Variant report

Variant	nsv568916
Chromosome Location	chr15:32968923-33023951
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:32992683-32993284	HepG2	liver:	n/a	n/a
2	ARID3A	chr15:32968901-32970113	HepG2	liver:	n/a	n/a
3	ARID3A	chr15:32989290-32989712	K562	blood:	n/a	n/a
4	ARID3A	chr15:32993779-32993979	HepG2	liver:	n/a	n/a
5	ARID3A	chr15:32980253-32980742	HepG2	liver:	n/a	n/a
6	ATF2	chr15:33007413-33007823	GM12878	blood:	n/a	n/a
7	ATF3	chr15:32969327-32969797	A549	lung:	n/a	n/a
8	BACH1	chr15:33023053-33023176	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr15:33010995-33011445	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr15:33010235-33010617	H1-hESC	embryonic stem cell:	n/a	n/a
11	BATF	chr15:33007478-33007843	GM12878	blood:	n/a	n/a
12	BATF	chr15:33007468-33007849	GM12878	blood:	n/a	n/a
13	BATF	chr15:33015759-33016097	GM12878	blood:	n/a	n/a
14	BATF	chr15:33015690-33016119	GM12878	blood:	n/a	n/a
15	BATF	chr15:33015363-33015714	GM12878	blood:	n/a	n/a
16	BCL11A	chr15:33007430-33007809	GM12878	blood:	n/a	n/a
17	BCL11A	chr15:33015690-33016111	GM12878	blood:	n/a	chr15:33016005-33016014 chr15:33015775-33015784
18	BCL11A	chr15:33015778-33016035	GM12878	blood:	n/a	chr15:33016005-33016014
19	BCL3	chr15:32969243-32969938	A549	lung:	n/a	n/a
20	BCLAF1	chr15:33015721-33016200	GM12878	blood:	n/a	chr15:33016005-33016014 chr15:33015775-33015784
21	BHLHE40	chr15:32991097-32991627	HepG2	liver:	n/a	chr15:32991378-32991387 chr15:32991377-32991386 chr15:32991377-32991386 chr15:32991376-32991385 chr15:32991375-32991388 chr15:32991371-32991392
22	BHLHE40	chr15:32992683-32993266	HepG2	liver:	n/a	n/a
23	BHLHE40	chr15:32991210-32991553	K562	blood:	n/a	chr15:32991378-32991387 chr15:32991377-32991386 chr15:32991377-32991386 chr15:32991376-32991385 chr15:32991375-32991388 chr15:32991371-32991392
24	BHLHE40	chr15:33022963-33023334	K562	blood:	n/a	n/a
25	BHLHE40	chr15:32980219-32980822	HepG2	liver:	n/a	n/a
26	BHLHE40	chr15:32996279-32996375	A549	lung:	n/a	n/a
27	BRCA1	chr15:32992356-32992453	GM12878	blood:	n/a	n/a
28	CCNT2	chr15:33022997-33023204	K562	blood:	n/a	n/a
29	CEBPB	chr15:32969372-32969743	MCF-7	breast:	n/a	chr15:32969552-32969563
30	CEBPB	chr15:32974376-32975621	IMR90	lung:	n/a	chr15:32974966-32974979 chr15:32974967-32974978
31	CEBPB	chr15:32977788-32978131	IMR90	lung:	n/a	n/a
32	CEBPB	chr15:32979773-32980555	IMR90	lung:	n/a	n/a
33	CEBPB	chr15:32979663-32980788	A549	lung:	n/a	n/a
34	CEBPB	chr15:32980016-32980653	HepG2	liver:	n/a	n/a
35	CEBPB	chr15:32969360-32969909	A549	lung:	n/a	chr15:32969552-32969563
36	CEBPB	chr15:32969337-32969821	A549	lung:	n/a	chr15:32969552-32969563
37	CEBPB	chr15:33014097-33014256	HepG2	liver:	n/a	chr15:33014154-33014165 chr15:33014154-33014167
38	CEBPB	chr15:32969434-32969671	HepG2	liver:	n/a	chr15:32969552-32969563
39	CEBPB	chr15:32969366-32969945	HepG2	liver:	n/a	chr15:32969552-32969563
40	CEBPB	chr15:32969406-32969747	HepG2	liver:	n/a	chr15:32969552-32969563
41	CEBPB	chr15:32969368-32969757	MCF-7	breast:	n/a	chr15:32969552-32969563
42	CEBPB	chr15:32969364-32969839	HepG2	liver:	n/a	chr15:32969552-32969563
43	CEBPB	chr15:32969289-32970011	A549	lung:	n/a	chr15:32969552-32969563
44	CEBPB	chr15:33020629-33020943	IMR90	lung:	n/a	n/a
45	CEBPB	chr15:32969383-32969719	K562	blood:	n/a	chr15:32969552-32969563
46	CEBPB	chr15:32974701-32975230	A549	lung:	n/a	chr15:32974966-32974979 chr15:32974967-32974978
47	CEBPB	chr15:32975888-32976938	IMR90	lung:	n/a	n/a
48	CEBPB	chr15:33001958-33002217	IMR90	lung:	n/a	n/a
49	CEBPB	chr15:32969373-32969937	IMR90	lung:	n/a	chr15:32969552-32969563
50	CEBPB	chr15:32969369-32969830	Hela-S3	cervix:	n/a	chr15:32969552-32969563

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:33009531-33009581	NB4	blood:	n/a
2	chr15:33006030-33006080	T-47D	breast:	n/a
3	chr15:33011166-33011216	HRE	kidney:	n/a
4	chr15:33009531-33009581	ECC-1	luminal epithelium:	n/a
5	chr15:33013972-33014022	HRPEpiC	eye:	n/a
6	chr15:33023586-33023636	GM12878	blood:	n/a
7	chr15:33011441-33011491	HCM	heart:	n/a
8	chr15:33010399-33010449	Hepatocyte	liver:	n/a
9	chr15:32983650-32983700	Hela-S3	cervix:	n/a
10	chr15:33023586-33023636	HL-60	blood:	n/a
11	chr15:33011166-33011216	K562	blood:	n/a
12	chr15:33011166-33011216	ProgFib	skin:	n/a
13	chr15:33006030-33006080	AG10803	skin:	n/a
14	chr15:33010536-33010586	AG04450	lung:	fetal
15	chr15:33010399-33010449	U87	brain:	n/a
16	chr15:33023237-33023287	RPTEC	kidney:	n/a
17	chr15:32984867-32984917	HL-60	blood:	n/a
18	chr15:33009409-33009459	HNPCEpiC	eye:	n/a
19	chr15:33011441-33011491	GM12891	blood:	n/a
20	chr15:33010143-33010193	HCPEpiC	choroid plexus:	n/a
21	chr15:33006030-33006080	GM06990	blood:	n/a
22	chr15:33009498-33009548	T-47D	breast:	n/a
23	chr15:33010143-33010193	LNCaP	prostate:	n/a
24	chr15:32999748-32999798	GM12878	blood:	n/a
25	chr15:33011441-33011491	ovcar-3	ovarian:	n/a
26	chr15:33010143-33010193	K562	blood:	n/a
27	chr15:33010399-33010449	ECC-1	luminal epithelium:	n/a
28	chr15:32984867-32984917	AoSMC	blood vessel:	n/a
29	chr15:33023586-33023636	U87	brain:	n/a
30	chr15:33009531-33009581	MCF-7	breast:	n/a
31	chr15:33013972-33014022	GM19239	blood:	n/a
32	chr15:32983650-32983700	SK-N-SH_RA	brain:	n/a
33	chr15:33012608-33012658	ovcar-3	ovarian:	n/a
34	chr15:33010399-33010449	AG09309	skin:	n/a
35	chr15:32999748-32999798	AG04449	skin:	fetal
36	chr15:33013972-33014022	Caco-2	colon:	n/a
37	chr15:33011166-33011216	H1-hESC	embryonic stem cell:	embryo
38	chr15:33011185-33011235	HepG2	liver:	n/a
39	chr15:33009531-33009581	HRE	kidney:	n/a
40	chr15:33009531-33009581	HRPEpiC	eye:	n/a
41	chr15:33023586-33023636	GM06990	blood:	n/a
42	chr15:33010399-33010449	RPTEC	kidney:	n/a
43	chr15:33023586-33023636	SK-N-SH	brain:	n/a
44	chr15:33011185-33011235	AG09309	skin:	n/a
45	chr15:33010536-33010586	HAEpiC	amniotic membrane:	n/a
46	chr15:32983650-32983700	ProgFib	skin:	n/a
47	chr15:33011695-33011745	HL-60	blood:	n/a
48	chr15:33012608-33012658	HNPCEpiC	eye:	n/a
49	chr15:33011695-33011745	AG04449	skin:	fetal
50	chr15:33006030-33006080	BE2_C	brain:	n/a

No.	Distal block	Cell Line	Cell type
1	chr15:33002373..33004292-chr15:33005569..33008001,2	K562	blood:
2	chr15:32962834..32965663-chr15:32971694..32973378,2	MCF-7	breast:
3	chr15:32958760..32961462-chr15:33012988..33014927,2	K562	blood:
4	chr15:32979184..32981622-chr15:32988121..32990602,2	K562	blood:
5	chr15:33023317..33025031-chr15:33032090..33034527,2	MCF-7	breast:
6	chr15:32979184..32981622-chr15:32988121..32990602,2	K562	blood:
7	chr15:33002373..33004292-chr15:33005569..33008001,2	K562	blood:

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FMN1-1	chr15:33009471-33011208	ENSG00000259721.1
2	lnc-FMN1-1	chr15:33010302-33010565	ENSG00000259721.1
3	lnc-FMN1-1	chr15:33010746-33011055	ENSG00000259721.1
4	lnc-GREM1-1	chr15:32983911-32984505	NONHSAT041523
5	lnc-FMN1-1	chr15:33010746-33011066	NR_109767
6	lnc-GREM1-1	chr15:32976617-32976870	NONHSAT041523
7	lnc-FMN1-1	chr15:33010302-33010565	NR_109767

Variant related genes	Relation type
ENSG00000259721	TF binding region
GREM1	TF binding region
SCG5	TF binding region
ENSG00000241818	TF binding region
ENSG00000259721	CpG island
GREM1	CpG island
SCG5	CpG island
ENSG00000241818	CpG island
ENSG00000241818	chromatin interactions
ENSG00000166922	chromatin interactions

Extended variants
information (count: 2310 )
Associated
traits (count: 92 )

Variant overlapped rSNPs/rCNVs (count:2310 , 50 per page) page: 1 2 3 4 5 6 7 ... 47

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7170561	chr15:32968923-32968924	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs16964893	chr15:32968930-32968931	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs7170735	chr15:32968998-32968999	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs559939244	chr15:32969018-32969019	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs571963899	chr15:32969080-32969081	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs541255440	chr15:32969118-32969119	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs12898633	chr15:32969153-32969154	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs564444555	chr15:32969154-32969155	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs139725355	chr15:32969238-32969239	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs144272538	chr15:32969296-32969297	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs550176824	chr15:32969306-32969307	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs562146240	chr15:32969327-32969328	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs529420387	chr15:32969389-32969390	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs10519737	chr15:32969457-32969458	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs542214256	chr15:32969472-32969473	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs566278802	chr15:32969476-32969477	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs560727714	chr15:32969494-32969495	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs551785622	chr15:32969538-32969539	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs570358663	chr15:32969572-32969573	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs146591063	chr15:32969626-32969627	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs555756297	chr15:32969640-32969641	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs567788791	chr15:32969666-32969667	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs376299387	chr15:32969694-32969695	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs553511566	chr15:32969743-32969744	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs572136173	chr15:32969761-32969762	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs546024450	chr15:32969774-32969775	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs77317481	chr15:32969787-32969788	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs576320391	chr15:32969794-32969795	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
29	rs190894309	chr15:32969797-32969798	Enhancers Weak transcription Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs113893425	chr15:32969837-32969838	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs112857525	chr15:32969838-32969839	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs28688414	chr15:32969909-32969910	Enhancers Weak transcription Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs140020127	chr15:32970028-32970029	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs118136985	chr15:32970038-32970039	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs7177176	chr15:32970057-32970058	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
36	rs533344278	chr15:32970140-32970141	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs6494576	chr15:32970143-32970144	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs11633548	chr15:32970156-32970157	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs182654604	chr15:32970160-32970161	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs531258516	chr15:32970164-32970165	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs532288762	chr15:32970167-32970168	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs187978353	chr15:32970171-32970172	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs149761390	chr15:32970183-32970184	Enhancers Weak transcription Active TSS Flanking Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs16965041	chr15:32970201-32970202	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs553446337	chr15:32970241-32970242	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
46	rs6494577	chr15:32970262-32970263	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs539241301	chr15:32970285-32970286	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
48	rs537721248	chr15:32970332-32970333	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
49	rs17841121	chr15:32970333-32970334	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs145711709	chr15:32970350-32970351	Weak transcription Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:92)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	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
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Autism	17322880	CNVD
Prader-willi syndrome	19329560	CNVD
Autism	17999366	CNVD
Autism	17901113	CNVD
Neurodevelopmental disorder	17015230	CNVD
Autism	18414403	CNVD
Neurocytoma	17123091	CNVD
Mental retardation	18923513	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
Gastrointestinal stromal cancer	20818650	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	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
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Autism	19521722	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Autism	19050728	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	18990708	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Schizophrenia	19443537	CNVD
Epilepsy	20923578	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Olfactory neuroblastoma	18408657	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Pancreatic cancer	17952125	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:1196 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:32952200-32972800	Weak transcription	Fetal Brain Female	brain
2	chr15:32956200-32973800	Weak transcription	HSMM	muscle
3	chr15:32961200-32976200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr15:32961200-32980200	Weak transcription	Thymus	Thymus
5	chr15:32961600-32969400	Weak transcription	NH-A	brain
6	chr15:32962600-32969400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr15:32962600-32969600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr15:32963000-32974200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
9	chr15:32963200-32969600	Weak transcription	Hela-S3	cervix
10	chr15:32963400-32969600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
11	chr15:32963600-32969400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr15:32963800-32969400	Weak transcription	HUES6 Cell Line	embryonic stem cell
13	chr15:32964200-32969400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr15:32964600-32990800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr15:32964800-32969000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
16	chr15:32964800-32993800	Weak transcription	Fetal Brain Male	brain
17	chr15:32965000-32969400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
18	chr15:32965000-32974000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr15:32965000-32983600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
20	chr15:32967000-32969600	Weak transcription	Esophagus	oesophagus
21	chr15:32967600-32969400	Enhancers	A549	lung
22	chr15:32967800-32969800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
23	chr15:32967800-32969800	Enhancers	Brain Angular Gyrus	brain
24	chr15:32967800-32970000	Enhancers	Brain Hippocampus Middle	brain
25	chr15:32967800-32970200	Enhancers	Brain Inferior Temporal Lobe	brain
26	chr15:32967800-32970200	Enhancers	Brain Substantia Nigra	brain
27	chr15:32968000-32969400	Weak transcription	NHDF-Ad	bronchial
28	chr15:32968000-32970000	Enhancers	Brain Anterior Caudate	brain
29	chr15:32968200-32969400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
30	chr15:32968200-32969400	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr15:32968200-32969400	Weak transcription	Osteobl	bone
32	chr15:32968200-32969800	Enhancers	Pancreatic Islets	Pancreatic Islet
33	chr15:32968200-32970000	Enhancers	Cortex derived primary cultured neurospheres	brain
34	chr15:32968200-32970200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:32968400-32969400	Enhancers	HepG2	liver
36	chr15:32968400-32969600	Enhancers	Liver	Liver
37	chr15:32968400-32969600	Weak transcription	Stomach Smooth Muscle	stomach
38	chr15:32968800-32969200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr15:32968800-32969600	Weak transcription	Brain Cingulate Gyrus	brain
40	chr15:32968800-32972800	Weak transcription	Brain Germinal Matrix	brain
41	chr15:32968800-32974000	Weak transcription	NHEK	skin
42	chr15:32968800-32974200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr15:32968800-32974200	Weak transcription	Duodenum Smooth Muscle	Duodenum
44	chr15:32969000-32970200	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
45	chr15:32969200-32970200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr15:32969400-32969600	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
47	chr15:32969400-32969800	Enhancers	Fetal Intestine Small	intestine
48	chr15:32969400-32969800	Active TSS	HepG2	liver
49	chr15:32969400-32970000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
50	chr15:32969400-32970000	Enhancers	H9 Cell Line	embryonic stem cell

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