Variant report

Variant	nsv1061776
Chromosome Location	chr17:46737526-46781977
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:741)
CpG islands
(count:488)
Chromatin interactive
region (count:32)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:741 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:46749100-46749225	HepG2	liver:	n/a	n/a
2	ATF2	chr17:46749092-46749366	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr17:46755667-46756098	H1-hESC	embryonic stem cell:	n/a	n/a
4	BCLAF1	chr17:46749085-46749377	GM12878	blood:	n/a	chr17:46749158-46749167
5	BHLHE40	chr17:46755814-46756094	K562	blood:	n/a	chr17:46755955-46755971
6	BRCA1	chr17:46756009-46756032	HepG2	liver:	n/a	n/a
7	BRCA1	chr17:46755860-46756069	H1-hESC	embryonic stem cell:	n/a	n/a
8	CCNT2	chr17:46755799-46756128	K562	blood:	n/a	chr17:46756112-46756121
9	CEBPB	chr17:46755847-46756217	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr17:46754550-46754874	Hela-S3	cervix:	n/a	n/a
11	CEBPB	chr17:46754477-46754981	A549	lung:	n/a	chr17:46754919-46754932
12	CEBPB	chr17:46754615-46754895	K562	blood:	n/a	n/a
13	CEBPB	chr17:46754582-46754855	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr17:46754583-46754848	HepG2	liver:	n/a	n/a
15	CEBPB	chr17:46754495-46754902	MCF-7	breast:	n/a	n/a
16	CEBPB	chr17:46754523-46754901	A549	lung:	n/a	n/a
17	CEBPB	chr17:46754540-46754875	IMR90	lung:	n/a	n/a
18	CHD2	chr17:46755909-46756145	HepG2	liver:	n/a	n/a
19	CREB1	chr17:46755800-46756175	A549	lung:	n/a	n/a
20	CREB1	chr17:46749093-46749281	A549	lung:	n/a	n/a
21	CTCF	chr17:46740560-46740710	HMF	breast:	n/a	n/a
22	CTCF	chr17:46740560-46740710	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr17:46755551-46756655	SK-N-SH	brain:	n/a	chr17:46755959-46755977
24	CTCF	chr17:46755613-46755667	GM13977	blood:	n/a	n/a
25	CTCF	chr17:46755900-46756050	HEK293	kidney:	n/a	chr17:46755959-46755977
26	CTCF	chr17:46749100-46749250	GM12869	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
27	CTCF	chr17:46749060-46749210	GM12873	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
28	CTCF	chr17:46755733-46756138	A549	lung:	n/a	chr17:46755959-46755977
29	CTCF	chr17:46755880-46756030	AoAF	blood vessel:	n/a	chr17:46755959-46755977
30	CTCF	chr17:46749060-46749210	NHEK	skin:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
31	CTCF	chr17:46755900-46756050	GM12871	blood:	n/a	chr17:46755959-46755977
32	CTCF	chr17:46755737-46756175	K562	blood:	n/a	chr17:46755959-46755977
33	CTCF	chr17:46740568-46740820	MCF-7	breast:	n/a	n/a
34	CTCF	chr17:46740580-46740730	A549	lung:	n/a	n/a
35	CTCF	chr17:46749060-46749210	GM12875	blood:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
36	CTCF	chr17:46749120-46749270	WI-38	lung:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
37	CTCF	chr17:46740620-46740770	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr17:46748995-46749363	T-47D	breast:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
39	CTCF	chr17:46741040-46741190	Caco-2	colon:	n/a	n/a
40	CTCF	chr17:46755940-46756090	HCFaa	heart:	n/a	chr17:46755959-46755977
41	CTCF	chr17:46740660-46740810	AG09309	skin:	n/a	n/a
42	CTCF	chr17:46740580-46740730	BJ	skin:	n/a	n/a
43	CTCF	chr17:46755795-46756105	GM19239	blood:	n/a	chr17:46755959-46755977
44	CTCF	chr17:46749053-46749054	Fibrobl	skin:	n/a	n/a
45	CTCF	chr17:46740639-46740752	HepG2	liver:	n/a	n/a
46	CTCF	chr17:46781680-46781830	GM12870	blood:	n/a	n/a
47	CTCF	chr17:46740557-46740729	GM12878	blood:	n/a	n/a
48	CTCF	chr17:46754300-46754450	HEK293	kidney:	n/a	n/a
49	CTCF	chr17:46755900-46756050	HMF	breast:	n/a	chr17:46755959-46755977
50	CTCF	chr17:46740580-46740730	HBMEC	blood vessel:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46755566-46755616	AG09309	skin:	n/a
2	chr17:46753282-46753332	GM06990	blood:	n/a
3	chr17:46756094-46756144	HRPEpiC	eye:	n/a
4	chr17:46756001-46756051	Jurkat	blood:	n/a
5	chr17:46755566-46755616	GM12878	blood:	n/a
6	chr17:46758520-46758570	U87	brain:	n/a
7	chr17:46756001-46756051	SK-N-MC	brain:	n/a
8	chr17:46755566-46755616	HCPEpiC	choroid plexus:	n/a
9	chr17:46756094-46756144	PrEC	prostate:	n/a
10	chr17:46758520-46758570	CMK	blood:	n/a
11	chr17:46755786-46755836	NH-A	brain:	n/a
12	chr17:46756001-46756051	BJ	skin:	n/a
13	chr17:46753282-46753332	T-47D	breast:	n/a
14	chr17:46756094-46756144	NH-A	brain:	n/a
15	chr17:46755422-46755472	HMEC	breast:	n/a
16	chr17:46755719-46755769	NHDF-neo	bronchial:	n/a
17	chr17:46755422-46755472	HCM	heart:	n/a
18	chr17:46755719-46755769	HCM	heart:	n/a
19	chr17:46758520-46758570	ProgFib	skin:	n/a
20	chr17:46756001-46756051	K562	blood:	n/a
21	chr17:46755566-46755616	BJ	skin:	n/a
22	chr17:46753282-46753332	HUVEC	blood vessel:	n/a
23	chr17:46758520-46758570	Jurkat	blood:	n/a
24	chr17:46755422-46755472	HEK293	kidney:	embryo
25	chr17:46756094-46756144	HCPEpiC	choroid plexus:	n/a
26	chr17:46756094-46756144	SAEC	small airway:	n/a
27	chr17:46756094-46756144	HCM	heart:	n/a
28	chr17:46758520-46758570	HEK293	kidney:	embryo
29	chr17:46755422-46755472	HAEpiC	amniotic membrane:	n/a
30	chr17:46755422-46755472	MCF10A-Er-Src	breast:	n/a
31	chr17:46755422-46755472	ProgFib	skin:	n/a
32	chr17:46756094-46756144	HAEpiC	amniotic membrane:	n/a
33	chr17:46755719-46755769	HCT-116	colon:	n/a
34	chr17:46753282-46753332	IMR90	lung:	fetal
35	chr17:46755566-46755616	NT2-D1	testis:	n/a
36	chr17:46755422-46755472	HUVEC	blood vessel:	n/a
37	chr17:46755719-46755769	HepG2	liver:	n/a
38	chr17:46755786-46755836	HIPEpiC	eye:	n/a
39	chr17:46753282-46753332	MCF-7	breast:	n/a
40	chr17:46756001-46756051	GM12891	blood:	n/a
41	chr17:46756001-46756051	AG09309	skin:	n/a
42	chr17:46758520-46758570	Caco-2	colon:	n/a
43	chr17:46755786-46755836	MCF-7	breast:	n/a
44	chr17:46756001-46756051	HepG2	liver:	n/a
45	chr17:46755422-46755472	PANC-1	pancreas:	n/a
46	chr17:46756001-46756051	T-47D	breast:	n/a
47	chr17:46758520-46758570	HIPEpiC	eye:	n/a
48	chr17:46756094-46756144	SK-N-MC	brain:	n/a
49	chr17:46755719-46755769	HPAEpiC	pulmonary alveolar:	n/a
50	chr17:46755719-46755769	AG04450	lung:	fetal

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
2	chr17:46748726..46749588-chr17:46801756..46802493,2	K562	blood:
3	chr17:46779621..46782109-chr17:46788288..46789802,2	K562	blood:
4	chr17:46748727..46749627-chr17:46867991..46868777,6	MCF-7	breast:
5	chr17:46735946..46737803-chr17:46738310..46740797,2	MCF-7	breast:
6	chr17:46748703..46749676-chr17:46867980..46869288,6	K562	blood:
7	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
8	chr17:46755434..46756698-chr17:46954846..46957173,15	K562	blood:
9	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:
10	chr17:46713679..46714197-chr17:46749118..46749636,2	MCF-7	breast:
11	chr17:46754810..46756534-chr17:46956012..46957174,7	MCF-7	breast:
12	chr17:46706915..46708436-chr17:46753619..46755678,2	K562	blood:
13	chr17:46702462..46704437-chr17:46745558..46748045,2	K562	blood:
14	chr17:46755541..46756386-chr17:46881997..46882806,2	MCF-7	breast:
15	chr17:46749070..46750038-chr17:46868565..46869067,2	MCF-7	breast:
16	chr17:46753552..46755878-chr17:46875165..46876959,2	K562	blood:
17	chr17:46735946..46737803-chr17:46738310..46740797,2	MCF-7	breast:
18	chr17:46693389..46695056-chr17:46744998..46747380,2	K562	blood:
19	chr17:46679617..46680600-chr17:46748738..46749566,2	K562	blood:
20	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
21	chr17:46680120..46680636-chr17:46740659..46741505,2	K562	blood:
22	chr17:46755482..46756508-chr17:46867920..46869021,7	K562	blood:
23	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
24	chr17:46755112..46756375-chr17:46868085..46869415,8	MCF-7	breast:
25	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
26	chr17:46709730..46712661-chr17:46739293..46740902,2	K562	blood:
27	chr17:46749857..46752584-chr17:46924851..46927771,2	K562	blood:
28	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:
29	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
30	chr17:46755465..46756352-chr17:46801247..46802560,4	MCF-7	breast:
31	chr17:46755465..46756849-chr17:46867926..46869081,19	MCF-7	breast:
32	chr17:46748711..46749583-chr17:46956106..46956875,4	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CALCOCO2-4	chr17:46777978-46778062	XLOC_012226
2	lnc-CALCOCO2-4	chr17:46760729-46760779	ENSG00000262745.1
3	lnc-CALCOCO2-4	chr17:46777974-46778058	ENSG00000262745.1
4	lnc-CALCOCO2-4	chr17:46781363-46781655	XLOC_012226
5	lnc-CALCOCO2-4	chr17:46781363-46781844	ENSG00000262745.1
6	lnc-PRAC-1	chr17:46768478-46769056	NONHSAT054466
7	lnc-CALCOCO2-12	chr17:46773611-46774931	ucscGeneNc_uc002itt_1
8	lnc-CALCOCO2-12	chr17:46769075-46770280	ucscGeneNc_uc002itt_1
9	lnc-CALCOCO2-12	chr17:46771967-46772084	ucscGeneNc_uc002itt_1

No data

Variant related genes	Relation type
RPL9P28	TF binding region
ENSG00000244649	TF binding region
ENSG00000244559	TF binding region
ENSG00000262745	TF binding region
RPL9P28	CpG island
ENSG00000244649	CpG island
ENSG00000244559	CpG island
ENSG00000262745	CpG island
ENSG00000210741	chromatin interactions
ENSG00000233101	chromatin interactions
ENSG00000136436	chromatin interactions
ENSG00000170689	chromatin interactions
ENSG00000260027	chromatin interactions
ENSG00000263602	chromatin interactions
ZNF828	miRNA target sites
ZNFX1	miRNA target sites

Extended variants
information (count: 1642 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1642 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs549543157	chr17:46737554-46737555	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs73324267	chr17:46737642-46737643	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs72831814	chr17:46737687-46737688	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs552302888	chr17:46737727-46737728	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs144783285	chr17:46737733-46737734	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs535272168	chr17:46737755-46737756	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs555140391	chr17:46737796-46737797	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs559441437	chr17:46737812-46737813	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140006367	chr17:46737823-46737824	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs375264159	chr17:46737845-46737846	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143904837	chr17:46737847-46737848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs545754004	chr17:46737868-46737869	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs568368460	chr17:46737888-46737889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs559463517	chr17:46737921-46737922	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs529149986	chr17:46737936-46737937	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs115273605	chr17:46737964-46737965	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs533114874	chr17:46737981-46737982	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs145108214	chr17:46737983-46737984	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs540899133	chr17:46737998-46737999	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529989697	chr17:46738050-46738051	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs561119276	chr17:46738091-46738092	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs529813835	chr17:46738142-46738143	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs71377383	chr17:46738152-46738153	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs147249119	chr17:46738161-46738162	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs79734901	chr17:46738224-46738225	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs188856435	chr17:46738266-46738267	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs377680522	chr17:46738277-46738278	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs532153402	chr17:46738283-46738284	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs371238401	chr17:46738320-46738321	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs374150134	chr17:46738325-46738326	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181311642	chr17:46738331-46738332	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs548186216	chr17:46738338-46738339	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs534685121	chr17:46738339-46738340	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547944135	chr17:46738341-46738342	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112269042	chr17:46738366-46738367	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs569200787	chr17:46738380-46738381	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs371003423	chr17:46738382-46738383	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs62064611	chr17:46738431-46738432	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs531234023	chr17:46738445-46738446	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs113451991	chr17:46738461-46738462	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs186373672	chr17:46738473-46738474	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs552930892	chr17:46738501-46738502	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs551640919	chr17:46738502-46738503	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs573037883	chr17:46738553-46738554	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs542322636	chr17:46738587-46738588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs562010045	chr17:46738609-46738610	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs574577360	chr17:46738615-46738616	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs543210632	chr17:46738630-46738631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs563614155	chr17:46738638-46738639	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs367628044	chr17:46738671-46738672	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Acute lymphoblastic leukemia	21339820	CNVD

Chromatin state (count:333 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46725400-46739000	Weak transcription	Sigmoid Colon	Sigmoid Colon
2	chr17:46725600-46749000	Weak transcription	A549	lung
3	chr17:46732600-46748800	Weak transcription	Rectal Mucosa Donor 31	rectum
4	chr17:46737200-46740600	Weak transcription	Rectal Mucosa Donor 29	rectum
5	chr17:46740600-46740800	Enhancers	Rectal Mucosa Donor 29	rectum
6	chr17:46740800-46741000	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr17:46743800-46744600	Bivalent Enhancer	HepG2	liver
8	chr17:46744200-46744400	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
9	chr17:46744200-46744400	Bivalent Enhancer	Stomach Mucosa	stomach
10	chr17:46746400-46746600	Bivalent Enhancer	Primary mononuclear cells fromperipheralblood	Blood
11	chr17:46748000-46748200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
12	chr17:46748200-46749200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr17:46748800-46749000	Enhancers	Rectal Mucosa Donor 31	rectum
14	chr17:46748800-46749200	Bivalent Enhancer	Primary T helper naive cells fromperipheralblood	blood
15	chr17:46748800-46749200	Enhancers	Primary T helper cells PMA-I stimulated	--
16	chr17:46748800-46749200	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
17	chr17:46748800-46749600	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
18	chr17:46749000-46749200	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
19	chr17:46749000-46749200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr17:46749000-46749200	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
21	chr17:46749000-46749200	Bivalent Enhancer	Primary T regulatory cells fromperipheralblood	blood
22	chr17:46749000-46749200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
23	chr17:46749000-46749200	Enhancers	Liver	Liver
24	chr17:46749000-46749200	Enhancers	Brain Germinal Matrix	brain
25	chr17:46749000-46749200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
26	chr17:46749000-46749200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
27	chr17:46749000-46749200	Active TSS	HSMM	muscle
28	chr17:46749000-46749400	Bivalent Enhancer	Primary Natural Killer cells fromperipheralblood	blood
29	chr17:46749000-46749400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
30	chr17:46749000-46749400	Active TSS	Rectal Mucosa Donor 31	rectum
31	chr17:46749000-46749400	Active TSS	A549	lung
32	chr17:46749000-46749400	Active TSS	HSMMtube	muscle
33	chr17:46749000-46749600	Bivalent Enhancer	Primary monocytes fromperipheralblood	blood
34	chr17:46749000-46749600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
35	chr17:46749000-46749600	Flanking Bivalent TSS/Enh	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr17:46749000-46749600	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
37	chr17:46749000-46749600	Active TSS	Brain Inferior Temporal Lobe	brain
38	chr17:46749000-46749800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr17:46749000-46749800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
40	chr17:46749200-46749400	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr17:46749200-46749400	Bivalent Enhancer	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
42	chr17:46749200-46749400	Flanking Active TSS	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr17:46749200-46749400	Bivalent/Poised TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr17:46749200-46749400	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
45	chr17:46749200-46749400	Bivalent/Poised TSS	iPS-18 Cell Line	embryonic stem cell
46	chr17:46749200-46749400	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr17:46749200-46749400	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr17:46749200-46749400	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
49	chr17:46749200-46749400	Bivalent Enhancer	Primary hematopoietic stem cells	blood
50	chr17:46749200-46749400	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood

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