Variant report

Variant	nsv3419
Chromosome Location	chr20:52637581-52672115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:232)
CpG islands
(count:0)
Chromatin interactive
region (count:57)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:232 , 50 per page) page: 1 2 3 4 5

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr20:52660800-52661065	K562	blood:	n/a	n/a
2	ATF2	chr20:52660603-52661076	GM12878	blood:	n/a	n/a
3	ATF2	chr20:52660569-52661110	GM12878	blood:	n/a	n/a
4	ATF3	chr20:52660702-52661099	K562	blood:	n/a	n/a
5	BATF	chr20:52660645-52661119	GM12878	blood:	n/a	n/a
6	BATF	chr20:52660667-52661056	GM12878	blood:	n/a	n/a
7	BCL11A	chr20:52660768-52661068	GM12878	blood:	n/a	chr20:52660971-52660980 chr20:52660970-52660979
8	BHLHE40	chr20:52660756-52661015	K562	blood:	n/a	n/a
9	BRCA1	chr20:52660410-52660416	HepG2	liver:	n/a	n/a
10	CBX3	chr20:52660708-52661021	K562	blood:	n/a	n/a
11	CBX3	chr20:52660706-52661028	K562	blood:	n/a	n/a
12	CCNT2	chr20:52663681-52664125	K562	blood:	n/a	n/a
13	CCNT2	chr20:52660716-52661053	K562	blood:	n/a	n/a
14	CEBPB	chr20:52660694-52661096	A549	lung:	n/a	n/a
15	CEBPB	chr20:52660644-52661125	K562	blood:	n/a	n/a
16	CEBPB	chr20:52659371-52659387	HepG2	liver:	n/a	chr20:52659372-52659385 chr20:52659372-52659383
17	CEBPB	chr20:52663571-52663913	K562	blood:	n/a	n/a
18	CEBPB	chr20:52660557-52661108	K562	blood:	n/a	n/a
19	CEBPB	chr20:52658684-52661814	MCF-7	breast:	n/a	chr20:52659372-52659385 chr20:52659372-52659383 chr20:52659617-52659629
20	CEBPB	chr20:52660758-52660996	K562	blood:	n/a	n/a
21	CEBPB	chr20:52660834-52661014	A549	lung:	n/a	n/a
22	CEBPB	chr20:52652599-52652817	A549	lung:	n/a	chr20:52652797-52652809
23	CEBPB	chr20:52660901-52660966	HepG2	liver:	n/a	n/a
24	CEBPB	chr20:52660784-52661093	IMR90	lung:	n/a	n/a
25	CEBPB	chr20:52658997-52661146	MCF-7	breast:	n/a	chr20:52659372-52659385 chr20:52659372-52659383 chr20:52659617-52659629
26	CEBPB	chr20:52663588-52663955	K562	blood:	n/a	n/a
27	CEBPD	chr20:52660650-52661087	K562	blood:	n/a	n/a
28	CEBPD	chr20:52660584-52661091	K562	blood:	n/a	n/a
29	CTCF	chr20:52660299-52660420	MCF-7	breast:	n/a	n/a
30	CTCF	chr20:52660280-52660430	GM12878	blood:	n/a	n/a
31	CTCF	chr20:52660440-52660590	NHDF-neo	bronchial:	n/a	n/a
32	CTCF	chr20:52660317-52660409	MCF-7	breast:	n/a	n/a
33	CTCF	chr20:52641580-52641730	K562	blood:	n/a	n/a
34	CTCF	chr20:52660260-52660410	GM12864	blood:	n/a	n/a
35	CTCF	chr20:52656980-52657130	NHDF-neo	bronchial:	n/a	n/a
36	CTCF	chr20:52660260-52660529	A549	lung:	n/a	n/a
37	CTCF	chr20:52660292-52660481	K562	blood:	n/a	n/a
38	CTCF	chr20:52660317-52660412	MCF-7	breast:	n/a	n/a
39	CTCF	chr20:52660320-52660470	GM06990	blood:	n/a	n/a
40	CTCF	chr20:52660358-52660382	NHEK	skin:	n/a	n/a
41	CTCF	chr20:52660280-52660430	Caco-2	colon:	n/a	n/a
42	CTCF	chr20:52671227-52671258	ProgFib	skin:	n/a	n/a
43	CTCF	chr20:52660360-52660430	Hela-S3	cervix:	n/a	n/a
44	CTCF	chr20:52660258-52660510	GM12878	blood:	n/a	n/a
45	CTCF	chr20:52660360-52660510	NHDF-neo	bronchial:	n/a	n/a
46	CTCF	chr20:52660335-52660379	A549	lung:	n/a	n/a
47	CTCF	chr20:52644962-52644976	ProgFib	skin:	n/a	n/a
48	CTCF	chr20:52660295-52660417	GM12891	blood:	n/a	n/a
49	CTCF	chr20:52660320-52660470	AoAF	blood vessel:	n/a	n/a
50	CTCF	chr20:52660300-52660450	GM12873	blood:	n/a	n/a

No data

(count:57 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr20:52641892..52642874-chr8:145597609..145598579,2	MCF-7	breast:
2	chr10:6752413..6755027-chr20:52637066..52638701,2	MCF-7	breast:
3	chr20:52666267..52667791-chr20:52670697..52672738,2	K562	blood:
4	chr20:52637066..52638758-chr20:52814521..52816313,2	MCF-7	breast:
5	chr20:52556030..52560309-chr20:52671948..52677336,4	K562	blood:
6	chr17:69373468..69375354-chr20:52636085..52637962,2	MCF-7	breast:
7	chr20:52655188..52657937-chr20:55839006..55840900,2	MCF-7	breast:
8	chr20:52640367..52641889-chr20:52645625..52647973,2	K562	blood:
9	chr20:52646106..52649105-chr20:52656818..52659729,2	MCF-7	breast:
10	chr17:57917278..57919596-chr20:52653625..52656516,2	MCF-7	breast:
11	chr17:59805932..59807613-chr20:52665362..52667872,2	MCF-7	breast:
12	chr20:52645173..52647456-chr8:56684089..56685719,2	MCF-7	breast:
13	chr20:52637571..52639350-chr20:52639396..52641959,2	K562	blood:
14	chr20:52666267..52667791-chr20:52670697..52672738,2	K562	blood:
15	chr20:52659902..52660887-chr20:52678920..52680381,7	MCF-7	breast:
16	chr17:57915947..57917652-chr20:52646723..52649567,2	MCF-7	breast:
17	chr20:52646106..52649105-chr20:52656818..52659729,2	MCF-7	breast:
18	chr19:11025812..11027987-chr20:52653374..52655752,2	MCF-7	breast:
19	chr20:52648757..52649473-chr5:157170244..157171208,2	MCF-7	breast:
20	chr1:121484253..121484817-chr20:52659977..52660776,2	MCF-7	breast:
21	chr20:52671492..52674058-chr20:55837796..55841174,3	MCF-7	breast:
22	chr17:56735097..56736691-chr20:52662317..52665029,2	MCF-7	breast:
23	chr17:56708938..56711128-chr20:52668141..52671621,3	MCF-7	breast:
24	chr20:52669724..52670230-chr20:52678961..52679874,2	MCF-7	breast:
25	chr17:56707799..56710607-chr20:52642228..52644941,3	MCF-7	breast:
26	chr20:52638922..52641694-chr20:52671102..52673075,2	MCF-7	breast:
27	chr20:52647368..52649299-chr20:52654193..52656329,2	MCF-7	breast:
28	chr20:52628739..52630363-chr20:52636022..52638678,2	K562	blood:
29	chr20:52637587..52640113-chr20:52663021..52665849,2	MCF-7	breast:
30	chr20:52557746..52563146-chr20:52657006..52659772,4	MCF-7	breast:
31	chr20:52626505..52628533-chr20:52652801..52654568,2	MCF-7	breast:
32	chr20:52666156..52668326-chr20:52673321..52675547,2	K562	blood:
33	chr2:99769202..99772000-chr20:52646224..52647934,2	MCF-7	breast:
34	chr20:52643210..52646138-chr20:52658422..52660423,2	K562	blood:
35	chr20:52671848..52674033-chr20:55841179..55843003,2	MCF-7	breast:
36	chr17:57920665..57924197-chr20:52662636..52665586,3	MCF-7	breast:
37	chr20:52646516..52648390-chr3:62045905..62047422,2	MCF-7	breast:
38	chr20:52621471..52622138-chr20:52658585..52659278,2	MCF-7	breast:
39	chr20:52647368..52649299-chr20:52654193..52656329,2	MCF-7	breast:
40	chr20:52637408..52640155-chr20:52655059..52656752,2	MCF-7	breast:
41	chr17:56707459..56709744-chr20:52669878..52671451,2	MCF-7	breast:
42	chr20:52637587..52640113-chr20:52663021..52665849,2	MCF-7	breast:
43	chr17:56736044..56738825-chr20:52668683..52672447,3	MCF-7	breast:
44	chr20:52642833..52647245-chr20:52651317..52656592,5	MCF-7	breast:
45	chr20:52637571..52639350-chr20:52639396..52641959,2	K562	blood:
46	chr20:52638922..52641694-chr20:52671102..52673075,2	MCF-7	breast:
47	chr17:57917127..57917905-chr20:52639454..52640219,2	MCF-7	breast:
48	chr20:45987538..45989784-chr20:52646421..52648098,2	MCF-7	breast:
49	chr20:52643673..52645639-chr20:52687051..52688962,2	MCF-7	breast:
50	chr20:52640020..52640592-chr20:52673395..52674189,2	MCF-7	breast:

No data

Variant related genes	Relation type
BCAS1	TF binding region
ENSG00000101132	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000137574	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000273155	chromatin interactions
ENSG00000144182	chromatin interactions
ENSG00000167904	chromatin interactions
ENSG00000101144	chromatin interactions
ENSG00000226308	chromatin interactions
ENSG00000236352	chromatin interactions
ENSG00000135951	chromatin interactions
ENSG00000155858	chromatin interactions
ENSG00000064787	chromatin interactions
ENSG00000173137	chromatin interactions

Extended variants
information (count: 1459 )
Associated
traits (count: 84 )

Variant overlapped rSNPs/rCNVs (count:1459 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs369652365	chr20:52637588-52637589	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs539560988	chr20:52637590-52637591	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543251924	chr20:52637649-52637650	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs556574632	chr20:52637652-52637653	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs192284702	chr20:52637712-52637713	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs140767530	chr20:52637725-52637726	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs554938622	chr20:52637753-52637754	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs574762065	chr20:52637785-52637786	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs558277427	chr20:52637809-52637810	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs540505111	chr20:52637903-52637904	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs113307674	chr20:52637911-52637912	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs208388	chr20:52637917-52637918	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs563492495	chr20:52637937-52637938	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs545581790	chr20:52637950-52637951	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs147803145	chr20:52637978-52637979	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs531847459	chr20:52637982-52637983	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs548355636	chr20:52637993-52637994	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs114044006	chr20:52637996-52637997	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs187781253	chr20:52638019-52638020	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs191139642	chr20:52638073-52638074	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs570762576	chr20:52638168-52638169	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs142488896	chr20:52638186-52638187	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs550048564	chr20:52638238-52638239	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs570120411	chr20:52638265-52638266	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs370543531	chr20:52638296-52638297	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs374127245	chr20:52638300-52638301	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs2299716	chr20:52638393-52638394	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs146777745	chr20:52638399-52638400	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs184551924	chr20:52638400-52638401	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369126116	chr20:52638407-52638408	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373397709	chr20:52638424-52638425	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs139577586	chr20:52638443-52638444	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs534088125	chr20:52638472-52638473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554060213	chr20:52638477-52638478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs576809079	chr20:52638530-52638531	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs545771496	chr20:52638538-52638539	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556017043	chr20:52638549-52638550	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs138939079	chr20:52638570-52638571	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs541492521	chr20:52638589-52638590	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs114707707	chr20:52638619-52638620	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs369024104	chr20:52638658-52638659	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs527835661	chr20:52638661-52638662	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs149443400	chr20:52638665-52638666	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs564793796	chr20:52638672-52638673	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs533205167	chr20:52638680-52638681	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs550127681	chr20:52638703-52638704	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs189318558	chr20:52638705-52638706	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs192898133	chr20:52638706-52638707	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs208386	chr20:52638714-52638715	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
50	rs540871691	chr20:52638718-52638719	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:84)

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
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
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:214 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:52566400-52644800	Weak transcription	Gastric	stomach
2	chr20:52618800-52644400	Weak transcription	Rectal Mucosa Donor 29	rectum
3	chr20:52631400-52641400	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
4	chr20:52633800-52638600	Weak transcription	Brain Cingulate Gyrus	brain
5	chr20:52633800-52641200	Weak transcription	Brain Angular Gyrus	brain
6	chr20:52634000-52638600	Weak transcription	Brain Anterior Caudate	brain
7	chr20:52634800-52645400	Weak transcription	Fetal Lung	lung
8	chr20:52635800-52641800	Enhancers	Brain Substantia Nigra	brain
9	chr20:52636000-52641200	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr20:52636600-52640600	Weak transcription	Stomach Mucosa	stomach
11	chr20:52637000-52637600	Strong transcription	Rectal Mucosa Donor 31	rectum
12	chr20:52637200-52638800	Enhancers	Brain Hippocampus Middle	brain
13	chr20:52637600-52640400	Weak transcription	Rectal Mucosa Donor 31	rectum
14	chr20:52638600-52638800	Enhancers	Brain Anterior Caudate	brain
15	chr20:52638600-52639200	Enhancers	Brain Cingulate Gyrus	brain
16	chr20:52638800-52639400	Weak transcription	Brain Anterior Caudate	brain
17	chr20:52638800-52640000	Weak transcription	Brain Hippocampus Middle	brain
18	chr20:52639200-52640800	Weak transcription	Brain Cingulate Gyrus	brain
19	chr20:52639400-52640200	Enhancers	Brain Anterior Caudate	brain
20	chr20:52639600-52641000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
21	chr20:52640000-52640600	Enhancers	Brain Hippocampus Middle	brain
22	chr20:52640200-52641000	Weak transcription	NHDF-Ad	bronchial
23	chr20:52640200-52641200	Weak transcription	Brain Anterior Caudate	brain
24	chr20:52640400-52642200	Strong transcription	Rectal Mucosa Donor 31	rectum
25	chr20:52640600-52641400	Genic enhancers	Brain Hippocampus Middle	brain
26	chr20:52640600-52641600	Strong transcription	Stomach Mucosa	stomach
27	chr20:52640800-52642000	Enhancers	Brain Cingulate Gyrus	brain
28	chr20:52640800-52643800	Enhancers	Fetal Brain Male	brain
29	chr20:52641000-52641400	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
30	chr20:52641000-52642000	Enhancers	NHDF-Ad	bronchial
31	chr20:52641000-52643200	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
32	chr20:52641000-52643400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr20:52641200-52641400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
34	chr20:52641200-52641400	Enhancers	Brain Angular Gyrus	brain
35	chr20:52641200-52641400	Flanking Active TSS	Brain Anterior Caudate	brain
36	chr20:52641200-52641400	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
37	chr20:52641200-52641600	Enhancers	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
38	chr20:52641200-52641600	Enhancers	Brain Inferior Temporal Lobe	brain
39	chr20:52641200-52642000	Enhancers	HSMMtube	muscle
40	chr20:52641200-52642400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr20:52641200-52642400	Enhancers	Osteobl	bone
42	chr20:52641200-52644400	Enhancers	Cortex derived primary cultured neurospheres	brain
43	chr20:52641400-52641600	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
44	chr20:52641400-52641800	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
45	chr20:52641400-52641800	Weak transcription	Brain Angular Gyrus	brain
46	chr20:52641400-52641800	Enhancers	Fetal Kidney	kidney
47	chr20:52641400-52642000	Enhancers	Colon Smooth Muscle	Colon
48	chr20:52641400-52642400	Flanking Active TSS	Brain Hippocampus Middle	brain
49	chr20:52641400-52642600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr20:52641400-52642600	Enhancers	NH-A	brain

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