Variant report

Variant	nsv902324
Chromosome Location	chr14:104399640-104464809
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:431)
CpG islands
(count:429)
Chromatin interactive
region (count:39)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:431 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr14:104409999-104410408	K562	blood:	n/a	n/a
2	ATF3	chr14:104410083-104410329	K562	blood:	n/a	n/a
3	BACH1	chr14:104410119-104410343	K562	blood:	n/a	n/a
4	BHLHE40	chr14:104400049-104400535	HepG2	liver:	n/a	n/a
5	BHLHE40	chr14:104408483-104408814	K562	blood:	n/a	n/a
6	BHLHE40	chr14:104430418-104430483	K562	blood:	n/a	n/a
7	BHLHE40	chr14:104410093-104410571	K562	blood:	n/a	n/a
8	BHLHE40	chr14:104439749-104439766	K562	blood:	n/a	n/a
9	CBX3	chr14:104413306-104413742	HCT-116	colon:	n/a	n/a
10	CBX3	chr14:104455396-104455737	K562	blood:	n/a	n/a
11	CBX3	chr14:104455307-104455762	HCT-116	colon:	n/a	n/a
12	CBX3	chr14:104455399-104455697	K562	blood:	n/a	n/a
13	CBX3	chr14:104455372-104455863	HCT-116	colon:	n/a	n/a
14	CCNT2	chr14:104410065-104410335	K562	blood:	n/a	n/a
15	CEBPB	chr14:104409092-104409159	A549	lung:	n/a	chr14:104409123-104409134
16	CEBPB	chr14:104415826-104416016	A549	lung:	n/a	n/a
17	CEBPB	chr14:104463259-104463336	HepG2	liver:	n/a	chr14:104463301-104463312
18	CEBPB	chr14:104409979-104410421	K562	blood:	n/a	n/a
19	CEBPB	chr14:104462480-104462693	HepG2	liver:	n/a	chr14:104462571-104462582
20	CEBPB	chr14:104410030-104410490	K562	blood:	n/a	n/a
21	CEBPB	chr14:104415806-104416079	Hela-S3	cervix:	n/a	n/a
22	CEBPB	chr14:104438295-104438485	HepG2	liver:	n/a	chr14:104438309-104438320
23	CEBPB	chr14:104414087-104414287	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:104423536-104423707	HepG2	liver:	n/a	n/a
25	CEBPB	chr14:104399460-104399814	Hela-S3	cervix:	n/a	n/a
26	CHD2	chr14:104439639-104439825	K562	blood:	n/a	n/a
27	CREB1	chr14:104409903-104410407	K562	blood:	n/a	n/a
28	CREB1	chr14:104409903-104410532	K562	blood:	n/a	n/a
29	CTCF	chr14:104446980-104447130	GM12871	blood:	n/a	n/a
30	CTCF	chr14:104446980-104447130	HA-sp	spinal cord:	n/a	n/a
31	CTCF	chr14:104462617-104462640	Lung_OC	lung:	n/a	n/a
32	CTCF	chr14:104446980-104447130	BJ	skin:	n/a	n/a
33	CTCF	chr14:104446940-104447090	HRPEpiC	eye:	n/a	n/a
34	CTCF	chr14:104446980-104447130	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr14:104456436-104456512	MCF-7	breast:	n/a	n/a
36	CTCF	chr14:104446980-104447130	NHDF-neo	bronchial:	n/a	n/a
37	CTCF	chr14:104446980-104447130	MCF-7	breast:	n/a	n/a
38	CTCF	chr14:104447065-104447263	H1-hESC	embryonic stem cell:	n/a	n/a
39	CTCF	chr14:104446940-104447090	HPF	lung:	n/a	n/a
40	CTCF	chr14:104446963-104447177	T-47D	breast:	n/a	n/a
41	CTCF	chr14:104447033-104447260	NHEK	skin:	n/a	n/a
42	CTCF	chr14:104447010-104447275	A549	lung:	n/a	n/a
43	CTCF	chr14:104447031-104447313	IMR90	lung:	n/a	n/a
44	CTCF	chr14:104446980-104447130	HCT-116	colon:	n/a	n/a
45	CTCF	chr14:104446890-104447401	K562	blood:	n/a	n/a
46	CTCF	chr14:104456472-104456510	NHEK	skin:	n/a	n/a
47	CTCF	chr14:104446980-104447130	GM12865	blood:	n/a	n/a
48	CTCF	chr14:104447071-104447264	HUVEC	blood vessel:	n/a	n/a
49	CTCF	chr14:104446980-104447130	HFF	foreskin:	n/a	n/a
50	CTCF	chr14:104446980-104447130	GM12875	blood:	n/a	n/a

(count:429 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:104436418-104436468	HRPEpiC	eye:	n/a
2	chr14:104436947-104436997	ovcar-3	ovarian:	n/a
3	chr14:104436418-104436468	HRPEpiC	eye:	n/a
4	chr14:104436947-104436997	ovcar-3	ovarian:	n/a
5	chr14:104440623-104440673	HepG2	liver:	n/a
6	chr14:104436947-104436997	HCT-116	colon:	n/a
7	chr14:104436947-104436997	AG10803	skin:	n/a
8	chr14:104436161-104436211	SK-N-SH_RA	brain:	n/a
9	chr14:104436161-104436211	ECC-1	luminal epithelium:	n/a
10	chr14:104436418-104436468	HCT-116	colon:	n/a
11	chr14:104436418-104436468	BE2_C	brain:	n/a
12	chr14:104436161-104436211	NB4	blood:	n/a
13	chr14:104440854-104440904	SK-N-SH_RA	brain:	n/a
14	chr14:104440854-104440904	A549	lung:	n/a
15	chr14:104436161-104436211	GM06990	blood:	n/a
16	chr14:104440623-104440673	GM12891	blood:	n/a
17	chr14:104440854-104440904	Hela-S3	cervix:	n/a
18	chr14:104436418-104436468	AG10803	skin:	n/a
19	chr14:104422055-104422105	GM12891	blood:	n/a
20	chr14:104436057-104436107	PANC-1	pancreas:	n/a
21	chr14:104436418-104436468	HPAEpiC	pulmonary alveolar:	n/a
22	chr14:104422055-104422105	IMR90	lung:	fetal
23	chr14:104436161-104436211	GM12878	blood:	n/a
24	chr14:104436947-104436997	GM06990	blood:	n/a
25	chr14:104436161-104436211	PrEC	prostate:	n/a
26	chr14:104440623-104440673	BJ	skin:	n/a
27	chr14:104440854-104440904	NT2-D1	testis:	n/a
28	chr14:104436947-104436997	A549	lung:	n/a
29	chr14:104436057-104436107	HCT-116	colon:	n/a
30	chr14:104436947-104436997	AG04450	lung:	fetal
31	chr14:104436161-104436211	MCF10A-Er-Src	breast:	n/a
32	chr14:104436418-104436468	MCF-7	breast:	n/a
33	chr14:104440623-104440673	SK-N-SH	brain:	n/a
34	chr14:104440623-104440673	AG04450	lung:	fetal
35	chr14:104440854-104440904	HRE	kidney:	n/a
36	chr14:104440854-104440904	AoSMC	blood vessel:	n/a
37	chr14:104436161-104436211	PFSK-1	brain:	n/a
38	chr14:104436161-104436211	HRPEpiC	eye:	n/a
39	chr14:104436947-104436997	AG09319	gingival:	n/a
40	chr14:104436947-104436997	Hela-S3	cervix:	n/a
41	chr14:104440623-104440673	PrEC	prostate:	n/a
42	chr14:104436418-104436468	NHDF-neo	bronchial:	n/a
43	chr14:104440854-104440904	SK-N-MC	brain:	n/a
44	chr14:104436057-104436107	SAEC	small airway:	n/a
45	chr14:104440623-104440673	GM12892	blood:	n/a
46	chr14:104436057-104436107	AoSMC	blood vessel:	n/a
47	chr14:104436161-104436211	GM12891	blood:	n/a
48	chr14:104436161-104436211	HRCEpiC	kidney:	n/a
49	chr14:104440623-104440673	NHBE	bronchial:	n/a
50	chr14:104436418-104436468	GM12892	blood:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:104400120..104402233-chr14:104410455..104413050,2	MCF-7	breast:
2	chr14:104367293..104369155-chr14:104426158..104428921,2	K562	blood:
3	chr14:104408709..104411499-chr14:104426104..104427639,2	MCF-7	breast:
4	chr14:104422761..104424603-chr14:104427460..104430127,2	MCF-7	breast:
5	chr14:104408709..104411499-chr14:104426104..104427639,2	MCF-7	breast:
6	chr14:104461660..104464310-chr14:104577569..104579522,2	MCF-7	breast:
7	chr14:104391863..104393842-chr14:104396870..104399828,2	K562	blood:
8	chr14:104419063..104421166-chr14:104423566..104426306,2	MCF-7	breast:
9	chr14:104178828..104180421-chr14:104438971..104440971,2	K562	blood:
10	chr14:104399690..104401761-chr14:104403081..104405618,2	K562	blood:
11	chr14:104386060..104387762-chr14:104425498..104427108,2	MCF-7	breast:
12	chr14:104399690..104401761-chr14:104403081..104405618,2	K562	blood:
13	chr14:104400120..104402233-chr14:104410455..104413050,2	MCF-7	breast:
14	chr14:104383824..104386788-chr14:104411318..104413343,3	K562	blood:
15	chr14:104418207..104420448-chr14:104423783..104426563,2	MCF-7	breast:
16	chr14:104394897..104396539-chr14:104399297..104402064,2	MCF-7	breast:
17	chr14:104393603..104397064-chr14:104407702..104410726,3	K562	blood:
18	chr14:104391025..104393220-chr14:104438159..104440643,2	MCF-7	breast:
19	chr14:104363448..104365054-chr14:104402588..104404294,2	MCF-7	breast:
20	chr14:104389161..104391143-chr14:104411439..104413629,2	K562	blood:
21	chr14:104403831..104408776-chr14:104408810..104412826,6	K562	blood:
22	chr14:104233292..104236251-chr14:104461397..104463914,2	MCF-7	breast:
23	chr14:104312474..104314028-chr14:104433639..104437208,3	MCF-7	breast:
24	chr14:104418207..104420448-chr14:104423783..104426563,2	MCF-7	breast:
25	chr14:104402966..104405877-chr14:104408428..104410944,2	K562	blood:
26	chr14:104385987..104387958-chr14:104398361..104401155,2	MCF-7	breast:
27	chr14:104399167..104401671-chr14:104406191..104408805,2	K562	blood:
28	chr14:104395726..104398249-chr14:104421446..104423004,2	K562	blood:
29	chr14:104383824..104385771-chr14:104411318..104413343,2	K562	blood:
30	chr14:104461872..104464135-chr14:104467416..104470134,3	K562	blood:
31	chr14:104419063..104421166-chr14:104423566..104426306,2	MCF-7	breast:
32	chr14:104447828..104450385-chr14:104462611..104464716,2	MCF-7	breast:
33	chr14:104422761..104424603-chr14:104427460..104430127,2	MCF-7	breast:
34	chr14:104403769..104405537-chr14:104408994..104411713,3	MCF-7	breast:
35	chr14:104408381..104410627-chr14:104437148..104438734,2	MCF-7	breast:
36	chr14:104459245..104461701-chr4:2817391..2818995,2	MCF-7	breast:
37	chr14:104403769..104405537-chr14:104408994..104411713,3	MCF-7	breast:
38	chr14:104447828..104450385-chr14:104462611..104464716,2	MCF-7	breast:
39	chr14:104393603..104396242-chr14:104407114..104410000,4	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C14orf2-1	chr14:104398863-104400802	l_1076_chr14:104398227-104400802_kidney

No data

Variant related genes	Relation type
ENSG00000264439	TF binding region
RD3L	TF binding region
TDRD9	TF binding region
ENSG00000264439	CpG island
RD3L	CpG island
TDRD9	CpG island
ENSG00000088808	chromatin interactions
ENSG00000269963	chromatin interactions
ENSG00000156411	chromatin interactions
ENSG00000227729	chromatin interactions
ENSG00000156414	chromatin interactions
ENSG00000166183	chromatin interactions

Extended variants
information (count: 2626 )
Associated
traits (count: 101 )

Variant overlapped rSNPs/rCNVs (count:2626 , 50 per page) page: 1 2 3 4 5 6 7 ... 53

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17792891	chr14:104399640-104399641	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	mRNA abundance
2	rs35660478	chr14:104399645-104399646	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs540364478	chr14:104399648-104399649	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
4	rs560219138	chr14:104399658-104399659	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs190144661	chr14:104399662-104399663	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs538262488	chr14:104399684-104399685	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs17095276	chr14:104399702-104399703	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
8	rs562406899	chr14:104399725-104399726	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
9	rs531486460	chr14:104399750-104399751	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
10	rs574909490	chr14:104399787-104399788	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
11	rs140545894	chr14:104399901-104399902	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
12	rs117726739	chr14:104400034-104400035	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
13	rs533823964	chr14:104400035-104400036	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
14	rs547131204	chr14:104400037-104400038	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
15	rs570583629	chr14:104400103-104400104	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
16	rs181039486	chr14:104400104-104400105	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
17	rs577121244	chr14:104400114-104400115	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
18	rs554054731	chr14:104400136-104400137	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
19	rs6576012	chr14:104400159-104400160	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
20	rs569501956	chr14:104400200-104400201	Enhancers Flanking Active TSS Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
21	rs538155528	chr14:104400208-104400209	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
22	rs547601124	chr14:104400258-104400259	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
23	rs535447319	chr14:104400274-104400275	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
24	rs549520943	chr14:104400292-104400293	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
25	rs186054800	chr14:104400297-104400298	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
26	rs150451488	chr14:104400369-104400370	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
27	rs574704518	chr14:104400436-104400437	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
28	rs191804678	chr14:104400455-104400456	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
29	rs113387681	chr14:104400466-104400467	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
30	rs141240968	chr14:104400476-104400477	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
31	rs545926166	chr14:104400479-104400480	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
32	rs113111113	chr14:104400501-104400502	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
33	rs531580449	chr14:104400546-104400547	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
34	rs28461376	chr14:104400559-104400560	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
35	rs377711451	chr14:104400619-104400620	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
36	rs562025659	chr14:104400640-104400641	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
37	rs527264669	chr14:104400701-104400702	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
38	rs547385666	chr14:104400731-104400732	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
39	rs1744308	chr14:104400785-104400786	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
40	rs570497642	chr14:104400790-104400791	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
41	rs537749794	chr14:104400802-104400803	Enhancers Weak transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
42	rs146879424	chr14:104400812-104400813	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs549951280	chr14:104400825-104400826	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
44	rs569466150	chr14:104400837-104400838	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs115321195	chr14:104400838-104400839	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs150751588	chr14:104400846-104400847	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs568754851	chr14:104400883-104400884	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs533904631	chr14:104400887-104400888	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs540921644	chr14:104400906-104400907	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs113143361	chr14:104400945-104400946	Enhancers Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:101)

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
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
T-cell lymphomas	22341440	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
early-passage human iPS cells	21368824	CNVD
Amyotrophic lateral sclerosis	20685689	CNVD

Chromatin state (count:170 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:104395000-104401200	Weak transcription	Spleen	Spleen
2	chr14:104396200-104399800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr14:104396600-104400600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
4	chr14:104397000-104399800	Enhancers	Primary hematopoietic stem cells	blood
5	chr14:104397400-104400400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr14:104397800-104400800	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
7	chr14:104398400-104400600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
8	chr14:104398600-104404600	Weak transcription	Left Ventricle	heart
9	chr14:104399200-104400000	Flanking Active TSS	NHEK	skin
10	chr14:104399400-104399800	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
11	chr14:104399400-104399800	Flanking Active TSS	Foreskin Keratinocyte Primary Cells skin03	Skin
12	chr14:104399400-104399800	Enhancers	Hela-S3	cervix
13	chr14:104399400-104399800	Flanking Active TSS	HMEC	breast
14	chr14:104399400-104400000	Flanking Active TSS	Primary monocytes fromperipheralblood	blood
15	chr14:104399600-104399800	Enhancers	Colonic Mucosa	Colon
16	chr14:104399600-104399800	Flanking Active TSS	HepG2	liver
17	chr14:104399600-104399800	Enhancers	HUVEC	blood vessel
18	chr14:104399600-104400000	Weak transcription	Primary B cells from cord blood	blood
19	chr14:104399600-104402000	Enhancers	Primary hematopoietic stem cells short term culture	blood
20	chr14:104399800-104400000	Enhancers	Primary neutrophils fromperipheralblood	blood
21	chr14:104399800-104400000	Enhancers	HepG2	liver
22	chr14:104399800-104400000	Enhancers	Monocytes-CD14+_RO01746	blood
23	chr14:104399800-104400600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
24	chr14:104399800-104400600	Enhancers	HMEC	breast
25	chr14:104400000-104400200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
26	chr14:104400000-104400200	Enhancers	HUVEC	blood vessel
27	chr14:104400000-104400400	Enhancers	Primary B cells from cord blood	blood
28	chr14:104400000-104400400	Flanking Active TSS	HepG2	liver
29	chr14:104400000-104400600	Enhancers	Fetal Intestine Large	intestine
30	chr14:104400000-104400600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
31	chr14:104400000-104400800	Enhancers	Fetal Intestine Small	intestine
32	chr14:104400000-104400800	Enhancers	NHEK	skin
33	chr14:104400000-104402000	Enhancers	Primary monocytes fromperipheralblood	blood
34	chr14:104400200-104400600	Enhancers	Rectal Mucosa Donor 31	rectum
35	chr14:104400200-104400600	Enhancers	Sigmoid Colon	Sigmoid Colon
36	chr14:104400200-104403000	Enhancers	Primary neutrophils fromperipheralblood	blood
37	chr14:104400400-104400600	Enhancers	Colonic Mucosa	Colon
38	chr14:104400400-104401400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
39	chr14:104400400-104401600	Enhancers	HepG2	liver
40	chr14:104400600-104401600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
41	chr14:104400600-104402600	Enhancers	Monocytes-CD14+_RO01746	blood
42	chr14:104401200-104401800	Active TSS	Spleen	Spleen
43	chr14:104401600-104401800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
44	chr14:104401600-104402000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
45	chr14:104401600-104403200	Weak transcription	HepG2	liver
46	chr14:104401800-104404400	Weak transcription	Spleen	Spleen
47	chr14:104402000-104403000	Weak transcription	Primary monocytes fromperipheralblood	blood
48	chr14:104402600-104408400	Weak transcription	Monocytes-CD14+_RO01746	blood
49	chr14:104403000-104403200	Enhancers	Primary monocytes fromperipheralblood	blood
50	chr14:104403000-104404200	Weak transcription	Primary neutrophils fromperipheralblood	blood

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