Variant report

Variant	nsv457203
Chromosome Location	chr15:74308940-74347723
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1090)
CpG islands
(count:1162)
Chromatin interactive
region (count:43)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:1090 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:74346647-74346653	HepG2	liver:	n/a	n/a
2	BACH1	chr15:74341088-74341114	K562	blood:	n/a	n/a
3	BHLHE40	chr15:74340720-74340942	HepG2	liver:	n/a	n/a
4	BHLHE40	chr15:74346490-74346777	GM12878	blood:	n/a	n/a
5	BHLHE40	chr15:74346445-74346835	K562	blood:	n/a	n/a
6	BHLHE40	chr15:74325395-74325601	K562	blood:	n/a	n/a
7	BHLHE40	chr15:74340725-74340894	K562	blood:	n/a	n/a
8	BRCA1	chr15:74340715-74340980	H1-hESC	embryonic stem cell:	n/a	n/a
9	BRCA1	chr15:74346498-74346776	Hela-S3	cervix:	n/a	n/a
10	CEBPB	chr15:74343522-74344134	MCF-7	breast:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
11	CEBPB	chr15:74331722-74331903	K562	blood:	n/a	chr15:74331738-74331755
12	CEBPB	chr15:74329215-74329505	H1-hESC	embryonic stem cell:	n/a	n/a
13	CEBPB	chr15:74343677-74344044	HepG2	liver:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
14	CEBPB	chr15:74343643-74344166	IMR90	lung:	n/a	chr15:74344139-74344151 chr15:74343850-74343863 chr15:74343851-74343862
15	CEBPB	chr15:74343647-74344063	ECC-1	luminal epithelium:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
16	CEBPB	chr15:74344307-74344473	HepG2	liver:	n/a	n/a
17	CEBPB	chr15:74343664-74344051	ECC-1	luminal epithelium:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
18	CEBPB	chr15:74346176-74346712	Hela-S3	cervix:	n/a	n/a
19	CEBPB	chr15:74315635-74315835	HepG2	liver:	n/a	chr15:74315727-74315738
20	CEBPB	chr15:74343690-74344002	K562	blood:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
21	CEBPB	chr15:74343604-74344093	MCF-7	breast:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
22	CEBPB	chr15:74346156-74346504	HepG2	liver:	n/a	n/a
23	CEBPB	chr15:74343739-74343944	K562	blood:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
24	CEBPB	chr15:74343686-74344039	A549	lung:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
25	CEBPB	chr15:74346185-74346432	MCF-7	breast:	n/a	n/a
26	CEBPB	chr15:74343573-74344417	Hela-S3	cervix:	n/a	chr15:74344139-74344151 chr15:74343850-74343863 chr15:74343851-74343862
27	CEBPB	chr15:74346192-74346715	H1-hESC	embryonic stem cell:	n/a	n/a
28	CEBPB	chr15:74346163-74346689	IMR90	lung:	n/a	n/a
29	CEBPB	chr15:74346273-74346391	A549	lung:	n/a	n/a
30	CEBPB	chr15:74346153-74346685	K562	blood:	n/a	n/a
31	CEBPB	chr15:74343670-74344040	K562	blood:	n/a	chr15:74343850-74343863 chr15:74343851-74343862
32	CEBPD	chr15:74331684-74332044	K562	blood:	n/a	n/a
33	CEBPD	chr15:74331597-74332133	K562	blood:	n/a	n/a
34	CHD1	chr15:74340561-74341012	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr15:74343668-74344044	Hela-S3	cervix:	n/a	n/a
36	CHD2	chr15:74340700-74341035	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr15:74346522-74346606	GM12878	blood:	n/a	n/a
38	CHD2	chr15:74346411-74346774	Hela-S3	cervix:	n/a	n/a
39	CTCF	chr15:74346429-74346687	GM19240	blood:	n/a	chr15:74346534-74346555 chr15:74346535-74346543 chr15:74346532-74346550 chr15:74346535-74346548 chr15:74346534-74346542
40	CTCF	chr15:74329260-74329410	NHEK	skin:	n/a	chr15:74329390-74329408
41	CTCF	chr15:74329340-74329490	NHDF-neo	bronchial:	n/a	chr15:74329390-74329408
42	CTCF	chr15:74344490-74344491	GM10266	blood:	n/a	n/a
43	CTCF	chr15:74329300-74329450	WI-38	lung:	n/a	chr15:74329390-74329408
44	CTCF	chr15:74340787-74340968	HepG2	liver:	n/a	chr15:74340895-74340911 chr15:74340897-74340910 chr15:74340896-74340917 chr15:74340894-74340912 chr15:74340897-74340910
45	CTCF	chr15:74346500-74346650	GM12865	blood:	n/a	chr15:74346534-74346555 chr15:74346535-74346543 chr15:74346532-74346550 chr15:74346535-74346548 chr15:74346534-74346542
46	CTCF	chr15:74329195-74329468	A549	lung:	n/a	chr15:74329390-74329408
47	CTCF	chr15:74346457-74346649	HepG2	liver:	n/a	chr15:74346534-74346555 chr15:74346535-74346543 chr15:74346532-74346550 chr15:74346535-74346548 chr15:74346534-74346542
48	CTCF	chr15:74340524-74340720	GM12892	blood:	n/a	n/a
49	CTCF	chr15:74332760-74332910	AG04449	skin:	n/a	n/a
50	CTCF	chr15:74346500-74346650	GM12801	blood:	n/a	chr15:74346534-74346555 chr15:74346535-74346543 chr15:74346532-74346550 chr15:74346535-74346548 chr15:74346534-74346542

(count:1162 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:74314816-74314866	HRE	kidney:	n/a
2	chr15:74315710-74315760	BJ	skin:	n/a
3	chr15:74314816-74314866	HCM	heart:	n/a
4	chr15:74314816-74314866	HRE	kidney:	n/a
5	chr15:74315710-74315760	BJ	skin:	n/a
6	chr15:74314816-74314866	HCM	heart:	n/a
7	chr15:74335673-74335723	SK-N-SH	brain:	n/a
8	chr15:74315710-74315760	HEEpiC	esophagus:	n/a
9	chr15:74315331-74315381	HCPEpiC	choroid plexus:	n/a
10	chr15:74315331-74315381	T-47D	breast:	n/a
11	chr15:74315179-74315229	BE2_C	brain:	n/a
12	chr15:74315179-74315229	MCF-7	breast:	n/a
13	chr15:74334701-74334751	HepG2	liver:	n/a
14	chr15:74315710-74315760	HAEpiC	amniotic membrane:	n/a
15	chr15:74344979-74345029	U87	brain:	n/a
16	chr15:74343476-74343526	SKMC	muscle:	n/a
17	chr15:74314816-74314866	HEEpiC	esophagus:	n/a
18	chr15:74315179-74315229	NT2-D1	testis:	n/a
19	chr15:74335673-74335723	HCT-116	colon:	n/a
20	chr15:74346033-74346083	NT2-D1	testis:	n/a
21	chr15:74315179-74315229	GM12891	blood:	n/a
22	chr15:74314816-74314866	ProgFib	skin:	n/a
23	chr15:74315331-74315381	MCF10A-Er-Src	breast:	n/a
24	chr15:74318422-74318472	AG04449	skin:	fetal
25	chr15:74315539-74315589	PFSK-1	brain:	n/a
26	chr15:74315331-74315381	HNPCEpiC	eye:	n/a
27	chr15:74317780-74317830	MCF-7	breast:	n/a
28	chr15:74317780-74317830	IMR90	lung:	fetal
29	chr15:74346033-74346083	AG09309	skin:	n/a
30	chr15:74315331-74315381	GM12878	blood:	n/a
31	chr15:74315539-74315589	BJ	skin:	n/a
32	chr15:74343476-74343526	Hepatocyte	liver:	n/a
33	chr15:74339856-74339906	HRPEpiC	eye:	n/a
34	chr15:74328425-74328475	CMK	blood:	n/a
35	chr15:74346033-74346083	ECC-1	luminal epithelium:	n/a
36	chr15:74314816-74314866	AG09319	gingival:	n/a
37	chr15:74345103-74345153	MCF-7	breast:	n/a
38	chr15:74318422-74318472	LNCaP	prostate:	n/a
39	chr15:74317259-74317309	SAEC	small airway:	n/a
40	chr15:74335673-74335723	A549	lung:	n/a
41	chr15:74315179-74315229	AG10803	skin:	n/a
42	chr15:74312279-74312329	HRPEpiC	eye:	n/a
43	chr15:74346033-74346083	GM12892	blood:	n/a
44	chr15:74317259-74317309	GM19239	blood:	n/a
45	chr15:74315710-74315760	GM12892	blood:	n/a
46	chr15:74345103-74345153	SKMC	muscle:	n/a
47	chr15:74312279-74312329	GM19239	blood:	n/a
48	chr15:74315331-74315381	HL-60	blood:	n/a
49	chr15:74317259-74317309	Hepatocyte	liver:	n/a
50	chr15:74315539-74315589	HCT-116	colon:	n/a

(count:43 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:74224754..74226933-chr15:74339515..74341343,2	MCF-7	breast:
2	chr15:74282640..74284615-chr15:74313984..74316844,2	MCF-7	breast:
3	chr15:74264982..74265988-chr15:74340408..74341918,5	K562	blood:
4	chr15:74330729..74333109-chr15:74334617..74337154,3	K562	blood:
5	chr15:74176824..74179799-chr15:74328543..74330066,2	MCF-7	breast:
6	chr15:74265052..74265856-chr15:74340481..74341404,2	MCF-7	breast:
7	chr15:74243215..74244120-chr15:74328879..74329879,2	MCF-7	breast:
8	chr15:74265318..74265924-chr15:74340447..74341070,3	MCF-7	breast:
9	chr15:74284477..74286185-chr15:74319336..74321648,2	MCF-7	breast:
10	chr15:74346287..74347045-chr15:74614632..74615538,3	MCF-7	breast:
11	chr15:74284343..74287090-chr15:74322488..74325455,2	K562	blood:
12	chr15:74328869..74331984-chr15:74335288..74339582,4	MCF-7	breast:
13	chr15:74314012..74317004-chr15:74331925..74334688,2	K562	blood:
14	chr15:74284750..74286727-chr15:74339557..74341307,2	K562	blood:
15	chr15:57668365..57669086-chr15:74345790..74346310,2	HCT-116	colon:
16	chr15:74265011..74265899-chr15:74328914..74329841,6	MCF-7	breast:
17	chr15:74265025..74265814-chr15:74329334..74329841,2	K562	blood:
18	chr15:74340832..74341338-chr15:74614392..74615111,2	K562	blood:
19	chr15:74346506..74347022-chr15:74612599..74613302,2	MCF-7	breast:
20	chr15:74330729..74333109-chr15:74334617..74337154,3	K562	blood:
21	chr15:74328869..74331984-chr15:74335288..74339582,4	MCF-7	breast:
22	chr15:74264967..74265911-chr15:74346172..74346877,2	MCF-7	breast:
23	chr15:74264988..74266186-chr15:74328671..74329935,19	MCF-7	breast:
24	chr15:74340758..74341346-chr15:74614631..74615308,2	MCF-7	breast:
25	chr15:74346480..74347030-chr15:74612757..74613449,2	MCF-7	breast:
26	chr15:74340833..74341392-chr15:74600254..74600808,2	MCF-7	breast:
27	chr15:74346036..74347051-chr15:74419547..74420472,4	MCF-7	breast:
28	chr15:74303068..74303808-chr15:74316250..74317180,2	MCF-7	breast:
29	chr15:74283820..74286284-chr15:74308005..74310945,2	MCF-7	breast:
30	chr15:74218748..74221720-chr15:74327759..74329413,2	MCF-7	breast:
31	chr15:74310869..74312553-chr15:74315639..74317174,2	MCF-7	breast:
32	chr15:74334928..74336787-chr15:74343703..74345975,2	MCF-7	breast:
33	chr15:74346094..74347046-chr15:74614640..74615508,4	K562	blood:
34	chr15:74264224..74266446-chr15:74328782..74330811,3	MCF-7	breast:
35	chr15:74311100..74312963-chr15:74315126..74316880,2	MCF-7	breast:
36	chr15:74310869..74312553-chr15:74315639..74317174,2	MCF-7	breast:
37	chr15:74314012..74317004-chr15:74331925..74334688,2	K562	blood:
38	chr15:74282684..74284862-chr15:74339446..74341891,2	K562	blood:
39	chr15:74312798..74315530-chr15:74325452..74327125,2	K562	blood:
40	chr15:74346274..74346810-chr15:74666060..74666858,2	MCF-7	breast:
41	chr15:74277650..74279742-chr15:74319526..74321446,2	MCF-7	breast:
42	chr15:74301606..74304928-chr15:74311289..74313632,4	MCF-7	breast:
43	chr15:74334928..74336787-chr15:74343703..74345975,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ISLR2-2	chr15:74335330-74335683	NONHSAT047197
2	lnc-ISLR2-3	chr15:74325497-74325546	NONHSAT047195
3	lnc-ISLR2-3	chr15:74325510-74325718	NONHSAT047196
4	lnc-ISLR2-3	chr15:74324736-74325056	NONHSAT047195
5	lnc-ISLR2-2	chr15:74333670-74333911	NONHSAT047197
6	lnc-PML-2	chr15:74346640-74347125	XLOC_011309

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	PML	hsa-miR-378a-3p	chr15:74335348-74335368

Variant related genes	Relation type
PML	TF binding region
PML	CpG island
ENSG00000128849	chromatin interactions
ENSG00000129038	chromatin interactions
ENSG00000261801	chromatin interactions
ENSG00000167178	chromatin interactions
ENSG00000067221	chromatin interactions
ENSG00000140464	chromatin interactions
MAML1	miRNA target sites

Extended variants
information (count: 1455 )
Associated
traits (count: 72 )

Variant overlapped rSNPs/rCNVs (count:1455 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4886844	chr15:74308940-74308941	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs536080899	chr15:74308978-74308979	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs570901808	chr15:74309076-74309077	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs201224633	chr15:74309093-74309094	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs535120869	chr15:74309099-74309100	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs547070848	chr15:74309105-74309106	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs535665071	chr15:74309133-74309134	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs371838639	chr15:74309177-74309178	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs568579219	chr15:74309186-74309187	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs374833746	chr15:74309205-74309206	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs184085276	chr15:74309207-74309208	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs576236107	chr15:74309229-74309230	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs549457883	chr15:74309261-74309262	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557251653	chr15:74309272-74309273	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs543068798	chr15:74309298-74309299	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs186942672	chr15:74309326-74309327	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs12910596	chr15:74309373-74309374	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs12910581	chr15:74309385-74309386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs372711911	chr15:74309413-74309414	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs12911984	chr15:74309472-74309473	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
21	rs551265981	chr15:74309495-74309496	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574212300	chr15:74309627-74309628	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542034299	chr15:74309630-74309631	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs563938875	chr15:74309635-74309636	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs546286631	chr15:74309672-74309673	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs369671350	chr15:74309699-74309700	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs531104448	chr15:74309713-74309714	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs571455649	chr15:74309726-74309727	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs12917179	chr15:74309727-74309728	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs377524496	chr15:74309785-74309786	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12324916	chr15:74309800-74309801	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs566879611	chr15:74309801-74309802	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs373081911	chr15:74309813-74309814	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs138089719	chr15:74309858-74309859	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs540620915	chr15:74309871-74309872	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs375972169	chr15:74309932-74309933	Weak transcription Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs529417809	chr15:74310080-74310081	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs548065910	chr15:74310121-74310122	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs78237933	chr15:74310145-74310146	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376334324	chr15:74310195-74310196	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375486561	chr15:74310225-74310226	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs192980787	chr15:74310317-74310318	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs558388187	chr15:74310324-74310325	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs570427429	chr15:74310385-74310386	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs564551086	chr15:74310398-74310399	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs532122174	chr15:74310440-74310441	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs552575105	chr15:74310443-74310444	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs574431388	chr15:74310459-74310460	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs556872104	chr15:74310506-74310507	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541951720	chr15:74310539-74310540	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:72)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	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
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
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
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Breast cancer	17133270	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Gastrointestinal stromal cancer	20877625	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Prostate cancer	16573809	CNVD
Autism	17322880	CNVD
phobic disorder	16773131	CNVD
Autism	21480499	CNVD
Disorders of sex development	22290220	CNVD
Mental retardation	19951919	CNVD
Mental retardation	16773131	CNVD
T-cell lymphomas	19863542	CNVD
15q24 microdeletion syndrome	22180641	CNVD
15q24 microdeletion syndrome	19921647	CNVD
Disease	22216833	CNVD
Mental retardation	17360722	CNVD
15q24 microdeletion syndrome	22216833	CNVD
15q24 microdeletion syndrome	22283845	CNVD
Developmental delay	17932688	CNVD
craniofacial dysmorphism	17932688	CNVD
digital and genital abnormalities	17932688	CNVD
Breast cancer	21364760	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Bipolar disorder	19114987	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1710 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:74288200-74331000	Weak transcription	Fetal Heart	heart
2	chr15:74289800-74331000	Weak transcription	Pancreatic Islets	Pancreatic Islet
3	chr15:74290000-74314800	Weak transcription	Brain Cingulate Gyrus	brain
4	chr15:74291000-74311200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
5	chr15:74291000-74314800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr15:74291000-74315000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr15:74291000-74315200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
8	chr15:74291800-74314800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr15:74292000-74315200	Weak transcription	Fetal Brain Female	brain
10	chr15:74292000-74329200	Weak transcription	Fetal Brain Male	brain
11	chr15:74296600-74315200	Weak transcription	HUES48 Cell Line	embryonic stem cell
12	chr15:74296800-74315200	Weak transcription	Brain Germinal Matrix	brain
13	chr15:74297000-74315200	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr15:74297000-74315600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr15:74298200-74311200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr15:74299200-74315400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
17	chr15:74299400-74315400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
18	chr15:74300000-74314800	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr15:74300400-74315800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr15:74300600-74315200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr15:74300800-74315200	Weak transcription	H9 Cell Line	embryonic stem cell
22	chr15:74300800-74315200	Weak transcription	Brain Inferior Temporal Lobe	brain
23	chr15:74300800-74315200	Weak transcription	Placenta Amnion	Placenta Amnion
24	chr15:74300800-74326000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
25	chr15:74302400-74312800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
26	chr15:74302400-74331000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr15:74303600-74331600	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr15:74303800-74315000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
29	chr15:74304000-74314800	Weak transcription	Brain Hippocampus Middle	brain
30	chr15:74304000-74314800	Weak transcription	NH-A	brain
31	chr15:74304000-74315200	Weak transcription	Brain Anterior Caudate	brain
32	chr15:74304000-74315200	Weak transcription	Brain Substantia Nigra	brain
33	chr15:74304000-74315200	Weak transcription	Psoas Muscle	Psoas
34	chr15:74304000-74326000	Weak transcription	Fetal Kidney	kidney
35	chr15:74304200-74311200	Weak transcription	K562	blood
36	chr15:74304200-74311200	Weak transcription	NHDF-Ad	bronchial
37	chr15:74304200-74314400	Weak transcription	Dnd41	blood
38	chr15:74304200-74314600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
39	chr15:74304200-74314800	Weak transcription	Ovary	ovary
40	chr15:74304200-74314800	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr15:74304200-74315000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
42	chr15:74304200-74315000	Weak transcription	Skeletal Muscle Female	skeletal muscle
43	chr15:74304200-74315200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr15:74304200-74315200	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
45	chr15:74304200-74315200	Weak transcription	Colonic Mucosa	Colon
46	chr15:74304200-74315200	Weak transcription	Fetal Lung	lung
47	chr15:74304200-74315200	Weak transcription	Gastric	stomach
48	chr15:74304200-74315200	Weak transcription	Pancreas	Pancrea
49	chr15:74304200-74315400	Weak transcription	Brain Angular Gyrus	brain
50	chr15:74304200-74316800	Weak transcription	Right Atrium	heart

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