Variant report

Variant	nsv904336
Chromosome Location	chr15:72145937-72329906
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:455)
CpG islands
(count:61)
Chromatin interactive
region (count:52)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:455 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:72301633-72301833	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:72212595-72212649	K562	blood:	n/a	n/a
3	ARID3A	chr15:72254936-72255089	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:72283644-72283708	K562	blood:	n/a	n/a
5	ARID3A	chr15:72213921-72213933	K562	blood:	n/a	n/a
6	ATF2	chr15:72206368-72206921	GM12878	blood:	n/a	n/a
7	BACH1	chr15:72222151-72222156	K562	blood:	n/a	n/a
8	BATF	chr15:72172137-72172404	GM12878	blood:	n/a	n/a
9	BATF	chr15:72172158-72172394	GM12878	blood:	n/a	n/a
10	BATF	chr15:72206431-72206854	GM12878	blood:	n/a	chr15:72206656-72206667
11	BATF	chr15:72206435-72206822	GM12878	blood:	n/a	chr15:72206656-72206667
12	BATF	chr15:72166614-72167024	GM12878	blood:	n/a	n/a
13	BCL11A	chr15:72206377-72206869	GM12878	blood:	n/a	n/a
14	BCL11A	chr15:72232433-72232749	GM12878	blood:	n/a	chr15:72232503-72232512
15	BCL11A	chr15:72206400-72206839	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:72229896-72230301	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:72229951-72230355	GM12878	blood:	n/a	n/a
18	BCL3	chr15:72206413-72206809	GM12878	blood:	n/a	n/a
19	BHLHE40	chr15:72168244-72168288	GM12878	blood:	n/a	n/a
20	BHLHE40	chr15:72166665-72166809	GM12878	blood:	n/a	n/a
21	BHLHE40	chr15:72230009-72230471	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:72232438-72232555	GM12878	blood:	n/a	n/a
23	BHLHE40	chr15:72183574-72183575	K562	blood:	n/a	n/a
24	CBX3	chr15:72223707-72223865	K562	blood:	n/a	n/a
25	CEBPB	chr15:72243415-72243732	IMR90	lung:	n/a	chr15:72243539-72243551
26	CEBPB	chr15:72157924-72158099	K562	blood:	n/a	n/a
27	CEBPB	chr15:72228588-72228918	HepG2	liver:	n/a	chr15:72228745-72228756
28	CEBPB	chr15:72294733-72294775	A549	lung:	n/a	n/a
29	CEBPB	chr15:72228611-72228922	A549	lung:	n/a	chr15:72228745-72228756
30	CEBPB	chr15:72234477-72234640	HepG2	liver:	n/a	chr15:72234521-72234532
31	CEBPB	chr15:72273080-72273270	K562	blood:	n/a	n/a
32	CEBPB	chr15:72290617-72290786	A549	lung:	n/a	n/a
33	CEBPB	chr15:72229831-72229991	A549	lung:	n/a	chr15:72229885-72229896
34	CEBPB	chr15:72247752-72248035	IMR90	lung:	n/a	n/a
35	CEBPB	chr15:72307627-72307787	K562	blood:	n/a	n/a
36	CEBPB	chr15:72179288-72179290	A549	lung:	n/a	n/a
37	CEBPB	chr15:72229773-72230036	IMR90	lung:	n/a	chr15:72229885-72229896
38	CEBPB	chr15:72229819-72229998	HepG2	liver:	n/a	chr15:72229885-72229896
39	CHD1	chr15:72166676-72166792	GM12878	blood:	n/a	n/a
40	CREB1	chr15:72267886-72268367	ECC-1	luminal epithelium:	n/a	n/a
41	CTCF	chr15:72163938-72163954	MCF-7	breast:	n/a	n/a
42	CTCF	chr15:72192683-72192728	GM13977	blood:	n/a	n/a
43	CTCF	chr15:72268300-72268570	GM12864	blood:	n/a	n/a
44	CTCF	chr15:72301850-72301853	Kidney_OC	kidney:	n/a	n/a
45	CTCF	chr15:72233690-72233741	GM12891	blood:	n/a	n/a
46	CTCF	chr15:72264565-72264600	ProgFib	skin:	n/a	n/a
47	CTCF	chr15:72306200-72306350	GM12871	blood:	n/a	n/a
48	CTCF	chr15:72213308-72213341	GM20000	blood:	n/a	n/a
49	CTCF	chr15:72328880-72329030	MCF-7	breast:	n/a	n/a
50	CTCF	chr15:72218574-72218639	Fibrobl	skin:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:72178118-72178168	HRCEpiC	kidney:	n/a
2	chr15:72178118-72178168	HAEpiC	amniotic membrane:	n/a
3	chr15:72178118-72178168	PANC-1	pancreas:	n/a
4	chr15:72178118-72178168	NH-A	brain:	n/a
5	chr15:72178118-72178168	HIPEpiC	eye:	n/a
6	chr15:72178118-72178168	AG10803	skin:	n/a
7	chr15:72178118-72178168	H1-hESC	embryonic stem cell:	embryo
8	chr15:72178118-72178168	HCM	heart:	n/a
9	chr15:72178118-72178168	HepG2	liver:	n/a
10	chr15:72178118-72178168	ECC-1	luminal epithelium:	n/a
11	chr15:72178118-72178168	BE2_C	brain:	n/a
12	chr15:72178118-72178168	PFSK-1	brain:	n/a
13	chr15:72178118-72178168	GM12892	blood:	n/a
14	chr15:72178118-72178168	LNCaP	prostate:	n/a
15	chr15:72178118-72178168	SKMC	muscle:	n/a
16	chr15:72178118-72178168	NHBE	bronchial:	n/a
17	chr15:72178118-72178168	MCF10A-Er-Src	breast:	n/a
18	chr15:72178118-72178168	GM06990	blood:	n/a
19	chr15:72178118-72178168	Hela-S3	cervix:	n/a
20	chr15:72178118-72178168	HEEpiC	esophagus:	n/a
21	chr15:72178118-72178168	GM12878	blood:	n/a
22	chr15:72178118-72178168	ovcar-3	ovarian:	n/a
23	chr15:72178118-72178168	U87	brain:	n/a
24	chr15:72178118-72178168	NT2-D1	testis:	n/a
25	chr15:72178118-72178168	SK-N-SH_RA	brain:	n/a
26	chr15:72178118-72178168	K562	blood:	n/a
27	chr15:72178118-72178168	BJ	skin:	n/a
28	chr15:72178118-72178168	HUVEC	blood vessel:	n/a
29	chr15:72178118-72178168	HMEC	breast:	n/a
30	chr15:72178118-72178168	HPAEpiC	pulmonary alveolar:	n/a
31	chr15:72178118-72178168	AoSMC	blood vessel:	n/a
32	chr15:72178118-72178168	AG04450	lung:	fetal
33	chr15:72178118-72178168	SK-N-SH	brain:	n/a
34	chr15:72178118-72178168	SAEC	small airway:	n/a
35	chr15:72178118-72178168	AG09319	gingival:	n/a
36	chr15:72178118-72178168	Hepatocyte	liver:	n/a
37	chr15:72178118-72178168	T-47D	breast:	n/a
38	chr15:72178118-72178168	HRPEpiC	eye:	n/a
39	chr15:72178118-72178168	NB4	blood:	n/a
40	chr15:72178118-72178168	MCF-7	breast:	n/a
41	chr15:72178118-72178168	HCF	heart:	n/a
42	chr15:72178118-72178168	AG09309	skin:	n/a
43	chr15:72178118-72178168	IMR90	lung:	fetal
44	chr15:72178118-72178168	A549	lung:	n/a
45	chr15:72178118-72178168	CMK	blood:	n/a
46	chr15:72178118-72178168	HNPCEpiC	eye:	n/a
47	chr15:72178118-72178168	GM12891	blood:	n/a
48	chr15:72178118-72178168	Caco-2	colon:	n/a
49	chr15:72178118-72178168	HCT-116	colon:	n/a
50	chr15:72178118-72178168	ProgFib	skin:	n/a

(count:52 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:72204090..72205988-chr15:72208798..72210918,2	K562	blood:
2	chr15:72176973..72179854-chr15:72407858..72409826,2	MCF-7	breast:
3	chr15:72177869..72180074-chr15:72180572..72182469,2	MCF-7	breast:
4	chr15:72297045..72298608-chr15:72298736..72301156,2	MCF-7	breast:
5	chr15:72324783..72327632-chr15:72328181..72330697,2	MCF-7	breast:
6	chr15:72173982..72176259-chr15:72181202..72184060,3	K562	blood:
7	chr15:72190232..72191910-chr15:72203994..72206448,2	MCF-7	breast:
8	chr15:72262124..72264073-chr15:72266768..72269290,2	K562	blood:
9	chr15:72262884..72265663-chr15:72272089..72274316,2	K562	blood:
10	chr15:72284044..72286331-chr15:72302500..72304124,2	K562	blood:
11	chr15:72297045..72298608-chr15:72298736..72301156,2	MCF-7	breast:
12	chr15:72229730..72230693-chr8:133827437..133828301,2	MCF-7	breast:
13	chr15:72251993..72253607-chr15:72256657..72258901,2	K562	blood:
14	chr15:72262124..72264016-chr15:72266000..72268268,2	K562	blood:
15	chr15:72168681..72170784-chr15:72179926..72181699,2	MCF-7	breast:
16	chr15:72324783..72327632-chr15:72328181..72330697,2	MCF-7	breast:
17	chr15:72132772..72134478-chr15:72147156..72150104,2	MCF-7	breast:
18	chr15:72274005..72275804-chr15:72283955..72286549,2	MCF-7	breast:
19	chr15:72274005..72275804-chr15:72283955..72286549,2	MCF-7	breast:
20	chr15:72318371..72321046-chr15:72324463..72327168,2	K562	blood:
21	chr15:72204090..72205988-chr15:72208798..72210918,2	K562	blood:
22	chr15:72197435..72199145-chr15:72206196..72207927,2	K562	blood:
23	chr15:72287720..72291695-chr15:72296118..72297805,3	MCF-7	breast:
24	chr15:72183241..72185017-chr15:72188166..72190098,2	MCF-7	breast:
25	chr15:72225351..72227489-chr15:72231458..72233712,2	K562	blood:
26	chr15:72282427..72284925-chr15:72286751..72289211,2	K562	blood:
27	chr15:72282427..72284925-chr15:72286751..72289211,2	K562	blood:
28	chr15:72322441..72324750-chr15:72328303..72329981,2	MCF-7	breast:
29	chr15:72183241..72185017-chr15:72188166..72190098,2	MCF-7	breast:
30	chr15:72328208..72329058-chr5:83308083..83308842,2	MCF-7	breast:
31	chr15:72292779..72294305-chr15:72296375..72298824,2	K562	blood:
32	chr15:72173982..72176259-chr15:72181202..72184060,3	K562	blood:
33	chr15:72284044..72286331-chr15:72302500..72304124,2	K562	blood:
34	chr15:72225351..72227489-chr15:72231458..72233712,2	K562	blood:
35	chr15:72318371..72321046-chr15:72324463..72327168,2	K562	blood:
36	chr15:72180763..72183209-chr15:72189285..72191973,2	MCF-7	breast:
37	chr15:72249559..72254389-chr15:72257826..72261874,6	MCF-7	breast:
38	chr15:72296226..72298848-chr15:72307966..72310000,2	K562	blood:
39	chr15:72143069..72145942-chr15:72153528..72155127,2	K562	blood:
40	chr15:72197435..72199145-chr15:72206196..72207927,2	K562	blood:
41	chr15:72262124..72264073-chr15:72266768..72269290,2	K562	blood:
42	chr15:72292779..72294305-chr15:72296375..72298824,2	K562	blood:
43	chr15:72138309..72141068-chr15:72175580..72177408,2	MCF-7	breast:
44	chr15:72180763..72183209-chr15:72189285..72191973,2	MCF-7	breast:
45	chr15:72187197..72189830-chr15:72197152..72199761,2	K562	blood:
46	chr15:72322441..72324750-chr15:72328303..72329981,2	MCF-7	breast:
47	chr15:72287720..72291695-chr15:72296118..72297805,3	MCF-7	breast:
48	chr15:72296226..72298848-chr15:72307966..72310000,2	K562	blood:
49	chr15:72249559..72254389-chr15:72257826..72261874,6	MCF-7	breast:
50	chr15:72187197..72189830-chr15:72197152..72199761,2	K562	blood:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SENP8-1	chr15:72286034-72286129	ENSG00000261632.1
2	lnc-SENP8-1	chr15:72264547-72264658	ENSG00000261632.1
3	lnc-GRAMD2-4	chr15:72185803-72186119	NONHSAT047057
4	lnc-GRAMD2-4	chr15:72189802-72190154	NONHSAT047057
5	lnc-SENP8-1	chr15:72291354-72291421	ENSG00000261632.1
6	lnc-SENP8-1	chr15:72328856-72329030	ENSG00000261632.1

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	MYO9A	hsa-let-7c-5p	chr15:72183618-72183640

Variant related genes	Relation type
RNA5SP399	TF binding region
ENSG00000261632	TF binding region
MYO9A	TF binding region
RNA5SP399	CpG island
ENSG00000261632	CpG island
MYO9A	CpG island
ENSG00000166192	chromatin interactions
ENSG00000067225	chromatin interactions
ENSG00000066933	chromatin interactions
ENSG00000261632	chromatin interactions

Extended variants
information (count: 6280 )
Associated
traits (count: 81 )

Variant overlapped rSNPs/rCNVs (count:6280 , 50 per page) page: 1 2 3 4 5 6 7 ... 126

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs982752	chr15:72145937-72145938	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs114238755	chr15:72145971-72145972	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs560667089	chr15:72145993-72145994	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs114932023	chr15:72146043-72146044	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs35084706	chr15:72146061-72146062	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs576300417	chr15:72146119-72146120	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs543722618	chr15:72146127-72146128	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs543191614	chr15:72146171-72146172	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs565135567	chr15:72146175-72146176	Weak transcription Strong transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs74545441	chr15:72146257-72146258	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs143457272	chr15:72146267-72146268	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs559439935	chr15:72146300-72146301	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs530138763	chr15:72146351-72146352	Weak transcription Strong transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs113416873	chr15:72146396-72146397	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs570147266	chr15:72146410-72146411	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs369817600	chr15:72146420-72146421	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs191378072	chr15:72146423-72146424	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs571036525	chr15:72146470-72146471	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs371721298	chr15:72146478-72146479	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs137865547	chr15:72146497-72146498	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs28630701	chr15:72146534-72146535	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs565507322	chr15:72146559-72146560	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs148839084	chr15:72146562-72146563	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs557313234	chr15:72146584-72146585	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs535830873	chr15:72146589-72146590	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs34791308	chr15:72146622-72146623	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs115844073	chr15:72146661-72146662	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372093588	chr15:72146703-72146704	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs145718155	chr15:72146728-72146729	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs376947878	chr15:72146735-72146736	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs543154074	chr15:72146801-72146802	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs148948301	chr15:72146816-72146817	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs372047607	chr15:72146827-72146828	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs369446662	chr15:72146841-72146842	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs200455358	chr15:72146844-72146845	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs143713074	chr15:72146846-72146847	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs148236635	chr15:72146865-72146866	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs146161400	chr15:72146915-72146916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs369955315	chr15:72146943-72146944	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs575792399	chr15:72146959-72146960	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs559614265	chr15:72146960-72146961	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs539773367	chr15:72146962-72146963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530049811	chr15:72146976-72146977	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs542219731	chr15:72146991-72146992	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs563717213	chr15:72147021-72147022	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs531013897	chr15:72147026-72147027	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2306579	chr15:72147033-72147034	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs369390837	chr15:72147036-72147037	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs570931554	chr15:72147096-72147097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs528701693	chr15:72147160-72147161	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:81)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Melanoma	18172304	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
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
Autism	20678247	CNVD
Retinoblastoma	21504564	CNVD
Matthew-Wood syndrome	21085971	CNVD
Myelofibrosis	22110671	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Urothelial cell carcinoma	18451213	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Mental retardation	17621639	CNVD
Autism	20808228	CNVD
Breast cancer	21364760	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Urothelial carcinoma	21177765	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD
Melanoma	20877625	CNVD
Epilepsy	22083797	CNVD

Chromatin state (count:2732 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:72114600-72190600	Weak transcription	Pancreas	Pancrea
2	chr15:72115800-72147000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr15:72116400-72147000	Weak transcription	Pancreatic Islets	Pancreatic Islet
4	chr15:72119200-72171800	Weak transcription	Psoas Muscle	Psoas
5	chr15:72120600-72147400	Weak transcription	Small Intestine	intestine
6	chr15:72122200-72189400	Weak transcription	Right Ventricle	heart
7	chr15:72122400-72195000	Weak transcription	NHEK	skin
8	chr15:72122600-72171800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
9	chr15:72122600-72185200	Weak transcription	Esophagus	oesophagus
10	chr15:72122600-72195800	Weak transcription	Gastric	stomach
11	chr15:72129200-72148000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
12	chr15:72131200-72148200	Strong transcription	Placenta	Placenta
13	chr15:72131600-72147000	Strong transcription	Fetal Muscle Leg	muscle
14	chr15:72131800-72192800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr15:72134000-72149000	Strong transcription	Breast Myoepithelial Primary Cells	Breast
16	chr15:72135200-72146600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
17	chr15:72135200-72147600	Strong transcription	Primary T cells from cord blood	blood
18	chr15:72136200-72148400	Strong transcription	Primary B cells from peripheral blood	blood
19	chr15:72136200-72148400	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr15:72136200-72149000	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr15:72136400-72147000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
22	chr15:72136400-72147000	Strong transcription	Adipose Nuclei	Adipose
23	chr15:72136400-72148400	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
24	chr15:72136600-72146600	Strong transcription	Fetal Muscle Trunk	muscle
25	chr15:72136800-72146400	Strong transcription	Duodenum Smooth Muscle	Duodenum
26	chr15:72136800-72146400	Strong transcription	Monocytes-CD14+_RO01746	blood
27	chr15:72136800-72147000	Strong transcription	Primary B cells from cord blood	blood
28	chr15:72137000-72156400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
29	chr15:72137800-72146000	Strong transcription	Fetal Lung	lung
30	chr15:72137800-72147000	Strong transcription	Stomach Smooth Muscle	stomach
31	chr15:72138200-72146200	Strong transcription	Primary T helper cells PMA-I stimulated	--
32	chr15:72138200-72172400	Weak transcription	HUVEC	blood vessel
33	chr15:72138400-72146200	Strong transcription	Sigmoid Colon	Sigmoid Colon
34	chr15:72138400-72146200	Strong transcription	Skeletal Muscle Female	skeletal muscle
35	chr15:72138400-72146400	Strong transcription	Skeletal Muscle Male	skeletal muscle
36	chr15:72138400-72146600	Strong transcription	Primary T helper cells fromperipheralblood	blood
37	chr15:72138400-72147000	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr15:72138600-72146200	Strong transcription	Left Ventricle	heart
39	chr15:72138600-72147000	Strong transcription	Liver	Liver
40	chr15:72138800-72146200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr15:72138800-72146800	Weak transcription	K562	blood
42	chr15:72139600-72146400	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr15:72139600-72146800	Strong transcription	Duodenum Mucosa	Duodenum
44	chr15:72140200-72171800	Weak transcription	HMEC	breast
45	chr15:72141200-72146400	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
46	chr15:72141400-72174200	Weak transcription	Fetal Brain Male	brain
47	chr15:72141600-72147000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr15:72142000-72146400	Strong transcription	Rectal Mucosa Donor 31	rectum
49	chr15:72142600-72150800	Weak transcription	HSMM	muscle
50	chr15:72142600-72151200	Weak transcription	HSMMtube	muscle

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