Variant report

Variant	esv3388313
Chromosome Location	chr18:28583296-28693160
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1051)
CpG islands
(count:2079)
Chromatin interactive
region (count:88)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1051 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:28681172-28681372	K562	blood:	n/a	n/a
2	ARID3A	chr18:28681767-28681934	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:28681381-28681402	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:28682324-28682635	HepG2	liver:	n/a	n/a
5	ARID3A	chr18:28682894-28683193	K562	blood:	n/a	n/a
6	ARID3A	chr18:28682320-28682542	K562	blood:	n/a	n/a
7	ARID3A	chr18:28626536-28626549	K562	blood:	n/a	n/a
8	ARID3A	chr18:28638602-28639276	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:28591334-28591717	HepG2	liver:	n/a	n/a
10	ATF1	chr18:28683257-28683748	K562	blood:	n/a	n/a
11	ATF2	chr18:28641878-28642432	GM12878	blood:	n/a	n/a
12	ATF2	chr18:28641762-28642485	GM12878	blood:	n/a	n/a
13	ATF2	chr18:28644069-28644441	GM12878	blood:	n/a	n/a
14	ATF2	chr18:28643982-28644530	GM12878	blood:	n/a	n/a
15	ATF3	chr18:28591243-28591882	HCT-116	colon:	n/a	n/a
16	ATF3	chr18:28591311-28591800	A549	lung:	n/a	n/a
17	ATF3	chr18:28591305-28591765	HCT-116	colon:	n/a	n/a
18	BACH1	chr18:28621452-28621945	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr18:28622835-28622968	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr18:28625753-28625790	K562	blood:	n/a	n/a
21	BACH1	chr18:28654125-28654223	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr18:28622505-28622509	H1-hESC	embryonic stem cell:	n/a	n/a
23	BATF	chr18:28630609-28630927	GM12878	blood:	n/a	chr18:28630793-28630801 chr18:28630771-28630782
24	BATF	chr18:28644099-28644529	GM12878	blood:	n/a	chr18:28644282-28644293
25	BATF	chr18:28644079-28644420	GM12878	blood:	n/a	chr18:28644282-28644293
26	BCL11A	chr18:28644099-28644453	GM12878	blood:	n/a	n/a
27	BCL3	chr18:28591319-28591753	A549	lung:	n/a	n/a
28	BCL3	chr18:28644087-28644381	GM12878	blood:	n/a	n/a
29	BCL3	chr18:28641839-28642386	GM12878	blood:	n/a	n/a
30	BCL3	chr18:28644069-28644521	GM12878	blood:	n/a	n/a
31	BCLAF1	chr18:28644038-28644550	GM12878	blood:	n/a	n/a
32	BHLHE40	chr18:28611018-28611124	K562	blood:	n/a	n/a
33	BHLHE40	chr18:28644116-28644316	GM12878	blood:	n/a	n/a
34	BHLHE40	chr18:28681020-28681939	HepG2	liver:	n/a	n/a
35	BHLHE40	chr18:28675101-28675130	K562	blood:	n/a	n/a
36	BHLHE40	chr18:28679783-28680484	K562	blood:	n/a	n/a
37	BHLHE40	chr18:28685681-28685956	K562	blood:	n/a	n/a
38	BHLHE40	chr18:28680962-28681342	GM12878	blood:	n/a	n/a
39	BHLHE40	chr18:28680791-28682761	K562	blood:	n/a	chr18:28682426-28682442 chr18:28682001-28682017
40	BHLHE40	chr18:28643724-28643732	GM12878	blood:	n/a	n/a
41	BRCA1	chr18:28680858-28681012	H1-hESC	embryonic stem cell:	n/a	n/a
42	BRCA1	chr18:28669420-28669423	GM12878	blood:	n/a	n/a
43	BRCA1	chr18:28682353-28682554	HepG2	liver:	n/a	n/a
44	CBX3	chr18:28681094-28681435	K562	blood:	n/a	n/a
45	CBX3	chr18:28591194-28591886	HCT-116	colon:	n/a	n/a
46	CCNT2	chr18:28680912-28683139	K562	blood:	n/a	chr18:28681229-28681238 chr18:28681714-28681723
47	CCNT2	chr18:28679833-28679937	K562	blood:	n/a	n/a
48	CCNT2	chr18:28629262-28629572	K562	blood:	n/a	n/a
49	CEBPB	chr18:28637017-28637308	HepG2	liver:	n/a	chr18:28637161-28637172
50	CEBPB	chr18:28639017-28639155	HepG2	liver:	n/a	n/a

(count:2079 , 50 per page) page: 1 2 3 4 5 6 7 ... 42

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:28623090-28623140	ovcar-3	ovarian:	n/a
2	chr18:28623874-28623924	NHBE	bronchial:	n/a
3	chr18:28623090-28623140	SK-N-SH_RA	brain:	n/a
4	chr18:28622876-28622926	HRCEpiC	kidney:	n/a
5	chr18:28682497-28682547	SKMC	muscle:	n/a
6	chr18:28623090-28623140	ovcar-3	ovarian:	n/a
7	chr18:28623874-28623924	NHBE	bronchial:	n/a
8	chr18:28623090-28623140	SK-N-SH_RA	brain:	n/a
9	chr18:28622876-28622926	HRCEpiC	kidney:	n/a
10	chr18:28682497-28682547	SKMC	muscle:	n/a
11	chr18:28623874-28623924	HAEpiC	amniotic membrane:	n/a
12	chr18:28621985-28622035	AoSMC	blood vessel:	n/a
13	chr18:28622200-28622250	SK-N-SH	brain:	n/a
14	chr18:28682828-28682878	U87	brain:	n/a
15	chr18:28622024-28622074	PrEC	prostate:	n/a
16	chr18:28624074-28624124	GM12892	blood:	n/a
17	chr18:28682345-28682395	HNPCEpiC	eye:	n/a
18	chr18:28621985-28622035	T-47D	breast:	n/a
19	chr18:28681689-28681739	ECC-1	luminal epithelium:	n/a
20	chr18:28683794-28683844	HEK293	kidney:	embryo
21	chr18:28624074-28624124	HCPEpiC	choroid plexus:	n/a
22	chr18:28682408-28682458	PrEC	prostate:	n/a
23	chr18:28622474-28622524	PFSK-1	brain:	n/a
24	chr18:28682345-28682395	MCF-7	breast:	n/a
25	chr18:28623874-28623924	NH-A	brain:	n/a
26	chr18:28625997-28626047	HEK293	kidney:	embryo
27	chr18:28622940-28622990	HMEC	breast:	n/a
28	chr18:28685799-28685849	RPTEC	kidney:	n/a
29	chr18:28623060-28623110	HRCEpiC	kidney:	n/a
30	chr18:28682229-28682279	HCM	heart:	n/a
31	chr18:28622200-28622250	T-47D	breast:	n/a
32	chr18:28683425-28683475	MCF10A-Er-Src	breast:	n/a
33	chr18:28622918-28622968	Caco-2	colon:	n/a
34	chr18:28623874-28623924	GM12892	blood:	n/a
35	chr18:28622474-28622524	RPTEC	kidney:	n/a
36	chr18:28658043-28658093	HMEC	breast:	n/a
37	chr18:28682345-28682395	NT2-D1	testis:	n/a
38	chr18:28682497-28682547	NT2-D1	testis:	n/a
39	chr18:28682408-28682458	HRCEpiC	kidney:	n/a
40	chr18:28681689-28681739	A549	lung:	n/a
41	chr18:28622918-28622968	MCF-7	breast:	n/a
42	chr18:28624074-28624124	BJ	skin:	n/a
43	chr18:28622593-28622643	GM12891	blood:	n/a
44	chr18:28621985-28622035	GM12878	blood:	n/a
45	chr18:28622024-28622074	HRPEpiC	eye:	n/a
46	chr18:28623874-28623924	NT2-D1	testis:	n/a
47	chr18:28685799-28685849	HIPEpiC	eye:	n/a
48	chr18:28622474-28622524	U87	brain:	n/a
49	chr18:28622813-28622863	HEEpiC	esophagus:	n/a
50	chr18:28681121-28681171	H1-hESC	embryonic stem cell:	embryo

(count:88 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:28592790..28595531-chr18:28608278..28610485,2	MCF-7	breast:
2	chr18:28665512..28667530-chr18:28670151..28672364,2	K562	blood:
3	chr18:28641189..28643310-chr18:28664453..28667293,2	K562	blood:
4	chr18:28614001..28615580-chr18:28618945..28620521,2	K562	blood:
5	chr18:28670381..28673006-chr18:28687292..28689679,2	K562	blood:
6	chr18:28592790..28595531-chr18:28608278..28610485,2	MCF-7	breast:
7	chr18:28667749..28669756-chr18:28680920..28683845,2	K562	blood:
8	chr18:28678241..28681068-chr18:28692831..28695270,2	K562	blood:
9	chr18:28594117..28596433-chr18:28615710..28618191,2	MCF-7	breast:
10	chr18:28682670..28684930-chr18:28689763..28691596,2	K562	blood:
11	chr18:28683460..28685615-chr18:28686180..28687685,2	MCF-7	breast:
12	chr18:28627195..28629881-chr18:28637008..28639341,2	MCF-7	breast:
13	chr18:28663717..28665312-chr18:28679601..28681471,2	K562	blood:
14	chr18:28620876..28623818-chr18:28658735..28661003,2	K562	blood:
15	chr18:28627031..28630994-chr18:28632365..28635393,5	K562	blood:
16	chr18:28596389..28598653-chr18:28602652..28604800,3	K562	blood:
17	chr18:28652105..28654902-chr18:28682018..28683959,2	K562	blood:
18	chr18:28606015..28608013-chr18:28608927..28611177,2	MCF-7	breast:
19	chr18:28606623..28609017-chr18:28636811..28638702,2	K562	blood:
20	chr18:28684191..28685989-chr18:28784874..28786377,2	MCF-7	breast:
21	chr18:28640333..28642657-chr18:28648234..28652025,3	K562	blood:
22	chr18:28669945..28672658-chr18:28679021..28683884,6	K562	blood:
23	chr18:28689571..28692235-chr18:28693758..28695428,2	K562	blood:
24	chr18:28653486..28654988-chr18:28657389..28659058,2	K562	blood:
25	chr18:28640728..28642575-chr18:28644774..28647318,2	K562	blood:
26	chr18:28627031..28630994-chr18:28632365..28635393,5	K562	blood:
27	chr18:28680521..28683192-chr18:28685125..28687786,4	MCF-7	breast:
28	chr18:28606623..28609017-chr18:28636811..28638702,2	K562	blood:
29	chr18:28682778..28684607-chr18:28773976..28775884,2	MCF-7	breast:
30	chr18:28692982..28695806-chr18:28698647..28700392,2	K562	blood:
31	chr18:28640728..28642575-chr18:28644774..28647318,2	K562	blood:
32	chr18:28673150..28676508-chr18:28678975..28681813,4	K562	blood:
33	chr18:28680382..28683219-chr18:28685108..28688486,3	MCF-7	breast:
34	chr18:28681172..28683355-chr18:28689605..28692486,2	K562	blood:
35	chr18:28626792..28630994-chr18:28631279..28635393,6	K562	blood:
36	chr18:28652105..28654902-chr18:28682018..28683959,2	K562	blood:
37	chr18:28604790..28606677-chr18:28608390..28611343,2	K562	blood:
38	chr18:28680816..28682711-chr18:29076315..29078384,2	K562	blood:
39	chr18:28641189..28643310-chr18:28664453..28667293,2	K562	blood:
40	chr18:28683460..28685615-chr18:28686180..28687685,2	MCF-7	breast:
41	chr18:28665512..28667530-chr18:28670151..28672364,2	K562	blood:
42	chr18:28651842..28653529-chr18:28655723..28658009,2	MCF-7	breast:
43	chr18:28638090..28639722-chr18:28640416..28641974,2	K562	blood:
44	chr18:28636549..28638858-chr18:28710603..28713057,2	K562	blood:
45	chr18:28660094..28661732-chr18:28665344..28667098,2	K562	blood:
46	chr18:28627929..28630084-chr18:28631591..28634323,2	MCF-7	breast:
47	chr18:28622482..28623001-chrX:152864333..152864870,2	MCF-7	breast:
48	chr18:28642756..28645487-chr18:28647010..28648822,3	K562	blood:
49	chr18:28655509..28657780-chr18:28673533..28675759,2	K562	blood:
50	chr18:28604790..28606677-chr18:28608390..28611343,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSG1-10	chr18:28607207-28607445	uc_428_+
2	lnc-DSG1-2	chr18:28683086-28683157	ENSG00000265888.1
3	lnc-DSG1-2	chr18:28681551-28681686	ENSG00000265888.1
4	lnc-DSC2-1	chr18:28638806-28639359	ENSG00000261521.1
5	lnc-DSC2-2	chr18:28607207-28607445	uc_428_-

No data

Variant related genes	Relation type
DSC3	TF binding region
ENSG00000265888	TF binding region
DSC2	TF binding region
ENSG00000261521	TF binding region
ENSG00000238376	TF binding region
DSC3	CpG island
ENSG00000265888	CpG island
DSC2	CpG island
ENSG00000261521	CpG island
ENSG00000238376	CpG island
ENSG00000266521	chromatin interactions
ENSG00000238376	chromatin interactions
ENSG00000261521	chromatin interactions
ENSG00000134755	chromatin interactions
ENSG00000263698	chromatin interactions
ENSG00000265888	chromatin interactions
ENSG00000134762	chromatin interactions
ENSG00000251562	chromatin interactions
ENSG00000046604	chromatin interactions
ENSG00000147382	chromatin interactions
ENSG00000270117	chromatin interactions
ENSG00000260081	chromatin interactions
ENSG00000206737	chromatin interactions

Extended variants
information (count: 4318 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:4318 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs537780954	chr18:28583297-28583298	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs572681587	chr18:28583300-28583301	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs146987237	chr18:28583337-28583338	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs181315438	chr18:28583345-28583346	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs541471270	chr18:28583346-28583347	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs138070686	chr18:28583359-28583360	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs143735764	chr18:28583391-28583392	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs146268271	chr18:28583414-28583415	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs76062217	chr18:28583415-28583416	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs138921206	chr18:28583486-28583487	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs550090839	chr18:28583548-28583549	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs568373433	chr18:28583619-28583620	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs529052083	chr18:28583699-28583700	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs547628404	chr18:28583723-28583724	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs566954516	chr18:28583724-28583725	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs534314938	chr18:28583741-28583742	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs558676521	chr18:28583784-28583785	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs141858917	chr18:28583787-28583788	Weak transcription Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs374798746	chr18:28583846-28583847	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs371289004	chr18:28583849-28583850	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs537859066	chr18:28583866-28583867	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs1313581	chr18:28583870-28583871	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs185318070	chr18:28583880-28583881	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs535621901	chr18:28583892-28583893	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs555017959	chr18:28583895-28583896	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs571788402	chr18:28583906-28583907	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs55727134	chr18:28583919-28583920	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs371997117	chr18:28583920-28583921	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs1908138	chr18:28583938-28583939	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs575952719	chr18:28583944-28583945	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs190172520	chr18:28583951-28583952	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs575965631	chr18:28583953-28583954	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs561930567	chr18:28583965-28583966	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs1313582	chr18:28583981-28583982	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs115929701	chr18:28584027-28584028	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs139800375	chr18:28584028-28584029	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs527772600	chr18:28584133-28584134	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs552598278	chr18:28584148-28584149	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs138482790	chr18:28584168-28584169	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs181961800	chr18:28584185-28584186	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs372346117	chr18:28584188-28584189	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs200793068	chr18:28584209-28584210	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs141990544	chr18:28584253-28584254	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs375469420	chr18:28584257-28584258	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs549782185	chr18:28584259-28584260	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs115141451	chr18:28584268-28584269	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs200263083	chr18:28584281-28584282	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs553943587	chr18:28584308-28584309	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs372055903	chr18:28584315-28584316	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs367811987	chr18:28584320-28584321	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

Disease	PMID	Source
Esophageal squamous carcinoma	18350619	CNVD
Follicular lymphoma	20505157	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	18923191	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Medulloblastoma	21979893	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Trisomy 18 syndrome	17576883	CNVD
lymphocytic leukemia	21291569	CNVD
Barrett''s syndrome	19417022	CNVD
Ewing''s sarcoma	17952124	CNVD
Multiple myeloma	17550852	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Glioblastoma multiforme	21922591	CNVD
Melanoma	18172304	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Lung cancer	18438408	CNVD
18q deletion syndrome	19533772	CNVD
Acute myeloid leukemia	16864856	CNVD
Colorectal cancer	21102417	CNVD
Colorectal cancer	20709793	CNVD
Pancreatic cancer	21811562	CNVD
Basal cell lymphoma	21115979	CNVD
Mucosa-associated lymphoid tissue lymphomas	21459788	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
colon cancer	17210682	CNVD
Breast cancer	21785460	CNVD
Hepatocellular carcinoma	16750200	CNVD
Prostate cancer	16573809	CNVD
Autism	16446308	CNVD
Colorectal cancer	19359472	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	18056178	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Metanephric adenoma	20802469	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	17133270	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Colorectal cancer	16774939	CNVD
Colorectal cancer	21297112	CNVD
Myelofibrosis	22110671	CNVD
Colorectal cancer	21645411	CNVD
Glioblastoma multiforme	17002787	CNVD
Cancer	21183584	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	16912164	CNVD
Renal cell carcinoma	19150565	CNVD
Multiple myeloma	16616336	CNVD
Colorectal cancer	19150955	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21364760	CNVD
Melanoma	20877625	CNVD
Breast cancer	22522925	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1339 , 50 per page) page: 1 2 3 4 5 6 7 ... 27

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28566200-28600600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
2	chr18:28573200-28590600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr18:28573400-28591000	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
4	chr18:28575400-28585200	Weak transcription	Esophagus	oesophagus
5	chr18:28579000-28584600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
6	chr18:28579200-28583400	Weak transcription	Placenta Amnion	Placenta Amnion
7	chr18:28582200-28587000	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr18:28582800-28583400	Strong transcription	NHEK	skin
9	chr18:28582800-28585800	Strong transcription	HMEC	breast
10	chr18:28583400-28583800	Genic enhancers	NHEK	skin
11	chr18:28583400-28585000	Enhancers	Placenta Amnion	Placenta Amnion
12	chr18:28583800-28590800	Strong transcription	NHEK	skin
13	chr18:28584600-28587400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
14	chr18:28585000-28585800	Genic enhancers	Placenta Amnion	Placenta Amnion
15	chr18:28585200-28585800	Strong transcription	Esophagus	oesophagus
16	chr18:28585800-28586600	Strong transcription	Placenta Amnion	Placenta Amnion
17	chr18:28585800-28588000	Weak transcription	HMEC	breast
18	chr18:28585800-28600600	Weak transcription	Esophagus	oesophagus
19	chr18:28586000-28586600	Enhancers	Gastric	stomach
20	chr18:28586600-28591200	Weak transcription	Placenta Amnion	Placenta Amnion
21	chr18:28587000-28590600	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
22	chr18:28587400-28588000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
23	chr18:28588000-28588600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
24	chr18:28588000-28588800	Strong transcription	HMEC	breast
25	chr18:28588600-28595400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
26	chr18:28588800-28590600	Weak transcription	HMEC	breast
27	chr18:28590600-28590800	Genic enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
28	chr18:28590600-28591400	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
29	chr18:28590600-28591400	Enhancers	NH-A	brain
30	chr18:28590600-28592400	Enhancers	HMEC	breast
31	chr18:28590800-28591000	Enhancers	A549	lung
32	chr18:28590800-28591200	Genic enhancers	NHEK	skin
33	chr18:28590800-28591600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr18:28590800-28592200	Enhancers	Stomach Mucosa	stomach
35	chr18:28591000-28591400	Genic enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
36	chr18:28591000-28591400	Flanking Active TSS	A549	lung
37	chr18:28591200-28591600	Enhancers	Placenta Amnion	Placenta Amnion
38	chr18:28591200-28592400	Enhancers	NHEK	skin
39	chr18:28591400-28592200	Enhancers	A549	lung
40	chr18:28591400-28592400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
41	chr18:28591400-28593600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
42	chr18:28591600-28594000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
43	chr18:28591600-28595800	Weak transcription	Placenta Amnion	Placenta Amnion
44	chr18:28592400-28592600	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
45	chr18:28592400-28594000	Weak transcription	HMEC	breast
46	chr18:28592400-28595600	Weak transcription	NHEK	skin
47	chr18:28592600-28614800	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
48	chr18:28593600-28611600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr18:28594000-28601200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
50	chr18:28594000-28611800	Strong transcription	HMEC	breast

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