Variant report

Variant	nsv904216
Chromosome Location	chr15:51631479-51739808
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1533)
CpG islands
(count:1100)
Chromatin interactive
region (count:130)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1533 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:51694163-51694171	K562	blood:	n/a	n/a
2	ARID3A	chr15:51661016-51661260	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:51673389-51673726	K562	blood:	n/a	n/a
4	ARID3A	chr15:51715479-51715733	K562	blood:	n/a	n/a
5	ARID3A	chr15:51695561-51695844	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:51673350-51673766	HepG2	liver:	n/a	n/a
7	ARID3A	chr15:51675080-51675297	HepG2	liver:	n/a	n/a
8	ATF2	chr15:51640893-51641346	GM12878	blood:	n/a	n/a
9	ATF2	chr15:51640773-51641403	GM12878	blood:	n/a	n/a
10	BACH1	chr15:51694223-51694232	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:51696717-51696732	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:51673559-51673565	K562	blood:	n/a	n/a
13	BACH1	chr15:51633839-51634450	H1-hESC	embryonic stem cell:	n/a	n/a
14	BATF	chr15:51640863-51641311	GM12878	blood:	n/a	n/a
15	BATF	chr15:51661579-51661847	GM12878	blood:	n/a	n/a
16	BATF	chr15:51678274-51678508	GM12878	blood:	n/a	n/a
17	BATF	chr15:51640910-51641299	GM12878	blood:	n/a	n/a
18	BCL11A	chr15:51640911-51641332	GM12878	blood:	n/a	n/a
19	BCL11A	chr15:51640937-51641271	GM12878	blood:	n/a	n/a
20	BCL3	chr15:51640965-51641259	GM12878	blood:	n/a	n/a
21	BCLAF1	chr15:51640794-51641430	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:51673395-51673852	K562	blood:	n/a	n/a
23	BHLHE40	chr15:51675185-51675304	K562	blood:	n/a	n/a
24	BHLHE40	chr15:51694121-51694439	K562	blood:	n/a	n/a
25	BHLHE40	chr15:51658568-51658587	K562	blood:	n/a	n/a
26	BHLHE40	chr15:51738546-51738749	GM12878	blood:	n/a	n/a
27	BRCA1	chr15:51696286-51696297	Hela-S3	cervix:	n/a	n/a
28	BRCA1	chr15:51694129-51694383	H1-hESC	embryonic stem cell:	n/a	n/a
29	BRCA1	chr15:51717119-51717187	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr15:51736991-51737380	K562	blood:	n/a	n/a
31	CBX3	chr15:51715524-51716064	K562	blood:	n/a	n/a
32	CEBPB	chr15:51649194-51649456	K562	blood:	n/a	n/a
33	CEBPB	chr15:51682495-51682694	HepG2	liver:	n/a	chr15:51682609-51682622 chr15:51682611-51682620 chr15:51682610-51682621
34	CEBPB	chr15:51660841-51661705	IMR90	lung:	n/a	chr15:51661490-51661503 chr15:51661492-51661503 chr15:51661492-51661503
35	CEBPB	chr15:51640843-51641441	GM12878	blood:	n/a	n/a
36	CEBPB	chr15:51738529-51739082	HCT-116	colon:	n/a	n/a
37	CEBPB	chr15:51673559-51673645	K562	blood:	n/a	n/a
38	CEBPB	chr15:51723485-51723691	K562	blood:	n/a	chr15:51723548-51723559
39	CEBPB	chr15:51683246-51683553	H1-hESC	embryonic stem cell:	n/a	n/a
40	CEBPB	chr15:51649263-51649392	HepG2	liver:	n/a	n/a
41	CEBPB	chr15:51658999-51659564	A549	lung:	n/a	n/a
42	CEBPB	chr15:51716939-51717240	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr15:51659022-51659860	MCF-7	breast:	n/a	n/a
44	CEBPB	chr15:51640971-51641320	GM12878	blood:	n/a	n/a
45	CEBPB	chr15:51719306-51719481	HepG2	liver:	n/a	n/a
46	CEBPB	chr15:51717910-51718114	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr15:51723429-51723618	IMR90	lung:	n/a	chr15:51723548-51723559
48	CEBPB	chr15:51632766-51633073	HepG2	liver:	n/a	chr15:51632919-51632930
49	CEBPB	chr15:51659117-51659422	A549	lung:	n/a	n/a
50	CEBPB	chr15:51639491-51639645	K562	blood:	n/a	n/a

(count:1100 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:51634039-51634089	K562	blood:	n/a
2	chr15:51633821-51633871	NB4	blood:	n/a
3	chr15:51634039-51634089	K562	blood:	n/a
4	chr15:51633821-51633871	NB4	blood:	n/a
5	chr15:51634250-51634300	SK-N-SH_RA	brain:	n/a
6	chr15:51633821-51633871	MCF-7	breast:	n/a
7	chr15:51632905-51632955	HepG2	liver:	n/a
8	chr15:51695713-51695763	Caco-2	colon:	n/a
9	chr15:51633430-51633480	MCF10A-Er-Src	breast:	n/a
10	chr15:51660650-51660700	MCF-7	breast:	n/a
11	chr15:51695713-51695763	HRPEpiC	eye:	n/a
12	chr15:51631687-51631737	BJ	skin:	n/a
13	chr15:51633704-51633754	IMR90	lung:	fetal
14	chr15:51633816-51633866	SAEC	small airway:	n/a
15	chr15:51669526-51669576	AG09319	gingival:	n/a
16	chr15:51633430-51633480	HEK293	kidney:	embryo
17	chr15:51632611-51632661	NHDF-neo	bronchial:	n/a
18	chr15:51632611-51632661	NB4	blood:	n/a
19	chr15:51669526-51669576	AG10803	skin:	n/a
20	chr15:51631687-51631737	NB4	blood:	n/a
21	chr15:51695713-51695763	HCPEpiC	choroid plexus:	n/a
22	chr15:51694383-51694433	Hepatocyte	liver:	n/a
23	chr15:51636552-51636602	Caco-2	colon:	n/a
24	chr15:51633430-51633480	ECC-1	luminal epithelium:	n/a
25	chr15:51634583-51634633	HCF	heart:	n/a
26	chr15:51636552-51636602	HRE	kidney:	n/a
27	chr15:51695713-51695763	MCF10A-Er-Src	breast:	n/a
28	chr15:51699392-51699442	HCT-116	colon:	n/a
29	chr15:51669526-51669576	NT2-D1	testis:	n/a
30	chr15:51634583-51634633	MCF10A-Er-Src	breast:	n/a
31	chr15:51669526-51669576	AG04449	skin:	fetal
32	chr15:51632905-51632955	HL-60	blood:	n/a
33	chr15:51633381-51633431	T-47D	breast:	n/a
34	chr15:51683249-51683299	SK-N-SH_RA	brain:	n/a
35	chr15:51634583-51634633	NH-A	brain:	n/a
36	chr15:51633430-51633480	HPAEpiC	pulmonary alveolar:	n/a
37	chr15:51669526-51669576	T-47D	breast:	n/a
38	chr15:51634039-51634089	HCPEpiC	choroid plexus:	n/a
39	chr15:51634039-51634089	PFSK-1	brain:	n/a
40	chr15:51695713-51695763	HepG2	liver:	n/a
41	chr15:51633816-51633866	LNCaP	prostate:	n/a
42	chr15:51699392-51699442	Hepatocyte	liver:	n/a
43	chr15:51669526-51669576	SK-N-SH	brain:	n/a
44	chr15:51634250-51634300	HNPCEpiC	eye:	n/a
45	chr15:51683249-51683299	ECC-1	luminal epithelium:	n/a
46	chr15:51633821-51633871	HCF	heart:	n/a
47	chr15:51634583-51634633	RPTEC	kidney:	n/a
48	chr15:51633381-51633431	HCPEpiC	choroid plexus:	n/a
49	chr15:51633821-51633871	MCF10A-Er-Src	breast:	n/a
50	chr15:51683249-51683299	AG10803	skin:	n/a

(count:130 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr15:51658520..51659654-chr15:51673214..51673922,3	MCF-7	breast:
2	chr15:51737006..51738600-chr15:51770041..51772007,2	MCF-7	breast:
3	chr15:51690409..51692139-chr15:51694758..51697390,2	K562	blood:
4	chr15:51659859..51663874-chr15:51668414..51672353,4	MCF-7	breast:
5	chr15:51455196..51455811-chr15:51674714..51675313,2	MCF-7	breast:
6	chr15:51629923..51631751-chr15:51631879..51634512,2	MCF-7	breast:
7	chr15:51454926..51455797-chr15:51673153..51673909,4	MCF-7	breast:
8	chr15:51651683..51656277-chr15:51657085..51661160,7	MCF-7	breast:
9	chr15:51521669..51522596-chr15:51674755..51675695,2	MCF-7	breast:
10	chr15:51578768..51579584-chr15:51674584..51675320,4	MCF-7	breast:
11	chr15:51633122..51636789-chr15:51637191..51639833,4	MCF-7	breast:
12	chr15:51573650..51574202-chr15:51695118..51695778,3	MCF-7	breast:
13	chr15:51633614..51635996-chr15:51658332..51660020,2	MCF-7	breast:
14	chr15:51660401..51662626-chr7:156685669..156687987,2	MCF-7	breast:
15	chr15:51573553..51574678-chr15:51674522..51675665,6	MCF-7	breast:
16	chr15:51727549..51728106-chr5:174151015..174151699,2	MCF-7	breast:
17	chr15:51690075..51690907-chr15:51716851..51717682,2	MCF-7	breast:
18	chr15:51654951..51657381-chr15:51671722..51675583,3	K562	blood:
19	chr15:51573015..51575119-chr15:51672522..51674124,19	MCF-7	breast:
20	chr15:51631962..51635284-chr15:51658030..51661576,5	MCF-7	breast:
21	chr15:51571944..51572724-chr15:51673082..51674003,2	MCF-7	breast:
22	chr15:51572199..51575130-chr15:51658067..51661201,3	MCF-7	breast:
23	chr15:51688961..51692300-chr15:51692695..51697004,4	MCF-7	breast:
24	chr15:51573701..51574203-chr15:51693816..51694736,2	K562	blood:
25	chr15:51613301..51614108-chr15:51673413..51674112,2	MCF-7	breast:
26	chr15:51633816..51636892-chr15:51670128..51672715,3	MCF-7	breast:
27	chr15:51648182..51651312-chr15:51657135..51660057,4	MCF-7	breast:
28	chr15:51521787..51522680-chr15:51673138..51674597,7	MCF-7	breast:
29	chr15:51672133..51674864-chr15:51676957..51679239,3	MCF-7	breast:
30	chr15:51693667..51695853-chr15:51915384..51917421,2	K562	blood:
31	chr15:51454781..51456161-chr15:51672829..51674093,16	MCF-7	breast:
32	chr12:49523938..49524712-chr15:51673098..51673696,2	MCF-7	breast:
33	chr15:51573458..51575048-chr15:51673491..51675129,2	MCF-7	breast:
34	chr15:51675621..51681279-chr15:51681874..51686494,6	MCF-7	breast:
35	chr15:51642370..51644642-chr15:51658744..51660938,2	MCF-7	breast:
36	chr15:51567204..51569192-chr15:51676110..51678309,2	MCF-7	breast:
37	chr15:51673613..51676825-chr15:51677424..51680901,4	K562	blood:
38	chr15:51678827..51682342-chr15:51683249..51685857,3	K562	blood:
39	chr15:51666016..51667942-chr15:51669809..51671705,2	K562	blood:
40	chr15:51694062..51694684-chr15:51881746..51882355,2	MCF-7	breast:
41	chr15:51673157..51673657-chr17:59494266..59494829,2	MCF-7	breast:
42	chr15:51678827..51682342-chr15:51683249..51685857,3	K562	blood:
43	chr15:51577515..51580026-chr15:51665371..51667352,2	MCF-7	breast:
44	chr15:51693668..51696563-chr15:51791743..51794551,3	MCF-7	breast:
45	chr15:51454803..51455765-chr15:51693822..51694605,5	MCF-7	breast:
46	chr15:51673486..51674048-chr15:51693999..51694751,2	MCF-7	breast:
47	chr15:51655989..51658966-chr15:51659678..51663133,3	K562	blood:
48	chr15:51578798..51579654-chr15:51695165..51696058,4	MCF-7	breast:
49	chr15:51577066..51580410-chr15:51672799..51675704,3	MCF-7	breast:
50	chr15:51693802..51694361-chr15:51791693..51792541,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GLDN-3	chr15:51706294-51706397	ENSG00000259678.1

No data

Variant related genes	Relation type
CYP19A1	TF binding region
ENSG00000259194	TF binding region
ENSG00000259678	TF binding region
GLDN	TF binding region
ENSG00000270378	TF binding region
CYP19A1	CpG island
ENSG00000259194	CpG island
ENSG00000259678	CpG island
GLDN	CpG island
ENSG00000270378	CpG island
ENSG00000120149	chromatin interactions
ENSG00000105983	chromatin interactions
ENSG00000259306	chromatin interactions
ENSG00000259194	chromatin interactions
ENSG00000259701	chromatin interactions
ENSG00000270378	chromatin interactions
ENSG00000104093	chromatin interactions
ENSG00000137869	chromatin interactions
ENSG00000186417	chromatin interactions

Extended variants
information (count: 4292 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:4292 , 50 per page) page: 1 2 3 4 5 6 7 ... 86

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs752760	chr15:51631479-51631480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs373840530	chr15:51631551-51631552	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs534417431	chr15:51631568-51631569	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs60070054	chr15:51631583-51631584	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs114188177	chr15:51631585-51631586	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs4257155	chr15:51631645-51631646	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs567936195	chr15:51631648-51631649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs538186932	chr15:51631649-51631650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs4257156	chr15:51631651-51631652	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs556115429	chr15:51631693-51631694	Weak transcription Enhancers	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs577634928	chr15:51631754-51631755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs146679667	chr15:51631764-51631765	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs139257932	chr15:51631787-51631788	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs572099061	chr15:51631792-51631793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs28757063	chr15:51631795-51631796	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs554508650	chr15:51631813-51631814	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs562060589	chr15:51631852-51631853	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs369695064	chr15:51631853-51631854	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs543768939	chr15:51631969-51631970	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs28757062	chr15:51632007-51632008	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs564847201	chr15:51632018-51632019	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs143077759	chr15:51632100-51632101	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs115836110	chr15:51632109-51632110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs574883569	chr15:51632124-51632125	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs150422751	chr15:51632166-51632167	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs529789429	chr15:51632196-51632197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs549536113	chr15:51632237-51632238	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs567789850	chr15:51632250-51632251	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs560620553	chr15:51632253-51632254	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs138235995	chr15:51632259-51632260	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs573830201	chr15:51632260-51632261	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs550076247	chr15:51632279-51632280	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs187383304	chr15:51632301-51632302	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs748838	chr15:51632323-51632324	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs553796200	chr15:51632401-51632402	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs562367325	chr15:51632402-51632403	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs748837	chr15:51632416-51632417	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs554728504	chr15:51632448-51632449	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs576181358	chr15:51632470-51632471	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs543708228	chr15:51632505-51632506	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs558902245	chr15:51632520-51632521	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs180804432	chr15:51632571-51632572	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs185767910	chr15:51632584-51632585	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs370372559	chr15:51632587-51632588	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs559117670	chr15:51632611-51632612	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs529771830	chr15:51632612-51632613	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs28757061	chr15:51632621-51632622	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs78300220	chr15:51632659-51632660	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs531796194	chr15:51632687-51632688	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs76559349	chr15:51632706-51632707	Enhancers Weak transcription	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	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
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
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	20877625	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1250 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:51627200-51632800	Weak transcription	Spleen	Spleen
2	chr15:51628400-51633000	Weak transcription	Brain Angular Gyrus	brain
3	chr15:51628400-51633400	Weak transcription	Adipose Nuclei	Adipose
4	chr15:51628600-51633000	Weak transcription	Brain Anterior Caudate	brain
5	chr15:51628800-51633000	Weak transcription	Brain Hippocampus Middle	brain
6	chr15:51628800-51633200	Weak transcription	Left Ventricle	heart
7	chr15:51628800-51633600	Weak transcription	Aorta	Aorta
8	chr15:51628800-51633600	Weak transcription	Right Atrium	heart
9	chr15:51630200-51633400	Weak transcription	Pancreas	Pancrea
10	chr15:51630400-51633000	Weak transcription	Right Ventricle	heart
11	chr15:51630800-51632200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
12	chr15:51630800-51633600	Enhancers	Placenta	Placenta
13	chr15:51631400-51633000	Weak transcription	Stomach Smooth Muscle	stomach
14	chr15:51632200-51633600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
15	chr15:51632800-51633200	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr15:51632800-51633800	Enhancers	Spleen	Spleen
17	chr15:51633000-51633200	Enhancers	Brain Anterior Caudate	brain
18	chr15:51633000-51633200	Enhancers	Brain Cingulate Gyrus	brain
19	chr15:51633000-51633200	Enhancers	Brain Hippocampus Middle	brain
20	chr15:51633000-51633400	Enhancers	Brain Angular Gyrus	brain
21	chr15:51633000-51633400	Enhancers	Right Ventricle	heart
22	chr15:51633000-51633400	Enhancers	Stomach Smooth Muscle	stomach
23	chr15:51633000-51633800	Enhancers	Placenta Amnion	Placenta Amnion
24	chr15:51633200-51633400	Bivalent Enhancer	Breast Myoepithelial Primary Cells	Breast
25	chr15:51633200-51633400	Flanking Active TSS	Brain Anterior Caudate	brain
26	chr15:51633200-51633400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
27	chr15:51633200-51633400	Enhancers	Brain Substantia Nigra	brain
28	chr15:51633200-51633400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
29	chr15:51633200-51633400	Flanking Bivalent TSS/Enh	Skeletal Muscle Female	skeletal muscle
30	chr15:51633200-51633600	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr15:51633200-51633600	Flanking Active TSS	Brain Cingulate Gyrus	brain
32	chr15:51633200-51633600	Flanking Active TSS	Brain Hippocampus Middle	brain
33	chr15:51633200-51633600	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
34	chr15:51633200-51633600	Enhancers	Left Ventricle	heart
35	chr15:51633200-51633600	Enhancers	Psoas Muscle	Psoas
36	chr15:51633200-51633600	Bivalent Enhancer	Rectal Mucosa Donor 31	rectum
37	chr15:51633200-51634000	Bivalent Enhancer	Stomach Mucosa	stomach
38	chr15:51633200-51634200	Bivalent Enhancer	Primary B cells from peripheral blood	blood
39	chr15:51633400-51633600	Bivalent Enhancer	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
40	chr15:51633400-51633600	Bivalent Enhancer	ES-UCSF4 Cell Line	embryonic stem cell
41	chr15:51633400-51633600	Flanking Bivalent TSS/Enh	Breast Myoepithelial Primary Cells	Breast
42	chr15:51633400-51633600	Bivalent Enhancer	Muscle Satellite Cultured Cells	--
43	chr15:51633400-51633600	Bivalent Enhancer	Ganglion Eminence derived primary cultured neurospheres	brain
44	chr15:51633400-51633600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr15:51633400-51633600	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr15:51633400-51633600	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr15:51633400-51633600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr15:51633400-51633600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr15:51633400-51633600	Flanking Active TSS	Brain Angular Gyrus	brain
50	chr15:51633400-51633600	Active TSS	Brain Anterior Caudate	brain

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