Variant report

Variant	nsv909613
Chromosome Location	chr18:44644530-44690107
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:843)
CpG islands
(count:916)
Chromatin interactive
region (count:30)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:843 , 50 per page) page: 1 2 3 4 5 6 7 ... 17

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr18:44684883-44685040	K562	blood:	n/a	n/a
2	ARID3A	chr18:44677824-44678132	K562	blood:	n/a	n/a
3	ATF2	chr18:44646738-44647341	GM12878	blood:	n/a	n/a
4	ATF2	chr18:44676480-44677442	GM12878	blood:	n/a	n/a
5	ATF2	chr18:44646731-44647251	GM12878	blood:	n/a	n/a
6	ATF3	chr18:44684823-44685126	K562	blood:	n/a	n/a
7	BACH1	chr18:44676328-44676759	H1-hESC	embryonic stem cell:	n/a	n/a
8	BATF	chr18:44646658-44647355	GM12878	blood:	n/a	n/a
9	BATF	chr18:44646695-44647275	GM12878	blood:	n/a	n/a
10	BATF	chr18:44689575-44690016	GM12878	blood:	n/a	n/a
11	BATF	chr18:44689580-44689951	GM12878	blood:	n/a	n/a
12	BCL11A	chr18:44646651-44647227	GM12878	blood:	n/a	n/a
13	BCL11A	chr18:44689553-44689930	GM12878	blood:	n/a	n/a
14	BCL3	chr18:44646767-44647250	GM12878	blood:	n/a	n/a
15	BCL3	chr18:44676634-44677320	A549	lung:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
16	BCL3	chr18:44676726-44677098	GM12878	blood:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
17	BCL3	chr18:44676555-44677346	A549	lung:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
18	BCLAF1	chr18:44689560-44690104	GM12878	blood:	n/a	n/a
19	BCLAF1	chr18:44676520-44677425	GM12878	blood:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
20	BCLAF1	chr18:44676300-44677253	GM12878	blood:	n/a	chr18:44676907-44676916 chr18:44676862-44676871 chr18:44676841-44676854
21	BCLAF1	chr18:44646802-44647168	GM12878	blood:	n/a	n/a
22	BHLHE40	chr18:44670436-44670781	K562	blood:	n/a	n/a
23	BHLHE40	chr18:44676328-44677091	GM12878	blood:	n/a	chr18:44676843-44676859
24	BHLHE40	chr18:44675924-44677495	K562	blood:	n/a	chr18:44676843-44676859
25	BHLHE40	chr18:44646804-44647255	GM12878	blood:	n/a	n/a
26	BRCA1	chr18:44676668-44677056	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr18:44676371-44676502	HepG2	liver:	n/a	n/a
28	BRCA1	chr18:44676397-44677399	Hela-S3	cervix:	n/a	n/a
29	BRCA1	chr18:44676951-44677167	HepG2	liver:	n/a	n/a
30	CBX3	chr18:44684698-44685113	K562	blood:	n/a	n/a
31	CCNT2	chr18:44677735-44678191	K562	blood:	n/a	n/a
32	CCNT2	chr18:44675920-44677117	K562	blood:	n/a	chr18:44676913-44676922
33	CEBPB	chr18:44662175-44662365	A549	lung:	n/a	chr18:44662297-44662308 chr18:44662299-44662308
34	CEBPB	chr18:44669615-44669871	MCF-7	breast:	n/a	n/a
35	CEBPB	chr18:44669574-44669892	ECC-1	luminal epithelium:	n/a	n/a
36	CEBPB	chr18:44669549-44669908	HepG2	liver:	n/a	n/a
37	CEBPB	chr18:44669549-44669919	K562	blood:	n/a	n/a
38	CEBPB	chr18:44684821-44685045	K562	blood:	n/a	n/a
39	CEBPB	chr18:44669609-44669819	A549	lung:	n/a	n/a
40	CEBPB	chr18:44677595-44677615	K562	blood:	n/a	n/a
41	CEBPB	chr18:44662148-44662455	HepG2	liver:	n/a	chr18:44662297-44662308 chr18:44662299-44662308
42	CEBPB	chr18:44669544-44669917	IMR90	lung:	n/a	n/a
43	CEBPB	chr18:44646616-44647359	GM12878	blood:	n/a	n/a
44	CEBPB	chr18:44669574-44669867	A549	lung:	n/a	n/a
45	CEBPB	chr18:44669651-44669824	HepG2	liver:	n/a	n/a
46	CEBPB	chr18:44669538-44669869	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr18:44684781-44685047	K562	blood:	n/a	n/a
48	CEBPB	chr18:44677836-44678149	K562	blood:	n/a	n/a
49	CEBPB	chr18:44669597-44669853	H1-hESC	embryonic stem cell:	n/a	n/a
50	CEBPB	chr18:44689472-44689948	IMR90	lung:	n/a	n/a

(count:916 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr18:44676672-44676722	PFSK-1	brain:	n/a
2	chr18:44676672-44676722	PFSK-1	brain:	n/a
3	chr18:44676757-44676807	HNPCEpiC	eye:	n/a
4	chr18:44676672-44676722	AoSMC	blood vessel:	n/a
5	chr18:44676421-44676471	HIPEpiC	eye:	n/a
6	chr18:44680380-44680430	IMR90	lung:	fetal
7	chr18:44676656-44676706	PrEC	prostate:	n/a
8	chr18:44676421-44676471	HCF	heart:	n/a
9	chr18:44677139-44677189	SAEC	small airway:	n/a
10	chr18:44676992-44677042	HIPEpiC	eye:	n/a
11	chr18:44676421-44676471	HRE	kidney:	n/a
12	chr18:44680380-44680430	PrEC	prostate:	n/a
13	chr18:44676764-44676814	SKMC	muscle:	n/a
14	chr18:44674172-44674222	AG09319	gingival:	n/a
15	chr18:44676656-44676706	HEK293	kidney:	embryo
16	chr18:44680380-44680430	NHBE	bronchial:	n/a
17	chr18:44676959-44677009	HRCEpiC	kidney:	n/a
18	chr18:44676764-44676814	K562	blood:	n/a
19	chr18:44644942-44644992	LNCaP	prostate:	n/a
20	chr18:44680380-44680430	H1-hESC	embryonic stem cell:	embryo
21	chr18:44644942-44644992	GM12892	blood:	n/a
22	chr18:44676764-44676814	GM19239	blood:	n/a
23	chr18:44676983-44677033	AG04449	skin:	fetal
24	chr18:44676992-44677042	SAEC	small airway:	n/a
25	chr18:44676959-44677009	SK-N-SH_RA	brain:	n/a
26	chr18:44676672-44676722	AG09309	skin:	n/a
27	chr18:44676656-44676706	HIPEpiC	eye:	n/a
28	chr18:44676962-44677012	HCPEpiC	choroid plexus:	n/a
29	chr18:44677553-44677603	HCF	heart:	n/a
30	chr18:44676421-44676471	K562	blood:	n/a
31	chr18:44677236-44677286	HPAEpiC	pulmonary alveolar:	n/a
32	chr18:44677553-44677603	HRE	kidney:	n/a
33	chr18:44676962-44677012	NB4	blood:	n/a
34	chr18:44680380-44680430	A549	lung:	n/a
35	chr18:44676992-44677042	U87	brain:	n/a
36	chr18:44676992-44677042	HCM	heart:	n/a
37	chr18:44676757-44676807	BE2_C	brain:	n/a
38	chr18:44676962-44677012	HCT-116	colon:	n/a
39	chr18:44676983-44677033	GM19239	blood:	n/a
40	chr18:44676672-44676722	SK-N-SH	brain:	n/a
41	chr18:44676764-44676814	SK-N-MC	brain:	n/a
42	chr18:44676983-44677033	A549	lung:	n/a
43	chr18:44677236-44677286	HRE	kidney:	n/a
44	chr18:44676672-44676722	PrEC	prostate:	n/a
45	chr18:44680380-44680430	AG04450	lung:	fetal
46	chr18:44676962-44677012	MCF10A-Er-Src	breast:	n/a
47	chr18:44674172-44674222	GM19239	blood:	n/a
48	chr18:44676764-44676814	Jurkat	blood:	n/a
49	chr18:44676672-44676722	HL-60	blood:	n/a
50	chr18:44676421-44676471	NH-A	brain:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr18:44675609..44678059-chr18:44682172..44686072,5	MCF-7	breast:
2	chr18:44685820..44687618-chr18:44709763..44711914,2	K562	blood:
3	chr18:44660900..44663835-chr18:44675479..44677959,3	MCF-7	breast:
4	chr18:44642698..44644448-chr18:44647501..44649189,2	K562	blood:
5	chr18:44676287..44678007-chr18:44686109..44688856,2	MCF-7	breast:
6	chr18:44664428..44666267-chr18:44672303..44675573,3	K562	blood:
7	chr18:44674746..44679194-chr18:44680542..44685924,9	K562	blood:
8	chr18:44676902..44678518-chr18:44699803..44701757,2	K562	blood:
9	chr17:79479596..79480269-chr18:44676737..44677238,2	HCT-116	colon:
10	chr18:44656520..44659372-chr18:44673623..44675752,2	K562	blood:
11	chr18:44668894..44671361-chr18:44675205..44677875,3	MCF-7	breast:
12	chr18:44648921..44650562-chr18:44675973..44678048,2	MCF-7	breast:
13	chr18:44675848..44678361-chr18:44699497..44704011,6	MCF-7	breast:
14	chr18:44664428..44666267-chr18:44672303..44675573,3	K562	blood:
15	chr18:44669254..44671555-chr18:44682680..44684488,2	K562	blood:
16	chr18:44660900..44663835-chr18:44675479..44677959,3	MCF-7	breast:
17	chr18:44663118..44666144-chr18:44673724..44676472,4	K562	blood:
18	chr18:44673432..44675834-chr18:44691617..44693277,2	MCF-7	breast:
19	chr18:44667945..44673232-chr18:44673754..44678571,7	MCF-7	breast:
20	chr18:44675461..44681646-chr18:44682135..44691602,15	MCF-7	breast:
21	chr18:44656520..44659372-chr18:44673623..44675752,2	K562	blood:
22	chr18:44687727..44690082-chr18:44690575..44692828,2	K562	blood:
23	chr18:44660861..44662516-chr18:44674947..44676839,2	K562	blood:
24	chr18:44687665..44690240-chr18:44700822..44702824,2	MCF-7	breast:
25	chr18:44666006..44667715-chr18:44675140..44677503,2	MCF-7	breast:
26	chr18:44669254..44671555-chr18:44682680..44684488,2	K562	blood:
27	chr18:44675372..44679287-chr18:44700113..44704114,10	MCF-7	breast:
28	chr18:44676561..44677117-chr21:38445057..38446026,2	Hela-S3	cervix:
29	chr18:44667492..44671272-chr18:44701185..44704416,3	MCF-7	breast:
30	chr18:44676438..44677089-chr4:99849867..99850574,2	HCT-116	colon:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KATNAL2-6	chr18:44663389-44663661	NONHSAT059155

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location
1	IER3IP1	hsa-miR-130b-3p	chr18:44682374-44682395
2	IER3IP1	hsa-miR-130b-3p	chr18:44682380-44682374
3	IER3IP1	hsa-miR-130b-3p	chr18:44682444-44682465
4	IER3IP1	hsa-miR-10a-5p	chr18:44682409-44682431
5	IER3IP1	hsa-miR-19b-3p	chr18:44682375-44682398
6	IER3IP1	hsa-miR-130b-3p	chr18:44682450-44682444

Variant related genes	Relation type
HDHD2	TF binding region
ENSG00000267800	TF binding region
HDHD2	CpG island
ENSG00000267800	CpG island
ENSG00000167220	chromatin interactions
ENSG00000182670	chromatin interactions
ENSG00000267228	chromatin interactions
ENSG00000267800	chromatin interactions
ENSG00000263923	chromatin interactions
ENSG00000229947	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000134049	chromatin interactions
ENSG00000151247	chromatin interactions
ENSG00000185808	chromatin interactions

Extended variants
information (count: 1755 )
Associated
traits (count: 88 )

Variant overlapped rSNPs/rCNVs (count:1755 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11876448	chr18:44644530-44644531	Weak transcription Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs79260308	chr18:44644541-44644542	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs183640515	chr18:44644553-44644554	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs569909592	chr18:44644602-44644603	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs188215088	chr18:44644620-44644621	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs558771760	chr18:44644635-44644636	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs145741848	chr18:44644638-44644639	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs117790209	chr18:44644698-44644699	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs554688070	chr18:44644736-44644737	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs574571046	chr18:44644756-44644757	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs543544736	chr18:44644787-44644788	Weak transcription Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs370743017	chr18:44644817-44644818	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs576976389	chr18:44644822-44644823	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs138298736	chr18:44644876-44644877	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs570856334	chr18:44644896-44644897	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs149572227	chr18:44644908-44644909	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs528802520	chr18:44644936-44644937	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs147401139	chr18:44644958-44644959	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs560899471	chr18:44644971-44644972	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs527917968	chr18:44644979-44644980	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs148279191	chr18:44644984-44644985	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs549951505	chr18:44644999-44645000	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs374723523	chr18:44645006-44645007	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs192920165	chr18:44645026-44645027	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs2635051	chr18:44645029-44645030	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs7239041	chr18:44645033-44645034	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs113706287	chr18:44645075-44645076	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs116312285	chr18:44645077-44645078	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs574784454	chr18:44645094-44645095	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs186859584	chr18:44645095-44645096	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
31	rs72905469	chr18:44645096-44645097	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs568156933	chr18:44645102-44645103	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs571719301	chr18:44645178-44645179	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs537050611	chr18:44645182-44645183	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs556994986	chr18:44645186-44645187	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs191360760	chr18:44645197-44645198	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs530198087	chr18:44645213-44645214	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs141296593	chr18:44645230-44645231	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs553316093	chr18:44645244-44645245	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs34581039	chr18:44645275-44645276	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs72905471	chr18:44645314-44645315	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs550357482	chr18:44645315-44645316	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs376945702	chr18:44645385-44645386	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs545952358	chr18:44645400-44645401	Weak transcription ZNF genes & repeats Strong transcription Enhancers Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs115556556	chr18:44645437-44645438	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs562901669	chr18:44645468-44645469	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs4609941	chr18:44645491-44645492	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
48	rs185019915	chr18:44645502-44645503	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs563339855	chr18:44645511-44645512	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs541738968	chr18:44645522-44645523	Weak transcription ZNF genes & repeats Strong transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:88)

Disease	PMID	Source
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
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
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
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
Invasive pancreatic ductal carcinoma	16982739	CNVD
Colorectal cancer	21297112	CNVD
Breast cancer	17603634	CNVD
Thyroid cancer	19087340	CNVD
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Colorectal cancer	19150955	CNVD
Acute myeloid leukemia	21251322	CNVD
Colorectal cancer	16912164	CNVD
Lung cancer	18438408	CNVD
Seminomas	18059402	CNVD
Breast cancer	16272173	CNVD
Breast cancer	17133270	CNVD
prenatal diagnosis	22389664	CNVD
Medulloblastoma	16783165	CNVD
Neuroblastoma	21508638	CNVD
Myelofibrosis	22110671	CNVD
Multiple myeloma	16461302	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Breast cancer	16397240	CNVD
Non-small cell lung cancer	21829676	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Pilomyxoid astrocytoma	17436254	CNVD
Mental retardation	21062444	CNVD
Cancer	21183584	CNVD
Burkitt''s lymphoma	18698080	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Cancer	17160897	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Gastric cancer	16891809	CNVD
Idiopathic thrombocytopenic purpura	19566914	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Basal cell lymphoma	17170743	CNVD
Follicular lymphoma	17170743	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16774939	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Lung cancer	21569311	CNVD
Prostate cancer	22341455	CNVD
Ependymoma	20639864	CNVD

Chromatin state (count:1528 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr18:44620800-44675400	Weak transcription	A549	lung
2	chr18:44621600-44674400	Weak transcription	Small Intestine	intestine
3	chr18:44624200-44654200	Weak transcription	Fetal Heart	heart
4	chr18:44626600-44664800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr18:44629200-44675800	Weak transcription	HUVEC	blood vessel
6	chr18:44630200-44646400	Strong transcription	Primary B cells from cord blood	blood
7	chr18:44630600-44660400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
8	chr18:44632000-44654200	Weak transcription	Pancreatic Islets	Pancreatic Islet
9	chr18:44632400-44675800	Weak transcription	Stomach Mucosa	stomach
10	chr18:44636200-44670600	Weak transcription	Pancreas	Pancrea
11	chr18:44636600-44661000	Weak transcription	Psoas Muscle	Psoas
12	chr18:44637000-44647000	Weak transcription	Fetal Brain Male	brain
13	chr18:44638400-44660800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr18:44639200-44662400	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
15	chr18:44639600-44660600	Weak transcription	NHLF	lung
16	chr18:44639600-44665000	Weak transcription	Colonic Mucosa	Colon
17	chr18:44639600-44666400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr18:44639800-44645000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr18:44639800-44654800	Weak transcription	HMEC	breast
20	chr18:44639800-44660600	Weak transcription	NH-A	brain
21	chr18:44639800-44660800	Weak transcription	Rectal Smooth Muscle	rectum
22	chr18:44640000-44645000	Weak transcription	Fetal Kidney	kidney
23	chr18:44640400-44662000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr18:44640600-44646200	Weak transcription	GM12878-XiMat	blood
25	chr18:44640600-44675600	Weak transcription	Placenta Amnion	Placenta Amnion
26	chr18:44640800-44662000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
27	chr18:44641000-44653800	Weak transcription	HSMM	muscle
28	chr18:44641000-44654200	Weak transcription	Brain Anterior Caudate	brain
29	chr18:44641000-44654800	Weak transcription	Hela-S3	cervix
30	chr18:44641200-44644800	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
31	chr18:44641200-44644800	Weak transcription	NHDF-Ad	bronchial
32	chr18:44641200-44645200	Weak transcription	HSMMtube	muscle
33	chr18:44641200-44654200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
34	chr18:44641200-44655600	Weak transcription	Fetal Brain Female	brain
35	chr18:44641200-44659600	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
36	chr18:44641600-44644800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
37	chr18:44641600-44645200	Weak transcription	Brain Hippocampus Middle	brain
38	chr18:44641600-44645800	Weak transcription	Fetal Lung	lung
39	chr18:44641600-44654000	Weak transcription	H1 Cell Line	embryonic stem cell
40	chr18:44641600-44654200	Weak transcription	Rectal Mucosa Donor 31	rectum
41	chr18:44641600-44654200	Weak transcription	Skeletal Muscle Male	skeletal muscle
42	chr18:44641600-44660400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
43	chr18:44641600-44670400	Weak transcription	HepG2	liver
44	chr18:44641600-44674000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
45	chr18:44641600-44675800	Weak transcription	Lung	lung
46	chr18:44641800-44644600	Weak transcription	Primary hematopoietic stem cells	blood
47	chr18:44641800-44644800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr18:44641800-44644800	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
49	chr18:44641800-44644800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
50	chr18:44641800-44644800	Weak transcription	Adipose Nuclei	Adipose

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