Variant report

Variant	nsv984510
Chromosome Location	chr17:17015688-17048858
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	chr17:17023369-17023532	K562	blood:	n/a	n/a
2	BHLHE40	chr17:17018195-17018476	GM12878	blood:	n/a	n/a
3	BHLHE40	chr17:17045280-17045419	GM12878	blood:	n/a	n/a
4	BRCA1	chr17:17044624-17044750	H1-hESC	embryonic stem cell:	n/a	n/a
5	CEBPB	chr17:17027288-17027572	A549	lung:	n/a	n/a
6	CEBPB	chr17:17027421-17027512	HepG2	liver:	n/a	n/a
7	CEBPB	chr17:17022955-17023332	IMR90	lung:	n/a	n/a
8	CHD2	chr17:17021808-17021963	HepG2	liver:	n/a	n/a
9	CREB1	chr17:17045227-17045491	A549	lung:	n/a	n/a
10	CTCF	chr17:17045260-17045410	AoAF	blood vessel:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
11	CTCF	chr17:17045260-17045410	AG04450	lung:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
12	CTCF	chr17:17032780-17032930	WERI-Rb-1	eye:	n/a	chr17:17032893-17032901
13	CTCF	chr17:17045260-17045410	GM12871	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
14	CTCF	chr17:17045240-17045390	HMF	breast:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
15	CTCF	chr17:17024480-17024630	HEEpiC	esophagus:	n/a	n/a
16	CTCF	chr17:17045200-17045350	GM12878	blood:	n/a	n/a
17	CTCF	chr17:17024660-17024810	A549	lung:	n/a	n/a
18	CTCF	chr17:17045220-17045370	A549	lung:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
19	CTCF	chr17:17045260-17045410	GM12866	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
20	CTCF	chr17:17045252-17045476	GM10266	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
21	CTCF	chr17:17045280-17045430	BJ	skin:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
22	CTCF	chr17:17045240-17045390	GM12867	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
23	CTCF	chr17:17045320-17045470	HRE	kidney:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
24	CTCF	chr17:17045260-17045410	GM12801	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
25	CTCF	chr17:17048621-17048788	GM19239	blood:	n/a	chr17:17048691-17048709 chr17:17048693-17048714
26	CTCF	chr17:17033460-17033610	MCF-7	breast:	n/a	n/a
27	CTCF	chr17:17024180-17024330	SK-N-SH_RA	brain:	n/a	n/a
28	CTCF	chr17:17023620-17023770	AG09319	gingival:	n/a	n/a
29	CTCF	chr17:17045260-17045410	MCF-7	breast:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
30	CTCF	chr17:17045320-17045470	GM12874	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
31	CTCF	chr17:17045240-17045390	HAc	cerebellar:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
32	CTCF	chr17:17045240-17045390	A549	lung:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
33	CTCF	chr17:17024060-17024210	NHLF	lung:	n/a	n/a
34	CTCF	chr17:17044100-17044250	HEEpiC	esophagus:	n/a	n/a
35	CTCF	chr17:17045125-17045514	HepG2	liver:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
36	CTCF	chr17:17033520-17033670	HEK293	kidney:	n/a	n/a
37	CTCF	chr17:17033522-17033641	Hela-S3	cervix:	n/a	n/a
38	CTCF	chr17:17045299-17045400	Medullo	brain:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
39	CTCF	chr17:17044540-17044690	HMF	breast:	n/a	chr17:17044676-17044689
40	CTCF	chr17:17045280-17045430	AG09319	gingival:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
41	CTCF	chr17:17040250-17040254	GM19240	blood:	n/a	n/a
42	CTCF	chr17:17045215-17045512	K562	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
43	CTCF	chr17:17045132-17045530	A549	lung:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
44	CTCF	chr17:17044120-17044270	HRE	kidney:	n/a	n/a
45	CTCF	chr17:17045147-17045567	K562	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
46	CTCF	chr17:17033521-17033643	GM10266	blood:	n/a	n/a
47	CTCF	chr17:17024626-17024726	K562	blood:	n/a	n/a
48	CTCF	chr17:17033447-17033751	A549	lung:	n/a	n/a
49	CTCF	chr17:17045233-17045503	GM12891	blood:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366
50	CTCF	chr17:17045260-17045410	SK-N-SH_RA	brain:	n/a	chr17:17045349-17045365 chr17:17045351-17045364 chr17:17045348-17045366

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17030253-17030303	NT2-D1	testis:	n/a
2	chr17:17047044-17047094	ProgFib	skin:	n/a
3	chr17:17030253-17030303	NT2-D1	testis:	n/a
4	chr17:17047044-17047094	ProgFib	skin:	n/a
5	chr17:17047044-17047094	HAEpiC	amniotic membrane:	n/a
6	chr17:17023057-17023107	HPAEpiC	pulmonary alveolar:	n/a
7	chr17:17047044-17047094	K562	blood:	n/a
8	chr17:17030253-17030303	HUVEC	blood vessel:	n/a
9	chr17:17023057-17023107	PFSK-1	brain:	n/a
10	chr17:17047044-17047094	HCPEpiC	choroid plexus:	n/a
11	chr17:17035777-17035827	HRE	kidney:	n/a
12	chr17:17023057-17023107	GM19239	blood:	n/a
13	chr17:17030253-17030303	RPTEC	kidney:	n/a
14	chr17:17044218-17044268	HMEC	breast:	n/a
15	chr17:17044218-17044268	HCF	heart:	n/a
16	chr17:17046995-17047045	ProgFib	skin:	n/a
17	chr17:17044218-17044268	Hepatocyte	liver:	n/a
18	chr17:17035777-17035827	HUVEC	blood vessel:	n/a
19	chr17:17023057-17023107	HIPEpiC	eye:	n/a
20	chr17:17023057-17023107	HCT-116	colon:	n/a
21	chr17:17023057-17023107	BE2_C	brain:	n/a
22	chr17:17035777-17035827	NHDF-neo	bronchial:	n/a
23	chr17:17044218-17044268	ovcar-3	ovarian:	n/a
24	chr17:17046995-17047045	Jurkat	blood:	n/a
25	chr17:17035777-17035827	GM12891	blood:	n/a
26	chr17:17023057-17023107	NHBE	bronchial:	n/a
27	chr17:17035777-17035827	NH-A	brain:	n/a
28	chr17:17035777-17035827	PANC-1	pancreas:	n/a
29	chr17:17047044-17047094	HRCEpiC	kidney:	n/a
30	chr17:17047044-17047094	HRPEpiC	eye:	n/a
31	chr17:17030253-17030303	HNPCEpiC	eye:	n/a
32	chr17:17044218-17044268	GM19239	blood:	n/a
33	chr17:17023057-17023107	NHDF-neo	bronchial:	n/a
34	chr17:17046995-17047045	HPAEpiC	pulmonary alveolar:	n/a
35	chr17:17047044-17047094	T-47D	breast:	n/a
36	chr17:17030253-17030303	HAEpiC	amniotic membrane:	n/a
37	chr17:17046995-17047045	Caco-2	colon:	n/a
38	chr17:17035777-17035827	AG09319	gingival:	n/a
39	chr17:17035777-17035827	ovcar-3	ovarian:	n/a
40	chr17:17030253-17030303	HRPEpiC	eye:	n/a
41	chr17:17035777-17035827	HCM	heart:	n/a
42	chr17:17046995-17047045	PANC-1	pancreas:	n/a
43	chr17:17047044-17047094	HepG2	liver:	n/a
44	chr17:17035777-17035827	T-47D	breast:	n/a
45	chr17:17047044-17047094	H1-hESC	embryonic stem cell:	embryo
46	chr17:17046995-17047045	HUVEC	blood vessel:	n/a
47	chr17:17047044-17047094	Hepatocyte	liver:	n/a
48	chr17:17030253-17030303	HCT-116	colon:	n/a
49	chr17:17046995-17047045	ECC-1	luminal epithelium:	n/a
50	chr17:17044218-17044268	H1-hESC	embryonic stem cell:	embryo

No.	Distal block	Cell Line	Cell type
1	chr17:17043821..17046160-chr17:17108071..17109890,2	MCF-7	breast:
2	chr17:17014229..17016435-chr17:17023401..17025123,2	K562	blood:
3	chr17:17023341..17025432-chr17:17027098..17029128,3	K562	blood:
4	chr17:17032608..17034755-chr17:17042355..17044187,2	K562	blood:
5	chr17:16990508..16991413-chr17:17037250..17038091,2	MCF-7	breast:
6	chr17:17023341..17025938-chr17:17027098..17030092,2	K562	blood:
7	chr17:17010273..17011801-chr17:17020537..17022736,2	K562	blood:
8	chr17:17046258..17049165-chr17:17140105..17142277,2	K562	blood:
9	chr17:17008907..17011801-chr17:17020811..17022736,2	K562	blood:
10	chr17:17038716..17041244-chr17:17042490..17044095,2	K562	blood:
11	chr17:17041998..17043566-chr17:17047044..17048728,2	MCF-7	breast:
12	chr17:17023341..17025432-chr17:17027098..17029128,3	K562	blood:
13	chr17:16954318..16955958-chr17:17023185..17024868,2	MCF-7	breast:
14	chr17:17008754..17011646-chr17:17017494..17019040,2	MCF-7	breast:
15	chr17:17028360..17030286-chr17:17031836..17034332,2	MCF-7	breast:
16	chr17:17041998..17043566-chr17:17047044..17048728,2	MCF-7	breast:
17	chr17:17042215..17045044-chr17:17066488..17068871,2	K562	blood:
18	chr17:17022152..17024534-chr17:17033092..17034855,2	MCF-7	breast:
19	chr17:17016476..17019464-chr17:17021686..17024565,2	K562	blood:
20	chr17:17014229..17016435-chr17:17023401..17025123,2	K562	blood:
21	chr17:17041398..17043468-chr17:17045137..17047861,3	K562	blood:
22	chr17:17026085..17028374-chr17:17031939..17033619,2	K562	blood:
23	chr17:17014931..17017643-chr17:17019821..17021328,2	K562	blood:
24	chr17:17030511..17032760-chr17:17032782..17034676,2	MCF-7	breast:
25	chr17:16991616..16993705-chr17:17019243..17022141,2	MCF-7	breast:
26	chr17:17041398..17043468-chr17:17045137..17047861,3	K562	blood:
27	chr17:17026085..17028374-chr17:17031939..17033619,2	K562	blood:
28	chr17:17022152..17024534-chr17:17033092..17034855,2	MCF-7	breast:
29	chr17:17017540..17019089-chr17:17022012..17023742,2	MCF-7	breast:
30	chr17:17045331..17046239-chr17:17216672..17217525,2	K562	blood:
31	chr17:17011246..17012755-chr17:17014614..17017121,2	K562	blood:
32	chr17:17020278..17022879-chr17:17024939..17027865,2	K562	blood:
33	chr17:17017540..17019089-chr17:17022012..17023742,2	MCF-7	breast:
34	chr17:17032608..17034755-chr17:17042355..17044187,2	K562	blood:
35	chr17:17020278..17022879-chr17:17024939..17027865,2	K562	blood:
36	chr17:17030511..17032760-chr17:17032782..17034676,2	MCF-7	breast:
37	chr17:16904876..16905537-chr17:17045251..17045788,2	MCF-7	breast:
38	chr17:17014931..17017643-chr17:17019821..17021328,2	K562	blood:
39	chr17:17028360..17030286-chr17:17031836..17034332,2	MCF-7	breast:
40	chr17:17011485..17013573-chr17:17019778..17021863,2	MCF-7	breast:
41	chr17:16904469..16905319-chr17:17033142..17034016,2	MCF-7	breast:
42	chr17:17011246..17012827-chr17:17014614..17017458,3	K562	blood:
43	chr17:17016476..17019464-chr17:17021686..17024565,2	K562	blood:
44	chr17:17023341..17025938-chr17:17027098..17030092,2	K562	blood:
45	chr17:17047306..17049744-chr17:17082516..17085207,2	K562	blood:
46	chr17:17006139..17008392-chr17:17014164..17016773,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C17orf84-2	chr17:17044809-17045074	NONHSAT146048
2	lnc-C17orf84-2	chr17:17045324-17045626	NONHSAT146048

Variant related genes	Relation type
MPRIP	TF binding region
MPRIP	CpG island
ENSG00000179598	chromatin interactions
ENSG00000154803	chromatin interactions
ENSG00000133030	chromatin interactions
ENSG00000264187	chromatin interactions

Extended variants
information (count: 1267 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:1267 , 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	rs151303005	chr17:17015688-17015689	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs554205970	chr17:17015710-17015711	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs76440905	chr17:17015718-17015719	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs187178103	chr17:17015764-17015765	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs542284267	chr17:17015792-17015793	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs569920294	chr17:17015805-17015806	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs535650811	chr17:17015808-17015809	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs562487452	chr17:17015822-17015823	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs140630843	chr17:17015850-17015851	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs567801030	chr17:17015859-17015860	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs113500398	chr17:17015862-17015863	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs575747014	chr17:17015878-17015879	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs533815460	chr17:17015885-17015886	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs544675850	chr17:17015913-17015914	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs140533351	chr17:17015932-17015933	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs553512643	chr17:17015966-17015967	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs527524981	chr17:17015974-17015975	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs11870483	chr17:17016012-17016013	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs376162008	chr17:17016047-17016048	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs529986675	chr17:17016055-17016056	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs549126757	chr17:17016061-17016062	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs370509606	chr17:17016080-17016081	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs538348627	chr17:17016098-17016099	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs551861481	chr17:17016100-17016101	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs192111403	chr17:17016120-17016121	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs534173576	chr17:17016127-17016128	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149698604	chr17:17016149-17016150	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs574285202	chr17:17016151-17016152	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs536914914	chr17:17016168-17016169	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs12450213	chr17:17016203-17016204	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs572871343	chr17:17016212-17016213	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs575584796	chr17:17016262-17016263	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs368425143	chr17:17016293-17016294	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs117803938	chr17:17016311-17016312	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs571788286	chr17:17016330-17016331	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs114710308	chr17:17016337-17016338	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs376619884	chr17:17016381-17016382	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs576350510	chr17:17016384-17016385	Weak transcription Enhancers Genic enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs561104934	chr17:17016434-17016435	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs529968566	chr17:17016435-17016436	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs542033854	chr17:17016444-17016445	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs562882326	chr17:17016472-17016473	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs531776904	chr17:17016478-17016479	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs551794032	chr17:17016520-17016521	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs571796114	chr17:17016573-17016574	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs8064296	chr17:17016607-17016608	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs8065260	chr17:17016685-17016686	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs541486731	chr17:17016691-17016692	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs567818149	chr17:17016692-17016693	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs536548269	chr17:17016709-17016710	Weak transcription Enhancers	n/a	n/a	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
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
Breast cancer	22522925	CNVD
Lung adenocarcinoma	21935476	CNVD

Chromatin state (count:1475 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16997000-17016600	Enhancers	Left Ventricle	heart
2	chr17:16998200-17016200	Enhancers	Fetal Heart	heart
3	chr17:16998600-17016600	Enhancers	Skeletal Muscle Female	skeletal muscle
4	chr17:17000200-17018200	Weak transcription	NH-A	brain
5	chr17:17002600-17023200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr17:17006200-17033000	Weak transcription	Primary neutrophils fromperipheralblood	blood
7	chr17:17006800-17016600	Enhancers	Right Ventricle	heart
8	chr17:17007400-17016600	Enhancers	Pancreas	Pancrea
9	chr17:17007600-17016600	Enhancers	Right Atrium	heart
10	chr17:17007800-17021000	Weak transcription	HepG2	liver
11	chr17:17008000-17017200	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr17:17008400-17016600	Enhancers	Placenta	Placenta
13	chr17:17009200-17025200	Enhancers	Brain Anterior Caudate	brain
14	chr17:17009400-17016000	Enhancers	Esophagus	oesophagus
15	chr17:17009400-17016200	Genic enhancers	A549	lung
16	chr17:17009400-17016600	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr17:17009400-17020600	Enhancers	Lung	lung
18	chr17:17009800-17017000	Enhancers	Brain Angular Gyrus	brain
19	chr17:17010000-17032000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
20	chr17:17010200-17016200	Enhancers	Gastric	stomach
21	chr17:17010200-17017200	Enhancers	Primary T helper cells fromperipheralblood	blood
22	chr17:17010200-17021600	Weak transcription	Dnd41	blood
23	chr17:17010200-17025000	Enhancers	Primary T cells fromperipheralblood	blood
24	chr17:17010200-17025000	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
25	chr17:17010400-17024000	Enhancers	Primary B cells from peripheral blood	blood
26	chr17:17010400-17025200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr17:17010800-17016400	Enhancers	Fetal Muscle Trunk	muscle
28	chr17:17011000-17019200	Enhancers	Primary B cells from cord blood	blood
29	chr17:17011200-17028800	Weak transcription	Fetal Brain Female	brain
30	chr17:17011400-17021600	Weak transcription	Aorta	Aorta
31	chr17:17011600-17017000	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr17:17011800-17017800	Weak transcription	Cortex derived primary cultured neurospheres	brain
33	chr17:17011800-17018400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr17:17012000-17035200	Weak transcription	HUES64 Cell Line	embryonic stem cell
35	chr17:17012200-17018000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
36	chr17:17012400-17016200	Weak transcription	GM12878-XiMat	blood
37	chr17:17012400-17018000	Weak transcription	H1 Cell Line	embryonic stem cell
38	chr17:17012400-17018000	Weak transcription	Brain Germinal Matrix	brain
39	chr17:17012600-17016200	Enhancers	Stomach Smooth Muscle	stomach
40	chr17:17012600-17016400	Genic enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr17:17012600-17023600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
42	chr17:17012800-17017800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
43	chr17:17013200-17016000	Enhancers	Stomach Mucosa	stomach
44	chr17:17013200-17017800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr17:17013600-17016200	Genic enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr17:17013600-17016400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr17:17013600-17017800	Weak transcription	Liver	Liver
48	chr17:17013600-17018600	Weak transcription	Primary hematopoietic stem cells	blood
49	chr17:17014000-17017800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
50	chr17:17014000-17017800	Weak transcription	Small Intestine	intestine

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