Variant report

Variant	nsv908704
Chromosome Location	chr17:66925324-66959710
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	chr17:66951429-66951869	K562	blood:	n/a	n/a
2	ARID3A	chr17:66934164-66934682	HepG2	liver:	n/a	n/a
3	ATF1	chr17:66951343-66951843	K562	blood:	n/a	n/a
4	ATF3	chr17:66951415-66951687	K562	blood:	n/a	n/a
5	BRCA1	chr17:66957235-66957255	HepG2	liver:	n/a	n/a
6	CEBPB	chr17:66952202-66952390	K562	blood:	n/a	n/a
7	CEBPB	chr17:66946779-66947429	K562	blood:	n/a	chr17:66947347-66947358
8	CEBPB	chr17:66950796-66951137	Hela-S3	cervix:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
9	CEBPB	chr17:66950797-66951135	A549	lung:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
10	CEBPB	chr17:66950789-66951122	H1-hESC	embryonic stem cell:	n/a	chr17:66950969-66950978 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
11	CEBPB	chr17:66950799-66951062	K562	blood:	n/a	chr17:66950969-66950978 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
12	CEBPB	chr17:66950722-66951085	A549	lung:	n/a	chr17:66950969-66950978 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
13	CEBPB	chr17:66938012-66938194	HepG2	liver:	n/a	chr17:66938120-66938131
14	CEBPB	chr17:66950544-66951220	K562	blood:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
15	CEBPB	chr17:66934423-66934641	HepG2	liver:	n/a	n/a
16	CEBPB	chr17:66950744-66951170	K562	blood:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
17	CEBPB	chr17:66950794-66951153	HepG2	liver:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
18	CEBPB	chr17:66950782-66951157	IMR90	lung:	n/a	chr17:66950969-66950978 chr17:66951113-66951124 chr17:66950967-66950980 chr17:66950968-66950979 chr17:66950967-66950980 chr17:66950967-66950978 chr17:66951113-66951124 chr17:66950969-66950978 chr17:66950969-66950978 chr17:66950969-66950978
19	CEBPB	chr17:66938010-66938212	A549	lung:	n/a	chr17:66938120-66938131
20	CEBPB	chr17:66937950-66938271	K562	blood:	n/a	chr17:66938120-66938131
21	CEBPB	chr17:66949911-66950058	K562	blood:	n/a	n/a
22	CREB1	chr17:66951280-66951875	K562	blood:	n/a	n/a
23	CREB1	chr17:66951252-66951984	K562	blood:	n/a	n/a
24	CTCF	chr17:66957560-66957710	NHEK	skin:	n/a	n/a
25	CTCF	chr17:66957800-66957950	NHLF	lung:	n/a	chr17:66957863-66957872
26	CTCF	chr17:66957720-66957870	NHEK	skin:	n/a	n/a
27	CTCF	chr17:66949860-66950010	HPAF	blood vessel:	n/a	n/a
28	CTCF	chr17:66949820-66949970	HCM	heart:	n/a	n/a
29	CTCF	chr17:66949860-66950010	HCPEpiC	choroid plexus:	n/a	n/a
30	CTCF	chr17:66949880-66950030	HPAF	blood vessel:	n/a	n/a
31	CTCF	chr17:66957845-66957892	NHEK	skin:	n/a	chr17:66957863-66957872
32	CTCF	chr17:66949880-66950030	AoAF	blood vessel:	n/a	n/a
33	CTCF	chr17:66949880-66950030	HCPEpiC	choroid plexus:	n/a	n/a
34	CTCF	chr17:66949860-66950010	HMF	breast:	n/a	n/a
35	CTCF	chr17:66949840-66949990	HMF	breast:	n/a	n/a
36	CTCF	chr17:66949880-66950030	HBMEC	blood vessel:	n/a	n/a
37	CTCF	chr17:66949886-66949994	K562	blood:	n/a	n/a
38	CTCF	chr17:66957720-66957870	HepG2	liver:	n/a	n/a
39	CTCF	chr17:66957760-66957910	GM12873	blood:	n/a	chr17:66957863-66957872
40	CUX1	chr17:66951385-66952018	K562	blood:	n/a	n/a
41	CUX1	chr17:66946818-66947179	K562	blood:	n/a	n/a
42	CUX1	chr17:66949352-66949458	K562	blood:	n/a	n/a
43	E2F4	chr17:66928967-66929167	MCF10A-Er-Src	breast:	n/a	n/a
44	ELF1	chr17:66951472-66951687	K562	blood:	n/a	n/a
45	EP300	chr17:66951410-66951719	GM12878	blood:	n/a	n/a
46	EP300	chr17:66951302-66951700	K562	blood:	n/a	chr17:66951328-66951342
47	EP300	chr17:66934215-66934661	HepG2	liver:	n/a	n/a
48	EP300	chr17:66934204-66934760	HepG2	liver:	n/a	n/a
49	FOS	chr17:66937943-66938142	MCF10A-Er-Src	breast:	n/a	chr17:66938069-66938077 chr17:66938070-66938077
50	FOS	chr17:66935293-66935687	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr17:66925642-66925692	GM12878	blood:	n/a
2	chr17:66925642-66925692	PFSK-1	brain:	n/a
3	chr17:66926513-66926563	HMEC	breast:	n/a
4	chr17:66926513-66926563	HIPEpiC	eye:	n/a
5	chr17:66950545-66950595	HL-60	blood:	n/a
6	chr17:66942706-66942756	ProgFib	skin:	n/a
7	chr17:66942706-66942756	NH-A	brain:	n/a
8	chr17:66942706-66942756	HEK293	kidney:	embryo
9	chr17:66942706-66942756	U87	brain:	n/a
10	chr17:66925642-66925692	NT2-D1	testis:	n/a
11	chr17:66926513-66926563	HRE	kidney:	n/a
12	chr17:66951572-66951622	IMR90	lung:	fetal
13	chr17:66925642-66925692	Caco-2	colon:	n/a
14	chr17:66942706-66942756	Hela-S3	cervix:	n/a
15	chr17:66926513-66926563	HAEpiC	amniotic membrane:	n/a
16	chr17:66942706-66942756	RPTEC	kidney:	n/a
17	chr17:66951572-66951622	AG09319	gingival:	n/a
18	chr17:66925642-66925692	BJ	skin:	n/a
19	chr17:66942706-66942756	NHBE	bronchial:	n/a
20	chr17:66926513-66926563	GM19239	blood:	n/a
21	chr17:66926513-66926563	NH-A	brain:	n/a
22	chr17:66950545-66950595	Caco-2	colon:	n/a
23	chr17:66951572-66951622	NHDF-neo	bronchial:	n/a
24	chr17:66925642-66925692	H1-hESC	embryonic stem cell:	embryo
25	chr17:66950545-66950595	CMK	blood:	n/a
26	chr17:66942706-66942756	NB4	blood:	n/a
27	chr17:66951572-66951622	ECC-1	luminal epithelium:	n/a
28	chr17:66925642-66925692	GM12892	blood:	n/a
29	chr17:66926513-66926563	Caco-2	colon:	n/a
30	chr17:66925642-66925692	PrEC	prostate:	n/a
31	chr17:66950545-66950595	HEEpiC	esophagus:	n/a
32	chr17:66942706-66942756	Caco-2	colon:	n/a
33	chr17:66925642-66925692	HEEpiC	esophagus:	n/a
34	chr17:66951572-66951622	BJ	skin:	n/a
35	chr17:66926513-66926563	AG04449	skin:	fetal
36	chr17:66925642-66925692	SKMC	muscle:	n/a
37	chr17:66942706-66942756	HRCEpiC	kidney:	n/a
38	chr17:66925642-66925692	ovcar-3	ovarian:	n/a
39	chr17:66926513-66926563	A549	lung:	n/a
40	chr17:66926513-66926563	U87	brain:	n/a
41	chr17:66926513-66926563	NT2-D1	testis:	n/a
42	chr17:66951572-66951622	HUVEC	blood vessel:	n/a
43	chr17:66942706-66942756	AG09309	skin:	n/a
44	chr17:66951572-66951622	ProgFib	skin:	n/a
45	chr17:66926513-66926563	IMR90	lung:	fetal
46	chr17:66926513-66926563	HRCEpiC	kidney:	n/a
47	chr17:66942706-66942756	GM06990	blood:	n/a
48	chr17:66926513-66926563	HCPEpiC	choroid plexus:	n/a
49	chr17:66942706-66942756	SK-N-SH	brain:	n/a
50	chr17:66926513-66926563	NHBE	bronchial:	n/a

No.	Distal block	Cell Line	Cell type
1	chr1:150945529..150947119-chr17:66926338..66928766,2	MCF-7	breast:
2	chr17:66924075..66929120-chr17:66931843..66935523,4	K562	blood:
3	chr17:66956572..66959212-chr17:67192982..67195972,2	K562	blood:
4	chr13:89843854..89844646-chr17:66927017..66927781,2	MCF-7	breast:

Variant related genes	Relation type
ABCA8	TF binding region
ABCA8	CpG island
ENSG00000143418	chromatin interactions
ENSG00000141338	chromatin interactions
ENSG00000231073	chromatin interactions

Extended variants
information (count: 1384 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:1384 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4147979	chr17:66925324-66925325	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs75793037	chr17:66925328-66925329	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs112947975	chr17:66925334-66925335	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs143207789	chr17:66925340-66925341	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs551606920	chr17:66925370-66925371	Weak transcription Strong transcription Genic enhancers Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs369668312	chr17:66925404-66925405	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs370719463	chr17:66925416-66925417	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs138929169	chr17:66925417-66925418	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs142822217	chr17:66925450-66925451	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs545033371	chr17:66925487-66925488	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs549088089	chr17:66925509-66925510	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs567624605	chr17:66925579-66925580	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs76738302	chr17:66925592-66925593	Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs556572390	chr17:66925642-66925643	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
15	rs113602844	chr17:66925670-66925671	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
16	rs190836676	chr17:66925673-66925674	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
17	rs4147978	chr17:66925674-66925675	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs558015179	chr17:66925680-66925681	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
19	rs375018927	chr17:66925684-66925685	Weak transcription Strong transcription Enhancers	CpG island	1 gene(s)	Overlapped CNVs	n/a
20	rs147262358	chr17:66925703-66925704	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs138825406	chr17:66925723-66925724	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs540491916	chr17:66925729-66925730	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs181049116	chr17:66925753-66925754	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs376987031	chr17:66925774-66925775	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs149397233	chr17:66925803-66925804	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs370078649	chr17:66925823-66925824	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs573542578	chr17:66925824-66925825	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs114603216	chr17:66925840-66925841	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs187336407	chr17:66925871-66925872	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs571015346	chr17:66925888-66925889	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs4147977	chr17:66925910-66925911	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs4147976	chr17:66925923-66925924	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs560345179	chr17:66925974-66925975	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs4147975	chr17:66926017-66926018	Weak transcription Strong transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs147400868	chr17:66926049-66926050	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs532750959	chr17:66926092-66926093	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs531726906	chr17:66926104-66926105	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs201863594	chr17:66926128-66926129	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs549944536	chr17:66926130-66926131	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs192063089	chr17:66926169-66926170	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs537398823	chr17:66926179-66926180	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs67234002	chr17:66926181-66926182	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs539164060	chr17:66926197-66926198	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs554328317	chr17:66926202-66926203	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs539544013	chr17:66926271-66926272	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs566636597	chr17:66926314-66926315	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs533754999	chr17:66926323-66926324	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs138028825	chr17:66926390-66926391	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs111793514	chr17:66926394-66926395	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs141668278	chr17:66926513-66926514	Weak transcription Strong transcription	CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	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
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
Endometrioid adenocarcinoma	16974079	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Neuroblastoma	18923191	CNVD
Bladder cancer	21909424	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
Ewing''s sarcoma	22429812	CNVD
Prostate cancer	18632612	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Breast cancer	21509527	CNVD
Chordoma	18071362	CNVD
Cancer	16751803	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Breast cancer	21523713	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Medulloblastoma	16783165	CNVD
Breast cancer	21785460	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	16397240	CNVD
Breast cancer	17603634	CNVD
Urothelial carcinoma	18382360	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Breast cancer	21858162	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
Cancer	21129771	CNVD
Congenital generalized hypertrichosis terminalis	19463983	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
XY gonadal dysgenesis	20685758	CNVD
Gingival hyperplasia	19463983	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Neuroblastoma	20406844	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16417655	CNVD
Breast cancer	21045282	CNVD
Epilepsy	22083797	CNVD
Sezary syndrome	18413736	CNVD
Honadal dysgenesis	21408189	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:307 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:66906600-66927400	Weak transcription	Aorta	Aorta
2	chr17:66906800-66928200	Weak transcription	Rectal Mucosa Donor 31	rectum
3	chr17:66907000-66940800	Weak transcription	Spleen	Spleen
4	chr17:66908000-66949000	Weak transcription	Right Ventricle	heart
5	chr17:66908200-66930000	Weak transcription	Brain Angular Gyrus	brain
6	chr17:66912400-66928400	Weak transcription	Colon Smooth Muscle	Colon
7	chr17:66914400-66930200	Weak transcription	Stomach Smooth Muscle	stomach
8	chr17:66916200-66934200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
9	chr17:66916200-66949000	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr17:66916200-66949400	Weak transcription	Fetal Muscle Leg	muscle
11	chr17:66916400-66928800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr17:66916400-66938600	Weak transcription	Psoas Muscle	Psoas
13	chr17:66916400-66949200	Weak transcription	Muscle Satellite Cultured Cells	--
14	chr17:66916400-66949400	Weak transcription	Osteobl	bone
15	chr17:66921000-66927000	Weak transcription	Fetal Muscle Trunk	muscle
16	chr17:66921200-66941000	Weak transcription	Fetal Heart	heart
17	chr17:66923000-66939000	Weak transcription	K562	blood
18	chr17:66923400-66932600	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
19	chr17:66923400-66936600	Weak transcription	Duodenum Smooth Muscle	Duodenum
20	chr17:66923400-66938600	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
21	chr17:66923600-66927000	Weak transcription	Brain Hippocampus Middle	brain
22	chr17:66923600-66928400	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
23	chr17:66923600-66932000	Weak transcription	Brain Anterior Caudate	brain
24	chr17:66923600-66932000	Weak transcription	Fetal Stomach	stomach
25	chr17:66923800-66932000	Weak transcription	Brain Cingulate Gyrus	brain
26	chr17:66924400-66925600	Genic enhancers	Liver	Liver
27	chr17:66924400-66925800	Strong transcription	Ovary	ovary
28	chr17:66924600-66927000	Weak transcription	Fetal Lung	lung
29	chr17:66924600-66927800	Weak transcription	Adipose Nuclei	Adipose
30	chr17:66924600-66928400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
31	chr17:66925000-66925400	Strong transcription	Left Ventricle	heart
32	chr17:66925200-66925400	Enhancers	Esophagus	oesophagus
33	chr17:66925200-66925600	Weak transcription	Brain Substantia Nigra	brain
34	chr17:66925400-66927000	Weak transcription	Left Ventricle	heart
35	chr17:66925400-66927200	Weak transcription	Esophagus	oesophagus
36	chr17:66925600-66925800	Enhancers	Brain Substantia Nigra	brain
37	chr17:66925600-66930800	Strong transcription	Liver	Liver
38	chr17:66925800-66926000	Weak transcription	Ovary	ovary
39	chr17:66925800-66926800	Weak transcription	Brain Substantia Nigra	brain
40	chr17:66926000-66927200	Strong transcription	Ovary	ovary
41	chr17:66926800-66927400	Enhancers	Brain Substantia Nigra	brain
42	chr17:66927000-66927200	Genic enhancers	Brain Hippocampus Middle	brain
43	chr17:66927000-66927200	Strong transcription	Fetal Muscle Trunk	muscle
44	chr17:66927000-66927400	Strong transcription	Left Ventricle	heart
45	chr17:66927000-66927600	Strong transcription	Fetal Lung	lung
46	chr17:66927000-66927800	Enhancers	HepG2	liver
47	chr17:66927200-66927400	Enhancers	Brain Hippocampus Middle	brain
48	chr17:66927200-66927400	Enhancers	Esophagus	oesophagus
49	chr17:66927200-66927400	Genic enhancers	Ovary	ovary
50	chr17:66927200-66937400	Weak transcription	Fetal Muscle Trunk	muscle

The 2.0 version of rSNPBase

Variant report

Quick Search:

what's new

Quick links