Variant report

Variant	esv18025
Chromosome Location	chr20:52464720-52486135
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:203)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

No data

(count:203 , 50 per page) page: 1 2 3 4 5

No.	Distal block	Cell Line	Cell type
1	chr20:52462638..52464808-chr3:62850144..62851891,3	MCF-7	breast:
2	chr17:57932184..57934585-chr20:52473101..52475297,2	MCF-7	breast:
3	chr20:52471901..52491673-chr20:55835708..55845674,34	MCF-7	breast:
4	chr11:10328570..10330547-chr20:52480919..52483206,2	MCF-7	breast:
5	chr20:52194976..52196071-chr20:52485853..52487276,31	MCF-7	breast:
6	chr20:52233059..52233901-chr20:52486110..52486787,2	MCF-7	breast:
7	chr20:52481454..52483306-chr8:125857851..125859697,2	MCF-7	breast:
8	chr20:52384341..52385045-chr20:52486093..52486635,2	MCF-7	breast:
9	chr20:52476210..52479178-chr20:52479229..52481158,2	K562	blood:
10	chr17:57913904..57917268-chr20:52480979..52484930,6	MCF-7	breast:
11	chr20:52368902..52371159-chr20:52471406..52474415,3	K562	blood:
12	chr20:52480919..52483362-chr7:155436504..155438211,2	MCF-7	breast:
13	chr20:46133845..46135512-chr20:52480481..52482213,2	MCF-7	breast:
14	chr20:52476198..52478320-chr20:52482797..52484408,2	K562	blood:
15	chr20:52482856..52483578-chr20:52531496..52532508,5	MCF-7	breast:
16	chr20:52476210..52479178-chr20:52479229..52481158,2	K562	blood:
17	chr17:79480745..79482983-chr20:52482594..52484140,2	MCF-7	breast:
18	chr17:59474412..59476108-chr20:52481688..52483520,2	MCF-7	breast:
19	chr20:52278383..52278965-chr20:52482508..52483417,2	MCF-7	breast:
20	chr17:57923074..57925214-chr20:52484890..52487156,2	MCF-7	breast:
21	chr20:52482155..52484312-chr9:130323428..130324987,2	MCF-7	breast:
22	chr17:57969168..57971185-chr20:52467018..52469521,2	MCF-7	breast:
23	chr20:52479441..52482415-chr3:186499654..186502146,2	MCF-7	breast:
24	chr17:59652154..59652890-chr20:52480568..52481434,2	MCF-7	breast:
25	chr20:52479837..52482598-chr22:27915640..27918350,2	MCF-7	breast:
26	chr20:52195092..52195876-chr20:52480230..52481887,4	MCF-7	breast:
27	chr1:114470967..114472634-chr20:52479813..52481526,2	MCF-7	breast:
28	chr20:52355095..52355945-chr20:52486074..52486806,2	MCF-7	breast:
29	chr20:52209805..52211171-chr20:52486045..52486721,5	MCF-7	breast:
30	chr17:59471125..59471637-chr20:52485944..52486582,2	MCF-7	breast:
31	chr17:59490690..59492764-chr20:52480509..52482719,2	MCF-7	breast:
32	chr12:53341666..53344368-chr20:52478824..52481024,2	MCF-7	breast:
33	chr20:52402271..52403940-chr20:52480276..52481396,7	MCF-7	breast:
34	chr20:52480111..52481859-chr6:21593030..21595290,2	MCF-7	breast:
35	chr17:59939092..59941762-chr20:52481316..52482941,2	MCF-7	breast:
36	chr20:45947037..45948893-chr20:52482561..52484356,2	MCF-7	breast:
37	chr2:200715652..200716231-chr20:52486094..52486752,2	MCF-7	breast:
38	chr20:52210538..52211147-chr20:52485992..52486693,2	MCF-7	breast:
39	chr12:58138537..58140112-chr20:52481997..52483617,2	MCF-7	breast:
40	chr20:49302292..49303982-chr20:52481386..52483714,2	MCF-7	breast:
41	chr20:52373784..52374675-chr20:52482911..52483518,2	MCF-7	breast:
42	chr20:52482329..52484682-chr5:35145735..35147970,2	MCF-7	breast:
43	chr20:49327701..49329366-chr20:52480366..52482846,2	MCF-7	breast:
44	chr17:57920817..57923301-chr20:52482910..52485730,2	MCF-7	breast:
45	chr20:52481826..52484212-chr20:55825219..55827860,2	MCF-7	breast:
46	chr20:52478179..52488683-chr20:55835744..55846940,26	MCF-7	breast:
47	chr20:52464485..52466366-chr20:52684074..52686854,2	MCF-7	breast:
48	chr20:52402635..52403327-chr20:52480213..52481045,2	MCF-7	breast:
49	chr20:52485674..52487205-chr20:52555803..52557075,17	MCF-7	breast:
50	chr20:52469682..52472418-chr20:52551027..52553100,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TSHZ2-4	chr20:52465059-52465091	NONHSAT080405
2	lnc-TSHZ2-4	chr20:52465950-52466616	NONHSAT080405
3	lnc-TSHZ2-4	chr20:52464584-52464747	XLOC_013570
4	lnc-TSHZ2-4	chr20:52468733-52468982	NONHSAT080405
5	lnc-TSHZ2-4	chr20:52464362-52465029	NONHSAT080405
6	lnc-TSHZ2-4	chr20:52466270-52466442	XLOC_013570
7	lnc-TSHZ2-4	chr20:52464562-52464737	XLOC_013570
8	lnc-PFDN4-6	chr20:52470249-52470254	NONHSAT080408
9	lnc-PFDN4-6	chr20:52469245-52470170	NONHSAT080408

No data

Variant related genes	Relation type
ENSG00000111057	chromatin interactions
ENSG00000103227	chromatin interactions
ENSG00000155366	chromatin interactions
ENSG00000101115	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000124766	chromatin interactions
ENSG00000168298	chromatin interactions
ENSG00000150756	chromatin interactions
ENSG00000263826	chromatin interactions
ENSG00000267100	chromatin interactions
ENSG00000129351	chromatin interactions
ENSG00000180573	chromatin interactions
ENSG00000184640	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000260793	chromatin interactions
ENSG00000229848	chromatin interactions
ENSG00000201524	chromatin interactions
ENSG00000135452	chromatin interactions
ENSG00000082701	chromatin interactions
ENSG00000267131	chromatin interactions
ENSG00000184863	chromatin interactions
ENSG00000241721	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000242622	chromatin interactions
ENSG00000114850	chromatin interactions
ENSG00000267882	chromatin interactions
ENSG00000265595	chromatin interactions
ENSG00000108312	chromatin interactions
ENSG00000163636	chromatin interactions
ENSG00000179818	chromatin interactions
ENSG00000180596	chromatin interactions
ENSG00000170832	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000136492	chromatin interactions
ENSG00000156976	chromatin interactions
ENSG00000267280	chromatin interactions
ENSG00000127124	chromatin interactions
ENSG00000235527	chromatin interactions
ENSG00000046647	chromatin interactions
ENSG00000202538	chromatin interactions
ENSG00000064787	chromatin interactions
ENSG00000101040	chromatin interactions
ENSG00000226124	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000169564	chromatin interactions
ENSG00000108424	chromatin interactions
ENSG00000126756	chromatin interactions
ENSG00000121068	chromatin interactions
ENSG00000158373	chromatin interactions
ENSG00000235448	chromatin interactions
ENSG00000163349	chromatin interactions
ENSG00000150753	chromatin interactions
ENSG00000170421	chromatin interactions
ENSG00000267064	chromatin interactions
ENSG00000216895	chromatin interactions
ENSG00000062716	chromatin interactions
ENSG00000013288	chromatin interactions
ENSG00000106069	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000133805	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000184924	chromatin interactions
ENSG00000171940	chromatin interactions
ENSG00000101144	chromatin interactions
TARBP1	miRNA target sites

Extended variants
information (count: 1272 )
Associated
traits (count: 82 )

Variant overlapped rSNPs/rCNVs (count:1272 , 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	rs570922451	chr20:52464752-52464753	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs376865712	chr20:52464769-52464770	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs552727391	chr20:52464795-52464796	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs538464469	chr20:52464825-52464826	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs371193336	chr20:52464851-52464852	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs558671974	chr20:52464928-52464929	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs189733594	chr20:52464951-52464952	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
8	rs181335776	chr20:52464966-52464967	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs186709345	chr20:52464976-52464977	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs720387	chr20:52465049-52465050	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs6013815	chr20:52465147-52465148	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs374050648	chr20:52465178-52465179	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs6064011	chr20:52465203-52465204	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
14	rs142734837	chr20:52465206-52465207	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs573190211	chr20:52465292-52465293	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs375161544	chr20:52465330-52465331	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs190620437	chr20:52465371-52465372	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs374376488	chr20:52465429-52465430	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs183173772	chr20:52465433-52465434	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
20	rs561270580	chr20:52465465-52465466	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs116912460	chr20:52465502-52465503	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs527709399	chr20:52465504-52465505	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs547770180	chr20:52465516-52465517	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs186302848	chr20:52465544-52465545	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs76339671	chr20:52465558-52465559	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs372062702	chr20:52465566-52465567	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs138378381	chr20:52465582-52465583	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs571863202	chr20:52465583-52465584	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs369725298	chr20:52465584-52465585	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs77168585	chr20:52465585-52465586	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs142685654	chr20:52465586-52465587	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs72491043	chr20:52465588-52465589	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs6097633	chr20:52465633-52465634	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs558149073	chr20:52465645-52465646	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs556372818	chr20:52465647-52465648	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs371298489	chr20:52465649-52465650	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs537621861	chr20:52465650-52465651	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
38	rs73622259	chr20:52465742-52465743	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
39	rs554464044	chr20:52465775-52465776	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs148732715	chr20:52465781-52465782	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs542077704	chr20:52465806-52465807	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs533553928	chr20:52465807-52465808	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs553305291	chr20:52465841-52465842	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs142349125	chr20:52465863-52465864	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs191047010	chr20:52465869-52465870	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs151195105	chr20:52465909-52465910	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs79001089	chr20:52465914-52465915	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs200640090	chr20:52465915-52465916	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs539057583	chr20:52465925-52465926	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs376754987	chr20:52465932-52465933	Weak transcription Enhancers	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:961 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52450400-52465200	Enhancers	Primary T helper cells fromperipheralblood	blood
2	chr20:52450600-52465200	Enhancers	Primary T cells fromperipheralblood	blood
3	chr20:52452400-52465200	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
4	chr20:52453600-52480200	Weak transcription	Small Intestine	intestine
5	chr20:52455000-52464800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
6	chr20:52456600-52468400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr20:52456600-52476200	Weak transcription	Gastric	stomach
8	chr20:52458400-52466200	Enhancers	Fetal Thymus	thymus
9	chr20:52458800-52465200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
10	chr20:52459000-52466600	Enhancers	Primary monocytes fromperipheralblood	blood
11	chr20:52459400-52465200	Enhancers	Primary T helper naive cells from peripheral blood	blood
12	chr20:52459600-52468400	Weak transcription	Rectal Mucosa Donor 31	rectum
13	chr20:52459600-52472600	Weak transcription	Rectal Mucosa Donor 29	rectum
14	chr20:52462400-52465000	Enhancers	HepG2	liver
15	chr20:52462800-52468200	Weak transcription	Osteobl	bone
16	chr20:52463000-52468400	Weak transcription	Muscle Satellite Cultured Cells	--
17	chr20:52463000-52474000	Weak transcription	A549	lung
18	chr20:52463200-52464800	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
19	chr20:52463200-52465200	Enhancers	Primary hematopoietic stem cells	blood
20	chr20:52463200-52465200	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
21	chr20:52463200-52465200	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
22	chr20:52463400-52464800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
23	chr20:52463400-52464800	Enhancers	Brain Anterior Caudate	brain
24	chr20:52463400-52465000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
25	chr20:52463600-52465000	Enhancers	Brain Substantia Nigra	brain
26	chr20:52463600-52465000	Flanking Active TSS	GM12878-XiMat	blood
27	chr20:52464200-52465200	Enhancers	K562	blood
28	chr20:52464200-52465600	Enhancers	Thymus	Thymus
29	chr20:52464200-52468600	Weak transcription	NHEK	skin
30	chr20:52464400-52465200	Enhancers	Primary T cells from cord blood	blood
31	chr20:52464400-52465200	Enhancers	Primary hematopoietic stem cells short term culture	blood
32	chr20:52464400-52465200	Enhancers	Primary T helper cells PMA-I stimulated	--
33	chr20:52464400-52465200	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
34	chr20:52464400-52465200	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
35	chr20:52464400-52465200	Enhancers	Primary T killer memory cells from peripheral blood	blood
36	chr20:52464400-52465200	Enhancers	Sigmoid Colon	Sigmoid Colon
37	chr20:52464400-52465400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr20:52464400-52465400	Enhancers	Dnd41	blood
39	chr20:52464400-52466400	Enhancers	Primary T helper naive cells fromperipheralblood	blood
40	chr20:52464400-52467600	Enhancers	Primary B cells from peripheral blood	blood
41	chr20:52464400-52468000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
42	chr20:52464400-52472400	Weak transcription	Fetal Stomach	stomach
43	chr20:52464600-52467200	Enhancers	Primary B cells from cord blood	blood
44	chr20:52464600-52472800	Weak transcription	Cortex derived primary cultured neurospheres	brain
45	chr20:52464600-52474200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
46	chr20:52464800-52465200	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
47	chr20:52464800-52467400	Enhancers	Primary neutrophils fromperipheralblood	blood
48	chr20:52465000-52465400	Enhancers	GM12878-XiMat	blood
49	chr20:52465000-52468400	Weak transcription	HepG2	liver
50	chr20:52465200-52467400	Enhancers	Monocytes-CD14+_RO01746	blood

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