Variant report

Variant	nsv569580
Chromosome Location	chr15:57629099-57767982
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1599)
CpG islands
(count:1711)
Chromatin interactive
region (count:60)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1599 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:57675122-57675478	K562	blood:	n/a	n/a
2	ARID3A	chr15:57709023-57709306	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:57698812-57699080	HepG2	liver:	n/a	n/a
4	ARID3A	chr15:57683674-57684095	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:57673166-57673314	HepG2	liver:	n/a	n/a
6	ARID3A	chr15:57767593-57767849	HepG2	liver:	n/a	n/a
7	ATF1	chr15:57739082-57739221	K562	blood:	n/a	n/a
8	ATF1	chr15:57675232-57675432	K562	blood:	n/a	n/a
9	ATF2	chr15:57677951-57678684	H1-hESC	embryonic stem cell:	n/a	n/a
10	ATF2	chr15:57677879-57679030	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr15:57648804-57649568	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr15:57632631-57633314	A549	lung:	n/a	chr15:57632639-57632653
13	BACH1	chr15:57649168-57649224	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:57668896-57669038	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:57678068-57678736	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:57738064-57738618	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:57738124-57738415	K562	blood:	n/a	n/a
18	BCL11A	chr15:57648928-57649135	H1-hESC	embryonic stem cell:	n/a	n/a
19	BCL11A	chr15:57648891-57649186	H1-hESC	embryonic stem cell:	n/a	n/a
20	BHLHE40	chr15:57630053-57630386	K562	blood:	n/a	n/a
21	BHLHE40	chr15:57632888-57633189	GM12878	blood:	n/a	n/a
22	BHLHE40	chr15:57675229-57675611	K562	blood:	n/a	n/a
23	BHLHE40	chr15:57632538-57632713	K562	blood:	n/a	n/a
24	BHLHE40	chr15:57683205-57684026	HepG2	liver:	n/a	n/a
25	BRCA1	chr15:57632912-57633179	H1-hESC	embryonic stem cell:	n/a	chr15:57633088-57633095
26	BRCA1	chr15:57649151-57649161	H1-hESC	embryonic stem cell:	n/a	n/a
27	CBX3	chr15:57630036-57630325	K562	blood:	n/a	n/a
28	CCNT2	chr15:57675201-57675501	K562	blood:	n/a	n/a
29	CEBPB	chr15:57719550-57719876	HepG2	liver:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
30	CEBPB	chr15:57719529-57719914	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
31	CEBPB	chr15:57755052-57755277	HepG2	liver:	n/a	chr15:57755215-57755226
32	CEBPB	chr15:57649017-57649179	H1-hESC	embryonic stem cell:	n/a	n/a
33	CEBPB	chr15:57683760-57684057	HepG2	liver:	n/a	n/a
34	CEBPB	chr15:57669218-57669407	HepG2	liver:	n/a	chr15:57669334-57669345
35	CEBPB	chr15:57759160-57759196	A549	lung:	n/a	n/a
36	CEBPB	chr15:57719370-57720131	A549	lung:	n/a	chr15:57719713-57719726 chr15:57719713-57719724 chr15:57719714-57719725 chr15:57719713-57719724 chr15:57719713-57719726
37	CEBPB	chr15:57688268-57688424	A549	lung:	n/a	n/a
38	CEBPB	chr15:57664441-57664787	H1-hESC	embryonic stem cell:	n/a	n/a
39	CEBPB	chr15:57753678-57754168	MCF-7	breast:	n/a	n/a
40	CEBPB	chr15:57737280-57737551	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:57633910-57634220	K562	blood:	n/a	chr15:57634043-57634056
42	CEBPB	chr15:57753700-57754104	MCF-7	breast:	n/a	n/a
43	CEBPB	chr15:57645093-57645295	A549	lung:	n/a	n/a
44	CEBPB	chr15:57664442-57664743	A549	lung:	n/a	n/a
45	CEBPB	chr15:57669187-57669508	H1-hESC	embryonic stem cell:	n/a	chr15:57669334-57669345
46	CEBPB	chr15:57645104-57645259	HepG2	liver:	n/a	n/a
47	CEBPB	chr15:57669133-57669500	HepG2	liver:	n/a	chr15:57669334-57669345
48	CEBPB	chr15:57767622-57767921	HepG2	liver:	n/a	n/a
49	CEBPB	chr15:57644830-57645208	K562	blood:	n/a	chr15:57644878-57644889
50	CEBPB	chr15:57669326-57669420	K562	blood:	n/a	chr15:57669334-57669345

(count:1711 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:57737942-57737992	MCF-7	breast:	n/a
2	chr15:57668539-57668589	AG04449	skin:	fetal
3	chr15:57668895-57668945	T-47D	breast:	n/a
4	chr15:57737942-57737992	MCF-7	breast:	n/a
5	chr15:57668539-57668589	AG04449	skin:	fetal
6	chr15:57668895-57668945	T-47D	breast:	n/a
7	chr15:57731648-57731698	PANC-1	pancreas:	n/a
8	chr15:57668247-57668297	HepG2	liver:	n/a
9	chr15:57668552-57668602	K562	blood:	n/a
10	chr15:57669165-57669215	PFSK-1	brain:	n/a
11	chr15:57724857-57724907	LNCaP	prostate:	n/a
12	chr15:57668039-57668089	HUVEC	blood vessel:	n/a
13	chr15:57731648-57731698	SK-N-SH_RA	brain:	n/a
14	chr15:57664490-57664540	HEEpiC	esophagus:	n/a
15	chr15:57682357-57682407	BJ	skin:	n/a
16	chr15:57731055-57731105	NT2-D1	testis:	n/a
17	chr15:57671034-57671084	U87	brain:	n/a
18	chr15:57719252-57719302	PrEC	prostate:	n/a
19	chr15:57668247-57668297	HRE	kidney:	n/a
20	chr15:57647657-57647707	ECC-1	luminal epithelium:	n/a
21	chr15:57668247-57668297	K562	blood:	n/a
22	chr15:57731166-57731216	HAEpiC	amniotic membrane:	n/a
23	chr15:57669165-57669215	BJ	skin:	n/a
24	chr15:57677507-57677557	HCPEpiC	choroid plexus:	n/a
25	chr15:57668547-57668597	CMK	blood:	n/a
26	chr15:57680479-57680529	HCPEpiC	choroid plexus:	n/a
27	chr15:57671034-57671084	ECC-1	luminal epithelium:	n/a
28	chr15:57731648-57731698	MCF-7	breast:	n/a
29	chr15:57719252-57719302	BE2_C	brain:	n/a
30	chr15:57695943-57695993	AG10803	skin:	n/a
31	chr15:57682357-57682407	NH-A	brain:	n/a
32	chr15:57668087-57668137	ovcar-3	ovarian:	n/a
33	chr15:57668087-57668137	HL-60	blood:	n/a
34	chr15:57682357-57682407	RPTEC	kidney:	n/a
35	chr15:57731055-57731105	HMEC	breast:	n/a
36	chr15:57695943-57695993	HIPEpiC	eye:	n/a
37	chr15:57719922-57719972	SK-N-MC	brain:	n/a
38	chr15:57731648-57731698	Hepatocyte	liver:	n/a
39	chr15:57731108-57731158	HRE	kidney:	n/a
40	chr15:57729383-57729433	HRE	kidney:	n/a
41	chr15:57731166-57731216	K562	blood:	n/a
42	chr15:57695943-57695993	HRE	kidney:	n/a
43	chr15:57719922-57719972	NT2-D1	testis:	n/a
44	chr15:57731108-57731158	HCT-116	colon:	n/a
45	chr15:57680479-57680529	HMEC	breast:	n/a
46	chr15:57668895-57668945	GM12892	blood:	n/a
47	chr15:57668812-57668862	HAEpiC	amniotic membrane:	n/a
48	chr15:57668552-57668602	Hela-S3	cervix:	n/a
49	chr15:57664490-57664540	GM12891	blood:	n/a
50	chr15:57668812-57668862	PANC-1	pancreas:	n/a

(count:60 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:57633114..57634635-chr15:57634661..57636364,2	K562	blood:
2	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
3	chr15:57668435..57670141-chr15:57674647..57676838,2	MCF-7	breast:
4	chr15:57667349..57669479-chr15:57681702..57683974,2	K562	blood:
5	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:
6	chr15:57745679..57747449-chr15:57751511..57754366,2	MCF-7	breast:
7	chr15:57632559..57633182-chr15:57833877..57834693,3	K562	blood:
8	chr15:57632947..57633501-chr15:57834811..57835609,2	MCF-7	breast:
9	chr15:57705802..57707350-chr15:57713092..57715307,2	K562	blood:
10	chr15:57637995..57638567-chr15:57798058..57798880,2	MCF-7	breast:
11	chr15:57632396..57633185-chr15:57798175..57798849,2	MCF-7	breast:
12	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
13	chr15:57627655..57630463-chr15:57790410..57793260,2	K562	blood:
14	chr15:57662175..57664160-chr15:57665608..57668558,2	K562	blood:
15	chr15:57614506..57616256-chr15:57638929..57640760,2	K562	blood:
16	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:
17	chr15:57614320..57618855-chr15:57629284..57632959,4	K562	blood:
18	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
19	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
20	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
21	chr15:57632774..57633483-chr15:57818149..57819070,2	K562	blood:
22	chr15:57632576..57633293-chr15:57834178..57834896,2	MCF-7	breast:
23	chr15:57708825..57710984-chr15:57719096..57721370,2	K562	blood:
24	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
25	chr15:57720476..57722936-chr15:57724611..57727742,3	K562	blood:
26	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
27	chr15:57636178..57637065-chr15:57819415..57820032,2	MCF-7	breast:
28	chr15:57632542..57633554-chr15:57819095..57820390,12	K562	blood:
29	chr15:57653032..57655514-chr15:57656834..57658857,2	K562	blood:
30	chr15:57753396..57757139-chr15:57762848..57768344,4	K562	blood:
31	chr15:57750506..57752282-chr15:57753554..57755712,2	K562	blood:
32	chr15:57632179..57633491-chr15:57795201..57795781,4	K562	blood:
33	chr15:57631137..57633998-chr15:57818191..57820623,2	K562	blood:
34	chr15:57668102..57670225-chr15:57677163..57679480,2	MCF-7	breast:
35	chr15:57731299..57732946-chr15:57744601..57746731,2	MCF-7	breast:
36	chr15:57632602..57633486-chr15:57819385..57820825,7	MCF-7	breast:
37	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
38	chr15:57637767..57638513-chr15:57664087..57664757,2	MCF-7	breast:
39	chr15:57676218..57678168-chr15:57687344..57689139,2	K562	blood:
40	chr15:57632854..57634984-chr15:57638024..57640746,3	K562	blood:
41	chr15:57698192..57700092-chr15:57702299..57704451,2	K562	blood:
42	chr15:57627482..57629792-chr15:57631496..57634850,3	K562	blood:
43	chr15:57760042..57761755-chr15:57765442..57768496,3	K562	blood:
44	chr15:57761779..57763343-chr15:57766139..57768515,2	K562	blood:
45	chr15:57637629..57639520-chr15:57818149..57819741,2	MCF-7	breast:
46	chr15:57720229..57721976-chr15:57725417..57727742,2	K562	blood:
47	chr15:57667871..57669464-chr15:57819823..57821848,2	MCF-7	breast:
48	chr15:57632756..57633581-chr15:57818988..57820292,4	MCF-7	breast:
49	chr1:121483186..121485028-chr15:57701904..57703998,2	MCF-7	breast:
50	chr15:57703606..57706122-chr15:57710560..57712105,2	MCF-7	breast:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CGNL1-2	chr15:57689122-57689304	NONHSAT044073
2	lnc-CGNL1-2	chr15:57699171-57699474	NONHSAT044073
3	lnc-CGNL1-2	chr15:57686151-57686289	NONHSAT044073
4	lnc-CGNL1-2	chr15:57668165-57668468	NONHSAT044072
5	lnc-CGNL1-2	chr15:57698164-57698262	NONHSAT044073
6	lnc-CGNL1-2	chr15:57694859-57694912	NONHSAT044073
7	lnc-CGNL1-2	chr15:57730183-57730215	NONHSAT044072
8	lnc-CGNL1-2	chr15:57690539-57690628	NONHSAT044073
9	lnc-CGNL1-2	chr15:57669344-57669363	NONHSAT044073
10	lnc-CGNL1-2	chr15:57669124-57669363	NONHSAT044072
11	lnc-ALDH1A2-6	chr15:57741444-57741697	expReg_chr15_4576_-
12	lnc-CGNL1-2	chr15:57694217-57694236	NONHSAT044073

No data

Variant related genes	Relation type
CGNL1	TF binding region
RNU6-844P	TF binding region
CGNL1	CpG island
RNU6-844P	CpG island
ENSG00000261265	chromatin interactions
ENSG00000260870	chromatin interactions
ENSG00000128849	chromatin interactions

Extended variants
information (count: 6373 )
Associated
traits (count: 64 )

Variant overlapped rSNPs/rCNVs (count:6373 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2544141	chr15:57629099-57629100	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs558971781	chr15:57629107-57629108	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs145591087	chr15:57629115-57629116	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs375172288	chr15:57629116-57629117	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs113002333	chr15:57629119-57629120	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs28691795	chr15:57629129-57629130	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
7	rs574597794	chr15:57629168-57629169	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs113718510	chr15:57629172-57629173	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs190681684	chr15:57629194-57629195	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs72736068	chr15:57629196-57629197	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs546110376	chr15:57629246-57629247	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559402819	chr15:57629248-57629249	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs138095313	chr15:57629260-57629261	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs2591056	chr15:57629283-57629284	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs377301243	chr15:57629301-57629302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs561504221	chr15:57629366-57629367	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs182419406	chr15:57629408-57629409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs549985233	chr15:57629411-57629412	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs142774159	chr15:57629465-57629466	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs538674519	chr15:57629499-57629500	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs7498037	chr15:57629556-57629557	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
22	rs558939266	chr15:57629569-57629570	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs566248933	chr15:57629582-57629583	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs535297204	chr15:57629594-57629595	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs555240605	chr15:57629672-57629673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs575080700	chr15:57629706-57629707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569142500	chr15:57629728-57629729	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs374288272	chr15:57629750-57629751	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs546142722	chr15:57629763-57629764	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs76514577	chr15:57629821-57629822	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs113298934	chr15:57629832-57629833	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs576836392	chr15:57629853-57629854	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs79852227	chr15:57629892-57629893	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs377372052	chr15:57629907-57629908	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs559254354	chr15:57629924-57629925	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572809964	chr15:57629980-57629981	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs114040873	chr15:57629981-57629982	Weak transcription Enhancers Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs150181211	chr15:57630006-57630007	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs568823339	chr15:57630010-57630011	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs538099729	chr15:57630100-57630101	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs138721155	chr15:57630109-57630110	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs370692981	chr15:57630116-57630117	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs563655028	chr15:57630146-57630147	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs557873140	chr15:57630161-57630162	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs552301910	chr15:57630180-57630181	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs566072982	chr15:57630184-57630185	Weak transcription Enhancers Flanking Bivalent TSS/Enh	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535385201	chr15:57630234-57630235	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs577936111	chr15:57630315-57630316	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs568703538	chr15:57630365-57630366	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs537262036	chr15:57630404-57630405	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:64)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	21129771	CNVD
Breast cancer	16272173	CNVD
Hepatocellular carcinoma	16750200	CNVD
Abnormal phenotypes	18644119	CNVD
Cancer	16751803	CNVD
Esophageal adenocarcinoma	18820669	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Pancreatic cancer	17952125	CNVD
Ovarian cancer	21781307	CNVD

Chromatin state (count:2581 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:57613000-57635400	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr15:57618600-57632000	Weak transcription	Spleen	Spleen
3	chr15:57622800-57629800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr15:57625200-57632000	Enhancers	HUVEC	blood vessel
5	chr15:57626600-57632600	Enhancers	Fetal Muscle Trunk	muscle
6	chr15:57626600-57633400	Enhancers	Fetal Muscle Leg	muscle
7	chr15:57626800-57630000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr15:57627000-57629800	Weak transcription	HSMM	muscle
9	chr15:57627000-57630000	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr15:57627000-57631000	Weak transcription	Placenta Amnion	Placenta Amnion
11	chr15:57627000-57633000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
12	chr15:57627200-57629600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
13	chr15:57627200-57630000	Weak transcription	Duodenum Mucosa	Duodenum
14	chr15:57627200-57630000	Weak transcription	NH-A	brain
15	chr15:57627200-57635400	Weak transcription	H1 Cell Line	embryonic stem cell
16	chr15:57627200-57635400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr15:57627400-57630200	Weak transcription	HSMMtube	muscle
18	chr15:57627400-57635400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
19	chr15:57627600-57629800	Weak transcription	Stomach Mucosa	stomach
20	chr15:57627600-57668200	Weak transcription	Right Atrium	heart
21	chr15:57627800-57629200	Weak transcription	Adipose Nuclei	Adipose
22	chr15:57628000-57630000	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr15:57628200-57629400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
24	chr15:57628200-57629400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
25	chr15:57628200-57629400	Weak transcription	Fetal Stomach	stomach
26	chr15:57628200-57629400	Weak transcription	Lung	lung
27	chr15:57628200-57629400	Weak transcription	Skeletal Muscle Male	skeletal muscle
28	chr15:57628200-57629600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
29	chr15:57628200-57629800	Weak transcription	K562	blood
30	chr15:57628200-57632000	Weak transcription	Fetal Kidney	kidney
31	chr15:57628200-57632600	Weak transcription	Fetal Heart	heart
32	chr15:57628400-57629400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
33	chr15:57628400-57629400	Weak transcription	Fetal Intestine Large	intestine
34	chr15:57628400-57630000	Weak transcription	Fetal Intestine Small	intestine
35	chr15:57629200-57631200	Enhancers	Adipose Nuclei	Adipose
36	chr15:57629400-57629600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
37	chr15:57629400-57629600	Enhancers	Lung	lung
38	chr15:57629400-57630400	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr15:57629400-57630600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr15:57629400-57630600	Enhancers	Primary hematopoietic stem cells short term culture	blood
41	chr15:57629400-57631600	Enhancers	Fetal Stomach	stomach
42	chr15:57629600-57630200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr15:57629600-57630200	Weak transcription	Lung	lung
44	chr15:57629600-57630600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr15:57629600-57638000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr15:57629800-57630000	Bivalent Enhancer	HepG2	liver
47	chr15:57629800-57630200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
48	chr15:57629800-57630200	Enhancers	Stomach Smooth Muscle	stomach
49	chr15:57629800-57630200	Enhancers	K562	blood
50	chr15:57629800-57630600	Enhancers	Primary hematopoietic stem cells	blood

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