Variant report

Variant	nsv960419
Chromosome Location	chr17:15470653-15494148
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:115)
CpG islands
(count:61)
Chromatin interactive
region (count:1)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:115 , 50 per page) page: 1 2 3

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BATF	chr17:15492808-15493262	GM12878	blood:	n/a	chr17:15492991-15492999 chr17:15493146-15493154
2	BATF	chr17:15492845-15493213	GM12878	blood:	n/a	chr17:15492991-15492999 chr17:15493146-15493154
3	BCL11A	chr17:15492818-15493314	GM12878	blood:	n/a	n/a
4	BCL11A	chr17:15492851-15493235	GM12878	blood:	n/a	n/a
5	BHLHE40	chr17:15492799-15492963	GM12878	blood:	n/a	n/a
6	CEBPB	chr17:15492770-15493365	GM12878	blood:	n/a	chr17:15493176-15493187
7	CTCF	chr17:15492052-15492058	HepG2	liver:	n/a	n/a
8	CTCF	chr17:15477300-15477450	MCF-7	breast:	n/a	n/a
9	CTCF	chr17:15492000-15492150	HepG2	liver:	n/a	n/a
10	CTCF	chr17:15477319-15477405	MCF-7	breast:	n/a	n/a
11	CTCF	chr17:15477296-15477349	Medullo	brain:	n/a	n/a
12	CTCF	chr17:15492052-15492129	MCF-7	breast:	n/a	n/a
13	CTCF	chr17:15477320-15477470	AG10803	skin:	n/a	n/a
14	CTCF	chr17:15477220-15477370	HEEpiC	esophagus:	n/a	n/a
15	CTCF	chr17:15492000-15492150	HEK293	kidney:	n/a	n/a
16	CTCF	chr17:15477080-15477230	NHEK	skin:	n/a	n/a
17	CTCF	chr17:15477302-15477415	MCF-7	breast:	n/a	n/a
18	CTCF	chr17:15477120-15477270	SAEC	small airway:	n/a	n/a
19	CTCF	chr17:15492352-15492380	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr17:15477226-15477378	K562	blood:	n/a	n/a
21	CTCF	chr17:15477309-15477377	HepG2	liver:	n/a	n/a
22	CTCF	chr17:15477280-15477408	H1-hESC	embryonic stem cell:	n/a	n/a
23	CTCF	chr17:15492364-15492412	MCF-7	breast:	n/a	n/a
24	CTCF	chr17:15492000-15492150	HEEpiC	esophagus:	n/a	n/a
25	CTCF	chr17:15477360-15477510	HMEC	breast:	n/a	n/a
26	CTCF	chr17:15477340-15477490	HCPEpiC	choroid plexus:	n/a	n/a
27	CTCF	chr17:15472258-15472324	GM13976	blood:	n/a	n/a
28	CTCF	chr17:15477271-15477430	NHEK	skin:	n/a	n/a
29	CTCF	chr17:15477313-15477376	ProgFib	skin:	n/a	n/a
30	CTCF	chr17:15477280-15477430	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr17:15477220-15477370	HCPEpiC	choroid plexus:	n/a	n/a
32	CTCF	chr17:15477220-15477370	HCFaa	heart:	n/a	n/a
33	CTCF	chr17:15492000-15492150	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr17:15477295-15477405	MCF-7	breast:	n/a	n/a
35	CTCF	chr17:15477304-15477388	MCF-7	breast:	n/a	n/a
36	CTCF	chr17:15477306-15477409	MCF-7	breast:	n/a	n/a
37	CTCF	chr17:15492043-15492128	K562	blood:	n/a	n/a
38	CTCF	chr17:15477320-15477340	HUVEC	blood vessel:	n/a	n/a
39	CTCF	chr17:15477328-15477380	Fibrobl	skin:	n/a	n/a
40	CTCF	chr17:15477080-15477230	HMEC	breast:	n/a	n/a
41	CTCF	chr17:15477340-15477490	HAc	cerebellar:	n/a	n/a
42	CTCF	chr17:15491980-15492130	NHEK	skin:	n/a	n/a
43	CTCF	chr17:15477233-15477483	LNCaP	prostate:	n/a	n/a
44	CTCF	chr17:15477218-15477477	LNCaP	prostate:	n/a	n/a
45	CTCF	chr17:15486717-15486807	MCF-7	breast:	n/a	n/a
46	CTCF	chr17:15492046-15492073	LNCaP	prostate:	n/a	n/a
47	CTCF	chr17:15477080-15477230	HCM	heart:	n/a	n/a
48	CTCF	chr17:15477288-15477414	K562	blood:	n/a	n/a
49	CTCF	chr17:15491940-15492090	MCF-7	breast:	n/a	n/a
50	CTCF	chr17:15477320-15477470	HUVEC	blood vessel:	n/a	n/a

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:15492168-15492218	SK-N-SH	brain:	n/a
2	chr17:15492168-15492218	NHDF-neo	bronchial:	n/a
3	chr17:15492168-15492218	AG10803	skin:	n/a
4	chr17:15492168-15492218	GM12878	blood:	n/a
5	chr17:15492168-15492218	BJ	skin:	n/a
6	chr17:15492168-15492218	SKMC	muscle:	n/a
7	chr17:15492168-15492218	NB4	blood:	n/a
8	chr17:15492168-15492218	A549	lung:	n/a
9	chr17:15492168-15492218	GM12891	blood:	n/a
10	chr17:15492168-15492218	SK-N-MC	brain:	n/a
11	chr17:15492168-15492218	HRCEpiC	kidney:	n/a
12	chr17:15492168-15492218	AG04450	lung:	fetal
13	chr17:15492168-15492218	MCF10A-Er-Src	breast:	n/a
14	chr17:15492168-15492218	RPTEC	kidney:	n/a
15	chr17:15492168-15492218	ECC-1	luminal epithelium:	n/a
16	chr17:15492168-15492218	Jurkat	blood:	n/a
17	chr17:15492168-15492218	AG04449	skin:	fetal
18	chr17:15492168-15492218	H1-hESC	embryonic stem cell:	embryo
19	chr17:15492168-15492218	GM12892	blood:	n/a
20	chr17:15492168-15492218	SK-N-SH_RA	brain:	n/a
21	chr17:15492168-15492218	PFSK-1	brain:	n/a
22	chr17:15492168-15492218	HCM	heart:	n/a
23	chr17:15492168-15492218	BE2_C	brain:	n/a
24	chr17:15492168-15492218	LNCaP	prostate:	n/a
25	chr17:15492168-15492218	HEEpiC	esophagus:	n/a
26	chr17:15492168-15492218	HCF	heart:	n/a
27	chr17:15492168-15492218	PrEC	prostate:	n/a
28	chr17:15492168-15492218	Hela-S3	cervix:	n/a
29	chr17:15492168-15492218	AG09309	skin:	n/a
30	chr17:15492168-15492218	HepG2	liver:	n/a
31	chr17:15492168-15492218	T-47D	breast:	n/a
32	chr17:15492168-15492218	HAEpiC	amniotic membrane:	n/a
33	chr17:15492168-15492218	HRE	kidney:	n/a
34	chr17:15492168-15492218	AG09319	gingival:	n/a
35	chr17:15492168-15492218	PANC-1	pancreas:	n/a
36	chr17:15492168-15492218	HMEC	breast:	n/a
37	chr17:15492168-15492218	HCT-116	colon:	n/a
38	chr17:15492168-15492218	K562	blood:	n/a
39	chr17:15492168-15492218	HRPEpiC	eye:	n/a
40	chr17:15492168-15492218	HL-60	blood:	n/a
41	chr17:15492168-15492218	NHBE	bronchial:	n/a
42	chr17:15492168-15492218	NH-A	brain:	n/a
43	chr17:15492168-15492218	HUVEC	blood vessel:	n/a
44	chr17:15492168-15492218	MCF-7	breast:	n/a
45	chr17:15492168-15492218	IMR90	lung:	fetal
46	chr17:15492168-15492218	AoSMC	blood vessel:	n/a
47	chr17:15492168-15492218	GM06990	blood:	n/a
48	chr17:15492168-15492218	HNPCEpiC	eye:	n/a
49	chr17:15492168-15492218	SAEC	small airway:	n/a
50	chr17:15492168-15492218	ProgFib	skin:	n/a

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

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:14078689..14080446-chr17:15474904..15476529,2	MCF-7	breast:

No data

Variant related genes	Relation type
TVP23C-CDRT4	TF binding region
TVP23C	TF binding region
ENSG00000181464	TF binding region
ENSG00000252129	TF binding region
ENSG00000223544	TF binding region
TVP23C-CDRT4	CpG island
TVP23C	CpG island
ENSG00000181464	CpG island
ENSG00000252129	CpG island
ENSG00000223544	CpG island

Extended variants
information (count: 266 )
Associated
traits (count: 130 )

Variant overlapped rSNPs/rCNVs (count:266 , 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	rs539192819	chr17:15471631-15471632	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a
2	rs559294178	chr17:15471673-15471674	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a
3	rs572772622	chr17:15471680-15471681	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a
4	rs541477474	chr17:15471708-15471709	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a
5	rs561250640	chr17:15471720-15471721	Inactive region	TF binding region	3 gene(s)	Overlapped CNVs	n/a
6	rs549854933	chr17:15472272-15472273	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs569601470	chr17:15472279-15472280	Inactive region	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs236803	chr17:15475601-15475602	Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs190600082	chr17:15475627-15475628	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs2856134	chr17:15475660-15475661	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs2856220	chr17:15475712-15475713	Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs559367330	chr17:15475713-15475714	Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs148774235	chr17:15475772-15475773	Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs541573128	chr17:15475783-15475784	Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs561779447	chr17:15475787-15475788	Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs531018260	chr17:15475795-15475796	Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs550761397	chr17:15475821-15475822	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2258057	chr17:15475844-15475845	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs564483291	chr17:15475849-15475850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs397843319	chr17:15475854-15475855	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs533432736	chr17:15475887-15475888	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs552104860	chr17:15475888-15475889	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs566775433	chr17:15475908-15475909	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs368269594	chr17:15475909-15475910	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs2856219	chr17:15475927-15475928	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs531493703	chr17:15476155-15476156	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs549218800	chr17:15476182-15476183	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs236802	chr17:15476190-15476191	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs2258072	chr17:15476257-15476258	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs557177283	chr17:15476279-15476280	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs181130174	chr17:15476300-15476301	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs140356976	chr17:15476353-15476354	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs114023663	chr17:15476409-15476410	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs553267436	chr17:15476454-15476455	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs567890754	chr17:15476458-15476459	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs541759690	chr17:15476469-15476470	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs144293824	chr17:15476514-15476515	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs533771786	chr17:15476612-15476613	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs2258077	chr17:15476640-15476641	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs185571785	chr17:15476655-15476656	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs2258129	chr17:15476676-15476677	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs544440591	chr17:15476702-15476703	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs115884569	chr17:15476707-15476708	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs533323097	chr17:15476811-15476812	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs190607372	chr17:15476837-15476838	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs200651119	chr17:15476854-15476855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs140073856	chr17:15476900-15476901	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs76241828	chr17:15477010-15477011	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182894144	chr17:15477108-15477109	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs186121324	chr17:15477151-15477152	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:130)

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
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Type 1 diabetes	21085585	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:75 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:15475600-15475800	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr17:15475800-15477000	Weak transcription	HUES48 Cell Line	embryonic stem cell
3	chr17:15476400-15477200	Enhancers	HUES6 Cell Line	embryonic stem cell
4	chr17:15476400-15477400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr17:15476400-15477400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr17:15476600-15477200	Enhancers	iPS-15b Cell Line	embryonic stem cell
7	chr17:15476600-15477400	Enhancers	Cortex derived primary cultured neurospheres	brain
8	chr17:15476600-15477400	Enhancers	Brain Germinal Matrix	brain
9	chr17:15477000-15477400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr17:15477000-15477400	Enhancers	HUES48 Cell Line	embryonic stem cell
11	chr17:15477000-15477400	Enhancers	Brain Angular Gyrus	brain
12	chr17:15477000-15477400	Enhancers	Fetal Brain Female	brain
13	chr17:15487000-15487200	Enhancers	Primary neutrophils fromperipheralblood	blood
14	chr17:15489800-15490200	Enhancers	HMEC	breast
15	chr17:15489800-15490200	Enhancers	NHEK	skin
16	chr17:15490000-15490600	Enhancers	Primary hematopoietic stem cells short term culture	blood
17	chr17:15490000-15492400	Weak transcription	A549	lung
18	chr17:15490400-15490600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
19	chr17:15490600-15491400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
20	chr17:15490600-15492200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
21	chr17:15491400-15491600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
22	chr17:15491400-15491600	Enhancers	Primary T helper cells PMA-I stimulated	--
23	chr17:15491400-15491600	ZNF genes & repeats	Esophagus	oesophagus
24	chr17:15491400-15491800	Enhancers	Fetal Intestine Large	intestine
25	chr17:15491400-15492200	Enhancers	Fetal Thymus	thymus
26	chr17:15491400-15492600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
27	chr17:15491400-15492800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
28	chr17:15491600-15492600	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr17:15491600-15501800	Weak transcription	Esophagus	oesophagus
30	chr17:15491800-15493000	Weak transcription	Primary T helper cells PMA-I stimulated	--
31	chr17:15492200-15492400	Enhancers	Primary T helper naive cells from peripheral blood	blood
32	chr17:15492200-15494200	Weak transcription	Fetal Thymus	thymus
33	chr17:15492200-15495400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
34	chr17:15492200-15497000	Enhancers	Primary T cells fromperipheralblood	blood
35	chr17:15492200-15497000	Enhancers	Primary hematopoietic stem cells short term culture	blood
36	chr17:15492400-15492600	Enhancers	Primary T killer memory cells from peripheral blood	blood
37	chr17:15492400-15492800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr17:15492400-15493000	Strong transcription	A549	lung
39	chr17:15492400-15493600	Bivalent Enhancer	Primary B cells from peripheral blood	blood
40	chr17:15492400-15493600	Enhancers	HUVEC	blood vessel
41	chr17:15492400-15493800	Enhancers	Primary neutrophils fromperipheralblood	blood
42	chr17:15492400-15494800	Enhancers	Dnd41	blood
43	chr17:15492400-15495600	Enhancers	Primary T killer naive cells fromperipheralblood	blood
44	chr17:15492600-15492800	Enhancers	Primary hematopoietic stem cells	blood
45	chr17:15492600-15492800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
46	chr17:15492600-15492800	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood
47	chr17:15492600-15492800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
48	chr17:15492600-15493200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
49	chr17:15492800-15493200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
50	chr17:15492800-15493200	Enhancers	Primary T regulatory cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links