Variant report

Variant	esv3360998
Chromosome Location	chr18:28693111-28881812
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2005)
CpG islands
(count:183)
Chromatin interactive
region (count:78)
LncRNA
region (count:12)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2005 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:28821782-28822715	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:28842330-28842415	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:28858551-28859115	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:28786901-28787118	K562	blood:	n/a	n/a
5	ARID3A	chr18:28765531-28765956	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:28805562-28805905	HepG2	liver:	n/a	n/a
7	ARID3A	chr18:28854874-28855326	HepG2	liver:	n/a	n/a
8	ARID3A	chr18:28823228-28823291	HepG2	liver:	n/a	n/a
9	ARID3A	chr18:28810479-28810946	HepG2	liver:	n/a	n/a
10	ARID3A	chr18:28812776-28814046	HepG2	liver:	n/a	n/a
11	ARID3A	chr18:28846518-28846844	HepG2	liver:	n/a	n/a
12	ARID3A	chr18:28823598-28825480	HepG2	liver:	n/a	n/a
13	ARID3A	chr18:28786695-28787188	HepG2	liver:	n/a	n/a
14	ATF1	chr18:28740860-28740988	K562	blood:	n/a	n/a
15	ATF2	chr18:28810440-28810906	GM12878	blood:	n/a	n/a
16	ATF2	chr18:28786643-28787026	GM12878	blood:	n/a	n/a
17	ATF2	chr18:28810371-28810995	GM12878	blood:	n/a	n/a
18	ATF2	chr18:28809265-28810245	GM12878	blood:	n/a	n/a
19	ATF2	chr18:28847993-28848583	GM12878	blood:	n/a	n/a
20	ATF2	chr18:28847983-28848560	GM12878	blood:	n/a	n/a
21	ATF2	chr18:28786658-28787100	GM12878	blood:	n/a	n/a
22	BACH1	chr18:28825094-28825221	H1-hESC	embryonic stem cell:	n/a	n/a
23	BACH1	chr18:28821980-28822264	H1-hESC	embryonic stem cell:	n/a	n/a
24	BATF	chr18:28810466-28810820	GM12878	blood:	n/a	chr18:28810692-28810703 chr18:28810693-28810703
25	BATF	chr18:28777573-28777856	GM12878	blood:	n/a	chr18:28777703-28777714
26	BATF	chr18:28786692-28787085	GM12878	blood:	n/a	n/a
27	BATF	chr18:28809924-28810148	GM12878	blood:	n/a	n/a
28	BATF	chr18:28841815-28842103	GM12878	blood:	n/a	n/a
29	BATF	chr18:28786666-28787028	GM12878	blood:	n/a	n/a
30	BATF	chr18:28809724-28810114	GM12878	blood:	n/a	n/a
31	BATF	chr18:28810511-28810849	GM12878	blood:	n/a	chr18:28810692-28810703 chr18:28810693-28810703
32	BATF	chr18:28846850-28847074	GM12878	blood:	n/a	chr18:28847003-28847014
33	BATF	chr18:28835963-28836257	GM12878	blood:	n/a	n/a
34	BATF	chr18:28848171-28848447	GM12878	blood:	n/a	n/a
35	BATF	chr18:28765654-28765897	GM12878	blood:	n/a	chr18:28765731-28765742
36	BATF	chr18:28846865-28847153	GM12878	blood:	n/a	chr18:28847003-28847014
37	BCL11A	chr18:28786715-28787150	GM12878	blood:	n/a	n/a
38	BCL11A	chr18:28810490-28810848	GM12878	blood:	n/a	chr18:28810547-28810556
39	BCL11A	chr18:28848132-28848421	GM12878	blood:	n/a	n/a
40	BCL3	chr18:28829104-28829522	GM12878	blood:	n/a	n/a
41	BCL3	chr18:28841757-28842063	GM12878	blood:	n/a	n/a
42	BCL3	chr18:28848148-28848413	GM12878	blood:	n/a	n/a
43	BCL3	chr18:28786634-28787074	GM12878	blood:	n/a	n/a
44	BCL3	chr18:28847999-28848435	GM12878	blood:	n/a	n/a
45	BCL3	chr18:28725775-28726022	GM12878	blood:	n/a	n/a
46	BCLAF1	chr18:28832446-28832801	GM12878	blood:	n/a	n/a
47	BCLAF1	chr18:28848154-28848485	GM12878	blood:	n/a	n/a
48	BCLAF1	chr18:28786699-28787044	GM12878	blood:	n/a	n/a
49	BCLAF1	chr18:28810493-28810859	GM12878	blood:	n/a	chr18:28810547-28810556
50	BHLHE40	chr18:28813808-28814156	GM12878	blood:	n/a	n/a

(count:183 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:28743074-28743124	HCF	heart:	n/a
2	chr18:28737288-28737338	U87	brain:	n/a
3	chr18:28737288-28737338	NH-A	brain:	n/a
4	chr18:28737288-28737338	MCF-7	breast:	n/a
5	chr18:28742633-28742683	NHBE	bronchial:	n/a
6	chr18:28742633-28742683	ProgFib	skin:	n/a
7	chr18:28742633-28742683	AG10803	skin:	n/a
8	chr18:28742633-28742683	SK-N-SH_RA	brain:	n/a
9	chr18:28742633-28742683	CMK	blood:	n/a
10	chr18:28737288-28737338	BJ	skin:	n/a
11	chr18:28742633-28742683	HCM	heart:	n/a
12	chr18:28742633-28742683	GM12892	blood:	n/a
13	chr18:28737288-28737338	RPTEC	kidney:	n/a
14	chr18:28737288-28737338	HEK293	kidney:	embryo
15	chr18:28742633-28742683	MCF-7	breast:	n/a
16	chr18:28737288-28737338	H1-hESC	embryonic stem cell:	embryo
17	chr18:28742633-28742683	Caco-2	colon:	n/a
18	chr18:28742633-28742683	SKMC	muscle:	n/a
19	chr18:28742633-28742683	IMR90	lung:	fetal
20	chr18:28742633-28742683	ovcar-3	ovarian:	n/a
21	chr18:28737288-28737338	HPAEpiC	pulmonary alveolar:	n/a
22	chr18:28742633-28742683	HAEpiC	amniotic membrane:	n/a
23	chr18:28742633-28742683	NB4	blood:	n/a
24	chr18:28737288-28737338	GM12891	blood:	n/a
25	chr18:28743074-28743124	PFSK-1	brain:	n/a
26	chr18:28743074-28743124	ProgFib	skin:	n/a
27	chr18:28742633-28742683	NT2-D1	testis:	n/a
28	chr18:28737288-28737338	Jurkat	blood:	n/a
29	chr18:28743074-28743124	BJ	skin:	n/a
30	chr18:28742633-28742683	PFSK-1	brain:	n/a
31	chr18:28743074-28743124	HRPEpiC	eye:	n/a
32	chr18:28742633-28742683	K562	blood:	n/a
33	chr18:28737288-28737338	NHDF-neo	bronchial:	n/a
34	chr18:28743074-28743124	T-47D	breast:	n/a
35	chr18:28737288-28737338	Hela-S3	cervix:	n/a
36	chr18:28743074-28743124	NT2-D1	testis:	n/a
37	chr18:28737288-28737338	AG04450	lung:	fetal
38	chr18:28743074-28743124	HCM	heart:	n/a
39	chr18:28742633-28742683	HUVEC	blood vessel:	n/a
40	chr18:28743074-28743124	GM19239	blood:	n/a
41	chr18:28742633-28742683	SK-N-MC	brain:	n/a
42	chr18:28743074-28743124	SK-N-MC	brain:	n/a
43	chr18:28743074-28743124	PANC-1	pancreas:	n/a
44	chr18:28737288-28737338	CMK	blood:	n/a
45	chr18:28737288-28737338	T-47D	breast:	n/a
46	chr18:28743074-28743124	ovcar-3	ovarian:	n/a
47	chr18:28743074-28743124	H1-hESC	embryonic stem cell:	embryo
48	chr18:28737288-28737338	HCM	heart:	n/a
49	chr18:28743074-28743124	PrEC	prostate:	n/a
50	chr18:28742633-28742683	GM06990	blood:	n/a

(count:78 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr18:28781990..28784653-chr18:28785130..28789773,4	MCF-7	breast:
2	chr18:28846335..28847118-chr18:29086087..29086880,3	MCF-7	breast:
3	chr18:28681468..28683863-chr18:28849493..28851108,2	K562	blood:
4	chr18:28681327..28682828-chr18:28692315..28694009,2	K562	blood:
5	chr18:28763439..28766393-chr18:28769672..28771413,2	K562	blood:
6	chr18:28733790..28735614-chr18:28744987..28747684,2	MCF-7	breast:
7	chr18:28775974..28778249-chr18:28784606..28787686,3	K562	blood:
8	chr18:28783058..28785177-chr18:28785602..28787795,2	K562	blood:
9	chr18:28805153..28808185-chr18:28812239..28815732,4	K562	blood:
10	chr18:28681730..28682478-chr18:28821729..28822531,3	MCF-7	breast:
11	chr18:28767376..28769243-chr18:28777763..28779276,2	MCF-7	breast:
12	chr18:28778678..28780623-chr18:28785152..28786878,2	MCF-7	breast:
13	chr18:28821250..28823567-chr18:28859683..28862005,2	MCF-7	breast:
14	chr18:28736989..28739079-chr18:28820985..28823154,2	MCF-7	breast:
15	chr18:28680359..28682735-chr18:28766413..28769030,2	MCF-7	breast:
16	chr18:28682778..28684607-chr18:28773976..28775884,2	MCF-7	breast:
17	chr18:28786550..28787203-chr18:28821650..28822453,3	MCF-7	breast:
18	chr18:28680863..28683275-chr18:28786590..28789100,4	MCF-7	breast:
19	chr18:28679651..28682372-chr18:28736748..28738693,2	MCF-7	breast:
20	chr18:28786065..28788187-chr18:29077621..29079237,2	MCF-7	breast:
21	chr18:28733790..28735614-chr18:28744987..28747684,2	MCF-7	breast:
22	chr18:28779290..28779920-chr18:28821622..28822442,2	MCF-7	breast:
23	chr18:28789661..28791901-chr18:28794620..28797352,2	MCF-7	breast:
24	chr18:28821250..28823567-chr18:28859683..28862005,2	MCF-7	breast:
25	chr18:28707023..28709640-chr18:28710441..28712736,2	K562	blood:
26	chr18:28773850..28776194-chr18:28777418..28780175,2	MCF-7	breast:
27	chr18:28680611..28682147-chr18:28768511..28770649,2	K562	blood:
28	chr18:28692982..28695806-chr18:28698647..28700392,2	K562	blood:
29	chr18:28682311..28684139-chr18:28820172..28823004,2	MCF-7	breast:
30	chr18:28787689..28790379-chr18:28808328..28810205,2	MCF-7	breast:
31	chr18:28781545..28784523-chr18:28786005..28788278,2	MCF-7	breast:
32	chr18:28680633..28683180-chr18:28821248..28824915,4	MCF-7	breast:
33	chr18:28682071..28683929-chr18:28735459..28737121,2	MCF-7	breast:
34	chr18:28778678..28780623-chr18:28785152..28786878,2	MCF-7	breast:
35	chr18:28789661..28791901-chr18:28794620..28797352,2	MCF-7	breast:
36	chr18:28787689..28790379-chr18:28808328..28810205,2	MCF-7	breast:
37	chr18:28855249..28856898-chr18:28857462..28860362,2	MCF-7	breast:
38	chr18:28684191..28685989-chr18:28784874..28786377,2	MCF-7	breast:
39	chr18:28771150..28772798-chr18:28773593..28775966,2	MCF-7	breast:
40	chr18:28805153..28808185-chr18:28812239..28815732,4	K562	blood:
41	chr18:28681300..28683140-chr18:28753934..28756361,2	MCF-7	breast:
42	chr18:28873035..28874705-chr18:28881375..28882997,2	MCF-7	breast:
43	chr18:28836169..28838870-chr18:28845508..28848292,2	K562	blood:
44	chr18:28786778..28788708-chr18:29017378..29018896,2	MCF-7	breast:
45	chr18:28773850..28776194-chr18:28777418..28780175,2	MCF-7	breast:
46	chr18:28763439..28766393-chr18:28769672..28771413,2	K562	blood:
47	chr18:28767376..28769243-chr18:28777763..28779276,2	MCF-7	breast:
48	chr18:28741766..28744685-chr18:28746539..28748634,2	MCF-7	breast:
49	chr18:28836169..28838870-chr18:28845508..28848292,2	K562	blood:
50	chr18:28820916..28822485-chr18:29145187..29146692,2	K562	blood:

(count:12 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-DSG1-8	chr18:28830287-28830407	NONHSAT058811
2	lnc-DSG1-9	chr18:28755037-28755148	NONHSAT058810
3	lnc-DSG1-8	chr18:28830962-28831367	NONHSAT058812
4	lnc-DSG1-9	chr18:28753383-28753720	NONHSAT058810
5	lnc-DSG1-7	chr18:28867478-28867603	NONHSAT058813
6	lnc-DSG1-8	chr18:28830962-28831251	NONHSAT058811
7	lnc-DSG1-2	chr18:28742498-28742752	ENSG00000265888.1
8	lnc-DSG1-7	chr18:28866469-28866554	NONHSAT058813
9	lnc-DSG1-8	chr18:28808080-28808173	NONHSAT058811
10	lnc-DSG1-7	chr18:28853309-28855721	NONHSAT058813
11	lnc-DSG1-8	chr18:28830290-28830510	NONHSAT058812
12	lnc-DSG1-2	chr18:28730762-28730851	ENSG00000265888.1

No data

Variant related genes	Relation type
ENSG00000263698	TF binding region
DSC1	TF binding region
ENSG00000263698	CpG island
DSC1	CpG island
ENSG00000046604	chromatin interactions
ENSG00000263698	chromatin interactions
ENSG00000265888	chromatin interactions
ENSG00000134765	chromatin interactions
ENSG00000134755	chromatin interactions

Extended variants
information (count: 7358 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:7358 , 50 per page) page: 1 2 3 4 5 6 7 ... 148

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs117184801	chr18:28693124-28693125	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs574626406	chr18:28693139-28693140	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs147448749	chr18:28693150-28693151	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs560334876	chr18:28693151-28693152	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs527477558	chr18:28693161-28693162	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs540761070	chr18:28693237-28693238	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs544347909	chr18:28693287-28693288	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs11877153	chr18:28693322-28693323	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs190687706	chr18:28693333-28693334	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs386802090	chr18:28693421-28693422	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs35330628	chr18:28693422-28693423	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs73954506	chr18:28693423-28693424	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs548593577	chr18:28693443-28693444	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs182727899	chr18:28693468-28693469	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs187804484	chr18:28693532-28693533	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs1790669	chr18:28693553-28693554	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs191297263	chr18:28693580-28693581	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs1790670	chr18:28693601-28693602	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs537450446	chr18:28693611-28693612	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs77481081	chr18:28693696-28693697	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs562823378	chr18:28693711-28693712	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs1626700	chr18:28693728-28693729	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs535773249	chr18:28693745-28693746	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs183360002	chr18:28693755-28693756	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1790671	chr18:28693779-28693780	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs35100309	chr18:28693863-28693864	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs386802091	chr18:28693898-28693899	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs114795651	chr18:28693900-28693901	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs577365485	chr18:28693902-28693903	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs112987251	chr18:28693968-28693969	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs544714409	chr18:28694036-28694037	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138403997	chr18:28694037-28694038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs530028049	chr18:28694048-28694049	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs1790673	chr18:28694052-28694053	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
35	rs560587124	chr18:28694104-28694105	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs552730406	chr18:28694107-28694108	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs1790674	chr18:28694215-28694216	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs552306387	chr18:28694239-28694240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs78286901	chr18:28694241-28694242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs537588057	chr18:28694243-28694244	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs531840517	chr18:28694294-28694295	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs549594108	chr18:28694304-28694305	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs568074002	chr18:28694305-28694306	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs535080328	chr18:28694342-28694343	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs549389198	chr18:28694376-28694377	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs1790675	chr18:28694379-28694380	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
47	rs528176637	chr18:28694384-28694385	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs370117107	chr18:28694390-28694391	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs186885764	chr18:28694421-28694422	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs558031475	chr18:28694423-28694424	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Pancreatic cancer	21811587	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:1547 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:28691800-28694600	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr18:28694400-28694600	Enhancers	Pancreas	Pancrea
3	chr18:28697800-28698000	Enhancers	ES-I3 Cell Line	embryonic stem cell
4	chr18:28698200-28699200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
5	chr18:28698600-28699600	Enhancers	H9 Cell Line	embryonic stem cell
6	chr18:28698600-28699800	Enhancers	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr18:28698800-28699600	Enhancers	HUES48 Cell Line	embryonic stem cell
8	chr18:28698800-28700000	Enhancers	iPS-18 Cell Line	embryonic stem cell
9	chr18:28699000-28699400	Enhancers	iPS-15b Cell Line	embryonic stem cell
10	chr18:28699000-28699600	Enhancers	HUES64 Cell Line	embryonic stem cell
11	chr18:28699000-28699600	Enhancers	iPS-20b Cell Line	embryonic stem cell
12	chr18:28699000-28699800	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr18:28699200-28699600	Enhancers	ES-I3 Cell Line	embryonic stem cell
14	chr18:28700400-28703000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
15	chr18:28700600-28701200	Enhancers	Stomach Mucosa	stomach
16	chr18:28700800-28701000	Enhancers	GM12878-XiMat	blood
17	chr18:28703000-28703200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
18	chr18:28703200-28708200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
19	chr18:28706400-28706800	Enhancers	Brain Anterior Caudate	brain
20	chr18:28706600-28709400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
21	chr18:28709400-28710400	Strong transcription	Breast Myoepithelial Primary Cells	Breast
22	chr18:28709600-28710600	Enhancers	Right Ventricle	heart
23	chr18:28710400-28711200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr18:28710600-28740800	Weak transcription	Primary T cells from cord blood	blood
25	chr18:28711200-28712600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
26	chr18:28712600-28726200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
27	chr18:28714600-28715000	Enhancers	Placenta Amnion	Placenta Amnion
28	chr18:28715000-28717400	Weak transcription	Placenta Amnion	Placenta Amnion
29	chr18:28717400-28717800	Enhancers	Placenta Amnion	Placenta Amnion
30	chr18:28725800-28726200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
31	chr18:28726200-28726600	Strong transcription	Breast Myoepithelial Primary Cells	Breast
32	chr18:28726200-28726600	ZNF genes & repeats	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr18:28726600-28727200	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr18:28726600-28730000	Weak transcription	Breast Myoepithelial Primary Cells	Breast
35	chr18:28726600-28734000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr18:28730000-28730400	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
37	chr18:28730000-28730400	ZNF genes & repeats	Gastric	stomach
38	chr18:28730000-28730400	ZNF genes & repeats	Pancreas	Pancrea
39	chr18:28730000-28730600	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
40	chr18:28730000-28730600	ZNF genes & repeats	Esophagus	oesophagus
41	chr18:28730400-28740800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
42	chr18:28730600-28737400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
43	chr18:28730600-28742600	Weak transcription	Esophagus	oesophagus
44	chr18:28733400-28742000	Weak transcription	Primary T helper cells PMA-I stimulated	--
45	chr18:28733800-28734400	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
46	chr18:28734000-28734400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr18:28734000-28734400	Enhancers	Fetal Heart	heart
48	chr18:28734200-28735000	Enhancers	NHEK	skin
49	chr18:28734400-28735200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
50	chr18:28734400-28741400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast

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