Variant report

Variant	nsv1063833
Chromosome Location	chr17:20088333-20206601
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1397)
CpG islands
(count:673)
Chromatin interactive
region (count:58)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1397 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:20110439-20111125	K562	blood:	n/a	n/a
2	ARID3A	chr17:20093309-20093612	K562	blood:	n/a	n/a
3	ARID3A	chr17:20193406-20193703	HepG2	liver:	n/a	n/a
4	ARID3A	chr17:20129142-20129366	K562	blood:	n/a	n/a
5	ARID3A	chr17:20130052-20130393	K562	blood:	n/a	n/a
6	ATF1	chr17:20166977-20167251	K562	blood:	n/a	n/a
7	ATF2	chr17:20130036-20130451	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr17:20088179-20088586	K562	blood:	n/a	n/a
9	BACH1	chr17:20164107-20164272	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr17:20119585-20119856	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr17:20090476-20090702	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr17:20184460-20184504	K562	blood:	n/a	n/a
13	BACH1	chr17:20127222-20127526	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr17:20088046-20088596	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr17:20137775-20138041	GM12878	blood:	n/a	n/a
16	BATF	chr17:20132266-20132473	GM12878	blood:	n/a	n/a
17	BCL11A	chr17:20107250-20107565	GM12878	blood:	n/a	n/a
18	BCL3	chr17:20139141-20139466	GM12878	blood:	n/a	chr17:20139361-20139370
19	BCL3	chr17:20140911-20141229	GM12878	blood:	n/a	n/a
20	BCL3	chr17:20130009-20130507	A549	lung:	n/a	n/a
21	BCL3	chr17:20140915-20141180	GM12878	blood:	n/a	n/a
22	BCL3	chr17:20109832-20110342	A549	lung:	n/a	n/a
23	BHLHE40	chr17:20166944-20167199	K562	blood:	n/a	n/a
24	BHLHE40	chr17:20170764-20171148	K562	blood:	n/a	n/a
25	BHLHE40	chr17:20170769-20171135	GM12878	blood:	n/a	n/a
26	BHLHE40	chr17:20088371-20088669	K562	blood:	n/a	n/a
27	BHLHE40	chr17:20130089-20130330	K562	blood:	n/a	n/a
28	BRCA1	chr17:20109414-20110344	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr17:20099360-20100278	Hela-S3	cervix:	n/a	n/a
30	CBX3	chr17:20098014-20098369	K562	blood:	n/a	n/a
31	CBX3	chr17:20088305-20088635	K562	blood:	n/a	n/a
32	CBX3	chr17:20108390-20108652	K562	blood:	n/a	n/a
33	CBX3	chr17:20098102-20098357	K562	blood:	n/a	n/a
34	CBX3	chr17:20099554-20100007	K562	blood:	n/a	n/a
35	CCNT2	chr17:20088331-20088604	K562	blood:	n/a	n/a
36	CCNT2	chr17:20110580-20111009	K562	blood:	n/a	chr17:20110783-20110803
37	CEBPB	chr17:20093359-20093679	K562	blood:	n/a	n/a
38	CEBPB	chr17:20175668-20175868	A549	lung:	n/a	n/a
39	CEBPB	chr17:20131087-20131750	A549	lung:	n/a	n/a
40	CEBPB	chr17:20200598-20200793	Hela-S3	cervix:	n/a	chr17:20200701-20200712
41	CEBPB	chr17:20180974-20180981	K562	blood:	n/a	n/a
42	CEBPB	chr17:20162132-20162442	A549	lung:	n/a	chr17:20162293-20162302 chr17:20162292-20162303
43	CEBPB	chr17:20099654-20099980	IMR90	lung:	n/a	chr17:20099827-20099838
44	CEBPB	chr17:20106217-20106703	A549	lung:	n/a	chr17:20106536-20106553
45	CEBPB	chr17:20109316-20110735	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr17:20111624-20112149	K562	blood:	n/a	chr17:20111954-20111965
47	CEBPB	chr17:20109944-20110619	A549	lung:	n/a	n/a
48	CEBPB	chr17:20130126-20131679	IMR90	lung:	n/a	chr17:20130630-20130641
49	CEBPB	chr17:20200540-20200895	HepG2	liver:	n/a	chr17:20200701-20200712
50	CEBPB	chr17:20173356-20173646	IMR90	lung:	n/a	chr17:20173508-20173519

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:20165967-20166017	HUVEC	blood vessel:	n/a
2	chr17:20105626-20105676	AG04450	lung:	fetal
3	chr17:20165967-20166017	HUVEC	blood vessel:	n/a
4	chr17:20105626-20105676	AG04450	lung:	fetal
5	chr17:20156940-20156990	Hela-S3	cervix:	n/a
6	chr17:20140352-20140402	HNPCEpiC	eye:	n/a
7	chr17:20187457-20187507	HEK293	kidney:	embryo
8	chr17:20171047-20171097	K562	blood:	n/a
9	chr17:20156940-20156990	SKMC	muscle:	n/a
10	chr17:20120115-20120165	HMEC	breast:	n/a
11	chr17:20187457-20187507	HCF	heart:	n/a
12	chr17:20105626-20105676	HPAEpiC	pulmonary alveolar:	n/a
13	chr17:20120115-20120165	RPTEC	kidney:	n/a
14	chr17:20128997-20129047	SKMC	muscle:	n/a
15	chr17:20156940-20156990	HRCEpiC	kidney:	n/a
16	chr17:20171047-20171097	GM12878	blood:	n/a
17	chr17:20203992-20204042	HepG2	liver:	n/a
18	chr17:20165967-20166017	GM12891	blood:	n/a
19	chr17:20120115-20120165	HNPCEpiC	eye:	n/a
20	chr17:20187457-20187507	BE2_C	brain:	n/a
21	chr17:20105626-20105676	PFSK-1	brain:	n/a
22	chr17:20165967-20166017	MCF-7	breast:	n/a
23	chr17:20140352-20140402	HMEC	breast:	n/a
24	chr17:20203992-20204042	NHBE	bronchial:	n/a
25	chr17:20171047-20171097	ProgFib	skin:	n/a
26	chr17:20105626-20105676	HMEC	breast:	n/a
27	chr17:20156940-20156990	HepG2	liver:	n/a
28	chr17:20120115-20120165	SAEC	small airway:	n/a
29	chr17:20120115-20120165	NHDF-neo	bronchial:	n/a
30	chr17:20187457-20187507	K562	blood:	n/a
31	chr17:20165967-20166017	K562	blood:	n/a
32	chr17:20180146-20180196	RPTEC	kidney:	n/a
33	chr17:20165967-20166017	Hela-S3	cervix:	n/a
34	chr17:20120115-20120165	SK-N-MC	brain:	n/a
35	chr17:20105626-20105676	AG10803	skin:	n/a
36	chr17:20180146-20180196	HCM	heart:	n/a
37	chr17:20105626-20105676	HIPEpiC	eye:	n/a
38	chr17:20140352-20140402	GM12891	blood:	n/a
39	chr17:20140352-20140402	CMK	blood:	n/a
40	chr17:20107320-20107370	H1-hESC	embryonic stem cell:	embryo
41	chr17:20105626-20105676	SK-N-SH	brain:	n/a
42	chr17:20156940-20156990	AoSMC	blood vessel:	n/a
43	chr17:20107320-20107370	SAEC	small airway:	n/a
44	chr17:20107320-20107370	HCM	heart:	n/a
45	chr17:20105626-20105676	H1-hESC	embryonic stem cell:	embryo
46	chr17:20203992-20204042	AG10803	skin:	n/a
47	chr17:20105626-20105676	BJ	skin:	n/a
48	chr17:20180146-20180196	HRPEpiC	eye:	n/a
49	chr17:20105626-20105676	AG09319	gingival:	n/a
50	chr17:20140352-20140402	HCPEpiC	choroid plexus:	n/a

(count:58 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr17:20058383..20060895-chr17:20129200..20131943,2	K562	blood:
2	chr17:20057192..20060270-chr17:20108096..20110844,3	K562	blood:
3	chr17:20089910..20092717-chr17:20126449..20128094,2	MCF-7	breast:
4	chr17:20056629..20058673-chr17:20092649..20094964,2	MCF-7	breast:
5	chr17:20144551..20147091-chr17:20150035..20152753,2	MCF-7	breast:
6	chr17:20129853..20130435-chr17:20223856..20224752,2	MCF-7	breast:
7	chr17:20144551..20147091-chr17:20150035..20152753,2	MCF-7	breast:
8	chr17:20080334..20082016-chr17:20102428..20104693,2	MCF-7	breast:
9	chr17:20108645..20112421-chr17:20113678..20117792,3	MCF-7	breast:
10	chr17:20090600..20093131-chr17:20093995..20097468,3	MCF-7	breast:
11	chr17:20109966..20112285-chr17:20118187..20119843,2	MCF-7	breast:
12	chr17:20144165..20146631-chr17:20158234..20160364,2	MCF-7	breast:
13	chr17:20025221..20027004-chr17:20127712..20130710,2	MCF-7	breast:
14	chr17:20159792..20163252-chr17:20165134..20168652,3	MCF-7	breast:
15	chr17:20109966..20112285-chr17:20118187..20119843,2	MCF-7	breast:
16	chr17:20113360..20115266-chr17:20118185..20120021,2	K562	blood:
17	chr17:20183025..20185353-chr17:20193031..20195779,2	MCF-7	breast:
18	chr17:20114496..20116993-chr17:20117575..20120257,2	MCF-7	breast:
19	chr17:20187206..20188805-chr17:20191022..20192770,2	K562	blood:
20	chr17:20170501..20172130-chr17:20175746..20177689,2	MCF-7	breast:
21	chr17:20058693..20060833-chr17:20107962..20111201,3	MCF-7	breast:
22	chr17:20144165..20146631-chr17:20158234..20160364,2	MCF-7	breast:
23	chr17:20092981..20095104-chr17:20106076..20107735,2	MCF-7	breast:
24	chr17:20088001..20089506-chr17:20108427..20110013,2	MCF-7	breast:
25	chr17:20116998..20118634-chr17:20126553..20129376,2	K562	blood:
26	chr17:20058426..20061680-chr17:20114068..20117694,3	MCF-7	breast:
27	chr17:20170600..20173338-chr17:20176185..20177778,2	K562	blood:
28	chr17:20058977..20061113-chr17:20127273..20129010,3	MCF-7	breast:
29	chr17:20108704..20111495-chr17:20125977..20128241,2	MCF-7	breast:
30	chr17:20170600..20173338-chr17:20176185..20177778,2	K562	blood:
31	chr17:20092728..20094832-chr17:20098161..20099795,2	K562	blood:
32	chr17:20187206..20188805-chr17:20191022..20192770,2	K562	blood:
33	chr17:20090600..20093131-chr17:20093995..20097468,3	MCF-7	breast:
34	chr17:20080906..20083704-chr17:20086823..20088345,2	MCF-7	breast:
35	chr17:20114496..20116993-chr17:20117575..20120257,2	MCF-7	breast:
36	chr17:20105840..20107350-chr17:20109491..20112046,2	MCF-7	breast:
37	chr17:20109094..20109672-chr17:20129868..20130670,2	K562	blood:
38	chr17:20092728..20094832-chr17:20098161..20099795,2	K562	blood:
39	chr17:20097809..20099634-chr17:20110030..20112138,2	K562	blood:
40	chr17:20057342..20059768-chr17:20130709..20132708,3	MCF-7	breast:
41	chr17:20164807..20165435-chr17:20223847..20224473,2	MCF-7	breast:
42	chr17:20116998..20118634-chr17:20126553..20129376,2	K562	blood:
43	chr17:20024691..20025538-chr17:20129010..20129692,3	MCF-7	breast:
44	chr17:20086231..20089170-chr17:20090433..20092897,2	MCF-7	breast:
45	chr17:20193195..20195348-chr17:20196222..20198766,2	MCF-7	breast:
46	chr17:20096735..20100140-chr17:20107698..20112138,4	K562	blood:
47	chr17:20099390..20102374-chr17:20106721..20109465,2	MCF-7	breast:
48	chr17:20058170..20060902-chr17:20103752..20106651,2	MCF-7	breast:
49	chr17:20170501..20172130-chr17:20175746..20177689,2	MCF-7	breast:
50	chr17:20092981..20095104-chr17:20106076..20107735,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SPECC1-1	chr17:20088395-20088499	ENSG00000263494.1

No data

Variant related genes	Relation type
ENSG00000263494	TF binding region
RNU6-1057P	TF binding region
SPECC1	TF binding region
ENSG00000263494	CpG island
RNU6-1057P	CpG island
SPECC1	CpG island
ENSG00000154898	chromatin interactions
ENSG00000252971	chromatin interactions
ENSG00000263494	chromatin interactions
ENSG00000128487	chromatin interactions

Extended variants
information (count: 4530 )
Associated
traits (count: 153 )

Variant overlapped rSNPs/rCNVs (count:4530 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs554429125	chr17:20088356-20088357	Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs568274743	chr17:20088431-20088432	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
3	rs59649893	chr17:20088435-20088436	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
4	rs2107565	chr17:20088492-20088493	Enhancers Weak transcription	Chromatin interactive region lncRNA	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs576873353	chr17:20088513-20088514	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs151048733	chr17:20088550-20088551	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs2243732	chr17:20088589-20088590	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs572842206	chr17:20088598-20088599	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs541776691	chr17:20088599-20088600	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539281466	chr17:20088653-20088654	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs183872510	chr17:20088663-20088664	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs142330165	chr17:20088683-20088684	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs146621601	chr17:20088688-20088689	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs563859559	chr17:20088690-20088691	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374626778	chr17:20088712-20088713	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs187146253	chr17:20088752-20088753	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs139105984	chr17:20088769-20088770	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs72830179	chr17:20088770-20088771	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs143648839	chr17:20088783-20088784	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs548126083	chr17:20088787-20088788	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs568255205	chr17:20088815-20088816	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs371398424	chr17:20088816-20088817	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs537311941	chr17:20088844-20088845	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs576273171	chr17:20088871-20088872	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs550504223	chr17:20088885-20088886	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs570596070	chr17:20088894-20088895	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs539555167	chr17:20088909-20088910	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs553085521	chr17:20088910-20088911	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150127654	chr17:20088916-20088917	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs535438112	chr17:20088987-20088988	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs191526981	chr17:20088991-20088992	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs374800822	chr17:20089063-20089064	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs182633628	chr17:20089083-20089084	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs200226070	chr17:20089132-20089133	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs544068216	chr17:20089164-20089165	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs563747660	chr17:20089178-20089179	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368615945	chr17:20089361-20089362	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs545922099	chr17:20089371-20089372	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs56749995	chr17:20089452-20089453	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs540790215	chr17:20089533-20089534	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs77051996	chr17:20089554-20089555	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs149335352	chr17:20089576-20089577	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs574261871	chr17:20089630-20089631	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs143021200	chr17:20089635-20089636	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs530734972	chr17:20089671-20089672	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs117119016	chr17:20089714-20089715	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs570588407	chr17:20089774-20089775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs539618576	chr17:20089818-20089819	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs191544873	chr17:20089852-20089853	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs566561035	chr17:20089858-20089859	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:153)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Chronic lymphocytic leukemia	21546498	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
Acute promyelocytic leukemia	19109227	CNVD
T-cell prolymphocytic leukemia	19278963	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
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
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
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
Autism	22543975	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:3538 , 50 per page) page: 1 2 3 4 5 6 7 ... 71

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:20060800-20092200	Weak transcription	Fetal Intestine Small	intestine
2	chr17:20062000-20090400	Weak transcription	Aorta	Aorta
3	chr17:20075800-20090800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
4	chr17:20078000-20089800	Weak transcription	Spleen	Spleen
5	chr17:20078600-20090400	Weak transcription	Muscle Satellite Cultured Cells	--
6	chr17:20079200-20088400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr17:20080400-20092200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr17:20080400-20092400	Weak transcription	Sigmoid Colon	Sigmoid Colon
9	chr17:20082800-20088400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
10	chr17:20082800-20092400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
11	chr17:20084200-20092000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
12	chr17:20084400-20092200	Weak transcription	Brain Germinal Matrix	brain
13	chr17:20085600-20093800	Enhancers	Brain Substantia Nigra	brain
14	chr17:20085800-20088600	Enhancers	Hela-S3	cervix
15	chr17:20085800-20089000	Enhancers	A549	lung
16	chr17:20086000-20092200	Weak transcription	Rectal Mucosa Donor 31	rectum
17	chr17:20086000-20092600	Enhancers	Cortex derived primary cultured neurospheres	brain
18	chr17:20086600-20092000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
19	chr17:20087400-20089000	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr17:20087400-20089200	Enhancers	Primary monocytes fromperipheralblood	blood
21	chr17:20087400-20092200	Enhancers	Brain Angular Gyrus	brain
22	chr17:20087600-20088400	Enhancers	NH-A	brain
23	chr17:20087600-20088600	Enhancers	ES-I3 Cell Line	embryonic stem cell
24	chr17:20087600-20088600	Enhancers	iPS-15b Cell Line	embryonic stem cell
25	chr17:20087600-20088600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr17:20087600-20088600	Enhancers	Osteobl	bone
27	chr17:20087600-20088800	Enhancers	HUES48 Cell Line	embryonic stem cell
28	chr17:20087600-20088800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
29	chr17:20087600-20089000	Enhancers	HUES6 Cell Line	embryonic stem cell
30	chr17:20087600-20089000	Enhancers	Monocytes-CD14+_RO01746	blood
31	chr17:20087600-20089200	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
32	chr17:20087600-20091400	Enhancers	Brain Anterior Caudate	brain
33	chr17:20087600-20091600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
34	chr17:20087600-20092200	Enhancers	Brain Cingulate Gyrus	brain
35	chr17:20087600-20092400	Enhancers	Brain Hippocampus Middle	brain
36	chr17:20087800-20088800	Enhancers	ES-WA7 Cell Line	embryonic stem cell
37	chr17:20087800-20089000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr17:20087800-20089200	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr17:20087800-20089200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
40	chr17:20087800-20089200	Enhancers	Brain Inferior Temporal Lobe	brain
41	chr17:20087800-20091000	Enhancers	iPS-18 Cell Line	embryonic stem cell
42	chr17:20088000-20088400	Enhancers	Fetal Brain Female	brain
43	chr17:20088200-20088400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr17:20088200-20088600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr17:20088200-20088800	Enhancers	H1 Cell Line	embryonic stem cell
46	chr17:20088200-20088800	Enhancers	H9 Cell Line	embryonic stem cell
47	chr17:20088200-20088800	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr17:20088200-20088800	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr17:20088200-20088800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr17:20088200-20088800	Enhancers	Ovary	ovary

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