Variant report

Variant	nsv902449
Chromosome Location	chr14:105617891-105682527
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2698)
CpG islands
(count:3604)
Chromatin interactive
region (count:185)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2698 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105635551-105635751	K562	blood:	n/a	n/a
2	ARID3A	chr14:105646970-105647099	K562	blood:	n/a	n/a
3	ATF3	chr14:105647476-105647754	K562	blood:	n/a	n/a
4	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
5	ATF3	chr14:105647408-105647698	GM12878	blood:	n/a	n/a
6	ATF3	chr14:105665582-105665772	K562	blood:	n/a	n/a
7	ATF3	chr14:105647527-105647695	GM12878	blood:	n/a	n/a
8	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:105650175-105650256	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:105663077-105663199	H1-hESC	embryonic stem cell:	n/a	n/a
11	BACH1	chr14:105662435-105662753	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr14:105669384-105669662	H1-hESC	embryonic stem cell:	n/a	n/a
13	BACH1	chr14:105647431-105647661	H1-hESC	embryonic stem cell:	n/a	n/a
14	BACH1	chr14:105635446-105635818	H1-hESC	embryonic stem cell:	n/a	n/a
15	BCL3	chr14:105668099-105668659	A549	lung:	n/a	chr14:105668189-105668198
16	BCL3	chr14:105667847-105668627	A549	lung:	n/a	chr14:105667887-105667896 chr14:105668189-105668198 chr14:105667888-105667897
17	BCL3	chr14:105670617-105671440	A549	lung:	n/a	n/a
18	BCL3	chr14:105668932-105669779	A549	lung:	n/a	n/a
19	BCL3	chr14:105681691-105682038	GM12878	blood:	n/a	n/a
20	BCL3	chr14:105669015-105669647	A549	lung:	n/a	n/a
21	BCL3	chr14:105681677-105681921	GM12878	blood:	n/a	n/a
22	BHLHE40	chr14:105670862-105671194	HepG2	liver:	n/a	n/a
23	BHLHE40	chr14:105641106-105641239	GM12878	blood:	n/a	n/a
24	BHLHE40	chr14:105673381-105673508	K562	blood:	n/a	n/a
25	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
26	BHLHE40	chr14:105647471-105647910	GM12878	blood:	n/a	chr14:105647556-105647572
27	BHLHE40	chr14:105635049-105635625	K562	blood:	n/a	n/a
28	BHLHE40	chr14:105647446-105647893	K562	blood:	n/a	chr14:105647556-105647572
29	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
30	BRCA1	chr14:105663594-105663903	Hela-S3	cervix:	n/a	n/a
31	CBX3	chr14:105654397-105654814	K562	blood:	n/a	n/a
32	CBX3	chr14:105635458-105635833	K562	blood:	n/a	n/a
33	CBX3	chr14:105665434-105665804	K562	blood:	n/a	n/a
34	CBX3	chr14:105654534-105654767	K562	blood:	n/a	n/a
35	CCNT2	chr14:105672167-105672351	K562	blood:	n/a	n/a
36	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
37	CCNT2	chr14:105665556-105665715	K562	blood:	n/a	n/a
38	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
39	CCNT2	chr14:105673513-105673600	K562	blood:	n/a	n/a
40	CCNT2	chr14:105662979-105663291	K562	blood:	n/a	n/a
41	CCNT2	chr14:105647484-105647639	K562	blood:	n/a	n/a
42	CEBPB	chr14:105671141-105671144	Hela-S3	cervix:	n/a	n/a
43	CEBPB	chr14:105663593-105663880	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr14:105669556-105669564	HepG2	liver:	n/a	n/a
45	CEBPB	chr14:105646836-105646884	K562	blood:	n/a	n/a
46	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
47	CHD1	chr14:105673884-105674043	H1-hESC	embryonic stem cell:	n/a	n/a
48	CHD2	chr14:105633690-105633737	Hela-S3	cervix:	n/a	n/a
49	CHD2	chr14:105663633-105663886	Hela-S3	cervix:	n/a	n/a
50	CHD2	chr14:105662873-105662997	H1-hESC	embryonic stem cell:	n/a	n/a

(count:3604 , 50 per page) page: 1 2 3 4 5 6 7 ... 73

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105676908-105676958	AG04450	lung:	fetal
2	chr14:105660876-105660926	AG10803	skin:	n/a
3	chr14:105620358-105620408	SK-N-SH	brain:	n/a
4	chr14:105635706-105635756	BE2_C	brain:	n/a
5	chr14:105649747-105649797	IMR90	lung:	fetal
6	chr14:105676908-105676958	AG04450	lung:	fetal
7	chr14:105660876-105660926	AG10803	skin:	n/a
8	chr14:105620358-105620408	SK-N-SH	brain:	n/a
9	chr14:105635706-105635756	BE2_C	brain:	n/a
10	chr14:105649747-105649797	IMR90	lung:	fetal
11	chr14:105648224-105648274	AoSMC	blood vessel:	n/a
12	chr14:105677543-105677593	HIPEpiC	eye:	n/a
13	chr14:105657710-105657760	H1-hESC	embryonic stem cell:	embryo
14	chr14:105619634-105619684	ovcar-3	ovarian:	n/a
15	chr14:105676908-105676958	ovcar-3	ovarian:	n/a
16	chr14:105670754-105670804	NH-A	brain:	n/a
17	chr14:105648697-105648747	MCF-7	breast:	n/a
18	chr14:105620358-105620408	ECC-1	luminal epithelium:	n/a
19	chr14:105662787-105662837	BE2_C	brain:	n/a
20	chr14:105635706-105635756	HCPEpiC	choroid plexus:	n/a
21	chr14:105669480-105669530	SAEC	small airway:	n/a
22	chr14:105648697-105648747	AG09319	gingival:	n/a
23	chr14:105651786-105651836	SK-N-SH	brain:	n/a
24	chr14:105655178-105655228	HCT-116	colon:	n/a
25	chr14:105663478-105663528	AoSMC	blood vessel:	n/a
26	chr14:105676686-105676736	HAEpiC	amniotic membrane:	n/a
27	chr14:105619634-105619684	IMR90	lung:	fetal
28	chr14:105648024-105648074	T-47D	breast:	n/a
29	chr14:105667508-105667558	Hela-S3	cervix:	n/a
30	chr14:105669480-105669530	HL-60	blood:	n/a
31	chr14:105635208-105635258	NT2-D1	testis:	n/a
32	chr14:105625577-105625627	SAEC	small airway:	n/a
33	chr14:105663019-105663069	IMR90	lung:	fetal
34	chr14:105677543-105677593	SK-N-MC	brain:	n/a
35	chr14:105635769-105635819	GM06990	blood:	n/a
36	chr14:105635763-105635813	HAEpiC	amniotic membrane:	n/a
37	chr14:105635763-105635813	HRPEpiC	eye:	n/a
38	chr14:105663093-105663143	PrEC	prostate:	n/a
39	chr14:105635763-105635813	ovcar-3	ovarian:	n/a
40	chr14:105622992-105623042	GM19239	blood:	n/a
41	chr14:105634387-105634437	PFSK-1	brain:	n/a
42	chr14:105676846-105676896	HL-60	blood:	n/a
43	chr14:105657710-105657760	GM12892	blood:	n/a
44	chr14:105648697-105648747	ovcar-3	ovarian:	n/a
45	chr14:105624483-105624533	ECC-1	luminal epithelium:	n/a
46	chr14:105635769-105635819	AG09309	skin:	n/a
47	chr14:105635769-105635819	HIPEpiC	eye:	n/a
48	chr14:105635081-105635131	AG09319	gingival:	n/a
49	chr14:105635706-105635756	NHDF-neo	bronchial:	n/a
50	chr14:105677543-105677593	HRE	kidney:	n/a

(count:185 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr14:105556861..105558363-chr14:105628903..105631842,2	K562	blood:
2	chr14:105659714..105661407-chr14:105665604..105667882,2	K562	blood:
3	chr14:105620302..105622152-chr14:105646136..105647731,2	MCF-7	breast:
4	chr14:105635244..105636129-chr14:105665708..105667054,3	K562	blood:
5	chr14:105556907..105557905-chr14:105631981..105632717,2	MCF-7	breast:
6	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
7	chr14:105636616..105638377-chr14:105781844..105784159,2	K562	blood:
8	chr14:105667951..105671831-chr14:105672268..105675254,4	K562	blood:
9	chr14:105669895..105672499-chr14:105780191..105782899,2	MCF-7	breast:
10	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
11	chr14:105668626..105670243-chr14:105732918..105735863,2	MCF-7	breast:
12	chr14:105647532..105649524-chr14:105654465..105656702,2	MCF-7	breast:
13	chr14:105647951..105651045-chr14:105657056..105659475,3	MCF-7	breast:
14	chr14:105638805..105642866-chr14:105643000..105645474,4	K562	blood:
15	chr14:105486956..105489375-chr14:105652100..105655755,4	MCF-7	breast:
16	chr14:105556904..105557457-chr14:105630667..105631594,2	MCF-7	breast:
17	chr14:105605939..105608674-chr14:105628049..105630309,2	K562	blood:
18	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:
19	chr14:105681198..105683564-chr14:105712338..105715416,3	MCF-7	breast:
20	chr14:105441844..105444735-chr14:105632724..105634694,2	MCF-7	breast:
21	chr14:105611401..105614212-chr14:105625101..105627298,2	MCF-7	breast:
22	chr14:105670331..105671987-chr14:105672268..105674643,2	K562	blood:
23	chr14:105268465..105270651-chr14:105635461..105637238,2	K562	blood:
24	chr14:105668621..105671368-chr14:105688558..105691360,2	K562	blood:
25	chr14:105559890..105560867-chr14:105633779..105634301,2	MCF-7	breast:
26	chr14:105647774..105650762-chr14:105651625..105655733,5	MCF-7	breast:
27	chr14:105636897..105638962-chr14:105660422..105663007,2	MCF-7	breast:
28	chr14:105555328..105560254-chr14:105631379..105635555,5	MCF-7	breast:
29	chr14:105583616..105585913-chr14:105629918..105634007,5	MCF-7	breast:
30	chr14:105667108..105669624-chr14:105818365..105820045,2	K562	blood:
31	chr14:105438558..105440399-chr14:105616229..105618880,2	MCF-7	breast:
32	chr14:105539437..105542411-chr14:105625371..105627547,2	K562	blood:
33	chr14:105618086..105620322-chr14:105622917..105625684,2	MCF-7	breast:
34	chr14:105665162..105667358-chr14:105780436..105782662,2	MCF-7	breast:
35	chr14:105671811..105674041-chr14:105933944..105936633,2	MCF-7	breast:
36	chr14:105670960..105673149-chr14:105739734..105742723,2	MCF-7	breast:
37	chr14:105635510..105639334-chr14:105658974..105662269,3	K562	blood:
38	chr14:105649676..105651978-chr14:105660260..105663010,3	K562	blood:
39	chr14:105629335..105630135-chr14:105669031..105669954,2	K562	blood:
40	chr14:105568093..105570383-chr14:105666909..105669878,2	K562	blood:
41	chr14:105635176..105636125-chr14:105747875..105748809,5	K562	blood:
42	chr14:105668719..105671355-chr14:105765771..105767767,2	MCF-7	breast:
43	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
44	chr14:105671389..105673472-chr14:105681134..105682646,2	K562	blood:
45	chr14:105667141..105669666-chr14:105676688..105678333,2	K562	blood:
46	chr14:105637173..105640162-chr14:105646187..105648550,3	MCF-7	breast:
47	chr14:105645461..105647244-chr14:105649629..105652172,2	MCF-7	breast:
48	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
49	chr14:105667782..105668766-chr14:105818459..105819088,3	MCF-7	breast:
50	chr14:105633713..105635633-chr7:75987137..75988852,2	K562	blood:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-1	chr14:105639787-105640155	ENSG00000257816.1
2	lnc-BTBD6-1	chr14:105639541-105639584	ENSG00000257816.1
3	lnc-BTBD6-3	chr14:105682370-105682401	NONHSAT040337
4	lnc-BTBD6-3	chr14:105681490-105682260	NONHSAT040337

No data

Variant related genes	Relation type
BRF1	TF binding region
NUDT14	TF binding region
JAG2	TF binding region
ENSG00000257622	TF binding region
BRF1	CpG island
NUDT14	CpG island
JAG2	CpG island
ENSG00000257622	CpG island
ENSG00000140104	chromatin interactions
ENSG00000185567	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000183828	chromatin interactions
ENSG00000256498	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000182979	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000226174	chromatin interactions
ENSG00000170027	chromatin interactions
ENSG00000257556	chromatin interactions

Extended variants
information (count: 2667 )
Associated
traits (count: 115 )

Variant overlapped rSNPs/rCNVs (count:2667 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2293806	chr14:105617891-105617892	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587755543	chr14:105617895-105617896	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs587650444	chr14:105617899-105617900	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs587703640	chr14:105617902-105617903	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs373476148	chr14:105617921-105617922	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs374907421	chr14:105617926-105617927	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs200292411	chr14:105617933-105617934	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs369643590	chr14:105617948-105617949	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs373182983	chr14:105617949-105617950	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs190677466	chr14:105617952-105617953	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs202151324	chr14:105617991-105617992	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs200420004	chr14:105617992-105617993	Weak transcription Strong transcription Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs35006456	chr14:105618009-105618010	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs199655385	chr14:105618014-105618015	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs150988866	chr14:105618018-105618019	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs140813175	chr14:105618019-105618020	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs373042386	chr14:105618042-105618043	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs377080908	chr14:105618063-105618064	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs112847453	chr14:105618074-105618075	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs587625775	chr14:105618095-105618096	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs587651513	chr14:105618136-105618137	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs182915705	chr14:105618140-105618141	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs367930670	chr14:105618172-105618173	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs587614311	chr14:105618184-105618185	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs187981259	chr14:105618203-105618204	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs587753763	chr14:105618214-105618215	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs200732629	chr14:105618266-105618267	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs377309230	chr14:105618268-105618269	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs147044294	chr14:105618271-105618272	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs144763428	chr14:105618295-105618296	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs146825603	chr14:105618297-105618298	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs140609711	chr14:105618302-105618303	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs369610323	chr14:105618303-105618304	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs201502188	chr14:105618304-105618305	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs145660902	chr14:105618312-105618313	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs113354175	chr14:105618317-105618318	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs587684377	chr14:105618319-105618320	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs199563269	chr14:105618348-105618349	Weak transcription Strong transcription Bivalent Enhancer Genic enhancers Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs76850057	chr14:105618429-105618430	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs376091870	chr14:105618430-105618431	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587744023	chr14:105618433-105618434	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs370031844	chr14:105618436-105618437	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs199832800	chr14:105618437-105618438	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs201919806	chr14:105618459-105618460	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs76684207	chr14:105618460-105618461	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371553658	chr14:105618476-105618477	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs201026401	chr14:105618482-105618483	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs374713574	chr14:105618483-105618484	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs147670846	chr14:105618516-105618517	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs138120492	chr14:105618517-105618518	Weak transcription Strong transcription Bivalent Enhancer Enhancers Genic enhancers Flanking Active TSS	CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:115)

Disease	PMID	Source
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
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	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
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
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	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
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Oligozoospermia	20877625	CNVD
Sertoli-cell only syndrome	20877625	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	20369283	CNVD

Chromatin state (count:2826 , 50 per page) page: 1 2 3 4 5 6 7 ... 57

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105602800-105629800	Weak transcription	K562	blood
2	chr14:105606800-105618000	Weak transcription	Psoas Muscle	Psoas
3	chr14:105606800-105619600	Weak transcription	Stomach Smooth Muscle	stomach
4	chr14:105606800-105631600	Weak transcription	Hela-S3	cervix
5	chr14:105607000-105618200	Strong transcription	Gastric	stomach
6	chr14:105607000-105621600	Weak transcription	Duodenum Mucosa	Duodenum
7	chr14:105607200-105619600	Weak transcription	Colonic Mucosa	Colon
8	chr14:105607400-105619200	Strong transcription	Pancreas	Pancrea
9	chr14:105607600-105625400	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
10	chr14:105607600-105632000	Weak transcription	Brain Angular Gyrus	brain
11	chr14:105608000-105618000	Strong transcription	Adipose Nuclei	Adipose
12	chr14:105608800-105618400	Strong transcription	Lung	lung
13	chr14:105609400-105631400	Weak transcription	HUES6 Cell Line	embryonic stem cell
14	chr14:105609600-105618800	Weak transcription	Placenta	Placenta
15	chr14:105609600-105622000	Weak transcription	Sigmoid Colon	Sigmoid Colon
16	chr14:105610000-105631400	Weak transcription	HUVEC	blood vessel
17	chr14:105610200-105625200	Strong transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
18	chr14:105612800-105621000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
19	chr14:105613400-105623000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr14:105613400-105631400	Weak transcription	Brain Anterior Caudate	brain
21	chr14:105613600-105618400	Weak transcription	HSMMtube	muscle
22	chr14:105613600-105619200	Strong transcription	Breast Myoepithelial Primary Cells	Breast
23	chr14:105613600-105631400	Weak transcription	Brain Inferior Temporal Lobe	brain
24	chr14:105613800-105631400	Weak transcription	Brain Cingulate Gyrus	brain
25	chr14:105614000-105620200	Weak transcription	Fetal Brain Female	brain
26	chr14:105614000-105621600	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
27	chr14:105614000-105622000	Weak transcription	Brain Hippocampus Middle	brain
28	chr14:105614600-105619000	Strong transcription	Fetal Stomach	stomach
29	chr14:105615200-105621600	Weak transcription	Esophagus	oesophagus
30	chr14:105615200-105625600	Weak transcription	A549	lung
31	chr14:105615800-105618400	Weak transcription	Left Ventricle	heart
32	chr14:105615800-105633200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
33	chr14:105616000-105618000	Weak transcription	Fetal Intestine Small	intestine
34	chr14:105616000-105619000	Weak transcription	Spleen	Spleen
35	chr14:105616000-105621800	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
36	chr14:105616000-105623600	Weak transcription	NHEK	skin
37	chr14:105616000-105623800	Weak transcription	HMEC	breast
38	chr14:105616200-105619000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr14:105616200-105619600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
40	chr14:105617000-105618400	Genic enhancers	Fetal Muscle Trunk	muscle
41	chr14:105617000-105619600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
42	chr14:105617600-105618200	Strong transcription	Brain Germinal Matrix	brain
43	chr14:105617600-105618200	Genic enhancers	Skeletal Muscle Male	skeletal muscle
44	chr14:105617600-105618400	Genic enhancers	Fetal Muscle Leg	muscle
45	chr14:105617800-105618200	Genic enhancers	Skeletal Muscle Female	skeletal muscle
46	chr14:105617800-105618400	Weak transcription	Right Ventricle	heart
47	chr14:105617800-105620600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr14:105618000-105618600	Weak transcription	Adipose Nuclei	Adipose
49	chr14:105618000-105618800	Bivalent Enhancer	Foreskin Fibroblast Primary Cells skin02	Skin
50	chr14:105618000-105618800	Strong transcription	Fetal Intestine Small	intestine

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