Variant report

Variant	nsv470580
Chromosome Location	chr17:18029857-18060192
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1091)
CpG islands
(count:305)
Chromatin interactive
region (count:70)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1091 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:18046421-18046669	K562	blood:	n/a	n/a
2	ARID3A	chr17:18041673-18042165	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:18044390-18044917	K562	blood:	n/a	n/a
4	ARID3A	chr17:18044477-18044878	HepG2	liver:	n/a	n/a
5	BACH1	chr17:18047347-18047455	H1-hESC	embryonic stem cell:	n/a	n/a
6	BHLHE40	chr17:18043279-18043577	K562	blood:	n/a	n/a
7	BHLHE40	chr17:18057445-18057622	K562	blood:	n/a	n/a
8	BHLHE40	chr17:18043300-18043453	GM12878	blood:	n/a	n/a
9	BHLHE40	chr17:18046481-18046647	K562	blood:	n/a	n/a
10	BRCA1	chr17:18041647-18042000	HepG2	liver:	n/a	n/a
11	BRCA1	chr17:18057440-18057572	GM12878	blood:	n/a	n/a
12	BRCA1	chr17:18057042-18057466	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr17:18056835-18057016	K562	blood:	n/a	n/a
14	CEBPB	chr17:18046553-18046933	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr17:18057274-18057483	HepG2	liver:	n/a	n/a
16	CEBPB	chr17:18057203-18057565	HepG2	liver:	n/a	n/a
17	CEBPB	chr17:18056804-18057664	IMR90	lung:	n/a	n/a
18	CEBPB	chr17:18056806-18057580	K562	blood:	n/a	n/a
19	CEBPB	chr17:18057280-18057511	A549	lung:	n/a	n/a
20	CEBPB	chr17:18046693-18046871	HepG2	liver:	n/a	n/a
21	CEBPB	chr17:18046610-18046956	HepG2	liver:	n/a	n/a
22	CEBPB	chr17:18041694-18041932	Hela-S3	cervix:	n/a	chr17:18041823-18041834
23	CEBPB	chr17:18057263-18057496	K562	blood:	n/a	n/a
24	CEBPB	chr17:18032664-18032829	HepG2	liver:	n/a	chr17:18032723-18032734
25	CEBPB	chr17:18032567-18032894	Hela-S3	cervix:	n/a	chr17:18032723-18032734
26	CEBPB	chr17:18041615-18042147	HepG2	liver:	n/a	chr17:18041823-18041834
27	CEBPB	chr17:18056831-18057090	K562	blood:	n/a	n/a
28	CEBPB	chr17:18056803-18057637	H1-hESC	embryonic stem cell:	n/a	n/a
29	CEBPB	chr17:18057202-18057628	MCF-7	breast:	n/a	n/a
30	CEBPB	chr17:18046407-18046987	K562	blood:	n/a	n/a
31	CEBPB	chr17:18032538-18032905	A549	lung:	n/a	chr17:18032723-18032734
32	CEBPB	chr17:18032587-18032844	H1-hESC	embryonic stem cell:	n/a	chr17:18032723-18032734
33	CEBPB	chr17:18041496-18042198	HepG2	liver:	n/a	chr17:18041823-18041834
34	CEBPB	chr17:18041690-18041916	HepG2	liver:	n/a	chr17:18041823-18041834
35	CEBPB	chr17:18032598-18032908	K562	blood:	n/a	chr17:18032723-18032734
36	CEBPB	chr17:18032551-18032908	HepG2	liver:	n/a	chr17:18032723-18032734
37	CEBPB	chr17:18032482-18032907	IMR90	lung:	n/a	chr17:18032723-18032734
38	CEBPB	chr17:18041553-18042047	HepG2	liver:	n/a	chr17:18041823-18041834
39	CEBPD	chr17:18041683-18041943	HepG2	liver:	n/a	n/a
40	CEBPD	chr17:18041633-18041921	HepG2	liver:	n/a	n/a
41	CHD1	chr17:18055892-18055969	H1-hESC	embryonic stem cell:	n/a	n/a
42	CHD1	chr17:18056912-18057230	H1-hESC	embryonic stem cell:	n/a	n/a
43	CHD2	chr17:18042148-18042267	HepG2	liver:	n/a	n/a
44	CHD2	chr17:18056978-18057325	H1-hESC	embryonic stem cell:	n/a	n/a
45	CHD2	chr17:18057046-18057245	K562	blood:	n/a	n/a
46	CHD2	chr17:18044401-18044601	K562	blood:	n/a	n/a
47	CHD2	chr17:18047050-18047079	HepG2	liver:	n/a	n/a
48	CREB1	chr17:18043326-18043621	A549	lung:	n/a	n/a
49	CREB1	chr17:18032339-18032677	A549	lung:	n/a	n/a
50	CTCF	chr17:18043327-18043524	GM12878	blood:	n/a	chr17:18043423-18043444 chr17:18043421-18043439 chr17:18043424-18043437

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:18057145-18057195	HUVEC	blood vessel:	n/a
2	chr17:18046564-18046614	SK-N-SH	brain:	n/a
3	chr17:18057215-18057265	ovcar-3	ovarian:	n/a
4	chr17:18046564-18046614	HRPEpiC	eye:	n/a
5	chr17:18044452-18044502	SK-N-SH_RA	brain:	n/a
6	chr17:18046564-18046614	GM19239	blood:	n/a
7	chr17:18057079-18057129	GM19239	blood:	n/a
8	chr17:18057145-18057195	Caco-2	colon:	n/a
9	chr17:18044452-18044502	SK-N-SH	brain:	n/a
10	chr17:18057215-18057265	T-47D	breast:	n/a
11	chr17:18057215-18057265	AG10803	skin:	n/a
12	chr17:18046564-18046614	LNCaP	prostate:	n/a
13	chr17:18057145-18057195	BE2_C	brain:	n/a
14	chr17:18044452-18044502	HCT-116	colon:	n/a
15	chr17:18057145-18057195	SK-N-SH_RA	brain:	n/a
16	chr17:18057215-18057265	NB4	blood:	n/a
17	chr17:18046564-18046614	RPTEC	kidney:	n/a
18	chr17:18044452-18044502	HNPCEpiC	eye:	n/a
19	chr17:18057145-18057195	HNPCEpiC	eye:	n/a
20	chr17:18057215-18057265	MCF-7	breast:	n/a
21	chr17:18057145-18057195	AG09309	skin:	n/a
22	chr17:18057145-18057195	ProgFib	skin:	n/a
23	chr17:18057145-18057195	NH-A	brain:	n/a
24	chr17:18057215-18057265	PrEC	prostate:	n/a
25	chr17:18057079-18057129	NHDF-neo	bronchial:	n/a
26	chr17:18057215-18057265	NHBE	bronchial:	n/a
27	chr17:18044452-18044502	HEK293	kidney:	embryo
28	chr17:18046564-18046614	Jurkat	blood:	n/a
29	chr17:18046564-18046614	A549	lung:	n/a
30	chr17:18057079-18057129	HepG2	liver:	n/a
31	chr17:18057145-18057195	Jurkat	blood:	n/a
32	chr17:18057079-18057129	AG04449	skin:	fetal
33	chr17:18044452-18044502	HMEC	breast:	n/a
34	chr17:18057079-18057129	Hela-S3	cervix:	n/a
35	chr17:18057215-18057265	A549	lung:	n/a
36	chr17:18057145-18057195	GM12892	blood:	n/a
37	chr17:18044452-18044502	Caco-2	colon:	n/a
38	chr17:18057079-18057129	K562	blood:	n/a
39	chr17:18044452-18044502	BJ	skin:	n/a
40	chr17:18044452-18044502	HepG2	liver:	n/a
41	chr17:18057215-18057265	HRE	kidney:	n/a
42	chr17:18044452-18044502	AoSMC	blood vessel:	n/a
43	chr17:18057079-18057129	RPTEC	kidney:	n/a
44	chr17:18044452-18044502	Jurkat	blood:	n/a
45	chr17:18057215-18057265	GM06990	blood:	n/a
46	chr17:18057079-18057129	BE2_C	brain:	n/a
47	chr17:18057215-18057265	SAEC	small airway:	n/a
48	chr17:18057145-18057195	BJ	skin:	n/a
49	chr17:18057079-18057129	A549	lung:	n/a
50	chr17:18057215-18057265	HL-60	blood:	n/a

(count:70 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:18036844..18039575-chr17:18086899..18088977,2	K562	blood:
2	chr17:18042232..18044800-chr17:18055136..18057841,3	K562	blood:
3	chr17:18039531..18041825-chr17:18044151..18046470,2	K562	blood:
4	chr17:18049467..18051833-chr17:18057367..18059688,2	MCF-7	breast:
5	chr17:18042232..18044129-chr17:18055136..18056759,2	K562	blood:
6	chr17:18052063..18054995-chr17:18074493..18076431,2	K562	blood:
7	chr17:18054836..18057146-chr17:18057563..18061410,3	MCF-7	breast:
8	chr17:18044679..18047861-chr17:18085770..18088322,3	MCF-7	breast:
9	chr17:18046909..18048719-chr17:18053512..18055928,2	K562	blood:
10	chr17:18029147..18031463-chr17:18032320..18035257,3	K562	blood:
11	chr17:18044305..18045021-chr17:18059355..18060391,3	MCF-7	breast:
12	chr17:18042232..18044129-chr17:18055136..18056759,2	K562	blood:
13	chr17:18039043..18041825-chr17:18043264..18046470,4	K562	blood:
14	chr17:18007764..18010490-chr17:18045760..18048651,2	MCF-7	breast:
15	chr13:114999940..115000764-chr17:18056683..18057332,2	HCT-116	colon:
16	chr17:18055989..18058847-chr17:18059352..18061809,2	K562	blood:
17	chr17:18035401..18038176-chr17:18084988..18086618,2	MCF-7	breast:
18	chr17:18031771..18034328-chr17:18038844..18040628,2	MCF-7	breast:
19	chr17:18056639..18059705-chr17:18061625..18064659,3	MCF-7	breast:
20	chr17:18048504..18050762-chr17:18055124..18057185,2	MCF-7	breast:
21	chr17:18031305..18033778-chr17:18084971..18087031,2	MCF-7	breast:
22	chr17:18057350..18061680-chr17:18083813..18088656,8	K562	blood:
23	chr17:18026105..18028759-chr17:18029242..18030867,2	K562	blood:
24	chr12:66523833..66524533-chr17:18043009..18043721,2	MCF-7	breast:
25	chr17:18034463..18036913-chr17:18059459..18061391,2	MCF-7	breast:
26	chr17:18036589..18038167-chr17:18040097..18042014,2	K562	blood:
27	chr17:18044150..18045078-chr17:18059256..18060265,3	MCF-7	breast:
28	chr17:18050664..18054288-chr17:18086112..18089564,5	K562	blood:
29	chr17:18034621..18036345-chr17:18038369..18041119,2	K562	blood:
30	chr17:18044317..18045124-chr17:18086070..18086665,2	MCF-7	breast:
31	chr17:18044115..18044841-chr17:18120469..18121362,2	K562	blood:
32	chr17:18041836..18044896-chr17:18058231..18061380,3	K562	blood:
33	chr17:18044305..18045021-chr17:18059355..18060391,3	MCF-7	breast:
34	chr17:18042805..18044736-chr17:18086569..18089339,2	K562	blood:
35	chr17:18048504..18050762-chr17:18055124..18057185,2	MCF-7	breast:
36	chr17:18042115..18044970-chr17:18226720..18228381,2	MCF-7	breast:
37	chr17:18034463..18036913-chr17:18059459..18061391,2	MCF-7	breast:
38	chr17:18020795..18023670-chr17:18040460..18042465,2	K562	blood:
39	chr17:18036589..18038167-chr17:18040097..18042014,2	K562	blood:
40	chr17:18045055..18047545-chr17:18085965..18089684,5	K562	blood:
41	chr17:18059602..18061497-chr17:18162404..18165342,2	MCF-7	breast:
42	chr17:18032210..18034004-chr17:18085274..18087745,2	K562	blood:
43	chr17:18029147..18031463-chr17:18032320..18035257,3	K562	blood:
44	chr17:18043317..18043875-chr17:18059389..18059944,2	MCF-7	breast:
45	chr17:18023938..18027022-chr17:18030857..18033750,4	MCF-7	breast:
46	chr17:18042232..18044800-chr17:18055136..18057841,3	K562	blood:
47	chr17:18034621..18036345-chr17:18038369..18041119,2	K562	blood:
48	chr17:18043317..18043875-chr17:18059389..18059944,2	MCF-7	breast:
49	chr17:18020446..18022435-chr17:18029700..18032433,2	MCF-7	breast:
50	chr17:18044909..18046948-chr17:18057322..18059132,2	K562	blood:

No data

Variant related genes	Relation type
ENSG00000238691	TF binding region
MYO15A	TF binding region
ENSG00000238691	CpG island
MYO15A	CpG island
ENSG00000108591	chromatin interactions
ENSG00000176994	chromatin interactions
ENSG00000130177	chromatin interactions
ENSG00000139233	chromatin interactions
ENSG00000177302	chromatin interactions
ENSG00000177427	chromatin interactions
ENSG00000141034	chromatin interactions
ENSG00000239335	chromatin interactions
ENSG00000091542	chromatin interactions
ENSG00000091536	chromatin interactions
ENSG00000238691	chromatin interactions
ENSG00000267350	chromatin interactions
ENSG00000266677	chromatin interactions

Extended variants
information (count: 1274 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:1274 , 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	rs854791	chr17:18029857-18029858	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs147231478	chr17:18030014-18030015	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs9899727	chr17:18030032-18030033	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs150847766	chr17:18030038-18030039	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs189308777	chr17:18030081-18030082	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs201667235	chr17:18030091-18030092	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs369087707	chr17:18030129-18030130	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs373041935	chr17:18030144-18030145	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs377070697	chr17:18030147-18030148	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs139329625	chr17:18030148-18030149	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs369760532	chr17:18030150-18030151	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs557186938	chr17:18030171-18030172	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs576985725	chr17:18030180-18030181	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs374190062	chr17:18030188-18030189	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs372425620	chr17:18030204-18030205	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs854792	chr17:18030240-18030241	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs143363422	chr17:18030283-18030284	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs572197779	chr17:18030298-18030299	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs541071322	chr17:18030351-18030352	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs370914309	chr17:18030356-18030357	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113394958	chr17:18030382-18030383	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561101869	chr17:18030393-18030394	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs374088232	chr17:18030399-18030400	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs146245515	chr17:18030426-18030427	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs374131038	chr17:18030435-18030436	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs199511042	chr17:18030436-18030437	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs192570479	chr17:18030446-18030447	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs372116433	chr17:18030447-18030448	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs374336846	chr17:18030462-18030463	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs368407094	chr17:18030463-18030464	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs370707928	chr17:18030473-18030474	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs532765171	chr17:18030478-18030479	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs371873646	chr17:18030502-18030503	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs552797261	chr17:18030513-18030514	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs854793	chr17:18030524-18030525	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	mRNA abundance
36	rs369435764	chr17:18030527-18030528	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs528172739	chr17:18030547-18030548	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548204271	chr17:18030596-18030597	Enhancers Weak transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs567980110	chr17:18030634-18030635	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs184421726	chr17:18030693-18030694	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs73979301	chr17:18030705-18030706	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs181232273	chr17:18030848-18030849	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs854794	chr17:18030852-18030853	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs552744353	chr17:18030922-18030923	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs547459837	chr17:18030970-18030971	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs115463904	chr17:18031005-18031006	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs534791418	chr17:18031053-18031054	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186505440	chr17:18031089-18031090	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs76347380	chr17:18031100-18031101	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs533426248	chr17:18031139-18031140	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:160)

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
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
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Sezary syndrome	18413736	CNVD
Medulloblastoma	16783165	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:700 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:18010600-18030400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr17:18028000-18034600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:18029400-18031800	Weak transcription	Gastric	stomach
4	chr17:18030400-18030600	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr17:18030400-18030600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
6	chr17:18031400-18032000	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
7	chr17:18031800-18032800	Enhancers	Placenta	Placenta
8	chr17:18031800-18032800	Enhancers	Gastric	stomach
9	chr17:18032000-18032200	Active TSS	Osteobl	bone
10	chr17:18032000-18032600	Bivalent Enhancer	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr17:18032000-18032600	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
12	chr17:18032000-18033000	Enhancers	Stomach Mucosa	stomach
13	chr17:18032200-18032400	Enhancers	Osteobl	bone
14	chr17:18032400-18032800	Active TSS	Osteobl	bone
15	chr17:18032600-18032800	Flanking Bivalent TSS/Enh	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr17:18032600-18033000	Enhancers	Liver	Liver
17	chr17:18033000-18040200	Weak transcription	Liver	Liver
18	chr17:18033800-18034800	Bivalent/Poised TSS	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr17:18033800-18035000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
20	chr17:18034600-18035400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr17:18034800-18035000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr17:18034800-18035200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
23	chr17:18035000-18039400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr17:18035400-18035800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
25	chr17:18035800-18036000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr17:18036000-18039000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr17:18036200-18036800	Bivalent Enhancer	HepG2	liver
28	chr17:18039000-18039200	Flanking Bivalent TSS/Enh	H1 Derived Mesenchymal Stem Cells	ES cell derived
29	chr17:18039000-18039400	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
30	chr17:18039000-18040000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
31	chr17:18039200-18039600	Enhancers	ES-I3 Cell Line	embryonic stem cell
32	chr17:18039200-18039600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr17:18039400-18039800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
34	chr17:18039400-18040000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
35	chr17:18039600-18041600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr17:18039600-18046800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
37	chr17:18039800-18040000	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr17:18039800-18046200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr17:18040000-18041400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
40	chr17:18040000-18043400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
41	chr17:18040200-18044800	Enhancers	Liver	Liver
42	chr17:18040400-18041400	Enhancers	HepG2	liver
43	chr17:18040600-18056000	Weak transcription	Gastric	stomach
44	chr17:18040800-18056400	Weak transcription	Right Atrium	heart
45	chr17:18041400-18041800	Flanking Active TSS	HepG2	liver
46	chr17:18041400-18043400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr17:18041600-18041800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
48	chr17:18041600-18041800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
49	chr17:18041600-18041800	Enhancers	Fetal Intestine Small	intestine
50	chr17:18041600-18045000	Enhancers	Placenta	Placenta

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