Variant report

Variant	nsv544214
Chromosome Location	chr20:23415029-23565333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1147)
CpG islands
(count:2629)
Chromatin interactive
region (count:45)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1147 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:23488216-23488283	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:23426293-23426601	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:23550890-23551138	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:23422511-23422806	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:23416561-23416867	HepG2	liver:	n/a	n/a
6	ATF1	chr20:23417323-23417566	K562	blood:	n/a	n/a
7	ATF2	chr20:23513756-23514081	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr20:23507823-23507979	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr20:23422462-23422769	GM12878	blood:	n/a	n/a
10	BATF	chr20:23478200-23478493	GM12878	blood:	n/a	n/a
11	BATF	chr20:23509691-23510055	GM12878	blood:	n/a	chr20:23509889-23509900 chr20:23509906-23509917
12	BATF	chr20:23440154-23440332	GM12878	blood:	n/a	chr20:23440243-23440254
13	BATF	chr20:23495915-23496215	GM12878	blood:	n/a	n/a
14	BATF	chr20:23495900-23496255	GM12878	blood:	n/a	n/a
15	BATF	chr20:23511849-23512071	GM12878	blood:	n/a	n/a
16	BCL11A	chr20:23513851-23514075	H1-hESC	embryonic stem cell:	n/a	n/a
17	BCL11A	chr20:23513761-23514166	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL3	chr20:23456839-23457441	GM12878	blood:	n/a	n/a
19	BCL3	chr20:23425378-23425971	GM12878	blood:	n/a	n/a
20	BCL3	chr20:23456780-23457368	GM12878	blood:	n/a	n/a
21	BCL3	chr20:23506840-23507065	GM12878	blood:	n/a	n/a
22	BCL3	chr20:23425339-23425976	GM12878	blood:	n/a	n/a
23	BCL3	chr20:23516024-23516292	GM12878	blood:	n/a	n/a
24	BHLHE40	chr20:23427304-23427533	K562	blood:	n/a	n/a
25	BHLHE40	chr20:23426259-23426863	HepG2	liver:	n/a	n/a
26	BHLHE40	chr20:23427279-23427535	GM12878	blood:	n/a	n/a
27	BHLHE40	chr20:23422567-23422798	K562	blood:	n/a	n/a
28	BHLHE40	chr20:23422476-23422794	GM12878	blood:	n/a	n/a
29	BHLHE40	chr20:23426616-23426748	K562	blood:	n/a	n/a
30	BHLHE40	chr20:23427237-23427550	HepG2	liver:	n/a	n/a
31	BRCA1	chr20:23454055-23454315	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr20:23510630-23510647	GM12878	blood:	n/a	n/a
33	BRCA1	chr20:23422574-23422690	HepG2	liver:	n/a	n/a
34	BRCA1	chr20:23523709-23523728	GM12878	blood:	n/a	n/a
35	CEBPB	chr20:23523470-23523817	HepG2	liver:	n/a	chr20:23523648-23523659 chr20:23523647-23523658 chr20:23523649-23523658
36	CEBPB	chr20:23474028-23474368	K562	blood:	n/a	chr20:23474176-23474187
37	CEBPB	chr20:23427308-23427620	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr20:23422526-23422826	IMR90	lung:	n/a	n/a
39	CEBPB	chr20:23416564-23416889	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:23435874-23436147	A549	lung:	n/a	chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436004-23436015 chr20:23436006-23436015 chr20:23436005-23436016
41	CEBPB	chr20:23515699-23515853	HepG2	liver:	n/a	n/a
42	CEBPB	chr20:23435881-23436117	K562	blood:	n/a	chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436004-23436015 chr20:23436006-23436015 chr20:23436005-23436016
43	CEBPB	chr20:23506064-23506151	HepG2	liver:	n/a	n/a
44	CEBPB	chr20:23473969-23474249	HepG2	liver:	n/a	chr20:23474176-23474187
45	CEBPB	chr20:23538255-23538343	HepG2	liver:	n/a	n/a
46	CEBPB	chr20:23427329-23427625	A549	lung:	n/a	n/a
47	CEBPB	chr20:23499478-23499579	HepG2	liver:	n/a	chr20:23499522-23499533
48	CEBPB	chr20:23498469-23498679	A549	lung:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
49	CEBPB	chr20:23550852-23551260	HepG2	liver:	n/a	chr20:23551082-23551095 chr20:23551055-23551066 chr20:23551055-23551066
50	CEBPB	chr20:23471614-23471730	HepG2	liver:	n/a	n/a

(count:2629 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23550632-23550682	NHBE	bronchial:	n/a
2	chr20:23433608-23433658	A549	lung:	n/a
3	chr20:23420355-23420405	SK-N-MC	brain:	n/a
4	chr20:23420200-23420250	AG09319	gingival:	n/a
5	chr20:23548991-23549041	SKMC	muscle:	n/a
6	chr20:23419162-23419212	T-47D	breast:	n/a
7	chr20:23550632-23550682	NHBE	bronchial:	n/a
8	chr20:23433608-23433658	A549	lung:	n/a
9	chr20:23420355-23420405	SK-N-MC	brain:	n/a
10	chr20:23420200-23420250	AG09319	gingival:	n/a
11	chr20:23548991-23549041	SKMC	muscle:	n/a
12	chr20:23419162-23419212	T-47D	breast:	n/a
13	chr20:23549467-23549517	Caco-2	colon:	n/a
14	chr20:23471737-23471787	AG10803	skin:	n/a
15	chr20:23550632-23550682	HRCEpiC	kidney:	n/a
16	chr20:23433349-23433399	GM12892	blood:	n/a
17	chr20:23420121-23420171	HEK293	kidney:	embryo
18	chr20:23434086-23434136	HCT-116	colon:	n/a
19	chr20:23549525-23549575	Jurkat	blood:	n/a
20	chr20:23498941-23498991	SK-N-SH_RA	brain:	n/a
21	chr20:23420121-23420171	HMEC	breast:	n/a
22	chr20:23471711-23471761	PrEC	prostate:	n/a
23	chr20:23550632-23550682	PANC-1	pancreas:	n/a
24	chr20:23545938-23545988	PANC-1	pancreas:	n/a
25	chr20:23549467-23549517	AG10803	skin:	n/a
26	chr20:23549522-23549572	BJ	skin:	n/a
27	chr20:23548991-23549041	MCF10A-Er-Src	breast:	n/a
28	chr20:23545938-23545988	HMEC	breast:	n/a
29	chr20:23549525-23549575	SKMC	muscle:	n/a
30	chr20:23471627-23471677	MCF10A-Er-Src	breast:	n/a
31	chr20:23549522-23549572	HEEpiC	esophagus:	n/a
32	chr20:23433349-23433399	T-47D	breast:	n/a
33	chr20:23420379-23420429	GM06990	blood:	n/a
34	chr20:23471627-23471677	NHBE	bronchial:	n/a
35	chr20:23549455-23549505	NT2-D1	testis:	n/a
36	chr20:23419162-23419212	GM12878	blood:	n/a
37	chr20:23419120-23419170	HEK293	kidney:	embryo
38	chr20:23499644-23499694	Hela-S3	cervix:	n/a
39	chr20:23550632-23550682	HNPCEpiC	eye:	n/a
40	chr20:23498941-23498991	HepG2	liver:	n/a
41	chr20:23470461-23470511	U87	brain:	n/a
42	chr20:23549467-23549517	Hela-S3	cervix:	n/a
43	chr20:23550668-23550718	IMR90	lung:	fetal
44	chr20:23550632-23550682	BJ	skin:	n/a
45	chr20:23471627-23471677	HPAEpiC	pulmonary alveolar:	n/a
46	chr20:23433608-23433658	HRCEpiC	kidney:	n/a
47	chr20:23550632-23550682	SK-N-MC	brain:	n/a
48	chr20:23471693-23471743	SKMC	muscle:	n/a
49	chr20:23549467-23549517	GM06990	blood:	n/a
50	chr20:23548991-23549041	K562	blood:	n/a

(count:45 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:23415427..23417677-chr20:23422614..23424382,2	K562	blood:
2	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:
3	chr20:23430353..23432292-chr20:23432999..23435596,2	MCF-7	breast:
4	chr20:23330412..23330928-chr20:23426987..23427635,2	MCF-7	breast:
5	chr20:23426981..23427599-chr20:23487754..23488340,2	MCF-7	breast:
6	chr20:23495614..23498073-chr20:23499354..23501428,2	MCF-7	breast:
7	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
8	chr20:23415648..23417559-chr20:23421207..23423158,2	MCF-7	breast:
9	chr20:23342185..23344395-chr20:23415797..23420151,3	K562	blood:
10	chr20:23429806..23432217-chr20:23436004..23438997,2	K562	blood:
11	chr20:23547114..23549526-chr20:23565217..23567174,2	MCF-7	breast:
12	chr20:23494582..23497425-chr20:23497787..23500282,2	MCF-7	breast:
13	chr20:23422166..23423021-chr20:23565222..23566039,3	MCF-7	breast:
14	chr20:23459835..23462068-chr20:23463876..23466517,2	MCF-7	breast:
15	chr20:23422154..23423090-chr20:23586925..23587808,6	MCF-7	breast:
16	chr20:23422636..23423138-chr9:129901794..129902375,2	MCF-7	breast:
17	chr20:23400976..23401856-chr20:23422235..23423058,2	MCF-7	breast:
18	chr20:23426981..23427599-chr20:23487754..23488340,2	MCF-7	breast:
19	chr20:23427640..23430149-chr20:23434541..23436355,2	MCF-7	breast:
20	chr20:23459835..23462068-chr20:23463876..23466517,2	MCF-7	breast:
21	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
22	chr20:23428863..23430535-chr20:23433558..23435826,2	K562	blood:
23	chr20:23422547..23423488-chr20:23586916..23587742,4	K562	blood:
24	chr20:23461901..23463918-chr20:23618342..23620994,2	MCF-7	breast:
25	chr20:23434496..23436579-chr20:23437423..23440853,3	K562	blood:
26	chr20:23426997..23427916-chr20:23586801..23588394,7	MCF-7	breast:
27	chr20:23427640..23430149-chr20:23434541..23436355,2	MCF-7	breast:
28	chr20:23422153..23424654-chr20:23586384..23588911,4	MCF-7	breast:
29	chr20:23329921..23332820-chr20:23421116..23423226,2	MCF-7	breast:
30	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
31	chr20:23428863..23430535-chr20:23433558..23435826,2	K562	blood:
32	chr20:23421799..23423146-chr20:23586414..23588198,22	MCF-7	breast:
33	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:
34	chr20:23336129..23338538-chr20:23416708..23418719,2	K562	blood:
35	chr20:23340941..23343437-chr20:23505184..23507656,2	MCF-7	breast:
36	chr20:23454015..23456705-chr20:23459387..23462774,3	MCF-7	breast:
37	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
38	chr20:23330602..23332708-chr20:23549852..23552530,2	MCF-7	breast:
39	chr20:23415427..23417677-chr20:23422614..23424382,2	K562	blood:
40	chr20:23422166..23423021-chr20:23565222..23566039,3	MCF-7	breast:
41	chr20:23402010..23403710-chr20:23413584..23415342,2	K562	blood:
42	chr20:23415648..23417559-chr20:23421207..23423158,2	MCF-7	breast:
43	chr20:23482103..23484253-chr20:23488282..23490217,2	MCF-7	breast:
44	chr20:23342324..23344912-chr20:23496142..23497648,2	MCF-7	breast:
45	chr20:23482103..23484253-chr20:23488282..23490217,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CST9LP1-2	chr20:23499254-23499667	XLOC_013694
2	lnc-CST9LP1-2	chr20:23498841-23499170	XLOC_013694
3	lnc-CST8-1	chr20:23484643-23484689	XLOC_013490
4	lnc-CST8-1	chr20:23487411-23487749	NONHSAT079066
5	lnc-CST9LP1-2	chr20:23498840-23499170	NONHSAT079070
6	lnc-CST8-2	chr20:23517371-23517422	NONHSAT079074
7	lnc-CST8-1	chr20:23487412-23487749	XLOC_013490
8	lnc-CST9LP1-2	chr20:23499254-23499661	XLOC_013694
9	lnc-CST8-2	chr20:23514835-23514945	NONHSAT079074
10	lnc-CST8-1	chr20:23484350-23484430	XLOC_013490
11	lnc-CST8-1	chr20:23484642-23484689	NONHSAT079066
12	lnc-CST8-1	chr20:23487412-23487749	XLOC_013490
13	lnc-CST9LP1-2	chr20:23495374-23495498	XLOC_013694
14	lnc-CST9LP1-1	chr20:23497521-23498706	ENSG00000260202.1
15	lnc-CST8-1	chr20:23484305-23484689	NONHSAT079064
16	lnc-CST8-2	chr20:23499763-23500121	NONHSAT079074
17	lnc-CST8-1	chr20:23487412-23487716	NONHSAT079064
18	lnc-CST9LP1-2	chr20:23499253-23499667	NONHSAT079070

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	CST9L	hsa-miR-132-3p	chr20:23545479-23545501

Variant related genes	Relation type
ENSG00000200208	TF binding region
ENSG00000260202	TF binding region
CST9LP1	TF binding region
CST8	TF binding region
CST13P	TF binding region
CSTL1	TF binding region
ENSG00000204658	TF binding region
CST11	TF binding region
CST9L	TF binding region
CST12P	TF binding region
ENSG00000200208	CpG island
ENSG00000260202	CpG island
CST9LP1	CpG island
CST8	CpG island
CST13P	CpG island
CSTL1	CpG island
ENSG00000204658	CpG island
CST11	CpG island
CST9L	CpG island
CST12P	CpG island
ENSG00000226344	chromatin interactions
ENSG00000101439	chromatin interactions
ENSG00000101435	chromatin interactions
ENSG00000232645	chromatin interactions
ENSG00000125831	chromatin interactions
ENSG00000200208	chromatin interactions
ENSG00000125812	chromatin interactions
ENSG00000173335	chromatin interactions
ENSG00000260202	chromatin interactions
ENSG00000234832	chromatin interactions
ENSG00000132661	chromatin interactions
ENSG00000125814	chromatin interactions
ENSG00000204663	chromatin interactions
LPGAT1	miRNA target sites

Extended variants
information (count: 6519 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:6519 , 50 per page) page: 1 2 3 4 5 6 7 ... 131

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs556113228	chr20:23415045-23415046	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs76660502	chr20:23415096-23415097	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs530258710	chr20:23415132-23415133	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs181996943	chr20:23415144-23415145	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs558637802	chr20:23415212-23415213	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs79002964	chr20:23415217-23415218	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs376553453	chr20:23415245-23415246	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs572092404	chr20:23415250-23415251	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs577307112	chr20:23415257-23415258	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs564754410	chr20:23415278-23415279	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs6076074	chr20:23415332-23415333	Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374301941	chr20:23415363-23415364	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs113363534	chr20:23415371-23415372	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs543990078	chr20:23415408-23415409	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs553629786	chr20:23415421-23415422	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs563768031	chr20:23415439-23415440	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs148467009	chr20:23415445-23415446	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs115375940	chr20:23415491-23415492	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs118111533	chr20:23415539-23415540	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs8183442	chr20:23415563-23415564	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs79924031	chr20:23415581-23415582	Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs372372677	chr20:23415630-23415631	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs373674405	chr20:23415633-23415634	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs556314997	chr20:23415679-23415680	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs569751856	chr20:23415687-23415688	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs2424554	chr20:23415867-23415868	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs555186423	chr20:23415872-23415873	Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs559487134	chr20:23415989-23415990	Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs572204609	chr20:23416044-23416045	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541002389	chr20:23416051-23416052	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs557830570	chr20:23416106-23416107	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs6106652	chr20:23416154-23416155	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs79065375	chr20:23416176-23416177	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs549830519	chr20:23416182-23416183	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529486615	chr20:23416222-23416223	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs376422367	chr20:23416274-23416275	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs559408397	chr20:23416280-23416281	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs543447456	chr20:23416340-23416341	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs73303378	chr20:23416390-23416391	Enhancers Weak transcription Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs551358740	chr20:23416414-23416415	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs142681219	chr20:23416430-23416431	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs533214236	chr20:23416442-23416443	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs549827876	chr20:23416443-23416444	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs569796310	chr20:23416452-23416453	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs184452087	chr20:23416459-23416460	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs549226056	chr20:23416477-23416478	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs565775104	chr20:23416497-23416498	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs150578040	chr20:23416503-23416504	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs189209605	chr20:23416525-23416526	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs577566608	chr20:23416534-23416535	Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:660 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23414400-23415600	Enhancers	HepG2	liver
2	chr20:23415600-23416000	Enhancers	Fetal Brain Female	brain
3	chr20:23415600-23417600	Flanking Active TSS	HepG2	liver
4	chr20:23415800-23416000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
5	chr20:23415800-23416000	Enhancers	Ovary	ovary
6	chr20:23415800-23417400	Enhancers	Pancreas	Pancrea
7	chr20:23415800-23417800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
8	chr20:23415800-23417800	Enhancers	Fetal Muscle Trunk	muscle
9	chr20:23416000-23416400	Weak transcription	Fetal Brain Female	brain
10	chr20:23416000-23416800	Weak transcription	Ovary	ovary
11	chr20:23416200-23416400	Enhancers	Liver	Liver
12	chr20:23416400-23416600	Enhancers	Brain Anterior Caudate	brain
13	chr20:23416400-23416600	Enhancers	Brain Cingulate Gyrus	brain
14	chr20:23416400-23416600	Enhancers	Brain Hippocampus Middle	brain
15	chr20:23416400-23416600	Enhancers	Brain Inferior Temporal Lobe	brain
16	chr20:23416400-23416600	Enhancers	Brain Substantia Nigra	brain
17	chr20:23416400-23417200	Enhancers	Right Ventricle	heart
18	chr20:23416400-23417400	Flanking Active TSS	Liver	Liver
19	chr20:23416400-23417600	Enhancers	Brain Angular Gyrus	brain
20	chr20:23416400-23417600	Enhancers	Fetal Brain Male	brain
21	chr20:23416400-23417600	Enhancers	Fetal Brain Female	brain
22	chr20:23416400-23417800	Enhancers	Fetal Intestine Small	intestine
23	chr20:23416400-23417800	Enhancers	Stomach Mucosa	stomach
24	chr20:23416600-23417000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
25	chr20:23416600-23417200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr20:23416600-23417200	Enhancers	Breast Myoepithelial Primary Cells	Breast
27	chr20:23416600-23417200	Flanking Active TSS	Brain Anterior Caudate	brain
28	chr20:23416600-23417200	Flanking Active TSS	Brain Cingulate Gyrus	brain
29	chr20:23416600-23417200	Enhancers	Placenta	Placenta
30	chr20:23416600-23417200	Enhancers	Fetal Stomach	stomach
31	chr20:23416600-23417200	Enhancers	Rectal Mucosa Donor 31	rectum
32	chr20:23416600-23417400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
33	chr20:23416600-23417400	Flanking Active TSS	Brain Substantia Nigra	brain
34	chr20:23416600-23417400	Enhancers	Fetal Lung	lung
35	chr20:23416600-23417600	Flanking Active TSS	Brain Hippocampus Middle	brain
36	chr20:23416600-23417600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr20:23416600-23417600	Enhancers	Fetal Muscle Leg	muscle
38	chr20:23416600-23417600	Enhancers	Left Ventricle	heart
39	chr20:23416600-23417800	Enhancers	Right Atrium	heart
40	chr20:23416800-23417000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr20:23416800-23417000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
42	chr20:23416800-23417000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr20:23416800-23417200	Enhancers	Gastric	stomach
44	chr20:23416800-23417200	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr20:23416800-23417600	Enhancers	Colonic Mucosa	Colon
46	chr20:23416800-23417600	Enhancers	Skeletal Muscle Male	skeletal muscle
47	chr20:23416800-23417800	Enhancers	Fetal Intestine Large	intestine
48	chr20:23416800-23417800	Enhancers	Ovary	ovary
49	chr20:23417000-23417600	Enhancers	K562	blood
50	chr20:23417000-23422800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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