Variant report

Variant	esv1004208
Chromosome Location	chr17:17136933-17147885
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:676)
CpG islands
(count:977)
Chromatin interactive
region (count:36)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:676 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:17140527-17141159	HepG2	liver:	n/a	chr17:17140923-17140939
2	ARID3A	chr17:17140432-17141098	K562	blood:	n/a	chr17:17140923-17140939
3	ATF2	chr17:17140380-17140829	H1-hESC	embryonic stem cell:	n/a	n/a
4	ATF2	chr17:17140213-17141106	GM12878	blood:	n/a	n/a
5	ATF3	chr17:17140342-17140609	K562	blood:	n/a	n/a
6	ATF3	chr17:17140793-17141195	H1-hESC	embryonic stem cell:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
7	ATF3	chr17:17140905-17141092	HepG2	liver:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
8	ATF3	chr17:17140309-17141244	A549	lung:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
9	ATF3	chr17:17140882-17141111	K562	blood:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
10	ATF3	chr17:17140781-17141234	GM12878	blood:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
11	ATF3	chr17:17140900-17141123	GM12878	blood:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
12	ATF3	chr17:17140726-17141276	H1-hESC	embryonic stem cell:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
13	ATF3	chr17:17140718-17141275	HepG2	liver:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
14	ATF3	chr17:17140366-17141111	A549	lung:	n/a	chr17:17140984-17141004 chr17:17140995-17141004
15	BACH1	chr17:17140447-17141284	K562	blood:	n/a	n/a
16	BACH1	chr17:17140301-17141230	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL3	chr17:17140331-17141192	A549	lung:	n/a	chr17:17140536-17140549 chr17:17140651-17140664
18	BCL3	chr17:17139434-17141322	A549	lung:	n/a	chr17:17140536-17140549 chr17:17140323-17140336 chr17:17140651-17140664
19	BHLHE40	chr17:17140304-17141176	A549	lung:	n/a	chr17:17140993-17141006 chr17:17140989-17141010 chr17:17140996-17141005 chr17:17140995-17141004 chr17:17140994-17141003 chr17:17140995-17141004
20	BHLHE40	chr17:17138759-17138915	K562	blood:	n/a	n/a
21	BHLHE40	chr17:17139680-17141236	K562	blood:	n/a	chr17:17140993-17141006 chr17:17140989-17141010 chr17:17140996-17141005 chr17:17140995-17141004 chr17:17140994-17141003 chr17:17140995-17141004
22	BHLHE40	chr17:17139947-17141220	GM12878	blood:	n/a	chr17:17140993-17141006 chr17:17140989-17141010 chr17:17140996-17141005 chr17:17140995-17141004 chr17:17140994-17141003 chr17:17140995-17141004
23	BHLHE40	chr17:17139555-17141266	HepG2	liver:	n/a	chr17:17140993-17141006 chr17:17140989-17141010 chr17:17140996-17141005 chr17:17140995-17141004 chr17:17140994-17141003 chr17:17140995-17141004
24	BRCA1	chr17:17140363-17141149	Hela-S3	cervix:	n/a	n/a
25	BRCA1	chr17:17140422-17141074	GM12878	blood:	n/a	n/a
26	BRCA1	chr17:17140368-17141150	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr17:17140262-17141015	HepG2	liver:	n/a	n/a
28	CCNT2	chr17:17141565-17141765	K562	blood:	n/a	n/a
29	CCNT2	chr17:17140924-17141145	K562	blood:	n/a	n/a
30	CCNT2	chr17:17140171-17140721	K562	blood:	n/a	chr17:17140293-17140302
31	CEBPB	chr17:17140357-17141348	A549	lung:	n/a	n/a
32	CEBPB	chr17:17140511-17141189	K562	blood:	n/a	n/a
33	CEBPB	chr17:17139499-17139862	Hela-S3	cervix:	n/a	n/a
34	CEBPB	chr17:17140326-17141073	GM12878	blood:	n/a	n/a
35	CEBPB	chr17:17139551-17139765	HepG2	liver:	n/a	n/a
36	CEBPB	chr17:17139528-17139848	K562	blood:	n/a	n/a
37	CEBPB	chr17:17140831-17141247	MCF-7	breast:	n/a	n/a
38	CEBPB	chr17:17140563-17141187	Hela-S3	cervix:	n/a	n/a
39	CEBPD	chr17:17140883-17141203	HepG2	liver:	n/a	n/a
40	CEBPD	chr17:17140917-17141130	HepG2	liver:	n/a	n/a
41	CHD1	chr17:17138651-17141410	IMR90	lung:	n/a	n/a
42	CHD1	chr17:17140340-17141205	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD1	chr17:17140097-17141254	GM12878	blood:	n/a	n/a
44	CHD2	chr17:17140190-17140696	HepG2	liver:	n/a	n/a
45	CHD2	chr17:17140290-17140730	K562	blood:	n/a	n/a
46	CHD2	chr17:17140364-17141171	Hela-S3	cervix:	n/a	n/a
47	CHD2	chr17:17140260-17141169	GM12878	blood:	n/a	n/a
48	CREB1	chr17:17140168-17140797	A549	lung:	n/a	n/a
49	CREB1	chr17:17140882-17141259	A549	lung:	n/a	n/a
50	CTCF	chr17:17140481-17140617	GM12878	blood:	n/a	n/a

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17140685-17140735	AoSMC	blood vessel:	n/a
2	chr17:17140685-17140735	AoSMC	blood vessel:	n/a
3	chr17:17137465-17137515	T-47D	breast:	n/a
4	chr17:17140219-17140269	RPTEC	kidney:	n/a
5	chr17:17144298-17144348	U87	brain:	n/a
6	chr17:17137465-17137515	BE2_C	brain:	n/a
7	chr17:17140633-17140683	NT2-D1	testis:	n/a
8	chr17:17140570-17140620	ECC-1	luminal epithelium:	n/a
9	chr17:17139986-17140036	HRE	kidney:	n/a
10	chr17:17137465-17137515	K562	blood:	n/a
11	chr17:17140597-17140647	AG09309	skin:	n/a
12	chr17:17140633-17140683	HNPCEpiC	eye:	n/a
13	chr17:17141020-17141070	HMEC	breast:	n/a
14	chr17:17139986-17140036	AG04449	skin:	fetal
15	chr17:17140558-17140608	GM19239	blood:	n/a
16	chr17:17140580-17140630	SAEC	small airway:	n/a
17	chr17:17140597-17140647	NB4	blood:	n/a
18	chr17:17140597-17140647	HIPEpiC	eye:	n/a
19	chr17:17141047-17141097	HNPCEpiC	eye:	n/a
20	chr17:17144298-17144348	MCF10A-Er-Src	breast:	n/a
21	chr17:17140463-17140513	A549	lung:	n/a
22	chr17:17139986-17140036	HCM	heart:	n/a
23	chr17:17144298-17144348	HCM	heart:	n/a
24	chr17:17140463-17140513	Caco-2	colon:	n/a
25	chr17:17141047-17141097	ovcar-3	ovarian:	n/a
26	chr17:17140219-17140269	HPAEpiC	pulmonary alveolar:	n/a
27	chr17:17140580-17140630	HEEpiC	esophagus:	n/a
28	chr17:17140463-17140513	Hepatocyte	liver:	n/a
29	chr17:17140493-17140543	HPAEpiC	pulmonary alveolar:	n/a
30	chr17:17140493-17140543	HCF	heart:	n/a
31	chr17:17140633-17140683	RPTEC	kidney:	n/a
32	chr17:17141047-17141097	NB4	blood:	n/a
33	chr17:17140580-17140630	AG10803	skin:	n/a
34	chr17:17140084-17140134	SAEC	small airway:	n/a
35	chr17:17137465-17137515	AG10803	skin:	n/a
36	chr17:17140570-17140620	NH-A	brain:	n/a
37	chr17:17140570-17140620	BE2_C	brain:	n/a
38	chr17:17140084-17140134	NB4	blood:	n/a
39	chr17:17139986-17140036	AG04450	lung:	fetal
40	chr17:17137465-17137515	AG04450	lung:	fetal
41	chr17:17139986-17140036	AG10803	skin:	n/a
42	chr17:17141047-17141097	HepG2	liver:	n/a
43	chr17:17140343-17140393	GM12878	blood:	n/a
44	chr17:17141020-17141070	AG09309	skin:	n/a
45	chr17:17140633-17140683	K562	blood:	n/a
46	chr17:17140558-17140608	PFSK-1	brain:	n/a
47	chr17:17140084-17140134	HCPEpiC	choroid plexus:	n/a
48	chr17:17139986-17140036	NHDF-neo	bronchial:	n/a
49	chr17:17140558-17140608	MCF10A-Er-Src	breast:	n/a
50	chr17:17140558-17140608	HAEpiC	amniotic membrane:	n/a

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr17:17107445..17110008-chr17:17138195..17140495,3	K562	blood:
2	chr17:17140058..17141717-chr17:17149806..17152339,2	MCF-7	breast:
3	chr17:17121039..17123215-chr17:17134749..17137620,2	K562	blood:
4	chr17:17131671..17134526-chr17:17137834..17141080,5	MCF-7	breast:
5	chr17:17107449..17109941-chr17:17138935..17142587,4	MCF-7	breast:
6	chr17:17139508..17142367-chr17:17182538..17186121,3	MCF-7	breast:
7	chr13:111805704..111806343-chr17:17140161..17140763,2	HCT-116	colon:
8	chr17:17126964..17129201-chr17:17139091..17140803,2	MCF-7	breast:
9	chr17:17138850..17142014-chr17:17149192..17152269,3	K562	blood:
10	chr17:17142608..17144134-chr17:17146092..17148091,2	K562	blood:
11	chr17:17146996..17149508-chr17:17150450..17152248,2	K562	blood:
12	chr17:17139773..17141689-chr17:17147238..17149246,2	MCF-7	breast:
13	chr17:17140695..17143255-chr17:17151117..17153823,2	MCF-7	breast:
14	chr17:17139597..17142266-chr17:17398056..17400275,2	MCF-7	breast:
15	chr17:17139354..17141733-chr17:17143268..17148053,6	MCF-7	breast:
16	chr17:17135445..17137036-chr17:17206485..17208759,2	K562	blood:
17	chr17:17140568..17141073-chr7:69416276..69416797,2	HCT-116	colon:
18	chr17:17126262..17128515-chr17:17140252..17142748,2	MCF-7	breast:
19	chr17:17139635..17142575-chr17:17144486..17149716,4	K562	blood:
20	chr17:17109583..17111343-chr17:17139423..17141092,2	MCF-7	breast:
21	chr17:17134971..17137251-chr17:17137733..17141244,3	K562	blood:
22	chr17:17107449..17110459-chr17:17138885..17140924,4	K562	blood:
23	chr17:17137888..17140600-chr17:17205281..17208205,3	MCF-7	breast:
24	chr17:17141498..17143338-chr17:17206126..17208099,2	K562	blood:
25	chr17:17138742..17142464-chr17:17205516..17208012,3	MCF-7	breast:
26	chr17:17135534..17137524-chr17:17138995..17141355,2	MCF-7	breast:
27	chr17:17139354..17141733-chr17:17143268..17148053,6	MCF-7	breast:
28	chr17:17134971..17137251-chr17:17137733..17141244,3	K562	blood:
29	chr17:17138230..17139977-chr17:17206965..17208705,2	K562	blood:
30	chr17:17138280..17141930-chr17:17183181..17187644,4	MCF-7	breast:
31	chr17:17138181..17140588-chr17:17182569..17184810,2	K562	blood:
32	chr17:17142608..17144134-chr17:17146092..17148091,2	K562	blood:
33	chr17:17142459..17145077-chr17:17167559..17169849,2	K562	blood:
34	chr17:17135534..17137524-chr17:17138995..17141355,2	MCF-7	breast:
35	chr17:17139635..17142575-chr17:17144486..17149716,4	K562	blood:
36	chr17:17103497..17105821-chr17:17140669..17142216,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-COPS3-1	chr17:17138747-17139432	ENSG00000266498.1

No data

Variant related genes	Relation type
ENSG00000226359	TF binding region
ENSG00000264187	TF binding region
FLCN	TF binding region
ENSG00000266498	TF binding region
ENSG00000265109	TF binding region
ENSG00000226359	CpG island
ENSG00000264187	CpG island
FLCN	CpG island
ENSG00000266498	CpG island
ENSG00000265109	CpG island
ENSG00000102606	chromatin interactions
ENSG00000264187	chromatin interactions
ENSG00000205309	chromatin interactions
ENSG00000108551	chromatin interactions
ENSG00000154803	chromatin interactions
ENSG00000266498	chromatin interactions
ENSG00000226359	chromatin interactions
ENSG00000179598	chromatin interactions
ENSG00000265109	chromatin interactions
ENSG00000141030	chromatin interactions

Extended variants
information (count: 461 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:461 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs565180253	chr17:17136961-17136962	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs527637572	chr17:17137001-17137002	Weak transcription Enhancers Strong transcription	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs34208211	chr17:17137054-17137055	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs533020285	chr17:17137071-17137072	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs374236806	chr17:17137110-17137111	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs567714789	chr17:17137203-17137204	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs372683304	chr17:17137231-17137232	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs549991024	chr17:17137302-17137303	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs8079562	chr17:17137306-17137307	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
10	rs187016533	chr17:17137307-17137308	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs548629503	chr17:17137360-17137361	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs138890259	chr17:17137380-17137381	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs190217043	chr17:17137397-17137398	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs534571960	chr17:17137417-17137418	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs8079892	chr17:17137492-17137493	Weak transcription Enhancers Genic enhancers Strong transcription	CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs111444648	chr17:17137521-17137522	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs574611571	chr17:17137522-17137523	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs543526231	chr17:17137524-17137525	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs563512080	chr17:17137525-17137526	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs147858994	chr17:17137526-17137527	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs386795904	chr17:17137527-17137528	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs386795905	chr17:17137528-17137529	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs139807532	chr17:17137529-17137530	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs199672078	chr17:17137530-17137531	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs559559154	chr17:17137536-17137537	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs375429199	chr17:17137675-17137676	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs547740891	chr17:17137715-17137716	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs200106813	chr17:17137781-17137782	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs8079971	chr17:17137811-17137812	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs530167256	chr17:17137872-17137873	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs139600743	chr17:17137929-17137930	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs571895847	chr17:17137949-17137950	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs149324031	chr17:17138013-17138014	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs113630550	chr17:17138014-17138015	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs8065774	chr17:17138159-17138160	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
36	rs368013798	chr17:17138167-17138168	Weak transcription Enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs566330779	chr17:17138204-17138205	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
38	rs369894087	chr17:17138207-17138208	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
39	rs371911802	chr17:17138209-17138210	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
40	rs534983132	chr17:17138218-17138219	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
41	rs376531540	chr17:17138221-17138222	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
42	rs369841791	chr17:17138238-17138239	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
43	rs145061409	chr17:17138261-17138262	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
44	rs8067200	chr17:17138288-17138289	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
45	rs537187777	chr17:17138295-17138296	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
46	rs376026949	chr17:17138317-17138318	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
47	rs182152167	chr17:17138329-17138330	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
48	rs369223545	chr17:17138334-17138335	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
49	rs373930686	chr17:17138343-17138344	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
50	rs8066090	chr17:17138381-17138382	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:161)

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
Pancreatic cancer	21811587	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
Breast cancer	22522925	CNVD
Melanoma	20877625	CNVD

Chromatin state (count:800 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17113800-17137600	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
2	chr17:17115200-17139600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
3	chr17:17126200-17138600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr17:17128600-17138800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
5	chr17:17129400-17138800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr17:17130000-17139000	Weak transcription	Fetal Kidney	kidney
7	chr17:17130600-17138600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr17:17132400-17138800	Weak transcription	Primary hematopoietic stem cells	blood
9	chr17:17133400-17138600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
10	chr17:17133400-17138600	Weak transcription	Rectal Smooth Muscle	rectum
11	chr17:17133600-17138600	Weak transcription	K562	blood
12	chr17:17133600-17138800	Weak transcription	Stomach Mucosa	stomach
13	chr17:17135000-17138800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr17:17135200-17138800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr17:17135400-17138600	Weak transcription	Primary T helper naive cells from peripheral blood	blood
16	chr17:17135400-17138800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr17:17135400-17138800	Weak transcription	HUVEC	blood vessel
18	chr17:17135400-17139000	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
19	chr17:17135400-17139400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
20	chr17:17135600-17138600	Weak transcription	Fetal Lung	lung
21	chr17:17135600-17138800	Weak transcription	Fetal Brain Male	brain
22	chr17:17135600-17139000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr17:17135800-17137400	Weak transcription	Fetal Heart	heart
24	chr17:17135800-17138600	Weak transcription	HSMM	muscle
25	chr17:17135800-17138800	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
26	chr17:17135800-17138800	Weak transcription	Esophagus	oesophagus
27	chr17:17135800-17138800	Weak transcription	Right Ventricle	heart
28	chr17:17135800-17138800	Weak transcription	Thymus	Thymus
29	chr17:17136000-17138600	Weak transcription	Muscle Satellite Cultured Cells	--
30	chr17:17136000-17138600	Weak transcription	Fetal Brain Female	brain
31	chr17:17136000-17138800	Weak transcription	H1 Cell Line	embryonic stem cell
32	chr17:17136000-17138800	Weak transcription	Colonic Mucosa	Colon
33	chr17:17136000-17138800	Weak transcription	Psoas Muscle	Psoas
34	chr17:17136000-17138800	Weak transcription	Small Intestine	intestine
35	chr17:17136200-17137200	Weak transcription	Ovary	ovary
36	chr17:17136200-17137400	Weak transcription	Adipose Nuclei	Adipose
37	chr17:17136200-17137400	Weak transcription	Brain Substantia Nigra	brain
38	chr17:17136200-17137400	Weak transcription	Gastric	stomach
39	chr17:17136200-17137600	Weak transcription	Pancreas	Pancrea
40	chr17:17136200-17138000	Strong transcription	Fetal Intestine Small	intestine
41	chr17:17136200-17138400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
42	chr17:17136200-17138400	Weak transcription	Spleen	Spleen
43	chr17:17136200-17138600	Weak transcription	H9 Cell Line	embryonic stem cell
44	chr17:17136200-17138600	Weak transcription	Primary neutrophils fromperipheralblood	blood
45	chr17:17136200-17138600	Weak transcription	Primary B cells from cord blood	blood
46	chr17:17136200-17138600	Weak transcription	Primary B cells from peripheral blood	blood
47	chr17:17136200-17138600	Weak transcription	Primary T helper cells PMA-I stimulated	--
48	chr17:17136200-17138600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
49	chr17:17136200-17138600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr17:17136200-17138600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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