Variant report

Variant	nsv828747
Chromosome Location	chr20:52475762-52484076
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:0)
CpG islands
(count:0)
Chromatin interactive
region (count:132)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:132 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr16:27419619..27422309-chr20:52480366..52482215,2	MCF-7	breast:
2	chr20:52403738..52404269-chr20:52481124..52481895,2	MCF-7	breast:
3	chr20:52480471..52483179-chr9:129365694..129367894,2	MCF-7	breast:
4	chr20:52480111..52481859-chr6:21593030..21595290,2	MCF-7	breast:
5	chr20:52482302..52483839-chr20:52727165..52730009,2	MCF-7	breast:
6	chr20:52403342..52404336-chr20:52481470..52481988,2	MCF-7	breast:
7	chr20:52480563..52482351-chr9:126090029..126091702,2	MCF-7	breast:
8	chr17:43867694..43870674-chr20:52481399..52483362,2	MCF-7	breast:
9	chr20:52403400..52404343-chr20:52480514..52481175,2	MCF-7	breast:
10	chr17:57920817..57923301-chr20:52482910..52485730,2	MCF-7	breast:
11	chr20:52481752..52485242-chr20:55845808..55850200,8	MCF-7	breast:
12	chr20:52482155..52484312-chr9:130323428..130324987,2	MCF-7	breast:
13	chr20:49327701..49329366-chr20:52480366..52482846,2	MCF-7	breast:
14	chr17:57913904..57917268-chr20:52480979..52484930,6	MCF-7	breast:
15	chr20:52481918..52484276-chr20:55753867..55756347,2	MCF-7	breast:
16	chr20:52210166..52211054-chr20:52480725..52481577,3	MCF-7	breast:
17	chr1:114471512..114474044-chr20:52481463..52484304,2	MCF-7	breast:
18	chr17:56734789..56738046-chr20:52480985..52484877,5	MCF-7	breast:
19	chr17:59939831..59941756-chr20:52478044..52481154,3	MCF-7	breast:
20	chr20:52368202..52371256-chr20:52472915..52475847,3	K562	blood:
21	chr20:52403315..52403970-chr20:52482550..52483200,2	MCF-7	breast:
22	chr20:52462487..52463357-chr20:52481724..52482466,3	MCF-7	breast:
23	chr20:52480308..52482647-chr3:156271373..156273715,2	MCF-7	breast:
24	chr17:45746021..45748218-chr20:52482710..52484284,3	MCF-7	breast:
25	chr20:52367063..52367873-chr20:52481613..52482604,2	MCF-7	breast:
26	chr20:52479441..52482415-chr3:186499654..186502146,2	MCF-7	breast:
27	chr17:56707643..56709532-chr20:52480297..52482944,2	MCF-7	breast:
28	chr17:75282518..75284568-chr20:52482187..52484117,2	MCF-7	breast:
29	chr13:42535349..42537267-chr20:52481642..52484433,2	MCF-7	breast:
30	chr20:50414398..50417627-chr20:52478226..52480048,3	MCF-7	breast:
31	chr20:52462474..52463337-chr20:52480867..52481393,2	MCF-7	breast:
32	chr20:52483037..52485677-chr9:12813088..12815674,2	MCF-7	breast:
33	chr20:52478179..52488683-chr20:55835744..55846940,26	MCF-7	breast:
34	chr17:56706335..56710914-chr20:52478718..52484082,7	MCF-7	breast:
35	chr17:42297720..42299653-chr20:52481879..52484305,2	MCF-7	breast:
36	chr20:49358154..49361002-chr20:52481386..52484444,3	MCF-7	breast:
37	chr20:52278292..52278903-chr20:52480742..52481616,3	MCF-7	breast:
38	chr20:52402667..52403323-chr20:52481515..52482169,2	MCF-7	breast:
39	chr20:45988422..45990533-chr20:52480760..52483220,2	MCF-7	breast:
40	chr20:52483421..52485868-chr20:55831559..55834264,2	MCF-7	breast:
41	chr20:52482856..52483578-chr20:52531496..52532508,5	MCF-7	breast:
42	chr13:28501323..28502030-chr20:52481842..52482437,2	MCF-7	breast:
43	chr20:52481326..52483442-chr4:6576919..6578844,2	MCF-7	breast:
44	chr20:52480919..52483362-chr7:155436504..155438211,2	MCF-7	breast:
45	chr20:52482916..52483597-chr20:52531915..52532688,3	MCF-7	breast:
46	chr12:120726893..120729772-chr20:52476403..52478337,2	MCF-7	breast:
47	chr20:52476331..52478777-chr20:52492357..52493924,2	K562	blood:
48	chr20:52479588..52482520-chr20:52814960..52817385,2	MCF-7	breast:
49	chr20:52481454..52483306-chr8:125857851..125859697,2	MCF-7	breast:
50	chr20:52372417..52373284-chr20:52482553..52483441,2	MCF-7	breast:

No data

Variant related genes	Relation type
ENSG00000235448	chromatin interactions
ENSG00000127124	chromatin interactions
ENSG00000267882	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000179818	chromatin interactions
ENSG00000263826	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000260793	chromatin interactions
ENSG00000103227	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000082701	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000229848	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000013288	chromatin interactions
ENSG00000155366	chromatin interactions
ENSG00000111057	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000101115	chromatin interactions
ENSG00000184924	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000114850	chromatin interactions
ENSG00000169564	chromatin interactions
ENSG00000106069	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000135452	chromatin interactions
ENSG00000235527	chromatin interactions
ENSG00000129351	chromatin interactions
ENSG00000046647	chromatin interactions
ENSG00000267100	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000184640	chromatin interactions
ENSG00000170832	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000216895	chromatin interactions
ENSG00000064787	chromatin interactions
ENSG00000184863	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000124766	chromatin interactions
ENSG00000136492	chromatin interactions

Extended variants
information (count: 634 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:634 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs73146535	chr20:52475764-52475765	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs58020297	chr20:52475795-52475796	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs142387119	chr20:52475811-52475812	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs74365704	chr20:52475825-52475826	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs80037225	chr20:52475827-52475828	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs202222916	chr20:52475835-52475836	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs554656953	chr20:52475839-52475840	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs73146537	chr20:52475849-52475850	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs574402678	chr20:52475852-52475853	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs540314053	chr20:52475896-52475897	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs6022805	chr20:52475912-52475913	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs554118015	chr20:52475922-52475923	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs192826866	chr20:52475962-52475963	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs577491719	chr20:52475976-52475977	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs6022806	chr20:52476025-52476026	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs6126992	chr20:52476042-52476043	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs66723113	chr20:52476051-52476052	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs531759200	chr20:52476071-52476072	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs62206591	chr20:52476072-52476073	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs185306789	chr20:52476078-52476079	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs62206592	chr20:52476090-52476091	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs76906401	chr20:52476103-52476104	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs114961392	chr20:52476104-52476105	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs562218884	chr20:52476143-52476144	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs386815145	chr20:52476160-52476161	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs78609519	chr20:52476162-52476163	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs62206593	chr20:52476167-52476168	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs79520917	chr20:52476173-52476174	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs73146540	chr20:52476179-52476180	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs567448994	chr20:52476213-52476214	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs117997024	chr20:52476251-52476252	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs67623449	chr20:52476254-52476255	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs140580688	chr20:52476266-52476267	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs150496200	chr20:52476272-52476273	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs79934682	chr20:52476280-52476281	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs75293681	chr20:52476292-52476293	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs78068331	chr20:52476310-52476311	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs75060216	chr20:52476314-52476315	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs386815146	chr20:52476332-52476333	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs77288308	chr20:52476333-52476334	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs75134459	chr20:52476337-52476338	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs75003913	chr20:52476345-52476346	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs73146542	chr20:52476360-52476361	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs73914607	chr20:52476391-52476392	Enhancers Weak transcription Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs568765961	chr20:52476409-52476410	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs73914608	chr20:52476410-52476411	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs62206594	chr20:52476420-52476421	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs13041552	chr20:52476430-52476431	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs13041973	chr20:52476431-52476432	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs73273910	chr20:52476492-52476493	Enhancers Weak transcription Bivalent Enhancer ZNF genes & repeats	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:82)

Disease	PMID	Source
Gastric cancer	17908304	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Urothelial carcinoma	21177765	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	21645411	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Melanoma	21693616	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Endometrial cancer	22040021	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Hepatocellular carcinoma	22174799	CNVD
colon cancer	17210682	CNVD
Colorectal cancer	20709793	CNVD
Breast cancer	22028636	CNVD
Breast cancer	21264507	CNVD
Thyroid cancer	19087340	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Colorectal cancer	19359472	CNVD
Gastric cancer	17167181	CNVD
Myeloproliferative neoplasm	19047681	CNVD
Breast cancer	17899364	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Breast cancer	17603634	CNVD
Melanoma	18172304	CNVD
Breast cancer	16608533	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17133270	CNVD
Oral cancer	21386901	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Ewing''s sarcoma	18628472	CNVD
Glioblastoma multiforme	18628472	CNVD
Leukemia	18628472	CNVD
Acute myeloid leukemia	20729466	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Myelodysplastic syndrome	21251322	CNVD
Ductal carcinoma	22052326	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Colorectal cancer	16774939	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Gastric cancer	20585902	CNVD
Ductal carcinoma	18381933	CNVD
Cancer	21129771	CNVD
Cancer	21183584	CNVD
Non-small cell lung cancer	20864512	CNVD
Ovarian cancer	22174824	CNVD
Lung cancer	16740712	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	16620391	CNVD
Okamoto syndrome	17623483	CNVD
Breast cancer	21858162	CNVD
Breast cancer	21785460	CNVD
Bladder cancer	21909424	CNVD
Biliary cancer	19435499	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Cervical cancer	16585170	CNVD
Ovarian cancer	20844748	CNVD
Hirschsprung''s Disease	21712996	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20459607	CNVD
Gastric cancer	18160780	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Medulloblastoma	16783165	CNVD

Chromatin state (count:540 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52453600-52480200	Weak transcription	Small Intestine	intestine
2	chr20:52456600-52476200	Weak transcription	Gastric	stomach
3	chr20:52468800-52476200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
4	chr20:52468800-52481400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
5	chr20:52472200-52476600	Enhancers	Rectal Mucosa Donor 31	rectum
6	chr20:52472400-52480800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
7	chr20:52473200-52480200	Weak transcription	Primary T helper cells PMA-I stimulated	--
8	chr20:52473400-52476200	Weak transcription	Placenta	Placenta
9	chr20:52473400-52476200	Weak transcription	Spleen	Spleen
10	chr20:52473600-52476400	Weak transcription	Monocytes-CD14+_RO01746	blood
11	chr20:52474000-52476600	Enhancers	Stomach Mucosa	stomach
12	chr20:52474200-52476600	Enhancers	Duodenum Mucosa	Duodenum
13	chr20:52474400-52476200	Weak transcription	H9 Cell Line	embryonic stem cell
14	chr20:52474600-52476200	Weak transcription	Aorta	Aorta
15	chr20:52474600-52480200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
16	chr20:52474600-52480200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr20:52474600-52481600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr20:52474800-52476200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
19	chr20:52474800-52476200	Weak transcription	HUES6 Cell Line	embryonic stem cell
20	chr20:52474800-52476200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr20:52474800-52476200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
22	chr20:52474800-52476200	Weak transcription	iPS-18 Cell Line	embryonic stem cell
23	chr20:52474800-52476200	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
24	chr20:52474800-52476200	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr20:52474800-52476200	Weak transcription	Fetal Muscle Leg	muscle
26	chr20:52474800-52476200	Weak transcription	Fetal Stomach	stomach
27	chr20:52474800-52476200	Weak transcription	Sigmoid Colon	Sigmoid Colon
28	chr20:52474800-52476200	Weak transcription	K562	blood
29	chr20:52474800-52476400	Weak transcription	HUES64 Cell Line	embryonic stem cell
30	chr20:52474800-52479600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
31	chr20:52474800-52480000	Weak transcription	Ovary	ovary
32	chr20:52474800-52480000	Weak transcription	A549	lung
33	chr20:52474800-52480200	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
34	chr20:52474800-52480200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
35	chr20:52474800-52480200	Weak transcription	Fetal Thymus	thymus
36	chr20:52474800-52480200	Weak transcription	Pancreas	Pancrea
37	chr20:52474800-52480800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
38	chr20:52474800-52480800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
39	chr20:52474800-52482000	Weak transcription	Thymus	Thymus
40	chr20:52474800-52482600	Weak transcription	Left Ventricle	heart
41	chr20:52475000-52476000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
42	chr20:52475000-52476200	Weak transcription	H1 Cell Line	embryonic stem cell
43	chr20:52475000-52476200	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
44	chr20:52475000-52476200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
45	chr20:52475000-52476200	Weak transcription	Fetal Lung	lung
46	chr20:52475000-52476200	Weak transcription	Rectal Mucosa Donor 29	rectum
47	chr20:52475000-52479600	Weak transcription	Fetal Kidney	kidney
48	chr20:52475000-52480000	Weak transcription	Duodenum Smooth Muscle	Duodenum
49	chr20:52475000-52480200	Weak transcription	Primary T cells from cord blood	blood
50	chr20:52475000-52480200	Weak transcription	Colonic Mucosa	Colon

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