Variant report

Variant	nsv566093
Chromosome Location	chr14:105274093-105321835
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1969)
CpG islands
(count:2811)
Chromatin interactive
region (count:124)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1969 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105282255-105282586	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:105287166-105287416	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:105282287-105282592	K562	blood:	n/a	n/a
4	ARID3A	chr14:105281624-105281816	HepG2	liver:	n/a	n/a
5	ATF2	chr14:105282156-105282881	GM12878	blood:	n/a	n/a
6	ATF2	chr14:105282258-105282694	GM12878	blood:	n/a	n/a
7	ATF2	chr14:105309952-105310298	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF3	chr14:105282142-105282595	H1-hESC	embryonic stem cell:	n/a	chr14:105282374-105282394
9	ATF3	chr14:105282205-105282632	K562	blood:	n/a	chr14:105282374-105282394
10	ATF3	chr14:105282165-105282657	HepG2	liver:	n/a	chr14:105282374-105282394
11	ATF3	chr14:105282145-105282742	A549	lung:	n/a	chr14:105282374-105282394
12	ATF3	chr14:105282214-105282545	K562	blood:	n/a	chr14:105282374-105282394
13	ATF3	chr14:105282230-105282441	GM12878	blood:	n/a	chr14:105282374-105282394
14	ATF3	chr14:105282177-105282704	GM12878	blood:	n/a	chr14:105282374-105282394
15	ATF3	chr14:105282172-105282754	A549	lung:	n/a	chr14:105282374-105282394
16	ATF3	chr14:105282202-105282572	HepG2	liver:	n/a	chr14:105282374-105282394
17	BACH1	chr14:105287096-105287337	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr14:105282176-105282497	K562	blood:	n/a	n/a
19	BACH1	chr14:105293388-105294331	H1-hESC	embryonic stem cell:	n/a	n/a
20	BACH1	chr14:105309848-105310593	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr14:105282309-105282857	H1-hESC	embryonic stem cell:	n/a	n/a
22	BATF	chr14:105282302-105282631	GM12878	blood:	n/a	n/a
23	BCL11A	chr14:105282271-105282551	GM12878	blood:	n/a	chr14:105282413-105282422 chr14:105282334-105282347
24	BCL3	chr14:105282119-105282782	A549	lung:	n/a	chr14:105282765-105282778 chr14:105282413-105282422 chr14:105282334-105282347
25	BCL3	chr14:105282005-105282935	A549	lung:	n/a	chr14:105282765-105282778 chr14:105282413-105282422 chr14:105282334-105282347 chr14:105282865-105282878 chr14:105282051-105282064 chr14:105282047-105282060
26	BCL3	chr14:105281471-105281936	A549	lung:	n/a	chr14:105281894-105281903
27	BCLAF1	chr14:105282160-105282651	K562	blood:	n/a	chr14:105282413-105282422 chr14:105282334-105282347
28	BCLAF1	chr14:105281873-105282818	GM12878	blood:	n/a	chr14:105282765-105282778 chr14:105281968-105281981 chr14:105282413-105282422 chr14:105282334-105282347 chr14:105281894-105281903 chr14:105282051-105282064 chr14:105282047-105282060
29	BCLAF1	chr14:105281530-105282813	GM12878	blood:	n/a	chr14:105282765-105282778 chr14:105281968-105281981 chr14:105282413-105282422 chr14:105282334-105282347 chr14:105281894-105281903 chr14:105282051-105282064 chr14:105282047-105282060
30	BCLAF1	chr14:105282177-105282764	K562	blood:	n/a	chr14:105282413-105282422 chr14:105282334-105282347
31	BHLHE40	chr14:105282117-105282639	A549	lung:	n/a	chr14:105282594-105282610 chr14:105282120-105282136 chr14:105282331-105282347 chr14:105282162-105282178
32	BHLHE40	chr14:105281557-105282786	GM12878	blood:	n/a	chr14:105282594-105282610 chr14:105282120-105282136 chr14:105282331-105282347 chr14:105282162-105282178
33	BHLHE40	chr14:105292777-105293009	GM12878	blood:	n/a	n/a
34	BHLHE40	chr14:105293954-105294144	K562	blood:	n/a	n/a
35	BHLHE40	chr14:105282143-105282369	HepG2	liver:	n/a	chr14:105282331-105282347 chr14:105282162-105282178
36	BHLHE40	chr14:105297149-105297499	HepG2	liver:	n/a	n/a
37	BHLHE40	chr14:105297136-105297489	K562	blood:	n/a	n/a
38	BHLHE40	chr14:105281624-105281804	HepG2	liver:	n/a	n/a
39	BHLHE40	chr14:105281677-105281864	A549	lung:	n/a	n/a
40	BHLHE40	chr14:105281588-105283026	K562	blood:	n/a	chr14:105282594-105282610 chr14:105282120-105282136 chr14:105282331-105282347 chr14:105282162-105282178
41	BHLHE40	chr14:105282069-105282781	HepG2	liver:	n/a	chr14:105282594-105282610 chr14:105282120-105282136 chr14:105282331-105282347 chr14:105282162-105282178
42	BHLHE40	chr14:105286963-105287348	HepG2	liver:	n/a	n/a
43	BHLHE40	chr14:105287068-105287325	K562	blood:	n/a	n/a
44	BHLHE40	chr14:105282300-105282574	HepG2	liver:	n/a	chr14:105282331-105282347
45	BRCA1	chr14:105281501-105281996	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr14:105282299-105282623	H1-hESC	embryonic stem cell:	n/a	n/a
47	BRCA1	chr14:105311936-105311956	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr14:105282263-105282780	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr14:105294006-105294178	H1-hESC	embryonic stem cell:	n/a	n/a
50	BRCA1	chr14:105282313-105282615	GM12878	blood:	n/a	n/a

(count:2811 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105302637-105302687	BE2_C	brain:	n/a
2	chr14:105310639-105310689	RPTEC	kidney:	n/a
3	chr14:105292332-105292382	SK-N-SH_RA	brain:	n/a
4	chr14:105303134-105303184	H1-hESC	embryonic stem cell:	embryo
5	chr14:105295832-105295882	HCF	heart:	n/a
6	chr14:105302637-105302687	BE2_C	brain:	n/a
7	chr14:105310639-105310689	RPTEC	kidney:	n/a
8	chr14:105292332-105292382	SK-N-SH_RA	brain:	n/a
9	chr14:105303134-105303184	H1-hESC	embryonic stem cell:	embryo
10	chr14:105295832-105295882	HCF	heart:	n/a
11	chr14:105310421-105310471	PANC-1	pancreas:	n/a
12	chr14:105318279-105318329	HEEpiC	esophagus:	n/a
13	chr14:105290118-105290168	AG04450	lung:	fetal
14	chr14:105302637-105302687	H1-hESC	embryonic stem cell:	embryo
15	chr14:105293878-105293928	AG09309	skin:	n/a
16	chr14:105281643-105281693	HCPEpiC	choroid plexus:	n/a
17	chr14:105288878-105288928	K562	blood:	n/a
18	chr14:105282271-105282321	PrEC	prostate:	n/a
19	chr14:105293067-105293117	GM06990	blood:	n/a
20	chr14:105309894-105309944	NHDF-neo	bronchial:	n/a
21	chr14:105310639-105310689	LNCaP	prostate:	n/a
22	chr14:105282271-105282321	GM12891	blood:	n/a
23	chr14:105293760-105293810	IMR90	lung:	fetal
24	chr14:105282974-105283024	AG09319	gingival:	n/a
25	chr14:105287408-105287458	AG10803	skin:	n/a
26	chr14:105293199-105293249	HPAEpiC	pulmonary alveolar:	n/a
27	chr14:105288878-105288928	A549	lung:	n/a
28	chr14:105281991-105282041	HEEpiC	esophagus:	n/a
29	chr14:105293067-105293117	SK-N-SH	brain:	n/a
30	chr14:105293199-105293249	H1-hESC	embryonic stem cell:	embryo
31	chr14:105286678-105286728	Hela-S3	cervix:	n/a
32	chr14:105287408-105287458	AG09319	gingival:	n/a
33	chr14:105310181-105310231	ECC-1	luminal epithelium:	n/a
34	chr14:105309812-105309862	Hela-S3	cervix:	n/a
35	chr14:105310921-105310971	GM12878	blood:	n/a
36	chr14:105310421-105310471	PrEC	prostate:	n/a
37	chr14:105310921-105310971	HUVEC	blood vessel:	n/a
38	chr14:105310639-105310689	HepG2	liver:	n/a
39	chr14:105318494-105318544	GM12891	blood:	n/a
40	chr14:105309352-105309402	SK-N-MC	brain:	n/a
41	chr14:105293199-105293249	Hela-S3	cervix:	n/a
42	chr14:105281643-105281693	CMK	blood:	n/a
43	chr14:105293578-105293628	HRE	kidney:	n/a
44	chr14:105287326-105287376	HRCEpiC	kidney:	n/a
45	chr14:105288120-105288170	Caco-2	colon:	n/a
46	chr14:105310639-105310689	HCT-116	colon:	n/a
47	chr14:105281991-105282041	GM12892	blood:	n/a
48	chr14:105318459-105318509	AG09309	skin:	n/a
49	chr14:105283180-105283230	MCF10A-Er-Src	breast:	n/a
50	chr14:105281991-105282041	NB4	blood:	n/a

(count:124 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:105311809..105313743-chr14:105332493..105335026,2	K562	blood:
2	chr14:105197416..105200391-chr14:105289343..105292189,2	MCF-7	breast:
3	chr14:105282319..105283214-chr3:19988588..19989090,2	Hela-S3	cervix:
4	chr14:105189864..105192391-chr14:105285849..105287579,2	MCF-7	breast:
5	chr14:105279760..105281975-chr14:105284516..105287260,2	K562	blood:
6	chr14:105281911..105282745-chr20:35233716..35234619,2	Hela-S3	cervix:
7	chr14:105309593..105311570-chr14:105314429..105316740,2	K562	blood:
8	chr14:105167254..105168944-chr14:105280807..105283484,2	K562	blood:
9	chr14:105199229..105201973-chr14:105280789..105282414,2	MCF-7	breast:
10	chr14:105292163..105294059-chr14:105311800..105314620,2	K562	blood:
11	chr14:105276873..105279342-chr14:105282954..105284515,2	K562	blood:
12	chr14:105193547..105195878-chr14:105280692..105283165,3	MCF-7	breast:
13	chr14:105189826..105192403-chr14:105291424..105294271,3	MCF-7	breast:
14	chr14:105280966..105282808-chr14:105292129..105294295,2	K562	blood:
15	chr14:105234738..105235318-chr14:105293407..105294201,2	K562	blood:
16	chr14:105196164..105197690-chr14:105281072..105283961,2	MCF-7	breast:
17	chr1:249153105..249153770-chr14:105282047..105282552,2	Hela-S3	cervix:
18	chr14:105265450..105268632-chr14:105270321..105274809,6	K562	blood:
19	chr1:180720385..180721345-chr14:105282463..105283068,2	Hela-S3	cervix:
20	chr14:105177553..105179620-chr14:105284148..105286152,2	K562	blood:
21	chr14:105318741..105320546-chr14:105320767..105322575,2	MCF-7	breast:
22	chr14:105268427..105271161-chr14:105291567..105294333,2	K562	blood:
23	chr14:105234579..105236355-chr14:105286684..105287712,12	MCF-7	breast:
24	chr14:105282552..105286026-chr14:105289483..105293569,5	K562	blood:
25	chr11:122016442..122016997-chr14:105280970..105281470,2	HCT-116	colon:
26	chr14:105190451..105191132-chr14:105286694..105287658,2	MCF-7	breast:
27	chr14:105308114..105313218-chr14:105327481..105332918,6	MCF-7	breast:
28	chr14:104094539..104096574-chr14:105280898..105283467,2	MCF-7	breast:
29	chr14:105190468..105192484-chr14:105291233..105293061,2	MCF-7	breast:
30	chr14:105218316..105220941-chr14:105310362..105313289,2	MCF-7	breast:
31	chr14:105234538..105236569-chr14:105286438..105288492,2	K562	blood:
32	chr14:105282292..105284225-chr14:105434347..105435910,2	MCF-7	breast:
33	chr14:105267306..105268128-chr14:105276242..105277034,2	MCF-7	breast:
34	chr14:105269532..105276799-chr14:105278912..105285805,20	K562	blood:
35	chr14:105290213..105292759-chr8:144821047..144823089,2	MCF-7	breast:
36	chr14:105318741..105320546-chr14:105320767..105322575,2	MCF-7	breast:
37	chr14:105280960..105282917-chr17:59489026..59491365,2	MCF-7	breast:
38	chr14:105289983..105292400-chr14:105295807..105297431,2	MCF-7	breast:
39	chr14:105218306..105221418-chr14:105291704..105295058,3	MCF-7	breast:
40	chr14:105280921..105283748-chr14:105368977..105371929,2	MCF-7	breast:
41	chr14:104444303..104447278-chr14:105280749..105282624,2	MCF-7	breast:
42	chr14:105264645..105268219-chr14:105292165..105294813,6	K562	blood:
43	chr14:105275614..105278023-chr17:32632159..32633680,2	MCF-7	breast:
44	chr14:105189943..105192068-chr14:105271473..105274094,2	MCF-7	breast:
45	chr14:105282326..105284059-chr14:105337774..105340057,2	MCF-7	breast:
46	chr14:105189504..105190527-chr14:105292721..105293350,3	MCF-7	breast:
47	chr14:105282332..105284186-chr14:105286769..105289212,2	K562	blood:
48	chr14:105281444..105284186-chr14:105287475..105289212,2	K562	blood:
49	chr14:105292878..105295272-chr14:105309126..105311348,2	MCF-7	breast:
50	chr14:105266435..105267408-chr14:105286766..105287693,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-AKT1-3	chr14:105297175-105297508	NONHSAT040287

No data

Variant related genes	Relation type
ENSG00000258811	TF binding region
RPS26P49	TF binding region
RPS2P4	TF binding region
LINC00638	TF binding region
ENSG00000258811	CpG island
RPS26P49	CpG island
RPS2P4	CpG island
LINC00638	CpG island
ENSG00000264439	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000185100	chromatin interactions
ENSG00000023287	chromatin interactions
ENSG00000184009	chromatin interactions
ENSG00000144566	chromatin interactions
ENSG00000203499	chromatin interactions
ENSG00000259067	chromatin interactions
ENSG00000142208	chromatin interactions
ENSG00000258701	chromatin interactions
ENSG00000229947	chromatin interactions
ENSG00000171163	chromatin interactions
ENSG00000258811	chromatin interactions
ENSG00000258430	chromatin interactions
ENSG00000227237	chromatin interactions
ENSG00000229848	chromatin interactions
ENSG00000203485	chromatin interactions
ENSG00000187013	chromatin interactions
ENSG00000101084	chromatin interactions
ENSG00000258858	chromatin interactions
ENSG00000099814	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000179627	chromatin interactions
ENSG00000126214	chromatin interactions
ENSG00000166428	chromatin interactions
ENSG00000184990	chromatin interactions

Extended variants
information (count: 1857 )
Associated
traits (count: 108 )

Variant overlapped rSNPs/rCNVs (count:1857 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56140226	chr14:105274093-105274094	Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs112633574	chr14:105274105-105274106	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs113688457	chr14:105274257-105274258	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs55983264	chr14:105274314-105274315	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs372936860	chr14:105274447-105274448	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs35636289	chr14:105274561-105274562	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs376200993	chr14:105274675-105274676	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs12888828	chr14:105274713-105274714	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs12888969	chr14:105274751-105274752	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs141584190	chr14:105274763-105274764	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs528036614	chr14:105274769-105274770	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs547663899	chr14:105274770-105274771	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs28690313	chr14:105274789-105274790	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs74090040	chr14:105274801-105274802	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
15	rs570067019	chr14:105274804-105274805	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs535441766	chr14:105274812-105274813	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs201644609	chr14:105274827-105274828	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs548995187	chr14:105274854-105274855	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs565635243	chr14:105274857-105274858	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs188129064	chr14:105274858-105274859	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557778874	chr14:105274907-105274908	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs192926365	chr14:105274924-105274925	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs67110142	chr14:105274945-105274946	Enhancers Weak transcription ZNF genes & repeats	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs556987680	chr14:105275027-105275028	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs573806238	chr14:105275044-105275045	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs542639112	chr14:105275056-105275057	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs138480105	chr14:105275077-105275078	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs572884961	chr14:105275087-105275088	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs541662547	chr14:105275088-105275089	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs12889796	chr14:105275106-105275107	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs564646376	chr14:105275123-105275124	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs533534193	chr14:105275128-105275129	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs550141270	chr14:105275153-105275154	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs563420004	chr14:105275196-105275197	Enhancers Weak transcription ZNF genes & repeats Bivalent Enhancer	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs184554373	chr14:105275215-105275216	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs368513238	chr14:105275250-105275251	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs115036672	chr14:105275251-105275252	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs534702963	chr14:105275275-105275276	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs200487954	chr14:105275310-105275311	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs144233319	chr14:105275319-105275320	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs111267305	chr14:105275322-105275323	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs561050521	chr14:105275323-105275324	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs201910967	chr14:105275325-105275326	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs71129252	chr14:105275343-105275344	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs11628510	chr14:105275365-105275366	Weak transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
46	rs140791612	chr14:105275386-105275387	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs537826071	chr14:105275426-105275427	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537225194	chr14:105275427-105275428	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556920978	chr14:105275430-105275431	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs567357309	chr14:105275436-105275437	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:108)

Disease	PMID	Source
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
small cell lung cancer	20016488	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Urothelial carcinoma	21177765	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD

Chromatin state (count:1740 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105268000-105280400	Weak transcription	Brain Inferior Temporal Lobe	brain
2	chr14:105268000-105281000	Weak transcription	Brain Substantia Nigra	brain
3	chr14:105268400-105280800	Weak transcription	HUVEC	blood vessel
4	chr14:105268400-105281400	Weak transcription	Brain Cingulate Gyrus	brain
5	chr14:105268600-105281200	Weak transcription	Primary hematopoietic stem cells	blood
6	chr14:105268600-105281600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
7	chr14:105268800-105281000	Weak transcription	Primary T cells from cord blood	blood
8	chr14:105269000-105279800	Weak transcription	Brain Germinal Matrix	brain
9	chr14:105269000-105280400	Weak transcription	GM12878-XiMat	blood
10	chr14:105269200-105280800	Weak transcription	Fetal Intestine Large	intestine
11	chr14:105269800-105281400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr14:105270000-105280600	Weak transcription	Rectal Mucosa Donor 29	rectum
13	chr14:105270000-105281400	Weak transcription	Colonic Mucosa	Colon
14	chr14:105270400-105280200	Weak transcription	Fetal Brain Female	brain
15	chr14:105271000-105280800	Weak transcription	Fetal Intestine Small	intestine
16	chr14:105272000-105280000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
17	chr14:105272200-105277000	Weak transcription	Fetal Stomach	stomach
18	chr14:105272200-105280800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
19	chr14:105272200-105281000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
20	chr14:105272200-105281400	Weak transcription	Esophagus	oesophagus
21	chr14:105272200-105281400	Weak transcription	Fetal Lung	lung
22	chr14:105272400-105280200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr14:105272400-105280400	Weak transcription	Brain Hippocampus Middle	brain
24	chr14:105272400-105281400	Weak transcription	Muscle Satellite Cultured Cells	--
25	chr14:105272400-105281400	Weak transcription	NHLF	lung
26	chr14:105272600-105276600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
27	chr14:105272600-105277000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
28	chr14:105272600-105280600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
29	chr14:105272600-105280600	Weak transcription	Fetal Heart	heart
30	chr14:105272600-105281000	Weak transcription	Stomach Smooth Muscle	stomach
31	chr14:105272600-105281400	Weak transcription	A549	lung
32	chr14:105272600-105281600	Weak transcription	Ovary	ovary
33	chr14:105272800-105280000	Weak transcription	Cortex derived primary cultured neurospheres	brain
34	chr14:105272800-105280000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr14:105272800-105281000	Weak transcription	Fetal Muscle Leg	muscle
36	chr14:105273000-105281000	Weak transcription	Lung	lung
37	chr14:105273200-105274800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
38	chr14:105273200-105274800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr14:105273200-105274800	Weak transcription	Pancreas	Pancrea
40	chr14:105273400-105275000	Weak transcription	Stomach Mucosa	stomach
41	chr14:105273800-105279800	Weak transcription	Spleen	Spleen
42	chr14:105273800-105280400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
43	chr14:105274000-105280400	Weak transcription	Brain Anterior Caudate	brain
44	chr14:105274000-105280600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
45	chr14:105274800-105275200	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
46	chr14:105274800-105275200	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr14:105274800-105275200	Enhancers	Pancreas	Pancrea
48	chr14:105275000-105275200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
49	chr14:105275000-105275200	Enhancers	Stomach Mucosa	stomach
50	chr14:105275200-105276600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived

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