Variant report

Variant	nsv833946
Chromosome Location	chr20:24320375-24490702
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:778)
CpG islands
(count:1404)
Chromatin interactive
region (count:22)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:778 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr20:24472860-24473548	H1-hESC	embryonic stem cell:	n/a	n/a
2	BACH1	chr20:24466302-24466502	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr20:24406265-24406582	H1-hESC	embryonic stem cell:	n/a	n/a
4	BATF	chr20:24389263-24389569	GM12878	blood:	n/a	n/a
5	BATF	chr20:24434656-24434832	GM12878	blood:	n/a	n/a
6	BATF	chr20:24483385-24483555	GM12878	blood:	n/a	n/a
7	BCL11A	chr20:24389120-24389396	GM12878	blood:	n/a	n/a
8	BCL3	chr20:24415916-24416156	GM12878	blood:	n/a	n/a
9	BCL3	chr20:24415845-24416289	GM12878	blood:	n/a	n/a
10	BHLHE40	chr20:24406210-24406229	GM12878	blood:	n/a	n/a
11	BHLHE40	chr20:24404449-24404662	GM12878	blood:	n/a	n/a
12	CEBPB	chr20:24413325-24413519	HepG2	liver:	n/a	n/a
13	CEBPB	chr20:24413312-24413524	A549	lung:	n/a	n/a
14	CEBPB	chr20:24449689-24449861	H1-hESC	embryonic stem cell:	n/a	n/a
15	CEBPB	chr20:24472938-24473351	MCF-7	breast:	n/a	chr20:24473182-24473193
16	CEBPB	chr20:24390022-24390286	HepG2	liver:	n/a	chr20:24390130-24390141 chr20:24390130-24390143
17	CEBPB	chr20:24463252-24463459	IMR90	lung:	n/a	chr20:24463321-24463332
18	CEBPB	chr20:24331452-24331786	IMR90	lung:	n/a	chr20:24331619-24331630 chr20:24331618-24331629
19	CEBPB	chr20:24349513-24349639	HepG2	liver:	n/a	n/a
20	CEBPB	chr20:24350949-24351238	HepG2	liver:	n/a	n/a
21	CEBPB	chr20:24331475-24331764	HepG2	liver:	n/a	chr20:24331619-24331630 chr20:24331618-24331629
22	CEBPB	chr20:24463168-24463440	HepG2	liver:	n/a	chr20:24463321-24463332
23	CEBPB	chr20:24472974-24473297	HepG2	liver:	n/a	chr20:24473182-24473193
24	CEBPB	chr20:24454101-24454229	A549	lung:	n/a	n/a
25	CEBPB	chr20:24353984-24354039	HepG2	liver:	n/a	chr20:24353999-24354010
26	CEBPB	chr20:24334411-24334508	HepG2	liver:	n/a	chr20:24334472-24334483
27	CEBPB	chr20:24463242-24463444	A549	lung:	n/a	chr20:24463321-24463332
28	CEBPB	chr20:24472875-24473238	K562	blood:	n/a	chr20:24473182-24473193
29	CEBPB	chr20:24472883-24473312	H1-hESC	embryonic stem cell:	n/a	chr20:24473182-24473193
30	CEBPB	chr20:24472960-24473202	K562	blood:	n/a	chr20:24473182-24473193
31	CEBPB	chr20:24429436-24429573	A549	lung:	n/a	n/a
32	CHD1	chr20:24450623-24450818	H1-hESC	embryonic stem cell:	n/a	n/a
33	CHD2	chr20:24450335-24450691	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr20:24426201-24426353	H1-hESC	embryonic stem cell:	n/a	n/a
35	CHD2	chr20:24449687-24449904	H1-hESC	embryonic stem cell:	n/a	n/a
36	CHD2	chr20:24424019-24424652	H1-hESC	embryonic stem cell:	n/a	n/a
37	CHD2	chr20:24443144-24443490	H1-hESC	embryonic stem cell:	n/a	n/a
38	CHD2	chr20:24472805-24473416	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTBP2	chr20:24449619-24450490	H1-hESC	embryonic stem cell:	n/a	n/a
40	CTBP2	chr20:24450695-24452117	H1-hESC	embryonic stem cell:	n/a	n/a
41	CTBP2	chr20:24423614-24425184	H1-hESC	embryonic stem cell:	n/a	n/a
42	CTCF	chr20:24441440-24441590	HA-sp	spinal cord:	n/a	n/a
43	CTCF	chr20:24441471-24441596	MCF-7	breast:	n/a	n/a
44	CTCF	chr20:24470480-24470630	BE2_C	brain:	n/a	chr20:24470548-24470561
45	CTCF	chr20:24473040-24473190	WERI-Rb-1	eye:	n/a	n/a
46	CTCF	chr20:24484380-24484530	HEK293	kidney:	n/a	n/a
47	CTCF	chr20:24460400-24460550	AG04449	skin:	n/a	n/a
48	CTCF	chr20:24433426-24433582	GM19238	blood:	n/a	n/a
49	CTCF	chr20:24412700-24412850	HCPEpiC	choroid plexus:	n/a	n/a
50	CTCF	chr20:24414479-24414482	GM10248	blood:	n/a	n/a

(count:1404 , 50 per page) page: 1 2 3 4 5 6 7 ... 29

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr20:24449804-24449854	HCT-116	colon:	n/a
2	chr20:24449804-24449854	HCT-116	colon:	n/a
3	chr20:24450353-24450403	MCF-7	breast:	n/a
4	chr20:24450361-24450411	HIPEpiC	eye:	n/a
5	chr20:24449704-24449754	ProgFib	skin:	n/a
6	chr20:24452091-24452141	HUVEC	blood vessel:	n/a
7	chr20:24449392-24449442	SK-N-SH	brain:	n/a
8	chr20:24449392-24449442	HRE	kidney:	n/a
9	chr20:24449865-24449915	HRPEpiC	eye:	n/a
10	chr20:24449734-24449784	Hepatocyte	liver:	n/a
11	chr20:24450353-24450403	SKMC	muscle:	n/a
12	chr20:24449865-24449915	GM12892	blood:	n/a
13	chr20:24450698-24450748	HNPCEpiC	eye:	n/a
14	chr20:24455463-24455513	K562	blood:	n/a
15	chr20:24448859-24448909	HRCEpiC	kidney:	n/a
16	chr20:24449668-24449718	SK-N-MC	brain:	n/a
17	chr20:24446527-24446577	A549	lung:	n/a
18	chr20:24451428-24451478	ECC-1	luminal epithelium:	n/a
19	chr20:24449865-24449915	PANC-1	pancreas:	n/a
20	chr20:24449392-24449442	ECC-1	luminal epithelium:	n/a
21	chr20:24449392-24449442	NHDF-neo	bronchial:	n/a
22	chr20:24449668-24449718	HCPEpiC	choroid plexus:	n/a
23	chr20:24450698-24450748	BJ	skin:	n/a
24	chr20:24450361-24450411	ECC-1	luminal epithelium:	n/a
25	chr20:24449916-24449966	GM06990	blood:	n/a
26	chr20:24449704-24449754	SK-N-MC	brain:	n/a
27	chr20:24451428-24451478	H1-hESC	embryonic stem cell:	embryo
28	chr20:24455463-24455513	MCF10A-Er-Src	breast:	n/a
29	chr20:24451769-24451819	HUVEC	blood vessel:	n/a
30	chr20:24452131-24452181	HRE	kidney:	n/a
31	chr20:24446527-24446577	CMK	blood:	n/a
32	chr20:24449668-24449718	NH-A	brain:	n/a
33	chr20:24451084-24451134	AG04450	lung:	fetal
34	chr20:24451084-24451134	HEK293	kidney:	embryo
35	chr20:24451518-24451568	Hela-S3	cervix:	n/a
36	chr20:24449760-24449810	Hepatocyte	liver:	n/a
37	chr20:24451428-24451478	AG10803	skin:	n/a
38	chr20:24450353-24450403	ovcar-3	ovarian:	n/a
39	chr20:24449916-24449966	PANC-1	pancreas:	n/a
40	chr20:24450698-24450748	PrEC	prostate:	n/a
41	chr20:24449704-24449754	NB4	blood:	n/a
42	chr20:24449760-24449810	Caco-2	colon:	n/a
43	chr20:24452091-24452141	A549	lung:	n/a
44	chr20:24451428-24451478	HRE	kidney:	n/a
45	chr20:24451084-24451134	AoSMC	blood vessel:	n/a
46	chr20:24449668-24449718	GM19239	blood:	n/a
47	chr20:24452036-24452086	K562	blood:	n/a
48	chr20:24449668-24449718	A549	lung:	n/a
49	chr20:24452091-24452141	LNCaP	prostate:	n/a
50	chr20:24449668-24449718	HPAEpiC	pulmonary alveolar:	n/a

(count:22 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr20:24461646..24463186-chr20:24463669..24465264,2	MCF-7	breast:
2	chr20:24347069..24348854-chr20:24350597..24353212,2	K562	blood:
3	chr20:24347069..24348854-chr20:24350597..24353212,2	K562	blood:
4	chr20:24458098..24460302-chr20:24472208..24475161,2	MCF-7	breast:
5	chr20:24337993..24340100-chr20:24340194..24343622,3	MCF-7	breast:
6	chr20:24434255..24436755-chr20:24440462..24442784,2	MCF-7	breast:
7	chr20:24434255..24436755-chr20:24440462..24442784,2	MCF-7	breast:
8	chr20:24462787..24464329-chr20:24469582..24472376,2	MCF-7	breast:
9	chr20:24346392..24348668-chr20:24354485..24357111,2	MCF-7	breast:
10	chr20:24458098..24460302-chr20:24472208..24475161,2	MCF-7	breast:
11	chr20:24420874..24424389-chr20:24442088..24445319,3	MCF-7	breast:
12	chr20:24420874..24424389-chr20:24442088..24445319,3	MCF-7	breast:
13	chr20:24448972..24451523-chr20:24462045..24463814,3	MCF-7	breast:
14	chr20:24337993..24340100-chr20:24340194..24343622,3	MCF-7	breast:
15	chr20:24344885..24347176-chr20:24347608..24349903,2	MCF-7	breast:
16	chr20:24363369..24365498-chr20:24749184..24751241,2	MCF-7	breast:
17	chr20:24147267..24149849-chr20:24336608..24338562,2	MCF-7	breast:
18	chr20:24441261..24441801-chr20:24580346..24581116,2	MCF-7	breast:
19	chr20:24462787..24464329-chr20:24469582..24472376,2	MCF-7	breast:
20	chr20:24461646..24463186-chr20:24463669..24465264,2	MCF-7	breast:
21	chr20:24344885..24347176-chr20:24347608..24349903,2	MCF-7	breast:
22	chr20:24346392..24348668-chr20:24354485..24357111,2	MCF-7	breast:

(count:6 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C20orf3-3	chr20:24472108-24472374	ENSG00000228539
2	lnc-SYNDIG1-5	chr20:24426027-24426950	NONHSAT079109
3	lnc-CST7-5	chr20:24466726-24466776	NONHSAT079110
4	lnc-C20orf3-3	chr20:24476057-24476435	ENSG00000228539
5	lnc-C20orf3-3	chr20:24482805-24482981	ENSG00000228539
6	lnc-CST7-5	chr20:24468399-24468664	NONHSAT079110

No data

Variant related genes	Relation type
GAPDHP53	TF binding region
SYNDIG1	TF binding region
ENSG00000228539	TF binding region
GAPDHP53	CpG island
SYNDIG1	CpG island
ENSG00000228539	CpG island
ENSG00000101463	chromatin interactions

Extended variants
information (count: 7428 )
Associated
traits (count: 59 )

Variant overlapped rSNPs/rCNVs (count:7428 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs112540989	chr20:24320394-24320395	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs577913152	chr20:24320403-24320404	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs55738719	chr20:24320414-24320415	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs543519600	chr20:24320433-24320434	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs563481215	chr20:24320506-24320507	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs56381548	chr20:24320510-24320511	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs572392414	chr20:24320529-24320530	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs371869963	chr20:24320533-24320534	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs370701463	chr20:24320539-24320540	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs189326518	chr20:24320574-24320575	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs375460328	chr20:24320652-24320653	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs369705645	chr20:24320656-24320657	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs372527885	chr20:24320688-24320689	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs180808298	chr20:24320697-24320698	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs187662897	chr20:24320711-24320712	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs530474588	chr20:24320774-24320775	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs542913313	chr20:24320826-24320827	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs190343540	chr20:24320894-24320895	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs113265453	chr20:24320917-24320918	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs185679754	chr20:24320929-24320930	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs115708625	chr20:24320943-24320944	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs28478956	chr20:24320949-24320950	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs536003767	chr20:24320968-24320969	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs369123375	chr20:24320999-24321000	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs190181342	chr20:24321039-24321040	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs538928363	chr20:24321050-24321051	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs558531318	chr20:24321077-24321078	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs575178726	chr20:24321089-24321090	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs531751312	chr20:24321224-24321225	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs182403257	chr20:24321238-24321239	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs149121738	chr20:24321262-24321263	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs573830268	chr20:24321281-24321282	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs549978569	chr20:24321289-24321290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs202001639	chr20:24321301-24321302	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76079339	chr20:24321304-24321305	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs73901974	chr20:24321322-24321323	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs142210282	chr20:24321330-24321331	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs545689893	chr20:24321388-24321389	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565478956	chr20:24321389-24321390	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs531211951	chr20:24321399-24321400	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs550632055	chr20:24321422-24321423	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs185398335	chr20:24321432-24321433	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs529838256	chr20:24321446-24321447	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs533024973	chr20:24321479-24321480	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs566667933	chr20:24321544-24321545	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs538498691	chr20:24321546-24321547	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs141498283	chr20:24321549-24321550	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs79775888	chr20:24321593-24321594	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs566459273	chr20:24321598-24321599	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs537731037	chr20:24321605-24321606	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:59)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	16272173	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Ewing''s sarcoma	21437220	CNVD
Oral cancer	19627613	CNVD
colon cancer	17210682	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	21080181	CNVD
Thyroid cancer	19087340	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Colorectal cancer	19359472	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Human rectal carcinomas	16397240	CNVD
Olfactory neuroblastoma	18408657	CNVD
Central neurocytomas	17123091	CNVD
Colorectal cancer	16272173	CNVD
Medulloblastoma	21979893	CNVD
Gastric cancer	17908304	CNVD
Urothelial carcinoma	21177765	CNVD
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Colorectal cancer	21645411	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Autism	22495311	CNVD
Renal cell carcinoma	18765545	CNVD
Alagille syndrome	17576883	CNVD
Anaplastic large cell lymphoma	18179710	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Cancer	21183584	CNVD
Myxofibrosarcoma	16751306	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Breast cancer	16608533	CNVD
Bladder cancer	21909424	CNVD
Esophageal cancer	21851588	CNVD
Breast cancer	17133270	CNVD
Thrombophilia	17576883	CNVD
Myelofibrosis	22110671	CNVD
Mental retardation	21062444	CNVD
Hepatocellular carcinoma	22174799	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chordoma	18071362	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	21364760	CNVD
Cancer	20164919	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1888 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr20:24316800-24322600	Enhancers	NHEK	skin
2	chr20:24317400-24322200	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
3	chr20:24317400-24322200	Enhancers	HMEC	breast
4	chr20:24317600-24320600	Enhancers	NH-A	brain
5	chr20:24317600-24322200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
6	chr20:24317800-24322600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr20:24318400-24321400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
8	chr20:24319600-24320600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
9	chr20:24320200-24320400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
10	chr20:24320400-24322800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
11	chr20:24321400-24322000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
12	chr20:24321800-24322200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
13	chr20:24322400-24323200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
14	chr20:24322600-24331400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr20:24322800-24323200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
16	chr20:24331000-24332200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr20:24331000-24332600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
18	chr20:24331400-24332400	Enhancers	NHEK	skin
19	chr20:24331400-24332600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr20:24331800-24332000	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
21	chr20:24331800-24332000	Enhancers	Ovary	ovary
22	chr20:24331800-24332400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
23	chr20:24331800-24332600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
24	chr20:24332000-24332400	Active TSS	Ovary	ovary
25	chr20:24332000-24332400	Enhancers	HMEC	breast
26	chr20:24332000-24341800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr20:24332400-24332600	Enhancers	Dnd41	blood
28	chr20:24332400-24333200	Enhancers	Brain Substantia Nigra	brain
29	chr20:24332400-24334000	Weak transcription	Ovary	ovary
30	chr20:24332600-24332800	Enhancers	Brain Hippocampus Middle	brain
31	chr20:24332600-24335000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
32	chr20:24332800-24334000	Weak transcription	Brain Hippocampus Middle	brain
33	chr20:24332800-24334200	Weak transcription	Dnd41	blood
34	chr20:24333000-24333200	Enhancers	Brain Cingulate Gyrus	brain
35	chr20:24333000-24334400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
36	chr20:24333200-24333400	Enhancers	Brain Angular Gyrus	brain
37	chr20:24333200-24337000	Weak transcription	Brain Cingulate Gyrus	brain
38	chr20:24333200-24337600	Weak transcription	Brain Substantia Nigra	brain
39	chr20:24333400-24339400	Weak transcription	Brain Angular Gyrus	brain
40	chr20:24333800-24334600	Enhancers	iPS-18 Cell Line	embryonic stem cell
41	chr20:24334000-24334200	Enhancers	Ovary	ovary
42	chr20:24334000-24334400	Enhancers	Brain Germinal Matrix	brain
43	chr20:24334000-24334400	Enhancers	Fetal Thymus	thymus
44	chr20:24334000-24338400	Enhancers	Brain Hippocampus Middle	brain
45	chr20:24334200-24334400	Enhancers	Brain Inferior Temporal Lobe	brain
46	chr20:24334200-24334600	Enhancers	Dnd41	blood
47	chr20:24334400-24334800	Weak transcription	Brain Germinal Matrix	brain
48	chr20:24334600-24339800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr20:24334800-24338000	Enhancers	Brain Germinal Matrix	brain
50	chr20:24335000-24335400	Enhancers	Fetal Intestine Small	intestine

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