Variant report

Variant	esv1803680
Chromosome Location	chr17:17408484-17426009
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BHLHE40	chr17:17412516-17412612	K562	blood:	n/a	n/a
2	BHLHE40	chr17:17415310-17415513	K562	blood:	n/a	n/a
3	CEBPB	chr17:17418817-17419159	IMR90	lung:	n/a	chr17:17418961-17418972 chr17:17418961-17418974 chr17:17418960-17418977 chr17:17418961-17418972
4	CEBPB	chr17:17418611-17418647	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr17:17410766-17411077	HepG2	liver:	n/a	chr17:17410908-17410921 chr17:17410908-17410919 chr17:17410910-17410919 chr17:17410908-17410921 chr17:17410910-17410921
6	CEBPB	chr17:17415261-17415620	IMR90	lung:	n/a	n/a
7	CEBPB	chr17:17418912-17419112	H1-hESC	embryonic stem cell:	n/a	chr17:17418961-17418972 chr17:17418961-17418974 chr17:17418960-17418977 chr17:17418961-17418972
8	CEBPB	chr17:17410796-17411057	A549	lung:	n/a	chr17:17410908-17410921 chr17:17410908-17410919 chr17:17410910-17410919 chr17:17410908-17410921 chr17:17410910-17410921
9	CEBPB	chr17:17410749-17411084	K562	blood:	n/a	chr17:17410908-17410921 chr17:17410908-17410919 chr17:17410910-17410919 chr17:17410908-17410921 chr17:17410910-17410921
10	CEBPB	chr17:17410775-17411042	IMR90	lung:	n/a	chr17:17410908-17410921 chr17:17410908-17410919 chr17:17410910-17410919 chr17:17410908-17410921 chr17:17410910-17410921
11	CHD1	chr17:17415120-17415691	IMR90	lung:	n/a	n/a
12	CHD1	chr17:17417622-17417643	H1-hESC	embryonic stem cell:	n/a	n/a
13	CHD2	chr17:17418476-17418657	H1-hESC	embryonic stem cell:	n/a	n/a
14	CTCF	chr17:17420260-17420410	HepG2	liver:	n/a	n/a
15	CTCF	chr17:17414740-17414890	GM12864	blood:	n/a	n/a
16	CTCF	chr17:17409038-17409046	H1-hESC	embryonic stem cell:	n/a	n/a
17	CTCF	chr17:17409047-17409104	H1-hESC	embryonic stem cell:	n/a	n/a
18	CTCF	chr17:17408940-17409090	HBMEC	blood vessel:	n/a	n/a
19	CTCF	chr17:17412972-17413114	MCF-7	breast:	n/a	chr17:17413036-17413052
20	CTCF	chr17:17414600-17414750	HRPEpiC	eye:	n/a	n/a
21	CTCF	chr17:17420240-17420390	GM12873	blood:	n/a	n/a
22	CTCF	chr17:17412760-17412914	Hela-S3	cervix:	n/a	n/a
23	CTCF	chr17:17414720-17414870	AG04449	skin:	n/a	chr17:17414739-17414757
24	CTCF	chr17:17415460-17415610	AG04449	skin:	n/a	chr17:17415473-17415486
25	CTCF	chr17:17413003-17413098	MCF-7	breast:	n/a	chr17:17413036-17413052
26	CTCF	chr17:17420300-17420450	WERI-Rb-1	eye:	n/a	n/a
27	CTCF	chr17:17414500-17414650	RPTEC	kidney:	n/a	chr17:17414557-17414570
28	CTCF	chr17:17414100-17414250	NB4	blood:	n/a	chr17:17414175-17414193 chr17:17414188-17414201
29	CTCF	chr17:17412656-17413260	K562	blood:	n/a	chr17:17412950-17412958 chr17:17412951-17412959 chr17:17413036-17413052
30	CTCF	chr17:17420240-17420390	HBMEC	blood vessel:	n/a	n/a
31	CTCF	chr17:17414620-17414770	BJ	skin:	n/a	chr17:17414739-17414757
32	CTCF	chr17:17414760-17414910	HRE	kidney:	n/a	n/a
33	CTCF	chr17:17415404-17415431	Fibrobl	skin:	n/a	n/a
34	CTCF	chr17:17413006-17413062	GM19239	blood:	n/a	chr17:17413036-17413052
35	CTCF	chr17:17420340-17420490	HEK293	kidney:	n/a	n/a
36	CTCF	chr17:17420260-17420410	MCF-7	breast:	n/a	n/a
37	CTCF	chr17:17415160-17415310	AoAF	blood vessel:	n/a	n/a
38	CTCF	chr17:17413000-17413150	A549	lung:	n/a	chr17:17413036-17413052
39	CTCF	chr17:17420320-17420470	Caco-2	colon:	n/a	n/a
40	CTCF	chr17:17414660-17414810	HRPEpiC	eye:	n/a	chr17:17414739-17414757
41	CTCF	chr17:17420300-17420450	SAEC	small airway:	n/a	n/a
42	CTCF	chr17:17415420-17415570	HCPEpiC	choroid plexus:	n/a	chr17:17415473-17415486
43	CTCF	chr17:17412940-17413090	HEK293	kidney:	n/a	chr17:17412950-17412958 chr17:17412951-17412959 chr17:17413036-17413052
44	CTCF	chr17:17413024-17413077	NHEK	skin:	n/a	chr17:17413036-17413052
45	CTCF	chr17:17414620-17414770	GM12869	blood:	n/a	chr17:17414739-17414757
46	CTCF	chr17:17414660-17414810	Hela-S3	cervix:	n/a	chr17:17414739-17414757
47	CTCF	chr17:17414688-17414784	GM12891	blood:	n/a	chr17:17414739-17414757
48	CTCF	chr17:17412920-17413070	GM12875	blood:	n/a	chr17:17412950-17412958 chr17:17412951-17412959 chr17:17413036-17413052
49	CTCF	chr17:17420380-17420530	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr17:17415438-17415442	Fibrobl	skin:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17409003-17409053	NHBE	bronchial:	n/a
2	chr17:17409003-17409053	K562	blood:	n/a
3	chr17:17418691-17418741	SAEC	small airway:	n/a
4	chr17:17414998-17415048	RPTEC	kidney:	n/a
5	chr17:17418691-17418741	HPAEpiC	pulmonary alveolar:	n/a
6	chr17:17414998-17415048	NHDF-neo	bronchial:	n/a
7	chr17:17414998-17415048	SKMC	muscle:	n/a
8	chr17:17414998-17415048	AG10803	skin:	n/a
9	chr17:17409003-17409053	HCM	heart:	n/a
10	chr17:17409003-17409053	HNPCEpiC	eye:	n/a
11	chr17:17409003-17409053	HCF	heart:	n/a
12	chr17:17414998-17415048	CMK	blood:	n/a
13	chr17:17414998-17415048	LNCaP	prostate:	n/a
14	chr17:17414998-17415048	HCT-116	colon:	n/a
15	chr17:17409003-17409053	NB4	blood:	n/a
16	chr17:17414998-17415048	HCPEpiC	choroid plexus:	n/a
17	chr17:17418691-17418741	GM19239	blood:	n/a
18	chr17:17409003-17409053	PFSK-1	brain:	n/a
19	chr17:17409003-17409053	HEK293	kidney:	embryo
20	chr17:17409003-17409053	MCF10A-Er-Src	breast:	n/a
21	chr17:17418691-17418741	HEEpiC	esophagus:	n/a
22	chr17:17418691-17418741	HCT-116	colon:	n/a
23	chr17:17418691-17418741	AG04450	lung:	fetal
24	chr17:17414998-17415048	BJ	skin:	n/a
25	chr17:17409003-17409053	Hela-S3	cervix:	n/a
26	chr17:17418691-17418741	HCF	heart:	n/a
27	chr17:17409003-17409053	NT2-D1	testis:	n/a
28	chr17:17409003-17409053	LNCaP	prostate:	n/a
29	chr17:17418691-17418741	SKMC	muscle:	n/a
30	chr17:17414998-17415048	HAEpiC	amniotic membrane:	n/a
31	chr17:17418691-17418741	HMEC	breast:	n/a
32	chr17:17414998-17415048	H1-hESC	embryonic stem cell:	embryo
33	chr17:17418691-17418741	HNPCEpiC	eye:	n/a
34	chr17:17414998-17415048	AG09309	skin:	n/a
35	chr17:17409003-17409053	NH-A	brain:	n/a
36	chr17:17409003-17409053	Caco-2	colon:	n/a
37	chr17:17414998-17415048	GM12892	blood:	n/a
38	chr17:17409003-17409053	GM12892	blood:	n/a
39	chr17:17414998-17415048	HL-60	blood:	n/a
40	chr17:17409003-17409053	BE2_C	brain:	n/a
41	chr17:17409003-17409053	HEEpiC	esophagus:	n/a
42	chr17:17409003-17409053	GM19239	blood:	n/a
43	chr17:17418691-17418741	HCM	heart:	n/a
44	chr17:17409003-17409053	GM12878	blood:	n/a
45	chr17:17409003-17409053	CMK	blood:	n/a
46	chr17:17414998-17415048	T-47D	breast:	n/a
47	chr17:17409003-17409053	ovcar-3	ovarian:	n/a
48	chr17:17414998-17415048	HRCEpiC	kidney:	n/a
49	chr17:17409003-17409053	H1-hESC	embryonic stem cell:	embryo
50	chr17:17414998-17415048	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:17254871..17257854-chr17:17406200..17408838,2	K562	blood:
2	chr17:17404753..17406377-chr17:17407243..17409547,3	K562	blood:
3	chr17:17349656..17350278-chr17:17417464..17418315,2	MCF-7	breast:
4	chr17:17405820..17407609-chr17:17411201..17413921,2	MCF-7	breast:
5	chr17:17415079..17418148-chr17:17445039..17448328,3	MCF-7	breast:
6	chr17:17412469..17415269-chr17:17430447..17432803,2	MCF-7	breast:
7	chr17:17414329..17416478-chr17:17418151..17420327,2	K562	blood:
8	chr17:17403140..17409448-chr17:17410177..17415726,8	K562	blood:
9	chr17:17396995..17404908-chr17:17406815..17414609,13	MCF-7	breast:
10	chr17:17400013..17403525-chr17:17411408..17414122,3	MCF-7	breast:
11	chr17:17417655..17420606-chr17:17424227..17426115,2	K562	blood:
12	chr17:17402799..17405333-chr17:17413416..17415879,2	K562	blood:
13	chr17:17422447..17424302-chr17:17424957..17427591,2	MCF-7	breast:
14	chr17:17417655..17420606-chr17:17424227..17426115,2	K562	blood:
15	chr17:17417278..17420062-chr17:17491860..17494692,3	MCF-7	breast:
16	chr17:17422447..17424302-chr17:17424957..17427591,2	MCF-7	breast:
17	chr17:17396965..17400190-chr17:17416535..17418625,3	MCF-7	breast:
18	chr17:17407715..17410629-chr17:17418150..17421035,2	MCF-7	breast:
19	chr17:17415416..17417029-chr17:17420667..17422439,2	MCF-7	breast:
20	chr17:17255931..17259232-chr17:17416483..17420040,4	K562	blood:
21	chr17:17418461..17420867-chr17:17565358..17567430,2	K562	blood:
22	chr17:17413540..17416682-chr17:17491858..17494964,3	MCF-7	breast:
23	chr17:17402735..17405355-chr17:17407250..17409232,2	K562	blood:
24	chr17:17414329..17416478-chr17:17418151..17420327,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MED9-1	chr17:17410665-17410931	ENSG00000265511.1
2	lnc-MED9-1	chr17:17411095-17411622	ENSG00000265511.1

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PEMT	hsa-miR-124-3p	chr17:17408974-17408994
2	PEMT	hsa-miR-124-3p	chr17:17408980-17408974

Variant related genes	Relation type
ENSG00000265511	TF binding region
PEMT	TF binding region
ENSG00000265511	CpG island
PEMT	CpG island
ENSG00000264666	chromatin interactions
ENSG00000133027	chromatin interactions
ENSG00000265511	chromatin interactions
ENSG00000108551	chromatin interactions

Extended variants
information (count: 733 )
Associated
traits (count: 162 )

Variant overlapped rSNPs/rCNVs (count:733 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1020696	chr17:17408484-17408485	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs576522351	chr17:17408571-17408572	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs545691041	chr17:17408587-17408588	Weak transcription Enhancers Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs565582890	chr17:17408620-17408621	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538234788	chr17:17408628-17408629	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs145023337	chr17:17408639-17408640	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs541607226	chr17:17408645-17408646	Weak transcription Enhancers Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs4646410	chr17:17408699-17408700	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs150938262	chr17:17408708-17408709	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs575181700	chr17:17408721-17408722	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs189503305	chr17:17408783-17408784	Weak transcription Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs532000938	chr17:17408814-17408815	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs70965429	chr17:17408824-17408825	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs552004865	chr17:17408848-17408849	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs192498877	chr17:17408881-17408882	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs534651950	chr17:17408891-17408892	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs537718150	chr17:17408946-17408947	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs548343501	chr17:17408960-17408961	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs554763232	chr17:17408994-17408995	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region miRNA target site	4 gene(s)	Overlapped CNVs	n/a
20	rs568197691	chr17:17408995-17408996	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs536708459	chr17:17409007-17409008	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs70965428	chr17:17409032-17409033	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs377124101	chr17:17409038-17409039	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs539041693	chr17:17409058-17409059	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs201604713	chr17:17409062-17409063	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs370372061	chr17:17409075-17409076	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs367695879	chr17:17409092-17409093	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs70965427	chr17:17409125-17409126	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs147868279	chr17:17409139-17409140	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs140621950	chr17:17409140-17409141	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs375372363	chr17:17409152-17409153	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs560374658	chr17:17409153-17409154	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs368528009	chr17:17409168-17409169	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs543087227	chr17:17409170-17409171	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs371281392	chr17:17409177-17409178	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs371984632	chr17:17409187-17409188	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs563049169	chr17:17409219-17409220	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs531940974	chr17:17409234-17409235	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs373217602	chr17:17409235-17409236	Weak transcription Enhancers Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs545384293	chr17:17409243-17409244	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs376679485	chr17:17409251-17409252	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs139498493	chr17:17409330-17409331	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs369411717	chr17:17409389-17409390	Weak transcription Enhancers Strong transcription Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs3816511	chr17:17409401-17409402	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs548201995	chr17:17409437-17409438	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs149699061	chr17:17409445-17409446	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs34890050	chr17:17409518-17409519	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs113940354	chr17:17409521-17409522	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375888743	chr17:17409522-17409523	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs376787997	chr17:17409545-17409546	Weak transcription Enhancers Genic enhancers Strong transcription	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:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17399600-17413800	Weak transcription	Dnd41	blood
2	chr17:17400600-17409800	Weak transcription	Esophagus	oesophagus
3	chr17:17400600-17410000	Weak transcription	Liver	Liver
4	chr17:17400600-17415200	Weak transcription	Ovary	ovary
5	chr17:17400600-17422000	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
6	chr17:17400800-17409000	Weak transcription	Right Ventricle	heart
7	chr17:17400800-17413000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
8	chr17:17400800-17419200	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr17:17401000-17411200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
10	chr17:17401000-17418800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
11	chr17:17401000-17425400	Weak transcription	Thymus	Thymus
12	chr17:17401200-17411000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
13	chr17:17401200-17415200	Weak transcription	Gastric	stomach
14	chr17:17401600-17409200	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr17:17405600-17408800	Enhancers	Fetal Muscle Leg	muscle
16	chr17:17405600-17412000	Enhancers	Fetal Muscle Trunk	muscle
17	chr17:17405800-17413200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr17:17406200-17415800	Enhancers	Fetal Heart	heart
19	chr17:17406600-17409000	Enhancers	Brain Inferior Temporal Lobe	brain
20	chr17:17406600-17414600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr17:17406800-17410600	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:17407000-17408800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
23	chr17:17407400-17409200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
24	chr17:17407400-17409600	Weak transcription	Skeletal Muscle Female	skeletal muscle
25	chr17:17407400-17409800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
26	chr17:17407400-17409800	Weak transcription	Right Atrium	heart
27	chr17:17407400-17425400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr17:17407800-17409200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr17:17407800-17418400	Weak transcription	Cortex derived primary cultured neurospheres	brain
30	chr17:17407800-17422600	Weak transcription	Brain Germinal Matrix	brain
31	chr17:17408000-17409600	Weak transcription	Brain Hippocampus Middle	brain
32	chr17:17408000-17409600	Strong transcription	Fetal Stomach	stomach
33	chr17:17408000-17410000	Weak transcription	Brain Anterior Caudate	brain
34	chr17:17408000-17410200	Weak transcription	Brain Cingulate Gyrus	brain
35	chr17:17408000-17411200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr17:17408000-17418200	Weak transcription	Fetal Brain Female	brain
37	chr17:17408000-17418400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr17:17408200-17409000	Weak transcription	Lung	lung
39	chr17:17408200-17409400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
40	chr17:17408200-17409400	Strong transcription	Fetal Intestine Small	intestine
41	chr17:17408200-17419200	Weak transcription	Pancreatic Islets	Pancreatic Islet
42	chr17:17408400-17408600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
43	chr17:17408400-17409200	Strong transcription	Foreskin Fibroblast Primary Cells skin02	Skin
44	chr17:17408400-17409600	Weak transcription	Brain Angular Gyrus	brain
45	chr17:17408400-17409800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
46	chr17:17408400-17410000	Weak transcription	Fetal Brain Male	brain
47	chr17:17408400-17417600	Weak transcription	H1 Cell Line	embryonic stem cell
48	chr17:17408800-17409400	Genic enhancers	Fetal Muscle Leg	muscle
49	chr17:17408800-17414400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
50	chr17:17409000-17409600	Weak transcription	Brain Inferior Temporal Lobe	brain

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