Variant report

Variant	esv3389518
Chromosome Location	chr17:45606828-45610526
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	BCL11A	chr17:45609110-45609438	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
2	BCLAF1	chr17:45609125-45609498	GM12878	blood:	n/a	chr17:45609227-45609236 chr17:45609179-45609192 chr17:45609236-45609245
3	CBX3	chr17:45609185-45609788	K562	blood:	n/a	n/a
4	CCNT2	chr17:45608329-45608370	K562	blood:	n/a	n/a
5	CEBPB	chr17:45609557-45609591	Hela-S3	cervix:	n/a	n/a
6	CEBPD	chr17:45608348-45608658	HepG2	liver:	n/a	n/a
7	CHD2	chr17:45608212-45608501	HepG2	liver:	n/a	n/a
8	CHD2	chr17:45608171-45608525	Hela-S3	cervix:	n/a	n/a
9	CREB1	chr17:45608212-45608653	A549	lung:	n/a	n/a
10	CTCF	chr17:45608264-45608280	GM13977	blood:	n/a	n/a
11	CTCF	chr17:45608674-45608723	MCF-7	breast:	n/a	n/a
12	CTCF	chr17:45609163-45609272	GM10248	blood:	n/a	n/a
13	CTCF	chr17:45608670-45608672	MCF-7	breast:	n/a	n/a
14	CTCF	chr17:45609146-45609247	GM19240	blood:	n/a	n/a
15	CTCF	chr17:45608677-45608717	Fibrobl	skin:	n/a	n/a
16	CTCF	chr17:45608622-45608710	Spleen_OC	spleen:	n/a	n/a
17	E2F4	chr17:45608301-45608415	MCF10A-Er-Src	breast:	n/a	chr17:45608389-45608398
18	E2F4	chr17:45609441-45609604	MCF10A-Er-Src	breast:	n/a	n/a
19	E2F6	chr17:45608254-45608467	K562	blood:	n/a	chr17:45608389-45608398
20	E2F6	chr17:45608192-45608625	K562	blood:	n/a	chr17:45608459-45608469 chr17:45608389-45608398 chr17:45608610-45608619 chr17:45608607-45608619
21	EBF1	chr17:45609270-45609512	GM12878	blood:	n/a	n/a
22	EBF1	chr17:45608125-45608837	GM12878	blood:	n/a	n/a
23	EGR1	chr17:45608386-45608617	GM12878	blood:	n/a	chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608503-45608517 chr17:45608521-45608535
24	EGR1	chr17:45608263-45608647	K562	blood:	n/a	chr17:45608609-45608619 chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608279-45608292 chr17:45608605-45608618 chr17:45608521-45608535
25	EGR1	chr17:45608321-45608635	K562	blood:	n/a	chr17:45608609-45608619 chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608605-45608618 chr17:45608521-45608535
26	EGR1	chr17:45608104-45608955	GM12878	blood:	n/a	chr17:45608609-45608619 chr17:45608408-45608417 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608203-45608227 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608279-45608292 chr17:45608605-45608618 chr17:45608521-45608535
27	EGR1	chr17:45608435-45608626	GM12878	blood:	n/a	chr17:45608609-45608619 chr17:45608546-45608556 chr17:45608477-45608491 chr17:45608610-45608620 chr17:45608503-45608517 chr17:45608605-45608618 chr17:45608521-45608535
28	EGR1	chr17:45609243-45609701	K562	blood:	n/a	chr17:45609549-45609562 chr17:45609550-45609560 chr17:45609549-45609562 chr17:45609388-45609403 chr17:45609548-45609563
29	ELF1	chr17:45608235-45608651	K562	blood:	n/a	chr17:45608392-45608404
30	ELF1	chr17:45608201-45608669	GM12878	blood:	n/a	chr17:45608392-45608404
31	ELF1	chr17:45608330-45608613	K562	blood:	n/a	chr17:45608392-45608404
32	EP300	chr17:45609301-45609491	GM12878	blood:	n/a	chr17:45609343-45609357
33	EP300	chr17:45609481-45609594	GM12878	blood:	n/a	n/a
34	FOS	chr17:45609954-45610163	MCF10A-Er-Src	breast:	n/a	n/a
35	FOS	chr17:45609954-45610153	MCF10A-Er-Src	breast:	n/a	n/a
36	FOSL2	chr17:45609235-45609780	HepG2	liver:	n/a	chr17:45609339-45609349
37	FOSL2	chr17:45607924-45608918	HepG2	liver:	n/a	chr17:45608611-45608620 chr17:45608547-45608556
38	FOXA1	chr17:45610515-45610997	HepG2	liver:	n/a	n/a
39	FOXM1	chr17:45609218-45609509	GM12878	blood:	n/a	n/a
40	FOXP2	chr17:45608141-45608503	PFSK-1	brain:	n/a	n/a
41	GTF2F1	chr17:45609440-45609521	Hela-S3	cervix:	n/a	n/a
42	HA-E2F1	chr17:45608041-45608420	MCF-7	breast:	n/a	chr17:45608389-45608398
43	HA-E2F1	chr17:45608167-45608595	Hela-S3	cervix:	n/a	chr17:45608459-45608469 chr17:45608389-45608398
44	HDAC2	chr17:45608263-45608486	HepG2	liver:	n/a	n/a
45	HEY1	chr17:45608472-45609062	K562	blood:	n/a	chr17:45608543-45608558
46	HEY1	chr17:45608118-45608398	K562	blood:	n/a	n/a
47	HEY1	chr17:45609103-45609767	K562	blood:	n/a	n/a
48	HEY1	chr17:45609121-45609712	HepG2	liver:	n/a	n/a
49	HEY1	chr17:45608086-45609001	K562	blood:	n/a	chr17:45608543-45608558
50	HEY1	chr17:45608444-45608937	HepG2	liver:	n/a	chr17:45608543-45608558

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:45608114-45608164	SAEC	small airway:	n/a
2	chr17:45608114-45608164	AG10803	skin:	n/a
3	chr17:45608823-45608873	PANC-1	pancreas:	n/a
4	chr17:45608315-45608365	HEEpiC	esophagus:	n/a
5	chr17:45608114-45608164	HNPCEpiC	eye:	n/a
6	chr17:45608315-45608365	HNPCEpiC	eye:	n/a
7	chr17:45608823-45608873	NHDF-neo	bronchial:	n/a
8	chr17:45608114-45608164	T-47D	breast:	n/a
9	chr17:45608315-45608365	HPAEpiC	pulmonary alveolar:	n/a
10	chr17:45608315-45608365	HIPEpiC	eye:	n/a
11	chr17:45608823-45608873	HMEC	breast:	n/a
12	chr17:45608114-45608164	GM19239	blood:	n/a
13	chr17:45609121-45609171	Caco-2	colon:	n/a
14	chr17:45608315-45608365	ProgFib	skin:	n/a
15	chr17:45609121-45609171	ProgFib	skin:	n/a
16	chr17:45609121-45609171	GM12878	blood:	n/a
17	chr17:45608114-45608164	HRE	kidney:	n/a
18	chr17:45608114-45608164	HUVEC	blood vessel:	n/a
19	chr17:45608823-45608873	AoSMC	blood vessel:	n/a
20	chr17:45609121-45609171	AG04450	lung:	fetal
21	chr17:45608823-45608873	HCF	heart:	n/a
22	chr17:45608823-45608873	Hepatocyte	liver:	n/a
23	chr17:45609121-45609171	CMK	blood:	n/a
24	chr17:45608823-45608873	PrEC	prostate:	n/a
25	chr17:45608315-45608365	GM12878	blood:	n/a
26	chr17:45608823-45608873	HCT-116	colon:	n/a
27	chr17:45608114-45608164	K562	blood:	n/a
28	chr17:45608315-45608365	K562	blood:	n/a
29	chr17:45608114-45608164	NH-A	brain:	n/a
30	chr17:45609121-45609171	GM12892	blood:	n/a
31	chr17:45608823-45608873	HEK293	kidney:	embryo
32	chr17:45608315-45608365	HRCEpiC	kidney:	n/a
33	chr17:45608114-45608164	PrEC	prostate:	n/a
34	chr17:45608823-45608873	U87	brain:	n/a
35	chr17:45608114-45608164	HIPEpiC	eye:	n/a
36	chr17:45608315-45608365	NHBE	bronchial:	n/a
37	chr17:45609121-45609171	NHDF-neo	bronchial:	n/a
38	chr17:45608823-45608873	GM06990	blood:	n/a
39	chr17:45608823-45608873	NHBE	bronchial:	n/a
40	chr17:45609121-45609171	SK-N-MC	brain:	n/a
41	chr17:45608114-45608164	HMEC	breast:	n/a
42	chr17:45609121-45609171	GM06990	blood:	n/a
43	chr17:45609121-45609171	AG10803	skin:	n/a
44	chr17:45608315-45608365	AG10803	skin:	n/a
45	chr17:45608823-45608873	K562	blood:	n/a
46	chr17:45608315-45608365	AG04450	lung:	fetal
47	chr17:45608315-45608365	ovcar-3	ovarian:	n/a
48	chr17:45608114-45608164	Hela-S3	cervix:	n/a
49	chr17:45609121-45609171	Hepatocyte	liver:	n/a
50	chr17:45608315-45608365	GM12892	blood:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr17:45569553..45571642-chr17:45608535..45610078,2	MCF-7	breast:
2	chr14:38063458..38065003-chr17:45607681..45609442,2	MCF-7	breast:

Variant related genes	Relation type
NPEPPS	TF binding region
NPEPPS	CpG island
ENSG00000129514	chromatin interactions
ENSG00000228782	chromatin interactions

Extended variants
information (count: 105 )
Associated
traits (count: 118 )

Variant overlapped rSNPs/rCNVs (count:105 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs569538747	chr17:45606898-45606899	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs113402409	chr17:45607023-45607024	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs111475713	chr17:45607033-45607034	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs533257101	chr17:45607095-45607096	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs200029608	chr17:45607102-45607103	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs201105590	chr17:45607103-45607104	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs202172308	chr17:45607104-45607105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs2611986	chr17:45607139-45607140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs186564653	chr17:45607167-45607168	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs200538359	chr17:45607285-45607286	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs566570982	chr17:45607288-45607289	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs2935187	chr17:45607292-45607293	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs2935186	chr17:45607293-45607294	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs191074635	chr17:45607312-45607313	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs536949363	chr17:45607316-45607317	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs558418730	chr17:45607351-45607352	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs578216226	chr17:45607367-45607368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs2935185	chr17:45607395-45607396	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs370406863	chr17:45607468-45607469	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs2935184	chr17:45607528-45607529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs3874910	chr17:45607563-45607564	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs2935183	chr17:45607572-45607573	Weak transcription	n/a	n/a	Overlapped CNVs	mRNA abundance disease
23	rs544006202	chr17:45607598-45607599	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs8065344	chr17:45607608-45607609	Weak transcription Active TSS Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs549295681	chr17:45607718-45607719	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs58886094	chr17:45607737-45607738	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs554876036	chr17:45607739-45607740	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs111749349	chr17:45607768-45607769	Weak transcription Active TSS Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs28457024	chr17:45607812-45607813	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs541774116	chr17:45607843-45607844	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs561331262	chr17:45607857-45607858	Weak transcription Enhancers Active TSS Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs370506237	chr17:45607898-45607899	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs544095873	chr17:45607902-45607903	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs563978078	chr17:45607905-45607906	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs567744912	chr17:45607938-45607939	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs532919187	chr17:45607944-45607945	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs546779605	chr17:45607975-45607976	Weak transcription Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs151301802	chr17:45608010-45608011	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs187536984	chr17:45608088-45608089	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs374573333	chr17:45608102-45608103	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs549395115	chr17:45608168-45608169	Enhancers Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs569256274	chr17:45608300-45608301	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs368401966	chr17:45608303-45608304	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs8077485	chr17:45608326-45608327	Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs571880226	chr17:45608342-45608343	Weak transcription Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs534357597	chr17:45608381-45608382	Weak transcription Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs552807092	chr17:45608511-45608512	Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs142358928	chr17:45608592-45608593	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs572926933	chr17:45608609-45608610	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs535178976	chr17:45608628-45608629	Weak transcription Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:118)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Ovarian cancer	22174824	CNVD
Melanoma	18172304	CNVD
Moyamoya disease	22323933	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ovarian cancer	21781307	CNVD
Colorectal cancer	21645411	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Medulloblastoma	21979893	CNVD
Cancer	20164919	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell lymphomas	19863542	CNVD
Cancer	16751803	CNVD
Chordoma	21602918	CNVD
Neurofibromatosis	20686819	CNVD
Peripheral nerve sheath tumors	20686819	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Neuroblastoma	18923524	CNVD
Neuroblastoma	17897457	CNVD
Neuroblastoma	17327916	CNVD
Breast cancer	21264507	CNVD
Endometrial cancer	22040021	CNVD
Neuroblastoma	21484798	CNVD
Breast cancer	22028636	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Acute myeloid leukemia	20724749	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Gastric cancer	17167181	CNVD
Breast cancer	19287154	CNVD
Leukemia	20874852	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	17533364	CNVD
Human rectal carcinomas	16397240	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	16608533	CNVD
Breast cancer	17457667	CNVD
Breast cancer	16951389	CNVD
Basal cell lymphoma	17053054	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22048815	CNVD
Breast cancer	17603634	CNVD
Follicular lymphoma	20505157	CNVD
Non-small cell lung cancer	20864512	CNVD
Cancer	21183584	CNVD
Cervical cancer	21062161	CNVD
Breast cancer	20953835	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
TAR Syndrome	17847015	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	17850661	CNVD
Breast cancer	19261255	CNVD
Lung cancer	16773561	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Basal-like breast cancer	18066063	CNVD
Breast cancer	20031965	CNVD
Colorectal cancer	19287155	CNVD
Hereditary breast	19566914	CNVD
Ovarian cancer	19047089	CNVD
Ovarian cancer	19566914	CNVD
Triple-negative breast cancer	18950515	CNVD
Breast cancer	16846527	CNVD
Bladder cancer	21909424	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	21251322	CNVD
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21364760	CNVD
Urothelial carcinoma	21177765	CNVD
Breast cancer	16397240	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	17217626	CNVD
Non-syndromic sensorineural hearing loss	21084979	CNVD
Autism	22817714	CNVD
Breast cancer	20409316	CNVD
Cancer	17160897	CNVD
Frontotemporal lobar degeneration	19640594	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	21509527	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:258 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:45604200-45608000	Weak transcription	ES-I3 Cell Line	embryonic stem cell
2	chr17:45607600-45607800	Enhancers	Placenta	Placenta
3	chr17:45607600-45607800	Enhancers	Dnd41	blood
4	chr17:45607600-45607800	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr17:45607600-45608000	Enhancers	Primary T cells fromperipheralblood	blood
6	chr17:45607600-45609400	Active TSS	Primary neutrophils fromperipheralblood	blood
7	chr17:45607600-45610800	Active TSS	A549	lung
8	chr17:45607800-45608000	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr17:45607800-45608000	Enhancers	Primary B cells from peripheral blood	blood
10	chr17:45607800-45608000	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
11	chr17:45607800-45608000	Enhancers	Cortex derived primary cultured neurospheres	brain
12	chr17:45607800-45608000	Enhancers	Fetal Muscle Leg	muscle
13	chr17:45607800-45608200	Enhancers	Primary B cells from cord blood	blood
14	chr17:45607800-45608200	Flanking Active TSS	Placenta	Placenta
15	chr17:45607800-45608200	Flanking Active TSS	Dnd41	blood
16	chr17:45607800-45609400	Active TSS	Primary T regulatory cells fromperipheralblood	blood
17	chr17:45607800-45609800	Active TSS	Monocytes-CD14+_RO01746	blood
18	chr17:45607800-45610000	Active TSS	Colonic Mucosa	Colon
19	chr17:45607800-45610200	Active TSS	Rectal Mucosa Donor 31	rectum
20	chr17:45607800-45610400	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr17:45608000-45608200	Enhancers	ES-I3 Cell Line	embryonic stem cell
22	chr17:45608000-45608200	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
23	chr17:45608000-45608200	Flanking Active TSS	Primary B cells from peripheral blood	blood
24	chr17:45608000-45608200	Flanking Active TSS	Primary T cells fromperipheralblood	blood
25	chr17:45608000-45608200	Enhancers	Primary hematopoietic stem cells short term culture	blood
26	chr17:45608000-45608200	Flanking Active TSS	Primary Natural Killer cells fromperipheralblood	blood
27	chr17:45608000-45608200	Flanking Active TSS	Cortex derived primary cultured neurospheres	brain
28	chr17:45608000-45608200	Flanking Active TSS	Fetal Muscle Leg	muscle
29	chr17:45608000-45608200	Enhancers	K562	blood
30	chr17:45608000-45608400	Active TSS	Brain Angular Gyrus	brain
31	chr17:45608000-45609200	Active TSS	Primary T helper naive cells fromperipheralblood	blood
32	chr17:45608000-45609200	Active TSS	Primary mononuclear cells fromperipheralblood	Blood
33	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells	blood
34	chr17:45608000-45609400	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
35	chr17:45608000-45609400	Active TSS	Primary T helper cells PMA-I stimulated	--
36	chr17:45608000-45609400	Active TSS	Primary T helper cells fromperipheralblood	blood
37	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
38	chr17:45608000-45609400	Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr17:45608000-45609400	Active TSS	Liver	Liver
40	chr17:45608000-45609600	Active TSS	Primary T helper naive cells from peripheral blood	blood
41	chr17:45608000-45609600	Active TSS	Primary T helper 17 cells PMA-I stimulated	--
42	chr17:45608000-45609600	Active TSS	Fetal Adrenal Gland	Adrenal Gland
43	chr17:45608000-45609600	Active TSS	Fetal Muscle Trunk	muscle
44	chr17:45608000-45609600	Active TSS	Fetal Thymus	thymus
45	chr17:45608000-45609800	Active TSS	ES-WA7 Cell Line	embryonic stem cell
46	chr17:45608000-45609800	Active TSS	Primary T cells from cord blood	blood
47	chr17:45608000-45609800	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
48	chr17:45608000-45609800	Active TSS	Primary T killer naive cells fromperipheralblood	blood
49	chr17:45608000-45609800	Active TSS	Colon Smooth Muscle	Colon
50	chr17:45608000-45610000	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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