Variant report

Variant	nsv457160
Chromosome Location	chr15:56273446-56320235
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1177)
CpG islands
(count:794)
Chromatin interactive
region (count:53)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1177 , 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	chr15:56286628-56286918	K562	blood:	n/a	n/a
2	ARID3A	chr15:56285218-56285455	K562	blood:	n/a	n/a
3	ARID3A	chr15:56290869-56290907	K562	blood:	n/a	n/a
4	ARID3A	chr15:56285729-56285953	HepG2	liver:	n/a	n/a
5	ATF1	chr15:56286965-56287213	K562	blood:	n/a	n/a
6	ATF1	chr15:56295967-56296197	K562	blood:	n/a	n/a
7	ATF1	chr15:56311295-56311472	K562	blood:	n/a	n/a
8	ATF1	chr15:56301135-56301199	K562	blood:	n/a	n/a
9	ATF3	chr15:56295943-56296234	K562	blood:	n/a	chr15:56296138-56296151
10	BACH1	chr15:56285350-56286282	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr15:56286927-56286969	K562	blood:	n/a	n/a
12	BHLHE40	chr15:56310014-56310402	HepG2	liver:	n/a	n/a
13	BHLHE40	chr15:56285172-56286542	K562	blood:	n/a	chr15:56285460-56285476
14	BHLHE40	chr15:56291015-56291031	K562	blood:	n/a	n/a
15	BHLHE40	chr15:56309879-56310348	K562	blood:	n/a	n/a
16	BHLHE40	chr15:56285538-56285951	GM12878	blood:	n/a	n/a
17	BHLHE40	chr15:56298674-56298896	HepG2	liver:	n/a	n/a
18	BRCA1	chr15:56285293-56285463	GM12878	blood:	n/a	n/a
19	BRCA1	chr15:56290670-56291397	Hela-S3	cervix:	n/a	n/a
20	BRCA1	chr15:56285563-56285941	Hela-S3	cervix:	n/a	n/a
21	BRCA1	chr15:56285288-56285308	H1-hESC	embryonic stem cell:	n/a	n/a
22	CBX3	chr15:56285682-56285992	K562	blood:	n/a	n/a
23	CBX3	chr15:56306949-56307149	K562	blood:	n/a	n/a
24	CBX3	chr15:56306952-56307210	K562	blood:	n/a	n/a
25	CCNT2	chr15:56285239-56286486	K562	blood:	n/a	n/a
26	CEBPB	chr15:56309053-56309130	K562	blood:	n/a	n/a
27	CEBPB	chr15:56290772-56291058	IMR90	lung:	n/a	chr15:56290913-56290926 chr15:56290913-56290924
28	CEBPB	chr15:56295983-56296187	A549	lung:	n/a	chr15:56296117-56296128
29	CEBPB	chr15:56297105-56297209	K562	blood:	n/a	n/a
30	CEBPB	chr15:56285127-56285219	K562	blood:	n/a	n/a
31	CEBPB	chr15:56296056-56296169	H1-hESC	embryonic stem cell:	n/a	chr15:56296117-56296128
32	CEBPB	chr15:56286775-56287121	A549	lung:	n/a	chr15:56286825-56286838
33	CEBPB	chr15:56295964-56296254	K562	blood:	n/a	chr15:56296117-56296128
34	CEBPB	chr15:56290525-56291437	Hela-S3	cervix:	n/a	chr15:56290913-56290926 chr15:56290913-56290924
35	CEBPB	chr15:56298541-56298913	IMR90	lung:	n/a	chr15:56298720-56298731
36	CEBPB	chr15:56295986-56296186	IMR90	lung:	n/a	chr15:56296117-56296128
37	CEBPB	chr15:56315403-56315553	HepG2	liver:	n/a	chr15:56315481-56315492
38	CEBPB	chr15:56298546-56298903	A549	lung:	n/a	chr15:56298720-56298731
39	CEBPB	chr15:56295902-56296342	K562	blood:	n/a	chr15:56296117-56296128
40	CEBPB	chr15:56291777-56292507	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr15:56298655-56298882	Hela-S3	cervix:	n/a	chr15:56298720-56298731
42	CEBPB	chr15:56295963-56296294	Hela-S3	cervix:	n/a	chr15:56296117-56296128
43	CEBPB	chr15:56285035-56287150	Hela-S3	cervix:	n/a	chr15:56286825-56286838 chr15:56286689-56286697
44	CEBPB	chr15:56315434-56315641	Hela-S3	cervix:	n/a	chr15:56315481-56315492
45	CEBPB	chr15:56290784-56291085	HepG2	liver:	n/a	chr15:56290913-56290926 chr15:56290913-56290924
46	CEBPB	chr15:56310153-56310358	HepG2	liver:	n/a	n/a
47	CEBPB	chr15:56298629-56298817	K562	blood:	n/a	chr15:56298720-56298731
48	CEBPB	chr15:56298629-56298888	HepG2	liver:	n/a	chr15:56298720-56298731
49	CEBPB	chr15:56290800-56290987	K562	blood:	n/a	chr15:56290913-56290926 chr15:56290913-56290924
50	CEBPB	chr15:56286883-56287057	K562	blood:	n/a	n/a

(count:794 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:56285741-56285791	ECC-1	luminal epithelium:	n/a
2	chr15:56285741-56285791	ECC-1	luminal epithelium:	n/a
3	chr15:56286067-56286117	ovcar-3	ovarian:	n/a
4	chr15:56286150-56286200	HCM	heart:	n/a
5	chr15:56286150-56286200	HNPCEpiC	eye:	n/a
6	chr15:56285761-56285811	AoSMC	blood vessel:	n/a
7	chr15:56285484-56285534	GM12878	blood:	n/a
8	chr15:56285741-56285791	BE2_C	brain:	n/a
9	chr15:56286336-56286386	T-47D	breast:	n/a
10	chr15:56285261-56285311	T-47D	breast:	n/a
11	chr15:56299380-56299430	GM12878	blood:	n/a
12	chr15:56299380-56299430	HCPEpiC	choroid plexus:	n/a
13	chr15:56285741-56285791	SK-N-MC	brain:	n/a
14	chr15:56285741-56285791	IMR90	lung:	fetal
15	chr15:56285741-56285791	CMK	blood:	n/a
16	chr15:56282277-56282327	NHBE	bronchial:	n/a
17	chr15:56286575-56286625	HepG2	liver:	n/a
18	chr15:56290261-56290311	HCF	heart:	n/a
19	chr15:56284168-56284218	LNCaP	prostate:	n/a
20	chr15:56285484-56285534	HCT-116	colon:	n/a
21	chr15:56286150-56286200	AG04450	lung:	fetal
22	chr15:56282277-56282327	HRE	kidney:	n/a
23	chr15:56286283-56286333	HRPEpiC	eye:	n/a
24	chr15:56285261-56285311	HAEpiC	amniotic membrane:	n/a
25	chr15:56282277-56282327	BJ	skin:	n/a
26	chr15:56299380-56299430	ovcar-3	ovarian:	n/a
27	chr15:56285741-56285791	MCF-7	breast:	n/a
28	chr15:56286067-56286117	Caco-2	colon:	n/a
29	chr15:56285484-56285534	HRCEpiC	kidney:	n/a
30	chr15:56285484-56285534	Hepatocyte	liver:	n/a
31	chr15:56299380-56299430	SK-N-SH_RA	brain:	n/a
32	chr15:56284168-56284218	PFSK-1	brain:	n/a
33	chr15:56286575-56286625	AoSMC	blood vessel:	n/a
34	chr15:56286067-56286117	SK-N-SH	brain:	n/a
35	chr15:56285761-56285811	T-47D	breast:	n/a
36	chr15:56286575-56286625	NT2-D1	testis:	n/a
37	chr15:56286067-56286117	HNPCEpiC	eye:	n/a
38	chr15:56284168-56284218	ProgFib	skin:	n/a
39	chr15:56286336-56286386	AG04449	skin:	fetal
40	chr15:56286150-56286200	NB4	blood:	n/a
41	chr15:56282277-56282327	HepG2	liver:	n/a
42	chr15:56286336-56286386	HCF	heart:	n/a
43	chr15:56290261-56290311	GM12892	blood:	n/a
44	chr15:56286575-56286625	HMEC	breast:	n/a
45	chr15:56286150-56286200	K562	blood:	n/a
46	chr15:56282277-56282327	CMK	blood:	n/a
47	chr15:56285741-56285791	HPAEpiC	pulmonary alveolar:	n/a
48	chr15:56285741-56285791	HCPEpiC	choroid plexus:	n/a
49	chr15:56286150-56286200	NH-A	brain:	n/a
50	chr15:56285261-56285311	GM12892	blood:	n/a

(count:53 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:56272827..56275263-chr15:56276968..56278689,2	MCF-7	breast:
2	chr15:56276877..56278529-chr15:56290959..56293005,2	MCF-7	breast:
3	chr15:56275489..56279024-chr15:56279462..56282619,5	K562	blood:
4	chr15:56279620..56282017-chr15:56535404..56538288,2	MCF-7	breast:
5	chr15:56275489..56279024-chr15:56279462..56282619,5	K562	blood:
6	chr15:56281891..56284127-chr15:56288031..56290159,2	K562	blood:
7	chr15:56286939..56288503-chr15:56293657..56295210,2	K562	blood:
8	chr15:56286068..56286594-chr15:56344895..56345645,2	MCF-7	breast:
9	chr15:56284954..56286880-chr15:56299616..56301777,2	K562	blood:
10	chr15:56304158..56307081-chr15:56310322..56313297,2	K562	blood:
11	chr15:56288413..56291274-chr15:56330655..56333525,2	MCF-7	breast:
12	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
13	chr15:56285803..56286769-chr7:144532503..144533132,2	HCT-116	colon:
14	chr1:100503143..100503837-chr15:56285483..56286241,2	Hela-S3	cervix:
15	chr15:56283971..56286834-chr15:56291176..56293680,2	K562	blood:
16	chr14:55737712..55738366-chr15:56285235..56286222,2	Hela-S3	cervix:
17	chr15:56284455..56287261-chr15:56299264..56302045,2	MCF-7	breast:
18	chr15:56284668..56287599-chr15:56288074..56291098,3	K562	blood:
19	chr15:56282101..56284524-chr15:56536077..56539290,3	MCF-7	breast:
20	chr1:145381291..145384278-chr15:56284107..56286728,2	MCF-7	breast:
21	chr15:56308090..56310952-chr15:56323916..56326374,2	MCF-7	breast:
22	chr15:56283238..56284535-chr15:56344426..56345460,6	MCF-7	breast:
23	chr15:56290100..56291758-chr15:56342391..56345191,2	MCF-7	breast:
24	chr15:56282892..56284804-chr15:56387312..56388901,2	MCF-7	breast:
25	chr15:56269452..56273528-chr15:56284245..56287674,5	MCF-7	breast:
26	chr1:152008878..152009756-chr15:56285598..56286362,2	Hela-S3	cervix:
27	chr15:56286939..56288503-chr15:56293657..56295210,2	K562	blood:
28	chr15:56281891..56284127-chr15:56288031..56290159,2	K562	blood:
29	chr15:56299007..56301700-chr15:56309609..56311858,2	MCF-7	breast:
30	chr15:56285499..56287418-chr15:56534884..56536553,2	K562	blood:
31	chr15:56292596..56295463-chr15:56332389..56335036,2	MCF-7	breast:
32	chr15:56309924..56310815-chr15:56344688..56345628,4	MCF-7	breast:
33	chr15:56271136..56275778-chr15:56283975..56288276,6	K562	blood:
34	chr15:56275489..56278398-chr15:56279462..56282619,4	K562	blood:
35	chr15:56286056..56286943-chr15:56344508..56345311,2	MCF-7	breast:
36	chr1:109234674..109235306-chr15:56285708..56286287,2	Hela-S3	cervix:
37	chr1:28994985..28995485-chr15:56285972..56286627,2	Hela-S3	cervix:
38	chr15:56281435..56283774-chr15:56390486..56392704,2	MCF-7	breast:
39	chr1:233748980..233749780-chr15:56285541..56286277,2	Hela-S3	cervix:
40	chr15:56272827..56275263-chr15:56276968..56278689,2	MCF-7	breast:
41	chr15:56271720..56275778-chr15:56283975..56286935,4	K562	blood:
42	chr15:56284455..56287261-chr15:56299264..56302045,2	MCF-7	breast:
43	chr15:56289959..56291765-chr15:56293575..56295875,2	K562	blood:
44	chr15:56285985..56288747-chr15:56326549..56330061,4	MCF-7	breast:
45	chr15:56290352..56292488-chr15:56331467..56333363,2	MCF-7	breast:
46	chr15:56304158..56307081-chr15:56310322..56313297,2	K562	blood:
47	chr15:56276877..56278529-chr15:56290959..56293005,2	MCF-7	breast:
48	chr15:56285724..56286656-chr8:8559373..8559873,2	Hela-S3	cervix:
49	chr15:56275489..56278398-chr15:56279462..56282619,4	K562	blood:
50	chr15:56309948..56310461-chr15:56538175..56538871,2	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RFX7-3	chr15:56285709-56285811	NONHSAT044012
2	lnc-RFX7-2	chr15:56305102-56305262	l_1162_chr15:56293600-56416163_liver
3	lnc-RFX7-2	chr15:56293601-56293799	l_1162_chr15:56293600-56416163_liver
4	lnc-RFX7-3	chr15:56279929-56280199	NONHSAT044012

No data

Variant related genes	Relation type
NEDD4	TF binding region
CNOT6LP1	TF binding region
NEDD4	CpG island
CNOT6LP1	CpG island
ENSG00000151575	chromatin interactions
ENSG00000069869	chromatin interactions
ENSG00000156875	chromatin interactions
ENSG00000230183	chromatin interactions
ENSG00000181827	chromatin interactions
ENSG00000134186	chromatin interactions
ENSG00000258413	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000163191	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000176305	chromatin interactions
ENSG00000162419	chromatin interactions
ENSG00000135750	chromatin interactions
ENSG00000178974	chromatin interactions
ENSG00000253958	chromatin interactions
ENSG00000196511	chromatin interactions

Extended variants
information (count: 1590 )
Associated
traits (count: 58 )

Variant overlapped rSNPs/rCNVs (count:1590 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs8029247	chr15:56273446-56273447	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs138606065	chr15:56273469-56273470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543278580	chr15:56273474-56273475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs189073212	chr15:56273504-56273505	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs373943992	chr15:56273510-56273511	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs141837287	chr15:56273519-56273520	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372671966	chr15:56273528-56273529	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs59382910	chr15:56273565-56273566	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs397735251	chr15:56273574-56273575	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs531546996	chr15:56273576-56273577	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs75434294	chr15:56273603-56273604	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs146285888	chr15:56273610-56273611	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs139514549	chr15:56273635-56273636	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs182473154	chr15:56273664-56273665	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs547599835	chr15:56273686-56273687	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs533956724	chr15:56273697-56273698	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs34774048	chr15:56273725-56273726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567827354	chr15:56273753-56273754	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs527687545	chr15:56273774-56273775	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs536828797	chr15:56273804-56273805	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs556822136	chr15:56273814-56273815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs570358048	chr15:56273833-56273834	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539002309	chr15:56273868-56273869	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs558484868	chr15:56273912-56273913	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs187044736	chr15:56273915-56273916	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs541090896	chr15:56273927-56273928	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554383637	chr15:56273932-56273933	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs576016225	chr15:56273981-56273982	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs574222209	chr15:56273992-56273993	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs4774839	chr15:56274074-56274075	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs563184943	chr15:56274078-56274079	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs570668792	chr15:56274079-56274080	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs532234986	chr15:56274115-56274116	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190668673	chr15:56274166-56274167	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181442686	chr15:56274174-56274175	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs527703527	chr15:56274187-56274188	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs547807791	chr15:56274227-56274228	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs567738349	chr15:56274259-56274260	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs144267521	chr15:56274301-56274302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs550387140	chr15:56274310-56274311	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs368192257	chr15:56274337-56274338	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs539272629	chr15:56274349-56274350	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs148749138	chr15:56274393-56274394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs565636048	chr15:56274396-56274397	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs555968785	chr15:56274418-56274419	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs567685146	chr15:56274440-56274441	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs11632974	chr15:56274443-56274444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs554192055	chr15:56274470-56274471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs574185348	chr15:56274477-56274478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs186086411	chr15:56274529-56274530	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:58)

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
Gastrointestinal stromal cancer	16982739	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
Acute lymphoblastic leukemia	21339820	CNVD
Gastric adenocarcinoma	19115996	CNVD
Congenital diaphragmatic hernia	21341218	CNVD
Holoprosencephaly	21359414	CNVD

Chromatin state (count:858 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:56229600-56282600	Weak transcription	NHLF	lung
2	chr15:56231400-56284200	Weak transcription	Stomach Smooth Muscle	stomach
3	chr15:56236200-56276000	Weak transcription	HUVEC	blood vessel
4	chr15:56236800-56282800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
5	chr15:56243200-56276200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
6	chr15:56248200-56285200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
7	chr15:56251600-56281600	Weak transcription	Osteobl	bone
8	chr15:56253600-56282400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
9	chr15:56257600-56281600	Weak transcription	Fetal Intestine Large	intestine
10	chr15:56257600-56283600	Weak transcription	Duodenum Smooth Muscle	Duodenum
11	chr15:56257600-56283800	Weak transcription	Primary T cells from cord blood	blood
12	chr15:56257800-56273800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
13	chr15:56262800-56274200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
14	chr15:56262800-56276200	Weak transcription	NHEK	skin
15	chr15:56262800-56276400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
16	chr15:56262800-56276600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr15:56262800-56276600	Weak transcription	HMEC	breast
18	chr15:56263000-56275400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
19	chr15:56263800-56282400	Weak transcription	Fetal Intestine Small	intestine
20	chr15:56269400-56282400	Weak transcription	Primary hematopoietic stem cells	blood
21	chr15:56270400-56281600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
22	chr15:56271000-56273800	Weak transcription	A549	lung
23	chr15:56272600-56274000	Enhancers	HSMM	muscle
24	chr15:56272600-56284200	Weak transcription	Lung	lung
25	chr15:56272800-56281600	Weak transcription	Psoas Muscle	Psoas
26	chr15:56273000-56273600	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr15:56273000-56281600	Weak transcription	Primary hematopoietic stem cells short term culture	blood
28	chr15:56273000-56283000	Weak transcription	HSMMtube	muscle
29	chr15:56273600-56274800	Enhancers	Muscle Satellite Cultured Cells	--
30	chr15:56273800-56274800	Enhancers	A549	lung
31	chr15:56273800-56277000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
32	chr15:56274000-56281600	Weak transcription	HSMM	muscle
33	chr15:56274200-56274400	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
34	chr15:56274200-56274400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
35	chr15:56274200-56274400	Enhancers	NH-A	brain
36	chr15:56274200-56274600	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr15:56274400-56283800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
38	chr15:56274400-56283800	Weak transcription	NH-A	brain
39	chr15:56274400-56284000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
40	chr15:56274600-56276200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
41	chr15:56274600-56278000	Weak transcription	Hela-S3	cervix
42	chr15:56274800-56282800	Weak transcription	Muscle Satellite Cultured Cells	--
43	chr15:56274800-56282800	Weak transcription	A549	lung
44	chr15:56275200-56276800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
45	chr15:56275400-56275600	Enhancers	Left Ventricle	heart
46	chr15:56275400-56276000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
47	chr15:56275400-56283000	Weak transcription	Cortex derived primary cultured neurospheres	brain
48	chr15:56275600-56284000	Weak transcription	Aorta	Aorta
49	chr15:56275600-56284200	Weak transcription	Left Ventricle	heart
50	chr15:56276000-56276400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin

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