Variant report

Variant	nsv1057992
Chromosome Location	chr20:23430887-23565333
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	chr20:23550890-23551138	HepG2	liver:	n/a	n/a
2	ARID3A	chr20:23488216-23488283	HepG2	liver:	n/a	n/a
3	ATF2	chr20:23513756-23514081	H1-hESC	embryonic stem cell:	n/a	n/a
4	BACH1	chr20:23507823-23507979	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr20:23440154-23440332	GM12878	blood:	n/a	chr20:23440243-23440254
6	BATF	chr20:23495915-23496215	GM12878	blood:	n/a	n/a
7	BATF	chr20:23511849-23512071	GM12878	blood:	n/a	n/a
8	BATF	chr20:23509691-23510055	GM12878	blood:	n/a	chr20:23509889-23509900 chr20:23509906-23509917
9	BATF	chr20:23478200-23478493	GM12878	blood:	n/a	n/a
10	BATF	chr20:23495900-23496255	GM12878	blood:	n/a	n/a
11	BCL11A	chr20:23513761-23514166	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr20:23513851-23514075	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL3	chr20:23456780-23457368	GM12878	blood:	n/a	n/a
14	BCL3	chr20:23516024-23516292	GM12878	blood:	n/a	n/a
15	BCL3	chr20:23456839-23457441	GM12878	blood:	n/a	n/a
16	BCL3	chr20:23506840-23507065	GM12878	blood:	n/a	n/a
17	BRCA1	chr20:23523709-23523728	GM12878	blood:	n/a	n/a
18	BRCA1	chr20:23454055-23454315	H1-hESC	embryonic stem cell:	n/a	n/a
19	BRCA1	chr20:23510630-23510647	GM12878	blood:	n/a	n/a
20	CEBPB	chr20:23523470-23523817	HepG2	liver:	n/a	chr20:23523648-23523659 chr20:23523647-23523658 chr20:23523649-23523658
21	CEBPB	chr20:23499478-23499579	HepG2	liver:	n/a	chr20:23499522-23499533
22	CEBPB	chr20:23498350-23498677	HepG2	liver:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
23	CEBPB	chr20:23523481-23523798	IMR90	lung:	n/a	chr20:23523648-23523659 chr20:23523647-23523658 chr20:23523649-23523658
24	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
25	CEBPB	chr20:23498438-23498523	H1-hESC	embryonic stem cell:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
26	CEBPB	chr20:23473969-23474249	HepG2	liver:	n/a	chr20:23474176-23474187
27	CEBPB	chr20:23498469-23498679	A549	lung:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
28	CEBPB	chr20:23550852-23551205	MCF-7	breast:	n/a	chr20:23551082-23551095 chr20:23551055-23551066 chr20:23551055-23551066
29	CEBPB	chr20:23523481-23523817	A549	lung:	n/a	chr20:23523648-23523659 chr20:23523647-23523658 chr20:23523649-23523658
30	CEBPB	chr20:23515699-23515853	HepG2	liver:	n/a	n/a
31	CEBPB	chr20:23474055-23474238	HepG2	liver:	n/a	chr20:23474176-23474187
32	CEBPB	chr20:23550852-23551260	HepG2	liver:	n/a	chr20:23551082-23551095 chr20:23551055-23551066 chr20:23551055-23551066
33	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
34	CEBPB	chr20:23488124-23488404	HepG2	liver:	n/a	chr20:23488287-23488298
35	CEBPB	chr20:23471614-23471730	HepG2	liver:	n/a	n/a
36	CEBPB	chr20:23474028-23474368	K562	blood:	n/a	chr20:23474176-23474187
37	CEBPB	chr20:23431788-23431941	HepG2	liver:	n/a	chr20:23431854-23431867 chr20:23431854-23431865 chr20:23431856-23431867
38	CEBPB	chr20:23498447-23498603	K562	blood:	n/a	chr20:23498501-23498510 chr20:23498499-23498512 chr20:23498500-23498511
39	CEBPB	chr20:23495956-23496320	MCF-7	breast:	n/a	n/a
40	CEBPB	chr20:23489894-23490054	HepG2	liver:	n/a	n/a
41	CEBPB	chr20:23473560-23473660	HepG2	liver:	n/a	chr20:23473570-23473581 chr20:23473570-23473583 chr20:23473570-23473583
42	CEBPB	chr20:23435843-23436158	HepG2	liver:	n/a	chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436006-23436015 chr20:23436004-23436015 chr20:23436006-23436015 chr20:23436005-23436016
43	CEBPB	chr20:23474040-23474347	HepG2	liver:	n/a	chr20:23474176-23474187
44	CEBPB	chr20:23538255-23538343	HepG2	liver:	n/a	n/a
45	CEBPB	chr20:23506064-23506151	HepG2	liver:	n/a	n/a
46	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
47	CEBPB	chr20:23474028-23474386	MCF-7	breast:	n/a	chr20:23474176-23474187
48	CHD2	chr20:23513861-23514356	H1-hESC	embryonic stem cell:	n/a	n/a
49	CTCF	chr20:23546926-23547151	K562	blood:	n/a	chr20:23547024-23547042 chr20:23547027-23547040 chr20:23547026-23547047
50	CTCF	chr20:23488021-23488385	K562	blood:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:23472171-23472221	HNPCEpiC	eye:	n/a
2	chr20:23432977-23433027	AG04450	lung:	fetal
3	chr20:23433349-23433399	MCF-7	breast:	n/a
4	chr20:23472171-23472221	HNPCEpiC	eye:	n/a
5	chr20:23432977-23433027	AG04450	lung:	fetal
6	chr20:23433349-23433399	MCF-7	breast:	n/a
7	chr20:23549522-23549572	HCPEpiC	choroid plexus:	n/a
8	chr20:23434086-23434136	PrEC	prostate:	n/a
9	chr20:23434279-23434329	AG09309	skin:	n/a
10	chr20:23433608-23433658	HCPEpiC	choroid plexus:	n/a
11	chr20:23434244-23434294	BE2_C	brain:	n/a
12	chr20:23545539-23545589	GM12891	blood:	n/a
13	chr20:23545938-23545988	HUVEC	blood vessel:	n/a
14	chr20:23434244-23434294	SK-N-SH	brain:	n/a
15	chr20:23500381-23500431	Jurkat	blood:	n/a
16	chr20:23434086-23434136	HRPEpiC	eye:	n/a
17	chr20:23433503-23433553	SK-N-SH_RA	brain:	n/a
18	chr20:23550632-23550682	HMEC	breast:	n/a
19	chr20:23498941-23498991	AG04450	lung:	fetal
20	chr20:23548991-23549041	AG04449	skin:	fetal
21	chr20:23548991-23549041	Hepatocyte	liver:	n/a
22	chr20:23434279-23434329	ProgFib	skin:	n/a
23	chr20:23472484-23472534	BE2_C	brain:	n/a
24	chr20:23549455-23549505	ovcar-3	ovarian:	n/a
25	chr20:23549495-23549545	ECC-1	luminal epithelium:	n/a
26	chr20:23545938-23545988	BE2_C	brain:	n/a
27	chr20:23549522-23549572	A549	lung:	n/a
28	chr20:23433503-23433553	GM12891	blood:	n/a
29	chr20:23550668-23550718	Jurkat	blood:	n/a
30	chr20:23499644-23499694	GM06990	blood:	n/a
31	chr20:23472171-23472221	HMEC	breast:	n/a
32	chr20:23549525-23549575	GM12892	blood:	n/a
33	chr20:23548991-23549041	BJ	skin:	n/a
34	chr20:23549525-23549575	SK-N-SH_RA	brain:	n/a
35	chr20:23545539-23545589	AG04449	skin:	fetal
36	chr20:23499644-23499694	SK-N-SH	brain:	n/a
37	chr20:23498937-23498987	GM06990	blood:	n/a
38	chr20:23549525-23549575	RPTEC	kidney:	n/a
39	chr20:23549467-23549517	AG04449	skin:	fetal
40	chr20:23472171-23472221	SKMC	muscle:	n/a
41	chr20:23550632-23550682	NH-A	brain:	n/a
42	chr20:23471737-23471787	HRPEpiC	eye:	n/a
43	chr20:23433503-23433553	HCT-116	colon:	n/a
44	chr20:23470461-23470511	NHDF-neo	bronchial:	n/a
45	chr20:23471737-23471787	AG09319	gingival:	n/a
46	chr20:23549455-23549505	MCF10A-Er-Src	breast:	n/a
47	chr20:23434279-23434329	AG04449	skin:	fetal
48	chr20:23472171-23472221	NHDF-neo	bronchial:	n/a
49	chr20:23545539-23545589	GM12878	blood:	n/a
50	chr20:23549455-23549505	SK-N-SH	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:
2	chr20:23482103..23484253-chr20:23488282..23490217,2	MCF-7	breast:
3	chr20:23482103..23484253-chr20:23488282..23490217,2	MCF-7	breast:
4	chr20:23459835..23462068-chr20:23463876..23466517,2	MCF-7	breast:
5	chr20:23434496..23436579-chr20:23437423..23440853,3	K562	blood:
6	chr20:23495614..23498073-chr20:23499354..23501428,2	MCF-7	breast:
7	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
8	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
9	chr20:23340941..23343437-chr20:23505184..23507656,2	MCF-7	breast:
10	chr20:23459835..23462068-chr20:23463876..23466517,2	MCF-7	breast:
11	chr20:23494582..23497425-chr20:23497787..23500282,2	MCF-7	breast:
12	chr20:23430353..23432292-chr20:23432999..23435596,2	MCF-7	breast:
13	chr20:23486686..23489080-chr20:23489324..23491431,2	MCF-7	breast:
14	chr20:23547114..23549526-chr20:23565217..23567174,2	MCF-7	breast:
15	chr20:23429806..23432217-chr20:23436004..23438997,2	K562	blood:
16	chr20:23422166..23423021-chr20:23565222..23566039,3	MCF-7	breast:
17	chr20:23428863..23430535-chr20:23433558..23435826,2	K562	blood:
18	chr20:23461901..23463918-chr20:23618342..23620994,2	MCF-7	breast:
19	chr20:23330602..23332708-chr20:23549852..23552530,2	MCF-7	breast:
20	chr20:23435629..23437264-chr20:23438674..23441153,2	MCF-7	breast:
21	chr20:23454015..23456705-chr20:23459387..23462774,3	MCF-7	breast:
22	chr20:23460080..23462432-chr20:23464977..23467863,2	K562	blood:
23	chr20:23342324..23344912-chr20:23496142..23497648,2	MCF-7	breast:
24	chr20:23426981..23427599-chr20:23487754..23488340,2	MCF-7	breast:
25	chr20:23427640..23430149-chr20:23434541..23436355,2	MCF-7	breast:

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

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

Extended variants
information (count: 5833 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:5833 , 50 per page) page: 1 2 3 4 5 6 7 ... 117

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs550464468	chr20:23430907-23430908	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574332534	chr20:23430934-23430935	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376857138	chr20:23430992-23430993	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs115144070	chr20:23430994-23430995	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs2273237	chr20:23431011-23431012	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
6	rs577660171	chr20:23431025-23431026	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs546372539	chr20:23431043-23431044	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs377350536	chr20:23431109-23431110	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs370445492	chr20:23431116-23431117	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs374560815	chr20:23431119-23431120	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs199961715	chr20:23431121-23431122	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs1055183	chr20:23431131-23431132	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs576508463	chr20:23431132-23431133	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs202073384	chr20:23431158-23431159	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs146499468	chr20:23431187-23431188	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140997818	chr20:23431197-23431198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs548414724	chr20:23431200-23431201	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs562237019	chr20:23431243-23431244	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs527669057	chr20:23431304-23431305	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs547809137	chr20:23431312-23431313	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs548018678	chr20:23431346-23431347	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs60264236	chr20:23431375-23431376	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs566649147	chr20:23431406-23431407	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs530279737	chr20:23431459-23431460	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186887306	chr20:23431527-23431528	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs199951329	chr20:23431632-23431633	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs377333263	chr20:23431635-23431636	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs2424560	chr20:23431665-23431666	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
29	rs551353019	chr20:23431712-23431713	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs533741369	chr20:23431723-23431724	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537680588	chr20:23431811-23431812	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs566608998	chr20:23431877-23431878	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs6083129	chr20:23431900-23431901	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs11471498	chr20:23431934-23431935	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs377480937	chr20:23431935-23431936	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs72536504	chr20:23431936-23431937	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs397810201	chr20:23431937-23431938	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs554355018	chr20:23431954-23431955	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377443799	chr20:23431980-23431981	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs368242142	chr20:23432035-23432036	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs35765813	chr20:23432048-23432049	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs191781074	chr20:23432086-23432087	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533551414	chr20:23432124-23432125	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs372138660	chr20:23432126-23432127	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs555630797	chr20:23432184-23432185	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs553733218	chr20:23432194-23432195	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs370595137	chr20:23432209-23432210	Enhancers Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs577573350	chr20:23432235-23432236	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs546535690	chr20:23432243-23432244	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs112032795	chr20:23432254-23432255	Enhancers Weak transcription	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	21364760	CNVD
Bipolar disorder	19114987	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:531 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

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	chr20:23423000-23432200	Weak transcription	HUES6 Cell Line	embryonic stem cell
4	chr20:23423800-23432200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr20:23427800-23431600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
6	chr20:23429600-23431200	Enhancers	Fetal Thymus	thymus
7	chr20:23430400-23436200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
8	chr20:23430600-23435200	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
9	chr20:23430800-23432000	Weak transcription	Primary T cells from cord blood	blood
10	chr20:23431200-23434000	Weak transcription	Fetal Thymus	thymus
11	chr20:23431800-23432000	Enhancers	Pancreas	Pancrea
12	chr20:23431800-23432400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr20:23432000-23434600	Weak transcription	Pancreas	Pancrea
14	chr20:23432200-23432600	Enhancers	HUES6 Cell Line	embryonic stem cell
15	chr20:23432200-23432600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
16	chr20:23432400-23433400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
17	chr20:23432600-23432800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr20:23432600-23433400	Weak transcription	HUES6 Cell Line	embryonic stem cell
19	chr20:23432600-23433400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr20:23432600-23446000	Weak transcription	H9 Cell Line	embryonic stem cell
21	chr20:23432800-23433000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr20:23433200-23433800	Enhancers	Fetal Stomach	stomach
23	chr20:23433400-23433600	Bivalent Enhancer	Stomach Smooth Muscle	stomach
24	chr20:23433400-23433800	Enhancers	ES-I3 Cell Line	embryonic stem cell
25	chr20:23433400-23434000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
26	chr20:23433400-23434200	Enhancers	HUES6 Cell Line	embryonic stem cell
27	chr20:23433400-23434200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
28	chr20:23433600-23434000	Enhancers	H1 Cell Line	embryonic stem cell
29	chr20:23433800-23437000	Weak transcription	Fetal Stomach	stomach
30	chr20:23434000-23434200	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
31	chr20:23434000-23434200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
32	chr20:23434000-23434200	Bivalent Enhancer	Primary T cells fromperipheralblood	blood
33	chr20:23434000-23440400	Enhancers	Fetal Thymus	thymus
34	chr20:23434200-23434600	Bivalent Enhancer	ES-WA7 Cell Line	embryonic stem cell
35	chr20:23434200-23434600	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
36	chr20:23434200-23434600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr20:23434200-23434800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr20:23434200-23435200	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr20:23434400-23434800	Enhancers	Esophagus	oesophagus
40	chr20:23434600-23434800	Bivalent/Poised TSS	ES-WA7 Cell Line	embryonic stem cell
41	chr20:23434600-23434800	ZNF genes & repeats	Pancreas	Pancrea
42	chr20:23434800-23435000	Enhancers	Gastric	stomach
43	chr20:23434800-23445200	Weak transcription	Esophagus	oesophagus
44	chr20:23435200-23439800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
45	chr20:23435400-23436400	Weak transcription	Primary T cells from cord blood	blood
46	chr20:23435600-23437400	Enhancers	Primary T cells fromperipheralblood	blood
47	chr20:23436000-23436800	Enhancers	Dnd41	blood
48	chr20:23436200-23436800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr20:23436200-23438000	Enhancers	Primary T killer naive cells fromperipheralblood	blood
50	chr20:23436200-23438000	Enhancers	Primary T killer memory cells from peripheral blood	blood

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