Variant report

Variant	nsv533857
Chromosome Location	chr8:112819659-113801258
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	chr8:113350397-113350810	HepG2	liver:	n/a	chr8:113350726-113350742
2	ARID3A	chr8:113477312-113477622	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:113038752-113039444	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:112976470-112976714	HepG2	liver:	n/a	n/a
5	ATF1	chr8:113500282-113500373	K562	blood:	n/a	n/a
6	ATF1	chr8:113711892-113712099	K562	blood:	n/a	n/a
7	ATF1	chr8:113041124-113041245	K562	blood:	n/a	n/a
8	ATF2	chr8:113407709-113408069	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr8:112929242-112929439	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr8:113114422-113114764	H1-hESC	embryonic stem cell:	n/a	n/a
11	BCL11A	chr8:113407778-113408009	H1-hESC	embryonic stem cell:	n/a	n/a
12	BCL11A	chr8:112929118-112929489	H1-hESC	embryonic stem cell:	n/a	n/a
13	BCL11A	chr8:113407703-113408043	H1-hESC	embryonic stem cell:	n/a	n/a
14	BCL11A	chr8:112929219-112929426	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr8:113623801-113624046	GM12878	blood:	n/a	n/a
16	BCL3	chr8:113472001-113472616	A549	lung:	n/a	n/a
17	BCL3	chr8:113472029-113472628	A549	lung:	n/a	n/a
18	BHLHE40	chr8:112980773-112980798	GM12878	blood:	n/a	n/a
19	CEBPB	chr8:112979555-112979799	H1-hESC	embryonic stem cell:	n/a	chr8:112979671-112979682
20	CEBPB	chr8:113200327-113200529	K562	blood:	n/a	chr8:113200412-113200423 chr8:113200411-113200424
21	CEBPB	chr8:113675839-113676180	Hela-S3	cervix:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
22	CEBPB	chr8:112949249-112949366	A549	lung:	n/a	chr8:112949283-112949294
23	CEBPB	chr8:113482822-113483178	Hela-S3	cervix:	n/a	chr8:113483052-113483065
24	CEBPB	chr8:112889690-112890032	IMR90	lung:	n/a	chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889855-112889868 chr8:112889855-112889866 chr8:112889855-112889868 chr8:112889857-112889866 chr8:112889857-112889868
25	CEBPB	chr8:112964083-112964229	HepG2	liver:	n/a	n/a
26	CEBPB	chr8:113219563-113219901	IMR90	lung:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
27	CEBPB	chr8:113219571-113219907	A549	lung:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
28	CEBPB	chr8:113022252-113022492	A549	lung:	n/a	chr8:113022392-113022403
29	CEBPB	chr8:112979559-112979838	A549	lung:	n/a	chr8:112979671-112979682
30	CEBPB	chr8:113447659-113448026	HepG2	liver:	n/a	chr8:113447842-113447853
31	CEBPB	chr8:113358923-113359044	A549	lung:	n/a	n/a
32	CEBPB	chr8:113675862-113676155	H1-hESC	embryonic stem cell:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
33	CEBPB	chr8:113219601-113219895	K562	blood:	n/a	chr8:113219724-113219733 chr8:113219723-113219734 chr8:113219722-113219733 chr8:113219722-113219735 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219724-113219733 chr8:113219722-113219735 chr8:113219689-113219697
34	CEBPB	chr8:113347479-113347753	HepG2	liver:	n/a	chr8:113347586-113347597
35	CEBPB	chr8:113322419-113322604	H1-hESC	embryonic stem cell:	n/a	n/a
36	CEBPB	chr8:113584173-113584544	HepG2	liver:	n/a	chr8:113584378-113584389 chr8:113584378-113584391 chr8:113584325-113584336 chr8:113584380-113584391
37	CEBPB	chr8:113038704-113039417	MCF-7	breast:	n/a	chr8:113039120-113039133
38	CEBPB	chr8:113163673-113163818	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr8:112979515-112979804	K562	blood:	n/a	chr8:112979671-112979682
40	CEBPB	chr8:113675831-113676188	HepG2	liver:	n/a	chr8:113675994-113676003 chr8:113675994-113676003 chr8:113675993-113676004 chr8:113675994-113676003 chr8:113675992-113676003 chr8:113675992-113676005 chr8:113675992-113676005 chr8:113675994-113676003
41	CEBPB	chr8:113124393-113124693	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr8:113022271-113022547	HepG2	liver:	n/a	chr8:113022392-113022403
43	CEBPB	chr8:113482783-113483181	HepG2	liver:	n/a	chr8:113483052-113483065
44	CEBPB	chr8:112963973-112964321	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr8:113016885-113017171	A549	lung:	n/a	n/a
46	CEBPB	chr8:113161150-113161370	H1-hESC	embryonic stem cell:	n/a	n/a
47	CEBPB	chr8:113242212-113242350	A549	lung:	n/a	n/a
48	CEBPB	chr8:113124367-113124716	IMR90	lung:	n/a	n/a
49	CEBPB	chr8:113158356-113158618	HepG2	liver:	n/a	chr8:113158502-113158513
50	CEBPB	chr8:112889693-112890005	HepG2	liver:	n/a	chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889857-112889866 chr8:112889855-112889868 chr8:112889855-112889866 chr8:112889855-112889868 chr8:112889857-112889866 chr8:112889857-112889868

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:113702707-113702757	IMR90	lung:	fetal
2	chr8:113702707-113702757	IMR90	lung:	fetal
3	chr8:112835665-112835715	HNPCEpiC	eye:	n/a
4	chr8:113145005-113145055	U87	brain:	n/a
5	chr8:113655561-113655611	CMK	blood:	n/a
6	chr8:113145005-113145055	HMEC	breast:	n/a
7	chr8:112835665-112835715	MCF-7	breast:	n/a
8	chr8:113049519-113049569	ProgFib	skin:	n/a
9	chr8:113656015-113656065	HepG2	liver:	n/a
10	chr8:113703176-113703226	HRPEpiC	eye:	n/a
11	chr8:113655436-113655486	HCPEpiC	choroid plexus:	n/a
12	chr8:113351420-113351470	HEEpiC	esophagus:	n/a
13	chr8:113655561-113655611	NT2-D1	testis:	n/a
14	chr8:113656015-113656065	GM12892	blood:	n/a
15	chr8:112906823-112906873	AG10803	skin:	n/a
16	chr8:113655436-113655486	SK-N-SH_RA	brain:	n/a
17	chr8:112906823-112906873	HRE	kidney:	n/a
18	chr8:113655436-113655486	NT2-D1	testis:	n/a
19	chr8:113702707-113702757	SK-N-SH_RA	brain:	n/a
20	chr8:113281175-113281225	SK-N-MC	brain:	n/a
21	chr8:113655561-113655611	NB4	blood:	n/a
22	chr8:113656015-113656065	Caco-2	colon:	n/a
23	chr8:113145005-113145055	PANC-1	pancreas:	n/a
24	chr8:113351420-113351470	RPTEC	kidney:	n/a
25	chr8:113703176-113703226	PANC-1	pancreas:	n/a
26	chr8:112835665-112835715	ECC-1	luminal epithelium:	n/a
27	chr8:113655436-113655486	HRE	kidney:	n/a
28	chr8:113703176-113703226	HCT-116	colon:	n/a
29	chr8:113145005-113145055	ProgFib	skin:	n/a
30	chr8:112835665-112835715	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:113049519-113049569	BJ	skin:	n/a
32	chr8:112906823-112906873	T-47D	breast:	n/a
33	chr8:113655436-113655486	RPTEC	kidney:	n/a
34	chr8:113145005-113145055	MCF-7	breast:	n/a
35	chr8:113656015-113656065	HCF	heart:	n/a
36	chr8:113703176-113703226	U87	brain:	n/a
37	chr8:113655561-113655611	LNCaP	prostate:	n/a
38	chr8:113351420-113351470	HPAEpiC	pulmonary alveolar:	n/a
39	chr8:113113972-113114022	A549	lung:	n/a
40	chr8:113049519-113049569	HepG2	liver:	n/a
41	chr8:113655436-113655486	AG04449	skin:	fetal
42	chr8:113281175-113281225	HEEpiC	esophagus:	n/a
43	chr8:113049519-113049569	Hepatocyte	liver:	n/a
44	chr8:113655561-113655611	HUVEC	blood vessel:	n/a
45	chr8:113703176-113703226	BJ	skin:	n/a
46	chr8:113702707-113702757	GM12892	blood:	n/a
47	chr8:113655561-113655611	HCT-116	colon:	n/a
48	chr8:113702707-113702757	HCM	heart:	n/a
49	chr8:113655436-113655486	NB4	blood:	n/a
50	chr8:113656015-113656065	AoSMC	blood vessel:	n/a

No.	Distal block	Cell Line	Cell type
1	chr8:112946524..112947507-chr8:113386902..113387446,2	MCF-7	breast:
2	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
3	chr8:113057607..113060468-chr8:113062471..113064373,2	MCF-7	breast:
4	chr8:113461648..113464072-chr8:113471155..113472872,2	MCF-7	breast:
5	chr8:113495952..113497684-chr8:113532113..113534940,2	MCF-7	breast:
6	chr8:112877538..112880401-chr8:112881600..112883445,2	K562	blood:
7	chr8:113730328..113732083-chr8:113748434..113750301,2	K562	blood:
8	chr8:113659187..113660730-chr8:113666931..113668583,2	MCF-7	breast:
9	chr8:113121132..113122642-chr8:113123330..113125697,2	MCF-7	breast:
10	chr8:113408283..113409229-chr8:113477372..113477931,2	MCF-7	breast:
11	chr8:112878252..112879995-chr8:113601916..113604196,2	MCF-7	breast:
12	chr8:112980405..112982694-chr8:112982938..112985443,2	MCF-7	breast:
13	chr8:113282212..113283944-chr8:113285167..113287640,2	MCF-7	breast:
14	chr8:113773909..113774597-chr8:114183855..114184506,4	MCF-7	breast:
15	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:
16	chr8:112976625..112977471-chr8:114449676..114450374,2	MCF-7	breast:
17	chr8:113774024..113774627-chr8:114390471..114391174,2	MCF-7	breast:
18	chr8:112919794..112922834-chr8:112924781..112927217,3	K562	blood:
19	chr8:113334749..113337746-chr8:113352582..113354421,2	MCF-7	breast:
20	chr8:112946373..112947269-chr8:113476964..113477520,2	MCF-7	breast:
21	chr8:113057607..113060468-chr8:113062471..113064373,2	MCF-7	breast:
22	chr8:112976314..112977253-chr8:113408305..113409151,3	MCF-7	breast:
23	chr8:113411416..113413911-chr8:113414434..113416216,2	MCF-7	breast:
24	chr8:113234003..113236007-chr8:113240691..113242262,2	MCF-7	breast:
25	chr8:112946524..112947507-chr8:113386902..113387446,2	MCF-7	breast:
26	chr8:112841029..112843004-chr8:112843259..112845025,2	MCF-7	breast:
27	chr8:113334749..113337746-chr8:113352582..113354421,2	MCF-7	breast:
28	chr8:112946373..112947269-chr8:113476964..113477520,2	MCF-7	breast:
29	chr8:102371552..102373757-chr8:113387253..113389057,2	MCF-7	breast:
30	chr8:113036903..113039112-chr8:113145309..113148146,2	K562	blood:
31	chr8:112877538..112880401-chr8:112881600..112883445,2	K562	blood:
32	chr8:112976579..112977386-chr8:113471922..113472710,2	MCF-7	breast:
33	chr8:112947101..112947938-chr8:113477362..113477935,2	MCF-7	breast:
34	chr8:113719443..113721302-chr8:113723054..113725365,2	K562	blood:
35	chr8:113774348..113777140-chr8:114064225..114066718,2	K562	blood:
36	chr8:113730328..113732083-chr8:113748434..113750301,2	K562	blood:
37	chr8:112946353..112947027-chr8:112976279..112976810,2	MCF-7	breast:
38	chr8:113623376..113625406-chr8:113626015..113627569,2	MCF-7	breast:
39	chr20:18661388..18664062-chr8:113586254..113588798,2	MCF-7	breast:
40	chr8:113036903..113039112-chr8:113145309..113148146,2	K562	blood:
41	chr8:112946353..112947027-chr8:112976279..112976810,2	MCF-7	breast:
42	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:
43	chr8:113656932..113658484-chr8:113659367..113661819,2	K562	blood:
44	chr8:112952038..112954490-chr8:112955048..112956799,2	K562	blood:
45	chr8:112976314..112977253-chr8:113408305..113409151,3	MCF-7	breast:
46	chr17:56736027..56736822-chr8:112887594..112888361,2	MCF-7	breast:
47	chr8:113648317..113650428-chr8:113651221..113653011,2	MCF-7	breast:
48	chr8:112878252..112879995-chr8:113601916..113604196,2	MCF-7	breast:
49	chr6:26214142..26215773-chr8:112896843..112899051,2	MCF-7	breast:
50	chr8:113536029..113539003-chr8:113540588..113542968,2	MCF-7	breast:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RP11-67H2.1.1-7	chr8:112837712-112837805	l_3669_chr8:112823382-112827015_testes
2	lnc-RP11-67H2.1.1-7	chr8:112837915-112838389	l_3669_chr8:112823382-112827015_testes
3	lnc-RP11-67H2.1.1-6	chr8:113551118-113551546	NONHSAT128340
4	lnc-RP11-67H2.1.1-7	chr8:112823383-112823488	l_3669_chr8:112823382-112827015_testes
5	lnc-RP11-67H2.1.1-7	chr8:112826847-112827015	l_3669_chr8:112823382-112827015_testes

miRNA name	Chromosome Location	mirBase accession
hsa-miR-2053	chr8:113655782-113655804	MIMAT0009978

Variant related genes	Relation type
RPL30P16	TF binding region
RNU4-37P	TF binding region
ENSG00000264794	TF binding region
CSMD3	TF binding region
ENSG00000238656	TF binding region
MIR2053	TF binding region
RPL30P16	CpG island
RNU4-37P	CpG island
ENSG00000264794	CpG island
CSMD3	CpG island
ENSG00000238656	CpG island
MIR2053	CpG island
ENSG00000202077	chromatin interactions
ENSG00000167986	chromatin interactions
ENSG00000149476	chromatin interactions

Extended variants
information (count: 21573 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:21573 , 50 per page) page: 1 2 3 4 5 6 7 ... 432

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs376033419	chr8:112819732-112819733	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs543057516	chr8:112819740-112819741	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs78574952	chr8:112819752-112819753	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs13272408	chr8:112819835-112819836	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs549286606	chr8:112819875-112819876	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs565521266	chr8:112819895-112819896	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185476070	chr8:112819896-112819897	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs76272396	chr8:112819906-112819907	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs547482709	chr8:112819928-112819929	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs140811877	chr8:112819929-112819930	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs73340382	chr8:112819937-112819938	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs556307046	chr8:112819967-112819968	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1397364	chr8:112819969-112819970	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs113014052	chr8:112819991-112819992	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs572645283	chr8:112820000-112820001	Weak transcription Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
16	rs556068988	chr8:112820052-112820053	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
17	rs189596088	chr8:112820066-112820067	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
18	rs541644616	chr8:112820072-112820073	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
19	rs535219737	chr8:112820093-112820094	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
20	rs370764474	chr8:112820137-112820138	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
21	rs557842890	chr8:112820161-112820162	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
22	rs180923466	chr8:112820162-112820163	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
23	rs73704874	chr8:112820186-112820187	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
24	rs541648164	chr8:112820197-112820198	Enhancers ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
25	rs1397363	chr8:112820204-112820205	ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs528916095	chr8:112820259-112820260	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
27	rs184344023	chr8:112820305-112820306	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
28	rs530206816	chr8:112820307-112820308	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
29	rs148499175	chr8:112820326-112820327	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
30	rs188569321	chr8:112820336-112820337	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
31	rs528231417	chr8:112820348-112820349	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
32	rs551178613	chr8:112820386-112820387	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
33	rs570584717	chr8:112820390-112820391	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
34	rs370433037	chr8:112820453-112820454	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
35	rs550286181	chr8:112820519-112820520	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
36	rs569943215	chr8:112820588-112820589	ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
37	rs4633090	chr8:112823394-112823395	Inactive region	lncRNA	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs540556494	chr8:112823404-112823405	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
39	rs181359064	chr8:112823457-112823458	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
40	rs570202791	chr8:112823465-112823466	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
41	rs532639224	chr8:112823476-112823477	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
42	rs534695864	chr8:112826206-112826207	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
43	rs557884626	chr8:112826210-112826211	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
44	rs190135204	chr8:112826211-112826212	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
45	rs148656519	chr8:112826213-112826214	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
46	rs563403459	chr8:112826232-112826233	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
47	rs530814924	chr8:112826265-112826266	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
48	rs115271954	chr8:112826285-112826286	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
49	rs550825347	chr8:112826344-112826345	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
50	rs559107428	chr8:112826346-112826347	Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Prostate cancer	22341455	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic cancer	17952125	CNVD
T-cell lymphomas	22341440	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:880 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112818200-112820000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:112818600-112820000	Weak transcription	HUES6 Cell Line	embryonic stem cell
3	chr8:112819800-112820200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr8:112820000-112820200	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
5	chr8:112820000-112820600	ZNF genes & repeats	HUES6 Cell Line	embryonic stem cell
6	chr8:112826200-112826800	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr8:112826400-112826600	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
8	chr8:112826400-112826800	Bivalent Enhancer	iPS DF 19.11 Cell Line	embryonic stem cell
9	chr8:112826600-112826800	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
10	chr8:112827400-112827600	Bivalent Enhancer	iPS DF 6.9 Cell Line	embryonic stem cell
11	chr8:112832800-112834000	Enhancers	Breast Myoepithelial Primary Cells	Breast
12	chr8:112833200-112833600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
13	chr8:112844200-112844800	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr8:112846000-112846400	Enhancers	iPS-18 Cell Line	embryonic stem cell
15	chr8:112851600-112851800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:112851600-112851800	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr8:112851600-112851800	ZNF genes & repeats	Pancreas	Pancrea
18	chr8:112851800-112857800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
19	chr8:112857800-112858000	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
20	chr8:112860400-112861000	Enhancers	Adipose Nuclei	Adipose
21	chr8:112870400-112870600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr8:112872600-112873000	Enhancers	Adipose Nuclei	Adipose
23	chr8:112872800-112873200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
24	chr8:112872800-112873200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr8:112872800-112873400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
26	chr8:112873000-112873600	Enhancers	Colon Smooth Muscle	Colon
27	chr8:112879400-112879600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
28	chr8:112900000-112900200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr8:112900200-112900800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:112900800-112901800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
31	chr8:112901000-112901600	Enhancers	iPS-18 Cell Line	embryonic stem cell
32	chr8:112901600-112906600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
33	chr8:112901800-112907200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
34	chr8:112905800-112907800	Enhancers	HUES48 Cell Line	embryonic stem cell
35	chr8:112906200-112907000	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr8:112906600-112907600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:112906600-112907600	Enhancers	HUES64 Cell Line	embryonic stem cell
38	chr8:112906600-112907600	Enhancers	iPS-18 Cell Line	embryonic stem cell
39	chr8:112907200-112909200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
40	chr8:112909800-112911200	ZNF genes & repeats	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
41	chr8:112910000-112912600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr8:112922000-112925200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
43	chr8:112928400-112928800	Bivalent Enhancer	HUES48 Cell Line	embryonic stem cell
44	chr8:112928400-112929400	Bivalent Enhancer	HUES64 Cell Line	embryonic stem cell
45	chr8:112928600-112929400	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
46	chr8:112928800-112929000	Flanking Bivalent TSS/Enh	HUES48 Cell Line	embryonic stem cell
47	chr8:112928800-112929200	Flanking Bivalent TSS/Enh	HUES6 Cell Line	embryonic stem cell
48	chr8:112928800-112929600	Bivalent Enhancer	H1 Cell Line	embryonic stem cell
49	chr8:112928800-112929600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
50	chr8:112928800-112929800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell

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