861172-30861222	HAEpiC	amniotic membrane:	n/a
12	chr15:30763199-30763249	HAEpiC	amniotic membrane:	n/a
13	chr15:30865191-30865241	NHDF-neo	bronchial:	n/a
14	chr15:30918328-30918378	MCF-7	breast:	n/a
15	chr15:30861172-30861222	AG10803	skin:	n/a
16	chr15:30685198-30685248	HepG2	liver:	n/a
17	chr15:30896060-30896110	HCT-116	colon:	n/a
18	chr15:30918595-30918645	AG09309	skin:	n/a
19	chr15:30866091-30866141	GM12878	blood:	n/a
20	chr15:30930499-30930549	GM12891	blood:	n/a
21	chr15:30920627-30920677	CMK	blood:	n/a
22	chr15:30763484-30763534	HRCEpiC	kidney:	n/a
23	chr15:30917958-30918008	HRCEpiC	kidney:	n/a
24	chr15:30896216-30896266	HCPEpiC	choroid plexus:	n/a
25	chr15:30866091-30866141	K562	blood:	n/a
26	chr15:30919020-30919070	HPAEpiC	pulmonary alveolar:	n/a
27	chr15:30677804-30677854	HPAEpiC	pulmonary alveolar:	n/a
28	chr15:30763487-30763537	GM12878	blood:	n/a
29	chr15:30685198-30685248	Jurkat	blood:	n/a
30	chr15:30865191-30865241	SK-N-SH	brain:	n/a
31	chr15:30919020-30919070	AG10803	skin:	n/a
32	chr15:30861172-30861222	HRE	kidney:	n/a
33	chr15:30699977-30700027	GM12878	blood:	n/a
34	chr15:30918339-30918389	NB4	blood:	n/a
35	chr15:30918339-30918389	SK-N-MC	brain:	n/a
36	chr15:30699977-30700027	Hela-S3	cervix:	n/a
37	chr15:30918595-30918645	NHDF-neo	bronchial:	n/a
38	chr15:30677804-30677854	Hepatocyte	liver:	n/a
39	chr15:30920627-30920677	NB4	blood:	n/a
40	chr15:30861172-30861222	SK-N-SH	brain:	n/a
41	chr15:30865191-30865241	BJ	skin:	n/a
42	chr15:30763484-30763534	IMR90	lung:	fetal
43	chr15:30685198-30685248	HRPEpiC	eye:	n/a
44	chr15:30685198-30685248	RPTEC	kidney:	n/a
45	chr15:30918065-30918115	HCT-116	colon:	n/a
46	chr15:30920627-30920677	HNPCEpiC	eye:	n/a
47	chr15:30866091-30866141	Caco-2	colon:	n/a
48	chr15:30917991-30918041	HCF	heart:	n/a
49	chr15:30861172-30861222	AG09309	skin:	n/a
50	chr15:30844060-30844110	BJ	skin:	n/a

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

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

(count:45 , 50 per page) page: 1

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

No data

Variant related genes	Relation type
ENSG00000270016	TF binding region
ENSG00000221723	TF binding region
ENSG00000247728	TF binding region
ENSG00000221593	TF binding region
ENSG00000207430	TF binding region
ENSG00000270055	TF binding region
RN7SL196P	TF binding region
ENSG00000238519	TF binding region
ENSG00000260693	TF binding region
GOLGA8R	TF binding region
RN7SL796P	TF binding region
DNM1P50	TF binding region
ENSG00000263070	TF binding region
ULK4P2	TF binding region
RN7SL628P	TF binding region
ENSG00000260784	TF binding region
GOLGA8H	TF binding region
ENSG00000252602	TF binding region
ENSG00000271333	TF binding region
ARHGAP11B	TF binding region
ENSG00000215302	TF binding region
ENSG00000221358	TF binding region
ENSG00000269930	TF binding region
ENSG00000269974	TF binding region
GOLGA8Q	TF binding region
CHRFAM7A	TF binding region
ENSG00000270016	CpG island
ENSG00000221723	CpG island
ENSG00000247728	CpG island
ENSG00000221593	CpG island
ENSG00000207430	CpG island
ENSG00000270055	CpG island
RN7SL196P	CpG island
ENSG00000238519	CpG island
ENSG00000260693	CpG island
GOLGA8R	CpG island
RN7SL796P	CpG island
DNM1P50	CpG island
ENSG00000263070	CpG island
ULK4P2	CpG island
RN7SL628P	CpG island
ENSG00000260784	CpG island
GOLGA8H	CpG island
ENSG00000252602	CpG island
ENSG00000271333	CpG island
ARHGAP11B	CpG island
ENSG00000215302	CpG island
ENSG00000221358	CpG island
ENSG00000269930	CpG island
ENSG00000269974	CpG island
GOLGA8Q	CpG island
CHRFAM7A	CpG island
ENSG00000244952	chromatin interactions
ENSG00000262728	chromatin interactions
ENSG00000135916	chromatin interactions
ENSG00000198826	chromatin interactions
TGFB2	miRNA target sites
PRKAB2	miRNA target sites

Extended variants
information (count: 2925 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:2925 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs574047180	chr15:30665610-30665611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543360102	chr15:30665612-30665613	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs557210989	chr15:30665648-30665649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs577008089	chr15:30665655-30665656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs367874015	chr15:30665674-30665675	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs141612625	chr15:30665726-30665727	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs371407074	chr15:30665727-30665728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs545954704	chr15:30665735-30665736	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs62016478	chr15:30665760-30665761	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs565410072	chr15:30665763-30665764	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs527805238	chr15:30665772-30665773	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs201961508	chr15:30665799-30665800	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs201888375	chr15:30665973-30665974	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs541512247	chr15:30666020-30666021	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561271363	chr15:30666039-30666040	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530064957	chr15:30666095-30666096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs550249339	chr15:30666121-30666122	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs560023484	chr15:30666166-30666167	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564006158	chr15:30666181-30666182	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs376362902	chr15:30666182-30666183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs532624938	chr15:30666210-30666211	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552337347	chr15:30666230-30666231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs565907263	chr15:30666252-30666253	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs534415008	chr15:30666462-30666463	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs547840299	chr15:30666538-30666539	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs567757693	chr15:30666587-30666588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs537045613	chr15:30666718-30666719	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs145786150	chr15:30666736-30666737	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs577049220	chr15:30666739-30666740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs542646429	chr15:30666750-30666751	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs553228628	chr15:30666754-30666755	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573031068	chr15:30666782-30666783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs560542903	chr15:30666786-30666787	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs201074366	chr15:30666938-30666939	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200260103	chr15:30666977-30666978	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs561360575	chr15:30666997-30666998	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs574787589	chr15:30667140-30667141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62016479	chr15:30667141-30667142	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs111460804	chr15:30667145-30667146	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs543778750	chr15:30667163-30667164	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs563861016	chr15:30667182-30667183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs532855669	chr15:30667187-30667188	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs552406659	chr15:30667222-30667223	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs559529349	chr15:30667231-30667232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563904325	chr15:30667256-30667257	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs147650661	chr15:30667257-30667258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs528651016	chr15:30667277-30667278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs374859171	chr15:30667693-30667694	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs151197193	chr15:30667705-30667706	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs568124941	chr15:30667715-30667716	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:952 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30654200-30668200	Weak transcription	Aorta	Aorta
2	chr15:30667000-30669400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
3	chr15:30668000-30668200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
4	chr15:30668000-30668200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr15:30668200-30668400	Flanking Bivalent TSS/Enh	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr15:30668200-30668400	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:30668200-30668400	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
8	chr15:30668200-30668400	Enhancers	Aorta	Aorta
9	chr15:30668200-30668400	ZNF genes & repeats	Fetal Kidney	kidney
10	chr15:30668200-30668400	Active TSS	Fetal Lung	lung
11	chr15:30668200-30668400	Enhancers	Gastric	stomach
12	chr15:30668200-30668400	ZNF genes & repeats	Pancreas	Pancrea
13	chr15:30668200-30668400	Enhancers	Spleen	Spleen
14	chr15:30685000-30685400	Active TSS	H1 Cell Line	embryonic stem cell
15	chr15:30685000-30685400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr15:30685000-30685400	Active TSS	HUES6 Cell Line	embryonic stem cell
17	chr15:30685000-30685400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr15:30685000-30685400	Active TSS	Primary neutrophils fromperipheralblood	blood
19	chr15:30685000-30685400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
20	chr15:30685000-30685400	Active TSS	Pancreas	Pancrea
21	chr15:30685000-30685400	Active TSS	Right Atrium	heart
22	chr15:30697800-30699800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
23	chr15:30698400-30699800	Weak transcription	Fetal Stomach	stomach
24	chr15:30698400-30712800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr15:30698800-30701200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr15:30698800-30701200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
27	chr15:30698800-30701200	Weak transcription	Placenta	Placenta
28	chr15:30699000-30701400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr15:30699000-30701400	Weak transcription	Liver	Liver
30	chr15:30699000-30701400	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr15:30699000-30701400	Weak transcription	Ovary	ovary
32	chr15:30699000-30701400	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr15:30699000-30701400	Weak transcription	Spleen	Spleen
34	chr15:30699600-30700000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
35	chr15:30699800-30700400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr15:30699800-30700400	Strong transcription	Fetal Stomach	stomach
37	chr15:30700000-30700200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr15:30700000-30700200	Enhancers	Brain Angular Gyrus	brain
39	chr15:30700000-30700200	ZNF genes & repeats	Esophagus	oesophagus
40	chr15:30700000-30700200	Enhancers	Pancreas	Pancrea
41	chr15:30700000-30700400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr15:30700200-30700400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr15:30700400-30701800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr15:30700400-30701800	Weak transcription	Fetal Stomach	stomach
45	chr15:30712800-30713200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr15:30712800-30713200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
47	chr15:30713200-30713400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:30762800-30763200	Active TSS	Fetal Thymus	thymus
49	chr15:30762800-30763600	Active TSS	Psoas Muscle	Psoas
50	chr15:30762800-30763600	Active TSS	Thymus	Thymus

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