Variant report

Variant	nsv1044912
Chromosome Location	chr15:30668453-30981033
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2905)
CpG islands
(count:1649)
Chromatin interactive
region (count:7)
LncRNA
region (count:46)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2905 , 50 per page) page: 1 2 3 4 5 6 7 ... 59

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:30917819-30918297	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:30917841-30918381	K562	blood:	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	chr15:30917709-30918426	GM12878	blood:	n/a	n/a
7	ATF2	chr15:30941959-30942874	GM12878	blood:	n/a	n/a
8	ATF2	chr15:30917808-30918347	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:30918103-30918425	H1-hESC	embryonic stem cell:	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	chr15:30763776-30764872	GM12878	blood:	n/a	n/a
13	BATF	chr15:30678631-30678956	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
14	BATF	chr15:30763589-30764924	GM12878	blood:	n/a	n/a
15	BATF	chr15:30691171-30691739	GM12878	blood:	n/a	n/a
16	BATF	chr15:30832414-30833216	GM12878	blood:	n/a	chr15:30833063-30833074
17	BATF	chr15:30793866-30794121	GM12878	blood:	n/a	n/a
18	BATF	chr15:30939410-30939698	GM12878	blood:	n/a	n/a
19	BATF	chr15:30880957-30881265	GM12878	blood:	n/a	n/a
20	BATF	chr15:30765283-30765578	GM12878	blood:	n/a	n/a
21	BATF	chr15:30858799-30859444	GM12878	blood:	n/a	n/a
22	BATF	chr15:30881037-30881316	GM12878	blood:	n/a	n/a
23	BATF	chr15:30829434-30829723	GM12878	blood:	n/a	n/a
24	BATF	chr15:30939417-30939718	GM12878	blood:	n/a	n/a
25	BATF	chr15:30871690-30872015	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
26	BATF	chr15:30716939-30717383	GM12878	blood:	n/a	n/a
27	BATF	chr15:30763002-30763213	GM12878	blood:	n/a	n/a
28	BATF	chr15:30832413-30833670	GM12878	blood:	n/a	chr15:30833063-30833074
29	BATF	chr15:30717407-30718307	GM12878	blood:	n/a	n/a
30	BATF	chr15:30917720-30918566	GM12878	blood:	n/a	n/a
31	BATF	chr15:30765290-30765504	GM12878	blood:	n/a	n/a
32	BATF	chr15:30942101-30942823	GM12878	blood:	n/a	n/a
33	BATF	chr15:30793879-30794120	GM12878	blood:	n/a	n/a
34	BATF	chr15:30942098-30942760	GM12878	blood:	n/a	n/a
35	BATF	chr15:30871617-30871985	GM12878	blood:	n/a	chr15:30871822-30871833 chr15:30871827-30871837 chr15:30871823-30871833
36	BATF	chr15:30720885-30721174	GM12878	blood:	n/a	n/a
37	BATF	chr15:30678661-30679029	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
38	BATF	chr15:30717393-30718193	GM12878	blood:	n/a	n/a
39	BCL11A	chr15:30692208-30692390	GM12878	blood:	n/a	n/a
40	BCL11A	chr15:30942112-30942840	GM12878	blood:	n/a	n/a
41	BCL11A	chr15:30880980-30881263	GM12878	blood:	n/a	n/a
42	BCL11A	chr15:30717394-30718057	GM12878	blood:	n/a	n/a
43	BCL11A	chr15:30918059-30918429	GM12878	blood:	n/a	chr15:30918103-30918112
44	BCL11A	chr15:30763771-30764696	GM12878	blood:	n/a	n/a
45	BCL11A	chr15:30678714-30679009	GM12878	blood:	n/a	chr15:30678847-30678856 chr15:30678892-30678901
46	BCL11A	chr15:30763746-30764847	GM12878	blood:	n/a	n/a
47	BCL11A	chr15:30793856-30794157	GM12878	blood:	n/a	n/a
48	BCL11A	chr15:30691441-30691613	GM12878	blood:	n/a	n/a
49	BCL11A	chr15:30832618-30833226	GM12878	blood:	n/a	n/a
50	BCL11A	chr15:30717383-30717989	GM12878	blood:	n/a	n/a

(count:1649 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30918313-30918363	SK-N-MC	brain:	n/a
2	chr15:30918313-30918363	HUVEC	blood vessel:	n/a
3	chr15:30918313-30918363	SK-N-MC	brain:	n/a
4	chr15:30918313-30918363	HUVEC	blood vessel:	n/a
5	chr15:30917958-30918008	NHDF-neo	bronchial:	n/a
6	chr15:30918313-30918363	AG09319	gingival:	n/a
7	chr15:30763484-30763534	NHDF-neo	bronchial:	n/a
8	chr15:30700112-30700162	HEEpiC	esophagus:	n/a
9	chr15:30677804-30677854	AG09309	skin:	n/a
10	chr15:30918313-30918363	Hepatocyte	liver:	n/a
11	chr15:30700112-30700162	HRCEpiC	kidney:	n/a
12	chr15:30917918-30917968	CMK	blood:	n/a
13	chr15:30918328-30918378	HRPEpiC	eye:	n/a
14	chr15:30917991-30918041	SK-N-SH_RA	brain:	n/a
15	chr15:30918313-30918363	GM06990	blood:	n/a
16	chr15:30699977-30700027	Caco-2	colon:	n/a
17	chr15:30918328-30918378	H1-hESC	embryonic stem cell:	embryo
18	chr15:30685198-30685248	HCT-116	colon:	n/a
19	chr15:30816232-30816282	AoSMC	blood vessel:	n/a
20	chr15:30866091-30866141	HIPEpiC	eye:	n/a
21	chr15:30763487-30763537	CMK	blood:	n/a
22	chr15:30763199-30763249	PFSK-1	brain:	n/a
23	chr15:30861172-30861222	HUVEC	blood vessel:	n/a
24	chr15:30918595-30918645	MCF-7	breast:	n/a
25	chr15:30918328-30918378	AG09319	gingival:	n/a
26	chr15:30865191-30865241	NT2-D1	testis:	n/a
27	chr15:30896216-30896266	NT2-D1	testis:	n/a
28	chr15:30866091-30866141	HCF	heart:	n/a
29	chr15:30917991-30918041	HNPCEpiC	eye:	n/a
30	chr15:30918595-30918645	PFSK-1	brain:	n/a
31	chr15:30917991-30918041	NT2-D1	testis:	n/a
32	chr15:30920627-30920677	GM12892	blood:	n/a
33	chr15:30918313-30918363	LNCaP	prostate:	n/a
34	chr15:30844060-30844110	HRPEpiC	eye:	n/a
35	chr15:30700112-30700162	NHDF-neo	bronchial:	n/a
36	chr15:30919020-30919070	A549	lung:	n/a
37	chr15:30844060-30844110	HMEC	breast:	n/a
38	chr15:30685198-30685248	AG04449	skin:	fetal
39	chr15:30918313-30918363	NHDF-neo	bronchial:	n/a
40	chr15:30866091-30866141	AG09319	gingival:	n/a
41	chr15:30816232-30816282	HMEC	breast:	n/a
42	chr15:30918065-30918115	AG04450	lung:	fetal
43	chr15:30763199-30763249	AG10803	skin:	n/a
44	chr15:30896060-30896110	K562	blood:	n/a
45	chr15:30896060-30896110	HCPEpiC	choroid plexus:	n/a
46	chr15:30866091-30866141	NHDF-neo	bronchial:	n/a
47	chr15:30763199-30763249	ProgFib	skin:	n/a
48	chr15:30865200-30865250	NHBE	bronchial:	n/a
49	chr15:30918595-30918645	LNCaP	prostate:	n/a
50	chr15:30861172-30861222	GM19239	blood:	n/a

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

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

(count:46 , 50 per page) page: 1

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

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
ENSG00000263070	TF binding region
ENSG00000260784	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
ENSG00000263070	CpG island
ENSG00000260784	CpG island
ENSG00000252602	CpG island
ENSG00000271333	CpG island
ENSG00000215302	CpG island
ENSG00000221358	CpG island
GOLGA8Q	CpG island
CHRFAM7A	CpG island
ENSG00000135916	chromatin interactions
ENSG00000262728	chromatin interactions
ENSG00000244952	chromatin interactions
ENSG00000198826	chromatin interactions
PRKAB2	miRNA target sites
TGFB2	miRNA target sites

Extended variants
information (count: 4257 )
Associated
traits (count: 146 )

Variant overlapped rSNPs/rCNVs (count:4257 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372837477	chr15:30668476-30668477	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs539750018	chr15:30668551-30668552	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs202206323	chr15:30668604-30668605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs553265334	chr15:30668639-30668640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs369198667	chr15:30668659-30668660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs62016480	chr15:30669109-30669110	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs200179246	chr15:30669218-30669219	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs200064591	chr15:30672561-30672562	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
9	rs373716749	chr15:30675294-30675295	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
10	rs377464096	chr15:30675471-30675472	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
11	rs202209324	chr15:30675505-30675506	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
12	rs112266675	chr15:30675512-30675513	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
13	rs200486343	chr15:30675552-30675553	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
14	rs570439947	chr15:30675565-30675566	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
15	rs532949924	chr15:30675575-30675576	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
16	rs201569187	chr15:30675581-30675582	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
17	rs545770202	chr15:30685162-30685163	Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs113122737	chr15:30685170-30685171	Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs372286970	chr15:30685858-30685859	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs374549942	chr15:30686087-30686088	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs548607680	chr15:30686088-30686089	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs28615614	chr15:30686090-30686091	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs553284643	chr15:30686094-30686095	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs28630485	chr15:30686102-30686103	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs2648258	chr15:30687539-30687540	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs2604810	chr15:30687564-30687565	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs200780727	chr15:30696650-30696651	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs201727454	chr15:30696657-30696658	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs199873891	chr15:30696658-30696659	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs200802447	chr15:30696661-30696662	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs201764346	chr15:30696669-30696670	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs199934957	chr15:30696678-30696679	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs201209007	chr15:30696682-30696683	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs193209666	chr15:30696687-30696688	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200190162	chr15:30696691-30696692	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs201102961	chr15:30696714-30696715	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs201766701	chr15:30696753-30696754	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs529227160	chr15:30696761-30696762	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs4102150	chr15:30696764-30696765	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs62016501	chr15:30698522-30698523	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs2648127	chr15:30699003-30699004	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs62016502	chr15:30699388-30699389	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs570594600	chr15:30699609-30699610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs200116715	chr15:30699639-30699640	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs372339894	chr15:30699660-30699661	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs376518315	chr15:30699678-30699679	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs539511738	chr15:30699687-30699688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs367793099	chr15:30699723-30699724	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs372054611	chr15:30699739-30699740	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs552968047	chr15:30699758-30699759	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:1220 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30667000-30669400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
2	chr15:30685000-30685400	Active TSS	H1 Cell Line	embryonic stem cell
3	chr15:30685000-30685400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:30685000-30685400	Active TSS	HUES6 Cell Line	embryonic stem cell
5	chr15:30685000-30685400	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
6	chr15:30685000-30685400	Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr15:30685000-30685400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
8	chr15:30685000-30685400	Active TSS	Pancreas	Pancrea
9	chr15:30685000-30685400	Active TSS	Right Atrium	heart
10	chr15:30697800-30699800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
11	chr15:30698400-30699800	Weak transcription	Fetal Stomach	stomach
12	chr15:30698400-30712800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
13	chr15:30698800-30701200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
14	chr15:30698800-30701200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
15	chr15:30698800-30701200	Weak transcription	Placenta	Placenta
16	chr15:30699000-30701400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
17	chr15:30699000-30701400	Weak transcription	Liver	Liver
18	chr15:30699000-30701400	Weak transcription	Duodenum Smooth Muscle	Duodenum
19	chr15:30699000-30701400	Weak transcription	Ovary	ovary
20	chr15:30699000-30701400	Weak transcription	Rectal Mucosa Donor 29	rectum
21	chr15:30699000-30701400	Weak transcription	Spleen	Spleen
22	chr15:30699600-30700000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
23	chr15:30699800-30700400	Strong transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:30699800-30700400	Strong transcription	Fetal Stomach	stomach
25	chr15:30700000-30700200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr15:30700000-30700200	Enhancers	Brain Angular Gyrus	brain
27	chr15:30700000-30700200	ZNF genes & repeats	Esophagus	oesophagus
28	chr15:30700000-30700200	Enhancers	Pancreas	Pancrea
29	chr15:30700000-30700400	Enhancers	H1 Cell Line	embryonic stem cell
30	chr15:30700200-30700400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
31	chr15:30700400-30701800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
32	chr15:30700400-30701800	Weak transcription	Fetal Stomach	stomach
33	chr15:30712800-30713200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
34	chr15:30712800-30713200	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
35	chr15:30713200-30713400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:30762800-30763200	Active TSS	Fetal Thymus	thymus
37	chr15:30762800-30763600	Active TSS	Psoas Muscle	Psoas
38	chr15:30762800-30763600	Active TSS	Thymus	Thymus
39	chr15:30763000-30763600	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr15:30763000-30763600	Active TSS	Cortex derived primary cultured neurospheres	brain
41	chr15:30763000-30763600	Active TSS	Right Ventricle	heart
42	chr15:30763000-30763600	Active TSS	NHLF	lung
43	chr15:30763000-30763600	Active TSS	Osteobl	bone
44	chr15:30763200-30763600	Active TSS	H1 Cell Line	embryonic stem cell
45	chr15:30763200-30763600	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:30763200-30763600	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr15:30763200-30763600	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
48	chr15:30763200-30763600	Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
49	chr15:30763200-30763600	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr15:30763200-30763600	Active TSS	HUES48 Cell Line	embryonic stem cell

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