Variant report

Variant	nsv541978
Chromosome Location	chr14:21602341-21847247
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:5782)
CpG islands
(count:2444)
Chromatin interactive
region (count:289)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:14)

(count:5782 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:21604159-21604455	K562	blood:	n/a	n/a
2	ARID3A	chr14:21770673-21771067	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:21766716-21766742	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:21788216-21788219	K562	blood:	n/a	n/a
5	ARID3A	chr14:21737436-21738247	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:21711256-21711587	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:21732200-21733006	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:21776279-21777397	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:21712624-21712985	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:21709409-21709593	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:21776552-21777534	K562	blood:	n/a	n/a
12	ARID3A	chr14:21736068-21736120	K562	blood:	n/a	n/a
13	ARID3A	chr14:21604119-21604443	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:21766152-21766244	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:21617164-21617199	K562	blood:	n/a	n/a
16	ARID3A	chr14:21747410-21747610	HepG2	liver:	n/a	n/a
17	ARID3A	chr14:21737195-21738158	K562	blood:	n/a	n/a
18	ARID3A	chr14:21711963-21711985	HepG2	liver:	n/a	n/a
19	ARID3A	chr14:21717162-21717278	K562	blood:	n/a	n/a
20	ARID3A	chr14:21697647-21697673	K562	blood:	n/a	n/a
21	ATF1	chr14:21776699-21777288	K562	blood:	n/a	n/a
22	ATF1	chr14:21623382-21623761	K562	blood:	n/a	n/a
23	ATF1	chr14:21737526-21738185	K562	blood:	n/a	n/a
24	ATF1	chr14:21653751-21653965	K562	blood:	n/a	n/a
25	ATF1	chr14:21785645-21785927	K562	blood:	n/a	n/a
26	ATF2	chr14:21727624-21728013	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr14:21736898-21737748	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr14:21671164-21671970	GM12878	blood:	n/a	n/a
29	ATF2	chr14:21735848-21738400	GM12878	blood:	n/a	n/a
30	ATF2	chr14:21776636-21777278	GM12878	blood:	n/a	n/a
31	ATF2	chr14:21726892-21727596	H1-hESC	embryonic stem cell:	n/a	n/a
32	ATF2	chr14:21732138-21732971	GM12878	blood:	n/a	n/a
33	ATF2	chr14:21785532-21786027	GM12878	blood:	n/a	n/a
34	ATF2	chr14:21736929-21737878	H1-hESC	embryonic stem cell:	n/a	n/a
35	ATF2	chr14:21731973-21733035	GM12878	blood:	n/a	n/a
36	ATF2	chr14:21674092-21674706	H1-hESC	embryonic stem cell:	n/a	n/a
37	ATF2	chr14:21735362-21735856	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr14:21729447-21729836	GM12878	blood:	n/a	n/a
39	ATF2	chr14:21672214-21673111	GM12878	blood:	n/a	n/a
40	ATF2	chr14:21775817-21777333	GM12878	blood:	n/a	n/a
41	ATF2	chr14:21729052-21729484	H1-hESC	embryonic stem cell:	n/a	n/a
42	ATF2	chr14:21776687-21777400	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF2	chr14:21669277-21669678	H1-hESC	embryonic stem cell:	n/a	n/a
44	ATF2	chr14:21731544-21732278	H1-hESC	embryonic stem cell:	n/a	n/a
45	ATF2	chr14:21730290-21730933	H1-hESC	embryonic stem cell:	n/a	n/a
46	ATF2	chr14:21671705-21673219	H1-hESC	embryonic stem cell:	n/a	n/a
47	ATF2	chr14:21673281-21674952	GM12878	blood:	n/a	n/a
48	ATF2	chr14:21737251-21738411	GM12878	blood:	n/a	n/a
49	ATF2	chr14:21735629-21736731	GM12878	blood:	n/a	n/a
50	BACH1	chr14:21604152-21604420	K562	blood:	n/a	n/a

(count:2444 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:21769240-21769290	IMR90	lung:	fetal
2	chr14:21769105-21769155	AG04450	lung:	fetal
3	chr14:21624639-21624689	RPTEC	kidney:	n/a
4	chr14:21738093-21738143	BE2_C	brain:	n/a
5	chr14:21769240-21769290	IMR90	lung:	fetal
6	chr14:21769105-21769155	AG04450	lung:	fetal
7	chr14:21624639-21624689	RPTEC	kidney:	n/a
8	chr14:21738093-21738143	BE2_C	brain:	n/a
9	chr14:21624049-21624099	HPAEpiC	pulmonary alveolar:	n/a
10	chr14:21820190-21820240	BE2_C	brain:	n/a
11	chr14:21623804-21623854	MCF-7	breast:	n/a
12	chr14:21755820-21755870	SK-N-SH	brain:	n/a
13	chr14:21738303-21738353	SK-N-SH	brain:	n/a
14	chr14:21679191-21679241	NHBE	bronchial:	n/a
15	chr14:21657028-21657078	HL-60	blood:	n/a
16	chr14:21738093-21738143	ECC-1	luminal epithelium:	n/a
17	chr14:21676297-21676347	HPAEpiC	pulmonary alveolar:	n/a
18	chr14:21737751-21737801	GM12892	blood:	n/a
19	chr14:21624639-21624689	HEEpiC	esophagus:	n/a
20	chr14:21656260-21656310	HRPEpiC	eye:	n/a
21	chr14:21625063-21625113	U87	brain:	n/a
22	chr14:21625173-21625223	Hepatocyte	liver:	n/a
23	chr14:21734410-21734460	SK-N-MC	brain:	n/a
24	chr14:21679191-21679241	HepG2	liver:	n/a
25	chr14:21737878-21737928	HIPEpiC	eye:	n/a
26	chr14:21765313-21765363	MCF10A-Er-Src	breast:	n/a
27	chr14:21625173-21625223	IMR90	lung:	fetal
28	chr14:21725703-21725753	IMR90	lung:	fetal
29	chr14:21772854-21772904	SK-N-SH_RA	brain:	n/a
30	chr14:21624049-21624099	LNCaP	prostate:	n/a
31	chr14:21769332-21769382	HCF	heart:	n/a
32	chr14:21623804-21623854	A549	lung:	n/a
33	chr14:21689119-21689169	HMEC	breast:	n/a
34	chr14:21738303-21738353	AG09309	skin:	n/a
35	chr14:21727471-21727521	Hela-S3	cervix:	n/a
36	chr14:21769240-21769290	ProgFib	skin:	n/a
37	chr14:21738093-21738143	HNPCEpiC	eye:	n/a
38	chr14:21624639-21624689	HCF	heart:	n/a
39	chr14:21756231-21756281	HMEC	breast:	n/a
40	chr14:21769379-21769429	HCT-116	colon:	n/a
41	chr14:21769379-21769429	AG04450	lung:	fetal
42	chr14:21737765-21737815	HCM	heart:	n/a
43	chr14:21624049-21624099	CMK	blood:	n/a
44	chr14:21738093-21738143	NHDF-neo	bronchial:	n/a
45	chr14:21737252-21737302	HCF	heart:	n/a
46	chr14:21704611-21704661	HIPEpiC	eye:	n/a
47	chr14:21738303-21738353	HL-60	blood:	n/a
48	chr14:21756231-21756281	MCF-7	breast:	n/a
49	chr14:21769240-21769290	GM12878	blood:	n/a
50	chr14:21737935-21737985	ProgFib	skin:	n/a

(count:289 , 50 per page) page: 1 2 3 4 5 6

No.	Distal block	Cell Line	Cell type
1	chr14:21811333..21813148-chr14:21813647..21817148,3	K562	blood:
2	chr14:21727359..21730774-chr14:21816654..21820383,4	K562	blood:
3	chr14:21726630..21729193-chr14:21742611..21744564,2	MCF-7	breast:
4	chr14:21785391..21787053-chr14:21851556..21854033,2	K562	blood:
5	chr14:21667283..21669208-chr14:21670633..21672838,2	MCF-7	breast:
6	chr14:21702152..21704976-chr14:21712747..21715545,2	MCF-7	breast:
7	chr14:21736279..21738855-chr14:21774365..21778910,7	K562	blood:
8	chr14:21817179..21819703-chr14:21826063..21828409,2	MCF-7	breast:
9	chr14:21667283..21669208-chr14:21670633..21672838,2	MCF-7	breast:
10	chr14:21678499..21681454-chr14:21736107..21737906,2	MCF-7	breast:
11	chr14:21700378..21702346-chr14:21819126..21821504,2	MCF-7	breast:
12	chr14:21682890..21684914-chr14:21686115..21687924,2	K562	blood:
13	chr14:21701295..21703897-chr14:21842847..21844816,2	K562	blood:
14	chr14:21836067..21840182-chr14:21848186..21853359,8	MCF-7	breast:
15	chr14:21651029..21652913-chr14:21654690..21656270,2	K562	blood:
16	chr14:21698449..21701323-chr14:21702052..21705538,3	MCF-7	breast:
17	chr14:21824475..21826488-chr14:21835956..21838723,2	K562	blood:
18	chr14:21834683..21837534-chr14:21840141..21842518,2	MCF-7	breast:
19	chr14:21813548..21815621-chr14:21836008..21837523,2	MCF-7	breast:
20	chr14:21733164..21734781-chr14:21745082..21746648,2	MCF-7	breast:
21	chr14:21649811..21651897-chr14:21658475..21660736,2	MCF-7	breast:
22	chr14:21730988..21732970-chr14:21824045..21825778,2	K562	blood:
23	chr14:21803371..21805126-chr14:21810991..21813516,2	K562	blood:
24	chr14:21820070..21822211-chr14:21844617..21847241,2	MCF-7	breast:
25	chr14:21700378..21702346-chr14:21819126..21821504,2	MCF-7	breast:
26	chr14:21678068..21679716-chr14:21682875..21685617,2	K562	blood:
27	chr14:21705289..21706946-chr14:21709944..21711637,2	MCF-7	breast:
28	chr14:21709277..21713584-chr14:21714708..21717034,3	K562	blood:
29	chr14:21690598..21692490-chr14:21705492..21708066,2	MCF-7	breast:
30	chr14:21737031..21737660-chr17:29297639..29298182,2	NB4	blood:
31	chr14:21700872..21703141-chr14:21723886..21726612,2	K562	blood:
32	chr14:21814371..21817924-chr14:21819365..21822480,4	K562	blood:
33	chr14:21725390..21727095-chr14:21852518..21854130,2	K562	blood:
34	chr14:21659338..21661906-chr14:21661938..21664120,2	MCF-7	breast:
35	chr14:21734939..21739093-chr14:21774613..21780791,11	K562	blood:
36	chr14:21725317..21729371-chr14:21774547..21778706,6	K562	blood:
37	chr14:21731095..21732813-chr14:21767081..21768936,2	K562	blood:
38	chr14:21733893..21736248-chr14:21775936..21778469,3	K562	blood:
39	chr14:21725773..21728367-chr14:21769503..21772392,2	MCF-7	breast:
40	chr14:21689585..21692266-chr14:21692375..21695207,2	MCF-7	breast:
41	chr14:21689585..21692266-chr14:21692375..21695207,2	MCF-7	breast:
42	chr14:21731613..21734582-chr14:21826282..21828114,3	MCF-7	breast:
43	chr14:21820226..21822237-chr14:21826339..21828894,2	K562	blood:
44	chr14:21736434..21738367-chr14:21826392..21828107,2	MCF-7	breast:
45	chr14:21732976..21734644-chr14:21771387..21772893,2	MCF-7	breast:
46	chr14:21730203..21732388-chr14:21795365..21797950,2	K562	blood:
47	chr14:21650511..21651012-chr3:158378169..158378669,2	Hela-S3	cervix:
48	chr14:21734765..21737618-chr14:21748763..21750396,2	K562	blood:
49	chr14:21775709..21778456-chr14:21815008..21816691,2	MCF-7	breast:
50	chr14:21713934..21716894-chr14:21726084..21727992,2	MCF-7	breast:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUPT16H-3	chr14:21737457-21737548	NONHSAT035670
2	lnc-HNRNPC-1	chr14:21668238-21673662	ENSG00000258441
3	lnc-C14orf176-4	chr14:21634450-21634520	ucscGeneNc_uc001wda_1
4	lnc-HNRNPC-1	chr14:21668621-21670092	ENSG00000251466
5	lnc-HNRNPC-2	chr14:21652500-21653118	NONHSAT035662
6	lnc-SUPT16H-3	chr14:21731152-21731988	NONHSAT035670
7	lnc-RPGRIP1-2	chr14:21668434-21668954	ENSG00000247386
8	lnc-SUPT16H-3	chr14:21737457-21737601	NONHSAT035669
9	lnc-HNRNPC-1	chr14:21674770-21675059	ENSG00000251466
10	lnc-HNRNPC-1	chr14:21674770-21675059	NONHSAT035664
11	lnc-SUPT16H-3	chr14:21731470-21731988	NONHSAT035669
12	lnc-HNRNPC-1	chr14:21674770-21675059	ENSG00000258441
13	lnc-HNRNPC-1	chr14:21668238-21670092	NONHSAT035664
14	lnc-RPGRIP1-2	chr14:21669731-21672514	ENSG00000247386
15	lnc-C14orf176-4	chr14:21634603-21634734	ucscGeneNc_uc001wda_1
16	lnc-HNRNPC-1	chr14:21668240-21672514	NONHSAT035665
17	lnc-SUPT16H-3	chr14:21730762-21730857	NONHSAT035669
18	lnc-HNRNPC-1	chr14:21668620-21670092	ENSG00000258441

No data

(count:14 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	HNRNPC	hsa-miR-142-3p	chr14:21678567-21678589
2	HNRNPC	hsa-miR-30c-5p	chr14:21678673-21678667
3	HNRNPC	hsa-miR-30c-5p	chr14:21678667-21678690
4	HNRNPC	hsa-miR-186-5p	chr14:21679345-21679339
5	HNRNPC	hsa-miR-335-5p	chr14:21679069-21679091
6	SUPT16H	hsa-miR-615-3p	chr14:21820188-21820211
7	HNRNPC	hsa-miR-186-5p	chr14:21679046-21679067
8	SUPT16H	hsa-miR-16-5p	chr14:21819925-21819945
9	HNRNPC	hsa-miR-186-5p	chr14:21679340-21679361
10	SUPT16H	hsa-miR-25-3p	chr14:21820642-21820664
11	HNRNPC	hsa-miR-142-3p	chr14:21678022-21678046
12	HNRNPC	hsa-let-7e-5p	chr14:21679132-21679153
13	SUPT16H	hsa-miR-16-5p	chr14:21819931-21819925
14	HNRNPC	hsa-miR-335-5p	chr14:21678975-21678999

Variant related genes	Relation type
LINC00641	TF binding region
OR5AU1	TF binding region
SUPT16H	TF binding region
RPGRIP1	TF binding region
HNRNPC	TF binding region
ENSG00000258906	TF binding region
ENSG00000259102	TF binding region
LINC00641	CpG island
OR5AU1	CpG island
SUPT16H	CpG island
RPGRIP1	CpG island
HNRNPC	CpG island
ENSG00000258906	CpG island
ENSG00000259102	CpG island
ENSG00000175866	chromatin interactions
ENSG00000181481	chromatin interactions
ENSG00000162415	chromatin interactions
ENSG00000129514	chromatin interactions
ENSG00000034510	chromatin interactions
ENSG00000143442	chromatin interactions
ENSG00000258906	chromatin interactions
ENSG00000232070	chromatin interactions
ENSG00000108423	chromatin interactions
ENSG00000204054	chromatin interactions
ENSG00000100888	chromatin interactions
ENSG00000124193	chromatin interactions
ENSG00000139865	chromatin interactions
ENSG00000108443	chromatin interactions
ENSG00000092201	chromatin interactions
ENSG00000092199	chromatin interactions
ENSG00000260830	chromatin interactions
ENSG00000102096	chromatin interactions
ENSG00000165795	chromatin interactions
ENSG00000165804	chromatin interactions
ENSG00000092200	chromatin interactions
ENSG00000109919	chromatin interactions
ENSG00000258441	chromatin interactions
GFPT2	miRNA target sites
RUNX2	miRNA target sites
MTA2	miRNA target sites
STK4	miRNA target sites

Extended variants
information (count: 9439 )
Associated
traits (count: 78 )

Variant overlapped rSNPs/rCNVs (count:9439 , 50 per page) page: 1 2 3 4 5 6 7 ... 189

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539273239	chr14:21602373-21602374	Active TSS Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs559274309	chr14:21602438-21602439	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs576056391	chr14:21602443-21602444	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs66535106	chr14:21602508-21602509	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs185404381	chr14:21602529-21602530	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs113069920	chr14:21602559-21602560	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs573559712	chr14:21602584-21602585	Enhancers Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs71410263	chr14:21602624-21602625	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs192695623	chr14:21602636-21602637	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs140620678	chr14:21602647-21602648	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs528255354	chr14:21602648-21602649	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs150340354	chr14:21602654-21602655	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs564833915	chr14:21602702-21602703	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs184501389	chr14:21602710-21602711	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs537743932	chr14:21602783-21602784	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs138051534	chr14:21602786-21602787	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs199817148	chr14:21602787-21602788	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs530059775	chr14:21602836-21602837	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs547033792	chr14:21602847-21602848	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs562748955	chr14:21602876-21602877	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112150643	chr14:21602909-21602910	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs115660704	chr14:21602959-21602960	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs574367613	chr14:21602964-21602965	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs74037716	chr14:21603006-21603007	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs534740169	chr14:21603109-21603110	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs535116315	chr14:21603165-21603166	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs569483896	chr14:21603197-21603198	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs556513900	chr14:21603237-21603238	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs538495194	chr14:21603273-21603274	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs143209695	chr14:21603279-21603280	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs573546830	chr14:21603290-21603291	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs537649013	chr14:21603301-21603302	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs189215638	chr14:21603358-21603359	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs553306881	chr14:21603376-21603377	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs181191526	chr14:21603379-21603380	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs572648353	chr14:21603408-21603409	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs556818906	chr14:21603410-21603411	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs544792542	chr14:21603461-21603462	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs200520040	chr14:21603466-21603467	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs371666671	chr14:21603467-21603468	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs375002825	chr14:21603468-21603469	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs564695065	chr14:21603469-21603470	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs530620748	chr14:21603470-21603471	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs199613522	chr14:21603472-21603473	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs139952527	chr14:21603473-21603474	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs201607447	chr14:21603474-21603475	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs60258396	chr14:21603477-21603478	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs68179904	chr14:21603478-21603479	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12886116	chr14:21603479-21603480	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs117103034	chr14:21603497-21603498	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:78)

Disease	PMID	Source
Cancer	20164920	CNVD
Esophageal cancer	21851588	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cone-rod dystrophy	18421352	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20067559	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
Breast cancer	17899364	CNVD
Colorectal cancer	16774939	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	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
Endometrioid adenocarcinoma	16974079	CNVD
Myelofibrosis	22110671	CNVD
Alzheimer''s disease	21482944	CNVD
Mental retardation	19951919	CNVD
Neuroblastoma	21899760	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Heart disease	21282601	CNVD
Esophageal cancer	20955586	CNVD
Neurodevelopmental disorder	22521361	CNVD
Lung cancer	16773561	CNVD
Multiple myeloma	16616336	CNVD
Cancer	17440070	CNVD
Breast cancer	16272173	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Epilepsy	20736978	CNVD
Mental retardation	20736978	CNVD
severe speech impairment	20736978	CNVD
speech impairment	20736978	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
small cell lung cancer	20016488	CNVD
Developmental delay	21147756	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
Cancer	20164919	CNVD
Breast cancer	21364760	CNVD
Mortal	21835882	CNVD
Williams Syndrome	20824207	CNVD
Breast cancer	21858162	CNVD
Schizophrenia	20967226	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Autism	22102821	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Neuroblastoma	19536264	CNVD
Schizophrenia	23813976	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Ewing''s sarcoma	18628472	CNVD
early-passage human iPS cells	21368824	CNVD
Rheumatoid arthritis	23223014	CNVD

Chromatin state (count:5276 , 50 per page) page: 1 2 3 4 5 6 7 ... 106

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:21601400-21602400	Enhancers	HUES48 Cell Line	embryonic stem cell
2	chr14:21601400-21604000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
3	chr14:21601600-21602400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
4	chr14:21601600-21602400	Enhancers	HUES64 Cell Line	embryonic stem cell
5	chr14:21601600-21602400	Enhancers	iPS-18 Cell Line	embryonic stem cell
6	chr14:21601600-21602400	Enhancers	K562	blood
7	chr14:21601600-21603800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
8	chr14:21601800-21602400	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
9	chr14:21602000-21602400	Active TSS	ES-I3 Cell Line	embryonic stem cell
10	chr14:21602200-21602400	Flanking Active TSS	iPS-20b Cell Line	embryonic stem cell
11	chr14:21602200-21602400	Enhancers	Hela-S3	cervix
12	chr14:21602200-21602600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr14:21602200-21603800	Weak transcription	iPS-15b Cell Line	embryonic stem cell
14	chr14:21602600-21603800	Weak transcription	Hela-S3	cervix
15	chr14:21603800-21604200	Enhancers	H1 Cell Line	embryonic stem cell
16	chr14:21603800-21604200	Enhancers	iPS-15b Cell Line	embryonic stem cell
17	chr14:21603800-21604200	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
18	chr14:21603800-21604200	Enhancers	Hela-S3	cervix
19	chr14:21604000-21604200	Enhancers	iPS-18 Cell Line	embryonic stem cell
20	chr14:21604000-21604200	Enhancers	iPS-20b Cell Line	embryonic stem cell
21	chr14:21604200-21605200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr14:21605200-21605400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
23	chr14:21610200-21610600	Active TSS	HepG2	liver
24	chr14:21623200-21623400	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
25	chr14:21623200-21624200	Enhancers	K562	blood
26	chr14:21628400-21628600	Enhancers	Pancreas	Pancrea
27	chr14:21631000-21631800	Enhancers	Fetal Lung	lung
28	chr14:21631200-21631400	Bivalent Enhancer	Fetal Kidney	kidney
29	chr14:21631400-21632200	Enhancers	Fetal Kidney	kidney
30	chr14:21631600-21632200	Enhancers	Fetal Adrenal Gland	Adrenal Gland
31	chr14:21631800-21632200	Flanking Active TSS	Fetal Lung	lung
32	chr14:21632200-21632600	Enhancers	Fetal Lung	lung
33	chr14:21632600-21633200	Weak transcription	Fetal Lung	lung
34	chr14:21633200-21634000	Enhancers	Fetal Lung	lung
35	chr14:21633400-21634400	Bivalent Enhancer	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr14:21634000-21634400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
37	chr14:21634400-21637400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
38	chr14:21636200-21636400	Bivalent Enhancer	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
39	chr14:21636400-21636600	Enhancers	HMEC	breast
40	chr14:21636600-21637000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
41	chr14:21636600-21637600	Weak transcription	HMEC	breast
42	chr14:21637000-21638400	Enhancers	Foreskin Melanocyte Primary Cells skin01	Skin
43	chr14:21637200-21637400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
44	chr14:21637400-21638200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:21637600-21638000	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
46	chr14:21637600-21638200	Enhancers	HMEC	breast
47	chr14:21637800-21638600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
48	chr14:21638400-21638600	Flanking Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
49	chr14:21638600-21639000	Bivalent Enhancer	HepG2	liver
50	chr14:21638600-21639600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin

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