Variant report

Variant	nsv960065
Chromosome Location	chr17:16758719-16789003
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	BATF	chr17:16788586-16788829	GM12878	blood:	n/a	chr17:16788732-16788742 chr17:16788731-16788742
2	BHLHE40	chr17:16776637-16776774	A549	lung:	n/a	n/a
3	BRCA1	chr17:16776669-16776811	H1-hESC	embryonic stem cell:	n/a	n/a
4	BRCA1	chr17:16764549-16764560	Hela-S3	cervix:	n/a	n/a
5	CEBPB	chr17:16768234-16768445	Hela-S3	cervix:	n/a	n/a
6	CEBPB	chr17:16781507-16781814	HepG2	liver:	n/a	chr17:16781621-16781632 chr17:16781621-16781634
7	CEBPB	chr17:16771631-16771906	A549	lung:	n/a	chr17:16771790-16771801
8	CEBPB	chr17:16763881-16764076	A549	lung:	n/a	chr17:16764008-16764019
9	CEBPB	chr17:16781616-16781809	IMR90	lung:	n/a	chr17:16781621-16781632 chr17:16781621-16781634
10	CEBPB	chr17:16764004-16764108	HepG2	liver:	n/a	chr17:16764008-16764019
11	CEBPB	chr17:16764555-16764730	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr17:16773866-16773956	A549	lung:	n/a	n/a
13	CEBPB	chr17:16771713-16771889	HepG2	liver:	n/a	chr17:16771790-16771801
14	CEBPB	chr17:16763876-16764183	Hela-S3	cervix:	n/a	chr17:16764008-16764019
15	CHD2	chr17:16764544-16764744	Hela-S3	cervix:	n/a	n/a
16	CTCF	chr17:16776560-16776710	HL-60	blood:	n/a	n/a
17	CTCF	chr17:16769190-16769328	Spleen_OC	spleen:	n/a	chr17:16769264-16769282
18	CTCF	chr17:16769260-16769410	HAc	cerebellar:	n/a	chr17:16769264-16769282
19	CTCF	chr17:16769320-16769470	AG10803	skin:	n/a	n/a
20	CTCF	chr17:16764623-16764825	Gliobla	brain:	n/a	n/a
21	CTCF	chr17:16776578-16776880	ECC-1	luminal epithelium:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
22	CTCF	chr17:16769320-16769470	AG09319	gingival:	n/a	n/a
23	CTCF	chr17:16769260-16769410	HRPEpiC	eye:	n/a	chr17:16769264-16769282
24	CTCF	chr17:16776660-16776810	HPAF	blood vessel:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
25	CTCF	chr17:16776596-16776811	HepG2	liver:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
26	CTCF	chr17:16782260-16782410	HVMF	connective:	n/a	chr17:16782386-16782407 chr17:16782387-16782400
27	CTCF	chr17:16769167-16769370	Kidney_OC	kidney:	n/a	chr17:16769264-16769282
28	CTCF	chr17:16775599-16775683	Spleen_OC	spleen:	n/a	n/a
29	CTCF	chr17:16788734-16788807	GM13976	blood:	n/a	n/a
30	CTCF	chr17:16776620-16776770	Caco-2	colon:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
31	CTCF	chr17:16776640-16776790	GM12875	blood:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
32	CTCF	chr17:16776640-16776790	HA-sp	spinal cord:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
33	CTCF	chr17:16765475-16765549	LNCaP	prostate:	n/a	n/a
34	CTCF	chr17:16783604-16783732	MCF-7	breast:	n/a	n/a
35	CTCF	chr17:16776549-16776871	IMR90	lung:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
36	CTCF	chr17:16764620-16764770	HRE	kidney:	n/a	n/a
37	CTCF	chr17:16788691-16788789	MCF-7	breast:	n/a	n/a
38	CTCF	chr17:16776469-16776895	H1-hESC	embryonic stem cell:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
39	CTCF	chr17:16769138-16769339	MCF-7	breast:	n/a	chr17:16769264-16769282
40	CTCF	chr17:16776660-16776810	HEEpiC	esophagus:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
41	CTCF	chr17:16776960-16777110	GM12864	blood:	n/a	n/a
42	CTCF	chr17:16776616-16776833	MCF-7	breast:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
43	CTCF	chr17:16768660-16768810	HCPEpiC	choroid plexus:	n/a	n/a
44	CTCF	chr17:16764620-16764770	HCT-116	colon:	n/a	n/a
45	CTCF	chr17:16769380-16769530	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr17:16769340-16769490	HPAF	blood vessel:	n/a	n/a
47	CTCF	chr17:16788700-16788817	HepG2	liver:	n/a	n/a
48	CTCF	chr17:16776600-16776750	GM12864	blood:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
49	CTCF	chr17:16776572-16776980	MCF-7	breast:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720
50	CTCF	chr17:16776620-16776770	GM12873	blood:	n/a	chr17:16776707-16776720 chr17:16776706-16776722 chr17:16776705-16776723 chr17:16776700-16776721 chr17:16776712-16776720 chr17:16776707-16776720

No.	Distal block	Cell Line	Cell type
1	chr17:16721818..16722353-chr17:16776583..16777108,2	MCF-7	breast:
2	chr17:16756059..16758999-chr17:16760586..16763495,2	K562	blood:
3	chr17:16784922..16787392-chr17:16982105..16984669,2	K562	blood:

Variant related genes	Relation type
ENSG00000205312	TF binding region
ENSG00000205312	chromatin interactions
ENSG00000229749	chromatin interactions

Extended variants
information (count: 1263 )
Associated
traits (count: 160 )

Variant overlapped rSNPs/rCNVs (count:1263 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs545789910	chr17:16758746-16758747	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs111365978	chr17:16758786-16758787	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs559145936	chr17:16758808-16758809	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs528207091	chr17:16758834-16758835	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs191577162	chr17:16758844-16758845	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs142966760	chr17:16758858-16758859	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs533126332	chr17:16758871-16758872	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs35768340	chr17:16758961-16758962	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs566677788	chr17:16759004-16759005	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs550454486	chr17:16759033-16759034	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs151097122	chr17:16759043-16759044	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs185146900	chr17:16759052-16759053	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs190085822	chr17:16759057-16759058	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs538607667	chr17:16759066-16759067	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs552555577	chr17:16759099-16759100	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs184842117	chr17:16759145-16759146	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs142532886	chr17:16759146-16759147	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs2882119	chr17:16759197-16759198	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs575076872	chr17:16759198-16759199	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs4034437	chr17:16759199-16759200	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs2882120	chr17:16759239-16759240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs147591430	chr17:16759243-16759244	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs190530074	chr17:16759311-16759312	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577623863	chr17:16759331-16759332	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs545449443	chr17:16759343-16759344	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs559323378	chr17:16759364-16759365	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs4034438	chr17:16759378-16759379	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs572782002	chr17:16759379-16759380	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs116955955	chr17:16759380-16759381	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2349285	chr17:16759405-16759406	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs3078339	chr17:16759437-16759438	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs2349286	chr17:16759439-16759440	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs541898445	chr17:16759473-16759474	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs561490333	chr17:16759496-16759497	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs530570136	chr17:16759525-16759526	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs3963147	chr17:16759534-16759535	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs550370397	chr17:16759547-16759548	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs4034439	chr17:16759564-16759565	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs564004529	chr17:16759567-16759568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs533277570	chr17:16759568-16759569	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs546605759	chr17:16759620-16759621	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs2089180	chr17:16759636-16759637	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs566050158	chr17:16759682-16759683	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs2089179	chr17:16759695-16759696	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs3963148	chr17:16759710-16759711	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs372060780	chr17:16759716-16759717	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs534750081	chr17:16759724-16759725	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs548659823	chr17:16759744-16759745	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs182192073	chr17:16759752-16759753	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs186824297	chr17:16759759-16759760	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:160)

Disease	PMID	Source
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
Melanoma	18172304	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
Oral squamous cell carcinoma	17134496	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
Colorectal cancer	16774939	CNVD
Pancreatic cancer	21811587	CNVD
Breast cancer	17001317	CNVD
Rhabdomyosarcoma	16790082	CNVD
Charcot-marie-tooth disease	16463004	CNVD
Osteosarcoma	22292074	CNVD
Breast cancer	17603634	CNVD
Charcot	16760730	CNVD
Mental retardation	17901693	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
ovarian endometriomas	16273235	CNVD
Ovarian cancer	21720365	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Gastric cancer	18160780	CNVD
Smith-Magenis syndrome	18923513	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16272173	CNVD
Austim spectrum disorder	21302340	CNVD
Autism	22492990	CNVD
Congenital abnormalities	21549014	CNVD
Developmental delay	18414209	CNVD
Developmental delay	21549014	CNVD
Epilepsy	20970697	CNVD
Mental retardation	18414209	CNVD
Mental retardation	21549014	CNVD
Smith-Magenis syndrome	21981782	CNVD
Smith-Magenis syndrome	20188345	CNVD
Smith-Magenis syndrome	16775514	CNVD
Smith-Magenis syndrome	22585170	CNVD
Smith-Magenis syndrome	22241247	CNVD
Autism	20970697	CNVD
Mental retardation	19951919	CNVD
Potocki-Lupski syndrome	21271655	CNVD
Potocki-lupski syndrome	17357070	CNVD
Potocki-lupski syndrome	20110824	CNVD
Potocki-lupski syndrome	18923514	CNVD
Potocki-lupski syndrome	22241247	CNVD
Potocki-lupski syndrome	20188345	CNVD
Schizophrenia	21399695	CNVD
Mental retardation	16773131	CNVD
Adenocarcinoma	19607727	CNVD
Squamous cell cancer	19607727	CNVD
Non-small cell lung cancer	21829676	CNVD
Glioblastoma multiforme	17002787	CNVD
Charcot-marie-tooth disease	22470819	CNVD
Neurofibromatosis	22470819	CNVD
Neuropathy	22470819	CNVD
Smith-Magenis syndrome	18301319	CNVD
Smith-Magenis syndrome	17357070	CNVD
Smith-Magenis syndrome	18469339	CNVD
Smith-Magenis syndrome	22241097	CNVD
Smith-Magenis syndrome	22470819	CNVD
Tourette syndrome	18923514	CNVD
Type 1 diabetes	22470819	CNVD
Potocki-lupski syndrome	18469339	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Neuropathy	17597781	CNVD
Hepatocellular carcinoma	16750200	CNVD
Neurodevelopmental disorder	17015230	CNVD
Smith-Magenis syndrome	17597781	CNVD
Potocki-lupski syndrome	18059269	CNVD
Potocki-lupski syndrome	17597781	CNVD
Mental retardation	17847001	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	20409316	CNVD
Breast cancer	21509527	CNVD
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:192 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:16754800-16761200	Weak transcription	Stomach Mucosa	stomach
2	chr17:16758200-16775200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr17:16758400-16760400	Enhancers	Fetal Intestine Large	intestine
4	chr17:16758400-16760600	Enhancers	Fetal Intestine Small	intestine
5	chr17:16758800-16759000	Enhancers	Small Intestine	intestine
6	chr17:16760000-16760400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
7	chr17:16760200-16760600	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr17:16760400-16762000	Weak transcription	Fetal Intestine Large	intestine
9	chr17:16760600-16761000	Weak transcription	Fetal Intestine Small	intestine
10	chr17:16761000-16761200	Enhancers	Fetal Intestine Small	intestine
11	chr17:16761200-16762000	Weak transcription	Fetal Intestine Small	intestine
12	chr17:16761200-16765200	Enhancers	Stomach Mucosa	stomach
13	chr17:16762000-16762200	Active TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
14	chr17:16762000-16762200	Enhancers	Gastric	stomach
15	chr17:16762000-16764800	Enhancers	Fetal Intestine Large	intestine
16	chr17:16762000-16765200	Enhancers	Fetal Intestine Small	intestine
17	chr17:16762200-16776800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr17:16762400-16763400	Weak transcription	Gastric	stomach
19	chr17:16762600-16763000	Enhancers	Duodenum Mucosa	Duodenum
20	chr17:16762600-16763000	Enhancers	A549	lung
21	chr17:16763000-16763400	Weak transcription	Duodenum Mucosa	Duodenum
22	chr17:16763000-16763400	Weak transcription	A549	lung
23	chr17:16763000-16765200	Enhancers	Hela-S3	cervix
24	chr17:16763400-16763800	Enhancers	Gastric	stomach
25	chr17:16763400-16764400	Enhancers	Duodenum Mucosa	Duodenum
26	chr17:16763400-16764800	Enhancers	A549	lung
27	chr17:16763400-16765000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr17:16763600-16764200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
29	chr17:16763600-16764600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
30	chr17:16763600-16764600	Enhancers	Esophagus	oesophagus
31	chr17:16763600-16765000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr17:16763800-16764600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr17:16763800-16765000	Enhancers	NHEK	skin
34	chr17:16764000-16765200	Enhancers	HMEC	breast
35	chr17:16764200-16764600	Enhancers	ES-I3 Cell Line	embryonic stem cell
36	chr17:16764200-16765000	Enhancers	NH-A	brain
37	chr17:16764200-16769600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
38	chr17:16764400-16769400	Weak transcription	Duodenum Mucosa	Duodenum
39	chr17:16764600-16767600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr17:16764600-16769800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
41	chr17:16764800-16768000	Weak transcription	Fetal Intestine Large	intestine
42	chr17:16764800-16769200	Weak transcription	A549	lung
43	chr17:16765000-16769200	Weak transcription	NHEK	skin
44	chr17:16765000-16769400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
45	chr17:16765000-16769800	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr17:16765200-16767200	Weak transcription	HMEC	breast
47	chr17:16765200-16767600	Weak transcription	Fetal Intestine Small	intestine
48	chr17:16765200-16769200	Weak transcription	Stomach Mucosa	stomach
49	chr17:16765200-16769200	Weak transcription	Hela-S3	cervix
50	chr17:16767200-16767400	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow

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