Variant report

Variant	esv1822745
Chromosome Location	chr15:30358034-30399178
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	chr15:30389882-30390529	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
7	CTCF	chr15:30367585-30367786	Kidney_OC	kidney:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
8	CTCF	chr15:30395806-30395979	GM20000	blood:	n/a	chr15:30395870-30395886
9	CTCF	chr15:30367620-30367770	BJ	skin:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
10	CTCF	chr15:30367600-30367750	HRPEpiC	eye:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
11	CTCF	chr15:30396000-30396150	GM12874	blood:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
12	CTCF	chr15:30367573-30367701	GM19238	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
13	CTCF	chr15:30395980-30396130	HepG2	liver:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
14	CTCF	chr15:30396000-30396150	HCPEpiC	choroid plexus:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
15	CTCF	chr15:30396056-30396069	K562	blood:	n/a	n/a
16	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
17	CTCF	chr15:30367620-30367770	NHDF-neo	bronchial:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
18	CTCF	chr15:30395980-30396130	AG09319	gingival:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
19	CTCF	chr15:30367660-30367810	K562	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
20	CTCF	chr15:30395980-30396130	WI-38	lung:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
21	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
22	CTCF	chr15:30395960-30396110	HA-sp	spinal cord:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
23	CTCF	chr15:30367560-30367710	HEK293	kidney:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
24	CTCF	chr15:30367545-30367777	Lung_OC	lung:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
25	CTCF	chr15:30367660-30367810	GM12872	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
26	CTCF	chr15:30367574-30367831	Pancreas_OC	pancreas:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
27	CTCF	chr15:30367600-30367750	HPAF	blood vessel:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
28	CTCF	chr15:30367600-30367750	WI-38	lung:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
29	CTCF	chr15:30385019-30385025	K562	blood:	n/a	n/a
30	CTCF	chr15:30367660-30367810	GM12873	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
31	CTCF	chr15:30393368-30393389	Lung_OC	lung:	n/a	n/a
32	CTCF	chr15:30390118-30390414	Spleen_OC	spleen:	n/a	chr15:30390267-30390288 chr15:30390197-30390206 chr15:30390275-30390285 chr15:30390274-30390287 chr15:30390272-30390290 chr15:30390273-30390289 chr15:30390278-30390287
33	CTCF	chr15:30367600-30367750	HMF	breast:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
34	CTCF	chr15:30367560-30367710	GM12865	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
35	CTCF	chr15:30367475-30367871	GM12878	blood:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
36	CTCF	chr15:30367600-30367750	HCPEpiC	choroid plexus:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
37	CTCF	chr15:30389874-30390463	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
38	CTCF	chr15:30367620-30367770	Caco-2	colon:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
39	CTCF	chr15:30383204-30383524	K562	blood:	n/a	chr15:30383403-30383411 chr15:30383400-30383418
40	CTCF	chr15:30396000-30396150	AG09319	gingival:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
41	CTCF	chr15:30367620-30367770	HPAF	blood vessel:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
42	CTCF	chr15:30367620-30367770	AG04449	skin:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
43	CTCF	chr15:30367620-30367770	AG09309	skin:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
44	CTCF	chr15:30367600-30367750	AoAF	blood vessel:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
45	CTCF	chr15:30367600-30367750	NHDF-neo	bronchial:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
46	CTCF	chr15:30367560-30367710	HCPEpiC	choroid plexus:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
47	CTCF	chr15:30396000-30396150	SK-N-SH_RA	brain:	n/a	chr15:30396032-30396041 chr15:30396083-30396096 chr15:30396028-30396041 chr15:30396028-30396041
48	CTCF	chr15:30367162-30368039	SK-N-SH	brain:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
49	CTCF	chr15:30367620-30367770	HRPEpiC	eye:	n/a	chr15:30367671-30367687 chr15:30367665-30367686 chr15:30367670-30367688
50	CTCF	chr15:30396000-30396150	GM12875	blood:	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	K562	blood:	n/a
2	chr15:30396121-30396171	NHBE	bronchial:	n/a
3	chr15:30396121-30396171	GM12891	blood:	n/a
4	chr15:30365409-30365459	PANC-1	pancreas:	n/a
5	chr15:30396121-30396171	HIPEpiC	eye:	n/a
6	chr15:30396500-30396550	BE2_C	brain:	n/a
7	chr15:30366335-30366385	AG04450	lung:	fetal
8	chr15:30396500-30396550	HRE	kidney:	n/a
9	chr15:30366335-30366385	HRCEpiC	kidney:	n/a
10	chr15:30366335-30366385	CMK	blood:	n/a
11	chr15:30396121-30396171	HRCEpiC	kidney:	n/a
12	chr15:30396500-30396550	ECC-1	luminal epithelium:	n/a
13	chr15:30366335-30366385	HEEpiC	esophagus:	n/a
14	chr15:30396121-30396171	PFSK-1	brain:	n/a
15	chr15:30366335-30366385	RPTEC	kidney:	n/a
16	chr15:30365409-30365459	HPAEpiC	pulmonary alveolar:	n/a
17	chr15:30396121-30396171	AG09309	skin:	n/a
18	chr15:30365409-30365459	HepG2	liver:	n/a
19	chr15:30396500-30396550	GM12892	blood:	n/a
20	chr15:30396121-30396171	GM12892	blood:	n/a
21	chr15:30396121-30396171	AG04449	skin:	fetal
22	chr15:30366335-30366385	Hela-S3	cervix:	n/a
23	chr15:30396121-30396171	RPTEC	kidney:	n/a
24	chr15:30366335-30366385	HUVEC	blood vessel:	n/a
25	chr15:30365409-30365459	HRPEpiC	eye:	n/a
26	chr15:30365409-30365459	AG10803	skin:	n/a
27	chr15:30365409-30365459	BJ	skin:	n/a
28	chr15:30396500-30396550	IMR90	lung:	fetal
29	chr15:30365409-30365459	HRE	kidney:	n/a
30	chr15:30366335-30366385	NHDF-neo	bronchial:	n/a
31	chr15:30396500-30396550	U87	brain:	n/a
32	chr15:30396500-30396550	PrEC	prostate:	n/a
33	chr15:30365409-30365459	HMEC	breast:	n/a
34	chr15:30366335-30366385	NH-A	brain:	n/a
35	chr15:30366335-30366385	HNPCEpiC	eye:	n/a
36	chr15:30396121-30396171	SK-N-MC	brain:	n/a
37	chr15:30366335-30366385	GM12878	blood:	n/a
38	chr15:30366335-30366385	BE2_C	brain:	n/a
39	chr15:30396121-30396171	HNPCEpiC	eye:	n/a
40	chr15:30365409-30365459	HCPEpiC	choroid plexus:	n/a
41	chr15:30366335-30366385	Caco-2	colon:	n/a
42	chr15:30396121-30396171	HEEpiC	esophagus:	n/a
43	chr15:30396500-30396550	A549	lung:	n/a
44	chr15:30365409-30365459	NH-A	brain:	n/a
45	chr15:30365409-30365459	Hela-S3	cervix:	n/a
46	chr15:30366335-30366385	HCM	heart:	n/a
47	chr15:30366335-30366385	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:30365409-30365459	PrEC	prostate:	n/a
49	chr15:30365409-30365459	NT2-D1	testis:	n/a
50	chr15:30396500-30396550	SK-N-SH_RA	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:29959926..29960944-chr15:30367131..30368208,4	K562	blood:
2	chr15:30039724..30040629-chr15:30367249..30368123,2	K562	blood:
3	chr15:30359405..30361703-chr15:30365403..30368382,2	MCF-7	breast:
4	chr15:30359405..30361703-chr15:30365403..30368382,2	MCF-7	breast:
5	chr15:30233133..30233805-chr15:30367233..30367920,2	MCF-7	breast:

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

Variant related genes	Relation type
ULK4P3	TF binding region
ENSG00000221250	TF binding region
RN7SL673P	TF binding region
ENSG00000229389	TF binding region
GOLGA8J	TF binding region
DNM1P28	TF binding region
ULK4P3	CpG island
ENSG00000221250	CpG island
RN7SL673P	CpG island
ENSG00000229389	CpG island
GOLGA8J	CpG island
DNM1P28	CpG island

Extended variants
information (count: 661 )
Associated
traits (count: 144 )

Variant overlapped rSNPs/rCNVs (count:661 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561788534	chr15:30358037-30358038	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs143650807	chr15:30358044-30358045	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs550681119	chr15:30358097-30358098	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs570503697	chr15:30358102-30358103	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs375016568	chr15:30358116-30358117	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs564402482	chr15:30358192-30358193	Weak transcription Flanking Active TSS Enhancers Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs528741984	chr15:30358274-30358275	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs547510592	chr15:30358320-30358321	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs117649799	chr15:30358323-30358324	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs8034350	chr15:30358337-30358338	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs11855254	chr15:30358339-30358340	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs529791282	chr15:30358358-30358359	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs11855283	chr15:30358363-30358364	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs568692310	chr15:30358410-30358411	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs8039415	chr15:30358426-30358427	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs557029708	chr15:30358456-30358457	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs141345026	chr15:30358467-30358468	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs539777606	chr15:30358510-30358511	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs36032883	chr15:30358517-30358518	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185263258	chr15:30358610-30358611	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs553404504	chr15:30358632-30358633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs573454667	chr15:30358647-30358648	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs150729488	chr15:30358649-30358650	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs562302830	chr15:30358656-30358657	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575899156	chr15:30358687-30358688	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139045660	chr15:30358809-30358810	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564125307	chr15:30358823-30358824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532801601	chr15:30358827-30358828	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs546542995	chr15:30358874-30358875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs149445500	chr15:30358903-30358904	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs9673078	chr15:30358915-30358916	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548853764	chr15:30358916-30358917	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs568755688	chr15:30358979-30358980	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs537600549	chr15:30359140-30359141	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs62016974	chr15:30359224-30359225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs200930986	chr15:30359230-30359231	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs62016975	chr15:30359329-30359330	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs550669149	chr15:30359376-30359377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs570889088	chr15:30359377-30359378	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs539470342	chr15:30359386-30359387	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs553359782	chr15:30359501-30359502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs573139188	chr15:30359532-30359533	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs536186032	chr15:30359638-30359639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs556093923	chr15:30359796-30359797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs575913752	chr15:30359802-30359803	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs565819976	chr15:30359843-30359844	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs544776795	chr15:30359849-30359850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs564187054	chr15:30359851-30359852	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs369772411	chr15:30359886-30359887	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs529760987	chr15:30359887-30359888	Weak transcription	n/a	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:175 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:30355000-30358200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
2	chr15:30355000-30358200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
3	chr15:30355200-30358200	Enhancers	Brain Substantia Nigra	brain
4	chr15:30355400-30358200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr15:30355800-30358200	Enhancers	Adipose Nuclei	Adipose
6	chr15:30357000-30358200	Flanking Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
7	chr15:30357200-30358200	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
8	chr15:30357200-30358200	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
9	chr15:30357200-30358200	Enhancers	Rectal Smooth Muscle	rectum
10	chr15:30357400-30358200	Enhancers	Liver	Liver
11	chr15:30357400-30358200	Active TSS	Brain Anterior Caudate	brain
12	chr15:30357400-30360000	Weak transcription	Right Atrium	heart
13	chr15:30357400-30360200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr15:30357400-30364000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
15	chr15:30357600-30358200	Flanking Active TSS	Brain Hippocampus Middle	brain
16	chr15:30357800-30358200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
17	chr15:30357800-30358200	Flanking Active TSS	Brain Angular Gyrus	brain
18	chr15:30357800-30358200	Enhancers	Stomach Smooth Muscle	stomach
19	chr15:30357800-30358200	Enhancers	Hela-S3	cervix
20	chr15:30357800-30358200	Flanking Active TSS	HSMM	muscle
21	chr15:30357800-30358200	Flanking Active TSS	HSMMtube	muscle
22	chr15:30358000-30358200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:30358000-30358200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:30358000-30358200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
25	chr15:30358000-30358200	Enhancers	A549	lung
26	chr15:30358000-30358200	Enhancers	NH-A	brain
27	chr15:30358000-30358200	Enhancers	NHEK	skin
28	chr15:30358000-30358200	Enhancers	Osteobl	bone
29	chr15:30358000-30358400	Enhancers	Muscle Satellite Cultured Cells	--
30	chr15:30358000-30359000	Weak transcription	Brain Cingulate Gyrus	brain
31	chr15:30358200-30358400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
32	chr15:30358200-30358400	Enhancers	HSMM	muscle
33	chr15:30358200-30358400	Enhancers	HSMMtube	muscle
34	chr15:30358200-30360200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
35	chr15:30358200-30367200	Weak transcription	Brain Anterior Caudate	brain
36	chr15:30358400-30360000	Weak transcription	HSMM	muscle
37	chr15:30358400-30360200	Weak transcription	Muscle Satellite Cultured Cells	--
38	chr15:30358400-30360200	Weak transcription	HSMMtube	muscle
39	chr15:30360000-30361200	Enhancers	HSMM	muscle
40	chr15:30360200-30360400	Enhancers	Muscle Satellite Cultured Cells	--
41	chr15:30360200-30360400	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr15:30360200-30360400	Enhancers	HSMMtube	muscle
43	chr15:30360200-30361000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
44	chr15:30360400-30364800	Weak transcription	HSMMtube	muscle
45	chr15:30360600-30360800	Active TSS	H9 Cell Line	embryonic stem cell
46	chr15:30360800-30361000	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
47	chr15:30360800-30361200	Enhancers	H1 Cell Line	embryonic stem cell
48	chr15:30361200-30364000	Weak transcription	HSMM	muscle
49	chr15:30361600-30362600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr15:30362800-30364800	Weak transcription	Brain Cingulate Gyrus	brain

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