Variant report

Variant	esv3324863
Chromosome Location	chr17:17900927-17905625
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	BHLHE40	chr17:17902736-17903824	HepG2	liver:	n/a	n/a
2	BHLHE40	chr17:17902747-17903165	K562	blood:	n/a	n/a
3	CEBPB	chr17:17902897-17903224	K562	blood:	n/a	n/a
4	CEBPB	chr17:17902851-17903208	IMR90	lung:	n/a	n/a
5	CEBPB	chr17:17905598-17905722	Hela-S3	cervix:	n/a	n/a
6	CTCF	chr17:17903140-17903290	GM12873	blood:	n/a	n/a
7	CTCF	chr17:17903080-17903230	HEK293	kidney:	n/a	n/a
8	CTCF	chr17:17903040-17903190	SAEC	small airway:	n/a	n/a
9	CTCF	chr17:17903080-17903230	HBMEC	blood vessel:	n/a	n/a
10	E2F6	chr17:17901896-17902064	K562	blood:	n/a	chr17:17901983-17901995
11	FOS	chr17:17905546-17905751	MCF10A-Er-Src	breast:	n/a	n/a
12	FOS	chr17:17905541-17905826	MCF10A-Er-Src	breast:	n/a	n/a
13	FOS	chr17:17905605-17905793	MCF10A-Er-Src	breast:	n/a	n/a
14	FOS	chr17:17905572-17905765	MCF10A-Er-Src	breast:	n/a	n/a
15	JUND	chr17:17902816-17903061	HepG2	liver:	n/a	chr17:17902903-17902914 chr17:17902904-17902914 chr17:17902901-17902912
16	MAX	chr17:17902904-17903291	K562	blood:	n/a	chr17:17903162-17903172
17	MAX	chr17:17903046-17903181	NB4	blood:	n/a	chr17:17903162-17903172
18	MXI1	chr17:17902644-17903476	IMR90	lung:	n/a	n/a
19	NR2C2	chr17:17903271-17903639	GM12878	blood:	n/a	n/a
20	NR2F2	chr17:17902763-17903164	K562	blood:	n/a	n/a
21	NR2F2	chr17:17902814-17903056	K562	blood:	n/a	n/a
22	POLR2A	chr17:17902925-17903735	H1-neurons	neurons:	n/a	n/a
23	POLR2A	chr17:17905243-17905424	HepG2	liver:	n/a	n/a
24	POLR2A	chr17:17903052-17903080	HepG2	liver:	n/a	n/a
25	POLR2A	chr17:17902169-17902175	MCF10A-Er-Src	breast:	n/a	n/a
26	POLR2A	chr17:17903019-17903781	H1-neurons	neurons:	n/a	n/a
27	POLR2A	chr17:17903086-17903639	HepG2	liver:	n/a	n/a
28	REST	chr17:17902180-17902474	PFSK-1	brain:	n/a	n/a
29	SPI1	chr17:17902926-17903051	K562	blood:	n/a	n/a
30	TAL1	chr17:17902849-17903186	K562	blood:	n/a	n/a
31	YY1	chr17:17902848-17903097	K562	blood:	n/a	n/a
32	ZNF263	chr17:17902518-17903076	HEK293-T-REx	kidney:	n/a	chr17:17902841-17902850

No.	Distal block	Cell Line	Cell type
1	chr17:17901299..17904242-chr17:17926943..17929821,2	MCF-7	breast:
2	chr17:17904155..17906615-chr17:17908063..17910293,2	K562	blood:
3	chr17:17903006..17906615-chr17:17908063..17910293,3	K562	blood:
4	chr17:17904327..17906012-chr17:17908673..17910250,2	MCF-7	breast:
5	chr17:17901247..17903124-chr17:17907149..17909889,2	MCF-7	breast:
6	chr17:17890810..17892818-chr17:17898808..17902213,3	K562	blood:
7	chr17:17894578..17897548-chr17:17899295..17901518,2	K562	blood:

Variant related genes	Relation type
ENSG00000201378	TF binding region
LRRC48	TF binding region
ENSG00000171953	chromatin interactions
ENSG00000171962	chromatin interactions

Extended variants
information (count: 196 )
Associated
traits (count: 158 )

Variant overlapped rSNPs/rCNVs (count:196 , 50 per page) page: 1 2 3 4

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs563141191	chr17:17900930-17900931	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs372168615	chr17:17900931-17900932	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs201027663	chr17:17900944-17900945	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs565776542	chr17:17900955-17900956	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs369441797	chr17:17900957-17900958	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs373059687	chr17:17900964-17900965	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs375038316	chr17:17900981-17900982	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs8071238	chr17:17900990-17900991	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
9	rs189010542	chr17:17900998-17900999	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs566014385	chr17:17901005-17901006	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs534894052	chr17:17901066-17901067	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs548132551	chr17:17901098-17901099	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs568237857	chr17:17901113-17901114	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs536359393	chr17:17901169-17901170	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs556576656	chr17:17901195-17901196	Weak transcription Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs551481831	chr17:17901202-17901203	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs576052624	chr17:17901216-17901217	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs181882496	chr17:17901225-17901226	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs147575209	chr17:17901234-17901235	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs572450510	chr17:17901282-17901283	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs541698398	chr17:17901374-17901375	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs374674322	chr17:17901378-17901379	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs369465487	chr17:17901429-17901430	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs142056788	chr17:17901454-17901455	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs543174236	chr17:17901466-17901467	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs563337468	chr17:17901496-17901497	Weak transcription Strong transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs566837858	chr17:17901536-17901537	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs186540937	chr17:17901571-17901572	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs150117369	chr17:17901583-17901584	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs559387260	chr17:17901584-17901585	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs112082871	chr17:17901590-17901591	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs548426741	chr17:17901652-17901653	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs556139637	chr17:17901751-17901752	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs190999341	chr17:17901796-17901797	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs537224818	chr17:17901798-17901799	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs550024101	chr17:17901870-17901871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368605236	chr17:17901880-17901881	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs145789429	chr17:17901883-17901884	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs35964205	chr17:17901903-17901904	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs117844159	chr17:17901928-17901929	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs181400099	chr17:17901936-17901937	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs8075189	chr17:17901946-17901947	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs76061573	chr17:17901989-17901990	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs148986777	chr17:17901990-17901991	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs574947766	chr17:17901999-17902000	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs544027493	chr17:17902000-17902001	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs535792519	chr17:17902006-17902007	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs557568806	chr17:17902079-17902080	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs28537385	chr17:17902135-17902136	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs545905371	chr17:17902220-17902221	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:158)

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
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
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
Ductal carcinoma	22052326	CNVD
Non-syndromic sensorineural hearing loss	18496225	CNVD
Autism	22543975	CNVD
Ovarian cancer	22355333	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:113 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr17:17876400-17903200	Weak transcription	Gastric	stomach
2	chr17:17876600-17914600	Weak transcription	Aorta	Aorta
3	chr17:17876800-17909400	Weak transcription	Brain Substantia Nigra	brain
4	chr17:17876800-17912000	Weak transcription	Colon Smooth Muscle	Colon
5	chr17:17881800-17908200	Weak transcription	Pancreas	Pancrea
6	chr17:17886800-17909400	Weak transcription	Duodenum Smooth Muscle	Duodenum
7	chr17:17886800-17913000	Weak transcription	Fetal Lung	lung
8	chr17:17889000-17907400	Weak transcription	Brain Anterior Caudate	brain
9	chr17:17890000-17907400	Weak transcription	Brain Germinal Matrix	brain
10	chr17:17892200-17908400	Weak transcription	Lung	lung
11	chr17:17892400-17910800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
12	chr17:17892600-17909800	Weak transcription	Brain Angular Gyrus	brain
13	chr17:17892800-17908000	Weak transcription	Spleen	Spleen
14	chr17:17894000-17903400	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr17:17894000-17920600	Weak transcription	Stomach Mucosa	stomach
16	chr17:17894600-17911400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
17	chr17:17895000-17903400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
18	chr17:17895200-17909600	Weak transcription	NHLF	lung
19	chr17:17898000-17909200	Weak transcription	Brain Cingulate Gyrus	brain
20	chr17:17898000-17910800	Weak transcription	Brain Hippocampus Middle	brain
21	chr17:17898200-17902400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr17:17898200-17908200	Weak transcription	Right Ventricle	heart
23	chr17:17898200-17908400	Weak transcription	Fetal Brain Female	brain
24	chr17:17898200-17909000	Weak transcription	Brain Inferior Temporal Lobe	brain
25	chr17:17898200-17918000	Weak transcription	Cortex derived primary cultured neurospheres	brain
26	chr17:17898200-17918000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
27	chr17:17898400-17902600	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
28	chr17:17898400-17902800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
29	chr17:17898400-17903000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
30	chr17:17898400-17905600	Weak transcription	NHDF-Ad	bronchial
31	chr17:17898400-17907400	Weak transcription	Fetal Muscle Leg	muscle
32	chr17:17898400-17910000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
33	chr17:17898400-17911400	Weak transcription	HSMM	muscle
34	chr17:17898600-17902400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr17:17898600-17902600	Weak transcription	Fetal Muscle Trunk	muscle
36	chr17:17898600-17902800	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
37	chr17:17898600-17908400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
38	chr17:17898600-17909800	Weak transcription	Adipose Nuclei	Adipose
39	chr17:17898600-17909800	Weak transcription	Ovary	ovary
40	chr17:17898600-17910600	Weak transcription	Placenta	Placenta
41	chr17:17898600-17910800	Weak transcription	Esophagus	oesophagus
42	chr17:17898600-17917600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
43	chr17:17898800-17908800	Weak transcription	NHEK	skin
44	chr17:17899000-17902400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
45	chr17:17899000-17904600	Weak transcription	Placenta Amnion	Placenta Amnion
46	chr17:17900000-17901200	Strong transcription	Fetal Intestine Small	intestine
47	chr17:17900000-17901200	Strong transcription	Fetal Stomach	stomach
48	chr17:17900000-17901200	Strong transcription	Stomach Smooth Muscle	stomach
49	chr17:17900200-17903400	Enhancers	Fetal Heart	heart
50	chr17:17900400-17902400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived

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