Variant report

Variant	nsv585723
Chromosome Location	chr20:23426648-23569400
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:931)
CpG islands
(count:2139)
Chromatin interactive
region (count:33)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:931 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:23566494-23567822	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:23488216-23488283	HepG2	liver:	n/a	n/a
3	ARID3A	chr20:23550890-23551138	HepG2	liver:	n/a	n/a
4	ATF2	chr20:23513756-23514081	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr20:23507823-23507979	H1-hESC	embryonic stem cell:	n/a	n/a
6	BATF	chr20:23511849-23512071	GM12878	blood:	n/a	n/a
7	BATF	chr20:23495900-23496255	GM12878	blood:	n/a	n/a
8	BATF	chr20:23495915-23496215	GM12878	blood:	n/a	n/a
9	BATF	chr20:23440154-23440332	GM12878	blood:	n/a	chr20:23440243-23440254
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	BCL11A	chr20:23513761-23514166	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr20:23513851-23514075	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL3	chr20:23516024-23516292	GM12878	blood:	n/a	n/a
15	BCL3	chr20:23456780-23457368	GM12878	blood:	n/a	n/a
16	BCL3	chr20:23456839-23457441	GM12878	blood:	n/a	n/a
17	BCL3	chr20:23506840-23507065	GM12878	blood:	n/a	n/a
18	BHLHE40	chr20:23567164-23567983	HepG2	liver:	n/a	n/a
19	BHLHE40	chr20:23426259-23426863	HepG2	liver:	n/a	n/a
20	BHLHE40	chr20:23427304-23427533	K562	blood:	n/a	n/a
21	BHLHE40	chr20:23427237-23427550	HepG2	liver:	n/a	n/a
22	BHLHE40	chr20:23427279-23427535	GM12878	blood:	n/a	n/a
23	BHLHE40	chr20:23426616-23426748	K562	blood:	n/a	n/a
24	BRCA1	chr20:23523709-23523728	GM12878	blood:	n/a	n/a
25	BRCA1	chr20:23566711-23566753	HepG2	liver:	n/a	n/a
26	BRCA1	chr20:23454055-23454315	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr20:23510630-23510647	GM12878	blood:	n/a	n/a
28	CEBPB	chr20:23498469-23498679	A549	lung:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
29	CEBPB	chr20:23474040-23474347	HepG2	liver:	n/a	chr20:23474176-23474187
30	CEBPB	chr20:23498447-23498603	K562	blood:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
31	CEBPB	chr20:23523470-23523817	HepG2	liver:	n/a	chr20:23523648-23523659 chr20:23523647-23523658 chr20:23523649-23523658
32	CEBPB	chr20:23427329-23427625	A549	lung:	n/a	n/a
33	CEBPB	chr20:23431788-23431941	HepG2	liver:	n/a	chr20:23431854-23431867 chr20:23431854-23431865 chr20:23431856-23431867
34	CEBPB	chr20:23474055-23474238	HepG2	liver:	n/a	chr20:23474176-23474187
35	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
36	CEBPB	chr20:23473969-23474249	HepG2	liver:	n/a	chr20:23474176-23474187
37	CEBPB	chr20:23498350-23498677	HepG2	liver:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
38	CEBPB	chr20:23473560-23473660	HepG2	liver:	n/a	chr20:23473570-23473581 chr20:23473570-23473583 chr20:23473570-23473583
39	CEBPB	chr20:23427229-23427681	MCF-7	breast:	n/a	n/a
40	CEBPB	chr20:23474028-23474386	MCF-7	breast:	n/a	chr20:23474176-23474187
41	CEBPB	chr20:23427308-23427620	H1-hESC	embryonic stem cell:	n/a	n/a
42	CEBPB	chr20:23427310-23427618	HepG2	liver:	n/a	n/a
43	CEBPB	chr20:23566692-23566933	HepG2	liver:	n/a	n/a
44	CEBPB	chr20:23474028-23474368	K562	blood:	n/a	chr20:23474176-23474187
45	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
46	CEBPB	chr20:23498438-23498523	H1-hESC	embryonic stem cell:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
47	CEBPB	chr20:23538255-23538343	HepG2	liver:	n/a	n/a
48	CEBPB	chr20:23506064-23506151	HepG2	liver:	n/a	n/a
49	CEBPB	chr20:23488124-23488404	HepG2	liver:	n/a	chr20:23488287-23488298
50	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

(count:2139 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23549495-23549545	HCF	heart:	n/a
2	chr20:23545938-23545988	ovcar-3	ovarian:	n/a
3	chr20:23545938-23545988	AG04449	skin:	fetal
4	chr20:23498937-23498987	IMR90	lung:	fetal
5	chr20:23549495-23549545	HCF	heart:	n/a
6	chr20:23545938-23545988	ovcar-3	ovarian:	n/a
7	chr20:23545938-23545988	AG04449	skin:	fetal
8	chr20:23498937-23498987	IMR90	lung:	fetal
9	chr20:23433608-23433658	HEK293	kidney:	embryo
10	chr20:23549455-23549505	T-47D	breast:	n/a
11	chr20:23500381-23500431	HMEC	breast:	n/a
12	chr20:23431120-23431170	T-47D	breast:	n/a
13	chr20:23433349-23433399	U87	brain:	n/a
14	chr20:23549522-23549572	AG10803	skin:	n/a
15	chr20:23470274-23470324	SK-N-SH	brain:	n/a
16	chr20:23549455-23549505	HRPEpiC	eye:	n/a
17	chr20:23499697-23499747	SKMC	muscle:	n/a
18	chr20:23549467-23549517	SK-N-MC	brain:	n/a
19	chr20:23550668-23550718	HL-60	blood:	n/a
20	chr20:23471969-23472019	GM12878	blood:	n/a
21	chr20:23471969-23472019	SK-N-SH_RA	brain:	n/a
22	chr20:23545938-23545988	HIPEpiC	eye:	n/a
23	chr20:23550632-23550682	Hela-S3	cervix:	n/a
24	chr20:23550668-23550718	AoSMC	blood vessel:	n/a
25	chr20:23549455-23549505	PrEC	prostate:	n/a
26	chr20:23470274-23470324	ECC-1	luminal epithelium:	n/a
27	chr20:23433503-23433553	CMK	blood:	n/a
28	chr20:23434086-23434136	MCF-7	breast:	n/a
29	chr20:23470461-23470511	HAEpiC	amniotic membrane:	n/a
30	chr20:23550632-23550682	BE2_C	brain:	n/a
31	chr20:23550446-23550496	A549	lung:	n/a
32	chr20:23498993-23499043	H1-hESC	embryonic stem cell:	embryo
33	chr20:23471737-23471787	GM19239	blood:	n/a
34	chr20:23549495-23549545	HEK293	kidney:	embryo
35	chr20:23471737-23471787	H1-hESC	embryonic stem cell:	embryo
36	chr20:23433349-23433399	HIPEpiC	eye:	n/a
37	chr20:23545539-23545589	BJ	skin:	n/a
38	chr20:23549455-23549505	SK-N-SH_RA	brain:	n/a
39	chr20:23549106-23549156	PANC-1	pancreas:	n/a
40	chr20:23545539-23545589	SK-N-SH	brain:	n/a
41	chr20:23433349-23433399	MCF10A-Er-Src	breast:	n/a
42	chr20:23432977-23433027	HCF	heart:	n/a
43	chr20:23549525-23549575	AG09309	skin:	n/a
44	chr20:23472484-23472534	AoSMC	blood vessel:	n/a
45	chr20:23500381-23500431	HCT-116	colon:	n/a
46	chr20:23433349-23433399	T-47D	breast:	n/a
47	chr20:23470274-23470324	GM06990	blood:	n/a
48	chr20:23472484-23472534	GM12878	blood:	n/a
49	chr20:23434244-23434294	NH-A	brain:	n/a
50	chr20:23550668-23550718	ovcar-3	ovarian:	n/a

(count:33 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:23329684..23331925-chr20:23566520..23568100,2	MCF-7	breast:
2	chr20:23434496..23436579-chr20:23437423..23440853,3	K562	blood:
3	chr20:23340941..23343437-chr20:23505184..23507656,2	MCF-7	breast:
4	chr20:23482103..23484253-chr20:23488282..23490217,2	MCF-7	breast:
5	chr20:23426997..23427916-chr20:23586801..23588394,7	MCF-7	breast:
6	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
7	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
8	chr20:23461901..23463918-chr20:23618342..23620994,2	MCF-7	breast:
9	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
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	chr20:23330412..23330928-chr20:23426987..23427635,2	MCF-7	breast:
14	chr20:23495614..23498073-chr20:23499354..23501428,2	MCF-7	breast:
15	chr20:23568486..23570139-chr9:92478980..92480480,2	MCF-7	breast:
16	chr20:23482103..23484253-chr20:23488282..23490217,2	MCF-7	breast:
17	chr20:23459835..23462068-chr20:23463876..23466517,2	MCF-7	breast:
18	chr20:23342324..23344912-chr20:23496142..23497648,2	MCF-7	breast:
19	chr20:23426981..23427599-chr20:23487754..23488340,2	MCF-7	breast:
20	chr20:23426981..23427599-chr20:23487754..23488340,2	MCF-7	breast:
21	chr20:23428863..23430535-chr20:23433558..23435826,2	K562	blood:
22	chr20:23422166..23423021-chr20:23565222..23566039,3	MCF-7	breast:
23	chr20:23427640..23430149-chr20:23434541..23436355,2	MCF-7	breast:
24	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
25	chr20:23459835..23462068-chr20:23463876..23466517,2	MCF-7	breast:
26	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:
27	chr20:23454015..23456705-chr20:23459387..23462774,3	MCF-7	breast:
28	chr20:23562870..23565685-chr20:23566645..23569407,3	K562	blood:
29	chr20:23430353..23432292-chr20:23432999..23435596,2	MCF-7	breast:
30	chr20:23330602..23332708-chr20:23549852..23552530,2	MCF-7	breast:
31	chr20:23428863..23430535-chr20:23433558..23435826,2	K562	blood:
32	chr20:23427640..23430149-chr20:23434541..23436355,2	MCF-7	breast:
33	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:

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

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

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
ENSG00000204658	TF binding region
ENSG00000260202	TF binding region
CST9LP1	TF binding region
CST11	TF binding region
CST8	TF binding region
CST9L	TF binding region
CST13P	TF binding region
CST12P	TF binding region
ENSG00000200208	CpG island
ENSG00000204658	CpG island
ENSG00000260202	CpG island
CST9LP1	CpG island
CST11	CpG island
CST8	CpG island
CST9L	CpG island
CST13P	CpG island
CST12P	CpG island
ENSG00000101439	chromatin interactions
ENSG00000125812	chromatin interactions
ENSG00000260202	chromatin interactions
ENSG00000200208	chromatin interactions
ENSG00000204663	chromatin interactions
ENSG00000234832	chromatin interactions
ENSG00000132661	chromatin interactions
ENSG00000226344	chromatin interactions
ENSG00000204658	chromatin interactions
ENSG00000101435	chromatin interactions
ENSG00000125831	chromatin interactions
LPGAT1	miRNA target sites

Extended variants
information (count: 6239 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:6239 , 50 per page) page: 1 2 3 4 5 6 7 ... 125

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs761724	chr20:23426648-23426649	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs539550076	chr20:23426668-23426669	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs556149595	chr20:23426696-23426697	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544318570	chr20:23426703-23426704	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs549442172	chr20:23426736-23426737	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs114061104	chr20:23426758-23426759	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs536125109	chr20:23426760-23426761	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs556071658	chr20:23426787-23426788	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs572741782	chr20:23426799-23426800	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs541254249	chr20:23426804-23426805	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs558337932	chr20:23426839-23426840	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs562895576	chr20:23426849-23426850	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs192876150	chr20:23426856-23426857	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs533292300	chr20:23426874-23426875	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552330748	chr20:23426890-23426891	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs373084775	chr20:23426891-23426892	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs367928723	chr20:23426903-23426904	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs543529874	chr20:23426924-23426925	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs2016859	chr20:23426936-23426937	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs551835901	chr20:23426949-23426950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs2405127	chr20:23426972-23426973	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
22	rs529233916	chr20:23426984-23426985	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs377639109	chr20:23427007-23427008	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs561832189	chr20:23427038-23427039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2004288	chr20:23427049-23427050	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs184123756	chr20:23427060-23427061	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs149868825	chr20:23427087-23427088	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs188131948	chr20:23427146-23427147	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs549920812	chr20:23427151-23427152	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs569804635	chr20:23427179-23427180	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs535438017	chr20:23427185-23427186	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs1076777	chr20:23427231-23427232	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs35205310	chr20:23427276-23427277	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs566200605	chr20:23427304-23427305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs6114088	chr20:23427330-23427331	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs558040453	chr20:23427331-23427332	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180675670	chr20:23427339-23427340	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs370022700	chr20:23427346-23427347	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs79594720	chr20:23427375-23427376	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs149053713	chr20:23427384-23427385	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs1076776	chr20:23427399-23427400	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
42	rs542604608	chr20:23427480-23427481	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs559706592	chr20:23427501-23427502	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs527548582	chr20:23427506-23427507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs73901874	chr20:23427544-23427545	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs564095730	chr20:23427559-23427560	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372018864	chr20:23427578-23427579	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs386813355	chr20:23427582-23427583	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs202073656	chr20:23427583-23427584	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs199851112	chr20:23427585-23427586	Enhancers Weak transcription	n/a	n/a	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
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:610 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:23417200-23434800	Weak transcription	Gastric	stomach
2	chr20:23417800-23441000	Weak transcription	Right Atrium	heart
3	chr20:23421200-23427200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
4	chr20:23423000-23432200	Weak transcription	HUES6 Cell Line	embryonic stem cell
5	chr20:23423800-23426800	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr20:23423800-23432200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr20:23425600-23426800	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
8	chr20:23425600-23427000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
9	chr20:23426000-23426800	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
10	chr20:23426000-23426800	Enhancers	NHDF-Ad	bronchial
11	chr20:23426000-23426800	Enhancers	NHLF	lung
12	chr20:23426000-23426800	Enhancers	Osteobl	bone
13	chr20:23426000-23427000	Enhancers	NHEK	skin
14	chr20:23426000-23427200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr20:23426000-23427400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
16	chr20:23426000-23427600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
17	chr20:23426000-23427600	Enhancers	HMEC	breast
18	chr20:23426000-23427600	Enhancers	NH-A	brain
19	chr20:23426200-23426800	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr20:23426200-23427000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr20:23426200-23427600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
22	chr20:23426200-23427800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr20:23426400-23427000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr20:23426400-23427400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
25	chr20:23426400-23427400	Enhancers	HepG2	liver
26	chr20:23426400-23427400	Enhancers	HSMM	muscle
27	chr20:23426400-23427600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr20:23426400-23427600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr20:23426400-23427600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr20:23426400-23429600	Weak transcription	Fetal Thymus	thymus
31	chr20:23426800-23427200	Enhancers	Placenta Amnion	Placenta Amnion
32	chr20:23427200-23427400	Enhancers	Brain Anterior Caudate	brain
33	chr20:23427200-23427400	Enhancers	Brain Inferior Temporal Lobe	brain
34	chr20:23427200-23427800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
35	chr20:23427200-23427800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr20:23427600-23429800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
37	chr20:23427800-23428800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
38	chr20:23427800-23431600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
39	chr20:23429600-23431200	Enhancers	Fetal Thymus	thymus
40	chr20:23429800-23430000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr20:23429800-23430400	Enhancers	GM12878-XiMat	blood
42	chr20:23429800-23430600	Enhancers	Primary T cells fromperipheralblood	blood
43	chr20:23429800-23430600	Enhancers	Primary hematopoietic stem cells short term culture	blood
44	chr20:23429800-23430600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr20:23429800-23430600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
46	chr20:23430000-23430200	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
47	chr20:23430000-23430400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
48	chr20:23430000-23430400	Enhancers	Monocytes-CD14+_RO01746	blood
49	chr20:23430000-23430600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr20:23430000-23430600	Enhancers	Dnd41	blood

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