Variant report

Variant	nsv907749
Chromosome Location	chr17:17417169-17448589
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:446)
CpG islands
(count:185)
Chromatin interactive
region (count:38)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:446 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:17441690-17442407	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:17432908-17432936	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:17437142-17437777	HepG2	liver:	n/a	n/a
4	BACH1	chr17:17441812-17442261	K562	blood:	n/a	n/a
5	BCL3	chr17:17441793-17442420	A549	lung:	n/a	chr17:17441938-17441947
6	BHLHE40	chr17:17437213-17437556	HepG2	liver:	n/a	n/a
7	BHLHE40	chr17:17437187-17437500	HepG2	liver:	n/a	n/a
8	BHLHE40	chr17:17437124-17437736	HepG2	liver:	n/a	n/a
9	BHLHE40	chr17:17440733-17440937	A549	lung:	n/a	n/a
10	BHLHE40	chr17:17441733-17442313	HepG2	liver:	n/a	n/a
11	BHLHE40	chr17:17440834-17441032	HepG2	liver:	n/a	n/a
12	BHLHE40	chr17:17440760-17441105	K562	blood:	n/a	n/a
13	CEBPB	chr17:17439295-17439542	Hela-S3	cervix:	n/a	n/a
14	CEBPB	chr17:17427121-17427414	ECC-1	luminal epithelium:	n/a	n/a
15	CEBPB	chr17:17441697-17442154	HepG2	liver:	n/a	chr17:17441819-17441830 chr17:17442081-17442093
16	CEBPB	chr17:17441837-17441903	Hela-S3	cervix:	n/a	n/a
17	CEBPB	chr17:17418817-17419159	IMR90	lung:	n/a	chr17:17418961-17418972 chr17:17418961-17418974 chr17:17418960-17418977 chr17:17418961-17418972
18	CEBPB	chr17:17439331-17439628	ECC-1	luminal epithelium:	n/a	n/a
19	CEBPB	chr17:17426556-17427464	ECC-1	luminal epithelium:	n/a	n/a
20	CEBPB	chr17:17418912-17419112	H1-hESC	embryonic stem cell:	n/a	chr17:17418961-17418972 chr17:17418961-17418974 chr17:17418960-17418977 chr17:17418961-17418972
21	CEBPB	chr17:17437178-17437635	HepG2	liver:	n/a	n/a
22	CEBPB	chr17:17437190-17437634	HepG2	liver:	n/a	n/a
23	CEBPB	chr17:17439213-17439763	ECC-1	luminal epithelium:	n/a	n/a
24	CEBPB	chr17:17418611-17418647	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPD	chr17:17437195-17437526	HepG2	liver:	n/a	n/a
26	CHD1	chr17:17417622-17417643	H1-hESC	embryonic stem cell:	n/a	n/a
27	CHD2	chr17:17418476-17418657	H1-hESC	embryonic stem cell:	n/a	n/a
28	CREB1	chr17:17439154-17439849	A549	lung:	n/a	n/a
29	CREB1	chr17:17439207-17439747	ECC-1	luminal epithelium:	n/a	n/a
30	CREB1	chr17:17439287-17439579	A549	lung:	n/a	n/a
31	CREB1	chr17:17439116-17439781	ECC-1	luminal epithelium:	n/a	n/a
32	CREB1	chr17:17437224-17437822	HepG2	liver:	n/a	n/a
33	CREB1	chr17:17442040-17442321	A549	lung:	n/a	n/a
34	CTCF	chr17:17426680-17426830	BJ	skin:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
35	CTCF	chr17:17426469-17426998	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
36	CTCF	chr17:17426649-17426839	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
37	CTCF	chr17:17420320-17420470	Caco-2	colon:	n/a	n/a
38	CTCF	chr17:17420240-17420390	HBMEC	blood vessel:	n/a	n/a
39	CTCF	chr17:17426700-17426850	AG04449	skin:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
40	CTCF	chr17:17437400-17437550	HEK293	kidney:	n/a	n/a
41	CTCF	chr17:17441380-17441615	H1-hESC	embryonic stem cell:	n/a	chr17:17441447-17441455 chr17:17441571-17441580
42	CTCF	chr17:17420300-17420450	SAEC	small airway:	n/a	n/a
43	CTCF	chr17:17420260-17420410	MCF-7	breast:	n/a	n/a
44	CTCF	chr17:17426660-17426810	BJ	skin:	n/a	chr17:17426732-17426745
45	CTCF	chr17:17437241-17437313	GM10266	blood:	n/a	n/a
46	CTCF	chr17:17426664-17426841	LNCaP	prostate:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
47	CTCF	chr17:17426720-17426870	MCF-7	breast:	n/a	chr17:17426732-17426745 chr17:17426803-17426816 chr17:17426800-17426818
48	CTCF	chr17:17420440-17420590	A549	lung:	n/a	n/a
49	CTCF	chr17:17439820-17439970	SK-N-SH_RA	brain:	n/a	n/a
50	CTCF	chr17:17441240-17441390	MCF-7	breast:	n/a	chr17:17441257-17441270

(count:185 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17426422-17426472	NH-A	brain:	n/a
2	chr17:17418691-17418741	NB4	blood:	n/a
3	chr17:17426422-17426472	NH-A	brain:	n/a
4	chr17:17418691-17418741	NB4	blood:	n/a
5	chr17:17426422-17426472	HEK293	kidney:	embryo
6	chr17:17440660-17440710	SK-N-MC	brain:	n/a
7	chr17:17426422-17426472	SKMC	muscle:	n/a
8	chr17:17440660-17440710	Hepatocyte	liver:	n/a
9	chr17:17418691-17418741	ProgFib	skin:	n/a
10	chr17:17440660-17440710	BE2_C	brain:	n/a
11	chr17:17426422-17426472	PFSK-1	brain:	n/a
12	chr17:17440660-17440710	AG09309	skin:	n/a
13	chr17:17418691-17418741	IMR90	lung:	fetal
14	chr17:17426422-17426472	LNCaP	prostate:	n/a
15	chr17:17418691-17418741	T-47D	breast:	n/a
16	chr17:17440660-17440710	PANC-1	pancreas:	n/a
17	chr17:17418691-17418741	AoSMC	blood vessel:	n/a
18	chr17:17418691-17418741	HCT-116	colon:	n/a
19	chr17:17440660-17440710	HRPEpiC	eye:	n/a
20	chr17:17418691-17418741	BE2_C	brain:	n/a
21	chr17:17440660-17440710	GM06990	blood:	n/a
22	chr17:17440660-17440710	NH-A	brain:	n/a
23	chr17:17440660-17440710	NHBE	bronchial:	n/a
24	chr17:17418691-17418741	HCM	heart:	n/a
25	chr17:17418691-17418741	AG09319	gingival:	n/a
26	chr17:17418691-17418741	HIPEpiC	eye:	n/a
27	chr17:17426422-17426472	Hela-S3	cervix:	n/a
28	chr17:17440660-17440710	SKMC	muscle:	n/a
29	chr17:17440660-17440710	MCF10A-Er-Src	breast:	n/a
30	chr17:17418691-17418741	HL-60	blood:	n/a
31	chr17:17440660-17440710	SAEC	small airway:	n/a
32	chr17:17418691-17418741	Hela-S3	cervix:	n/a
33	chr17:17426422-17426472	HPAEpiC	pulmonary alveolar:	n/a
34	chr17:17440660-17440710	HepG2	liver:	n/a
35	chr17:17418691-17418741	MCF10A-Er-Src	breast:	n/a
36	chr17:17440660-17440710	A549	lung:	n/a
37	chr17:17418691-17418741	ovcar-3	ovarian:	n/a
38	chr17:17418691-17418741	HRPEpiC	eye:	n/a
39	chr17:17440660-17440710	NT2-D1	testis:	n/a
40	chr17:17418691-17418741	AG09309	skin:	n/a
41	chr17:17426422-17426472	AG09319	gingival:	n/a
42	chr17:17418691-17418741	NH-A	brain:	n/a
43	chr17:17440660-17440710	SK-N-SH	brain:	n/a
44	chr17:17426422-17426472	HAEpiC	amniotic membrane:	n/a
45	chr17:17418691-17418741	SK-N-MC	brain:	n/a
46	chr17:17418691-17418741	HAEpiC	amniotic membrane:	n/a
47	chr17:17426422-17426472	GM12892	blood:	n/a
48	chr17:17426422-17426472	K562	blood:	n/a
49	chr17:17440660-17440710	Jurkat	blood:	n/a
50	chr17:17440660-17440710	U87	brain:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17434263..17436931-chr17:17447202..17448742,2	K562	blood:
2	chr17:17417655..17420606-chr17:17424227..17426115,2	K562	blood:
3	chr17:17418461..17420867-chr17:17565358..17567430,2	K562	blood:
4	chr17:17433024..17434546-chr17:17435138..17436947,2	K562	blood:
5	chr17:17255931..17259232-chr17:17416483..17420040,4	K562	blood:
6	chr17:17407715..17410629-chr17:17418150..17421035,2	MCF-7	breast:
7	chr17:17398006..17400229-chr17:17440042..17442151,2	MCF-7	breast:
8	chr17:17417278..17420062-chr17:17491860..17494692,3	MCF-7	breast:
9	chr17:17419916..17424407-chr17:17429833..17432704,4	K562	blood:
10	chr17:17349656..17350278-chr17:17417464..17418315,2	MCF-7	breast:
11	chr17:17432762..17434995-chr17:17447449..17449700,2	K562	blood:
12	chr17:17426329..17426903-chr17:17544918..17545575,2	MCF-7	breast:
13	chr17:17447568..17449636-chr17:17462055..17463779,2	MCF-7	breast:
14	chr17:17422447..17424302-chr17:17424957..17427591,2	MCF-7	breast:
15	chr17:17426099..17426869-chr17:17516971..17517681,2	MCF-7	breast:
16	chr17:17437526..17439818-chr17:17494409..17495948,2	MCF-7	breast:
17	chr17:17432762..17434995-chr17:17447449..17449700,2	K562	blood:
18	chr17:17440432..17443332-chr17:17443891..17446677,2	MCF-7	breast:
19	chr17:17441533..17443885-chr17:17465004..17467167,2	K562	blood:
20	chr17:17433024..17434546-chr17:17435138..17436947,2	K562	blood:
21	chr17:17417655..17420606-chr17:17424227..17426115,2	K562	blood:
22	chr17:17407803..17409915-chr17:17438402..17440835,2	K562	blood:
23	chr17:17440432..17443332-chr17:17443891..17446677,2	MCF-7	breast:
24	chr17:17431321..17433424-chr17:17436533..17438889,2	MCF-7	breast:
25	chr17:17396965..17400190-chr17:17416535..17418625,3	MCF-7	breast:
26	chr17:17434263..17436931-chr17:17447202..17448742,2	K562	blood:
27	chr17:17439547..17441948-chr17:17448069..17450989,2	MCF-7	breast:
28	chr17:17412469..17415269-chr17:17430447..17432803,2	MCF-7	breast:
29	chr17:17447456..17449744-chr17:17453079..17454836,2	K562	blood:
30	chr17:17415079..17418148-chr17:17445039..17448328,3	MCF-7	breast:
31	chr17:17431321..17433424-chr17:17436533..17438889,2	MCF-7	breast:
32	chr17:17439547..17441948-chr17:17448069..17450989,2	MCF-7	breast:
33	chr17:17414329..17416478-chr17:17418151..17420327,2	K562	blood:
34	chr17:17420339..17423033-chr17:17440049..17441973,2	MCF-7	breast:
35	chr17:17398028..17400526-chr17:17429314..17431940,2	MCF-7	breast:
36	chr17:17444761..17447453-chr17:17453663..17455413,2	K562	blood:
37	chr17:17415079..17418148-chr17:17445039..17448328,3	MCF-7	breast:
38	chr17:17422447..17424302-chr17:17424957..17427591,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RASD1-2	chr17:17447584-17449725	NONHSAT146094

No data

Variant related genes	Relation type
PEMT	TF binding region
PEMT	CpG island
ENSG00000133027	chromatin interactions
ENSG00000264666	chromatin interactions
ENSG00000108551	chromatin interactions

Extended variants
information (count: 1254 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:1254 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4646406	chr17:17417169-17417170	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146617501	chr17:17417226-17417227	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs535431508	chr17:17417262-17417263	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs547900181	chr17:17417296-17417297	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs371265688	chr17:17417301-17417302	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs70963038	chr17:17417339-17417340	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs575589975	chr17:17417383-17417384	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs141390328	chr17:17417421-17417422	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs557637200	chr17:17417493-17417494	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs577791973	chr17:17417494-17417495	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs545931341	chr17:17417523-17417524	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs559430874	chr17:17417543-17417544	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs182444324	chr17:17417546-17417547	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs528604638	chr17:17417554-17417555	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs70963037	chr17:17417594-17417595	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs12373156	chr17:17417606-17417607	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs547695218	chr17:17417637-17417638	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs375974144	chr17:17417676-17417677	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs369274293	chr17:17417677-17417678	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370700740	chr17:17417689-17417690	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570907063	chr17:17417709-17417710	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs66637059	chr17:17417808-17417809	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs76032188	chr17:17417832-17417833	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs566566676	chr17:17417833-17417834	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs535574453	chr17:17417840-17417841	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs56180978	chr17:17418035-17418036	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs549959697	chr17:17418049-17418050	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs568889154	chr17:17418073-17418074	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs537724645	chr17:17418098-17418099	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs148931455	chr17:17418119-17418120	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs577724554	chr17:17418138-17418139	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs371734784	chr17:17418211-17418212	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs12103816	chr17:17418298-17418299	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs553599249	chr17:17418304-17418305	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs572985095	chr17:17418310-17418311	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs570052643	chr17:17418316-17418317	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs76127135	chr17:17418384-17418385	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs70963036	chr17:17418392-17418393	Enhancers Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs70963035	chr17:17418412-17418413	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs12103822	chr17:17418432-17418433	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs114727915	chr17:17418444-17418445	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs555492719	chr17:17418488-17418489	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533499430	chr17:17418497-17418498	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs70963034	chr17:17418501-17418502	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs4646405	chr17:17418594-17418595	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs143927608	chr17:17418616-17418617	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs369447198	chr17:17418678-17418679	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs558021486	chr17:17418691-17418692	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs373176807	chr17:17418694-17418695	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs70963033	chr17:17418735-17418736	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:162)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Colorectal cancer	16774939	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	22183965	CNVD

Chromatin state (count:788 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17400600-17422000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
2	chr17:17400800-17419200	Weak transcription	Duodenum Smooth Muscle	Duodenum
3	chr17:17401000-17418800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr17:17401000-17425400	Weak transcription	Thymus	Thymus
5	chr17:17407400-17425400	Weak transcription	Stomach Smooth Muscle	stomach
6	chr17:17407800-17418400	Weak transcription	Cortex derived primary cultured neurospheres	brain
7	chr17:17407800-17422600	Weak transcription	Brain Germinal Matrix	brain
8	chr17:17408000-17418200	Weak transcription	Fetal Brain Female	brain
9	chr17:17408000-17418400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr17:17408200-17419200	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr17:17408400-17417600	Weak transcription	H1 Cell Line	embryonic stem cell
12	chr17:17410200-17418200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr17:17410200-17426400	Weak transcription	Fetal Intestine Large	intestine
14	chr17:17411000-17418400	Strong transcription	Fetal Intestine Small	intestine
15	chr17:17411000-17420000	Weak transcription	Pancreas	Pancrea
16	chr17:17411000-17428600	Weak transcription	Brain Hippocampus Middle	brain
17	chr17:17411000-17428600	Weak transcription	Right Atrium	heart
18	chr17:17411000-17428800	Weak transcription	Brain Anterior Caudate	brain
19	chr17:17411400-17417200	Weak transcription	Spleen	Spleen
20	chr17:17411400-17419200	Weak transcription	Right Ventricle	heart
21	chr17:17411400-17423000	Weak transcription	Lung	lung
22	chr17:17411400-17428600	Weak transcription	Brain Cingulate Gyrus	brain
23	chr17:17411600-17425600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
24	chr17:17412000-17418200	Weak transcription	Fetal Brain Male	brain
25	chr17:17413200-17437400	Weak transcription	Aorta	Aorta
26	chr17:17414000-17424000	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr17:17414400-17417600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
28	chr17:17415000-17417200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr17:17415000-17425800	Weak transcription	Dnd41	blood
30	chr17:17415000-17426000	Strong transcription	Liver	Liver
31	chr17:17415400-17425600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
32	chr17:17415600-17423400	Weak transcription	Ovary	ovary
33	chr17:17415600-17424000	Weak transcription	Gastric	stomach
34	chr17:17415800-17417600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
35	chr17:17415800-17417800	Weak transcription	Adipose Nuclei	Adipose
36	chr17:17415800-17417800	Weak transcription	Fetal Heart	heart
37	chr17:17415800-17418000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
38	chr17:17415800-17420000	Weak transcription	Stomach Mucosa	stomach
39	chr17:17416000-17417600	Weak transcription	HUES6 Cell Line	embryonic stem cell
40	chr17:17416000-17417800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
41	chr17:17416000-17418400	Weak transcription	HSMMtube	muscle
42	chr17:17416000-17418600	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr17:17416000-17421800	Weak transcription	Esophagus	oesophagus
44	chr17:17416200-17417400	Weak transcription	Fetal Stomach	stomach
45	chr17:17416200-17417600	Weak transcription	Fetal Muscle Trunk	muscle
46	chr17:17416200-17417600	Weak transcription	Fetal Muscle Leg	muscle
47	chr17:17416200-17418000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
48	chr17:17416200-17418200	Weak transcription	NH-A	brain
49	chr17:17416200-17418600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
50	chr17:17416200-17425600	Weak transcription	Primary hematopoietic stem cells	blood

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