Variant report

Variant	nsv974545
Chromosome Location	chr15:30373033-30401482
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	BACH1	chr15:30396041-30396079	H1-hESC	embryonic stem cell:	n/a	n/a
2	BATF	chr15:30389801-30390448	GM12878	blood:	n/a	n/a
3	BCL11A	chr15:30389938-30390215	GM12878	blood:	n/a	n/a
4	BCL11A	chr15:30390006-30390348	GM12878	blood:	n/a	chr15:30390232-30390245
5	CEBPB	chr15:30373008-30373220	A549	lung:	n/a	n/a
6	CTCF	chr15:30396000-30396150	AG04450	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
7	CTCF	chr15:30389935-30390438	Lung_OC	lung:	n/a	chr15:30390267-30390288 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
8	CTCF	chr15:30389952-30390002	LNCaP	prostate:	n/a	n/a
9	CTCF	chr15:30390232-30390346	GM19240	blood:	n/a	chr15:30390267-30390288 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
10	CTCF	chr15:30395995-30396164	A549	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
11	CTCF	chr15:30384837-30385269	K562	blood:	n/a	chr15:30384859-30384872
12	CTCF	chr15:30395761-30396017	Pancreas_OC	pancreas:	n/a	chr15:30395870-30395886
13	CTCF	chr15:30396020-30396170	HAc	cerebellar:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
14	CTCF	chr15:30395980-30396130	HEEpiC	esophagus:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
15	CTCF	chr15:30396020-30396170	HFF-Myc	foreskin:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
16	CTCF	chr15:30384819-30385131	A549	lung:	n/a	chr15:30384859-30384872
17	CTCF	chr15:30396000-30396150	HMEC	breast:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
18	CTCF	chr15:30395672-30396154	K562	blood:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
19	CTCF	chr15:30395980-30396130	HEK293	kidney:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
20	CTCF	chr15:30395570-30396241	A549	lung:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
21	CTCF	chr15:30395646-30396114	A549	lung:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
22	CTCF	chr15:30384846-30385122	A549	lung:	n/a	chr15:30384859-30384872
23	CTCF	chr15:30382431-30382515	GM13976	blood:	n/a	n/a
24	CTCF	chr15:30390125-30390413	GM13977	blood:	n/a	chr15:30390267-30390288 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
25	CTCF	chr15:30396020-30396170	GM12867	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
26	CTCF	chr15:30395920-30396070	WERI-Rb-1	eye:	n/a	chr15:30396032-30396041 chr15:30396028-30396041 chr15:30396028-30396041
27	CTCF	chr15:30390104-30390411	Kidney_OC	kidney:	n/a	chr15:30390267-30390288 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
28	CTCF	chr15:30389701-30390532	A549	lung:	n/a	chr15:30390267-30390288 chr15:30390441-30390462 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390439-30390457 chr15:30390273-30390289 chr15:30390278-30390287
29	CTCF	chr15:30395900-30396050	GM12864	blood:	n/a	chr15:30396032-30396041 chr15:30396028-30396041 chr15:30396028-30396041
30	CTCF	chr15:30390206-30390348	Gliobla	brain:	n/a	chr15:30390267-30390288 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
31	CTCF	chr15:30396020-30396170	GM12875	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
32	CTCF	chr15:30395980-30396130	HL-60	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
33	CTCF	chr15:30396121-30396134	Gliobla	brain:	n/a	n/a
34	CTCF	chr15:30395654-30396255	K562	blood:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
35	CTCF	chr15:30396000-30396150	HPF	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
36	CTCF	chr15:30395762-30396041	GM13977	blood:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396028-30396041 chr15:30396028-30396041
37	CTCF	chr15:30396020-30396170	GM12869	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
38	CTCF	chr15:30395980-30396130	SAEC	small airway:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
39	CTCF	chr15:30395751-30396095	K562	blood:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396028-30396041 chr15:30396028-30396041
40	CTCF	chr15:30390140-30390384	GM10248	blood:	n/a	chr15:30390267-30390288 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
41	CTCF	chr15:30396000-30396150	GM12874	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
42	CTCF	chr15:30395757-30396081	GM10248	blood:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396028-30396041 chr15:30396028-30396041
43	CTCF	chr15:30395640-30396096	A549	lung:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
44	CTCF	chr15:30383204-30383524	K562	blood:	n/a	chr15:30383403-30383411 chr15:30383400-30383418
45	CTCF	chr15:30395623-30396207	A549	lung:	n/a	chr15:30395870-30395886 chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
46	CTCF	chr15:30390187-30390351	A549	lung:	n/a	chr15:30390267-30390288 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
47	CTCF	chr15:30395773-30395988	Kidney_OC	kidney:	n/a	chr15:30395870-30395886
48	CTCF	chr15:30390249-30390329	HUVEC	blood vessel:	n/a	chr15:30390267-30390288 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
49	CTCF	chr15:30384995-30385056	A549	lung:	n/a	n/a
50	CTCF	chr15:30395960-30396110	HEK293	kidney:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:30396500-30396550	SK-N-MC	brain:	n/a
2	chr15:30396500-30396550	GM12892	blood:	n/a
3	chr15:30396500-30396550	NHDF-neo	bronchial:	n/a
4	chr15:30396500-30396550	AG10803	skin:	n/a
5	chr15:30396121-30396171	NB4	blood:	n/a
6	chr15:30396121-30396171	U87	brain:	n/a
7	chr15:30396500-30396550	PANC-1	pancreas:	n/a
8	chr15:30396121-30396171	SKMC	muscle:	n/a
9	chr15:30396500-30396550	Hela-S3	cervix:	n/a
10	chr15:30396500-30396550	CMK	blood:	n/a
11	chr15:30396121-30396171	SK-N-SH_RA	brain:	n/a
12	chr15:30396500-30396550	HRPEpiC	eye:	n/a
13	chr15:30396121-30396171	HRPEpiC	eye:	n/a
14	chr15:30396121-30396171	Hela-S3	cervix:	n/a
15	chr15:30396121-30396171	BJ	skin:	n/a
16	chr15:30396500-30396550	HEK293	kidney:	embryo
17	chr15:30396500-30396550	SK-N-SH_RA	brain:	n/a
18	chr15:30396121-30396171	BE2_C	brain:	n/a
19	chr15:30396500-30396550	IMR90	lung:	fetal
20	chr15:30396500-30396550	SKMC	muscle:	n/a
21	chr15:30396500-30396550	BJ	skin:	n/a
22	chr15:30396121-30396171	K562	blood:	n/a
23	chr15:30396500-30396550	HCT-116	colon:	n/a
24	chr15:30396500-30396550	NT2-D1	testis:	n/a
25	chr15:30396500-30396550	HL-60	blood:	n/a
26	chr15:30396500-30396550	HNPCEpiC	eye:	n/a
27	chr15:30396121-30396171	A549	lung:	n/a
28	chr15:30396500-30396550	U87	brain:	n/a
29	chr15:30396500-30396550	GM19239	blood:	n/a
30	chr15:30396121-30396171	HepG2	liver:	n/a
31	chr15:30396500-30396550	GM12878	blood:	n/a
32	chr15:30396500-30396550	PFSK-1	brain:	n/a
33	chr15:30396121-30396171	HRE	kidney:	n/a
34	chr15:30396500-30396550	AG09309	skin:	n/a
35	chr15:30396500-30396550	GM06990	blood:	n/a
36	chr15:30396121-30396171	HAEpiC	amniotic membrane:	n/a
37	chr15:30396121-30396171	NT2-D1	testis:	n/a
38	chr15:30396121-30396171	HIPEpiC	eye:	n/a
39	chr15:30396500-30396550	AG09319	gingival:	n/a
40	chr15:30396121-30396171	IMR90	lung:	fetal
41	chr15:30396121-30396171	HCT-116	colon:	n/a
42	chr15:30396500-30396550	Hepatocyte	liver:	n/a
43	chr15:30396121-30396171	LNCaP	prostate:	n/a
44	chr15:30396500-30396550	LNCaP	prostate:	n/a
45	chr15:30396500-30396550	AG04449	skin:	fetal
46	chr15:30396121-30396171	AoSMC	blood vessel:	n/a
47	chr15:30396121-30396171	HCPEpiC	choroid plexus:	n/a
48	chr15:30396121-30396171	SK-N-MC	brain:	n/a
49	chr15:30396121-30396171	HNPCEpiC	eye:	n/a
50	chr15:30396500-30396550	K562	blood:	n/a

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AC120045.3-4	chr15:30383854-30384132	NONHSAT041327

Variant related genes	Relation type
ENSG00000207432	TF binding region
RN7SL673P	TF binding region
ULK4P3	TF binding region
GOLGA8J	TF binding region
DNM1P28	TF binding region
ENSG00000221250	TF binding region
ENSG00000207432	CpG island
RN7SL673P	CpG island
ULK4P3	CpG island
GOLGA8J	CpG island
DNM1P28	CpG island
ENSG00000221250	CpG island

Extended variants
information (count: 89 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:89 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs530920917	chr15:30373047-30373048	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs551005884	chr15:30373055-30373056	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs138574025	chr15:30373066-30373067	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs149640352	chr15:30373097-30373098	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs547353780	chr15:30373107-30373108	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs567146289	chr15:30373151-30373152	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs536118001	chr15:30373152-30373153	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs184431443	chr15:30373178-30373179	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs189315853	chr15:30373181-30373182	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs181413366	chr15:30373190-30373191	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs371921268	chr15:30373192-30373193	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs144256530	chr15:30373204-30373205	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs74011042	chr15:30373225-30373226	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs533527053	chr15:30373226-30373227	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs141388496	chr15:30373234-30373235	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs7162296	chr15:30373242-30373243	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs542869079	chr15:30373244-30373245	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs184799336	chr15:30373257-30373258	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs7180120	chr15:30373287-30373288	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
20	rs7178171	chr15:30373297-30373298	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs201522049	chr15:30373309-30373310	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs576182300	chr15:30373325-30373326	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs544420510	chr15:30373349-30373350	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs564557858	chr15:30373353-30373354	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs561328777	chr15:30373404-30373405	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs540651448	chr15:30373447-30373448	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs199826827	chr15:30373464-30373465	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs560481729	chr15:30373473-30373474	Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs4441249	chr15:30373507-30373508	Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs565489656	chr15:30373521-30373522	Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs181499237	chr15:30373524-30373525	Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs7162482	chr15:30373531-30373532	Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs531922646	chr15:30373571-30373572	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs551094364	chr15:30373572-30373573	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs538935252	chr15:30374850-30374851	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs552494115	chr15:30374861-30374862	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs376192256	chr15:30374988-30374989	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs62016979	chr15:30375254-30375255	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs113205019	chr15:30375852-30375853	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs201354967	chr15:30380151-30380152	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs370864009	chr15:30380279-30380280	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs541634095	chr15:30380356-30380357	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs561289791	chr15:30380379-30380380	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs548375584	chr15:30380876-30380877	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs568116179	chr15:30380953-30380954	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs536801641	chr15:30381002-30381003	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs559438285	chr15:30382433-30382434	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs557597282	chr15:30383616-30383617	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs563984175	chr15:30383856-30383857	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
50	rs532949353	chr15:30383909-30383910	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a

Variant related diseases (count:144)

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
Autism	20531469	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
Autism	22543975	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
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD

Chromatin state (count:81 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30372600-30373600	Enhancers	Muscle Satellite Cultured Cells	--
2	chr15:30372800-30373400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr15:30372800-30373600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
4	chr15:30373200-30373400	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
5	chr15:30373200-30373400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:30373200-30373400	Enhancers	HSMMtube	muscle
7	chr15:30373200-30373400	Enhancers	Osteobl	bone
8	chr15:30395800-30396000	Active TSS	HMEC	breast
9	chr15:30395800-30396200	Active TSS	Primary neutrophils fromperipheralblood	blood
10	chr15:30395800-30396200	Active TSS	Primary B cells from peripheral blood	blood
11	chr15:30395800-30396200	Active TSS	Colonic Mucosa	Colon
12	chr15:30395800-30396200	Active TSS	Gastric	stomach
13	chr15:30395800-30396400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
14	chr15:30395800-30396400	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
15	chr15:30395800-30396400	Active TSS	HUES48 Cell Line	embryonic stem cell
16	chr15:30395800-30396400	Active TSS	Breast Myoepithelial Primary Cells	Breast
17	chr15:30395800-30396400	Active TSS	Muscle Satellite Cultured Cells	--
18	chr15:30395800-30396400	Active TSS	Cortex derived primary cultured neurospheres	brain
19	chr15:30395800-30396400	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
21	chr15:30395800-30396400	Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr15:30395800-30396400	Active TSS	Adipose Nuclei	Adipose
23	chr15:30395800-30396400	Active TSS	Esophagus	oesophagus
24	chr15:30395800-30396400	Active TSS	Fetal Brain Female	brain
25	chr15:30395800-30396400	Bivalent/Poised TSS	Fetal Stomach	stomach
26	chr15:30395800-30396400	Active TSS	Left Ventricle	heart
27	chr15:30395800-30396400	Active TSS	Rectal Mucosa Donor 31	rectum
28	chr15:30395800-30396400	Active TSS	Right Atrium	heart
29	chr15:30395800-30396400	Active TSS	Right Ventricle	heart
30	chr15:30395800-30396400	Active TSS	Thymus	Thymus
31	chr15:30395800-30396400	Active TSS	Spleen	Spleen
32	chr15:30395800-30396400	Active TSS	HepG2	liver
33	chr15:30395800-30396400	Active TSS	Monocytes-CD14+_RO01746	blood
34	chr15:30395800-30396600	Active TSS	H1 Cell Line	embryonic stem cell
35	chr15:30395800-30396600	Active TSS	HUES6 Cell Line	embryonic stem cell
36	chr15:30395800-30396600	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
37	chr15:30395800-30396600	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr15:30395800-30396600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
39	chr15:30395800-30396600	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr15:30395800-30396600	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr15:30395800-30396600	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr15:30395800-30396600	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
44	chr15:30395800-30396600	Active TSS	Pancreas	Pancrea
45	chr15:30395800-30396600	Active TSS	HUVEC	blood vessel
46	chr15:30395800-30396800	Active TSS	HUES64 Cell Line	embryonic stem cell
47	chr15:30395800-30396800	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:30396000-30396200	Bivalent/Poised TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
49	chr15:30396000-30396200	Active TSS	Primary Natural Killer cells fromperipheralblood	blood
50	chr15:30396000-30396200	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland

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