Variant report

Variant	nsv902435
Chromosome Location	chr14:105602619-105654606
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1498)
CpG islands
(count:4029)
Chromatin interactive
region (count:119)
LncRNA
region (count:2)
Mature miRNA
region (count: 2)
miRNA target
sites (count:2)

(count:1498 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

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	chr14:105647408-105647698	GM12878	blood:	n/a	n/a
4	ATF3	chr14:105633815-105634024	K562	blood:	n/a	n/a
5	ATF3	chr14:105647476-105647754	K562	blood:	n/a	n/a
6	ATF3	chr14:105647527-105647695	GM12878	blood:	n/a	n/a
7	BACH1	chr14:105635446-105635818	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:105650175-105650256	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:105634160-105634415	H1-hESC	embryonic stem cell:	n/a	n/a
10	BACH1	chr14:105647431-105647661	H1-hESC	embryonic stem cell:	n/a	n/a
11	BHLHE40	chr14:105635049-105635625	K562	blood:	n/a	n/a
12	BHLHE40	chr14:105633488-105634425	K562	blood:	n/a	chr14:105633626-105633642
13	BHLHE40	chr14:105641106-105641239	GM12878	blood:	n/a	n/a
14	BHLHE40	chr14:105647446-105647893	K562	blood:	n/a	chr14:105647556-105647572
15	BHLHE40	chr14:105647471-105647910	GM12878	blood:	n/a	chr14:105647556-105647572
16	BRCA1	chr14:105628806-105629067	HepG2	liver:	n/a	n/a
17	CBX3	chr14:105654397-105654814	K562	blood:	n/a	n/a
18	CBX3	chr14:105607430-105607762	K562	blood:	n/a	n/a
19	CBX3	chr14:105606324-105606692	K562	blood:	n/a	n/a
20	CBX3	chr14:105606276-105606713	K562	blood:	n/a	n/a
21	CBX3	chr14:105635458-105635833	K562	blood:	n/a	n/a
22	CBX3	chr14:105654534-105654767	K562	blood:	n/a	n/a
23	CCNT2	chr14:105647484-105647639	K562	blood:	n/a	n/a
24	CCNT2	chr14:105633598-105634394	K562	blood:	n/a	n/a
25	CCNT2	chr14:105634944-105635778	K562	blood:	n/a	chr14:105635426-105635435
26	CEBPB	chr14:105646836-105646884	K562	blood:	n/a	n/a
27	CEBPB	chr14:105631426-105631943	ECC-1	luminal epithelium:	n/a	n/a
28	CHD2	chr14:105634239-105634449	Hela-S3	cervix:	n/a	n/a
29	CHD2	chr14:105633690-105633737	Hela-S3	cervix:	n/a	n/a
30	CHD2	chr14:105632638-105632642	K562	blood:	n/a	n/a
31	CHD2	chr14:105635003-105635186	Hela-S3	cervix:	n/a	n/a
32	CHD2	chr14:105628806-105628928	HepG2	liver:	n/a	n/a
33	CHD2	chr14:105635604-105635860	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr14:105635288-105635741	K562	blood:	n/a	n/a
35	CHD2	chr14:105647556-105647857	Hela-S3	cervix:	n/a	n/a
36	CREB1	chr14:105634956-105635290	A549	lung:	n/a	n/a
37	CREB1	chr14:105603330-105603686	K562	blood:	n/a	n/a
38	CREB1	chr14:105633974-105634413	A549	lung:	n/a	n/a
39	CREB1	chr14:105647357-105647807	A549	lung:	n/a	n/a
40	CTCF	chr14:105603960-105604110	HepG2	liver:	n/a	chr14:105604072-105604085
41	CTCF	chr14:105654265-105654571	H1-hESC	embryonic stem cell:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654292-105654300 chr14:105654465-105654481
42	CTCF	chr14:105631571-105631603	GM19239	blood:	n/a	n/a
43	CTCF	chr14:105631700-105631850	MCF-7	breast:	n/a	n/a
44	CTCF	chr14:105628840-105628990	AG04449	skin:	n/a	n/a
45	CTCF	chr14:105635620-105635770	BJ	skin:	n/a	chr14:105635654-105635667 chr14:105635651-105635669
46	CTCF	chr14:105611538-105611710	NHEK	skin:	n/a	chr14:105611569-105611579 chr14:105611619-105611637 chr14:105611626-105611634
47	CTCF	chr14:105632400-105632550	NHEK	skin:	n/a	chr14:105632422-105632435
48	CTCF	chr14:105644460-105644610	HCT-116	colon:	n/a	n/a
49	CTCF	chr14:105634060-105634210	Hela-S3	cervix:	n/a	n/a
50	CTCF	chr14:105654380-105654530	NHEK	skin:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654465-105654481

(count:4029 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105617839-105617889	GM06990	blood:	n/a
2	chr14:105609516-105609566	SK-N-SH_RA	brain:	n/a
3	chr14:105634387-105634437	HNPCEpiC	eye:	n/a
4	chr14:105617839-105617889	GM06990	blood:	n/a
5	chr14:105609516-105609566	SK-N-SH_RA	brain:	n/a
6	chr14:105634387-105634437	HNPCEpiC	eye:	n/a
7	chr14:105609472-105609522	A549	lung:	n/a
8	chr14:105635706-105635756	HCPEpiC	choroid plexus:	n/a
9	chr14:105643522-105643572	LNCaP	prostate:	n/a
10	chr14:105617308-105617358	HMEC	breast:	n/a
11	chr14:105624483-105624533	HEEpiC	esophagus:	n/a
12	chr14:105622454-105622504	PANC-1	pancreas:	n/a
13	chr14:105612971-105613021	HepG2	liver:	n/a
14	chr14:105643522-105643572	GM12878	blood:	n/a
15	chr14:105635208-105635258	NT2-D1	testis:	n/a
16	chr14:105603153-105603203	HCT-116	colon:	n/a
17	chr14:105622312-105622362	H1-hESC	embryonic stem cell:	embryo
18	chr14:105612130-105612180	GM12891	blood:	n/a
19	chr14:105622992-105623042	U87	brain:	n/a
20	chr14:105622454-105622504	HNPCEpiC	eye:	n/a
21	chr14:105651786-105651836	MCF-7	breast:	n/a
22	chr14:105648024-105648074	MCF10A-Er-Src	breast:	n/a
23	chr14:105612787-105612837	HUVEC	blood vessel:	n/a
24	chr14:105617839-105617889	Hepatocyte	liver:	n/a
25	chr14:105620358-105620408	HEK293	kidney:	embryo
26	chr14:105609516-105609566	GM12892	blood:	n/a
27	chr14:105608567-105608617	H1-hESC	embryonic stem cell:	embryo
28	chr14:105613783-105613833	GM19239	blood:	n/a
29	chr14:105618482-105618532	RPTEC	kidney:	n/a
30	chr14:105608260-105608310	CMK	blood:	n/a
31	chr14:105622992-105623042	HEEpiC	esophagus:	n/a
32	chr14:105613783-105613833	HUVEC	blood vessel:	n/a
33	chr14:105647407-105647457	BE2_C	brain:	n/a
34	chr14:105620358-105620408	SKMC	muscle:	n/a
35	chr14:105615459-105615509	RPTEC	kidney:	n/a
36	chr14:105639304-105639354	NT2-D1	testis:	n/a
37	chr14:105617173-105617223	HRE	kidney:	n/a
38	chr14:105635208-105635258	HCF	heart:	n/a
39	chr14:105651786-105651836	IMR90	lung:	fetal
40	chr14:105647507-105647557	Caco-2	colon:	n/a
41	chr14:105617839-105617889	T-47D	breast:	n/a
42	chr14:105613783-105613833	GM06990	blood:	n/a
43	chr14:105608567-105608617	NB4	blood:	n/a
44	chr14:105619634-105619684	AG04450	lung:	fetal
45	chr14:105647507-105647557	AG10803	skin:	n/a
46	chr14:105612753-105612803	SAEC	small airway:	n/a
47	chr14:105647734-105647784	HCF	heart:	n/a
48	chr14:105647734-105647784	CMK	blood:	n/a
49	chr14:105616988-105617038	Caco-2	colon:	n/a
50	chr14:105635708-105635758	GM12891	blood:	n/a

(count:119 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
2	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
3	chr14:105512170..105512763-chr14:105653793..105654556,2	MCF-7	breast:
4	chr14:105633713..105635633-chr7:75987137..75988852,2	K562	blood:
5	chr14:105619466..105621170-chr14:105628840..105630613,2	MCF-7	breast:
6	chr14:105609926..105615692-chr14:105616858..105625128,9	K562	blood:
7	chr14:105632643..105634203-chr14:105776322..105778030,2	K562	blood:
8	chr14:105646294..105648744-chr14:105860219..105862499,2	MCF-7	breast:
9	chr14:105613142..105616306-chr14:105622290..105625169,3	K562	blood:
10	chr14:105647877..105649605-chr14:105663025..105665566,2	MCF-7	breast:
11	chr14:105631482..105635033-chr14:105765939..105767661,3	K562	blood:
12	chr14:105556528..105557420-chr14:105633531..105634669,3	MCF-7	breast:
13	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
14	chr14:105627527..105629912-chr14:105632611..105634539,3	MCF-7	breast:
15	chr14:105615698..105618053-chr14:105622347..105625638,3	MCF-7	breast:
16	chr14:105647774..105650762-chr14:105651625..105655733,5	MCF-7	breast:
17	chr14:105635244..105636129-chr14:105665708..105667054,3	K562	blood:
18	chr14:105602588..105606045-chr14:105617930..105622124,4	MCF-7	breast:
19	chr14:105556806..105557482-chr14:105648408..105649374,2	K562	blood:
20	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
21	chr14:105618156..105621334-chr14:105628329..105630360,3	K562	blood:
22	chr14:105191017..105193582-chr14:105615897..105618849,2	MCF-7	breast:
23	chr14:105610604..105613096-chr14:105619107..105620769,2	K562	blood:
24	chr14:105268465..105270651-chr14:105635461..105637238,2	K562	blood:
25	chr14:105646332..105648438-chr14:105653932..105656621,2	K562	blood:
26	chr14:105601373..105604174-chr14:105610785..105613135,3	MCF-7	breast:
27	chr14:105502174..105504922-chr14:105632204..105633983,2	MCF-7	breast:
28	chr14:105632764..105636922-chr14:105637769..105642057,5	MCF-7	breast:
29	chr14:105556047..105558699-chr14:105620485..105622825,2	K562	blood:
30	chr14:105634303..105636398-chr14:105650780..105653428,2	MCF-7	breast:
31	chr14:105556568..105557626-chr14:105644344..105645020,4	MCF-7	breast:
32	chr14:105650402..105652151-chr14:105657349..105659937,3	MCF-7	breast:
33	chr14:105645461..105647244-chr14:105649629..105652172,2	MCF-7	breast:
34	chr14:105550862..105553369-chr14:105650448..105653112,3	MCF-7	breast:
35	chr14:105615014..105617239-chr14:105619145..105622136,2	K562	blood:
36	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
37	chr14:105649547..105651849-chr14:105660128..105661657,2	MCF-7	breast:
38	chr14:105629335..105630135-chr14:105669031..105669954,2	K562	blood:
39	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
40	chr14:105613499..105615482-chr14:105618517..105620945,3	MCF-7	breast:
41	chr14:105635510..105639334-chr14:105658974..105662269,3	K562	blood:
42	chr14:105618326..105620016-chr14:105627831..105630426,2	MCF-7	breast:
43	chr14:105642956..105644640-chr14:105647161..105649743,2	MCF-7	breast:
44	chr14:105618326..105620016-chr14:105627831..105630426,2	MCF-7	breast:
45	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
46	chr14:105511711..105512332-chr14:105633666..105634346,2	MCF-7	breast:
47	chr14:105636897..105638962-chr14:105660422..105663007,2	MCF-7	breast:
48	chr14:105438558..105440399-chr14:105616229..105618880,2	MCF-7	breast:
49	chr14:105603827..105606395-chr14:105610368..105612251,2	MCF-7	breast:
50	chr14:105633069..105635536-chr14:105714407..105716304,2	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-1	chr14:105639541-105639584	ENSG00000257816.1
2	lnc-BTBD6-1	chr14:105639787-105640155	ENSG00000257816.1

miRNA name	Chromosome Location	mirBase accession
hsa-miR-6765-3p	chr14:105617115-105617135	MIMAT0027431
hsa-miR-6765-5p	chr14:105617177-105617201	MIMAT0027430

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	JAG2	hsa-miR-124-3p	chr14:105608227-105608246
2	JAG2	hsa-miR-124-3p	chr14:105608233-105608227

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

Extended variants
information (count: 2263 )
Associated
traits (count: 112 )

Variant overlapped rSNPs/rCNVs (count:2263 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2091918	chr14:105602619-105602620	Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs587770641	chr14:105602658-105602659	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs587620329	chr14:105602675-105602676	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs35025851	chr14:105602676-105602677	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs587628780	chr14:105602684-105602685	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs373526079	chr14:105602687-105602688	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs57347298	chr14:105602706-105602707	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs375738940	chr14:105602765-105602766	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs369762466	chr14:105602842-105602843	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs587693805	chr14:105602848-105602849	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs8009452	chr14:105602850-105602851	Genic enhancers Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs587648652	chr14:105602953-105602954	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs587701492	chr14:105602975-105602976	Genic enhancers Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs587763408	chr14:105603066-105603067	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs150077917	chr14:105603080-105603081	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs377146813	chr14:105603112-105603113	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs12885890	chr14:105603211-105603212	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs149211863	chr14:105603241-105603242	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs587684793	chr14:105603289-105603290	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs587743795	chr14:105603295-105603296	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs587598565	chr14:105603309-105603310	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs587678007	chr14:105603323-105603324	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs145126036	chr14:105603333-105603334	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs587634206	chr14:105603349-105603350	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs587669489	chr14:105603358-105603359	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs587738968	chr14:105603379-105603380	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs369506801	chr14:105603381-105603382	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs587614186	chr14:105603389-105603390	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs587650329	chr14:105603398-105603399	Enhancers Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs1022431	chr14:105603415-105603416	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs587751049	chr14:105603434-105603435	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs587620758	chr14:105603490-105603491	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs377498940	chr14:105603499-105603500	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs111358591	chr14:105603514-105603515	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs76791826	chr14:105603525-105603526	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs190122331	chr14:105603531-105603532	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs138970841	chr14:105603562-105603563	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs587662113	chr14:105603583-105603584	Enhancers Genic enhancers Bivalent Enhancer Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs181687030	chr14:105603607-105603608	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs186682919	chr14:105603667-105603668	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs587660025	chr14:105603737-105603738	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs587712028	chr14:105603742-105603743	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs2816670	chr14:105603749-105603750	Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs140648004	chr14:105603764-105603765	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs115574789	chr14:105603827-105603828	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs587600410	chr14:105603833-105603834	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs2816671	chr14:105603844-105603845	Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs370669579	chr14:105603883-105603884	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs587749031	chr14:105604004-105604005	Genic enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs2816672	chr14:105604011-105604012	Genic enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:112)

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
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	22237106	CNVD

Chromatin state (count:1850 , 50 per page) page: 1 2 3 4 5 6 7 ... 37

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105601400-105605800	Weak transcription	Pancreas	Pancrea
2	chr14:105602600-105605200	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:105602800-105603600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
4	chr14:105602800-105603600	Enhancers	Primary hematopoietic stem cells	blood
5	chr14:105602800-105629800	Weak transcription	K562	blood
6	chr14:105603000-105603600	Enhancers	H1 Cell Line	embryonic stem cell
7	chr14:105603400-105603600	Bivalent Enhancer	Fetal Muscle Trunk	muscle
8	chr14:105603600-105606000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:105603800-105605800	Weak transcription	A549	lung
10	chr14:105604200-105605800	Enhancers	Breast Myoepithelial Primary Cells	Breast
11	chr14:105604400-105606400	ZNF genes & repeats	Foreskin Melanocyte Primary Cells skin01	Skin
12	chr14:105604600-105605000	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr14:105604600-105608400	Weak transcription	Primary T cells from cord blood	blood
14	chr14:105604800-105605000	Enhancers	HMEC	breast
15	chr14:105604800-105605400	Enhancers	Esophagus	oesophagus
16	chr14:105605000-105606000	Weak transcription	HMEC	breast
17	chr14:105605200-105606400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
18	chr14:105605200-105606400	ZNF genes & repeats	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr14:105605600-105606200	Weak transcription	Skeletal Muscle Female	skeletal muscle
20	chr14:105605800-105607200	ZNF genes & repeats	Duodenum Smooth Muscle	Duodenum
21	chr14:105605800-105607200	ZNF genes & repeats	A549	lung
22	chr14:105605800-105607400	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin02	Skin
23	chr14:105605800-105607400	ZNF genes & repeats	Pancreas	Pancrea
24	chr14:105605800-105607600	ZNF genes & repeats	Brain Hippocampus Middle	brain
25	chr14:105605800-105607600	ZNF genes & repeats	Skeletal Muscle Male	skeletal muscle
26	chr14:105605800-105608600	ZNF genes & repeats	Breast Myoepithelial Primary Cells	Breast
27	chr14:105606000-105607000	ZNF genes & repeats	Fetal Muscle Trunk	muscle
28	chr14:105606000-105607200	ZNF genes & repeats	Fetal Brain Female	brain
29	chr14:105606000-105607200	ZNF genes & repeats	Fetal Muscle Leg	muscle
30	chr14:105606000-105607200	ZNF genes & repeats	HMEC	breast
31	chr14:105606000-105607400	ZNF genes & repeats	ES-UCSF4 Cell Line	embryonic stem cell
32	chr14:105606000-105607400	ZNF genes & repeats	Brain Germinal Matrix	brain
33	chr14:105606000-105607600	ZNF genes & repeats	Foreskin Keratinocyte Primary Cells skin03	Skin
34	chr14:105606200-105606400	ZNF genes & repeats	Skeletal Muscle Female	skeletal muscle
35	chr14:105606200-105607200	ZNF genes & repeats	Brain Inferior Temporal Lobe	brain
36	chr14:105606200-105607200	ZNF genes & repeats	Brain Dorsolateral Prefrontal Cortex	brain
37	chr14:105606200-105607200	ZNF genes & repeats	Right Ventricle	heart
38	chr14:105606200-105607600	ZNF genes & repeats	Brain Angular Gyrus	brain
39	chr14:105606200-105607600	ZNF genes & repeats	Brain Cingulate Gyrus	brain
40	chr14:105606200-105607600	ZNF genes & repeats	Fetal Stomach	stomach
41	chr14:105606400-105606800	ZNF genes & repeats	Hela-S3	cervix
42	chr14:105606400-105607200	ZNF genes & repeats	HSMM	muscle
43	chr14:105606400-105607600	ZNF genes & repeats	Adipose Nuclei	Adipose
44	chr14:105606400-105608000	ZNF genes & repeats	NHEK	skin
45	chr14:105606400-105608800	ZNF genes & repeats	Lung	lung
46	chr14:105606400-105617800	Strong transcription	Skeletal Muscle Female	skeletal muscle
47	chr14:105606600-105606800	ZNF genes & repeats	Left Ventricle	heart
48	chr14:105606600-105607000	ZNF genes & repeats	HUVEC	blood vessel
49	chr14:105606600-105607200	ZNF genes & repeats	Pancreatic Islets	Pancreatic Islet
50	chr14:105606600-105607400	ZNF genes & repeats	Brain Anterior Caudate	brain

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