Variant report

Variant	esv3375230
Chromosome Location	chr20:1446177-1448725
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	chr20:1447389-1448758	HepG2	liver:	n/a	chr20:1447465-1447480
2	ARID3A	chr20:1447391-1447663	K562	blood:	n/a	chr20:1447465-1447480
3	ATF1	chr20:1448243-1449093	K562	blood:	n/a	n/a
4	ATF2	chr20:1447270-1447655	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr20:1447282-1447876	GM12878	blood:	n/a	n/a
6	ATF2	chr20:1447328-1447693	GM12878	blood:	n/a	n/a
7	ATF3	chr20:1447212-1447820	A549	lung:	n/a	n/a
8	ATF3	chr20:1447390-1447742	K562	blood:	n/a	n/a
9	BACH1	chr20:1447270-1447720	K562	blood:	n/a	n/a
10	BACH1	chr20:1446826-1447663	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr20:1447381-1447709	GM12878	blood:	n/a	n/a
12	BCL3	chr20:1446987-1447748	A549	lung:	n/a	chr20:1447283-1447296 chr20:1447092-1447105 chr20:1447643-1447656 chr20:1447055-1447068 chr20:1447496-1447509 chr20:1447346-1447359 chr20:1447590-1447603 chr20:1447521-1447534
13	BCL3	chr20:1447102-1447868	A549	lung:	n/a	chr20:1447283-1447296 chr20:1447643-1447656 chr20:1447496-1447509 chr20:1447346-1447359 chr20:1447590-1447603 chr20:1447521-1447534
14	BCLAF1	chr20:1447328-1447903	K562	blood:	n/a	chr20:1447643-1447656 chr20:1447496-1447509 chr20:1447346-1447359 chr20:1447590-1447603 chr20:1447521-1447534
15	BCLAF1	chr20:1447205-1447897	GM12878	blood:	n/a	chr20:1447283-1447296 chr20:1447643-1447656 chr20:1447496-1447509 chr20:1447346-1447359 chr20:1447590-1447603 chr20:1447521-1447534
16	BCLAF1	chr20:1447252-1447850	GM12878	blood:	n/a	chr20:1447283-1447296 chr20:1447643-1447656 chr20:1447496-1447509 chr20:1447346-1447359 chr20:1447590-1447603 chr20:1447521-1447534
17	BCLAF1	chr20:1447327-1447742	K562	blood:	n/a	chr20:1447643-1447656 chr20:1447496-1447509 chr20:1447346-1447359 chr20:1447590-1447603 chr20:1447521-1447534
18	BHLHE40	chr20:1447197-1447811	GM12878	blood:	n/a	chr20:1447494-1447510 chr20:1447574-1447590
19	BHLHE40	chr20:1446983-1447944	HepG2	liver:	n/a	chr20:1447494-1447510 chr20:1447574-1447590 chr20:1447087-1447103
20	BHLHE40	chr20:1447084-1448616	K562	blood:	n/a	chr20:1447494-1447510 chr20:1447574-1447590 chr20:1447087-1447103
21	BRCA1	chr20:1447386-1448276	HepG2	liver:	n/a	n/a
22	BRCA1	chr20:1447396-1447704	GM12878	blood:	n/a	n/a
23	BRCA1	chr20:1447510-1447778	Hela-S3	cervix:	n/a	n/a
24	BRCA1	chr20:1447440-1447832	H1-hESC	embryonic stem cell:	n/a	n/a
25	BRCA1	chr20:1446643-1447190	Hela-S3	cervix:	n/a	n/a
26	CBX3	chr20:1447112-1447964	HCT-116	colon:	n/a	n/a
27	CBX3	chr20:1448379-1448792	K562	blood:	n/a	n/a
28	CBX3	chr20:1447335-1447977	K562	blood:	n/a	n/a
29	CBX3	chr20:1448267-1448821	K562	blood:	n/a	n/a
30	CCNT2	chr20:1448086-1448714	K562	blood:	n/a	n/a
31	CCNT2	chr20:1447011-1447828	K562	blood:	n/a	n/a
32	CEBPB	chr20:1447405-1447826	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr20:1448264-1448856	K562	blood:	n/a	n/a
34	CEBPB	chr20:1447317-1447726	Hela-S3	cervix:	n/a	n/a
35	CEBPB	chr20:1448402-1448780	HepG2	liver:	n/a	n/a
36	CEBPB	chr20:1447243-1447807	GM12878	blood:	n/a	n/a
37	CEBPB	chr20:1446524-1447102	Hela-S3	cervix:	n/a	n/a
38	CEBPB	chr20:1447411-1447716	K562	blood:	n/a	n/a
39	CEBPB	chr20:1448318-1448797	K562	blood:	n/a	n/a
40	CEBPB	chr20:1448445-1448748	H1-hESC	embryonic stem cell:	n/a	n/a
41	CEBPB	chr20:1447315-1447900	A549	lung:	n/a	n/a
42	CEBPB	chr20:1447467-1447688	HepG2	liver:	n/a	n/a
43	CEBPB	chr20:1448404-1448714	K562	blood:	n/a	n/a
44	CEBPB	chr20:1447398-1447620	HepG2	liver:	n/a	n/a
45	CEBPB	chr20:1448462-1448682	HepG2	liver:	n/a	n/a
46	CEBPD	chr20:1447277-1447815	K562	blood:	n/a	n/a
47	CEBPD	chr20:1447019-1447857	HepG2	liver:	n/a	n/a
48	CEBPD	chr20:1447300-1447780	HepG2	liver:	n/a	n/a
49	CHD1	chr20:1447173-1447619	H1-hESC	embryonic stem cell:	n/a	n/a
50	CHD1	chr20:1447224-1447695	GM12878	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:1448595-1448645	GM19239	blood:	n/a
2	chr20:1448419-1448469	HAEpiC	amniotic membrane:	n/a
3	chr20:1448595-1448645	AG10803	skin:	n/a
4	chr20:1448645-1448695	ovcar-3	ovarian:	n/a
5	chr20:1447728-1447778	SK-N-SH	brain:	n/a
6	chr20:1448498-1448548	RPTEC	kidney:	n/a
7	chr20:1448577-1448627	ovcar-3	ovarian:	n/a
8	chr20:1446937-1446987	RPTEC	kidney:	n/a
9	chr20:1448498-1448548	HEK293	kidney:	embryo
10	chr20:1448480-1448530	Hela-S3	cervix:	n/a
11	chr20:1448577-1448627	H1-hESC	embryonic stem cell:	embryo
12	chr20:1448637-1448687	SAEC	small airway:	n/a
13	chr20:1448577-1448627	SKMC	muscle:	n/a
14	chr20:1447874-1447924	Hepatocyte	liver:	n/a
15	chr20:1446937-1446987	AG10803	skin:	n/a
16	chr20:1448595-1448645	HEK293	kidney:	embryo
17	chr20:1448498-1448548	NB4	blood:	n/a
18	chr20:1448595-1448645	HUVEC	blood vessel:	n/a
19	chr20:1447728-1447778	BJ	skin:	n/a
20	chr20:1448645-1448695	HCPEpiC	choroid plexus:	n/a
21	chr20:1448480-1448530	HEK293	kidney:	embryo
22	chr20:1448480-1448530	ECC-1	luminal epithelium:	n/a
23	chr20:1447728-1447778	HCF	heart:	n/a
24	chr20:1448595-1448645	RPTEC	kidney:	n/a
25	chr20:1447287-1447337	HRPEpiC	eye:	n/a
26	chr20:1447728-1447778	H1-hESC	embryonic stem cell:	embryo
27	chr20:1447728-1447778	RPTEC	kidney:	n/a
28	chr20:1448645-1448695	HIPEpiC	eye:	n/a
29	chr20:1448577-1448627	PFSK-1	brain:	n/a
30	chr20:1448577-1448627	HRCEpiC	kidney:	n/a
31	chr20:1448595-1448645	IMR90	lung:	fetal
32	chr20:1448595-1448645	ProgFib	skin:	n/a
33	chr20:1448419-1448469	HEK293	kidney:	embryo
34	chr20:1447728-1447778	HAEpiC	amniotic membrane:	n/a
35	chr20:1448577-1448627	AoSMC	blood vessel:	n/a
36	chr20:1446937-1446987	HIPEpiC	eye:	n/a
37	chr20:1448637-1448687	K562	blood:	n/a
38	chr20:1448595-1448645	MCF-7	breast:	n/a
39	chr20:1446937-1446987	Caco-2	colon:	n/a
40	chr20:1448637-1448687	SK-N-SH	brain:	n/a
41	chr20:1448595-1448645	PrEC	prostate:	n/a
42	chr20:1448419-1448469	HMEC	breast:	n/a
43	chr20:1447874-1447924	PrEC	prostate:	n/a
44	chr20:1448437-1448487	HCF	heart:	n/a
45	chr20:1448480-1448530	MCF-7	breast:	n/a
46	chr20:1448480-1448530	HRCEpiC	kidney:	n/a
47	chr20:1447287-1447337	SK-N-MC	brain:	n/a
48	chr20:1448419-1448469	AG04450	lung:	fetal
49	chr20:1448437-1448487	NB4	blood:	n/a
50	chr20:1448480-1448530	MCF10A-Er-Src	breast:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:1436244..1441221-chr20:1444525..1448562,4	MCF-7	breast:
2	chr20:361485..363213-chr20:1446007..1447644,2	K562	blood:
3	chr20:1372232..1375944-chr20:1446656..1450761,3	MCF-7	breast:
4	chr20:1422183..1425116-chr20:1445369..1447221,2	K562	blood:
5	chr20:1304611..1307577-chr20:1447050..1450049,5	K562	blood:
6	chr20:1443012..1448397-chr20:1448655..1450616,4	MCF-7	breast:
7	chr20:1437321..1440209-chr20:1445376..1448458,3	MCF-7	breast:
8	chr20:1444656..1446589-chr20:1449305..1450879,2	K562	blood:
9	chr20:1446155..1447724-chr20:1468382..1469913,2	MCF-7	breast:
10	chr20:1306070..1308541-chr20:1446001..1448028,2	MCF-7	breast:
11	chr20:1372434..1374768-chr20:1446935..1449052,2	K562	blood:
12	chr20:1371233..1373934-chr20:1446935..1449162,2	K562	blood:
13	chr20:1447017..1447769-chr9:102583969..102584507,2	Hela-S3	cervix:
14	chr20:1304840..1306676-chr20:1447020..1448985,3	K562	blood:
15	chr20:1408581..1410916-chr20:1448637..1451105,2	K562	blood:

Variant related genes	Relation type
NSFL1C	TF binding region
NSFL1C	CpG island
ENSG00000125775	chromatin interactions
ENSG00000088832	chromatin interactions
ENSG00000234684	chromatin interactions
ENSG00000101255	chromatin interactions
ENSG00000119508	chromatin interactions
ENSG00000266085	chromatin interactions
ENSG00000088833	chromatin interactions

Extended variants
information (count: 101 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:101 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs541964835	chr20:1446192-1446193	Weak transcription Enhancers Transcr. at gene 5' and 3' Genic enhancers Strong transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs551891313	chr20:1446228-1446229	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs570476827	chr20:1446256-1446257	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs534700723	chr20:1446260-1446261	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs73891552	chr20:1446335-1446336	Flanking Active TSS Weak transcription Enhancers Active TSS Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs568231178	chr20:1446401-1446402	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs535659946	chr20:1446440-1446441	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs557178291	chr20:1446456-1446457	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs545607236	chr20:1446497-1446498	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs193111977	chr20:1446541-1446542	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs377496107	chr20:1446559-1446560	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs959813	chr20:1446580-1446581	Flanking Active TSS Enhancers Active TSS Weak transcription Flanking Bivalent TSS/Enh	Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs531127340	chr20:1446665-1446666	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
14	rs74759040	chr20:1446667-1446668	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
15	rs116832887	chr20:1446693-1446694	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
16	rs563390735	chr20:1446708-1446709	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
17	rs149596588	chr20:1446750-1446751	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
18	rs144280190	chr20:1446782-1446783	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
19	rs544488574	chr20:1446789-1446790	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
20	rs563151023	chr20:1446797-1446798	Active TSS Flanking Active TSS Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
21	rs114639658	chr20:1446835-1446836	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
22	rs140053719	chr20:1446843-1446844	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
23	rs146551859	chr20:1446881-1446882	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
24	rs183553602	chr20:1446885-1446886	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
25	rs528113741	chr20:1446889-1446890	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
26	rs546681258	chr20:1446905-1446906	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
27	rs188289708	chr20:1446947-1446948	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
28	rs535596208	chr20:1446955-1446956	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
29	rs556873961	chr20:1446974-1446975	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
30	rs564018819	chr20:1446977-1446978	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
31	rs375610653	chr20:1446997-1446998	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
32	rs539336093	chr20:1447024-1447025	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
33	rs558059448	chr20:1447081-1447082	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
34	rs572875378	chr20:1447098-1447099	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
35	rs540249019	chr20:1447107-1447108	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs555401375	chr20:1447114-1447115	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs573799768	chr20:1447120-1447121	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs544742133	chr20:1447125-1447126	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs530662605	chr20:1447157-1447158	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs533611587	chr20:1447238-1447239	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
41	rs545356646	chr20:1447274-1447275	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs560780705	chr20:1447277-1447278	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs528048970	chr20:1447344-1447345	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs201950996	chr20:1447347-1447348	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs568107056	chr20:1447358-1447359	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs528971127	chr20:1447479-1447480	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
47	rs550684410	chr20:1447516-1447517	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
48	rs193187422	chr20:1447545-1447546	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
49	rs368086398	chr20:1447552-1447553	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
50	rs371973889	chr20:1447563-1447564	Active TSS Weak transcription Enhancers Bivalent/Poised TSS	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Hodgkin''s lymphoma	18641027	CNVD
Myelofibrosis	22110671	CNVD
Intellectual disability	22045946	CNVD
Glioblastoma multiforme	22286061	CNVD
Hepatocellular carcinoma	22174799	CNVD
Colorectal cancer	19455253	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	17603634	CNVD
Colorectal cancer	19359472	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Intracranial aneurysm	16715129	CNVD
Colorectal cancer	16774939	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16397240	CNVD
abortions and stillbirths	19751515	CNVD
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
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
lymphocytic leukemia	21291569	CNVD
Acute myeloid leukemia	20729466	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Ewing''s sarcoma	17952124	CNVD
Oral cancer	21386901	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Melanoma	17363583	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD

Chromatin state (count:578 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:1431600-1446400	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
2	chr20:1433600-1446600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr20:1436600-1446400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr20:1437600-1446200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr20:1442000-1446600	Weak transcription	Aorta	Aorta
6	chr20:1442200-1446200	Weak transcription	H9 Cell Line	embryonic stem cell
7	chr20:1442800-1446200	Genic enhancers	Primary T helper cells PMA-I stimulated	--
8	chr20:1443400-1446400	Genic enhancers	Primary B cells from peripheral blood	blood
9	chr20:1443600-1446200	Enhancers	Primary T helper naive cells from peripheral blood	blood
10	chr20:1443600-1446400	Genic enhancers	Primary monocytes fromperipheralblood	blood
11	chr20:1444000-1446200	Enhancers	Primary T killer memory cells from peripheral blood	blood
12	chr20:1444400-1446200	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
13	chr20:1444400-1446200	Genic enhancers	Brain Angular Gyrus	brain
14	chr20:1444400-1446200	Genic enhancers	HMEC	breast
15	chr20:1444400-1446400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr20:1444400-1446400	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
17	chr20:1444400-1446400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
18	chr20:1444400-1446400	Genic enhancers	Lung	lung
19	chr20:1444600-1446200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
20	chr20:1444600-1446200	Genic enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr20:1444600-1446400	Genic enhancers	Primary T cells from cord blood	blood
22	chr20:1444600-1446400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
23	chr20:1444800-1446200	Genic enhancers	Rectal Mucosa Donor 31	rectum
24	chr20:1444800-1446200	Genic enhancers	Spleen	Spleen
25	chr20:1444800-1446200	Transcr. at gene 5' and 3'	GM12878-XiMat	blood
26	chr20:1444800-1446200	Genic enhancers	HUVEC	blood vessel
27	chr20:1444800-1446200	Genic enhancers	K562	blood
28	chr20:1444800-1446200	Genic enhancers	Osteobl	bone
29	chr20:1444800-1446400	Enhancers	Primary T helper cells fromperipheralblood	blood
30	chr20:1444800-1446400	Enhancers	Fetal Heart	heart
31	chr20:1445000-1446200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
32	chr20:1445000-1446200	Genic enhancers	Liver	Liver
33	chr20:1445000-1446200	Enhancers	Brain Substantia Nigra	brain
34	chr20:1445000-1446200	Genic enhancers	Esophagus	oesophagus
35	chr20:1445200-1446200	Weak transcription	HUES48 Cell Line	embryonic stem cell
36	chr20:1445200-1446200	Weak transcription	Fetal Thymus	thymus
37	chr20:1445200-1446400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr20:1445200-1446400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
39	chr20:1445200-1446400	Enhancers	Gastric	stomach
40	chr20:1445200-1446600	Enhancers	Pancreas	Pancrea
41	chr20:1445400-1446200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
42	chr20:1445400-1446200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr20:1445400-1446200	Enhancers	Right Ventricle	heart
44	chr20:1445400-1446400	Genic enhancers	Fetal Stomach	stomach
45	chr20:1445400-1446600	Flanking Active TSS	Breast Myoepithelial Primary Cells	Breast
46	chr20:1445600-1446200	Genic enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr20:1445600-1446200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
48	chr20:1445600-1446200	Genic enhancers	Primary mononuclear cells fromperipheralblood	Blood
49	chr20:1445600-1446200	Transcr. at gene 5' and 3'	Skeletal Muscle Male	skeletal muscle
50	chr20:1445600-1446200	Transcr. at gene 5' and 3'	Dnd41	blood

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