Variant report

Variant	nsv1319
Chromosome Location	chr14:67863561-67908725
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1235)
CpG islands
(count:732)
Chromatin interactive
region (count:69)
LncRNA
region (count:0)
Mature miRNA
region (count: 1)
miRNA target
sites (count:0)

(count:1235 , 50 per page) page: 1 2 3 4 5 6 7 ... 25

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:67882772-67883133	K562	blood:	n/a	n/a
2	ARID3A	chr14:67893813-67894102	K562	blood:	n/a	n/a
3	ARID3A	chr14:67906963-67907136	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:67893880-67894078	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:67863452-67863614	HepG2	liver:	n/a	chr14:67863519-67863535
6	ATF1	chr14:67882889-67883127	K562	blood:	n/a	n/a
7	ATF1	chr14:67893759-67894087	K562	blood:	n/a	n/a
8	ATF1	chr14:67885301-67885959	K562	blood:	n/a	n/a
9	ATF1	chr14:67880901-67881291	K562	blood:	n/a	n/a
10	ATF1	chr14:67888157-67888778	K562	blood:	n/a	n/a
11	ATF2	chr14:67886894-67887276	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF3	chr14:67886831-67887162	K562	blood:	n/a	chr14:67887063-67887077 chr14:67887067-67887078 chr14:67887065-67887076 chr14:67887067-67887078
13	ATF3	chr14:67880916-67881163	K562	blood:	n/a	chr14:67881043-67881057
14	ATF3	chr14:67882886-67883050	K562	blood:	n/a	n/a
15	ATF3	chr14:67880831-67881290	K562	blood:	n/a	chr14:67881043-67881057
16	ATF3	chr14:67885567-67885968	K562	blood:	n/a	n/a
17	BACH1	chr14:67893885-67894323	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr14:67885750-67885953	K562	blood:	n/a	n/a
19	BHLHE40	chr14:67886990-67887118	GM12878	blood:	n/a	n/a
20	BHLHE40	chr14:67895292-67895743	HepG2	liver:	n/a	n/a
21	BHLHE40	chr14:67893697-67894184	K562	blood:	n/a	n/a
22	BHLHE40	chr14:67885054-67886297	K562	blood:	n/a	n/a
23	BHLHE40	chr14:67893867-67894184	GM12878	blood:	n/a	n/a
24	BHLHE40	chr14:67896964-67897369	HepG2	liver:	n/a	chr14:67897203-67897212 chr14:67897198-67897219 chr14:67897204-67897213 chr14:67897204-67897213 chr14:67897205-67897214 chr14:67897202-67897215
25	BHLHE40	chr14:67897113-67897380	K562	blood:	n/a	chr14:67897203-67897212 chr14:67897198-67897219 chr14:67897204-67897213 chr14:67897204-67897213 chr14:67897205-67897214 chr14:67897202-67897215
26	BHLHE40	chr14:67888441-67888700	K562	blood:	n/a	n/a
27	BHLHE40	chr14:67877239-67877364	K562	blood:	n/a	n/a
28	BHLHE40	chr14:67895267-67895339	K562	blood:	n/a	n/a
29	BHLHE40	chr14:67875187-67875453	HepG2	liver:	n/a	n/a
30	BHLHE40	chr14:67880875-67881263	K562	blood:	n/a	n/a
31	BHLHE40	chr14:67886888-67887245	K562	blood:	n/a	n/a
32	BRCA1	chr14:67878786-67879074	Hela-S3	cervix:	n/a	n/a
33	BRCA1	chr14:67880590-67881302	Hela-S3	cervix:	n/a	n/a
34	CBX3	chr14:67886806-67887329	K562	blood:	n/a	n/a
35	CBX3	chr14:67882826-67883158	K562	blood:	n/a	n/a
36	CBX3	chr14:67880930-67881410	K562	blood:	n/a	n/a
37	CBX3	chr14:67885549-67886006	K562	blood:	n/a	n/a
38	CCNT2	chr14:67885204-67886122	K562	blood:	n/a	chr14:67885821-67885841 chr14:67885760-67885769
39	CEBPB	chr14:67881000-67881191	K562	blood:	n/a	n/a
40	CEBPB	chr14:67878603-67879265	Hela-S3	cervix:	n/a	n/a
41	CEBPB	chr14:67880479-67881463	Hela-S3	cervix:	n/a	n/a
42	CEBPB	chr14:67907217-67907763	MCF-7	breast:	n/a	n/a
43	CEBPB	chr14:67882783-67883178	K562	blood:	n/a	n/a
44	CEBPB	chr14:67884962-67885408	Hela-S3	cervix:	n/a	n/a
45	CEBPB	chr14:67882881-67883088	K562	blood:	n/a	n/a
46	CEBPB	chr14:67863376-67863633	Hela-S3	cervix:	n/a	n/a
47	CEBPB	chr14:67882881-67883017	HepG2	liver:	n/a	n/a
48	CEBPB	chr14:67882800-67883174	K562	blood:	n/a	n/a
49	CEBPB	chr14:67884408-67884692	IMR90	lung:	n/a	n/a
50	CEBPB	chr14:67888375-67888865	K562	blood:	n/a	n/a

(count:732 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67881521-67881571	CMK	blood:	n/a
2	chr14:67875438-67875488	AG04449	skin:	fetal
3	chr14:67881521-67881571	U87	brain:	n/a
4	chr14:67878690-67878740	PFSK-1	brain:	n/a
5	chr14:67881521-67881571	AG04449	skin:	fetal
6	chr14:67879126-67879176	HPAEpiC	pulmonary alveolar:	n/a
7	chr14:67878973-67879023	A549	lung:	n/a
8	chr14:67894263-67894313	Hela-S3	cervix:	n/a
9	chr14:67878535-67878585	NH-A	brain:	n/a
10	chr14:67879101-67879151	HEEpiC	esophagus:	n/a
11	chr14:67875438-67875488	HPAEpiC	pulmonary alveolar:	n/a
12	chr14:67894263-67894313	HMEC	breast:	n/a
13	chr14:67878535-67878585	PFSK-1	brain:	n/a
14	chr14:67879166-67879216	HRCEpiC	kidney:	n/a
15	chr14:67894263-67894313	H1-hESC	embryonic stem cell:	embryo
16	chr14:67879101-67879151	BJ	skin:	n/a
17	chr14:67878142-67878192	HNPCEpiC	eye:	n/a
18	chr14:67879385-67879435	GM12892	blood:	n/a
19	chr14:67878973-67879023	NH-A	brain:	n/a
20	chr14:67879126-67879176	HEK293	kidney:	embryo
21	chr14:67879126-67879176	IMR90	lung:	fetal
22	chr14:67894263-67894313	PFSK-1	brain:	n/a
23	chr14:67879126-67879176	H1-hESC	embryonic stem cell:	embryo
24	chr14:67879166-67879216	HNPCEpiC	eye:	n/a
25	chr14:67878142-67878192	GM06990	blood:	n/a
26	chr14:67879385-67879435	HRPEpiC	eye:	n/a
27	chr14:67894164-67894214	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:67878535-67878585	PANC-1	pancreas:	n/a
29	chr14:67894263-67894313	MCF-7	breast:	n/a
30	chr14:67875438-67875488	NH-A	brain:	n/a
31	chr14:67878535-67878585	AG04450	lung:	fetal
32	chr14:67894164-67894214	HNPCEpiC	eye:	n/a
33	chr14:67879126-67879176	PrEC	prostate:	n/a
34	chr14:67878535-67878585	ECC-1	luminal epithelium:	n/a
35	chr14:67875438-67875488	HMEC	breast:	n/a
36	chr14:67881521-67881571	AG04450	lung:	fetal
37	chr14:67878973-67879023	AG04450	lung:	fetal
38	chr14:67879101-67879151	CMK	blood:	n/a
39	chr14:67875438-67875488	AG09309	skin:	n/a
40	chr14:67894164-67894214	SKMC	muscle:	n/a
41	chr14:67878142-67878192	AG04450	lung:	fetal
42	chr14:67881521-67881571	GM12892	blood:	n/a
43	chr14:67881521-67881571	HCM	heart:	n/a
44	chr14:67875438-67875488	HUVEC	blood vessel:	n/a
45	chr14:67878690-67878740	HCM	heart:	n/a
46	chr14:67878690-67878740	SK-N-MC	brain:	n/a
47	chr14:67879166-67879216	NB4	blood:	n/a
48	chr14:67894164-67894214	HCPEpiC	choroid plexus:	n/a
49	chr14:67878690-67878740	HPAEpiC	pulmonary alveolar:	n/a
50	chr14:67879166-67879216	BJ	skin:	n/a

(count:69 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:67859950..67861959-chr14:67870386..67872536,2	MCF-7	breast:
2	chr14:67893686..67894409-chr14:68042268..68043216,2	MCF-7	breast:
3	chr14:67855990..67858620-chr14:67871680..67873516,2	MCF-7	breast:
4	chr14:67863179..67866921-chr14:67868694..67870858,3	K562	blood:
5	chr14:67893537..67894142-chr14:68027301..68027887,2	MCF-7	breast:
6	chr14:67880503..67882430-chr14:67981236..67983724,2	MCF-7	breast:
7	chr14:67869261..67871633-chr14:67875881..67878692,2	MCF-7	breast:
8	chr14:67894342..67897151-chr14:67998655..68001300,4	MCF-7	breast:
9	chr14:67878466..67878977-chr17:56708695..56709522,2	Hela-S3	cervix:
10	chr14:67886232..67888392-chr14:67891357..67894583,3	MCF-7	breast:
11	chr14:67894282..67896038-chr14:67906515..67908863,2	MCF-7	breast:
12	chr14:67857879..67859653-chr14:67862774..67864465,2	MCF-7	breast:
13	chr14:67902815..67903723-chr14:67913653..67914607,2	MCF-7	breast:
14	chr14:67894301..67896561-chr14:68133942..68135577,2	K562	blood:
15	chr14:67890575..67893217-chr14:68140093..68141986,3	MCF-7	breast:
16	chr14:67885208..67887110-chr14:68037117..68038888,2	MCF-7	breast:
17	chr14:67879811..67882553-chr14:67883761..67886791,3	K562	blood:
18	chr14:67898493..67900065-chr14:67902969..67905934,2	MCF-7	breast:
19	chr14:67884151..67886526-chr14:67911099..67913926,2	K562	blood:
20	chr14:67892898..67896980-chr14:68036813..68040978,4	MCF-7	breast:
21	chr14:67882986..67884493-chr14:67884717..67887136,2	K562	blood:
22	chr14:67898417..67901273-chr14:67903029..67904787,2	K562	blood:
23	chr14:67883319..67885734-chr14:67982122..67985064,2	K562	blood:
24	chr14:67899751..67904520-chr14:67905212..67909411,5	MCF-7	breast:
25	chr14:67886608..67887490-chr14:68037726..68038773,4	MCF-7	breast:
26	chr14:67893911..67894417-chr14:68084755..68085556,2	MCF-7	breast:
27	chr14:67893736..67894467-chr14:67999560..68000418,2	MCF-7	breast:
28	chr14:67886247..67889154-chr14:67992283..67994737,2	MCF-7	breast:
29	chr14:67858454..67860962-chr14:67864794..67867141,2	MCF-7	breast:
30	chr14:67869356..67872173-chr14:67872703..67875078,2	K562	blood:
31	chr14:67882986..67884493-chr14:67884717..67887136,2	K562	blood:
32	chr14:67898417..67901273-chr14:67903029..67904787,2	K562	blood:
33	chr12:7052685..7053680-chr14:67878710..67879228,2	Hela-S3	cervix:
34	chr14:67864065..67866921-chr14:67868694..67870402,2	K562	blood:
35	chr14:67893018..67896627-chr14:67990879..67994840,3	MCF-7	breast:
36	chr14:67893842..67894620-chr14:68037699..68038738,5	MCF-7	breast:
37	chr14:67903388..67905312-chr14:67950420..67951946,2	MCF-7	breast:
38	chr14:67879811..67882553-chr14:67883761..67886791,3	K562	blood:
39	chr14:67883599..67885949-chr14:67998710..68001599,3	MCF-7	breast:
40	chr14:67902688..67903597-chr14:67993100..67993768,2	MCF-7	breast:
41	chr14:67869356..67872173-chr14:67872703..67875078,2	K562	blood:
42	chr14:67878348..67879211-chr15:34659300..34659943,2	Hela-S3	cervix:
43	chr14:67893770..67894281-chr14:68047105..68047614,2	MCF-7	breast:
44	chr14:67893587..67894509-chr14:68037660..68039070,9	MCF-7	breast:
45	chr14:67878492..67879251-chr2:85765787..85766682,2	Hela-S3	cervix:
46	chr14:67880313..67882274-chr14:67888977..67891033,2	K562	blood:
47	chr14:67896135..67897890-chr14:67898329..67900959,2	MCF-7	breast:
48	chr14:67869261..67871633-chr14:67875881..67878692,2	MCF-7	breast:
49	chr14:67880313..67882274-chr14:67888977..67891033,2	K562	blood:
50	chr14:67893593..67894512-chr14:67993089..67993976,3	MCF-7	breast:

No data

miRNA name	Chromosome Location	mirBase accession
hsa-miR-5694	chr14:67908619-67908639	MIMAT0022487

No data

Variant related genes	Relation type
PLEK2	TF binding region
MIR5694	TF binding region
PLEK2	CpG island
MIR5694	CpG island
ENSG00000111678	chromatin interactions
ENSG00000265993	chromatin interactions
ENSG00000100558	chromatin interactions
ENSG00000134001	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000212195	chromatin interactions
ENSG00000100568	chromatin interactions
ENSG00000238923	chromatin interactions
ENSG00000054690	chromatin interactions
ENSG00000176454	chromatin interactions
ENSG00000198133	chromatin interactions
ENSG00000100554	chromatin interactions

Extended variants
information (count: 1600 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:1600 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs115017540	chr14:67863627-67863628	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs373261864	chr14:67863661-67863662	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs72102932	chr14:67863662-67863663	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs398118329	chr14:67863676-67863677	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs201731306	chr14:67863677-67863678	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs199880319	chr14:67863678-67863679	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs372171715	chr14:67863695-67863696	Weak transcription Enhancers Genic enhancers Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs140415301	chr14:67863716-67863717	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs374822584	chr14:67863722-67863723	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs7157211	chr14:67863724-67863725	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
11	rs368931158	chr14:67863729-67863730	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs573187075	chr14:67863775-67863776	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs368381209	chr14:67863806-67863807	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs7157704	chr14:67863822-67863823	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs572985961	chr14:67863828-67863829	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs558970397	chr14:67863838-67863839	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs577371061	chr14:67863850-67863851	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs6573770	chr14:67863873-67863874	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs565079979	chr14:67863882-67863883	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs532427634	chr14:67863908-67863909	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563193471	chr14:67863910-67863911	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs181329057	chr14:67863916-67863917	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs542521968	chr14:67863936-67863937	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs560759689	chr14:67863958-67863959	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs145293907	chr14:67863989-67863990	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs28441403	chr14:67863995-67863996	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
27	rs143141122	chr14:67864003-67864004	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs147061678	chr14:67864094-67864095	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532189330	chr14:67864107-67864108	Weak transcription Enhancers Genic enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs550393145	chr14:67864283-67864284	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs568688505	chr14:67864340-67864341	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs377760581	chr14:67864360-67864361	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs530157668	chr14:67864375-67864376	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs536191922	chr14:67864379-67864380	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs200854004	chr14:67864384-67864385	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs149487309	chr14:67864395-67864396	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs199994324	chr14:67864403-67864404	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147132197	chr14:67864405-67864406	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs566761421	chr14:67864436-67864437	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs374958171	chr14:67864437-67864438	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375438919	chr14:67864449-67864450	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs185648616	chr14:67864455-67864456	Enhancers Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11545999	chr14:67864504-67864505	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs140298217	chr14:67864517-67864518	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs531803543	chr14:67864518-67864519	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs202224196	chr14:67864528-67864529	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs372165036	chr14:67864533-67864534	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs544704170	chr14:67864540-67864541	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs374135507	chr14:67864546-67864547	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs556826501	chr14:67864564-67864565	Enhancers Weak transcription Strong transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:74)

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
Malignant peripheral nerve sheath tumor	18522746	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
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chordoma	21215367	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Hepatocellular carcinoma	16750200	CNVD

Chromatin state (count:1032 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67831200-67864600	Strong transcription	Duodenum Mucosa	Duodenum
2	chr14:67845000-67864800	Strong transcription	Hela-S3	cervix
3	chr14:67846000-67876200	Weak transcription	Stomach Mucosa	stomach
4	chr14:67849600-67864400	Weak transcription	Gastric	stomach
5	chr14:67850200-67878400	Weak transcription	Lung	lung
6	chr14:67852800-67865800	Strong transcription	HMEC	breast
7	chr14:67853800-67864600	Strong transcription	Fetal Intestine Small	intestine
8	chr14:67854200-67864400	Weak transcription	Left Ventricle	heart
9	chr14:67854200-67872000	Weak transcription	Small Intestine	intestine
10	chr14:67855200-67867400	Strong transcription	NHEK	skin
11	chr14:67855200-67875400	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
12	chr14:67858600-67867400	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
13	chr14:67859600-67876600	Weak transcription	Esophagus	oesophagus
14	chr14:67859800-67866600	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
15	chr14:67860000-67876400	Weak transcription	Placenta Amnion	Placenta Amnion
16	chr14:67860800-67878000	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr14:67861600-67864400	Strong transcription	Fetal Stomach	stomach
18	chr14:67861800-67863600	Enhancers	HUVEC	blood vessel
19	chr14:67861800-67864600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:67861800-67864600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
21	chr14:67862000-67876600	Weak transcription	Rectal Mucosa Donor 31	rectum
22	chr14:67862200-67863600	Enhancers	ES-WA7 Cell Line	embryonic stem cell
23	chr14:67862400-67863600	Enhancers	HUES6 Cell Line	embryonic stem cell
24	chr14:67862400-67863600	Enhancers	HSMMtube	muscle
25	chr14:67862400-67867000	Weak transcription	Colonic Mucosa	Colon
26	chr14:67862600-67863600	Enhancers	Muscle Satellite Cultured Cells	--
27	chr14:67862600-67864400	Weak transcription	Pancreas	Pancrea
28	chr14:67862800-67878400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr14:67863000-67864000	Enhancers	HSMM	muscle
30	chr14:67863000-67864200	Enhancers	Placenta	Placenta
31	chr14:67863200-67863600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr14:67863200-67863600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
33	chr14:67863200-67863600	Flanking Active TSS	Fetal Heart	heart
34	chr14:67863200-67863600	Strong transcription	Fetal Intestine Large	intestine
35	chr14:67863200-67863600	Enhancers	Fetal Lung	lung
36	chr14:67863200-67863600	Enhancers	NHDF-Ad	bronchial
37	chr14:67863200-67863600	Enhancers	Osteobl	bone
38	chr14:67863200-67863800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
39	chr14:67863200-67864600	Strong transcription	Rectal Mucosa Donor 29	rectum
40	chr14:67863200-67864800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
41	chr14:67863400-67863600	Enhancers	HUES64 Cell Line	embryonic stem cell
42	chr14:67863400-67863600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr14:67863400-67864200	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
44	chr14:67863400-67864600	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
45	chr14:67863400-67875800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
46	chr14:67863600-67864200	Genic enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr14:67863600-67864800	Enhancers	Fetal Heart	heart
48	chr14:67863600-67867600	Weak transcription	HSMMtube	muscle
49	chr14:67863600-67868200	Weak transcription	Fetal Intestine Large	intestine
50	chr14:67863800-67864200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin

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