Variant report

Variant	nsv1055457
Chromosome Location	chr18:29654978-29677371
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:953)
CpG islands
(count:1161)
Chromatin interactive
region (count:32)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:953 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:29671473-29672011	HepG2	liver:	n/a	n/a
2	ARID3A	chr18:29672621-29672760	HepG2	liver:	n/a	n/a
3	ARID3A	chr18:29675829-29676076	HepG2	liver:	n/a	n/a
4	ARID3A	chr18:29673359-29673884	K562	blood:	n/a	n/a
5	ARID3A	chr18:29670540-29670822	HepG2	liver:	n/a	n/a
6	ARID3A	chr18:29671653-29671722	K562	blood:	n/a	n/a
7	ATF1	chr18:29671608-29672725	K562	blood:	n/a	n/a
8	ATF2	chr18:29672238-29673045	GM12878	blood:	n/a	n/a
9	ATF2	chr18:29671493-29672135	GM12878	blood:	n/a	n/a
10	ATF2	chr18:29671514-29672075	GM12878	blood:	n/a	n/a
11	ATF2	chr18:29665082-29665449	GM12878	blood:	n/a	n/a
12	ATF2	chr18:29665004-29665523	GM12878	blood:	n/a	n/a
13	ATF3	chr18:29671643-29671995	K562	blood:	n/a	chr18:29671812-29671823 chr18:29671810-29671825 chr18:29671814-29671822 chr18:29671772-29671781 chr18:29671812-29671823
14	BACH1	chr18:29672455-29672620	H1-hESC	embryonic stem cell:	n/a	n/a
15	BATF	chr18:29672599-29672844	GM12878	blood:	n/a	n/a
16	BATF	chr18:29671727-29671953	GM12878	blood:	n/a	n/a
17	BCL11A	chr18:29665138-29665493	GM12878	blood:	n/a	n/a
18	BCL11A	chr18:29665198-29665428	GM12878	blood:	n/a	n/a
19	BCLAF1	chr18:29671581-29672203	GM12878	blood:	n/a	chr18:29671982-29671995 chr18:29671983-29671992
20	BCLAF1	chr18:29665091-29665449	GM12878	blood:	n/a	n/a
21	BCLAF1	chr18:29672572-29673015	GM12878	blood:	n/a	chr18:29672947-29672960 chr18:29672946-29672955 chr18:29672940-29672953
22	BCLAF1	chr18:29671454-29672193	GM12878	blood:	n/a	chr18:29671982-29671995 chr18:29671983-29671992
23	BCLAF1	chr18:29673033-29673725	GM12878	blood:	n/a	n/a
24	BCLAF1	chr18:29664942-29665471	GM12878	blood:	n/a	n/a
25	BHLHE40	chr18:29672447-29672717	HepG2	liver:	n/a	n/a
26	BHLHE40	chr18:29671724-29673057	HepG2	liver:	n/a	chr18:29672946-29672962 chr18:29671977-29671993 chr18:29671974-29671990
27	BHLHE40	chr18:29671631-29673783	K562	blood:	n/a	chr18:29672946-29672962 chr18:29671977-29671993 chr18:29671974-29671990
28	BHLHE40	chr18:29665096-29665408	GM12878	blood:	n/a	n/a
29	BHLHE40	chr18:29671540-29673692	GM12878	blood:	n/a	chr18:29672946-29672962 chr18:29671977-29671993 chr18:29671974-29671990
30	BHLHE40	chr18:29672415-29672941	A549	lung:	n/a	n/a
31	BRCA1	chr18:29671833-29671910	HepG2	liver:	n/a	n/a
32	BRCA1	chr18:29672610-29672932	GM12878	blood:	n/a	n/a
33	BRCA1	chr18:29671717-29671983	GM12878	blood:	n/a	n/a
34	BRCA1	chr18:29672674-29672854	HepG2	liver:	n/a	n/a
35	BRCA1	chr18:29672168-29672315	HepG2	liver:	n/a	n/a
36	BRCA1	chr18:29672395-29672879	Hela-S3	cervix:	n/a	n/a
37	BRCA1	chr18:29671503-29672004	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr18:29671668-29672012	H1-hESC	embryonic stem cell:	n/a	n/a
39	CBX3	chr18:29664909-29665472	HCT-116	colon:	n/a	n/a
40	CBX3	chr18:29671556-29672903	K562	blood:	n/a	n/a
41	CBX3	chr18:29664887-29665486	HCT-116	colon:	n/a	n/a
42	CCNT2	chr18:29671651-29673750	K562	blood:	n/a	chr18:29672596-29672605 chr18:29672293-29672302 chr18:29673658-29673678 chr18:29672990-29672999 chr18:29672227-29672236 chr18:29672862-29672871 chr18:29672637-29672646
43	CEBPB	chr18:29672535-29672854	HepG2	liver:	n/a	n/a
44	CEBPB	chr18:29658270-29658302	K562	blood:	n/a	n/a
45	CEBPB	chr18:29671690-29671933	H1-hESC	embryonic stem cell:	n/a	n/a
46	CEBPB	chr18:29660553-29660705	K562	blood:	n/a	chr18:29660614-29660625
47	CEBPB	chr18:29671641-29672023	Hela-S3	cervix:	n/a	n/a
48	CEBPB	chr18:29671749-29671870	HepG2	liver:	n/a	n/a
49	CEBPB	chr18:29664784-29665497	HCT-116	colon:	n/a	n/a
50	CEBPB	chr18:29672527-29672789	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1161 , 50 per page) page: 1 2 3 4 5 6 7 ... 24

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:29671618-29671668	T-47D	breast:	n/a
2	chr18:29672450-29672500	HRCEpiC	kidney:	n/a
3	chr18:29671618-29671668	T-47D	breast:	n/a
4	chr18:29672450-29672500	HRCEpiC	kidney:	n/a
5	chr18:29669225-29669275	HRCEpiC	kidney:	n/a
6	chr18:29671448-29671498	Hela-S3	cervix:	n/a
7	chr18:29672736-29672786	Hepatocyte	liver:	n/a
8	chr18:29670396-29670446	LNCaP	prostate:	n/a
9	chr18:29671984-29672034	PrEC	prostate:	n/a
10	chr18:29670396-29670446	U87	brain:	n/a
11	chr18:29672450-29672500	Hepatocyte	liver:	n/a
12	chr18:29671618-29671668	HEEpiC	esophagus:	n/a
13	chr18:29671448-29671498	HRCEpiC	kidney:	n/a
14	chr18:29673246-29673296	SK-N-SH_RA	brain:	n/a
15	chr18:29671448-29671498	AoSMC	blood vessel:	n/a
16	chr18:29672555-29672605	Hela-S3	cervix:	n/a
17	chr18:29672468-29672518	HCT-116	colon:	n/a
18	chr18:29672458-29672508	BJ	skin:	n/a
19	chr18:29671772-29671822	HCPEpiC	choroid plexus:	n/a
20	chr18:29672736-29672786	GM06990	blood:	n/a
21	chr18:29671767-29671817	PANC-1	pancreas:	n/a
22	chr18:29671767-29671817	GM12891	blood:	n/a
23	chr18:29672549-29672599	HRCEpiC	kidney:	n/a
24	chr18:29669225-29669275	HNPCEpiC	eye:	n/a
25	chr18:29669225-29669275	HRPEpiC	eye:	n/a
26	chr18:29672468-29672518	NB4	blood:	n/a
27	chr18:29672549-29672599	HCT-116	colon:	n/a
28	chr18:29672458-29672508	A549	lung:	n/a
29	chr18:29671772-29671822	NT2-D1	testis:	n/a
30	chr18:29672535-29672585	HCPEpiC	choroid plexus:	n/a
31	chr18:29671448-29671498	SK-N-SH	brain:	n/a
32	chr18:29673278-29673328	H1-hESC	embryonic stem cell:	embryo
33	chr18:29671767-29671817	HEK293	kidney:	embryo
34	chr18:29673278-29673328	Hepatocyte	liver:	n/a
35	chr18:29672535-29672585	H1-hESC	embryonic stem cell:	embryo
36	chr18:29671984-29672034	HCF	heart:	n/a
37	chr18:29672468-29672518	HEK293	kidney:	embryo
38	chr18:29671797-29671847	AG10803	skin:	n/a
39	chr18:29671772-29671822	HL-60	blood:	n/a
40	chr18:29671772-29671822	GM06990	blood:	n/a
41	chr18:29672736-29672786	PrEC	prostate:	n/a
42	chr18:29672736-29672786	ECC-1	luminal epithelium:	n/a
43	chr18:29677086-29677136	HNPCEpiC	eye:	n/a
44	chr18:29674872-29674922	RPTEC	kidney:	n/a
45	chr18:29669225-29669275	Caco-2	colon:	n/a
46	chr18:29672535-29672585	HIPEpiC	eye:	n/a
47	chr18:29672736-29672786	SK-N-SH_RA	brain:	n/a
48	chr18:29677086-29677136	NHDF-neo	bronchial:	n/a
49	chr18:29671448-29671498	NHBE	bronchial:	n/a
50	chr18:29672535-29672585	HCF	heart:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:29666841..29669333-chr18:29671631..29673559,3	MCF-7	breast:
2	chr18:29660336..29661951-chr18:29664954..29667841,2	K562	blood:
3	chr18:29598038..29600342-chr18:29668214..29669893,2	MCF-7	breast:
4	chr18:29672647..29674860-chr18:29703384..29706167,2	MCF-7	breast:
5	chr18:29521618..29525019-chr18:29670361..29672184,4	MCF-7	breast:
6	chr18:29660336..29661951-chr18:29664954..29667841,2	K562	blood:
7	chr18:29671504..29673421-chr18:30049351..30052237,2	K562	blood:
8	chr18:29656745..29659248-chr18:29670363..29672023,2	K562	blood:
9	chr17:42976409..42976919-chr18:29671871..29672426,2	Hela-S3	cervix:
10	chr12:120972120..120972749-chr18:29671926..29672687,2	Hela-S3	cervix:
11	chr11:62608032..62609663-chr18:29672517..29674072,2	MCF-7	breast:
12	chr18:29521537..29525393-chr18:29670839..29674328,7	K562	blood:
13	chr18:29653056..29654979-chr18:29671460..29672978,2	MCF-7	breast:
14	chr18:29521522..29523729-chr18:29672844..29674625,2	MCF-7	breast:
15	chr18:29521939..29525237-chr18:29670716..29673913,4	MCF-7	breast:
16	chr18:29654269..29657288-chr18:29670351..29673351,3	K562	blood:
17	chr18:29654269..29657288-chr18:29670351..29673351,3	K562	blood:
18	chr18:29671880..29672426-chrX:131157129..131157907,2	Hela-S3	cervix:
19	chr18:29662644..29667608-chr18:29668028..29673014,9	K562	blood:
20	chr18:29657548..29661977-chr18:29669149..29673484,4	K562	blood:
21	chr18:29520857..29524705-chr18:29670705..29674434,7	K562	blood:
22	chr18:29598540..29599388-chr18:29671670..29672456,2	Hela-S3	cervix:
23	chr18:29597506..29599866-chr18:29670953..29673378,4	MCF-7	breast:
24	chr18:29661516..29666367-chr18:29670429..29672911,6	MCF-7	breast:
25	chr18:29637884..29642506-chr18:29670649..29674281,4	K562	blood:
26	chr18:29671668..29674127-chr18:29674569..29677601,3	MCF-7	breast:
27	chr18:29670755..29674701-chr18:29702072..29706406,4	K562	blood:
28	chr17:73150233..73150854-chr18:29672091..29672842,2	HCT-116	colon:
29	chr18:29671417..29672347-chr20:42086520..42087354,2	Hela-S3	cervix:
30	chr11:65190111..65190616-chr18:29672226..29673180,2	Hela-S3	cervix:
31	chr18:29596689..29599956-chr18:29670764..29674475,6	MCF-7	breast:
32	chr18:29671926..29672642-chr3:159481391..159482087,2	Hela-S3	cervix:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-RNF125-4	chr18:29671865-29672198	NONHSAT058853
2	lnc-TRAPPC8-2	chr18:29671258-29671465	ENSG00000265008.1
3	lnc-TRAPPC8-2	chr18:29671818-29672082	ENSG00000265008.1
4	lnc-RNF125-4	chr18:29672663-29672849	NONHSAT058852
5	lnc-RNF125-4	chr18:29671847-29672198	NONHSAT058852
6	lnc-TRAPPC8-4	chr18:29655848-29656235	NONHSAT058850
7	lnc-RNF125-4	chr18:29672663-29672849	NONHSAT058853

No data

Variant related genes	Relation type
ENSG00000265008	TF binding region
ENSG00000238982	TF binding region
RNF138	TF binding region
ENSG00000214917	TF binding region
ENSG00000265008	CpG island
ENSG00000238982	CpG island
RNF138	CpG island
ENSG00000214917	CpG island
ENSG00000263917	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000245532	chromatin interactions
ENSG00000141441	chromatin interactions
ENSG00000214917	chromatin interactions
ENSG00000134758	chromatin interactions
ENSG00000108883	chromatin interactions
ENSG00000124193	chromatin interactions
ENSG00000022840	chromatin interactions
ENSG00000153339	chromatin interactions
ENSG00000250588	chromatin interactions
ENSG00000263393	chromatin interactions
ENSG00000167131	chromatin interactions
ENSG00000265063	chromatin interactions
ENSG00000263823	chromatin interactions
ENSG00000110871	chromatin interactions
ENSG00000265008	chromatin interactions
ENSG00000134602	chromatin interactions
ENSG00000101695	chromatin interactions
ENSG00000189159	chromatin interactions

Extended variants
information (count: 819 )
Associated
traits (count: 70 )

Variant overlapped rSNPs/rCNVs (count:819 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs79913702	chr18:29654981-29654982	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs117930139	chr18:29654998-29654999	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs549161825	chr18:29655000-29655001	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs55786778	chr18:29655025-29655026	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
5	rs374689133	chr18:29655031-29655032	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs115865306	chr18:29655033-29655034	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs186478530	chr18:29655044-29655045	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs551826502	chr18:29655100-29655101	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs564005789	chr18:29655133-29655134	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs76366917	chr18:29655149-29655150	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs77204840	chr18:29655166-29655167	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs76197443	chr18:29655207-29655208	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs535091078	chr18:29655209-29655210	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547091580	chr18:29655226-29655227	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs372633144	chr18:29655257-29655258	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs145264338	chr18:29655270-29655271	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs538820593	chr18:29655284-29655285	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs190917676	chr18:29655308-29655309	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs575452679	chr18:29655373-29655374	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs535879397	chr18:29655415-29655416	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs554515763	chr18:29655437-29655438	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs61392417	chr18:29655472-29655473	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
23	rs539969193	chr18:29655490-29655491	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs564627002	chr18:29655519-29655520	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs577862682	chr18:29655600-29655601	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs545536420	chr18:29655605-29655606	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs12953843	chr18:29655655-29655656	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs12970765	chr18:29655656-29655657	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs372552376	chr18:29655657-29655658	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs58194866	chr18:29655675-29655676	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs563836390	chr18:29655757-29655758	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs62093946	chr18:29655791-29655792	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs549128678	chr18:29655807-29655808	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs368784379	chr18:29655831-29655832	Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs114685118	chr18:29655856-29655857	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
36	rs201467176	chr18:29655891-29655892	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
37	rs528477206	chr18:29655896-29655897	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
38	rs562506513	chr18:29655902-29655903	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs547158677	chr18:29655907-29655908	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
40	rs530263359	chr18:29655944-29655945	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
41	rs571767753	chr18:29655961-29655962	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
42	rs375142679	chr18:29655973-29655974	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs538460706	chr18:29656000-29656001	Strong transcription Weak transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs889888	chr18:29656001-29656002	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs149749707	chr18:29656020-29656021	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
46	rs145595972	chr18:29656054-29656055	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs182390554	chr18:29656153-29656154	Weak transcription Strong transcription	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs28376309	chr18:29656251-29656252	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
49	rs200332934	chr18:29656266-29656267	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs566452118	chr18:29656287-29656288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:70)

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
Prostate cancer	22341455	CNVD

Chromatin state (count:1071 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:29602600-29664200	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr18:29604600-29656000	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
3	chr18:29626000-29657200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
4	chr18:29630000-29664400	Weak transcription	Fetal Muscle Leg	muscle
5	chr18:29630400-29664400	Weak transcription	Left Ventricle	heart
6	chr18:29630800-29658600	Weak transcription	Rectal Mucosa Donor 29	rectum
7	chr18:29631400-29671400	Weak transcription	Hela-S3	cervix
8	chr18:29640400-29664400	Weak transcription	Primary T killer memory cells from peripheral blood	blood
9	chr18:29640400-29664600	Weak transcription	Thymus	Thymus
10	chr18:29640600-29664600	Weak transcription	HUES48 Cell Line	embryonic stem cell
11	chr18:29642600-29664600	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
12	chr18:29644000-29664200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr18:29645600-29655800	Weak transcription	Right Ventricle	heart
14	chr18:29647000-29660200	Weak transcription	Primary B cells from peripheral blood	blood
15	chr18:29647000-29660400	Weak transcription	Fetal Thymus	thymus
16	chr18:29647000-29664400	Weak transcription	Liver	Liver
17	chr18:29648400-29664200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr18:29648400-29664400	Weak transcription	Rectal Mucosa Donor 31	rectum
19	chr18:29648600-29664200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
20	chr18:29648800-29658200	Weak transcription	Fetal Intestine Large	intestine
21	chr18:29649000-29664200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
22	chr18:29650000-29663000	Weak transcription	Adipose Nuclei	Adipose
23	chr18:29652200-29660400	Weak transcription	Fetal Intestine Small	intestine
24	chr18:29652400-29656800	Strong transcription	Primary T cells fromperipheralblood	blood
25	chr18:29652800-29663600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
26	chr18:29653000-29655800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
27	chr18:29653200-29655400	Strong transcription	Primary T cells from cord blood	blood
28	chr18:29653200-29656200	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
29	chr18:29653200-29656400	Strong transcription	Primary hematopoietic stem cells short term culture	blood
30	chr18:29653400-29655200	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr18:29654200-29664200	Weak transcription	Primary B cells from cord blood	blood
32	chr18:29654400-29660400	Weak transcription	Primary monocytes fromperipheralblood	blood
33	chr18:29654400-29660400	Weak transcription	Monocytes-CD14+_RO01746	blood
34	chr18:29654400-29661000	Weak transcription	Primary T helper cells PMA-I stimulated	--
35	chr18:29654400-29663600	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
36	chr18:29654400-29664400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr18:29654400-29664400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
38	chr18:29654600-29662800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
39	chr18:29654600-29663800	Weak transcription	Primary hematopoietic stem cells	blood
40	chr18:29654600-29663800	Weak transcription	Primary T helper cells fromperipheralblood	blood
41	chr18:29654600-29664400	Weak transcription	Duodenum Mucosa	Duodenum
42	chr18:29655200-29663000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr18:29655400-29664200	Weak transcription	Primary T cells from cord blood	blood
44	chr18:29655800-29663600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
45	chr18:29656000-29671400	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
46	chr18:29656200-29664400	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
47	chr18:29656400-29663200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
48	chr18:29656800-29664000	Weak transcription	Primary T cells fromperipheralblood	blood
49	chr18:29657600-29657800	Enhancers	Sigmoid Colon	Sigmoid Colon
50	chr18:29657800-29658400	Weak transcription	Sigmoid Colon	Sigmoid Colon

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