Variant report

Variant	nsv964381
Chromosome Location	chr20:23614805-23621846
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:509)
CpG islands
(count:550)
Chromatin interactive
region (count:18)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:509 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:23621811-23622269	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:23620842-23621041	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:23618404-23618721	HepG2	liver:	n/a	n/a
4	ATF3	chr20:23617868-23618151	K562	blood:	n/a	chr20:23618034-23618054
5	BACH1	chr20:23618423-23618424	H1-hESC	embryonic stem cell:	n/a	n/a
6	BACH1	chr20:23617950-23617995	K562	blood:	n/a	n/a
7	BHLHE40	chr20:23617968-23618683	K562	blood:	n/a	n/a
8	BHLHE40	chr20:23617931-23618730	HepG2	liver:	n/a	n/a
9	BRCA1	chr20:23618186-23618317	HepG2	liver:	n/a	n/a
10	BRCA1	chr20:23617846-23618137	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr20:23618527-23618641	HepG2	liver:	n/a	n/a
12	CBX3	chr20:23618501-23618797	K562	blood:	n/a	n/a
13	CBX3	chr20:23617792-23618151	K562	blood:	n/a	n/a
14	CCNT2	chr20:23617735-23618726	K562	blood:	n/a	chr20:23618218-23618227
15	CEBPB	chr20:23617999-23618136	Hela-S3	cervix:	n/a	n/a
16	CEBPB	chr20:23621800-23622359	HepG2	liver:	n/a	n/a
17	CEBPB	chr20:23616224-23616387	A549	lung:	n/a	chr20:23616308-23616319
18	CEBPB	chr20:23616136-23616481	HepG2	liver:	n/a	chr20:23616308-23616319
19	CEBPD	chr20:23618337-23618765	HepG2	liver:	n/a	n/a
20	CEBPD	chr20:23618028-23618896	HepG2	liver:	n/a	n/a
21	CHD2	chr20:23618273-23618295	GM12878	blood:	n/a	n/a
22	CHD2	chr20:23621806-23621957	HepG2	liver:	n/a	n/a
23	CHD2	chr20:23618037-23618801	HepG2	liver:	n/a	n/a
24	CHD2	chr20:23618309-23618706	K562	blood:	n/a	n/a
25	CHD2	chr20:23617302-23617461	HepG2	liver:	n/a	n/a
26	CHD2	chr20:23620828-23620840	HepG2	liver:	n/a	n/a
27	CHD2	chr20:23620270-23620273	HepG2	liver:	n/a	n/a
28	CHD2	chr20:23617948-23618829	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr20:23618110-23618783	H1-hESC	embryonic stem cell:	n/a	n/a
30	CREB1	chr20:23617881-23618717	A549	lung:	n/a	n/a
31	CREB1	chr20:23617875-23618301	K562	blood:	n/a	n/a
32	CREB1	chr20:23617839-23618866	HepG2	liver:	n/a	n/a
33	CREB1	chr20:23617837-23618352	H1-hESC	embryonic stem cell:	n/a	n/a
34	CTBP2	chr20:23617903-23618777	H1-hESC	embryonic stem cell:	n/a	n/a
35	CTCF	chr20:23617840-23617990	HRE	kidney:	n/a	n/a
36	CTCF	chr20:23617860-23618010	BJ	skin:	n/a	n/a
37	CTCF	chr20:23621560-23621710	GM12875	blood:	n/a	n/a
38	CTCF	chr20:23617860-23618010	HCPEpiC	choroid plexus:	n/a	n/a
39	CTCF	chr20:23618380-23618530	AG04449	skin:	n/a	n/a
40	CTCF	chr20:23617860-23618010	HBMEC	blood vessel:	n/a	n/a
41	CTCF	chr20:23617900-23618050	HRE	kidney:	n/a	n/a
42	CTCF	chr20:23616564-23616615	NHEK	skin:	n/a	n/a
43	CTCF	chr20:23617940-23618090	GM12874	blood:	n/a	n/a
44	CTCF	chr20:23617960-23618110	SK-N-SH_RA	brain:	n/a	n/a
45	CTCF	chr20:23617920-23618070	HMEC	breast:	n/a	n/a
46	CTCF	chr20:23618340-23618490	HUVEC	blood vessel:	n/a	n/a
47	CTCF	chr20:23618100-23618250	AG04449	skin:	n/a	chr20:23618236-23618249
48	CTCF	chr20:23621540-23621690	HepG2	liver:	n/a	n/a
49	CTCF	chr20:23616597-23616617	Kidney_OC	kidney:	n/a	n/a
50	CTCF	chr20:23617972-23618011	Pancreas_OC	pancreas:	n/a	n/a

(count:550 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23618481-23618531	AG10803	skin:	n/a
2	chr20:23618481-23618531	AG10803	skin:	n/a
3	chr20:23618055-23618105	BJ	skin:	n/a
4	chr20:23618348-23618398	BJ	skin:	n/a
5	chr20:23618481-23618531	T-47D	breast:	n/a
6	chr20:23618481-23618531	GM12891	blood:	n/a
7	chr20:23621136-23621186	ovcar-3	ovarian:	n/a
8	chr20:23618512-23618562	SAEC	small airway:	n/a
9	chr20:23621136-23621186	ECC-1	luminal epithelium:	n/a
10	chr20:23618481-23618531	HNPCEpiC	eye:	n/a
11	chr20:23618512-23618562	HCPEpiC	choroid plexus:	n/a
12	chr20:23618481-23618531	NH-A	brain:	n/a
13	chr20:23618481-23618531	NT2-D1	testis:	n/a
14	chr20:23618481-23618531	GM06990	blood:	n/a
15	chr20:23618348-23618398	U87	brain:	n/a
16	chr20:23618055-23618105	ProgFib	skin:	n/a
17	chr20:23619778-23619828	AG04450	lung:	fetal
18	chr20:23619525-23619575	HL-60	blood:	n/a
19	chr20:23618512-23618562	HEEpiC	esophagus:	n/a
20	chr20:23621136-23621186	MCF-7	breast:	n/a
21	chr20:23618055-23618105	RPTEC	kidney:	n/a
22	chr20:23617145-23617195	HEEpiC	esophagus:	n/a
23	chr20:23617145-23617195	HCT-116	colon:	n/a
24	chr20:23617145-23617195	T-47D	breast:	n/a
25	chr20:23618512-23618562	BE2_C	brain:	n/a
26	chr20:23618590-23618640	HCF	heart:	n/a
27	chr20:23618348-23618398	HPAEpiC	pulmonary alveolar:	n/a
28	chr20:23618512-23618562	HMEC	breast:	n/a
29	chr20:23619778-23619828	HCT-116	colon:	n/a
30	chr20:23618512-23618562	HepG2	liver:	n/a
31	chr20:23618481-23618531	AG04449	skin:	fetal
32	chr20:23618055-23618105	HEK293	kidney:	embryo
33	chr20:23618348-23618398	GM12892	blood:	n/a
34	chr20:23621136-23621186	HRCEpiC	kidney:	n/a
35	chr20:23618481-23618531	BJ	skin:	n/a
36	chr20:23618348-23618398	HAEpiC	amniotic membrane:	n/a
37	chr20:23617145-23617195	HRE	kidney:	n/a
38	chr20:23618512-23618562	AoSMC	blood vessel:	n/a
39	chr20:23618055-23618105	MCF10A-Er-Src	breast:	n/a
40	chr20:23618590-23618640	HCT-116	colon:	n/a
41	chr20:23618590-23618640	NT2-D1	testis:	n/a
42	chr20:23621136-23621186	AG04449	skin:	fetal
43	chr20:23617145-23617195	AG09309	skin:	n/a
44	chr20:23618590-23618640	CMK	blood:	n/a
45	chr20:23618590-23618640	T-47D	breast:	n/a
46	chr20:23619525-23619575	HCT-116	colon:	n/a
47	chr20:23618512-23618562	ovcar-3	ovarian:	n/a
48	chr20:23618512-23618562	T-47D	breast:	n/a
49	chr20:23618055-23618105	NB4	blood:	n/a
50	chr20:23617145-23617195	LNCaP	prostate:	n/a

(count:18 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:23615698..23619686-chr20:23620113..23624171,4	MCF-7	breast:
2	chr20:23608610..23615599-chr20:23616056..23619619,19	MCF-7	breast:
3	chr15:93425841..93426770-chr20:23617945..23618689,2	Hela-S3	cervix:
4	chr20:23608610..23615599-chr20:23616056..23619619,19	MCF-7	breast:
5	chr20:23618414..23619171-chr5:138940732..138941254,2	HCT-116	colon:
6	chr20:23604645..23607070-chr20:23613987..23616956,2	K562	blood:
7	chr20:23617167..23619413-chr20:62495612..62498216,2	MCF-7	breast:
8	chr20:23340884..23343229-chr20:23616953..23618725,2	K562	blood:
9	chr20:23618106..23618624-chr3:150320619..150321356,2	NB4	blood:
10	chr20:23619975..23621824-chr20:23630879..23635181,3	MCF-7	breast:
11	chr20:23616967..23620200-chr20:23620235..23623406,7	MCF-7	breast:
12	chr20:23615462..23617688-chr20:23624542..23627030,2	MCF-7	breast:
13	chr20:23617967..23620245-chr20:23621003..23622581,2	K562	blood:
14	chr20:23400787..23402892-chr20:23617355..23620191,2	MCF-7	breast:
15	chr20:23610507..23612555-chr20:23613561..23616038,2	MCF-7	breast:
16	chr20:23615491..23618366-chr20:23625789..23627708,2	MCF-7	breast:
17	chr20:23400310..23402508-chr20:23615661..23618868,3	MCF-7	breast:
18	chr20:23342009..23344759-chr20:23616093..23619702,3	MCF-7	breast:

No data

Variant related genes	Relation type
CST3	TF binding region
ENSG00000270001	TF binding region
CST3	CpG island
ENSG00000270001	CpG island
ENSG00000270001	chromatin interactions
ENSG00000131508	chromatin interactions
ENSG00000173575	chromatin interactions
ENSG00000272888	chromatin interactions
ENSG00000120742	chromatin interactions
ENSG00000101439	chromatin interactions
ENSG00000125812	chromatin interactions
ENSG00000198843	chromatin interactions
ENSG00000101150	chromatin interactions
ENSG00000125814	chromatin interactions

Extended variants
information (count: 328 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:328 , 50 per page) page: 1 2 3 4 5 6 7

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs547281031	chr20:23614814-23614815	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs374753427	chr20:23614827-23614828	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs190651735	chr20:23614851-23614852	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533080598	chr20:23614860-23614861	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs549907876	chr20:23614879-23614880	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs569766868	chr20:23614900-23614901	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs555528298	chr20:23614905-23614906	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs561668215	chr20:23614946-23614947	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs79996778	chr20:23614991-23614992	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs547324462	chr20:23615014-23615015	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs534643726	chr20:23615015-23615016	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs150531460	chr20:23615058-23615059	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs372181337	chr20:23615061-23615062	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs578159771	chr20:23615095-23615096	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs543778124	chr20:23615111-23615112	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs144403951	chr20:23615112-23615113	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs147812588	chr20:23615150-23615151	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs77618046	chr20:23615191-23615192	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3' Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs533067431	chr20:23615223-23615224	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs559461904	chr20:23615228-23615229	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs528464103	chr20:23615237-23615238	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs556369884	chr20:23615256-23615257	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs139677671	chr20:23615324-23615325	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs565145332	chr20:23615332-23615333	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs145279791	chr20:23615396-23615397	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs180949711	chr20:23615414-23615415	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs569843253	chr20:23615473-23615474	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs369623295	chr20:23615525-23615526	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs529134330	chr20:23615578-23615579	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549088657	chr20:23615593-23615594	Weak transcription Strong transcription Genic enhancers Enhancers Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs186370174	chr20:23615611-23615612	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs534708598	chr20:23615625-23615626	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs551325495	chr20:23615637-23615638	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs571179044	chr20:23615680-23615681	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs145116574	chr20:23615699-23615700	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs149133032	chr20:23615720-23615721	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs191182286	chr20:23615743-23615744	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs536496231	chr20:23615775-23615776	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs6138022	chr20:23615785-23615786	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs551047299	chr20:23615793-23615794	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs553154093	chr20:23615816-23615817	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs369774064	chr20:23615819-23615820	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs375553362	chr20:23615820-23615821	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs572961309	chr20:23615832-23615833	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs534663906	chr20:23615843-23615844	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs397838066	chr20:23615844-23615845	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs34749026	chr20:23615845-23615846	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs6083205	chr20:23615855-23615856	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs6138023	chr20:23615882-23615883	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs373571066	chr20:23615887-23615888	Weak transcription ZNF genes & repeats Transcr. at gene 5' and 3' Strong transcription Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Prostate cancer	18632612	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
small cell lung cancer	17426248	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:747 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23600600-23617000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr20:23602000-23616800	Weak transcription	H1 Cell Line	embryonic stem cell
3	chr20:23603800-23615400	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
4	chr20:23604000-23616600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
5	chr20:23604000-23616800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
6	chr20:23604200-23615000	Weak transcription	Brain Anterior Caudate	brain
7	chr20:23606600-23615200	Weak transcription	Brain Cingulate Gyrus	brain
8	chr20:23606600-23617000	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
9	chr20:23606800-23616600	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
10	chr20:23607000-23615000	Weak transcription	Colon Smooth Muscle	Colon
11	chr20:23607600-23615400	Weak transcription	Fetal Kidney	kidney
12	chr20:23609600-23615000	Weak transcription	HSMMtube	muscle
13	chr20:23609800-23616800	Weak transcription	Primary hematopoietic stem cells	blood
14	chr20:23610200-23616800	Weak transcription	HUES6 Cell Line	embryonic stem cell
15	chr20:23610200-23617000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
16	chr20:23610200-23617000	Weak transcription	K562	blood
17	chr20:23610400-23615400	Weak transcription	NHDF-Ad	bronchial
18	chr20:23610400-23616000	Weak transcription	Fetal Thymus	thymus
19	chr20:23610400-23616800	Weak transcription	HUES64 Cell Line	embryonic stem cell
20	chr20:23610400-23616800	Weak transcription	NH-A	brain
21	chr20:23610400-23618200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
22	chr20:23610600-23616800	Weak transcription	Hela-S3	cervix
23	chr20:23610800-23615200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
24	chr20:23610800-23616800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
25	chr20:23610800-23617400	Weak transcription	H9 Cell Line	embryonic stem cell
26	chr20:23611000-23615600	Weak transcription	Brain Inferior Temporal Lobe	brain
27	chr20:23611000-23616000	Strong transcription	Fetal Intestine Small	intestine
28	chr20:23611200-23615000	Weak transcription	Right Atrium	heart
29	chr20:23611200-23615800	Weak transcription	GM12878-XiMat	blood
30	chr20:23611400-23615600	Weak transcription	HUVEC	blood vessel
31	chr20:23612000-23615000	Strong transcription	Brain Germinal Matrix	brain
32	chr20:23612000-23615000	Genic enhancers	Skeletal Muscle Male	skeletal muscle
33	chr20:23612000-23615400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
34	chr20:23612000-23615600	Genic enhancers	Primary monocytes fromperipheralblood	blood
35	chr20:23612000-23615600	Strong transcription	Fetal Intestine Large	intestine
36	chr20:23612000-23617000	Genic enhancers	Fetal Muscle Trunk	muscle
37	chr20:23612200-23615000	Strong transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
38	chr20:23612200-23615000	Strong transcription	Liver	Liver
39	chr20:23612200-23615000	Strong transcription	Left Ventricle	heart
40	chr20:23612200-23615200	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
41	chr20:23612200-23615200	Strong transcription	Esophagus	oesophagus
42	chr20:23612200-23615400	Strong transcription	Duodenum Mucosa	Duodenum
43	chr20:23612200-23615400	Strong transcription	NHLF	lung
44	chr20:23612200-23615800	Strong transcription	IMR90 fetal lung fibroblasts Cell Line	lung
45	chr20:23612200-23615800	Strong transcription	Aorta	Aorta
46	chr20:23612200-23616200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr20:23612400-23615000	Strong transcription	A549	lung
48	chr20:23612400-23615200	Genic enhancers	HepG2	liver
49	chr20:23612400-23615800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr20:23612400-23616000	Strong transcription	Fetal Stomach	stomach

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