Variant report

Variant	nsv1041708
Chromosome Location	chr15:30444264-30779684
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr15:30716939-30717383	GM12878	blood:	n/a	n/a
2	BATF	chr15:30717393-30718193	GM12878	blood:	n/a	n/a
3	BATF	chr15:30763589-30764924	GM12878	blood:	n/a	n/a
4	BATF	chr15:30458984-30459268	GM12878	blood:	n/a	n/a
5	BATF	chr15:30691171-30691739	GM12878	blood:	n/a	n/a
6	BATF	chr15:30678661-30679029	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
7	BATF	chr15:30626382-30626790	GM12878	blood:	n/a	chr15:30626595-30626606
8	BATF	chr15:30459001-30459247	GM12878	blood:	n/a	n/a
9	BATF	chr15:30763002-30763213	GM12878	blood:	n/a	n/a
10	BATF	chr15:30765283-30765578	GM12878	blood:	n/a	n/a
11	BATF	chr15:30717407-30718307	GM12878	blood:	n/a	n/a
12	BATF	chr15:30765290-30765504	GM12878	blood:	n/a	n/a
13	BATF	chr15:30763776-30764872	GM12878	blood:	n/a	n/a
14	BATF	chr15:30678631-30678956	GM12878	blood:	n/a	chr15:30678848-30678858 chr15:30678844-30678854
15	BATF	chr15:30720885-30721174	GM12878	blood:	n/a	n/a
16	BATF	chr15:30626371-30626674	GM12878	blood:	n/a	chr15:30626595-30626606
17	BCL11A	chr15:30678714-30679009	GM12878	blood:	n/a	chr15:30678847-30678856 chr15:30678892-30678901
18	BCL11A	chr15:30763771-30764696	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:30763746-30764847	GM12878	blood:	n/a	n/a
20	BCL11A	chr15:30678698-30678949	GM12878	blood:	n/a	chr15:30678847-30678856 chr15:30678892-30678901
21	BCL11A	chr15:30765257-30765493	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:30692208-30692390	GM12878	blood:	n/a	n/a
23	BCL11A	chr15:30469390-30469696	GM12878	blood:	n/a	n/a
24	BCL11A	chr15:30717394-30718057	GM12878	blood:	n/a	n/a
25	BCL11A	chr15:30626396-30626697	GM12878	blood:	n/a	n/a
26	BCL11A	chr15:30717383-30717989	GM12878	blood:	n/a	n/a
27	BCL11A	chr15:30691441-30691613	GM12878	blood:	n/a	n/a
28	BCL11A	chr15:30626461-30626686	GM12878	blood:	n/a	n/a
29	BCL11A	chr15:30717095-30717386	GM12878	blood:	n/a	n/a
30	BCL11A	chr15:30465220-30465511	GM12878	blood:	n/a	n/a
31	BCL3	chr15:30668118-30668389	GM12878	blood:	n/a	n/a
32	BCL3	chr15:30668077-30668421	GM12878	blood:	n/a	n/a
33	BHLHE40	chr15:30762992-30763207	HepG2	liver:	n/a	chr15:30763129-30763145 chr15:30763138-30763154 chr15:30763154-30763170
34	CBX3	chr15:30762898-30763215	K562	blood:	n/a	n/a
35	CEBPB	chr15:30764256-30764822	GM12878	blood:	n/a	n/a
36	CEBPB	chr15:30488906-30489076	IMR90	lung:	n/a	n/a
37	CEBPD	chr15:30762900-30763294	K562	blood:	n/a	n/a
38	CHD2	chr15:30465233-30465388	GM12878	blood:	n/a	n/a
39	CHD2	chr15:30618331-30618661	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTCF	chr15:30465620-30465770	GM12873	blood:	n/a	chr15:30465736-30465754 chr15:30465731-30465752 chr15:30465730-30465737 chr15:30465737-30465753 chr15:30465738-30465751
41	CTCF	chr15:30554111-30554265	ProgFib	skin:	n/a	n/a
42	CTCF	chr15:30691252-30691517	Medullo	brain:	n/a	chr15:30691367-30691380 chr15:30691448-30691457 chr15:30691366-30691387 chr15:30691364-30691382 chr15:30691365-30691381 chr15:30691369-30691379 chr15:30691367-30691376
43	CTCF	chr15:30454948-30455312	A549	lung:	n/a	n/a
44	CTCF	chr15:30554105-30554615	GM19238	blood:	n/a	chr15:30554453-30554469 chr15:30554455-30554464 chr15:30554452-30554470 chr15:30554455-30554468 chr15:30554454-30554475 chr15:30554457-30554467 chr15:30554455-30554468
45	CTCF	chr15:30554279-30554609	GM12891	blood:	n/a	chr15:30554453-30554469 chr15:30554455-30554464 chr15:30554452-30554470 chr15:30554455-30554468 chr15:30554454-30554475 chr15:30554457-30554467 chr15:30554455-30554468
46	CTCF	chr15:30669031-30669228	K562	blood:	n/a	chr15:30669144-30669162
47	CTCF	chr15:30698059-30698377	K562	blood:	n/a	chr15:30698228-30698246 chr15:30698235-30698243
48	CTCF	chr15:30465235-30465955	A549	lung:	n/a	chr15:30465736-30465754 chr15:30465731-30465752 chr15:30465730-30465737 chr15:30465737-30465753 chr15:30465738-30465751
49	CTCF	chr15:30596417-30596526	Fibrobl	skin:	n/a	n/a
50	CTCF	chr15:30554253-30554617	K562	blood:	n/a	chr15:30554453-30554469 chr15:30554455-30554464 chr15:30554452-30554470 chr15:30554455-30554468 chr15:30554454-30554475 chr15:30554457-30554467 chr15:30554455-30554468

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30666736-30666786	HepG2	liver:	n/a
2	chr15:30515844-30515894	ECC-1	luminal epithelium:	n/a
3	chr15:30482157-30482207	SK-N-MC	brain:	n/a
4	chr15:30666736-30666786	HepG2	liver:	n/a
5	chr15:30515844-30515894	ECC-1	luminal epithelium:	n/a
6	chr15:30482157-30482207	SK-N-MC	brain:	n/a
7	chr15:30516906-30516956	HPAEpiC	pulmonary alveolar:	n/a
8	chr15:30484033-30484083	ECC-1	luminal epithelium:	n/a
9	chr15:30517601-30517651	HRCEpiC	kidney:	n/a
10	chr15:30484753-30484803	GM06990	blood:	n/a
11	chr15:30685198-30685248	PFSK-1	brain:	n/a
12	chr15:30489014-30489064	U87	brain:	n/a
13	chr15:30487914-30487964	CMK	blood:	n/a
14	chr15:30483647-30483697	ProgFib	skin:	n/a
15	chr15:30518064-30518114	AoSMC	blood vessel:	n/a
16	chr15:30517601-30517651	HAEpiC	amniotic membrane:	n/a
17	chr15:30516422-30516472	PFSK-1	brain:	n/a
18	chr15:30515844-30515894	HPAEpiC	pulmonary alveolar:	n/a
19	chr15:30484033-30484083	SK-N-SH	brain:	n/a
20	chr15:30685198-30685248	HEEpiC	esophagus:	n/a
21	chr15:30700112-30700162	HIPEpiC	eye:	n/a
22	chr15:30700112-30700162	PFSK-1	brain:	n/a
23	chr15:30517601-30517651	Jurkat	blood:	n/a
24	chr15:30518064-30518114	HCPEpiC	choroid plexus:	n/a
25	chr15:30486767-30486817	AG09309	skin:	n/a
26	chr15:30677804-30677854	GM19239	blood:	n/a
27	chr15:30482157-30482207	ProgFib	skin:	n/a
28	chr15:30666736-30666786	T-47D	breast:	n/a
29	chr15:30666736-30666786	Hela-S3	cervix:	n/a
30	chr15:30763487-30763537	NHDF-neo	bronchial:	n/a
31	chr15:30763484-30763534	BE2_C	brain:	n/a
32	chr15:30515162-30515212	AG04449	skin:	fetal
33	chr15:30677804-30677854	AG09319	gingival:	n/a
34	chr15:30520018-30520068	HRE	kidney:	n/a
35	chr15:30685198-30685248	GM12878	blood:	n/a
36	chr15:30516906-30516956	SKMC	muscle:	n/a
37	chr15:30484753-30484803	ProgFib	skin:	n/a
38	chr15:30763487-30763537	SKMC	muscle:	n/a
39	chr15:30516906-30516956	HEK293	kidney:	embryo
40	chr15:30484753-30484803	HEEpiC	esophagus:	n/a
41	chr15:30489014-30489064	MCF10A-Er-Src	breast:	n/a
42	chr15:30666736-30666786	HEEpiC	esophagus:	n/a
43	chr15:30515162-30515212	HUVEC	blood vessel:	n/a
44	chr15:30489014-30489064	SKMC	muscle:	n/a
45	chr15:30489014-30489064	HRE	kidney:	n/a
46	chr15:30483647-30483697	HCPEpiC	choroid plexus:	n/a
47	chr15:30517589-30517639	PrEC	prostate:	n/a
48	chr15:30666736-30666786	PrEC	prostate:	n/a
49	chr15:30511386-30511436	HEEpiC	esophagus:	n/a
50	chr15:30520018-30520068	T-47D	breast:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CHRFAM7A-3	chr15:30697514-30697792	NONHSAT041354
2	lnc-CHRFAM7A-2	chr15:30649969-30650976	ENSG00000270173.1
3	lnc-RP5-1086D14.3.1-1	chr15:30491478-30491534	ENSG00000225930.2
4	lnc-RP11-382B18.2.1-2	chr15:30679087-30679190	NONHSAT041347
5	lnc-CHRFAM7A-1	chr15:30462766-30462831	ENSG00000259906.1
6	lnc-RP11-382B18.2.1-2	chr15:30673906-30674079	NONHSAT041347
7	lnc-RP5-1086D14.3.1-1	chr15:30502620-30506743	ENSG00000225930.3
8	lnc-RP11-382B18.2.1-2	chr15:30675522-30675585	NONHSAT041347
9	lnc-CHRFAM7A-1	chr15:30462912-30462975	ENSG00000259906.1
10	lnc-RP11-382B18.2.1-2	chr15:30679066-30679190	NONHSAT041348
11	lnc-RP5-1086D14.3.1-1	chr15:30488239-30488317	ENSG00000225930.3
12	lnc-RP5-1086D14.3.1-1	chr15:30502611-30503009	ENSG00000225930.2
13	lnc-RP11-382B18.2.1-2	chr15:30675247-30675585	NONHSAT041348
14	lnc-AC026150.9.1-4	chr15:30749372-30751192	ucscGeneNc_uc001zhb_2
15	lnc-RP11-382B18.2.1-2	chr15:30672556-30672602	NONHSAT041347
16	lnc-AC026150.9.1-5	chr15:30702037-30703662	NONHSAT041356
17	lnc-RP5-1086D14.3.1-1	chr15:30488239-30488317	ENSG00000225930.2
18	lnc-CHRFAM7A-1	chr15:30471079-30472146	ENSG00000259906.1
19	lnc-CHRFAM7A-1	chr15:30471212-30471332	ENSG00000259906.1
20	lnc-RP5-1086D14.3.1-1	chr15:30502620-30504471	ENSG00000225930.2
21	lnc-RP5-1086D14.3.1-1	chr15:30491478-30491534	ENSG00000225930.3

Variant related genes	Relation type
ENSG00000221723	TF binding region
RN7SL196P	TF binding region
DNM1P30	TF binding region
RNU6-17P	TF binding region
ENSG00000259906	TF binding region
ENSG00000270055	TF binding region
ENSG00000238519	TF binding region
GOLGA8R	TF binding region
ENSG00000238783	TF binding region
ENSG00000263070	TF binding region
ENSG00000225930	TF binding region
ENSG00000270955	TF binding region
ENSG00000270173	TF binding region
ENSG00000271333	TF binding region
ENSG00000215302	TF binding region
ENSG00000259993	TF binding region
CHRFAM7A	TF binding region
ENSG00000261747	TF binding region
ENSG00000221723	CpG island
RN7SL196P	CpG island
DNM1P30	CpG island
RNU6-17P	CpG island
ENSG00000259906	CpG island
ENSG00000270055	CpG island
ENSG00000238519	CpG island
GOLGA8R	CpG island
ENSG00000238783	CpG island
ENSG00000263070	CpG island
ENSG00000225930	CpG island
ENSG00000270955	CpG island
ENSG00000270173	CpG island
ENSG00000271333	CpG island
ENSG00000215302	CpG island
ENSG00000259993	CpG island
CHRFAM7A	CpG island
ENSG00000261747	CpG island

Extended variants
information (count: 1407 )
Associated
traits (count: 145 )

Variant overlapped rSNPs/rCNVs (count:1407 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs536948056	chr15:30446836-30446837	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs559428327	chr15:30446842-30446843	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs368956199	chr15:30446846-30446847	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs556518900	chr15:30446856-30446857	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs529739394	chr15:30446871-30446872	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs538382524	chr15:30446877-30446878	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs558705722	chr15:30446890-30446891	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs572134773	chr15:30446910-30446911	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs529220141	chr15:30455216-30455217	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs147891250	chr15:30455225-30455226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569107387	chr15:30455234-30455235	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs181361420	chr15:30455237-30455238	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs371759050	chr15:30455241-30455242	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs537662962	chr15:30455280-30455281	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs150131515	chr15:30455289-30455290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs376235771	chr15:30455307-30455308	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs570961131	chr15:30455362-30455363	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs539936921	chr15:30455392-30455393	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs553444790	chr15:30455411-30455412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs2554217	chr15:30455419-30455420	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs143466504	chr15:30455440-30455441	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs137887506	chr15:30455441-30455442	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs62017027	chr15:30455461-30455462	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs555800690	chr15:30455504-30455505	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs575853491	chr15:30455513-30455514	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs544482211	chr15:30455578-30455579	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs564334030	chr15:30455584-30455585	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs369630568	chr15:30455597-30455598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs200438703	chr15:30455652-30455653	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs577356346	chr15:30455657-30455658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs540250296	chr15:30455900-30455901	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs62017028	chr15:30455911-30455912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs112340202	chr15:30456193-30456194	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs539922539	chr15:30456351-30456352	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs559743506	chr15:30456374-30456375	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs113654331	chr15:30456384-30456385	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs528905007	chr15:30456413-30456414	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs548932257	chr15:30456573-30456574	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs562652331	chr15:30456662-30456663	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs531590628	chr15:30456673-30456674	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs551649107	chr15:30456768-30456769	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs571458816	chr15:30456773-30456774	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs62017029	chr15:30456796-30456797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs201492866	chr15:30457025-30457026	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs562573560	chr15:30457086-30457087	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs199547275	chr15:30457088-30457089	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs547136420	chr15:30457136-30457137	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs566922526	chr15:30457529-30457530	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs535489791	chr15:30457530-30457531	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs555686065	chr15:30457569-30457570	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:145)

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
idiopathic generalized epilepsy	19843651	CNVD
Neuropsychiatric disorder	20506139	CNVD
Austim spectrum disorder	21302340	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	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
Non-syndromic sensorineural hearing loss	21293372	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

Chromatin state (count:512 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30455200-30455400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr15:30455200-30455600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
3	chr15:30455200-30455600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
4	chr15:30455200-30455600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr15:30455400-30465000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
6	chr15:30455600-30456000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr15:30455600-30456000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr15:30455600-30456000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
9	chr15:30456000-30457000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr15:30456000-30457000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:30456000-30457800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
12	chr15:30456400-30456800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
13	chr15:30456400-30457000	Enhancers	Primary T cells fromperipheralblood	blood
14	chr15:30456400-30457000	Enhancers	Primary T helper naive cells from peripheral blood	blood
15	chr15:30456400-30457000	Enhancers	Primary T helper cells fromperipheralblood	blood
16	chr15:30456600-30457000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
17	chr15:30458800-30459200	Enhancers	Pancreas	Pancrea
18	chr15:30459200-30465000	Weak transcription	Pancreas	Pancrea
19	chr15:30463800-30465000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
20	chr15:30464800-30465000	Weak transcription	Spleen	Spleen
21	chr15:30465000-30465200	Flanking Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr15:30465000-30465200	Enhancers	Primary T helper naive cells from peripheral blood	blood
23	chr15:30465000-30465200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr15:30465000-30465200	Enhancers	Primary T killer memory cells from peripheral blood	blood
25	chr15:30465000-30465400	Bivalent Enhancer	Brain Anterior Caudate	brain
26	chr15:30465000-30465400	Enhancers	Placenta Amnion	Placenta Amnion
27	chr15:30465000-30465400	Transcr. at gene 5' and 3'	Spleen	Spleen
28	chr15:30465000-30465600	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr15:30465000-30465600	ZNF genes & repeats	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr15:30465000-30465600	ZNF genes & repeats	H9 Cell Line	embryonic stem cell
31	chr15:30465000-30465600	ZNF genes & repeats	iPS DF 6.9 Cell Line	embryonic stem cell
32	chr15:30465000-30465600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
33	chr15:30465000-30465600	Enhancers	Primary hematopoietic stem cells short term culture	blood
34	chr15:30465000-30465600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
35	chr15:30465000-30465600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr15:30465000-30465600	Enhancers	Esophagus	oesophagus
37	chr15:30465000-30465600	ZNF genes & repeats	Fetal Kidney	kidney
38	chr15:30465000-30465600	ZNF genes & repeats	Gastric	stomach
39	chr15:30465000-30465600	ZNF genes & repeats	Lung	lung
40	chr15:30465000-30465600	Transcr. at gene 5' and 3'	Pancreas	Pancrea
41	chr15:30465200-30465400	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
42	chr15:30465200-30465400	Active TSS	Fetal Brain Male	brain
43	chr15:30465200-30465400	Flanking Bivalent TSS/Enh	Fetal Lung	lung
44	chr15:30465200-30465400	Bivalent Enhancer	Skeletal Muscle Male	skeletal muscle
45	chr15:30465200-30465400	Bivalent/Poised TSS	Stomach Mucosa	stomach
46	chr15:30465200-30465400	ZNF genes & repeats	NHLF	lung
47	chr15:30465200-30465600	Transcr. at gene 5' and 3'	H1 Derived Mesenchymal Stem Cells	ES cell derived
48	chr15:30465200-30465600	Enhancers	Primary B cells from peripheral blood	blood
49	chr15:30465200-30465600	Enhancers	Primary T cells from cord blood	blood
50	chr15:30465200-30465600	Enhancers	Primary hematopoietic stem cells	blood

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