Variant report

Variant	esv10193
Chromosome Location	chr1:171128845-171414611
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2999)
CpG islands
(count:2078)
Chromatin interactive
region (count:54)
LncRNA
region (count:22)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2999 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:171164886-171165350	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:171282992-171283290	K562	blood:	n/a	n/a
3	ARID3A	chr1:171130164-171130334	HepG2	liver:	n/a	n/a
4	ARID3A	chr1:171313681-171314019	HepG2	liver:	n/a	n/a
5	ARID3A	chr1:171195980-171196243	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:171282987-171283384	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:171220991-171221208	HepG2	liver:	n/a	n/a
8	ATF1	chr1:171405080-171405221	K562	blood:	n/a	n/a
9	ATF1	chr1:171282998-171283392	K562	blood:	n/a	n/a
10	ATF1	chr1:171392674-171392783	K562	blood:	n/a	n/a
11	ATF1	chr1:171366241-171366405	K562	blood:	n/a	n/a
12	ATF2	chr1:171282746-171283366	GM12878	blood:	n/a	n/a
13	ATF2	chr1:171282858-171283441	H1-hESC	embryonic stem cell:	n/a	n/a
14	ATF2	chr1:171189621-171190119	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr1:171282908-171283421	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr1:171282922-171283472	GM12878	blood:	n/a	n/a
17	ATF2	chr1:171189619-171190092	H1-hESC	embryonic stem cell:	n/a	n/a
18	ATF2	chr1:171221699-171222048	GM12878	blood:	n/a	n/a
19	ATF2	chr1:171255404-171255838	GM12878	blood:	n/a	n/a
20	ATF2	chr1:171189048-171189525	H1-hESC	embryonic stem cell:	n/a	n/a
21	ATF3	chr1:171410278-171410798	HCT-116	colon:	n/a	n/a
22	ATF3	chr1:171410438-171410824	HCT-116	colon:	n/a	n/a
23	BACH1	chr1:171220950-171221075	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr1:171257011-171257031	K562	blood:	n/a	n/a
25	BACH1	chr1:171189110-171190074	H1-hESC	embryonic stem cell:	n/a	n/a
26	BATF	chr1:171255504-171255766	GM12878	blood:	n/a	chr1:171255643-171255653 chr1:171255642-171255653
27	BATF	chr1:171255502-171255771	GM12878	blood:	n/a	chr1:171255643-171255653 chr1:171255642-171255653
28	BCL11A	chr1:171401209-171401460	H1-hESC	embryonic stem cell:	n/a	n/a
29	BCL11A	chr1:171189264-171189499	H1-hESC	embryonic stem cell:	n/a	n/a
30	BCL11A	chr1:171401181-171401466	H1-hESC	embryonic stem cell:	n/a	n/a
31	BHLHE40	chr1:171366177-171366387	K562	blood:	n/a	n/a
32	BHLHE40	chr1:171374405-171374466	K562	blood:	n/a	n/a
33	BHLHE40	chr1:171220868-171221290	GM12878	blood:	n/a	n/a
34	BHLHE40	chr1:171164973-171165296	HepG2	liver:	n/a	n/a
35	BHLHE40	chr1:171221707-171222078	GM12878	blood:	n/a	n/a
36	BHLHE40	chr1:171282485-171283453	GM12878	blood:	n/a	n/a
37	BHLHE40	chr1:171283039-171283350	K562	blood:	n/a	n/a
38	BHLHE40	chr1:171214633-171214797	GM12878	blood:	n/a	n/a
39	BHLHE40	chr1:171220920-171221219	K562	blood:	n/a	n/a
40	BRCA1	chr1:171195922-171196383	H1-hESC	embryonic stem cell:	n/a	n/a
41	BRCA1	chr1:171221013-171221018	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr1:171230700-171230712	H1-hESC	embryonic stem cell:	n/a	n/a
43	CBX3	chr1:171407411-171408095	HCT-116	colon:	n/a	n/a
44	CBX3	chr1:171282914-171283458	K562	blood:	n/a	n/a
45	CBX3	chr1:171407198-171408114	HCT-116	colon:	n/a	n/a
46	CEBPB	chr1:171282897-171283672	MCF-7	breast:	n/a	n/a
47	CEBPB	chr1:171226315-171226515	IMR90	lung:	n/a	chr1:171226386-171226397
48	CEBPB	chr1:171313671-171313951	HepG2	liver:	n/a	chr1:171313802-171313813 chr1:171313821-171313832 chr1:171313800-171313813 chr1:171313800-171313811
49	CEBPB	chr1:171335206-171335721	A549	lung:	n/a	chr1:171335411-171335420 chr1:171335358-171335367 chr1:171335356-171335367 chr1:171335358-171335367 chr1:171335411-171335420 chr1:171335358-171335367 chr1:171335411-171335420 chr1:171335358-171335367 chr1:171335409-171335422
50	CEBPB	chr1:171279855-171279891	A549	lung:	n/a	n/a

(count:2078 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:171156996-171157046	HIPEpiC	eye:	n/a
2	chr1:171217592-171217642	SK-N-SH_RA	brain:	n/a
3	chr1:171226993-171227043	GM19239	blood:	n/a
4	chr1:171226993-171227043	SKMC	muscle:	n/a
5	chr1:171156996-171157046	HIPEpiC	eye:	n/a
6	chr1:171217592-171217642	SK-N-SH_RA	brain:	n/a
7	chr1:171226993-171227043	GM19239	blood:	n/a
8	chr1:171226993-171227043	SKMC	muscle:	n/a
9	chr1:171226702-171226752	HCT-116	colon:	n/a
10	chr1:171153544-171153594	AG09309	skin:	n/a
11	chr1:171217189-171217239	HMEC	breast:	n/a
12	chr1:171179875-171179925	HEEpiC	esophagus:	n/a
13	chr1:171216346-171216396	HepG2	liver:	n/a
14	chr1:171283153-171283203	ProgFib	skin:	n/a
15	chr1:171154802-171154852	HNPCEpiC	eye:	n/a
16	chr1:171286961-171287011	SAEC	small airway:	n/a
17	chr1:171309093-171309143	HNPCEpiC	eye:	n/a
18	chr1:171306733-171306783	HAEpiC	amniotic membrane:	n/a
19	chr1:171283893-171283943	HPAEpiC	pulmonary alveolar:	n/a
20	chr1:171217592-171217642	NT2-D1	testis:	n/a
21	chr1:171285111-171285161	HL-60	blood:	n/a
22	chr1:171189771-171189821	GM12878	blood:	n/a
23	chr1:171156996-171157046	AG09319	gingival:	n/a
24	chr1:171154612-171154662	HRE	kidney:	n/a
25	chr1:171307312-171307362	NT2-D1	testis:	n/a
26	chr1:171216672-171216722	HCF	heart:	n/a
27	chr1:171220644-171220694	ProgFib	skin:	n/a
28	chr1:171268464-171268514	HNPCEpiC	eye:	n/a
29	chr1:171154612-171154662	K562	blood:	n/a
30	chr1:171216346-171216396	SK-N-MC	brain:	n/a
31	chr1:171227787-171227837	U87	brain:	n/a
32	chr1:171227787-171227837	Hepatocyte	liver:	n/a
33	chr1:171154475-171154525	LNCaP	prostate:	n/a
34	chr1:171283893-171283943	ovcar-3	ovarian:	n/a
35	chr1:171156996-171157046	K562	blood:	n/a
36	chr1:171407789-171407839	MCF10A-Er-Src	breast:	n/a
37	chr1:171217555-171217605	ovcar-3	ovarian:	n/a
38	chr1:171216346-171216396	AoSMC	blood vessel:	n/a
39	chr1:171282607-171282657	PrEC	prostate:	n/a
40	chr1:171226702-171226752	HMEC	breast:	n/a
41	chr1:171220575-171220625	T-47D	breast:	n/a
42	chr1:171282607-171282657	GM19239	blood:	n/a
43	chr1:171283893-171283943	GM12878	blood:	n/a
44	chr1:171283893-171283943	HEK293	kidney:	embryo
45	chr1:171179875-171179925	BE2_C	brain:	n/a
46	chr1:171283203-171283253	LNCaP	prostate:	n/a
47	chr1:171154475-171154525	GM12878	blood:	n/a
48	chr1:171282607-171282657	PFSK-1	brain:	n/a
49	chr1:171226702-171226752	HEEpiC	esophagus:	n/a
50	chr1:171156996-171157046	U87	brain:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr1:171177619..171179300-chr1:171182219..171184780,2	K562	blood:
2	chr1:171364064..171365565-chr1:171368281..171370640,2	MCF-7	breast:
3	chr1:171051388..171052230-chr1:171195968..171196512,2	MCF-7	breast:
4	chr1:170936285..170936841-chr1:171157519..171158468,2	MCF-7	breast:
5	chr1:171180730..171183096-chr4:189101938..189104230,2	MCF-7	breast:
6	chr1:171336787..171338408-chr1:171339776..171341532,2	MCF-7	breast:
7	chr1:171214140..171215314-chr1:171282380..171283602,18	MCF-7	breast:
8	chr1:171182864..171185763-chr1:171186408..171189341,2	MCF-7	breast:
9	chr1:171219588..171222803-chr1:171228778..171230564,3	K562	blood:
10	chr1:171258018..171259639-chr1:171260854..171263633,2	K562	blood:
11	chr1:171215395..171216956-chr1:171219667..171221307,2	MCF-7	breast:
12	chr1:171282676..171283284-chr1:171373985..171374977,4	MCF-7	breast:
13	chr1:171214240..171215269-chr1:171282376..171283601,7	MCF-7	breast:
14	chr1:170936062..170936908-chr1:171282571..171283243,3	MCF-7	breast:
15	chr1:171368098..171369611-chr1:171388402..171390157,2	MCF-7	breast:
16	chr1:171157094..171159925-chr1:171161242..171162761,2	K562	blood:
17	chr1:171243618..171245261-chr1:171253063..171254907,2	K562	blood:
18	chr1:171161907..171164775-chr1:171168366..171171218,2	K562	blood:
19	chr1:171216177..171217237-chr1:171282875..171283514,3	MCF-7	breast:
20	chr1:171308429..171309488-chr1:171373955..171374861,3	MCF-7	breast:
21	chr1:171404013..171405651-chr1:171411065..171412627,2	K562	blood:
22	chr1:171151483..171154581-chr1:171157949..171161924,3	MCF-7	breast:
23	chr1:171405355..171408089-chr1:171454758..171456497,2	MCF-7	breast:
24	chr1:171219827..171222241-chr1:171222983..171225833,3	MCF-7	breast:
25	chr1:171187797..171189835-chr1:171191564..171194285,2	MCF-7	breast:
26	chr1:171404013..171405651-chr1:171411065..171412627,2	K562	blood:
27	chr1:171157094..171159925-chr1:171161242..171162761,2	K562	blood:
28	chr1:171289560..171292319-chr1:171321362..171324920,3	K562	blood:
29	chr1:171223210..171225976-chr1:171227419..171229692,2	MCF-7	breast:
30	chr1:171049785..171051089-chr1:171157506..171158409,9	MCF-7	breast:
31	chr1:171219827..171222241-chr1:171222983..171225833,3	MCF-7	breast:
32	chr1:171223210..171225976-chr1:171227419..171229692,2	MCF-7	breast:
33	chr1:171392802..171395770-chr1:171453289..171456118,2	MCF-7	breast:
34	chr1:170935902..170936885-chr1:171195525..171196580,9	MCF-7	breast:
35	chr1:171195796..171196545-chr1:171282426..171283362,2	MCF-7	breast:
36	chr1:170935849..170936463-chr1:171282647..171283201,2	MCF-7	breast:
37	chr1:169861640..169863148-chr1:171232591..171235056,2	K562	blood:
38	chr1:171368098..171369611-chr1:171388402..171390157,2	MCF-7	breast:
39	chr1:171364064..171365565-chr1:171368281..171370640,2	MCF-7	breast:
40	chr1:171161907..171164775-chr1:171168366..171171218,2	K562	blood:
41	chr1:171256964..171257592-chr10:82834076..82834599,2	MCF-7	breast:
42	chr1:171258018..171259639-chr1:171260854..171263633,2	K562	blood:
43	chr1:171177619..171179300-chr1:171182219..171184780,2	K562	blood:
44	chr1:171050311..171050975-chr1:171195652..171196489,2	MCF-7	breast:
45	chr1:171219588..171221486-chr1:171228778..171230328,2	K562	blood:
46	chr1:171336787..171338408-chr1:171339776..171341532,2	MCF-7	breast:
47	chr1:171387474..171389314-chr1:171452671..171455451,2	MCF-7	breast:
48	chr1:171282676..171283284-chr1:171373985..171374977,4	MCF-7	breast:
49	chr1:171283686..171286081-chr1:171289789..171292342,2	K562	blood:
50	chr1:171050144..171051119-chr1:171195616..171196435,6	MCF-7	breast:

(count:22 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FMO4-2	chr1:171314228-171314459	NONHSAT007524
2	lnc-MYOC-6	chr1:171314244-171314446	NONHSAT007525
3	lnc-MYOC-1	chr1:171168386-171168654	ENSG00000225243.1
4	lnc-MYOC-3	chr1:171413838-171414102	NONHSAT007530
5	lnc-MYOC-2	chr1:171137243-171137327	ENSG00000231424.1
6	lnc-MYOC-2	chr1:171220662-171220933	ENSG00000231424.1
7	lnc-MYOC-2	chr1:171220662-171220933	ENSG00000231424.2
8	lnc-FMO4-3	chr1:171361368-171361929	NONHSAT007527
9	lnc-MYOC-1	chr1:171196790-171196927	ENSG00000225243.1
10	lnc-MYOC-2	chr1:171216720-171216862	ENSG00000231424.1
11	lnc-MYOC-1	chr1:171168383-171168654	ENSG00000225243.1
12	lnc-MYOC-1	chr1:171173030-171173127	ENSG00000225243.1
13	lnc-MYOC-5	chr1:171315090-171315408	NONHSAT007526
14	lnc-MYOC-1	chr1:171196790-171196864	ENSG00000225243.1
15	lnc-MYOC-1	chr1:171193136-171193423	ENSG00000225243.1
16	lnc-MYOC-2	chr1:171216719-171216862	ENSG00000231424.2
17	lnc-FMO2-1	chr1:171143143-171143447	NONHSAT007516
18	lnc-MYOC-1	chr1:171168386-171168654	ENSG00000225243.1
19	lnc-MYOC-4	chr1:171410851-171411265	NONHSAT007529
20	lnc-MYOC-1	chr1:171173030-171173127	ENSG00000225243.1
21	lnc-FMO2-1	chr1:171142663-171143015	NONHSAT007516
22	lnc-MYOC-4	chr1:171410062-171410336	NONHSAT007529

No data

Variant related genes	Relation type
FMO1	TF binding region
HMGB1P11	TF binding region
ENSG00000225243	TF binding region
FMO4	TF binding region
ENSG00000206692	TF binding region
RNU6-290P	TF binding region
FMO2	TF binding region
GM2AP2	TF binding region
ENSG00000231424	TF binding region
CYCSP53	TF binding region
TOP1P1	TF binding region
ENSG00000225704	TF binding region
FMO1	CpG island
HMGB1P11	CpG island
ENSG00000225243	CpG island
FMO4	CpG island
ENSG00000206692	CpG island
RNU6-290P	CpG island
FMO2	CpG island
GM2AP2	CpG island
ENSG00000231424	CpG island
CYCSP53	CpG island
TOP1P1	CpG island
ENSG00000225704	CpG island
ENSG00000000457	chromatin interactions
ENSG00000206692	chromatin interactions
ENSG00000094963	chromatin interactions
ENSG00000225243	chromatin interactions
ENSG00000231424	chromatin interactions
ENSG00000010932	chromatin interactions
ENSG00000076258	chromatin interactions
ENSG00000117523	chromatin interactions

Extended variants
information (count: 10233 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:10233 , 50 per page) page: 1 2 3 4 5 6 7 ... 205

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112993633	chr1:171128845-171128846	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs36114094	chr1:171128884-171128885	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs573471123	chr1:171128900-171128901	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375812820	chr1:171128947-171128948	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs561879368	chr1:171129002-171129003	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs561901865	chr1:171129021-171129022	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs191593448	chr1:171129038-171129039	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs111812440	chr1:171129090-171129091	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs527756833	chr1:171129175-171129176	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs559724409	chr1:171129207-171129208	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143743403	chr1:171129252-171129253	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs573340047	chr1:171129313-171129314	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs36028142	chr1:171129329-171129330	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs398049732	chr1:171129338-171129339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs1920150	chr1:171129422-171129423	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs151091235	chr1:171129437-171129438	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs534045626	chr1:171129572-171129573	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs549016744	chr1:171129608-171129609	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs188443948	chr1:171129653-171129654	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs570747616	chr1:171129726-171129727	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs556419970	chr1:171129727-171129728	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs545755049	chr1:171129751-171129752	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs56877584	chr1:171129757-171129758	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs575791251	chr1:171129838-171129839	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs539586670	chr1:171129872-171129873	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs140976260	chr1:171129904-171129905	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs540132514	chr1:171129933-171129934	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs146579349	chr1:171129935-171129936	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs139017965	chr1:171129941-171129942	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs562061642	chr1:171130000-171130001	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs201009054	chr1:171130044-171130045	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573869562	chr1:171130067-171130068	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs544378989	chr1:171130079-171130080	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs193033134	chr1:171130084-171130085	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs74548997	chr1:171130136-171130137	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs537086198	chr1:171130160-171130161	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs544780044	chr1:171130216-171130217	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs61814301	chr1:171130236-171130237	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs555977587	chr1:171130303-171130304	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs185576913	chr1:171130313-171130314	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
41	rs200384864	chr1:171130316-171130317	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs527303272	chr1:171130341-171130342	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
43	rs16864125	chr1:171130346-171130347	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs577520016	chr1:171130357-171130358	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
45	rs567543460	chr1:171130362-171130363	Enhancers Flanking Active TSS Weak transcription Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs202213595	chr1:171130455-171130456	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
47	rs549989513	chr1:171130487-171130488	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs571510730	chr1:171130501-171130502	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs539878011	chr1:171130517-171130518	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
50	rs557982447	chr1:171130520-171130521	Enhancers Weak transcription Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Hepatocellular carcinoma	16750200	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Breast cancer	21611746	CNVD
Neuroblastoma	18923191	CNVD
Soft tissue tumor	16732325	CNVD
Cancer	17060936	CNVD
Lung cancer	16740712	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Williams-beuren syndrome	16971481	CNVD
Developmental delay	21147756	CNVD
Burkitt''s lymphoma	20823134	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Lung cancer	18438408	CNVD
Breast cancer	20409316	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	21509527	CNVD

Chromatin state (count:2648 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:171121000-171129000	Weak transcription	Fetal Kidney	kidney
2	chr1:171121400-171130200	Weak transcription	Right Atrium	heart
3	chr1:171122000-171129400	Weak transcription	Adipose Nuclei	Adipose
4	chr1:171126600-171131600	Enhancers	Fetal Intestine Large	intestine
5	chr1:171126800-171131600	Enhancers	Fetal Intestine Small	intestine
6	chr1:171127800-171129800	Enhancers	Liver	Liver
7	chr1:171128800-171129000	Enhancers	Esophagus	oesophagus
8	chr1:171128800-171129000	Enhancers	Small Intestine	intestine
9	chr1:171128800-171130600	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr1:171128800-171130600	Enhancers	Fetal Stomach	stomach
11	chr1:171128800-171131200	Enhancers	Fetal Lung	lung
12	chr1:171129000-171129800	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
13	chr1:171129000-171130200	Weak transcription	Small Intestine	intestine
14	chr1:171129000-171130400	Enhancers	Breast Myoepithelial Primary Cells	Breast
15	chr1:171129000-171130600	Enhancers	Fetal Kidney	kidney
16	chr1:171129000-171130600	Enhancers	Ovary	ovary
17	chr1:171129000-171130600	Enhancers	Stomach Mucosa	stomach
18	chr1:171129000-171137600	Weak transcription	Esophagus	oesophagus
19	chr1:171129200-171130000	Enhancers	HUES48 Cell Line	embryonic stem cell
20	chr1:171129200-171130000	Enhancers	HUES64 Cell Line	embryonic stem cell
21	chr1:171129200-171130800	Enhancers	HepG2	liver
22	chr1:171129400-171129600	Enhancers	Lung	lung
23	chr1:171129400-171130000	Enhancers	Stomach Smooth Muscle	stomach
24	chr1:171129400-171130400	Enhancers	Adipose Nuclei	Adipose
25	chr1:171129400-171130600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
26	chr1:171129800-171130400	Enhancers	Cortex derived primary cultured neurospheres	brain
27	chr1:171129800-171130600	Flanking Active TSS	Liver	Liver
28	chr1:171130000-171130800	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
29	chr1:171130200-171130600	Enhancers	Duodenum Mucosa	Duodenum
30	chr1:171130200-171130600	Enhancers	Gastric	stomach
31	chr1:171130200-171130600	Enhancers	Right Atrium	heart
32	chr1:171130200-171130600	Enhancers	Small Intestine	intestine
33	chr1:171130200-171130800	Active TSS	Fetal Brain Male	brain
34	chr1:171130400-171130600	Enhancers	iPS-20b Cell Line	embryonic stem cell
35	chr1:171130400-171134600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
36	chr1:171130600-171131200	Enhancers	Liver	Liver
37	chr1:171130600-171134600	Weak transcription	Stomach Mucosa	stomach
38	chr1:171131200-171136000	Weak transcription	Fetal Lung	lung
39	chr1:171131600-171134800	Weak transcription	Fetal Intestine Small	intestine
40	chr1:171134400-171137600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
41	chr1:171134600-171137400	Enhancers	HMEC	breast
42	chr1:171134600-171137800	Enhancers	Stomach Mucosa	stomach
43	chr1:171134800-171137600	Enhancers	NHEK	skin
44	chr1:171135000-171137400	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
45	chr1:171136000-171136400	Enhancers	Fetal Lung	lung
46	chr1:171136400-171139000	Weak transcription	Fetal Lung	lung
47	chr1:171137600-171137800	Enhancers	Esophagus	oesophagus
48	chr1:171137800-171138400	Weak transcription	Esophagus	oesophagus
49	chr1:171137800-171142200	Weak transcription	Stomach Mucosa	stomach
50	chr1:171138400-171139200	Enhancers	Esophagus	oesophagus

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