Variant report

Variant	nsv569342
Chromosome Location	chr15:49529302-49549943
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:144)
CpG islands
(count:183)
Chromatin interactive
region (count:15)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:144 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr15:49535098-49535236	K562	blood:	n/a	n/a
2	ATF3	chr15:49535104-49535341	K562	blood:	n/a	n/a
3	BACH1	chr15:49535125-49535374	H1-hESC	embryonic stem cell:	n/a	n/a
4	BHLHE40	chr15:49535202-49535371	K562	blood:	n/a	n/a
5	CEBPB	chr15:49530234-49531016	IMR90	lung:	n/a	chr15:49530331-49530348
6	CEBPB	chr15:49530260-49530498	Hela-S3	cervix:	n/a	chr15:49530331-49530348
7	CEBPB	chr15:49529623-49529721	K562	blood:	n/a	chr15:49529629-49529642 chr15:49529629-49529642 chr15:49529631-49529642
8	CEBPB	chr15:49535064-49535390	IMR90	lung:	n/a	n/a
9	CEBPB	chr15:49547716-49548421	Hela-S3	cervix:	n/a	n/a
10	CTCF	chr15:49535220-49535370	HBMEC	blood vessel:	n/a	n/a
11	CTCF	chr15:49535180-49535330	HCPEpiC	choroid plexus:	n/a	n/a
12	CTCF	chr15:49531440-49531590	SAEC	small airway:	n/a	n/a
13	CTCF	chr15:49535160-49535310	HPAF	blood vessel:	n/a	n/a
14	CTCF	chr15:49549260-49549410	HRPEpiC	eye:	n/a	n/a
15	CTCF	chr15:49535060-49535210	AG09319	gingival:	n/a	n/a
16	CTCF	chr15:49542318-49542350	Lung_OC	lung:	n/a	n/a
17	CTCF	chr15:49529300-49529450	HCPEpiC	choroid plexus:	n/a	n/a
18	CTCF	chr15:49535160-49535310	HPF	lung:	n/a	n/a
19	CTCF	chr15:49535200-49535350	AG04450	lung:	n/a	n/a
20	CTCF	chr15:49533554-49533622	LNCaP	prostate:	n/a	n/a
21	CTCF	chr15:49535220-49535370	HCPEpiC	choroid plexus:	n/a	n/a
22	CTCF	chr15:49535180-49535330	HPF	lung:	n/a	n/a
23	CTCF	chr15:49548660-49548810	AoAF	blood vessel:	n/a	n/a
24	CTCF	chr15:49535140-49535290	HPAF	blood vessel:	n/a	n/a
25	CUX1	chr15:49537013-49537019	GM12878	blood:	n/a	n/a
26	EBF1	chr15:49536936-49536954	GM12878	blood:	n/a	n/a
27	EBF1	chr15:49541484-49541496	GM12878	blood:	n/a	n/a
28	EP300	chr15:49530392-49531184	SK-N-SH	brain:	n/a	n/a
29	EP300	chr15:49529875-49532539	SK-N-SH	brain:	n/a	chr15:49531958-49531972 chr15:49530330-49530344
30	EP300	chr15:49535143-49535405	SK-N-SH_RA	brain:	n/a	n/a
31	EP300	chr15:49529138-49529425	SK-N-SH_RA	brain:	n/a	n/a
32	EP300	chr15:49534225-49534386	K562	blood:	n/a	n/a
33	EP300	chr15:49529083-49529457	SK-N-SH_RA	brain:	n/a	chr15:49529129-49529143
34	EP300	chr15:49530432-49531029	SK-N-SH_RA	brain:	n/a	n/a
35	EP300	chr15:49530470-49530983	SK-N-SH_RA	brain:	n/a	n/a
36	EP300	chr15:49548114-49548408	Hela-S3	cervix:	n/a	n/a
37	EP300	chr15:49534747-49535605	SK-N-SH	brain:	n/a	n/a
38	EP300	chr15:49528810-49529738	SK-N-SH	brain:	n/a	chr15:49529630-49529644 chr15:49528939-49528949 chr15:49529129-49529143
39	EP300	chr15:49534748-49535905	SK-N-SH	brain:	n/a	n/a
40	EP300	chr15:49534945-49535446	SK-N-SH_RA	brain:	n/a	n/a
41	EP300	chr15:49530431-49531135	SK-N-SH	brain:	n/a	n/a
42	EP300	chr15:49535000-49535356	K562	blood:	n/a	n/a
43	FOS	chr15:49535101-49535407	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
44	FOS	chr15:49530687-49530829	MCF10A-Er-Src	breast:	n/a	n/a
45	FOS	chr15:49535152-49535398	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
46	FOS	chr15:49535118-49535318	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
47	FOS	chr15:49535137-49535318	MCF10A-Er-Src	breast:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
48	FOSL1	chr15:49535051-49535486	K562	blood:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
49	FOSL2	chr15:49534870-49535797	SK-N-SH	brain:	n/a	chr15:49535268-49535280 chr15:49535270-49535278 chr15:49535269-49535279
50	FOSL2	chr15:49530420-49531077	SK-N-SH	brain:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:49535972-49536022	SK-N-SH_RA	brain:	n/a
2	chr15:49535972-49536022	LNCaP	prostate:	n/a
3	chr15:49535972-49536022	ProgFib	skin:	n/a
4	chr15:49548794-49548844	LNCaP	prostate:	n/a
5	chr15:49535972-49536022	SK-N-SH	brain:	n/a
6	chr15:49534692-49534742	PANC-1	pancreas:	n/a
7	chr15:49548794-49548844	RPTEC	kidney:	n/a
8	chr15:49535972-49536022	HIPEpiC	eye:	n/a
9	chr15:49535972-49536022	PANC-1	pancreas:	n/a
10	chr15:49534692-49534742	T-47D	breast:	n/a
11	chr15:49535972-49536022	SK-N-MC	brain:	n/a
12	chr15:49535972-49536022	SAEC	small airway:	n/a
13	chr15:49534692-49534742	AG04449	skin:	fetal
14	chr15:49548794-49548844	HCF	heart:	n/a
15	chr15:49534692-49534742	BE2_C	brain:	n/a
16	chr15:49548794-49548844	ovcar-3	ovarian:	n/a
17	chr15:49534692-49534742	A549	lung:	n/a
18	chr15:49535972-49536022	NT2-D1	testis:	n/a
19	chr15:49548794-49548844	HRCEpiC	kidney:	n/a
20	chr15:49534692-49534742	AoSMC	blood vessel:	n/a
21	chr15:49535972-49536022	HCM	heart:	n/a
22	chr15:49548794-49548844	HCM	heart:	n/a
23	chr15:49534692-49534742	Hepatocyte	liver:	n/a
24	chr15:49548794-49548844	NHDF-neo	bronchial:	n/a
25	chr15:49548794-49548844	IMR90	lung:	fetal
26	chr15:49548794-49548844	AG09309	skin:	n/a
27	chr15:49548794-49548844	BE2_C	brain:	n/a
28	chr15:49548794-49548844	Caco-2	colon:	n/a
29	chr15:49535972-49536022	GM12892	blood:	n/a
30	chr15:49548794-49548844	SK-N-SH	brain:	n/a
31	chr15:49535972-49536022	HRPEpiC	eye:	n/a
32	chr15:49534692-49534742	PrEC	prostate:	n/a
33	chr15:49548794-49548844	ProgFib	skin:	n/a
34	chr15:49534692-49534742	SK-N-SH_RA	brain:	n/a
35	chr15:49535972-49536022	AoSMC	blood vessel:	n/a
36	chr15:49534692-49534742	LNCaP	prostate:	n/a
37	chr15:49548794-49548844	HUVEC	blood vessel:	n/a
38	chr15:49535972-49536022	ovcar-3	ovarian:	n/a
39	chr15:49534692-49534742	ovcar-3	ovarian:	n/a
40	chr15:49535972-49536022	HAEpiC	amniotic membrane:	n/a
41	chr15:49534692-49534742	NHDF-neo	bronchial:	n/a
42	chr15:49534692-49534742	IMR90	lung:	fetal
43	chr15:49548794-49548844	GM06990	blood:	n/a
44	chr15:49548794-49548844	PFSK-1	brain:	n/a
45	chr15:49534692-49534742	NT2-D1	testis:	n/a
46	chr15:49535972-49536022	GM12878	blood:	n/a
47	chr15:49548794-49548844	BJ	skin:	n/a
48	chr15:49548794-49548844	NT2-D1	testis:	n/a
49	chr15:49535972-49536022	Jurkat	blood:	n/a
50	chr15:49534692-49534742	GM12891	blood:	n/a

(count:15 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr15:49527930..49530105-chr15:49533812..49536591,2	MCF-7	breast:
2	chr15:49533559..49535647-chr15:49536094..49538086,2	K562	blood:
3	chr15:49527986..49530632-chr15:49532231..49535128,2	K562	blood:
4	chr15:49461247..49464422-chr15:49530030..49534036,3	K562	blood:
5	chr15:49527986..49530632-chr15:49532231..49535128,2	K562	blood:
6	chr15:49541585..49543251-chr15:49545018..49547358,2	K562	blood:
7	chr15:49541585..49543251-chr15:49545018..49547358,2	K562	blood:
8	chr15:49538461..49540714-chr15:49541925..49544059,3	K562	blood:
9	chr15:49538461..49540714-chr15:49541925..49544059,3	K562	blood:
10	chr15:49533559..49535647-chr15:49536094..49538086,2	K562	blood:
11	chr15:49470039..49472415-chr15:49535845..49538837,2	K562	blood:
12	chr15:49535482..49538280-chr15:49538929..49540490,2	K562	blood:
13	chr15:49535482..49538280-chr15:49538929..49540490,2	K562	blood:
14	chr15:49527930..49530105-chr15:49533812..49536591,2	MCF-7	breast:
15	chr15:49470915..49472999-chr15:49535845..49537993,2	K562	blood:

No data

Variant related genes	Relation type
GALK2	TF binding region
GALK2	CpG island
ENSG00000259545	chromatin interactions
ENSG00000156958	chromatin interactions
ENSG00000264210	chromatin interactions

Extended variants
information (count: 680 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:680 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs16962159	chr15:49529302-49529303	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75801154	chr15:49529333-49529334	Weak transcription Enhancers Flanking Active TSS Active TSS	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs190000446	chr15:49529509-49529510	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs182664750	chr15:49529529-49529530	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs147051170	chr15:49529539-49529540	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs372635518	chr15:49529540-49529541	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs188282129	chr15:49529546-49529547	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs541631188	chr15:49529559-49529560	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs192826344	chr15:49529562-49529563	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs555426536	chr15:49529568-49529569	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs183744969	chr15:49529642-49529643	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs148034343	chr15:49529643-49529644	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs202146763	chr15:49529646-49529647	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs141731693	chr15:49529647-49529648	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs540652929	chr15:49529651-49529652	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs112279985	chr15:49529696-49529697	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs562195896	chr15:49529713-49529714	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs538552648	chr15:49529734-49529735	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs188665914	chr15:49529745-49529746	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs550730722	chr15:49529766-49529767	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs377633402	chr15:49529829-49529830	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs371046030	chr15:49529830-49529831	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs569096008	chr15:49529862-49529863	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376017226	chr15:49529949-49529950	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
25	rs533278684	chr15:49529957-49529958	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs368575560	chr15:49529963-49529964	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs557136097	chr15:49529988-49529989	Weak transcription Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs16962163	chr15:49530006-49530007	Weak transcription Enhancers Flanking Active TSS	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs12908394	chr15:49530039-49530040	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs546497967	chr15:49530041-49530042	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs564652635	chr15:49530048-49530049	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs114049500	chr15:49530129-49530130	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs540306893	chr15:49530138-49530139	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs533902279	chr15:49530181-49530182	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs553253436	chr15:49530256-49530257	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs386783855	chr15:49530272-49530273	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs111875610	chr15:49530284-49530285	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs11632303	chr15:49530321-49530322	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
39	rs193232608	chr15:49530323-49530324	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs184825086	chr15:49530325-49530326	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs557844697	chr15:49530369-49530370	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs572798192	chr15:49530409-49530410	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs539820075	chr15:49530488-49530489	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs562422129	chr15:49530534-49530535	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs529596306	chr15:49530539-49530540	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs16962166	chr15:49530598-49530599	Weak transcription Enhancers Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs188122365	chr15:49530676-49530677	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs562790088	chr15:49530713-49530714	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs369470410	chr15:49530815-49530816	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs3105858	chr15:49530823-49530824	Enhancers Weak transcription Flanking Active TSS Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance

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
Acute lymphoblastic leukemia	22237106	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
Myelofibrosis	22110671	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Breast cancer	21364760	CNVD
Aromatase excess syndrome	21470988	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:596 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:49463600-49540200	Weak transcription	Colonic Mucosa	Colon
2	chr15:49487200-49531200	Weak transcription	HMEC	breast
3	chr15:49492000-49530200	Weak transcription	Stomach Smooth Muscle	stomach
4	chr15:49492000-49539400	Weak transcription	Small Intestine	intestine
5	chr15:49504200-49530800	Weak transcription	Fetal Thymus	thymus
6	chr15:49508800-49535800	Weak transcription	A549	lung
7	chr15:49510000-49541800	Weak transcription	NHEK	skin
8	chr15:49510200-49537000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
9	chr15:49510800-49534400	Weak transcription	Muscle Satellite Cultured Cells	--
10	chr15:49511400-49530600	Weak transcription	Rectal Mucosa Donor 29	rectum
11	chr15:49511800-49531400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr15:49511800-49532200	Weak transcription	Sigmoid Colon	Sigmoid Colon
13	chr15:49516000-49531400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr15:49518000-49535400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr15:49518000-49541000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
16	chr15:49518200-49548600	Weak transcription	Aorta	Aorta
17	chr15:49518600-49532000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
18	chr15:49518600-49557600	Weak transcription	Esophagus	oesophagus
19	chr15:49518800-49539200	Weak transcription	Ovary	ovary
20	chr15:49520400-49595600	Weak transcription	Right Ventricle	heart
21	chr15:49520600-49531200	Weak transcription	Primary T helper cells fromperipheralblood	blood
22	chr15:49520800-49531400	Weak transcription	Duodenum Smooth Muscle	Duodenum
23	chr15:49522000-49534600	Weak transcription	Fetal Muscle Trunk	muscle
24	chr15:49522000-49537800	Weak transcription	Skeletal Muscle Male	skeletal muscle
25	chr15:49522000-49538200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
26	chr15:49522000-49540400	Weak transcription	Stomach Mucosa	stomach
27	chr15:49522200-49531400	Weak transcription	Primary T cells fromperipheralblood	blood
28	chr15:49522200-49535000	Weak transcription	Left Ventricle	heart
29	chr15:49522400-49559400	Weak transcription	Pancreas	Pancrea
30	chr15:49522600-49534400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
31	chr15:49522600-49535200	Weak transcription	Gastric	stomach
32	chr15:49522800-49531400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr15:49523800-49534800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
34	chr15:49523800-49540200	Weak transcription	Spleen	Spleen
35	chr15:49524400-49530800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr15:49524600-49531400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
37	chr15:49524600-49531400	Weak transcription	Duodenum Mucosa	Duodenum
38	chr15:49524600-49531400	Weak transcription	Rectal Mucosa Donor 31	rectum
39	chr15:49524600-49535200	Weak transcription	Cortex derived primary cultured neurospheres	brain
40	chr15:49524600-49535200	Weak transcription	Placenta	Placenta
41	chr15:49524600-49535200	Weak transcription	Thymus	Thymus
42	chr15:49524600-49539200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr15:49524600-49544800	Weak transcription	Lung	lung
44	chr15:49524800-49530200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
45	chr15:49524800-49530600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
46	chr15:49524800-49530600	Weak transcription	Liver	Liver
47	chr15:49524800-49531400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
48	chr15:49525000-49530200	Weak transcription	HUES64 Cell Line	embryonic stem cell
49	chr15:49525000-49531400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
50	chr15:49525000-49534600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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