Variant report

Variant	nsv1320
Chromosome Location	chr14:67938724-67984157
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:665)
CpG islands
(count:1283)
Chromatin interactive
region (count:74)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:665 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:67954759-67955830	GM12878	blood:	n/a	n/a
2	ATF2	chr14:67954819-67955693	GM12878	blood:	n/a	n/a
3	ATF2	chr14:67959748-67960269	GM12878	blood:	n/a	n/a
4	BATF	chr14:67971660-67971865	GM12878	blood:	n/a	chr14:67971761-67971772
5	BATF	chr14:67954843-67955690	GM12878	blood:	n/a	n/a
6	BATF	chr14:67954916-67955636	GM12878	blood:	n/a	n/a
7	BCL11A	chr14:67954907-67955245	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
8	BCL11A	chr14:67954761-67955701	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
9	BCL11A	chr14:67955249-67955651	GM12878	blood:	n/a	n/a
10	BCL3	chr14:67954795-67955606	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
11	BCL3	chr14:67954848-67955694	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
12	BCLAF1	chr14:67954817-67955786	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
13	BCLAF1	chr14:67954691-67955722	GM12878	blood:	n/a	chr14:67955031-67955040 chr14:67955054-67955063
14	BHLHE40	chr14:67954835-67955721	GM12878	blood:	n/a	n/a
15	BHLHE40	chr14:67982506-67982510	K562	blood:	n/a	n/a
16	BHLHE40	chr14:67963909-67964086	K562	blood:	n/a	n/a
17	BRCA1	chr14:67981672-67981768	Hela-S3	cervix:	n/a	n/a
18	BRCA1	chr14:67980900-67981007	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr14:67959916-67960503	HCT-116	colon:	n/a	n/a
20	CBX3	chr14:67960035-67960357	K562	blood:	n/a	n/a
21	CBX3	chr14:67960033-67960467	K562	blood:	n/a	n/a
22	CCNT2	chr14:67981433-67981901	K562	blood:	n/a	chr14:67981809-67981818
23	CEBPB	chr14:67939661-67939765	HepG2	liver:	n/a	chr14:67939708-67939719
24	CEBPB	chr14:67983927-67984043	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr14:67956934-67957172	HepG2	liver:	n/a	chr14:67957015-67957026 chr14:67957062-67957073
26	CEBPB	chr14:67955284-67955597	GM12878	blood:	n/a	n/a
27	CEBPB	chr14:67976994-67977217	A549	lung:	n/a	chr14:67977110-67977121
28	CEBPB	chr14:67954924-67955210	GM12878	blood:	n/a	n/a
29	CEBPB	chr14:67976975-67977287	HepG2	liver:	n/a	chr14:67977110-67977121
30	CEBPB	chr14:67954719-67955853	GM12878	blood:	n/a	n/a
31	CEBPB	chr14:67969668-67970306	MCF-7	breast:	n/a	chr14:67970073-67970084
32	CHD2	chr14:67982200-67982334	GM12878	blood:	n/a	n/a
33	CHD2	chr14:67981488-67981752	GM12878	blood:	n/a	n/a
34	CHD2	chr14:67954787-67955724	GM12878	blood:	n/a	n/a
35	CHD2	chr14:67981380-67982108	Hela-S3	cervix:	n/a	chr14:67981903-67981913 chr14:67981946-67981956
36	CREB1	chr14:67954884-67955760	GM12878	blood:	n/a	n/a
37	CTCF	chr14:67983980-67984130	SAEC	small airway:	n/a	n/a
38	CTCF	chr14:67952488-67952668	H1-hESC	embryonic stem cell:	n/a	chr14:67952602-67952611
39	CTCF	chr14:67952608-67952614	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr14:67969740-67969890	WERI-Rb-1	eye:	n/a	n/a
41	CTCF	chr14:67952569-67952605	Hela-S3	cervix:	n/a	n/a
42	CTCF	chr14:67954840-67954990	GM12865	blood:	n/a	n/a
43	CTCF	chr14:67952580-67952730	GM12875	blood:	n/a	chr14:67952602-67952611
44	CTCF	chr14:67952521-67952686	HepG2	liver:	n/a	chr14:67952602-67952611
45	CTCF	chr14:67954860-67955150	GM12869	blood:	n/a	n/a
46	CTCF	chr14:67981998-67982009	GM12892	blood:	n/a	n/a
47	CTCF	chr14:67954940-67955090	GM12868	blood:	n/a	n/a
48	CTCF	chr14:67969788-67969791	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:67982260-67982410	WERI-Rb-1	eye:	n/a	n/a
50	CTCF	chr14:67983880-67984030	NHDF-neo	bronchial:	n/a	n/a

(count:1283 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67957839-67957889	PANC-1	pancreas:	n/a
2	chr14:67943755-67943805	HEEpiC	esophagus:	n/a
3	chr14:67957839-67957889	PANC-1	pancreas:	n/a
4	chr14:67943755-67943805	HEEpiC	esophagus:	n/a
5	chr14:67940178-67940228	HL-60	blood:	n/a
6	chr14:67981876-67981926	NHBE	bronchial:	n/a
7	chr14:67978224-67978274	LNCaP	prostate:	n/a
8	chr14:67982170-67982220	HCT-116	colon:	n/a
9	chr14:67982170-67982220	HMEC	breast:	n/a
10	chr14:67957839-67957889	Hela-S3	cervix:	n/a
11	chr14:67943755-67943805	BJ	skin:	n/a
12	chr14:67957839-67957889	HCT-116	colon:	n/a
13	chr14:67982430-67982480	GM06990	blood:	n/a
14	chr14:67943755-67943805	MCF-7	breast:	n/a
15	chr14:67982456-67982506	HEK293	kidney:	embryo
16	chr14:67982176-67982226	AG09309	skin:	n/a
17	chr14:67981637-67981687	AG09319	gingival:	n/a
18	chr14:67940669-67940719	AG09319	gingival:	n/a
19	chr14:67981637-67981687	MCF-7	breast:	n/a
20	chr14:67982152-67982202	Jurkat	blood:	n/a
21	chr14:67982456-67982506	Hela-S3	cervix:	n/a
22	chr14:67980422-67980472	SAEC	small airway:	n/a
23	chr14:67982176-67982226	PANC-1	pancreas:	n/a
24	chr14:67983484-67983534	HCT-116	colon:	n/a
25	chr14:67978224-67978274	HEEpiC	esophagus:	n/a
26	chr14:67978224-67978274	GM06990	blood:	n/a
27	chr14:67981515-67981565	HRCEpiC	kidney:	n/a
28	chr14:67941820-67941870	SK-N-SH_RA	brain:	n/a
29	chr14:67982146-67982196	NHDF-neo	bronchial:	n/a
30	chr14:67940178-67940228	SAEC	small airway:	n/a
31	chr14:67983484-67983534	BE2_C	brain:	n/a
32	chr14:67981637-67981687	HIPEpiC	eye:	n/a
33	chr14:67978224-67978274	SK-N-SH_RA	brain:	n/a
34	chr14:67983484-67983534	AoSMC	blood vessel:	n/a
35	chr14:67981876-67981926	MCF10A-Er-Src	breast:	n/a
36	chr14:67983484-67983534	MCF10A-Er-Src	breast:	n/a
37	chr14:67982456-67982506	PFSK-1	brain:	n/a
38	chr14:67982149-67982199	Hela-S3	cervix:	n/a
39	chr14:67982152-67982202	H1-hESC	embryonic stem cell:	embryo
40	chr14:67978224-67978274	SKMC	muscle:	n/a
41	chr14:67940178-67940228	Jurkat	blood:	n/a
42	chr14:67982430-67982480	ProgFib	skin:	n/a
43	chr14:67940669-67940719	HCM	heart:	n/a
44	chr14:67982176-67982226	GM12891	blood:	n/a
45	chr14:67982198-67982248	GM12892	blood:	n/a
46	chr14:67981876-67981926	PANC-1	pancreas:	n/a
47	chr14:67980422-67980472	SK-N-SH_RA	brain:	n/a
48	chr14:67982152-67982202	SK-N-SH_RA	brain:	n/a
49	chr14:67983484-67983534	NB4	blood:	n/a
50	chr14:67957839-67957889	NT2-D1	testis:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:67944442..67947234-chr14:67997536..68000572,3	MCF-7	breast:
2	chr14:67908929..67909688-chr14:67946732..67947393,3	MCF-7	breast:
3	chr14:67946842..67948505-chr14:67958854..67960376,2	MCF-7	breast:
4	chr14:67954053..67956925-chr14:67980005..67982672,2	MCF-7	breast:
5	chr14:67960402..67962099-chr14:67962938..67964502,2	MCF-7	breast:
6	chr14:67937786..67940325-chr14:67940798..67942852,2	MCF-7	breast:
7	chr14:67946462..67947472-chr14:68000220..68001028,4	MCF-7	breast:
8	chr14:67953372..67955912-chr14:67957756..67960248,2	K562	blood:
9	chr14:67939344..67942070-chr14:67946929..67950674,3	MCF-7	breast:
10	chr14:67908947..67909688-chr14:67946562..67947331,3	MCF-7	breast:
11	chr14:67908880..67909947-chr14:67946478..67947292,3	MCF-7	breast:
12	chr14:67976445..67980059-chr14:67998803..68001828,3	K562	blood:
13	chr14:67945430..67947453-chr14:67950590..67952638,3	MCF-7	breast:
14	chr14:67981445..67983281-chr15:99192294..99193975,2	MCF-7	breast:
15	chr14:67955748..67958630-chr14:67960758..67962478,3	MCF-7	breast:
16	chr14:67932881..67935193-chr14:67939104..67941762,2	MCF-7	breast:
17	chr10:97125145..97125859-chr14:67972267..67972944,2	MCF-7	breast:
18	chr14:67945105..67947990-chr14:67956817..67958766,2	MCF-7	breast:
19	chr14:67935396..67937435-chr14:67945472..67948247,2	MCF-7	breast:
20	chr14:67953824..67955734-chr14:67983233..67985363,2	MCF-7	breast:
21	chr14:67928466..67932816-chr14:67938653..67942762,5	MCF-7	breast:
22	chr14:67946481..67947300-chr14:67979982..67980806,3	MCF-7	breast:
23	chr14:67928246..67929078-chr14:67946550..67947331,3	MCF-7	breast:
24	chr14:67946842..67948505-chr14:67958854..67960376,2	MCF-7	breast:
25	chr14:67946762..67947287-chr14:67969455..67970025,2	MCF-7	breast:
26	chr14:67946150..67948174-chr14:67950017..67952096,2	MCF-7	breast:
27	chr14:67938787..67940976-chr14:67998285..68000377,3	MCF-7	breast:
28	chr14:67950772..67953650-chr14:67961025..67964119,3	MCF-7	breast:
29	chr14:67955748..67958630-chr14:67960758..67962478,3	MCF-7	breast:
30	chr14:67937786..67940325-chr14:67940798..67942852,2	MCF-7	breast:
31	chr14:67945315..67948095-chr14:67972222..67974425,2	MCF-7	breast:
32	chr14:67966981..67969114-chr14:68003205..68004722,2	MCF-7	breast:
33	chr14:67912569..67913643-chr14:67946452..67947328,6	MCF-7	breast:
34	chr14:67982264..67984804-chr14:68036407..68038355,2	MCF-7	breast:
35	chr14:67919473..67920342-chr14:67946537..67947177,3	MCF-7	breast:
36	chr14:67973423..67975623-chr14:67977106..67978835,2	MCF-7	breast:
37	chr14:67945641..67948338-chr14:67966357..67969353,2	MCF-7	breast:
38	chr14:67912599..67913704-chr14:67946532..67947321,6	MCF-7	breast:
39	chr14:67946762..67947287-chr14:67969455..67970025,2	MCF-7	breast:
40	chr14:67945641..67948338-chr14:67966357..67969353,2	MCF-7	breast:
41	chr14:67968272..67970276-chr14:67989655..67991450,2	MCF-7	breast:
42	chr14:67945315..67948095-chr14:67972222..67974425,2	MCF-7	breast:
43	chr14:67973423..67975623-chr14:67977106..67978835,2	MCF-7	breast:
44	chr14:67954443..67956751-chr14:67999962..68001506,2	MCF-7	breast:
45	chr14:67945819..67948998-chr14:67952251..67955708,4	MCF-7	breast:
46	chr14:67935565..67937568-chr14:67945579..67947744,3	MCF-7	breast:
47	chr14:67944168..67950756-chr14:67978926..67983400,9	MCF-7	breast:
48	chr14:67952500..67954302-chr14:67954353..67956306,2	K562	blood:
49	chr14:67903388..67905312-chr14:67950420..67951946,2	MCF-7	breast:
50	chr14:67966210..67968491-chr14:67971245..67973933,2	K562	blood:

No data

Variant related genes	Relation type
TMEM229B	TF binding region
TMEM229B	CpG island
ENSG00000054690	chromatin interactions
ENSG00000140443	chromatin interactions
ENSG00000198133	chromatin interactions
ENSG00000265993	chromatin interactions

Extended variants
information (count: 1807 )
Associated
traits (count: 71 )

Variant overlapped rSNPs/rCNVs (count:1807 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs540491634	chr14:67938744-67938745	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs115898085	chr14:67938756-67938757	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs182547635	chr14:67938785-67938786	Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs149619552	chr14:67938789-67938790	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs544303155	chr14:67938805-67938806	Weak transcription Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs2753607	chr14:67938818-67938819	Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
7	rs45446506	chr14:67938855-67938856	Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
8	rs3742865	chr14:67938866-67938867	Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
9	rs574193094	chr14:67938889-67938890	Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs146658137	chr14:67938959-67938960	Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs149230503	chr14:67938961-67938962	Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs28661609	chr14:67938988-67938989	Weak transcription Strong transcription Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs187157694	chr14:67939002-67939003	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs142451387	chr14:67939030-67939031	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs557136624	chr14:67939038-67939039	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs548931455	chr14:67939055-67939056	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs1316130	chr14:67939093-67939094	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs111674510	chr14:67939099-67939100	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs554487902	chr14:67939108-67939109	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs2478033	chr14:67939117-67939118	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs112425504	chr14:67939163-67939164	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs11845739	chr14:67939165-67939166	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs558767612	chr14:67939184-67939185	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs371665459	chr14:67939244-67939245	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs12435581	chr14:67939252-67939253	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs571328415	chr14:67939275-67939276	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs147080939	chr14:67939288-67939289	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530157682	chr14:67939289-67939290	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs138405831	chr14:67939294-67939295	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs560529816	chr14:67939299-67939300	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs140825049	chr14:67939312-67939313	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs372149991	chr14:67939324-67939325	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs527840023	chr14:67939376-67939377	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs142416483	chr14:67939382-67939383	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs190692646	chr14:67939388-67939389	Genic enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs568745683	chr14:67939419-67939420	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs532181682	chr14:67939424-67939425	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs373830523	chr14:67939436-67939437	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs114434496	chr14:67939459-67939460	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs17104363	chr14:67939483-67939484	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	disease
41	rs111748907	chr14:67939502-67939503	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs554492666	chr14:67939508-67939509	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs536366591	chr14:67939525-67939526	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs554605724	chr14:67939553-67939554	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs566550054	chr14:67939566-67939567	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs533988204	chr14:67939576-67939577	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs368047725	chr14:67939599-67939600	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs370039407	chr14:67939605-67939606	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs566386094	chr14:67939647-67939648	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs576709852	chr14:67939750-67939751	Genic enhancers Enhancers Strong transcription Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:71)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21044232	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Medulloblastoma	21979893	CNVD
Oral cancer	21386901	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Hepatocellular carcinoma	22174799	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	17899364	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
cataract	16735990	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:1479 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67928800-67946600	Weak transcription	Pancreas	Pancrea
2	chr14:67929600-67942600	Weak transcription	Lung	lung
3	chr14:67931200-67939600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr14:67931400-67939000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
5	chr14:67932000-67939600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
6	chr14:67932800-67939200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr14:67932800-67940000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
8	chr14:67933000-67954400	Weak transcription	Duodenum Smooth Muscle	Duodenum
9	chr14:67933200-67939400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
10	chr14:67934400-67939400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr14:67934600-67938800	Weak transcription	Primary T helper cells fromperipheralblood	blood
12	chr14:67934600-67939000	Weak transcription	Primary T helper cells PMA-I stimulated	--
13	chr14:67934600-67950600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
14	chr14:67934800-67939200	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
15	chr14:67934800-67946800	Weak transcription	Placenta	Placenta
16	chr14:67935000-67977200	Weak transcription	Brain Angular Gyrus	brain
17	chr14:67935200-67946800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr14:67935200-67952200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
19	chr14:67935400-67940200	Weak transcription	Fetal Intestine Large	intestine
20	chr14:67935400-67945200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
21	chr14:67936000-67939600	Weak transcription	Fetal Thymus	thymus
22	chr14:67936000-67952000	Weak transcription	Brain Substantia Nigra	brain
23	chr14:67937000-67939800	Weak transcription	Sigmoid Colon	Sigmoid Colon
24	chr14:67937400-67939000	Weak transcription	Monocytes-CD14+_RO01746	blood
25	chr14:67937400-67944800	Weak transcription	Primary hematopoietic stem cells	blood
26	chr14:67937400-67945000	Weak transcription	Colonic Mucosa	Colon
27	chr14:67937400-67945200	Strong transcription	Fetal Intestine Small	intestine
28	chr14:67937400-67951600	Weak transcription	Rectal Mucosa Donor 29	rectum
29	chr14:67937400-67954800	Weak transcription	Gastric	stomach
30	chr14:67937400-67955000	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
31	chr14:67937600-67940600	Strong transcription	Spleen	Spleen
32	chr14:67937600-67952000	Strong transcription	Primary T cells from cord blood	blood
33	chr14:67937600-67955000	Weak transcription	Brain Anterior Caudate	brain
34	chr14:67937800-67939400	Weak transcription	Primary monocytes fromperipheralblood	blood
35	chr14:67938000-67945600	Weak transcription	Adipose Nuclei	Adipose
36	chr14:67938200-67939600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
37	chr14:67938200-67940800	Strong transcription	Thymus	Thymus
38	chr14:67938200-67953400	Weak transcription	Brain Inferior Temporal Lobe	brain
39	chr14:67938400-67945000	Strong transcription	Primary T cells fromperipheralblood	blood
40	chr14:67938400-67951800	Weak transcription	Fetal Brain Female	brain
41	chr14:67938600-67939800	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
42	chr14:67938600-67940600	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
43	chr14:67938600-67940800	Strong transcription	Primary hematopoietic stem cells short term culture	blood
44	chr14:67938600-67940800	Strong transcription	Primary mononuclear cells fromperipheralblood	Blood
45	chr14:67938600-67944600	Strong transcription	Duodenum Mucosa	Duodenum
46	chr14:67938800-67939000	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
47	chr14:67938800-67947000	Strong transcription	Primary T helper cells fromperipheralblood	blood
48	chr14:67939000-67940600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr14:67939000-67940600	Strong transcription	Monocytes-CD14+_RO01746	blood
50	chr14:67939000-67943200	Strong transcription	Primary T helper cells PMA-I stimulated	--

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