Variant report

Variant	nsv575484
Chromosome Location	chr17:46749791-46780829
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:344)
CpG islands
(count:488)
Chromatin interactive
region (count:20)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:344 , 50 per page) page: 1 2 3 4 5 6 7

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr17:46755667-46756098	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr17:46755814-46756094	K562	blood:	n/a	chr17:46755955-46755971
3	BRCA1	chr17:46755860-46756069	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr17:46756009-46756032	HepG2	liver:	n/a	n/a
5	CCNT2	chr17:46755799-46756128	K562	blood:	n/a	chr17:46756112-46756121
6	CEBPB	chr17:46754523-46754901	A549	lung:	n/a	n/a
7	CEBPB	chr17:46754583-46754848	HepG2	liver:	n/a	n/a
8	CEBPB	chr17:46754540-46754875	IMR90	lung:	n/a	n/a
9	CEBPB	chr17:46754582-46754855	H1-hESC	embryonic stem cell:	n/a	n/a
10	CEBPB	chr17:46754615-46754895	K562	blood:	n/a	n/a
11	CEBPB	chr17:46754550-46754874	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr17:46754495-46754902	MCF-7	breast:	n/a	n/a
13	CEBPB	chr17:46755847-46756217	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr17:46754477-46754981	A549	lung:	n/a	chr17:46754919-46754932
15	CHD2	chr17:46755909-46756145	HepG2	liver:	n/a	n/a
16	CREB1	chr17:46755800-46756175	A549	lung:	n/a	n/a
17	CTCF	chr17:46755380-46755530	K562	blood:	n/a	chr17:46755421-46755434
18	CTCF	chr17:46755500-46755650	HFF	foreskin:	n/a	n/a
19	CTCF	chr17:46756320-46756470	GM12872	blood:	n/a	n/a
20	CTCF	chr17:46755880-46756030	K562	blood:	n/a	chr17:46755959-46755977
21	CTCF	chr17:46755585-46756271	K562	blood:	n/a	chr17:46755959-46755977
22	CTCF	chr17:46755900-46756050	RPTEC	kidney:	n/a	chr17:46755959-46755977
23	CTCF	chr17:46755880-46756030	SAEC	small airway:	n/a	chr17:46755959-46755977
24	CTCF	chr17:46755656-46756194	K562	blood:	n/a	chr17:46755959-46755977
25	CTCF	chr17:46755880-46756030	BJ	skin:	n/a	chr17:46755959-46755977
26	CTCF	chr17:46755880-46756030	AoAF	blood vessel:	n/a	chr17:46755959-46755977
27	CTCF	chr17:46755860-46756010	HVMF	connective:	n/a	chr17:46755959-46755977
28	CTCF	chr17:46755365-46757285	A549	lung:	n/a	chr17:46755959-46755977 chr17:46755421-46755434
29	CTCF	chr17:46755840-46755990	HVMF	connective:	n/a	chr17:46755959-46755977
30	CTCF	chr17:46755579-46756110	GM10266	blood:	n/a	chr17:46755959-46755977
31	CTCF	chr17:46755920-46756070	NHEK	skin:	n/a	chr17:46755959-46755977
32	CTCF	chr17:46755738-46756183	K562	blood:	n/a	chr17:46755959-46755977
33	CTCF	chr17:46748908-46749978	SK-N-SH	brain:	n/a	chr17:46749166-46749184 chr17:46749167-46749183 chr17:46749168-46749189 chr17:46749171-46749179
34	CTCF	chr17:46755620-46755694	GM12891	blood:	n/a	n/a
35	CTCF	chr17:46755761-46756174	IMR90	lung:	n/a	chr17:46755959-46755977
36	CTCF	chr17:46755880-46756030	HL-60	blood:	n/a	chr17:46755959-46755977
37	CTCF	chr17:46755860-46756010	HCT-116	colon:	n/a	chr17:46755959-46755977
38	CTCF	chr17:46755420-46755570	GM12864	blood:	n/a	chr17:46755421-46755434
39	CTCF	chr17:46756240-46756270	K562	blood:	n/a	n/a
40	CTCF	chr17:46755748-46756117	MCF-7	breast:	n/a	chr17:46755959-46755977
41	CTCF	chr17:46755824-46756093	Hela-S3	cervix:	n/a	chr17:46755959-46755977
42	CTCF	chr17:46755500-46755650	GM12870	blood:	n/a	n/a
43	CTCF	chr17:46755574-46755719	ProgFib	skin:	n/a	n/a
44	CTCF	chr17:46755828-46756077	HepG2	liver:	n/a	chr17:46755959-46755977
45	CTCF	chr17:46755840-46755990	RPTEC	kidney:	n/a	chr17:46755959-46755977
46	CTCF	chr17:46755860-46756010	MCF-7	breast:	n/a	chr17:46755959-46755977
47	CTCF	chr17:46755900-46756050	GM12868	blood:	n/a	chr17:46755959-46755977
48	CTCF	chr17:46755736-46755742	GM12892	blood:	n/a	n/a
49	CTCF	chr17:46755737-46756175	K562	blood:	n/a	chr17:46755959-46755977
50	CTCF	chr17:46755900-46756050	HMF	breast:	n/a	chr17:46755959-46755977

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:46755422-46755472	NH-A	brain:	n/a
2	chr17:46755786-46755836	HRE	kidney:	n/a
3	chr17:46755786-46755836	HAEpiC	amniotic membrane:	n/a
4	chr17:46755719-46755769	BJ	skin:	n/a
5	chr17:46756094-46756144	ECC-1	luminal epithelium:	n/a
6	chr17:46755719-46755769	Hela-S3	cervix:	n/a
7	chr17:46756094-46756144	CMK	blood:	n/a
8	chr17:46755786-46755836	HEEpiC	esophagus:	n/a
9	chr17:46755786-46755836	NT2-D1	testis:	n/a
10	chr17:46755566-46755616	IMR90	lung:	fetal
11	chr17:46755719-46755769	ProgFib	skin:	n/a
12	chr17:46755422-46755472	NB4	blood:	n/a
13	chr17:46755719-46755769	K562	blood:	n/a
14	chr17:46756001-46756051	K562	blood:	n/a
15	chr17:46753282-46753332	CMK	blood:	n/a
16	chr17:46755566-46755616	HL-60	blood:	n/a
17	chr17:46755719-46755769	NHBE	bronchial:	n/a
18	chr17:46756001-46756051	RPTEC	kidney:	n/a
19	chr17:46753282-46753332	HCM	heart:	n/a
20	chr17:46755566-46755616	HCF	heart:	n/a
21	chr17:46755786-46755836	AoSMC	blood vessel:	n/a
22	chr17:46755566-46755616	PANC-1	pancreas:	n/a
23	chr17:46758520-46758570	K562	blood:	n/a
24	chr17:46756001-46756051	HIPEpiC	eye:	n/a
25	chr17:46756001-46756051	BJ	skin:	n/a
26	chr17:46753282-46753332	GM19239	blood:	n/a
27	chr17:46758520-46758570	CMK	blood:	n/a
28	chr17:46755422-46755472	HepG2	liver:	n/a
29	chr17:46755786-46755836	BJ	skin:	n/a
30	chr17:46758520-46758570	AoSMC	blood vessel:	n/a
31	chr17:46756001-46756051	HRCEpiC	kidney:	n/a
32	chr17:46758520-46758570	ECC-1	luminal epithelium:	n/a
33	chr17:46755786-46755836	K562	blood:	n/a
34	chr17:46756001-46756051	MCF-7	breast:	n/a
35	chr17:46755566-46755616	SAEC	small airway:	n/a
36	chr17:46756094-46756144	ovcar-3	ovarian:	n/a
37	chr17:46756001-46756051	HCT-116	colon:	n/a
38	chr17:46755719-46755769	LNCaP	prostate:	n/a
39	chr17:46755566-46755616	MCF10A-Er-Src	breast:	n/a
40	chr17:46755719-46755769	CMK	blood:	n/a
41	chr17:46755786-46755836	HPAEpiC	pulmonary alveolar:	n/a
42	chr17:46755786-46755836	HRPEpiC	eye:	n/a
43	chr17:46758520-46758570	BJ	skin:	n/a
44	chr17:46755422-46755472	Hepatocyte	liver:	n/a
45	chr17:46756001-46756051	HUVEC	blood vessel:	n/a
46	chr17:46755566-46755616	Hepatocyte	liver:	n/a
47	chr17:46755719-46755769	HCM	heart:	n/a
48	chr17:46758520-46758570	BE2_C	brain:	n/a
49	chr17:46756094-46756144	LNCaP	prostate:	n/a
50	chr17:46756094-46756144	HepG2	liver:	n/a

(count:20 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
2	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:
3	chr17:46779621..46782109-chr17:46788288..46789802,2	K562	blood:
4	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
5	chr17:46754493..46757349-chr17:46765268..46767829,2	K562	blood:
6	chr17:46753552..46755878-chr17:46875165..46876959,2	K562	blood:
7	chr17:46706915..46708436-chr17:46753619..46755678,2	K562	blood:
8	chr17:46755434..46756698-chr17:46954846..46957173,15	K562	blood:
9	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
10	chr17:46770373..46774309-chr17:46775013..46779321,3	K562	blood:
11	chr17:46755541..46756386-chr17:46881997..46882806,2	MCF-7	breast:
12	chr17:46754810..46756534-chr17:46956012..46957174,7	MCF-7	breast:
13	chr17:46755465..46756849-chr17:46867926..46869081,19	MCF-7	breast:
14	chr17:46755482..46756508-chr17:46867920..46869021,7	K562	blood:
15	chr17:46755465..46756352-chr17:46801247..46802560,4	MCF-7	breast:
16	chr17:46755112..46756375-chr17:46868085..46869415,8	MCF-7	breast:
17	chr17:46748343..46750795-chr17:46752847..46755076,2	K562	blood:
18	chr17:46757300..46759092-chr17:46761138..46763617,2	K562	blood:
19	chr17:46749857..46752584-chr17:46924851..46927771,2	K562	blood:
20	chr17:46749070..46750038-chr17:46868565..46869067,2	MCF-7	breast:

(count:7 , 50 per page) page: 1

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

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
ENSG00000136436	chromatin interactions
ENSG00000263602	chromatin interactions
ZNF828	miRNA target sites

Extended variants
information (count: 1132 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:1132 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8074700	chr17:46749791-46749792	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance disease
2	rs548876428	chr17:46749799-46749800	Weak transcription Bivalent Enhancer Active TSS Flanking Active TSS Bivalent/Poised TSS Enhancers Flanking Bivalent TSS/Enh	n/a	n/a	Overlapped CNVs	n/a
3	rs191148967	chr17:46749815-46749816	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143919512	chr17:46749833-46749834	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs183363509	chr17:46749843-46749844	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs571289707	chr17:46749854-46749855	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533904769	chr17:46749901-46749902	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs553539394	chr17:46749936-46749937	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs574293153	chr17:46749982-46749983	Weak transcription Bivalent Enhancer Flanking Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536830415	chr17:46750007-46750008	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs77592156	chr17:46750025-46750026	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576786485	chr17:46750080-46750081	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs140389969	chr17:46750109-46750110	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs565293445	chr17:46750111-46750112	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs572319872	chr17:46750226-46750227	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs541521361	chr17:46750256-46750257	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187562681	chr17:46750308-46750309	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs529096367	chr17:46750350-46750351	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs548764935	chr17:46750391-46750392	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562472384	chr17:46750393-46750394	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs531487769	chr17:46750422-46750423	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs193081131	chr17:46750438-46750439	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs375219257	chr17:46750471-46750472	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs571223972	chr17:46750479-46750480	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs566978290	chr17:46750517-46750518	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs547509699	chr17:46750588-46750589	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs542409253	chr17:46750600-46750601	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567707737	chr17:46750644-46750645	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs371159010	chr17:46750645-46750646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs61204483	chr17:46750646-46750647	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs76380430	chr17:46750649-46750650	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs71144515	chr17:46750665-46750666	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs185472150	chr17:46750700-46750701	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555793749	chr17:46750743-46750744	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs115907532	chr17:46750753-46750754	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs188289694	chr17:46750767-46750768	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs576672280	chr17:46750785-46750786	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs539338823	chr17:46750814-46750815	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144250636	chr17:46750828-46750829	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs192975099	chr17:46750829-46750830	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs572416237	chr17:46750854-46750855	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs541058710	chr17:46750923-46750924	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs184017304	chr17:46750961-46750962	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs574572704	chr17:46750986-46750987	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs141056104	chr17:46750994-46750995	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs35287491	chr17:46751050-46751051	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs34534959	chr17:46751057-46751058	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs562359319	chr17:46751063-46751064	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531377315	chr17:46751075-46751076	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs549483547	chr17:46751135-46751136	Weak transcription	Chromatin interactive region	1 gene(s)	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:196 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:46749000-46749800	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
2	chr17:46749000-46749800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin01	Skin
3	chr17:46749200-46749800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
4	chr17:46749200-46749800	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
5	chr17:46749200-46749800	Bivalent/Poised TSS	Fetal Lung	lung
6	chr17:46749200-46749800	Bivalent/Poised TSS	Right Atrium	heart
7	chr17:46749200-46749800	Bivalent Enhancer	Stomach Mucosa	stomach
8	chr17:46749400-46749800	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr17:46749400-46749800	Enhancers	Placenta	Placenta
10	chr17:46749400-46749800	Active TSS	Rectal Smooth Muscle	rectum
11	chr17:46749600-46749800	Bivalent Enhancer	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
12	chr17:46749600-46749800	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
13	chr17:46749600-46749800	Bivalent Enhancer	iPS-18 Cell Line	embryonic stem cell
14	chr17:46749600-46749800	Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
15	chr17:46749600-46749800	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
16	chr17:46749600-46749800	Bivalent Enhancer	Cortex derived primary cultured neurospheres	brain
17	chr17:46749600-46749800	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr17:46749600-46749800	Flanking Bivalent TSS/Enh	Adipose Nuclei	Adipose
19	chr17:46749600-46749800	Enhancers	Brain Hippocampus Middle	brain
20	chr17:46749600-46749800	Enhancers	Colon Smooth Muscle	Colon
21	chr17:46749600-46749800	Enhancers	Duodenum Mucosa	Duodenum
22	chr17:46749600-46749800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
23	chr17:46749600-46749800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
24	chr17:46749600-46749800	Bivalent Enhancer	Fetal Muscle Leg	muscle
25	chr17:46749600-46749800	Active TSS	Rectal Mucosa Donor 29	rectum
26	chr17:46749600-46749800	Enhancers	A549	lung
27	chr17:46749600-46749800	Enhancers	Hela-S3	cervix
28	chr17:46749600-46749800	Bivalent Enhancer	HepG2	liver
29	chr17:46749600-46749800	Enhancers	NHEK	skin
30	chr17:46749600-46749800	Enhancers	NHLF	lung
31	chr17:46749600-46750000	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
32	chr17:46749600-46750000	Enhancers	Brain Substantia Nigra	brain
33	chr17:46749600-46750000	Bivalent Enhancer	Fetal Stomach	stomach
34	chr17:46749600-46751400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr17:46749600-46752800	Weak transcription	Rectal Mucosa Donor 31	rectum
36	chr17:46749800-46750000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
37	chr17:46749800-46750000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr17:46749800-46750000	Bivalent Enhancer	Adipose Nuclei	Adipose
39	chr17:46749800-46755400	Weak transcription	Rectal Mucosa Donor 29	rectum
40	chr17:46749800-46755600	Weak transcription	A549	lung
41	chr17:46750000-46755400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr17:46752800-46753000	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
43	chr17:46752800-46753600	Enhancers	Rectal Mucosa Donor 31	rectum
44	chr17:46753600-46755600	Weak transcription	Rectal Mucosa Donor 31	rectum
45	chr17:46754800-46755000	Flanking Bivalent TSS/Enh	iPS-15b Cell Line	embryonic stem cell
46	chr17:46755000-46755400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
47	chr17:46755000-46755800	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
48	chr17:46755000-46756000	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
49	chr17:46755400-46755600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
50	chr17:46755400-46755600	Bivalent/Poised TSS	H1 Cell Line	embryonic stem cell

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