Variant report

Variant	nsv522564
Chromosome Location	chr17:15592762-15608194
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:477)
CpG islands
(count:672)
Chromatin interactive
region (count:1)
LncRNA
region (count:10)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:477 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr17:15602736-15603024	HepG2	liver:	n/a	n/a
2	ATF1	chr17:15602817-15603017	K562	blood:	n/a	n/a
3	ATF2	chr17:15602639-15603127	GM12878	blood:	n/a	n/a
4	BACH1	chr17:15602905-15603025	H1-hESC	embryonic stem cell:	n/a	n/a
5	BATF	chr17:15602698-15603139	GM12878	blood:	n/a	n/a
6	BCL11A	chr17:15602570-15603218	GM12878	blood:	n/a	n/a
7	BHLHE40	chr17:15602795-15603168	GM12878	blood:	n/a	n/a
8	BHLHE40	chr17:15602827-15603100	K562	blood:	n/a	n/a
9	BRCA1	chr17:15602639-15603141	Hela-S3	cervix:	n/a	chr17:15602870-15602879
10	BRCA1	chr17:15602711-15603054	H1-hESC	embryonic stem cell:	n/a	chr17:15602870-15602879
11	BRCA1	chr17:15602708-15603099	GM12878	blood:	n/a	chr17:15602870-15602879
12	BRCA1	chr17:15602716-15603056	HepG2	liver:	n/a	chr17:15602870-15602879
13	CBX3	chr17:15602574-15603183	K562	blood:	n/a	n/a
14	CEBPB	chr17:15602806-15603183	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr17:15602980-15603199	HepG2	liver:	n/a	n/a
16	CEBPD	chr17:15602664-15602922	HepG2	liver:	n/a	n/a
17	CHD2	chr17:15602649-15603183	GM12878	blood:	n/a	chr17:15602870-15602879
18	CHD2	chr17:15602655-15603159	HepG2	liver:	n/a	chr17:15602870-15602879
19	CHD2	chr17:15602651-15603116	H1-hESC	embryonic stem cell:	n/a	chr17:15602870-15602879
20	CHD2	chr17:15602653-15603124	K562	blood:	n/a	chr17:15602870-15602879
21	CHD2	chr17:15602572-15603200	Hela-S3	cervix:	n/a	chr17:15602870-15602879
22	CREB1	chr17:15602741-15603081	A549	lung:	n/a	n/a
23	CREB1	chr17:15602820-15603076	HepG2	liver:	n/a	n/a
24	CREB1	chr17:15602714-15603177	A549	lung:	n/a	n/a
25	CREB1	chr17:15602822-15603091	GM12878	blood:	n/a	n/a
26	CTCF	chr17:15602780-15602930	AG04449	skin:	n/a	n/a
27	CTCF	chr17:15602903-15603098	Spleen_OC	spleen:	n/a	n/a
28	CTCF	chr17:15602840-15602990	SAEC	small airway:	n/a	n/a
29	CTCF	chr17:15599756-15599839	GM13976	blood:	n/a	n/a
30	CTCF	chr17:15602740-15602916	K562	blood:	n/a	n/a
31	CTCF	chr17:15602866-15602936	Kidney_OC	kidney:	n/a	n/a
32	CTCF	chr17:15602840-15602990	HRE	kidney:	n/a	n/a
33	CTCF	chr17:15602840-15602990	HBMEC	blood vessel:	n/a	n/a
34	CTCF	chr17:15602807-15603033	Lung_OC	lung:	n/a	n/a
35	CTCF	chr17:15602840-15602990	AG04449	skin:	n/a	n/a
36	CUX1	chr17:15602813-15603117	GM12878	blood:	n/a	n/a
37	E2F4	chr17:15592765-15592887	MCF10A-Er-Src	breast:	n/a	n/a
38	E2F4	chr17:15602831-15603058	MCF10A-Er-Src	breast:	n/a	chr17:15603029-15603038
39	E2F6	chr17:15602861-15603001	K562	blood:	n/a	n/a
40	EBF1	chr17:15602739-15603571	GM12878	blood:	n/a	n/a
41	EBF1	chr17:15603238-15603495	GM12878	blood:	n/a	n/a
42	EBF1	chr17:15602807-15603115	GM12878	blood:	n/a	n/a
43	ELF1	chr17:15602643-15603291	GM12878	blood:	n/a	n/a
44	ELF1	chr17:15602804-15603091	K562	blood:	n/a	n/a
45	ELF1	chr17:15602724-15603112	HepG2	liver:	n/a	n/a
46	ELF1	chr17:15602632-15603273	GM12878	blood:	n/a	n/a
47	ELF1	chr17:15602691-15603079	HepG2	liver:	n/a	n/a
48	ELK1	chr17:15602725-15603122	Hela-S3	cervix:	n/a	n/a
49	ELK1	chr17:15602806-15603085	GM12878	blood:	n/a	n/a
50	ELK4	chr17:15602738-15603121	Hela-S3	cervix:	n/a	n/a

(count:672 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15607775-15607825	U87	brain:	n/a
2	chr17:15607775-15607825	U87	brain:	n/a
3	chr17:15602873-15602923	GM12892	blood:	n/a
4	chr17:15602873-15602923	HCT-116	colon:	n/a
5	chr17:15603030-15603080	CMK	blood:	n/a
6	chr17:15602157-15602207	GM19239	blood:	n/a
7	chr17:15608091-15608141	PrEC	prostate:	n/a
8	chr17:15608033-15608083	NHDF-neo	bronchial:	n/a
9	chr17:15602880-15602930	NB4	blood:	n/a
10	chr17:15602157-15602207	LNCaP	prostate:	n/a
11	chr17:15602873-15602923	NHBE	bronchial:	n/a
12	chr17:15602157-15602207	AG04449	skin:	fetal
13	chr17:15602157-15602207	HepG2	liver:	n/a
14	chr17:15608091-15608141	GM12892	blood:	n/a
15	chr17:15608033-15608083	HCT-116	colon:	n/a
16	chr17:15608033-15608083	Hepatocyte	liver:	n/a
17	chr17:15607775-15607825	HMEC	breast:	n/a
18	chr17:15607775-15607825	HRE	kidney:	n/a
19	chr17:15602157-15602207	U87	brain:	n/a
20	chr17:15600659-15600709	CMK	blood:	n/a
21	chr17:15603030-15603080	SK-N-SH_RA	brain:	n/a
22	chr17:15603030-15603080	HL-60	blood:	n/a
23	chr17:15607775-15607825	HepG2	liver:	n/a
24	chr17:15603030-15603080	HEEpiC	esophagus:	n/a
25	chr17:15606456-15606506	Hepatocyte	liver:	n/a
26	chr17:15603984-15604034	BJ	skin:	n/a
27	chr17:15606456-15606506	GM12892	blood:	n/a
28	chr17:15602714-15602764	PANC-1	pancreas:	n/a
29	chr17:15603030-15603080	SK-N-MC	brain:	n/a
30	chr17:15602880-15602930	AG04449	skin:	fetal
31	chr17:15607775-15607825	SK-N-SH	brain:	n/a
32	chr17:15602714-15602764	PrEC	prostate:	n/a
33	chr17:15602714-15602764	NT2-D1	testis:	n/a
34	chr17:15607775-15607825	HEEpiC	esophagus:	n/a
35	chr17:15602880-15602930	NHDF-neo	bronchial:	n/a
36	chr17:15606456-15606506	A549	lung:	n/a
37	chr17:15603030-15603080	HCPEpiC	choroid plexus:	n/a
38	chr17:15602714-15602764	HCT-116	colon:	n/a
39	chr17:15602714-15602764	HCM	heart:	n/a
40	chr17:15607775-15607825	A549	lung:	n/a
41	chr17:15602873-15602923	SKMC	muscle:	n/a
42	chr17:15608091-15608141	Hepatocyte	liver:	n/a
43	chr17:15607775-15607825	HCPEpiC	choroid plexus:	n/a
44	chr17:15603030-15603080	HUVEC	blood vessel:	n/a
45	chr17:15602873-15602923	PANC-1	pancreas:	n/a
46	chr17:15602880-15602930	HEEpiC	esophagus:	n/a
47	chr17:15602157-15602207	MCF-7	breast:	n/a
48	chr17:15600659-15600709	AG09309	skin:	n/a
49	chr17:15602714-15602764	H1-hESC	embryonic stem cell:	embryo
50	chr17:15602157-15602207	A549	lung:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:15603099..15603617-chr17:18585233..18585750,2	HCT-116	colon:

(count:10 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZNF286A-7	chr17:15603054-15603091	NONHSAT145850
2	lnc-ZNF286A-7	chr17:15604466-15604544	NONHSAT145853
3	lnc-ZNF286A-7	chr17:15602895-15603091	NONHSAT145849
4	lnc-ZNF286A-7	chr17:15603449-15603991	NONHSAT145850
5	lnc-ZNF286A-7	chr17:15604466-15604614	NONHSAT145848
6	lnc-ZNF286A-7	chr17:15602891-15603091	NONHSAT145848
7	lnc-ZSWIM7-1	chr17:15596563-15596608	ENSG00000248550
8	lnc-ZNF286A-7	chr17:15603449-15603680	NONHSAT145848
9	lnc-ZNF286A-7	chr17:15603477-15603901	NONHSAT145853
10	lnc-ZNF286A-7	chr17:15603362-15603853	NONHSAT145849

No data

Variant related genes	Relation type
ENSG00000187607	TF binding region
ZNF286A	TF binding region
ENSG00000187607	CpG island
ZNF286A	CpG island
ENSG00000249459	chromatin interactions
PHF17	miRNA target sites

Extended variants
information (count: 263 )
Associated
traits (count: 126 )

Variant overlapped rSNPs/rCNVs (count:263 , 50 per page) page: 1 2 3 4 5 6

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs542653221	chr17:15596563-15596564	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
2	rs140710477	chr17:15596573-15596574	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
3	rs572175807	chr17:15596596-15596597	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
4	rs534681049	chr17:15596597-15596598	Inactive region	lncRNA	n/a	Overlapped CNVs	n/a
5	rs537842767	chr17:15599793-15599794	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs558145883	chr17:15599804-15599805	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs368325099	chr17:15599810-15599811	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs183363167	chr17:15599823-15599824	Inactive region	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs9907892	chr17:15600692-15600693	Inactive region	CpG island	2 gene(s)	Overlapped CNVs	n/a
10	rs181790888	chr17:15601244-15601245	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs202019497	chr17:15601245-15601246	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs555286839	chr17:15601273-15601274	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs373592628	chr17:15601289-15601290	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs144246068	chr17:15601301-15601302	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs376477077	chr17:15601328-15601329	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs536378231	chr17:15601419-15601420	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs375188928	chr17:15601422-15601423	Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs557628517	chr17:15601469-15601470	Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs2601935	chr17:15601472-15601473	Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs8074851	chr17:15601532-15601533	Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs368141203	chr17:15601551-15601552	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs2601936	chr17:15601552-15601553	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs577258479	chr17:15601629-15601630	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
24	rs2601937	chr17:15601659-15601660	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs147543985	chr17:15601661-15601662	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
26	rs2654310	chr17:15601669-15601670	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
27	rs140189843	chr17:15601679-15601680	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
28	rs552806755	chr17:15601687-15601688	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
29	rs573677385	chr17:15601693-15601694	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
30	rs542675046	chr17:15601694-15601695	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
31	rs562976972	chr17:15601765-15601766	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
32	rs576704805	chr17:15601839-15601840	Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
33	rs200252105	chr17:15601927-15601928	Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs545754451	chr17:15601961-15601962	Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs117200551	chr17:15601963-15601964	Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs2601938	chr17:15601968-15601969	Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527939724	chr17:15602005-15602006	Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs149896804	chr17:15602020-15602021	Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
39	rs144900028	chr17:15602054-15602055	Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs544680383	chr17:15602092-15602093	Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs144591084	chr17:15602127-15602128	Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs146770527	chr17:15602129-15602130	Enhancers Flanking Active TSS Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs550225908	chr17:15602316-15602317	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs569003779	chr17:15602415-15602416	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs2654303	chr17:15602429-15602430	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs537640136	chr17:15602437-15602438	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs55852375	chr17:15602456-15602457	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs55635803	chr17:15602459-15602460	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
49	rs551121312	chr17:15602526-15602527	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
50	rs571212645	chr17:15602560-15602561	Active TSS Enhancers Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:126)

Disease	PMID	Source
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	19435819	CNVD
Non-small cell lung cancer	19010865	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Colorectal cancer	16774939	CNVD
Hepatocellular carcinoma	18803288	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Burkitt''s lymphoma	19759907	CNVD
Wilms tumour	21544195	CNVD
Esophageal adenocarcinoma	18519675	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Medulloblastoma	21979893	CNVD
Breast cancer	16608533	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Chordoma	21602918	CNVD
Miller-Dieker syndrome	22283845	CNVD
Non-syndromic sensorineural hearing loss	17457615	CNVD
Cancer	22429812	CNVD
Chronic lymphocytic leukemia	21795749	CNVD
Ewing''s sarcoma	21437220	CNVD
Follicular lymphoma	19010834	CNVD
Colorectal cancer	20709793	CNVD
Acute myeloid leukemia	16864856	CNVD
Endometrial cancer	22040021	CNVD
Paraganglioma	21461997	CNVD
Pheochromocytoma	21461997	CNVD
Breast cancer	22028636	CNVD
Breast cancer	20837533	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
colon cancer	17210682	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Basal cell lymphoma	17053054	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Cancer	16751803	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Chronic lymphocytic leukemia	17971485	CNVD
Basal cell lymphoma	17170743	CNVD
Breast cancer	16461572	CNVD
Colorectal cancer	16272173	CNVD
Follicular lymphoma	17170743	CNVD
Human rectal carcinomas	16397240	CNVD
Breast cancer	17133270	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Moyamoya disease	22323933	CNVD
small cell lung cancer	20016488	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	21251322	CNVD
Myelodysplastic syndrome	21251322	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20724749	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Acute myeloid leukemia	17237825	CNVD
Colorectal cancer	21645411	CNVD
HIV/AIDS	22844521	CNVD
Psoriasis	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
HIV/AIDS	17953491	CNVD
HIV/AIDS	20877625	CNVD
Immune disease	21076436	CNVD
Rheumatoid arthritis	17953491	CNVD
Type 1 diabetes	17953491	CNVD
HIV/AIDS	15637236	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21781307	CNVD
Autism	22495311	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Neurofibromatosis	18196300	CNVD
Adenoid cystic carcinoma	18332873	CNVD
Multiple myeloma	16616336	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21509527	CNVD
Pancreatic cancer	21811587	CNVD
Autism	17322880	CNVD
Hereditary neuropathy with liability to pressure palsy	19521722	CNVD
Schizophrenia	19571808	CNVD
Schizophrenia	19955444	CNVD
Charcot-marie-tooth disease	18787571	CNVD
Breast cancer	20409316	CNVD
Autism	18414403	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Myelofibrosis	22110671	CNVD
Peripheral neuropathy	21193943	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	22958593	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	20844748	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
ovarian endometriomas	16273235	CNVD
Breast cancer	21858162	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	17142309	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Autism	22102821	CNVD
Gastric cancer	18160780	CNVD

Chromatin state (count:389 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15601200-15602400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
2	chr17:15601400-15602000	Enhancers	Dnd41	blood
3	chr17:15601400-15602000	Enhancers	GM12878-XiMat	blood
4	chr17:15601400-15602200	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
5	chr17:15601400-15602200	Enhancers	Primary T killer memory cells from peripheral blood	blood
6	chr17:15601400-15602200	Enhancers	A549	lung
7	chr17:15601400-15602200	Enhancers	HepG2	liver
8	chr17:15601400-15602400	Enhancers	Primary T cells fromperipheralblood	blood
9	chr17:15601800-15602000	Enhancers	Primary T cells from cord blood	blood
10	chr17:15602000-15602200	Enhancers	Primary T helper naive cells fromperipheralblood	blood
11	chr17:15602000-15602200	Enhancers	Primary T helper cells fromperipheralblood	blood
12	chr17:15602000-15602200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
13	chr17:15602000-15602200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
14	chr17:15602000-15602200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr17:15602000-15602400	Enhancers	Primary B cells from cord blood	blood
16	chr17:15602000-15602400	Flanking Active TSS	Primary T cells from cord blood	blood
17	chr17:15602000-15602400	Enhancers	Primary hematopoietic stem cells short term culture	blood
18	chr17:15602000-15602400	Enhancers	Primary T helper cells PMA-I stimulated	--
19	chr17:15602000-15602400	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
20	chr17:15602000-15602400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
21	chr17:15602000-15602400	Enhancers	Primary T killer naive cells fromperipheralblood	blood
22	chr17:15602000-15602400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr17:15602000-15602400	Enhancers	Fetal Thymus	thymus
24	chr17:15602000-15602400	Flanking Active TSS	GM12878-XiMat	blood
25	chr17:15602000-15602400	Enhancers	Hela-S3	cervix
26	chr17:15602000-15602400	Enhancers	K562	blood
27	chr17:15602000-15602400	Enhancers	NH-A	brain
28	chr17:15602000-15602600	Enhancers	Primary B cells from peripheral blood	blood
29	chr17:15602000-15602600	Flanking Active TSS	Dnd41	blood
30	chr17:15602000-15603400	Active TSS	Primary T helper naive cells from peripheral blood	blood
31	chr17:15602000-15603400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
32	chr17:15602200-15602400	Enhancers	HUES48 Cell Line	embryonic stem cell
33	chr17:15602200-15602400	Flanking Active TSS	Primary T helper cells fromperipheralblood	blood
34	chr17:15602200-15602400	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
35	chr17:15602200-15602400	Flanking Active TSS	Primary T killer memory cells from peripheral blood	blood
36	chr17:15602200-15602400	Enhancers	Cortex derived primary cultured neurospheres	brain
37	chr17:15602200-15602400	Enhancers	Brain Anterior Caudate	brain
38	chr17:15602200-15602400	Flanking Active TSS	HepG2	liver
39	chr17:15602200-15602400	Enhancers	NHDF-Ad	bronchial
40	chr17:15602200-15602400	Enhancers	NHEK	skin
41	chr17:15602200-15602600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 1	blood
42	chr17:15602200-15603000	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
43	chr17:15602200-15603400	Active TSS	Primary T helper naive cells fromperipheralblood	blood
44	chr17:15602200-15603400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
45	chr17:15602200-15603400	Active TSS	Skeletal Muscle Male	skeletal muscle
46	chr17:15602200-15603400	Active TSS	Thymus	Thymus
47	chr17:15602200-15603800	Active TSS	Duodenum Mucosa	Duodenum
48	chr17:15602200-15604000	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr17:15602200-15604000	Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
50	chr17:15602200-15604000	Active TSS	A549	lung

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links