Variant report

Variant	nsv1046970
Chromosome Location	chr15:53065114-53142386
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1182)
CpG islands
(count:4338)
Chromatin interactive
region (count:29)
LncRNA
region (count:27)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1182 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:53082218-53082726	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:53072684-53073202	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:53077296-53077584	HepG2	liver:	n/a	n/a
4	ATF2	chr15:53096969-53097302	H1-hESC	embryonic stem cell:	n/a	n/a
5	ATF2	chr15:53072294-53073257	GM12878	blood:	n/a	n/a
6	ATF2	chr15:53076172-53076686	H1-hESC	embryonic stem cell:	n/a	n/a
7	ATF2	chr15:53072301-53073212	GM12878	blood:	n/a	n/a
8	BACH1	chr15:53080571-53080771	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:53098308-53098367	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:53082775-53083015	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr15:53076053-53076451	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr15:53097811-53098098	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr15:53083442-53084110	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr15:53075540-53075823	H1-hESC	embryonic stem cell:	n/a	n/a
15	BACH1	chr15:53080077-53080277	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr15:53082150-53082339	H1-hESC	embryonic stem cell:	n/a	n/a
17	BACH1	chr15:53096002-53096582	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr15:53086711-53087039	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr15:53078728-53078986	H1-hESC	embryonic stem cell:	n/a	n/a
20	BATF	chr15:53072392-53072765	GM12878	blood:	n/a	n/a
21	BATF	chr15:53072306-53073200	GM12878	blood:	n/a	n/a
22	BCL11A	chr15:53072219-53072910	GM12878	blood:	n/a	chr15:53072401-53072409
23	BCL11A	chr15:53072380-53072869	GM12878	blood:	n/a	chr15:53072401-53072409
24	BCLAF1	chr15:53072432-53073030	GM12878	blood:	n/a	n/a
25	BHLHE40	chr15:53082647-53082860	GM12878	blood:	n/a	chr15:53082735-53082744 chr15:53082735-53082744 chr15:53082734-53082743
26	BHLHE40	chr15:53082092-53082932	HepG2	liver:	n/a	chr15:53082735-53082744 chr15:53082735-53082744 chr15:53082462-53082478 chr15:53082455-53082471 chr15:53082734-53082743
27	BHLHE40	chr15:53082633-53082846	K562	blood:	n/a	chr15:53082735-53082744 chr15:53082735-53082744 chr15:53082734-53082743
28	BRCA1	chr15:53071977-53072011	GM12878	blood:	n/a	n/a
29	BRCA1	chr15:53106288-53106461	Hela-S3	cervix:	n/a	n/a
30	CCNT2	chr15:53082422-53082718	K562	blood:	n/a	chr15:53082631-53082640
31	CCNT2	chr15:53076203-53076415	K562	blood:	n/a	n/a
32	CEBPB	chr15:53094308-53094599	HepG2	liver:	n/a	chr15:53094466-53094477 chr15:53094466-53094479 chr15:53094468-53094479
33	CEBPB	chr15:53116289-53117061	MCF-7	breast:	n/a	chr15:53116969-53116980
34	CEBPB	chr15:53116803-53117002	HepG2	liver:	n/a	chr15:53116969-53116980
35	CEBPB	chr15:53072470-53073069	A549	lung:	n/a	chr15:53072565-53072576
36	CEBPB	chr15:53116686-53117039	MCF-7	breast:	n/a	chr15:53116969-53116980
37	CEBPB	chr15:53094449-53094491	K562	blood:	n/a	chr15:53094466-53094477 chr15:53094466-53094479 chr15:53094468-53094479
38	CEBPB	chr15:53116784-53117148	HepG2	liver:	n/a	chr15:53116969-53116980
39	CEBPB	chr15:53072314-53073009	H1-hESC	embryonic stem cell:	n/a	chr15:53072565-53072576
40	CEBPB	chr15:53116834-53117087	HepG2	liver:	n/a	chr15:53116969-53116980
41	CEBPB	chr15:53116901-53117119	A549	lung:	n/a	chr15:53116969-53116980
42	CEBPB	chr15:53072274-53072957	GM12878	blood:	n/a	chr15:53072565-53072576
43	CEBPB	chr15:53116777-53117151	HepG2	liver:	n/a	chr15:53116969-53116980
44	CEBPB	chr15:53075756-53076401	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr15:53094304-53094546	A549	lung:	n/a	chr15:53094466-53094477 chr15:53094466-53094479 chr15:53094468-53094479
46	CEBPD	chr15:53082328-53082849	HepG2	liver:	n/a	n/a
47	CEBPD	chr15:53116877-53117012	HepG2	liver:	n/a	n/a
48	CEBPD	chr15:53078674-53079064	HepG2	liver:	n/a	n/a
49	CEBPD	chr15:53116757-53117027	HepG2	liver:	n/a	n/a
50	CEBPD	chr15:53081999-53082244	HepG2	liver:	n/a	n/a

(count:4338 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:53096854-53096904	GM19239	blood:	n/a
2	chr15:53090232-53090282	NH-A	brain:	n/a
3	chr15:53087599-53087649	HepG2	liver:	n/a
4	chr15:53079445-53079495	Caco-2	colon:	n/a
5	chr15:53082902-53082952	HCT-116	colon:	n/a
6	chr15:53101548-53101598	CMK	blood:	n/a
7	chr15:53096481-53096531	ovcar-3	ovarian:	n/a
8	chr15:53096854-53096904	GM19239	blood:	n/a
9	chr15:53090232-53090282	NH-A	brain:	n/a
10	chr15:53087599-53087649	HepG2	liver:	n/a
11	chr15:53079445-53079495	Caco-2	colon:	n/a
12	chr15:53082902-53082952	HCT-116	colon:	n/a
13	chr15:53101548-53101598	CMK	blood:	n/a
14	chr15:53096481-53096531	ovcar-3	ovarian:	n/a
15	chr15:53093405-53093455	K562	blood:	n/a
16	chr15:53090232-53090282	ECC-1	luminal epithelium:	n/a
17	chr15:53078121-53078171	MCF-7	breast:	n/a
18	chr15:53086726-53086776	PrEC	prostate:	n/a
19	chr15:53083135-53083185	NB4	blood:	n/a
20	chr15:53078063-53078113	ECC-1	luminal epithelium:	n/a
21	chr15:53086857-53086907	AG04449	skin:	fetal
22	chr15:53077609-53077659	BJ	skin:	n/a
23	chr15:53077609-53077659	LNCaP	prostate:	n/a
24	chr15:53098475-53098525	Hela-S3	cervix:	n/a
25	chr15:53081248-53081298	HPAEpiC	pulmonary alveolar:	n/a
26	chr15:53075877-53075927	HIPEpiC	eye:	n/a
27	chr15:53088156-53088206	HEK293	kidney:	embryo
28	chr15:53075825-53075875	HPAEpiC	pulmonary alveolar:	n/a
29	chr15:53093509-53093559	SK-N-SH	brain:	n/a
30	chr15:53087887-53087937	HRPEpiC	eye:	n/a
31	chr15:53093405-53093455	HepG2	liver:	n/a
32	chr15:53097649-53097699	HMEC	breast:	n/a
33	chr15:53079445-53079495	AG04449	skin:	fetal
34	chr15:53095823-53095873	CMK	blood:	n/a
35	chr15:53086630-53086680	ECC-1	luminal epithelium:	n/a
36	chr15:53097822-53097872	H1-hESC	embryonic stem cell:	embryo
37	chr15:53096816-53096866	PrEC	prostate:	n/a
38	chr15:53101548-53101598	AG04449	skin:	fetal
39	chr15:53084679-53084729	HCPEpiC	choroid plexus:	n/a
40	chr15:53083978-53084028	MCF-7	breast:	n/a
41	chr15:53093007-53093057	ovcar-3	ovarian:	n/a
42	chr15:53087599-53087649	NH-A	brain:	n/a
43	chr15:53096248-53096298	HCM	heart:	n/a
44	chr15:53087887-53087937	AoSMC	blood vessel:	n/a
45	chr15:53086968-53087018	PANC-1	pancreas:	n/a
46	chr15:53098257-53098307	HEEpiC	esophagus:	n/a
47	chr15:53097289-53097339	ovcar-3	ovarian:	n/a
48	chr15:53097060-53097110	SK-N-SH	brain:	n/a
49	chr15:53087316-53087366	HPAEpiC	pulmonary alveolar:	n/a
50	chr15:53087232-53087282	GM12892	blood:	n/a

(count:29 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:53088202..53091601-chr15:53093551..53096557,3	MCF-7	breast:
2	chr15:53075751..53076563-chr15:53489418..53490178,2	K562	blood:
3	chr15:53127363..53130328-chr15:53159239..53161065,2	MCF-7	breast:
4	chr15:53139577..53141179-chr15:53147410..53150139,2	MCF-7	breast:
5	chr15:53072465..53075963-chr15:53080706..53083147,3	MCF-7	breast:
6	chr15:53140110..53140838-chr5:122040574..122041537,2	MCF-7	breast:
7	chr15:51844973..51847549-chr15:53093703..53095676,2	MCF-7	breast:
8	chr15:53093578..53096252-chr15:53138309..53141218,2	MCF-7	breast:
9	chr15:53060401..53062540-chr15:53070993..53073276,2	MCF-7	breast:
10	chr15:53072756..53074429-chr15:53080987..53082654,2	MCF-7	breast:
11	chr15:53079161..53080673-chr15:53143168..53145503,2	MCF-7	breast:
12	chr15:53072253..53073288-chr15:54008890..54009735,3	MCF-7	breast:
13	chr15:53072756..53074429-chr15:53080987..53082654,2	MCF-7	breast:
14	chr15:53091716..53093481-chr15:53093879..53095531,2	MCF-7	breast:
15	chr13:45913793..45915528-chr15:53082604..53084932,2	MCF-7	breast:
16	chr15:53072465..53075963-chr15:53080706..53083147,3	MCF-7	breast:
17	chr15:53081655..53083909-chr15:53083926..53085751,2	K562	blood:
18	chr15:53098934..53100673-chr15:53103575..53106101,2	MCF-7	breast:
19	chr15:53104829..53105653-chr15:53489336..53490188,3	MCF-7	breast:
20	chr15:53078999..53085478-chr15:53088216..53096885,9	MCF-7	breast:
21	chr15:53079651..53082730-chr15:53114348..53117214,3	MCF-7	breast:
22	chr15:53091716..53093481-chr15:53093879..53095531,2	MCF-7	breast:
23	chr15:53081717..53084310-chr15:53084763..53086372,2	MCF-7	breast:
24	chr15:53088202..53091601-chr15:53093551..53096557,3	MCF-7	breast:
25	chr15:53093578..53096252-chr15:53138309..53141218,2	MCF-7	breast:
26	chr15:53076988..53078899-chr16:3071890..3073813,2	MCF-7	breast:
27	chr15:53098934..53100673-chr15:53103575..53106101,2	MCF-7	breast:
28	chr15:52611004..52613000-chr15:53076080..53077962,2	K562	blood:
29	chr15:53072513..53073379-chr15:53804086..53804809,3	MCF-7	breast:

(count:27 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ONECUT1-1	chr15:53098245-53098609	NONHSAT043955
2	lnc-ONECUT1-1	chr15:53092407-53093114	XLOC_011481
3	lnc-ONECUT1-1	chr15:53096691-53097142	XLOC_011481
4	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
5	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
6	lnc-ONECUT1-1	chr15:53096691-53096992	XLOC_011481
7	lnc-ONECUT1-1	chr15:53095405-53096044	XLOC_011481
8	lnc-ONECUT1-1	chr15:53096691-53096992	NONHSAT043955
9	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
10	lnc-ONECUT1-1	chr15:53096691-53097139	ENSG00000259203.1
11	lnc-ONECUT1-1	chr15:53096691-53097142	XLOC_011481
12	lnc-ONECUT1-1	chr15:53096406-53096494	NONHSAT043955
13	lnc-ONECUT1-1	chr15:53093811-53093844	ENSG00000259203.1
14	lnc-ONECUT1-1	chr15:53097866-53097962	XLOC_011481
15	lnc-ONECUT1-1	chr15:53095448-53096044	NONHSAT043955
16	lnc-MAPK6-18	chr15:53136240-53136402	l_1157_chr15:53136239-53171611_testes
17	lnc-FAM214A-1	chr15:53079204-53079324	NONHSAT043947
18	lnc-FAM214A-1	chr15:53079958-53080605	NONHSAT043947
19	lnc-ONECUT1-1	chr15:53096406-53096494	ENSG00000259203.1
20	lnc-ONECUT1-1	chr15:53097866-53097962	XLOC_011481
21	lnc-ONECUT1-1	chr15:53096406-53096494	XLOC_011481
22	lnc-MAPK6-11	chr15:53086548-53087549	XLOC_011257
23	lnc-MAPK6-11	chr15:53084847-53084886	XLOC_011257
24	lnc-ONECUT1-1	chr15:53095593-53096044	XLOC_011481
25	lnc-ONECUT1-1	chr15:53092221-53093114	XLOC_011481
26	lnc-FAM214A-1	chr15:53077922-53078166	NONHSAT043947
27	lnc-ONECUT1-1	chr15:53096691-53096992	XLOC_011481

No data

Variant related genes	Relation type
ONECUT1	TF binding region
ENSG00000259203	TF binding region
ONECUT1	CpG island
ENSG00000259203	CpG island
ENSG00000170919	chromatin interactions
ENSG00000251538	chromatin interactions
ENSG00000273149	chromatin interactions
ENSG00000169856	chromatin interactions
ENSG00000133112	chromatin interactions
LPHN2	miRNA target sites
HLA-A	miRNA target sites
FBXO28	miRNA target sites
CCND1	miRNA target sites

Extended variants
information (count: 2648 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:2648 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17652361	chr15:53065114-53065115	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs188376416	chr15:53065178-53065179	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
3	rs79439754	chr15:53065189-53065190	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
4	rs556900076	chr15:53065228-53065229	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
5	rs571565923	chr15:53065245-53065246	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
6	rs578216082	chr15:53065256-53065257	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
7	rs574266792	chr15:53065265-53065266	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
8	rs368634084	chr15:53065284-53065285	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
9	rs547605460	chr15:53065285-53065286	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
10	rs138101156	chr15:53065367-53065368	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
11	rs539282217	chr15:53065413-53065414	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
12	rs199865776	chr15:53065439-53065440	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
13	rs200861393	chr15:53065441-53065442	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
14	rs375888032	chr15:53065442-53065443	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
15	rs397759181	chr15:53065457-53065458	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
16	rs149505482	chr15:53065477-53065478	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
17	rs569720941	chr15:53065481-53065482	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
18	rs35916321	chr15:53065505-53065506	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
19	rs537096639	chr15:53065535-53065536	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
20	rs558257355	chr15:53065569-53065570	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
21	rs578221364	chr15:53065599-53065600	Weak transcription Enhancers Strong transcription Bivalent Enhancer	n/a	n/a	Overlapped CNVs	n/a
22	rs8036828	chr15:53065630-53065631	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs193284681	chr15:53065669-53065670	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs6493581	chr15:53065676-53065677	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs144079047	chr15:53065721-53065722	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs542779470	chr15:53065723-53065724	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs561052581	chr15:53065725-53065726	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs183933707	chr15:53065730-53065731	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs35374244	chr15:53065774-53065775	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs561298847	chr15:53065791-53065792	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs2440325	chr15:53065798-53065799	Weak transcription Enhancers Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs10083678	chr15:53065805-53065806	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs148636834	chr15:53065915-53065916	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs547398800	chr15:53065962-53065963	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564880491	chr15:53065974-53065975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs559652386	chr15:53065979-53065980	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs74012476	chr15:53065990-53065991	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs188935041	chr15:53066034-53066035	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs191286362	chr15:53066087-53066088	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs76536349	chr15:53066096-53066097	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs569400473	chr15:53066104-53066105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs559002176	chr15:53066106-53066107	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs143220593	chr15:53066108-53066109	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs529767817	chr15:53066120-53066121	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs534574464	chr15:53066128-53066129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs554050955	chr15:53066168-53066169	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs572359432	chr15:53066178-53066179	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs183481516	chr15:53066202-53066203	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs568358506	chr15:53066254-53066255	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs187162950	chr15:53066270-53066271	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

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
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17053054	CNVD
Breast cancer	22032731	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Hirschsprung''s Disease	21712996	CNVD
Myeloproliferative neoplasm	20015882	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
Ovarian clear cell carcinoma	21343371	CNVD
Myelofibrosis	22110671	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute monocytic leukemia	16498392	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD

Chromatin state (count:1918 , 50 per page) page: 1 2 3 4 5 6 7 ... 39

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:53045800-53070800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr15:53049600-53070600	Weak transcription	H9 Cell Line	embryonic stem cell
3	chr15:53059400-53072400	Weak transcription	HepG2	liver
4	chr15:53059800-53068200	Weak transcription	Pancreas	Pancrea
5	chr15:53063600-53066200	Strong transcription	Liver	Liver
6	chr15:53064600-53065600	Enhancers	NHEK	skin
7	chr15:53064800-53065200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
8	chr15:53065000-53065600	Bivalent Enhancer	Fetal Brain Male	brain
9	chr15:53065000-53065800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
10	chr15:53065000-53065800	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
11	chr15:53066200-53068200	Weak transcription	Liver	Liver
12	chr15:53068200-53069200	Genic enhancers	Liver	Liver
13	chr15:53068200-53069800	Genic enhancers	Pancreas	Pancrea
14	chr15:53069200-53070600	Weak transcription	Liver	Liver
15	chr15:53069800-53073000	Weak transcription	Pancreas	Pancrea
16	chr15:53070400-53070800	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr15:53070400-53071000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
18	chr15:53070600-53070800	Enhancers	iPS-18 Cell Line	embryonic stem cell
19	chr15:53070600-53071000	Enhancers	H9 Cell Line	embryonic stem cell
20	chr15:53070600-53071200	Enhancers	HUES6 Cell Line	embryonic stem cell
21	chr15:53070600-53071400	Enhancers	H1 Cell Line	embryonic stem cell
22	chr15:53070600-53073000	Enhancers	Liver	Liver
23	chr15:53070800-53071000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr15:53070800-53071000	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
25	chr15:53070800-53071000	Enhancers	HUES64 Cell Line	embryonic stem cell
26	chr15:53071000-53071200	Enhancers	iPS-20b Cell Line	embryonic stem cell
27	chr15:53071000-53072000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr15:53071000-53075400	Weak transcription	H9 Cell Line	embryonic stem cell
29	chr15:53071200-53072400	Weak transcription	HUES6 Cell Line	embryonic stem cell
30	chr15:53071400-53071800	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr15:53071800-53072200	Enhancers	Monocytes-CD14+_RO01746	blood
32	chr15:53071800-53072600	Enhancers	Primary monocytes fromperipheralblood	blood
33	chr15:53071800-53073000	Enhancers	H1 Cell Line	embryonic stem cell
34	chr15:53072000-53072200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr15:53072000-53072200	Enhancers	GM12878-XiMat	blood
36	chr15:53072000-53072400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr15:53072000-53072400	Bivalent Enhancer	A549	lung
38	chr15:53072000-53072800	Enhancers	Primary B cells from peripheral blood	blood
39	chr15:53072000-53073400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
40	chr15:53072000-53073400	Bivalent Enhancer	Primary hematopoietic stem cells short term culture	blood
41	chr15:53072200-53072600	Enhancers	Primary B cells from cord blood	blood
42	chr15:53072200-53072600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr15:53072200-53072600	Flanking Active TSS	GM12878-XiMat	blood
44	chr15:53072200-53072800	Enhancers	Primary hematopoietic stem cells	blood
45	chr15:53072200-53073400	Bivalent Enhancer	Colon Smooth Muscle	Colon
46	chr15:53072200-53073600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
47	chr15:53072400-53072600	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
48	chr15:53072400-53072600	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr15:53072400-53072600	Enhancers	Duodenum Mucosa	Duodenum
50	chr15:53072400-53072600	Bivalent Enhancer	Fetal Brain Female	brain

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