Variant report

Variant	nsv902058
Chromosome Location	chr14:67310195-67760538
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:3058)
CpG islands
(count:1712)
Chromatin interactive
region (count:172)
LncRNA
region (count:17)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:3058 , 50 per page) page: 1 2 3 4 5 6 7 ... 62

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:67584937-67585164	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:67511249-67511316	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:67604519-67604819	K562	blood:	n/a	n/a
4	ARID3A	chr14:67398824-67399024	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:67752645-67752887	K562	blood:	n/a	n/a
6	ARID3A	chr14:67708722-67709610	K562	blood:	n/a	n/a
7	ARID3A	chr14:67752600-67752882	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:67633083-67633392	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:67707890-67709331	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:67584896-67585229	K562	blood:	n/a	n/a
11	ARID3A	chr14:67426302-67426423	K562	blood:	n/a	n/a
12	ARID3A	chr14:67604512-67604786	HepG2	liver:	n/a	n/a
13	ATF1	chr14:67511991-67512190	K562	blood:	n/a	n/a
14	ATF1	chr14:67556844-67556968	K562	blood:	n/a	n/a
15	ATF1	chr14:67486765-67486805	K562	blood:	n/a	n/a
16	ATF1	chr14:67629420-67629620	K562	blood:	n/a	n/a
17	ATF1	chr14:67511217-67511586	K562	blood:	n/a	n/a
18	ATF1	chr14:67633109-67633311	K562	blood:	n/a	n/a
19	ATF2	chr14:67485387-67485875	GM12878	blood:	n/a	n/a
20	ATF2	chr14:67485530-67485788	GM12878	blood:	n/a	n/a
21	ATF2	chr14:67707487-67707860	H1-hESC	embryonic stem cell:	n/a	n/a
22	ATF2	chr14:67707601-67708011	GM12878	blood:	n/a	n/a
23	ATF2	chr14:67708095-67708783	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF3	chr14:67708083-67708286	K562	blood:	n/a	n/a
25	ATF3	chr14:67653804-67654380	HCT-116	colon:	n/a	n/a
26	BACH1	chr14:67633086-67633407	H1-hESC	embryonic stem cell:	n/a	n/a
27	BACH1	chr14:67707621-67708891	H1-hESC	embryonic stem cell:	n/a	n/a
28	BACH1	chr14:67708636-67708994	K562	blood:	n/a	n/a
29	BACH1	chr14:67653942-67654252	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr14:67498772-67499037	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr14:67707713-67707824	K562	blood:	n/a	n/a
32	BACH1	chr14:67735003-67735180	K562	blood:	n/a	n/a
33	BATF	chr14:67464772-67465078	GM12878	blood:	n/a	n/a
34	BATF	chr14:67446182-67446668	GM12878	blood:	n/a	n/a
35	BATF	chr14:67464730-67465080	GM12878	blood:	n/a	n/a
36	BATF	chr14:67446173-67446665	GM12878	blood:	n/a	n/a
37	BATF	chr14:67485470-67485766	GM12878	blood:	n/a	n/a
38	BCL11A	chr14:67485422-67485738	GM12878	blood:	n/a	chr14:67485656-67485665
39	BCL3	chr14:67708193-67708916	A549	lung:	n/a	chr14:67708552-67708561 chr14:67708550-67708563 chr14:67708264-67708277
40	BCLAF1	chr14:67708228-67708842	GM12878	blood:	n/a	chr14:67708552-67708561 chr14:67708550-67708563 chr14:67708264-67708277
41	BCLAF1	chr14:67708176-67708819	GM12878	blood:	n/a	chr14:67708552-67708561 chr14:67708550-67708563 chr14:67708264-67708277
42	BHLHE40	chr14:67707027-67708525	K562	blood:	n/a	chr14:67708011-67708027 chr14:67708016-67708032 chr14:67708008-67708024
43	BHLHE40	chr14:67707510-67708965	GM12878	blood:	n/a	chr14:67708011-67708027 chr14:67708016-67708032 chr14:67708008-67708024
44	BHLHE40	chr14:67633241-67633355	GM12878	blood:	n/a	n/a
45	BHLHE40	chr14:67511409-67511436	GM12878	blood:	n/a	n/a
46	BHLHE40	chr14:67707706-67708209	HepG2	liver:	n/a	chr14:67708011-67708027 chr14:67708016-67708032 chr14:67708008-67708024
47	BHLHE40	chr14:67485435-67485813	GM12878	blood:	n/a	n/a
48	BHLHE40	chr14:67385429-67385602	HepG2	liver:	n/a	n/a
49	BRCA1	chr14:67511829-67512028	GM12878	blood:	n/a	n/a
50	BRCA1	chr14:67511723-67511744	Hela-S3	cervix:	n/a	n/a

(count:1712 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:67647740-67647790	HCM	heart:	n/a
2	chr14:67708212-67708262	AG09309	skin:	n/a
3	chr14:67653661-67653711	Hela-S3	cervix:	n/a
4	chr14:67579178-67579228	HCT-116	colon:	n/a
5	chr14:67647740-67647790	HCM	heart:	n/a
6	chr14:67708212-67708262	AG09309	skin:	n/a
7	chr14:67653661-67653711	Hela-S3	cervix:	n/a
8	chr14:67579178-67579228	HCT-116	colon:	n/a
9	chr14:67708950-67709000	ovcar-3	ovarian:	n/a
10	chr14:67708177-67708227	HMEC	breast:	n/a
11	chr14:67708475-67708525	HCF	heart:	n/a
12	chr14:67708950-67709000	Hela-S3	cervix:	n/a
13	chr14:67707842-67707892	HIPEpiC	eye:	n/a
14	chr14:67707462-67707512	MCF10A-Er-Src	breast:	n/a
15	chr14:67655758-67655808	LNCaP	prostate:	n/a
16	chr14:67707842-67707892	HEK293	kidney:	embryo
17	chr14:67692701-67692751	AG10803	skin:	n/a
18	chr14:67692701-67692751	HPAEpiC	pulmonary alveolar:	n/a
19	chr14:67656241-67656291	Caco-2	colon:	n/a
20	chr14:67688261-67688311	SAEC	small airway:	n/a
21	chr14:67708311-67708361	HCT-116	colon:	n/a
22	chr14:67653661-67653711	NT2-D1	testis:	n/a
23	chr14:67707756-67707806	SK-N-SH	brain:	n/a
24	chr14:67707306-67707356	AG10803	skin:	n/a
25	chr14:67708311-67708361	A549	lung:	n/a
26	chr14:67656241-67656291	Hela-S3	cervix:	n/a
27	chr14:67707842-67707892	AG04450	lung:	fetal
28	chr14:67707462-67707512	HCM	heart:	n/a
29	chr14:67707756-67707806	NT2-D1	testis:	n/a
30	chr14:67708212-67708262	MCF-7	breast:	n/a
31	chr14:67752711-67752761	HPAEpiC	pulmonary alveolar:	n/a
32	chr14:67655478-67655528	U87	brain:	n/a
33	chr14:67688261-67688311	HPAEpiC	pulmonary alveolar:	n/a
34	chr14:67729501-67729551	SKMC	muscle:	n/a
35	chr14:67656082-67656132	HPAEpiC	pulmonary alveolar:	n/a
36	chr14:67656241-67656291	ProgFib	skin:	n/a
37	chr14:67707359-67707409	BE2_C	brain:	n/a
38	chr14:67656082-67656132	GM06990	blood:	n/a
39	chr14:67656082-67656132	ECC-1	luminal epithelium:	n/a
40	chr14:67655758-67655808	AoSMC	blood vessel:	n/a
41	chr14:67579178-67579228	ovcar-3	ovarian:	n/a
42	chr14:67710831-67710881	GM06990	blood:	n/a
43	chr14:67707306-67707356	RPTEC	kidney:	n/a
44	chr14:67579178-67579228	RPTEC	kidney:	n/a
45	chr14:67708475-67708525	AG10803	skin:	n/a
46	chr14:67692701-67692751	Jurkat	blood:	n/a
47	chr14:67707756-67707806	AG04449	skin:	fetal
48	chr14:67707756-67707806	SKMC	muscle:	n/a
49	chr14:67708311-67708361	IMR90	lung:	fetal
50	chr14:67656029-67656079	HIPEpiC	eye:	n/a

(count:172 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:67632611..67633531-chr14:67749102..67749903,3	MCF-7	breast:
2	chr14:67752656..67754395-chr14:67757275..67759401,2	K562	blood:
3	chr14:67722215..67724352-chr14:67724413..67726414,2	MCF-7	breast:
4	chr14:67707264..67709261-chr14:67712534..67714050,2	MCF-7	breast:
5	chr14:67700811..67702650-chr14:67710191..67712644,2	K562	blood:
6	chr14:67485290..67488265-chr14:67490060..67491590,2	K562	blood:
7	chr14:67399698..67402646-chr14:67452739..67454975,2	MCF-7	breast:
8	chr14:67406512..67408916-chr14:67410508..67412779,2	MCF-7	breast:
9	chr14:67712988..67715259-chr14:67715330..67718013,2	K562	blood:
10	chr14:67707666..67709746-chr14:67710366..67712436,2	K562	blood:
11	chr14:67403550..67406227-chr14:67406417..67408734,2	MCF-7	breast:
12	chr14:67631986..67632614-chr14:67707358..67708232,2	Hela-S3	cervix:
13	chr14:67371739..67373252-chr14:67382189..67384942,2	MCF-7	breast:
14	chr14:67674549..67677391-chr14:67814114..67816733,2	K562	blood:
15	chr14:67697366..67699727-chr14:67704401..67707161,2	MCF-7	breast:
16	chr14:67347067..67349521-chr14:67447070..67449089,2	MCF-7	breast:
17	chr14:67747069..67749404-chr14:67756666..67758453,2	MCF-7	breast:
18	chr14:67412874..67415398-chr14:67415571..67417462,2	MCF-7	breast:
19	chr14:67090929..67091438-chr14:67585122..67585749,2	MCF-7	breast:
20	chr14:67663302..67666275-chr14:67670215..67672411,3	K562	blood:
21	chr14:67605438..67607246-chr14:67649867..67652399,2	K562	blood:
22	chr14:67684726..67688779-chr14:67706181..67709859,3	K562	blood:
23	chr14:67665237..67668000-chr14:67705488..67708368,2	MCF-7	breast:
24	chr14:67440552..67442279-chr14:67447848..67450195,2	K562	blood:
25	chr14:67687798..67690741-chr14:67704286..67706160,2	K562	blood:
26	chr14:67722215..67724352-chr14:67724413..67726414,2	MCF-7	breast:
27	chr14:67632850..67634159-chr14:67752109..67753244,6	MCF-7	breast:
28	chr14:67448510..67450063-chr14:67450561..67453014,2	MCF-7	breast:
29	chr14:67452240..67454374-chr14:67454933..67457036,2	K562	blood:
30	chr14:67632611..67633531-chr14:67749102..67749903,3	MCF-7	breast:
31	chr14:67718314..67720012-chr14:67725841..67728702,2	K562	blood:
32	chr11:65627799..65628455-chr14:67706816..67707712,2	Hela-S3	cervix:
33	chr14:67440552..67442279-chr14:67447848..67450195,2	K562	blood:
34	chr14:67706036..67709545-chr14:67826326..67828458,4	MCF-7	breast:
35	chr14:66831468..66833127-chr14:67617476..67620347,2	MCF-7	breast:
36	chr14:67737210..67739382-chr14:67748000..67750840,3	MCF-7	breast:
37	chr14:67551144..67554191-chr14:67555429..67558378,3	K562	blood:
38	chr14:66962164..66962780-chr14:67602828..67603411,2	MCF-7	breast:
39	chr14:67477930..67479660-chr14:67487049..67490010,2	K562	blood:
40	chr14:67429713..67432459-chr14:67435741..67437652,2	K562	blood:
41	chr14:67708428..67708936-chr7:155436811..155437523,2	Hela-S3	cervix:
42	chr14:67752656..67754395-chr14:67757275..67759401,2	K562	blood:
43	chr14:66973188..66975200-chr14:67683675..67686251,2	K562	blood:
44	chr14:67715902..67717588-chr14:67725188..67728083,2	K562	blood:
45	chr14:67632964..67633724-chr14:67752369..67753140,3	K562	blood:
46	chr14:67447429..67450664-chr14:67451355..67453565,3	MCF-7	breast:
47	chr14:67663302..67666275-chr14:67670215..67672411,3	K562	blood:
48	chr14:67551962..67554191-chr14:67556025..67558378,2	K562	blood:
49	chr14:67563581..67565684-chr14:67566134..67568510,2	MCF-7	breast:
50	chr14:67486765..67488657-chr14:67488979..67491560,2	K562	blood:

(count:17 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM71D-1	chr14:67708059-67708250	NONHSAT037434
2	lnc-GPHN-2	chr14:67664006-67664074	NONHSAT037431
3	lnc-ATP6V1D-4	chr14:67697621-67697844	NONHSAT037433
4	lnc-FAM71D-1	chr14:67736418-67736481	NONHSAT037434
5	lnc-ATP6V1D-2	chr14:67435755-67436127	ENSG00000258490.1
6	lnc-FAM71D-1	chr14:67720921-67721027	NONHSAT037434
7	lnc-FAM71D-1	chr14:67708152-67708250	NONHSAT037435
8	lnc-ATP6V1D-4	chr14:67706007-67706180	NONHSAT037433
9	lnc-ATP6V1D-1	chr14:67649711-67649740	XLOC_011057
10	lnc-ATP6V1D-1	chr14:67652258-67652438	XLOC_011057
11	lnc-FAM71D-1	chr14:67736418-67738776	NONHSAT037435
12	lnc-MPP5-1	chr14:67695105-67695261	NONHSAT037432
13	lnc-GPHN-2	chr14:67669885-67670004	NONHSAT037431
14	lnc-ATP6V1D-2	chr14:67436393-67436533	ENSG00000258490.1
15	lnc-ATP6V1D-3	chr14:67726938-67727164	NONHSAT037436
16	lnc-MPP5-1	chr14:67694188-67694451	NONHSAT037432
17	lnc-GPHN-2	chr14:67664853-67665037	NONHSAT037431

No data

Variant related genes	Relation type
MPP5	TF binding region
FAM71D	TF binding region
ENSG00000258490	TF binding region
GPHN	TF binding region
ENSG00000258988	TF binding region
MPP5	CpG island
FAM71D	CpG island
ENSG00000258490	CpG island
GPHN	CpG island
ENSG00000258988	CpG island
ENSG00000171723	chromatin interactions
ENSG00000226471	chromatin interactions
ENSG00000258490	chromatin interactions
ENSG00000184863	chromatin interactions
ENSG00000199755	chromatin interactions
ENSG00000100219	chromatin interactions
ENSG00000172717	chromatin interactions
ENSG00000240972	chromatin interactions
ENSG00000112081	chromatin interactions
ENSG00000134001	chromatin interactions
ENSG00000172732	chromatin interactions
ENSG00000253716	chromatin interactions
ENSG00000006125	chromatin interactions
ENSG00000100554	chromatin interactions
ENSG00000072415	chromatin interactions
ENSG00000258988	chromatin interactions
ENSG00000181938	chromatin interactions
ENSG00000216895	chromatin interactions
ENSG00000054690	chromatin interactions

Extended variants
information (count: 15287 )
Associated
traits (count: 74 )

Variant overlapped rSNPs/rCNVs (count:15287 , 50 per page) page: 1 2 3 4 5 6 7 ... 306

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7156426	chr14:67310195-67310196	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs146148447	chr14:67310216-67310217	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs113388476	chr14:67310246-67310247	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs541709891	chr14:67310253-67310254	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs562628444	chr14:67310302-67310303	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs185700960	chr14:67310318-67310319	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs531014011	chr14:67310345-67310346	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs189972398	chr14:67310365-67310366	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs112078605	chr14:67310408-67310409	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs140164471	chr14:67310414-67310415	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs143820886	chr14:67310537-67310538	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs571931691	chr14:67310556-67310557	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs529261153	chr14:67310585-67310586	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs182525454	chr14:67310595-67310596	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs561691956	chr14:67310641-67310642	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs113059245	chr14:67310642-67310643	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs529999803	chr14:67310670-67310671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs146833199	chr14:67310677-67310678	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs117416925	chr14:67310690-67310691	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs370660143	chr14:67310769-67310770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs111822190	chr14:67310774-67310775	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs74790513	chr14:67310814-67310815	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs534838268	chr14:67310826-67310827	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs552943885	chr14:67310846-67310847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs578004466	chr14:67310853-67310854	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs72728688	chr14:67310864-67310865	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
27	rs187747556	chr14:67310947-67310948	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs377466169	chr14:67310971-67310972	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs113774275	chr14:67310991-67310992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs368259791	chr14:67311037-67311038	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs111384063	chr14:67311040-67311041	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs542742708	chr14:67311135-67311136	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs570625713	chr14:67311174-67311175	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs183859369	chr14:67311192-67311193	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs112158305	chr14:67311322-67311323	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs112957419	chr14:67311324-67311325	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs372301082	chr14:67311360-67311361	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs547176761	chr14:67311367-67311368	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs537907807	chr14:67311399-67311400	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs77661931	chr14:67311527-67311528	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs187400190	chr14:67311528-67311529	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs192044800	chr14:67311555-67311556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs530440014	chr14:67311607-67311608	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs184148343	chr14:67311622-67311623	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs113555859	chr14:67311626-67311627	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs549501239	chr14:67311657-67311658	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs111862118	chr14:67311659-67311660	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs186919443	chr14:67311672-67311673	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs549962393	chr14:67311767-67311768	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs77684770	chr14:67311884-67311885	Weak 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
Autism	22495309	CNVD
Breast cancer	21611746	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Glioma	20126413	CNVD

Chromatin state (count:4219 , 50 per page) page: 1 2 3 4 5 6 7 ... 85

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:67309000-67310200	Enhancers	Brain Anterior Caudate	brain
2	chr14:67309000-67310400	Enhancers	Brain Inferior Temporal Lobe	brain
3	chr14:67309000-67310400	Enhancers	Brain Substantia Nigra	brain
4	chr14:67309200-67310400	Enhancers	Brain Angular Gyrus	brain
5	chr14:67309600-67310200	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr14:67309600-67310200	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
7	chr14:67309600-67310200	Enhancers	Brain Dorsolateral Prefrontal Cortex	brain
8	chr14:67309600-67310400	Enhancers	Primary B cells from peripheral blood	blood
9	chr14:67309800-67310200	Flanking Active TSS	Brain Hippocampus Middle	brain
10	chr14:67309800-67310200	Enhancers	Left Ventricle	heart
11	chr14:67309800-67310200	Enhancers	Right Atrium	heart
12	chr14:67310000-67310400	Flanking Active TSS	Brain Cingulate Gyrus	brain
13	chr14:67310200-67310400	Enhancers	Brain Hippocampus Middle	brain
14	chr14:67310200-67326600	Weak transcription	Left Ventricle	heart
15	chr14:67317200-67317600	Enhancers	Primary B cells from peripheral blood	blood
16	chr14:67320200-67320400	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
17	chr14:67320400-67325800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
18	chr14:67321600-67326000	Weak transcription	Cortex derived primary cultured neurospheres	brain
19	chr14:67323600-67325800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
20	chr14:67323600-67325800	Weak transcription	NHEK	skin
21	chr14:67323600-67326000	Weak transcription	Duodenum Smooth Muscle	Duodenum
22	chr14:67323600-67327400	Weak transcription	Psoas Muscle	Psoas
23	chr14:67324000-67341400	Weak transcription	Breast Myoepithelial Primary Cells	Breast
24	chr14:67324200-67325400	Weak transcription	Fetal Stomach	stomach
25	chr14:67324400-67325200	Enhancers	Liver	Liver
26	chr14:67324400-67326400	Enhancers	HepG2	liver
27	chr14:67324600-67325000	ZNF genes & repeats	Pancreas	Pancrea
28	chr14:67324800-67325000	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
29	chr14:67324800-67325600	ZNF genes & repeats	Primary hematopoietic stem cells G-CSF-mobilized Female	--
30	chr14:67325000-67327400	Weak transcription	Pancreas	Pancrea
31	chr14:67325200-67326000	Weak transcription	Liver	Liver
32	chr14:67325400-67325600	ZNF genes & repeats	Fetal Stomach	stomach
33	chr14:67325400-67326000	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
34	chr14:67325800-67326200	Enhancers	NHEK	skin
35	chr14:67325800-67326400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr14:67326000-67326800	Enhancers	Liver	Liver
37	chr14:67334400-67334800	Enhancers	HUES48 Cell Line	embryonic stem cell
38	chr14:67334400-67334800	Enhancers	HUES6 Cell Line	embryonic stem cell
39	chr14:67334400-67334800	Enhancers	HUES64 Cell Line	embryonic stem cell
40	chr14:67334400-67334800	Enhancers	iPS-15b Cell Line	embryonic stem cell
41	chr14:67335000-67339600	Weak transcription	Esophagus	oesophagus
42	chr14:67335400-67336000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
43	chr14:67339000-67341600	Weak transcription	Stomach Smooth Muscle	stomach
44	chr14:67339600-67340800	ZNF genes & repeats	Esophagus	oesophagus
45	chr14:67339800-67340400	ZNF genes & repeats	Duodenum Mucosa	Duodenum
46	chr14:67339800-67340400	Enhancers	Right Ventricle	heart
47	chr14:67339800-67340800	ZNF genes & repeats	Liver	Liver
48	chr14:67340200-67341000	ZNF genes & repeats	Cortex derived primary cultured neurospheres	brain
49	chr14:67340600-67340800	ZNF genes & repeats	Dnd41	blood
50	chr14:67340800-67341400	ZNF genes & repeats	iPS-20b Cell Line	embryonic stem cell

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