Variant report

Variant	nsv912820
Chromosome Location	chr20:23406519-23578148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1308)
CpG islands
(count:2628)
Chromatin interactive
region (count:54)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1308 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:23416561-23416867	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:23426293-23426601	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:23566494-23567822	HepG2	liver:	n/a	n/a
4	ARID3A	chr20:23422511-23422806	HepG2	liver:	n/a	n/a
5	ARID3A	chr20:23488216-23488283	HepG2	liver:	n/a	n/a
6	ARID3A	chr20:23550890-23551138	HepG2	liver:	n/a	n/a
7	ATF1	chr20:23417323-23417566	K562	blood:	n/a	n/a
8	ATF2	chr20:23513756-23514081	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr20:23507823-23507979	H1-hESC	embryonic stem cell:	n/a	n/a
10	BATF	chr20:23422462-23422769	GM12878	blood:	n/a	n/a
11	BATF	chr20:23478200-23478493	GM12878	blood:	n/a	n/a
12	BATF	chr20:23495915-23496215	GM12878	blood:	n/a	n/a
13	BATF	chr20:23495900-23496255	GM12878	blood:	n/a	n/a
14	BATF	chr20:23440154-23440332	GM12878	blood:	n/a	chr20:23440243-23440254
15	BATF	chr20:23509691-23510055	GM12878	blood:	n/a	chr20:23509889-23509900 chr20:23509906-23509917
16	BATF	chr20:23511849-23512071	GM12878	blood:	n/a	n/a
17	BCL11A	chr20:23513851-23514075	H1-hESC	embryonic stem cell:	n/a	n/a
18	BCL11A	chr20:23513761-23514166	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL3	chr20:23456780-23457368	GM12878	blood:	n/a	n/a
20	BCL3	chr20:23506840-23507065	GM12878	blood:	n/a	n/a
21	BCL3	chr20:23425339-23425976	GM12878	blood:	n/a	n/a
22	BCL3	chr20:23516024-23516292	GM12878	blood:	n/a	n/a
23	BCL3	chr20:23456839-23457441	GM12878	blood:	n/a	n/a
24	BCL3	chr20:23425378-23425971	GM12878	blood:	n/a	n/a
25	BHLHE40	chr20:23567164-23567983	HepG2	liver:	n/a	n/a
26	BHLHE40	chr20:23426259-23426863	HepG2	liver:	n/a	n/a
27	BHLHE40	chr20:23427237-23427550	HepG2	liver:	n/a	n/a
28	BHLHE40	chr20:23427279-23427535	GM12878	blood:	n/a	n/a
29	BHLHE40	chr20:23422567-23422798	K562	blood:	n/a	n/a
30	BHLHE40	chr20:23422476-23422794	GM12878	blood:	n/a	n/a
31	BHLHE40	chr20:23427304-23427533	K562	blood:	n/a	n/a
32	BHLHE40	chr20:23426616-23426748	K562	blood:	n/a	n/a
33	BRCA1	chr20:23566711-23566753	HepG2	liver:	n/a	n/a
34	BRCA1	chr20:23422574-23422690	HepG2	liver:	n/a	n/a
35	BRCA1	chr20:23523709-23523728	GM12878	blood:	n/a	n/a
36	BRCA1	chr20:23510630-23510647	GM12878	blood:	n/a	n/a
37	BRCA1	chr20:23454055-23454315	H1-hESC	embryonic stem cell:	n/a	n/a
38	CEBPB	chr20:23499478-23499579	HepG2	liver:	n/a	chr20:23499522-23499533
39	CEBPB	chr20:23489894-23490054	HepG2	liver:	n/a	n/a
40	CEBPB	chr20:23419411-23419489	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:23427329-23427625	A549	lung:	n/a	n/a
42	CEBPB	chr20:23473969-23474249	HepG2	liver:	n/a	chr20:23474176-23474187
43	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
44	CEBPB	chr20:23538255-23538343	HepG2	liver:	n/a	n/a
45	CEBPB	chr20:23425753-23426005	HepG2	liver:	n/a	chr20:23425924-23425935
46	CEBPB	chr20:23425743-23426489	IMR90	lung:	n/a	chr20:23425924-23425935
47	CEBPB	chr20:23506064-23506151	HepG2	liver:	n/a	n/a
48	CEBPB	chr20:23498350-23498677	HepG2	liver:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
49	CEBPB	chr20:23435864-23436154	IMR90	lung:	n/a	chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436004-23436015 chr20:23436006-23436015 chr20:23436005-23436016
50	CEBPB	chr20:23427308-23427620	H1-hESC	embryonic stem cell:	n/a	n/a

(count:2628 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23433349-23433399	PFSK-1	brain:	n/a
2	chr20:23433608-23433658	K562	blood:	n/a
3	chr20:23549522-23549572	ProgFib	skin:	n/a
4	chr20:23470274-23470324	ovcar-3	ovarian:	n/a
5	chr20:23549495-23549545	HCPEpiC	choroid plexus:	n/a
6	chr20:23433349-23433399	PFSK-1	brain:	n/a
7	chr20:23433608-23433658	K562	blood:	n/a
8	chr20:23549522-23549572	ProgFib	skin:	n/a
9	chr20:23470274-23470324	ovcar-3	ovarian:	n/a
10	chr20:23549495-23549545	HCPEpiC	choroid plexus:	n/a
11	chr20:23499697-23499747	AG10803	skin:	n/a
12	chr20:23498937-23498987	PFSK-1	brain:	n/a
13	chr20:23419120-23419170	AG04449	skin:	fetal
14	chr20:23472484-23472534	Jurkat	blood:	n/a
15	chr20:23498993-23499043	Jurkat	blood:	n/a
16	chr20:23420200-23420250	HRPEpiC	eye:	n/a
17	chr20:23470274-23470324	GM19239	blood:	n/a
18	chr20:23498937-23498987	HRE	kidney:	n/a
19	chr20:23470461-23470511	ProgFib	skin:	n/a
20	chr20:23472484-23472534	AG04450	lung:	fetal
21	chr20:23433608-23433658	HCT-116	colon:	n/a
22	chr20:23433608-23433658	HepG2	liver:	n/a
23	chr20:23498937-23498987	NHDF-neo	bronchial:	n/a
24	chr20:23420121-23420171	NT2-D1	testis:	n/a
25	chr20:23472171-23472221	NHDF-neo	bronchial:	n/a
26	chr20:23549455-23549505	PrEC	prostate:	n/a
27	chr20:23471693-23471743	K562	blood:	n/a
28	chr20:23470274-23470324	CMK	blood:	n/a
29	chr20:23420200-23420250	PANC-1	pancreas:	n/a
30	chr20:23419162-23419212	BJ	skin:	n/a
31	chr20:23549467-23549517	SK-N-SH	brain:	n/a
32	chr20:23549467-23549517	HMEC	breast:	n/a
33	chr20:23434086-23434136	Hepatocyte	liver:	n/a
34	chr20:23471711-23471761	SAEC	small airway:	n/a
35	chr20:23500381-23500431	GM12878	blood:	n/a
36	chr20:23549522-23549572	SKMC	muscle:	n/a
37	chr20:23549467-23549517	HRE	kidney:	n/a
38	chr20:23498937-23498987	BE2_C	brain:	n/a
39	chr20:23420355-23420405	HL-60	blood:	n/a
40	chr20:23470274-23470324	GM06990	blood:	n/a
41	chr20:23433608-23433658	HAEpiC	amniotic membrane:	n/a
42	chr20:23499697-23499747	SK-N-SH_RA	brain:	n/a
43	chr20:23550446-23550496	A549	lung:	n/a
44	chr20:23471627-23471677	PFSK-1	brain:	n/a
45	chr20:23420109-23420159	BE2_C	brain:	n/a
46	chr20:23420200-23420250	SK-N-SH	brain:	n/a
47	chr20:23550668-23550718	HAEpiC	amniotic membrane:	n/a
48	chr20:23434086-23434136	MCF10A-Er-Src	breast:	n/a
49	chr20:23549455-23549505	HCT-116	colon:	n/a
50	chr20:23549455-23549505	SK-N-SH_RA	brain:	n/a

(count:54 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
2	chr20:23495614..23498073-chr20:23499354..23501428,2	MCF-7	breast:
3	chr10:38581321..38584038-chr20:23412027..23414957,2	K562	blood:
4	chr20:23575532..23578369-chr20:23585910..23588143,2	MCF-7	breast:
5	chr20:23415427..23417677-chr20:23422614..23424382,2	K562	blood:
6	chr20:23342324..23344912-chr20:23496142..23497648,2	MCF-7	breast:
7	chr20:23336129..23338538-chr20:23416708..23418719,2	K562	blood:
8	chr20:23428863..23430535-chr20:23433558..23435826,2	K562	blood:
9	chr20:23454015..23456705-chr20:23459387..23462774,3	MCF-7	breast:
10	chr20:23400976..23401856-chr20:23422235..23423058,2	MCF-7	breast:
11	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
12	chr20:23342185..23344395-chr20:23415797..23420151,3	K562	blood:
13	chr20:23398847..23400771-chr20:23575954..23577563,2	K562	blood:
14	chr20:23422166..23423021-chr20:23565222..23566039,3	MCF-7	breast:
15	chr20:23494582..23497425-chr20:23497787..23500282,2	MCF-7	breast:
16	chr20:23547114..23549526-chr20:23565217..23567174,2	MCF-7	breast:
17	chr20:23562870..23565685-chr20:23566645..23569407,3	K562	blood:
18	chr20:23426981..23427599-chr20:23487754..23488340,2	MCF-7	breast:
19	chr20:23461901..23463918-chr20:23618342..23620994,2	MCF-7	breast:
20	chr20:23422636..23423138-chr9:129901794..129902375,2	MCF-7	breast:
21	chr20:23428863..23430535-chr20:23433558..23435826,2	K562	blood:
22	chr20:23426997..23427916-chr20:23586801..23588394,7	MCF-7	breast:
23	chr20:23430353..23432292-chr20:23432999..23435596,2	MCF-7	breast:
24	chr20:23422154..23423090-chr20:23586925..23587808,6	MCF-7	breast:
25	chr20:23400281..23403754-chr20:23404807..23406566,3	MCF-7	breast:
26	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
27	chr20:23427640..23430149-chr20:23434541..23436355,2	MCF-7	breast:
28	chr20:23422547..23423488-chr20:23586916..23587742,4	K562	blood:
29	chr20:23400058..23403758-chr20:23404517..23407833,5	K562	blood:
30	chr20:23329921..23332820-chr20:23421116..23423226,2	MCF-7	breast:
31	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:
32	chr20:23329684..23331925-chr20:23566520..23568100,2	MCF-7	breast:
33	chr20:23422153..23424654-chr20:23586384..23588911,4	MCF-7	breast:
34	chr20:23482103..23484253-chr20:23488282..23490217,2	MCF-7	breast:
35	chr20:23568486..23570139-chr9:92478980..92480480,2	MCF-7	breast:
36	chr20:23340941..23343437-chr20:23505184..23507656,2	MCF-7	breast:
37	chr20:23422166..23423021-chr20:23565222..23566039,3	MCF-7	breast:
38	chr20:23330412..23330928-chr20:23426987..23427635,2	MCF-7	breast:
39	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
40	chr20:23330602..23332708-chr20:23549852..23552530,2	MCF-7	breast:
41	chr20:23402010..23403710-chr20:23413584..23415342,2	K562	blood:
42	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:
43	chr20:23459835..23462068-chr20:23463876..23466517,2	MCF-7	breast:
44	chr20:23415648..23417559-chr20:23421207..23423158,2	MCF-7	breast:
45	chr20:23426981..23427599-chr20:23487754..23488340,2	MCF-7	breast:
46	chr20:23434496..23436579-chr20:23437423..23440853,3	K562	blood:
47	chr20:23429806..23432217-chr20:23436004..23438997,2	K562	blood:
48	chr20:23402152..23403758-chr20:23404630..23407146,2	K562	blood:
49	chr20:23421799..23423146-chr20:23586414..23588198,22	MCF-7	breast:
50	chr20:23427640..23430149-chr20:23434541..23436355,2	MCF-7	breast:

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

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

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
NAPB	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
NAPB	CpG island
ENSG00000204658	CpG island
CST11	CpG island
CST9L	CpG island
CST12P	CpG island
ENSG00000101439	chromatin interactions
ENSG00000132661	chromatin interactions
ENSG00000101435	chromatin interactions
ENSG00000125812	chromatin interactions
ENSG00000260202	chromatin interactions
ENSG00000125814	chromatin interactions
ENSG00000204663	chromatin interactions
ENSG00000226344	chromatin interactions
ENSG00000232645	chromatin interactions
ENSG00000234832	chromatin interactions
ENSG00000173335	chromatin interactions
ENSG00000200208	chromatin interactions
ENSG00000204658	chromatin interactions
ENSG00000125831	chromatin interactions
LPGAT1	miRNA target sites

Extended variants
information (count: 7013 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:7013 , 50 per page) page: 1 2 3 4 5 6 7 ... 141

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6076072	chr20:23406519-23406520	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs544664381	chr20:23406542-23406543	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs531247433	chr20:23406595-23406596	Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs112831441	chr20:23406678-23406679	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561238874	chr20:23406715-23406716	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs531333748	chr20:23406744-23406745	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs574909483	chr20:23406753-23406754	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs540245441	chr20:23406756-23406757	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs560583877	chr20:23406761-23406762	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs528388545	chr20:23406766-23406767	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs6132612	chr20:23406771-23406772	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
12	rs565027004	chr20:23406781-23406782	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs571226894	chr20:23406790-23406791	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs530749158	chr20:23406792-23406793	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs550617069	chr20:23406805-23406806	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs13040409	chr20:23406811-23406812	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs567234223	chr20:23406817-23406818	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs144626521	chr20:23406847-23406848	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs370450489	chr20:23406848-23406849	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs538793087	chr20:23406900-23406901	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs145917568	chr20:23406951-23406952	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374864175	chr20:23406976-23406977	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs566139021	chr20:23406977-23406978	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs369261378	chr20:23406978-23406979	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs553646491	chr20:23407012-23407013	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs558842462	chr20:23407029-23407030	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs201116878	chr20:23407038-23407039	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs138485495	chr20:23407047-23407048	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs374851085	chr20:23407051-23407052	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs569073499	chr20:23407073-23407074	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs538036536	chr20:23407120-23407121	Inactive region	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs202238452	chr20:23407236-23407237	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs533319170	chr20:23407257-23407258	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs555170719	chr20:23407515-23407516	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369265178	chr20:23407522-23407523	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs574836974	chr20:23407574-23407575	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs192494917	chr20:23407740-23407741	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs199822656	chr20:23407789-23407790	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148149671	chr20:23413631-23413632	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs537720798	chr20:23413661-23413662	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs554861301	chr20:23413708-23413709	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs141086717	chr20:23413727-23413728	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs540015080	chr20:23413733-23413734	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187449798	chr20:23413734-23413735	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs57368405	chr20:23413804-23413805	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs545504817	chr20:23413805-23413806	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs150283290	chr20:23413810-23413811	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs542519775	chr20:23413814-23413815	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs531361676	chr20:23413905-23413906	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs560901113	chr20:23413934-23413935	Inactive region	Chromatin interactive region	1 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	22522925	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:724 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23406000-23406600	Enhancers	NHEK	skin
2	chr20:23414400-23415600	Enhancers	HepG2	liver
3	chr20:23415600-23416000	Enhancers	Fetal Brain Female	brain
4	chr20:23415600-23417600	Flanking Active TSS	HepG2	liver
5	chr20:23415800-23416000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
6	chr20:23415800-23416000	Enhancers	Ovary	ovary
7	chr20:23415800-23417400	Enhancers	Pancreas	Pancrea
8	chr20:23415800-23417800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
9	chr20:23415800-23417800	Enhancers	Fetal Muscle Trunk	muscle
10	chr20:23416000-23416400	Weak transcription	Fetal Brain Female	brain
11	chr20:23416000-23416800	Weak transcription	Ovary	ovary
12	chr20:23416200-23416400	Enhancers	Liver	Liver
13	chr20:23416400-23416600	Enhancers	Brain Anterior Caudate	brain
14	chr20:23416400-23416600	Enhancers	Brain Cingulate Gyrus	brain
15	chr20:23416400-23416600	Enhancers	Brain Hippocampus Middle	brain
16	chr20:23416400-23416600	Enhancers	Brain Inferior Temporal Lobe	brain
17	chr20:23416400-23416600	Enhancers	Brain Substantia Nigra	brain
18	chr20:23416400-23417200	Enhancers	Right Ventricle	heart
19	chr20:23416400-23417400	Flanking Active TSS	Liver	Liver
20	chr20:23416400-23417600	Enhancers	Brain Angular Gyrus	brain
21	chr20:23416400-23417600	Enhancers	Fetal Brain Male	brain
22	chr20:23416400-23417600	Enhancers	Fetal Brain Female	brain
23	chr20:23416400-23417800	Enhancers	Fetal Intestine Small	intestine
24	chr20:23416400-23417800	Enhancers	Stomach Mucosa	stomach
25	chr20:23416600-23417000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
26	chr20:23416600-23417200	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr20:23416600-23417200	Enhancers	Breast Myoepithelial Primary Cells	Breast
28	chr20:23416600-23417200	Flanking Active TSS	Brain Anterior Caudate	brain
29	chr20:23416600-23417200	Flanking Active TSS	Brain Cingulate Gyrus	brain
30	chr20:23416600-23417200	Enhancers	Placenta	Placenta
31	chr20:23416600-23417200	Enhancers	Fetal Stomach	stomach
32	chr20:23416600-23417200	Enhancers	Rectal Mucosa Donor 31	rectum
33	chr20:23416600-23417400	Flanking Active TSS	Brain Inferior Temporal Lobe	brain
34	chr20:23416600-23417400	Flanking Active TSS	Brain Substantia Nigra	brain
35	chr20:23416600-23417400	Enhancers	Fetal Lung	lung
36	chr20:23416600-23417600	Flanking Active TSS	Brain Hippocampus Middle	brain
37	chr20:23416600-23417600	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
38	chr20:23416600-23417600	Enhancers	Fetal Muscle Leg	muscle
39	chr20:23416600-23417600	Enhancers	Left Ventricle	heart
40	chr20:23416600-23417800	Enhancers	Right Atrium	heart
41	chr20:23416800-23417000	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr20:23416800-23417000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr20:23416800-23417000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr20:23416800-23417200	Enhancers	Gastric	stomach
45	chr20:23416800-23417200	Enhancers	Skeletal Muscle Female	skeletal muscle
46	chr20:23416800-23417600	Enhancers	Colonic Mucosa	Colon
47	chr20:23416800-23417600	Enhancers	Skeletal Muscle Male	skeletal muscle
48	chr20:23416800-23417800	Enhancers	Fetal Intestine Large	intestine
49	chr20:23416800-23417800	Enhancers	Ovary	ovary
50	chr20:23417000-23417600	Enhancers	K562	blood

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