Variant report

Variant	nsv543239
Chromosome Location	chr17:17580295-17599851
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	ARID3A	chr17:17595898-17596383	HepG2	liver:	n/a	n/a
2	ARID3A	chr17:17596946-17597137	HepG2	liver:	n/a	n/a
3	ARID3A	chr17:17586242-17586247	HepG2	liver:	n/a	n/a
4	ATF1	chr17:17585613-17585974	K562	blood:	n/a	chr17:17585767-17585781
5	ATF1	chr17:17586322-17586664	K562	blood:	n/a	n/a
6	ATF2	chr17:17585580-17585950	GM12878	blood:	n/a	chr17:17585767-17585781
7	ATF2	chr17:17595163-17595642	GM12878	blood:	n/a	n/a
8	ATF2	chr17:17586233-17586778	GM12878	blood:	n/a	chr17:17586493-17586504
9	ATF2	chr17:17586099-17586648	GM12878	blood:	n/a	chr17:17586493-17586504
10	ATF2	chr17:17585478-17586159	GM12878	blood:	n/a	chr17:17585767-17585781
11	ATF2	chr17:17594917-17595704	GM12878	blood:	n/a	n/a
12	ATF3	chr17:17585943-17586524	A549	lung:	n/a	chr17:17586492-17586505 chr17:17586495-17586502 chr17:17586491-17586506 chr17:17586493-17586504 chr17:17586491-17586504 chr17:17586495-17586505 chr17:17586280-17586289 chr17:17586492-17586502 chr17:17586494-17586505 chr17:17586493-17586506 chr17:17586495-17586505 chr17:17586492-17586505 chr17:17586383-17586392 chr17:17586492-17586503 chr17:17586492-17586502
13	ATF3	chr17:17586117-17586631	A549	lung:	n/a	chr17:17586492-17586505 chr17:17586495-17586502 chr17:17586491-17586506 chr17:17586493-17586504 chr17:17586491-17586504 chr17:17586495-17586505 chr17:17586280-17586289 chr17:17586492-17586502 chr17:17586494-17586505 chr17:17586493-17586506 chr17:17586495-17586505 chr17:17586492-17586505 chr17:17586383-17586392 chr17:17586492-17586503 chr17:17586492-17586502
14	ATF3	chr17:17596910-17597876	A549	lung:	n/a	chr17:17597706-17597720
15	ATF3	chr17:17589149-17589448	K562	blood:	n/a	n/a
16	BACH1	chr17:17589276-17589501	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr17:17586044-17586215	K562	blood:	n/a	n/a
18	BACH1	chr17:17584367-17586749	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr17:17585569-17585838	K562	blood:	n/a	n/a
20	BATF	chr17:17595232-17595559	GM12878	blood:	n/a	n/a
21	BCL11A	chr17:17595135-17595627	GM12878	blood:	n/a	n/a
22	BCL11A	chr17:17595199-17595619	GM12878	blood:	n/a	n/a
23	BCL3	chr17:17595469-17597852	A549	lung:	n/a	chr17:17597807-17597815 chr17:17597168-17597181
24	BCL3	chr17:17595166-17595648	GM12878	blood:	n/a	n/a
25	BCL3	chr17:17586177-17587192	A549	lung:	n/a	chr17:17586382-17586391 chr17:17586299-17586312
26	BCLAF1	chr17:17584462-17584939	GM12878	blood:	n/a	chr17:17584561-17584574 chr17:17584549-17584562 chr17:17584565-17584578 chr17:17584603-17584616
27	BCLAF1	chr17:17597120-17597647	GM12878	blood:	n/a	chr17:17597168-17597181
28	BCLAF1	chr17:17584367-17584924	GM12878	blood:	n/a	chr17:17584561-17584574 chr17:17584549-17584562 chr17:17584565-17584578 chr17:17584603-17584616
29	BCLAF1	chr17:17595192-17595664	GM12878	blood:	n/a	n/a
30	BCLAF1	chr17:17595074-17595632	GM12878	blood:	n/a	n/a
31	BCLAF1	chr17:17585689-17586615	GM12878	blood:	n/a	chr17:17586382-17586391 chr17:17585985-17585994 chr17:17586299-17586312
32	BCLAF1	chr17:17585420-17586561	GM12878	blood:	n/a	chr17:17585498-17585507 chr17:17586382-17586391 chr17:17585985-17585994 chr17:17586299-17586312 chr17:17585660-17585673 chr17:17585487-17585500
33	BCLAF1	chr17:17598062-17598501	GM12878	blood:	n/a	chr17:17598162-17598175
34	BHLHE40	chr17:17597493-17597798	K562	blood:	n/a	n/a
35	BHLHE40	chr17:17584501-17584891	GM12878	blood:	n/a	n/a
36	BHLHE40	chr17:17589178-17589467	K562	blood:	n/a	n/a
37	BHLHE40	chr17:17585556-17586618	GM12878	blood:	n/a	chr17:17585659-17585675
38	BHLHE40	chr17:17585609-17586621	K562	blood:	n/a	chr17:17585659-17585675
39	BHLHE40	chr17:17584605-17584640	K562	blood:	n/a	n/a
40	BRCA1	chr17:17584490-17584648	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr17:17585707-17585930	GM12878	blood:	n/a	n/a
42	BRCA1	chr17:17589214-17589450	Hela-S3	cervix:	n/a	n/a
43	BRCA1	chr17:17598525-17598723	HepG2	liver:	n/a	n/a
44	BRCA1	chr17:17597701-17597726	Hela-S3	cervix:	n/a	n/a
45	BRCA1	chr17:17596437-17596455	HepG2	liver:	n/a	n/a
46	BRCA1	chr17:17586336-17586840	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr17:17585621-17585886	Hela-S3	cervix:	n/a	n/a
48	CBX3	chr17:17597449-17597860	K562	blood:	n/a	n/a
49	CCNT2	chr17:17584483-17586765	K562	blood:	n/a	chr17:17586230-17586239 chr17:17586383-17586392 chr17:17586224-17586233 chr17:17585462-17585471
50	CCNT2	chr17:17597635-17598432	K562	blood:	n/a	chr17:17598162-17598171

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:17598354-17598404	Jurkat	blood:	n/a
2	chr17:17598354-17598404	Jurkat	blood:	n/a
3	chr17:17584403-17584453	PFSK-1	brain:	n/a
4	chr17:17584505-17584555	Caco-2	colon:	n/a
5	chr17:17584403-17584453	SK-N-SH_RA	brain:	n/a
6	chr17:17589471-17589521	AG09309	skin:	n/a
7	chr17:17584403-17584453	H1-hESC	embryonic stem cell:	embryo
8	chr17:17589471-17589521	K562	blood:	n/a
9	chr17:17598080-17598130	SKMC	muscle:	n/a
10	chr17:17589471-17589521	AoSMC	blood vessel:	n/a
11	chr17:17597625-17597675	HRCEpiC	kidney:	n/a
12	chr17:17596386-17596436	SK-N-SH_RA	brain:	n/a
13	chr17:17580647-17580697	SK-N-MC	brain:	n/a
14	chr17:17598080-17598130	ProgFib	skin:	n/a
15	chr17:17596386-17596436	MCF10A-Er-Src	breast:	n/a
16	chr17:17598503-17598553	AG04450	lung:	fetal
17	chr17:17585298-17585348	Hepatocyte	liver:	n/a
18	chr17:17586116-17586166	AG09319	gingival:	n/a
19	chr17:17594719-17594769	ECC-1	luminal epithelium:	n/a
20	chr17:17584505-17584555	SAEC	small airway:	n/a
21	chr17:17585774-17585824	HUVEC	blood vessel:	n/a
22	chr17:17584505-17584555	AoSMC	blood vessel:	n/a
23	chr17:17583879-17583929	HCM	heart:	n/a
24	chr17:17584403-17584453	AoSMC	blood vessel:	n/a
25	chr17:17594719-17594769	AG10803	skin:	n/a
26	chr17:17586474-17586524	AoSMC	blood vessel:	n/a
27	chr17:17583879-17583929	Jurkat	blood:	n/a
28	chr17:17589471-17589521	ECC-1	luminal epithelium:	n/a
29	chr17:17584505-17584555	HepG2	liver:	n/a
30	chr17:17596386-17596436	NHDF-neo	bronchial:	n/a
31	chr17:17598503-17598553	NH-A	brain:	n/a
32	chr17:17597825-17597875	GM12892	blood:	n/a
33	chr17:17586116-17586166	HCPEpiC	choroid plexus:	n/a
34	chr17:17598354-17598404	AG09319	gingival:	n/a
35	chr17:17596386-17596436	HCPEpiC	choroid plexus:	n/a
36	chr17:17585298-17585348	ECC-1	luminal epithelium:	n/a
37	chr17:17584403-17584453	GM19239	blood:	n/a
38	chr17:17584403-17584453	BJ	skin:	n/a
39	chr17:17598503-17598553	AG09309	skin:	n/a
40	chr17:17586474-17586524	PrEC	prostate:	n/a
41	chr17:17589471-17589521	SAEC	small airway:	n/a
42	chr17:17586474-17586524	MCF-7	breast:	n/a
43	chr17:17584505-17584555	NH-A	brain:	n/a
44	chr17:17586474-17586524	MCF10A-Er-Src	breast:	n/a
45	chr17:17594719-17594769	CMK	blood:	n/a
46	chr17:17586474-17586524	HRPEpiC	eye:	n/a
47	chr17:17580647-17580697	U87	brain:	n/a
48	chr17:17598080-17598130	LNCaP	prostate:	n/a
49	chr17:17597625-17597675	NH-A	brain:	n/a
50	chr17:17586116-17586166	NB4	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr17:17594258..17600676-chr17:17738917..17745175,15	MCF-7	breast:
2	chr17:17586455..17590031-chr17:17707371..17710346,3	MCF-7	breast:
3	chr17:17578367..17581846-chr17:17711367..17714822,4	MCF-7	breast:
4	chr17:17592512..17594577-chr17:17712221..17713832,2	MCF-7	breast:
5	chr17:17583537..17586679-chr17:17711908..17715201,3	MCF-7	breast:
6	chr17:17583519..17585283-chr17:17719170..17722055,2	MCF-7	breast:
7	chr17:17588749..17591653-chr17:17617007..17620668,3	K562	blood:
8	chr17:17592971..17596816-chr17:17655717..17659704,4	MCF-7	breast:
9	chr17:17597990..17601613-chr17:17723911..17725744,3	MCF-7	breast:
10	chr17:17596357..17599284-chr17:17741696..17744327,3	MCF-7	breast:
11	chr17:17592326..17594289-chr17:17629222..17631306,2	K562	blood:
12	chr17:17595705..17598118-chr17:17712618..17714167,2	MCF-7	breast:
13	chr17:17597749..17599526-chr17:17663082..17665675,2	MCF-7	breast:
14	chr17:17596840..17599239-chr17:17655841..17657576,2	MCF-7	breast:
15	chr17:17588060..17590556-chr17:17627029..17629581,4	K562	blood:
16	chr17:17589035..17591653-chr17:17618320..17620668,2	K562	blood:
17	chr17:17598092..17600072-chr17:17758359..17760671,2	MCF-7	breast:
18	chr17:17583924..17586191-chr17:17941715..17944094,3	K562	blood:
19	chr17:17596829..17599707-chr17:17608179..17611084,3	K562	blood:
20	chr17:17591306..17603641-chr17:17622226..17637880,43	MCF-7	breast:
21	chr17:17596418..17598751-chr17:17739588..17742563,3	K562	blood:
22	chr17:17576955..17580952-chr17:17581294..17585850,4	MCF-7	breast:
23	chr17:17588333..17591625-chr17:17738463..17742838,4	MCF-7	breast:
24	chr16:30389118..30389652-chr17:17597819..17598333,2	Hela-S3	cervix:
25	chr17:17584110..17584675-chr17:17763112..17763841,2	MCF-7	breast:
26	chr17:17583640..17587401-chr17:17713270..17717474,6	MCF-7	breast:
27	chr17:17583267..17584889-chr17:17715443..17717177,2	K562	blood:
28	chr17:17582120..17584481-chr17:17669635..17672296,2	K562	blood:
29	chr17:17584806..17586554-chr17:17724863..17727625,2	K562	blood:
30	chr17:17597022..17599037-chr17:57970421..57971942,2	MCF-7	breast:
31	chr1:28974279..28975242-chr17:17597910..17598840,2	Hela-S3	cervix:
32	chr17:17566041..17569411-chr17:17596920..17599764,3	MCF-7	breast:
33	chr17:17584674..17588119-chr17:17738170..17742427,6	K562	blood:
34	chr17:17588589..17591181-chr17:17627029..17629351,3	K562	blood:
35	chr17:17582541..17589441-chr17:17738170..17742091,10	K562	blood:
36	chr17:17565862..17568773-chr17:17588308..17590151,2	K562	blood:
37	chr17:17583267..17586800-chr17:17714001..17718221,4	K562	blood:
38	chr17:17596829..17599707-chr17:17608593..17611084,2	K562	blood:
39	chr17:17594795..17598773-chr17:17639856..17643137,4	MCF-7	breast:
40	chr17:17596273..17597839-chr17:17685487..17687747,2	MCF-7	breast:
41	chr17:17597397..17599561-chr17:17661548..17663067,2	MCF-7	breast:
42	chr17:17595881..17597399-chr17:17743800..17745983,2	K562	blood:
43	chr17:17594932..17600890-chr17:17651321..17655426,6	MCF-7	breast:
44	chr17:17584137..17584962-chr17:17739599..17740212,2	HCT-116	colon:
45	chr17:17571014..17573975-chr17:17596687..17598856,2	K562	blood:
46	chr17:17594067..17596408-chr17:17745227..17748218,2	MCF-7	breast:
47	chr17:17599477..17603323-chr17:17655564..17658131,3	MCF-7	breast:
48	chr17:17588968..17590942-chr17:17625144..17626762,2	K562	blood:
49	chr17:17583605..17586318-chr17:17753777..17755939,2	K562	blood:
50	chr17:17594054..17595929-chr17:17740676..17742731,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PEMT-1	chr17:17580889-17581002	XLOC_012408
2	lnc-MED9-4	chr17:17585043-17585107	NONHSAT146100
3	lnc-MED9-4	chr17:17586860-17588364	NONHSAT146100

Variant related genes	Relation type
SMCR2	TF binding region
RAI1	TF binding region
SMCR2	CpG island
RAI1	CpG island
ENSG00000237328	chromatin interactions
ENSG00000270103	chromatin interactions
ENSG00000141034	chromatin interactions
ENSG00000108557	chromatin interactions
ENSG00000259438	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000175662	chromatin interactions
ENSG00000180035	chromatin interactions
ENSG00000207839	chromatin interactions
ENSG00000171953	chromatin interactions
ENSG00000069956	chromatin interactions
ENSG00000072310	chromatin interactions
ZNF238	miRNA target sites

Extended variants
information (count: 707 )
Associated
traits (count: 161 )

Variant overlapped rSNPs/rCNVs (count:707 , 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	rs533454796	chr17:17580295-17580296	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs540552614	chr17:17580298-17580299	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs113939510	chr17:17580340-17580341	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs186892193	chr17:17580341-17580342	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs529410859	chr17:17580361-17580362	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs375658401	chr17:17580368-17580369	Bivalent Enhancer Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs549185510	chr17:17580406-17580407	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs568810530	chr17:17580442-17580443	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs150129409	chr17:17580474-17580475	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs551077757	chr17:17580498-17580499	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs115157982	chr17:17580546-17580547	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs534067455	chr17:17580621-17580622	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs62064075	chr17:17580647-17580648	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs576581322	chr17:17580648-17580649	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs567589693	chr17:17580679-17580680	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567133114	chr17:17580688-17580689	Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs368743101	chr17:17580698-17580699	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs573772386	chr17:17580801-17580802	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs191814000	chr17:17580826-17580827	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538897177	chr17:17580862-17580863	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs575641314	chr17:17580894-17580895	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs559098521	chr17:17580920-17580921	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs116426263	chr17:17580956-17580957	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs571056005	chr17:17580995-17580996	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs536750939	chr17:17581025-17581026	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs371352767	chr17:17581087-17581088	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs556597582	chr17:17581170-17581171	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs11655976	chr17:17581184-17581185	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138584214	chr17:17581201-17581202	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs149310262	chr17:17581228-17581229	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs143592454	chr17:17581244-17581245	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs375748366	chr17:17581341-17581342	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs374801090	chr17:17581393-17581394	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs537318362	chr17:17581416-17581417	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs369051528	chr17:17581417-17581418	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs138225874	chr17:17581421-17581422	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs563134852	chr17:17581436-17581437	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs373220810	chr17:17581444-17581445	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs573317323	chr17:17581468-17581469	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs531287267	chr17:17581470-17581471	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs542578276	chr17:17581500-17581501	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs200511489	chr17:17581541-17581542	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs370033801	chr17:17581555-17581556	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs374667585	chr17:17581559-17581560	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs202101365	chr17:17581563-17581564	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs200718651	chr17:17581567-17581568	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs145652281	chr17:17581568-17581569	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs11078395	chr17:17581571-17581572	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs200662118	chr17:17581573-17581574	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs56305276	chr17:17581575-17581576	Enhancers Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	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
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
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22543975	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Autism	19492091	CNVD

Chromatin state (count:1745 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17574800-17583600	Weak transcription	Rectal Mucosa Donor 31	rectum
2	chr17:17576600-17584000	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr17:17576600-17584200	Weak transcription	Right Atrium	heart
4	chr17:17576800-17581000	Weak transcription	Primary monocytes fromperipheralblood	blood
5	chr17:17576800-17584200	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr17:17577000-17584200	Weak transcription	Left Ventricle	heart
7	chr17:17578200-17581400	Enhancers	HMEC	breast
8	chr17:17578400-17580600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr17:17578400-17581400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
10	chr17:17578600-17580600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr17:17578600-17580800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr17:17578600-17580800	Enhancers	Fetal Thymus	thymus
13	chr17:17578600-17581400	Enhancers	Breast Myoepithelial Primary Cells	Breast
14	chr17:17578600-17581400	Enhancers	Primary hematopoietic stem cells short term culture	blood
15	chr17:17578600-17582000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
16	chr17:17578800-17580400	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
17	chr17:17578800-17580400	Enhancers	Hela-S3	cervix
18	chr17:17579000-17580400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
19	chr17:17579000-17580400	Enhancers	Primary hematopoietic stem cells	blood
20	chr17:17579000-17580400	Enhancers	Duodenum Mucosa	Duodenum
21	chr17:17579000-17580600	Enhancers	Primary T helper naive cells from peripheral blood	blood
22	chr17:17579000-17580600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
23	chr17:17579000-17580600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr17:17579000-17580600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
25	chr17:17579000-17581000	Enhancers	Primary T cells from cord blood	blood
26	chr17:17579000-17581000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
27	chr17:17579200-17580400	Enhancers	Primary neutrophils fromperipheralblood	blood
28	chr17:17579200-17580400	Enhancers	K562	blood
29	chr17:17579200-17580600	Enhancers	Primary T cells fromperipheralblood	blood
30	chr17:17579200-17580600	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr17:17579200-17580600	Enhancers	Thymus	Thymus
32	chr17:17579200-17580800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
33	chr17:17579200-17580800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
34	chr17:17579200-17581000	Enhancers	Fetal Heart	heart
35	chr17:17579200-17581400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
36	chr17:17579200-17581400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
37	chr17:17579200-17581400	Enhancers	HUVEC	blood vessel
38	chr17:17579400-17580400	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr17:17579400-17580400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
40	chr17:17579400-17580600	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
41	chr17:17579400-17580600	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr17:17579400-17580800	Enhancers	Primary T killer memory cells from peripheral blood	blood
43	chr17:17579400-17581200	Enhancers	Fetal Intestine Large	intestine
44	chr17:17579400-17581200	Enhancers	Spleen	Spleen
45	chr17:17579600-17580400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr17:17579600-17580600	Enhancers	Primary B cells from peripheral blood	blood
47	chr17:17579600-17581400	Enhancers	HepG2	liver
48	chr17:17579800-17580800	Weak transcription	Fetal Muscle Leg	muscle
49	chr17:17579800-17581200	Enhancers	NHEK	skin
50	chr17:17579800-17581400	Enhancers	GM12878-XiMat	blood

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