Variant report

Variant	nsv904417
Chromosome Location	chr15:77851535-77935992
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2130)
CpG islands
(count:2445)
Chromatin interactive
region (count:147)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2130 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:77926765-77927030	K562	blood:	n/a	n/a
2	ARID3A	chr15:77912745-77912914	K562	blood:	n/a	n/a
3	ARID3A	chr15:77861390-77861782	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:77925899-77926076	K562	blood:	n/a	n/a
5	ARID3A	chr15:77915025-77915043	K562	blood:	n/a	n/a
6	ATF2	chr15:77925762-77927046	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:77915941-77916411	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr15:77915698-77916516	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF2	chr15:77925461-77927008	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF3	chr15:77885188-77885374	K562	blood:	n/a	n/a
11	ATF3	chr15:77925857-77926179	GM12878	blood:	n/a	n/a
12	ATF3	chr15:77925817-77926099	H1-hESC	embryonic stem cell:	n/a	n/a
13	ATF3	chr15:77925732-77926191	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF3	chr15:77892250-77892522	K562	blood:	n/a	n/a
15	ATF3	chr15:77925754-77926241	A549	lung:	n/a	n/a
16	ATF3	chr15:77925816-77926085	K562	blood:	n/a	n/a
17	BACH1	chr15:77897153-77897255	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:77926761-77927026	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:77925619-77926520	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr15:77915577-77915777	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr15:77899147-77899415	H1-hESC	embryonic stem cell:	n/a	n/a
22	BCL3	chr15:77925412-77926262	A549	lung:	n/a	chr15:77925420-77925433
23	BCLAF1	chr15:77925737-77926107	GM12878	blood:	n/a	n/a
24	BCLAF1	chr15:77925756-77926123	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:77869841-77869966	K562	blood:	n/a	n/a
26	BHLHE40	chr15:77901103-77901302	K562	blood:	n/a	n/a
27	BHLHE40	chr15:77876682-77876905	K562	blood:	n/a	n/a
28	BHLHE40	chr15:77925834-77926167	GM12878	blood:	n/a	n/a
29	BHLHE40	chr15:77912708-77912955	K562	blood:	n/a	n/a
30	BHLHE40	chr15:77925559-77926179	K562	blood:	n/a	n/a
31	BHLHE40	chr15:77926780-77927016	K562	blood:	n/a	n/a
32	BHLHE40	chr15:77899292-77899363	K562	blood:	n/a	n/a
33	BHLHE40	chr15:77914524-77915734	K562	blood:	n/a	n/a
34	BHLHE40	chr15:77922594-77922636	K562	blood:	n/a	n/a
35	BHLHE40	chr15:77904325-77904461	K562	blood:	n/a	n/a
36	BRCA1	chr15:77925788-77926457	H1-hESC	embryonic stem cell:	n/a	n/a
37	BRCA1	chr15:77925929-77926145	GM12878	blood:	n/a	n/a
38	BRCA1	chr15:77925889-77926125	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr15:77915330-77915744	K562	blood:	n/a	n/a
40	CBX3	chr15:77892090-77892627	K562	blood:	n/a	n/a
41	CBX3	chr15:77913865-77914196	K562	blood:	n/a	n/a
42	CBX3	chr15:77897291-77897710	K562	blood:	n/a	n/a
43	CBX3	chr15:77926671-77927062	K562	blood:	n/a	n/a
44	CBX3	chr15:77916009-77916436	K562	blood:	n/a	n/a
45	CBX3	chr15:77925518-77926182	K562	blood:	n/a	n/a
46	CBX3	chr15:77912604-77913108	K562	blood:	n/a	n/a
47	CBX3	chr15:77914464-77915225	K562	blood:	n/a	n/a
48	CCNT2	chr15:77915680-77916061	K562	blood:	n/a	chr15:77915777-77915797 chr15:77916007-77916016
49	CCNT2	chr15:77914800-77915263	K562	blood:	n/a	n/a
50	CCNT2	chr15:77925101-77926149	K562	blood:	n/a	chr15:77925365-77925374

(count:2445 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:77910606-77910656	AG09309	skin:	n/a
2	chr15:77927361-77927411	HAEpiC	amniotic membrane:	n/a
3	chr15:77900788-77900838	AG10803	skin:	n/a
4	chr15:77925960-77926010	HCM	heart:	n/a
5	chr15:77935488-77935538	GM12892	blood:	n/a
6	chr15:77910606-77910656	AG09309	skin:	n/a
7	chr15:77927361-77927411	HAEpiC	amniotic membrane:	n/a
8	chr15:77900788-77900838	AG10803	skin:	n/a
9	chr15:77925960-77926010	HCM	heart:	n/a
10	chr15:77935488-77935538	GM12892	blood:	n/a
11	chr15:77857909-77857959	GM19239	blood:	n/a
12	chr15:77910606-77910656	RPTEC	kidney:	n/a
13	chr15:77889974-77890024	K562	blood:	n/a
14	chr15:77915770-77915820	ECC-1	luminal epithelium:	n/a
15	chr15:77927305-77927355	HMEC	breast:	n/a
16	chr15:77907530-77907580	SKMC	muscle:	n/a
17	chr15:77927305-77927355	AG10803	skin:	n/a
18	chr15:77925960-77926010	A549	lung:	n/a
19	chr15:77906127-77906177	SK-N-MC	brain:	n/a
20	chr15:77922677-77922727	BE2_C	brain:	n/a
21	chr15:77897134-77897184	NB4	blood:	n/a
22	chr15:77927305-77927355	PANC-1	pancreas:	n/a
23	chr15:77900788-77900838	SK-N-MC	brain:	n/a
24	chr15:77889974-77890024	Hela-S3	cervix:	n/a
25	chr15:77889974-77890024	T-47D	breast:	n/a
26	chr15:77857909-77857959	IMR90	lung:	fetal
27	chr15:77852897-77852947	HIPEpiC	eye:	n/a
28	chr15:77935488-77935538	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:77927305-77927355	HIPEpiC	eye:	n/a
30	chr15:77925892-77925942	U87	brain:	n/a
31	chr15:77928919-77928969	HNPCEpiC	eye:	n/a
32	chr15:77925960-77926010	HCF	heart:	n/a
33	chr15:77908135-77908185	SK-N-MC	brain:	n/a
34	chr15:77925892-77925942	HL-60	blood:	n/a
35	chr15:77898183-77898233	HCT-116	colon:	n/a
36	chr15:77908222-77908272	HCM	heart:	n/a
37	chr15:77896785-77896835	LNCaP	prostate:	n/a
38	chr15:77862098-77862148	Hela-S3	cervix:	n/a
39	chr15:77933785-77933835	HMEC	breast:	n/a
40	chr15:77862098-77862148	AG10803	skin:	n/a
41	chr15:77908135-77908185	AG09309	skin:	n/a
42	chr15:77900788-77900838	HCM	heart:	n/a
43	chr15:77908222-77908272	BE2_C	brain:	n/a
44	chr15:77922163-77922213	HCPEpiC	choroid plexus:	n/a
45	chr15:77925892-77925942	IMR90	lung:	fetal
46	chr15:77889974-77890024	HMEC	breast:	n/a
47	chr15:77857909-77857959	ECC-1	luminal epithelium:	n/a
48	chr15:77876657-77876707	GM19239	blood:	n/a
49	chr15:77906127-77906177	PANC-1	pancreas:	n/a
50	chr15:77889974-77890024	IMR90	lung:	fetal

(count:147 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:77410865..77411747-chr15:77876252..77877201,2	MCF-7	breast:
2	chr15:77912184..77913186-chr15:77925455..77926450,5	K562	blood:
3	chr15:77898597..77902901-chr15:77907031..77910421,4	K562	blood:
4	chr15:77912527..77913180-chr15:77925436..77926049,2	MCF-7	breast:
5	chr15:77924201..77925801-chr15:77929261..77931789,2	K562	blood:
6	chr15:77866782..77869407-chr15:77890484..77892735,2	MCF-7	breast:
7	chr15:77864365..77867025-chr15:77869640..77872108,2	MCF-7	breast:
8	chr15:77316379..77317255-chr15:77925626..77926458,2	MCF-7	breast:
9	chr15:77927989..77932022-chr15:77933693..77937176,6	K562	blood:
10	chr15:77888337..77891310-chr15:77900138..77902706,2	MCF-7	breast:
11	chr15:77904241..77907935-chr15:77912354..77915026,5	K562	blood:
12	chr15:77861324..77862294-chr15:77925777..77926357,2	K562	blood:
13	chr15:77925887..77926426-chr19:40734602..40735348,2	MCF-7	breast:
14	chr15:77876287..77878594-chr15:77925145..77926985,3	K562	blood:
15	chr15:77912184..77913186-chr15:77925455..77926450,5	K562	blood:
16	chr15:77884788..77887533-chr15:77890079..77892791,3	K562	blood:
17	chr15:77848438..77851266-chr15:77854844..77857960,3	MCF-7	breast:
18	chr15:77899424..77903075-chr15:77914224..77917029,3	K562	blood:
19	chr15:77925603..77926173-chr15:77946987..77947667,2	MCF-7	breast:
20	chr15:77899584..77901870-chr15:77910990..77913716,3	K562	blood:
21	chr15:77862030..77863568-chr15:77895689..77897664,2	MCF-7	breast:
22	chr15:77879443..77881773-chr15:77883698..77885210,2	K562	blood:
23	chr15:77894564..77896146-chr15:77898435..77900182,2	K562	blood:
24	chr15:77883341..77886336-chr15:77886431..77889031,3	MCF-7	breast:
25	chr15:77925435..77927439-chr15:78112259..78115090,22	K562	blood:
26	chr15:77925387..77926440-chr15:77951721..77952677,7	MCF-7	breast:
27	chr15:77908642..77910166-chr15:77913466..77916078,2	MCF-7	breast:
28	chr15:77478486..77479274-chr15:77925458..77926114,2	MCF-7	breast:
29	chr15:77478624..77479221-chr15:77923075..77923905,2	MCF-7	breast:
30	chr15:77839369..77839946-chr15:77923059..77923563,2	MCF-7	breast:
31	chr15:77922761..77925687-chr15:77933695..77936379,3	K562	blood:
32	chr15:77879891..77882724-chr15:77887714..77890230,2	K562	blood:
33	chr15:77884388..77887095-chr15:77890695..77892603,2	K562	blood:
34	chr15:77872896..77874517-chr15:77881445..77883437,2	K562	blood:
35	chr15:77925519..77926294-chr15:78162494..78163468,3	MCF-7	breast:
36	chr15:77925299..77927652-chr15:78112444..78114100,3	MCF-7	breast:
37	chr15:77835672..77836457-chr15:77876317..77877245,2	MCF-7	breast:
38	chr15:77856989..77859495-chr15:77861940..77865382,3	K562	blood:
39	chr15:77852881..77857213-chr15:77858380..77864202,5	K562	blood:
40	chr15:77884788..77887533-chr15:77890079..77892791,3	K562	blood:
41	chr15:77902198..77904238-chr15:77912623..77914841,2	K562	blood:
42	chr15:77879443..77881773-chr15:77883698..77885210,2	K562	blood:
43	chr15:77848268..77851249-chr15:77883793..77885346,2	MCF-7	breast:
44	chr15:77898597..77902901-chr15:77907031..77910421,4	K562	blood:
45	chr15:77904241..77907935-chr15:77912354..77915026,5	K562	blood:
46	chr15:77903485..77904267-chr15:77926396..77927267,2	MCF-7	breast:
47	chr15:77839042..77839906-chr15:77876314..77877043,2	MCF-7	breast:
48	chr15:77835573..77836399-chr15:77908014..77909056,3	MCF-7	breast:
49	chr15:77899424..77903075-chr15:77914224..77917029,3	K562	blood:
50	chr15:77835734..77836523-chr15:77909574..77910418,2	MCF-7	breast:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-HMG20A-2	chr15:77864907-77865081	ENSG00000259420.1
2	lnc-HMG20A-3	chr15:77934106-77934299	NR_045123
3	lnc-HMG20A-2	chr15:77900882-77901023	ENSG00000259420.1
4	lnc-HMG20A-2	chr15:77864907-77865206	ENSG00000259420.1
5	lnc-HMG20A-2	chr15:77864593-77864787	ENSG00000259420.1
6	lnc-HMG20A-2	chr15:77864593-77864787	ENSG00000259420.1
7	lnc-HMG20A-2	chr15:77861312-77861518	ENSG00000259420.1
8	lnc-HMG20A-3	chr15:77934106-77934299	ENSG00000259666.1
9	lnc-HMG20A-3	chr15:77934106-77934299	ENSG00000249469
10	lnc-HMG20A-2	chr15:77861312-77861518	ENSG00000259420.1

No data

Variant related genes	Relation type
ENSG00000259666	TF binding region
ENSG00000259420	TF binding region
LINGO1	TF binding region
ENSG00000259666	CpG island
ENSG00000259420	CpG island
LINGO1	CpG island
ENSG00000169783	chromatin interactions
ENSG00000259281	chromatin interactions
ENSG00000259666	chromatin interactions
ENSG00000259420	chromatin interactions
DDX3X	miRNA target sites

Extended variants
information (count: 3476 )
Associated
traits (count: 53 )

Variant overlapped rSNPs/rCNVs (count:3476 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2137111	chr15:77851535-77851536	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs571868998	chr15:77851548-77851549	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs532493949	chr15:77851557-77851558	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs146155539	chr15:77851560-77851561	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs191589580	chr15:77851659-77851660	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139100256	chr15:77851673-77851674	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs368400092	chr15:77851674-77851675	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564920533	chr15:77851742-77851743	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs112752646	chr15:77851747-77851748	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs554319116	chr15:77851803-77851804	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs182777067	chr15:77851813-77851814	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs536866588	chr15:77851820-77851821	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146173258	chr15:77851823-77851824	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs577066081	chr15:77851828-77851829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs28740786	chr15:77851845-77851846	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs188890113	chr15:77851857-77851858	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs530635218	chr15:77851904-77851905	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs139022539	chr15:77851921-77851922	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs149912999	chr15:77851937-77851938	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs74545682	chr15:77851940-77851941	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs543661301	chr15:77851953-77851954	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs565535130	chr15:77851964-77851965	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs532736397	chr15:77851967-77851968	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs547387028	chr15:77851972-77851973	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs78682688	chr15:77851975-77851976	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs193226455	chr15:77851977-77851978	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs12908292	chr15:77851982-77851983	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs570071150	chr15:77851984-77851985	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs537201544	chr15:77851986-77851987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs77621051	chr15:77851992-77851993	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs75605516	chr15:77851996-77851997	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs369462276	chr15:77852010-77852011	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs372937245	chr15:77852036-77852037	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs558481338	chr15:77852037-77852038	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs566396039	chr15:77852066-77852067	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs570715821	chr15:77852075-77852076	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs72744575	chr15:77852096-77852097	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs552989342	chr15:77852103-77852104	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs376035086	chr15:77852133-77852134	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs574451012	chr15:77852146-77852147	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs541870359	chr15:77852149-77852150	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556971143	chr15:77852150-77852151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs575255037	chr15:77852154-77852155	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs543989999	chr15:77852171-77852172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs565388331	chr15:77852210-77852211	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532816650	chr15:77852215-77852216	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs541357328	chr15:77852224-77852225	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs559634298	chr15:77852225-77852226	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs530006277	chr15:77852229-77852230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs548180277	chr15:77852246-77852247	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:53)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Wilms tumour	21544195	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
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Autism	17322880	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Lung cancer	18438408	CNVD
Myelofibrosis	22110671	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Papillary thyroid carcinoma	22161024	CNVD
Autism	21480499	CNVD
Breast cancer	17603634	CNVD
Acute myeloid leukemia	16864856	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
small cell lung cancer	20016488	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:2062 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:77848000-77855800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
2	chr15:77850000-77855400	Weak transcription	Brain Angular Gyrus	brain
3	chr15:77850000-77855800	Weak transcription	Brain Anterior Caudate	brain
4	chr15:77850200-77855600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr15:77850200-77857200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr15:77850200-77857400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr15:77850400-77855600	Weak transcription	Brain Hippocampus Middle	brain
8	chr15:77850600-77859600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
9	chr15:77851200-77857200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr15:77855400-77857800	Enhancers	Brain Angular Gyrus	brain
11	chr15:77855600-77857000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr15:77855600-77859400	Enhancers	Brain Hippocampus Middle	brain
13	chr15:77855600-77862600	Enhancers	Brain Cingulate Gyrus	brain
14	chr15:77855800-77857800	Enhancers	Brain Anterior Caudate	brain
15	chr15:77855800-77857800	Enhancers	Brain Substantia Nigra	brain
16	chr15:77855800-77858200	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr15:77855800-77858600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
18	chr15:77856000-77858200	Enhancers	Fetal Lung	lung
19	chr15:77856200-77856400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr15:77856400-77860400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
21	chr15:77856800-77858200	Enhancers	Cortex derived primary cultured neurospheres	brain
22	chr15:77857000-77857400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
23	chr15:77857000-77858400	Enhancers	Fetal Brain Male	brain
24	chr15:77857000-77859000	Enhancers	Brain Germinal Matrix	brain
25	chr15:77857200-77857800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
26	chr15:77857200-77859000	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr15:77857200-77862600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr15:77857400-77857600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
29	chr15:77857400-77857600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
30	chr15:77857400-77857600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
31	chr15:77857400-77857600	Enhancers	Placenta	Placenta
32	chr15:77857400-77857800	Enhancers	Fetal Brain Female	brain
33	chr15:77857400-77858200	Bivalent Enhancer	Fetal Stomach	stomach
34	chr15:77857400-77858400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
35	chr15:77857400-77858800	Enhancers	H1 Cell Line	embryonic stem cell
36	chr15:77857400-77859400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
37	chr15:77857400-77862000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
38	chr15:77857600-77857800	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr15:77857600-77859000	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr15:77857600-77860600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
41	chr15:77857600-77860800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr15:77857800-77858000	Enhancers	ES-WA7 Cell Line	embryonic stem cell
43	chr15:77857800-77858600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
44	chr15:77857800-77859200	Weak transcription	Brain Anterior Caudate	brain
45	chr15:77857800-77859400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr15:77857800-77859600	Weak transcription	Brain Angular Gyrus	brain
47	chr15:77857800-77859800	Weak transcription	Fetal Brain Female	brain
48	chr15:77857800-77860200	Weak transcription	Brain Substantia Nigra	brain
49	chr15:77858000-77858200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr15:77858000-77858600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell

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