Variant report

Variant	nsv1043033
Chromosome Location	chr14:31538984-31686696
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2528)
CpG islands
(count:1037)
Chromatin interactive
region (count:124)
LncRNA
region (count:3)
Mature miRNA
region (count: 0)
miRNA target
sites (count:1)

(count:2528 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:31676990-31677431	K562	blood:	n/a	n/a
2	ARID3A	chr14:31559886-31561386	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:31676703-31678030	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:31549348-31549622	K562	blood:	n/a	n/a
5	ARID3A	chr14:31561638-31561823	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:31551219-31551628	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:31669217-31669582	K562	blood:	n/a	n/a
8	ARID3A	chr14:31674388-31675448	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:31667026-31667216	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:31596940-31597257	HepG2	liver:	n/a	n/a
11	ARID3A	chr14:31551258-31551518	K562	blood:	n/a	n/a
12	ARID3A	chr14:31633342-31633560	HepG2	liver:	n/a	n/a
13	ARID3A	chr14:31573701-31573703	K562	blood:	n/a	n/a
14	ATF1	chr14:31669163-31669692	K562	blood:	n/a	n/a
15	ATF1	chr14:31677060-31677669	K562	blood:	n/a	n/a
16	ATF1	chr14:31560047-31560326	K562	blood:	n/a	n/a
17	ATF2	chr14:31677042-31678003	GM12878	blood:	n/a	n/a
18	ATF2	chr14:31676407-31678063	GM12878	blood:	n/a	n/a
19	ATF3	chr14:31677261-31677456	K562	blood:	n/a	n/a
20	ATF3	chr14:31676703-31677570	HepG2	liver:	n/a	n/a
21	ATF3	chr14:31676915-31677439	A549	lung:	n/a	n/a
22	BACH1	chr14:31551367-31551442	K562	blood:	n/a	n/a
23	BACH1	chr14:31551362-31551542	H1-hESC	embryonic stem cell:	n/a	n/a
24	BACH1	chr14:31677868-31678382	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr14:31677838-31678318	K562	blood:	n/a	n/a
26	BACH1	chr14:31676759-31677544	H1-hESC	embryonic stem cell:	n/a	n/a
27	BATF	chr14:31675862-31676128	GM12878	blood:	n/a	n/a
28	BATF	chr14:31674187-31674369	GM12878	blood:	n/a	n/a
29	BATF	chr14:31677421-31677753	GM12878	blood:	n/a	n/a
30	BATF	chr14:31674199-31674376	GM12878	blood:	n/a	n/a
31	BATF	chr14:31668869-31669082	GM12878	blood:	n/a	n/a
32	BATF	chr14:31676959-31677963	GM12878	blood:	n/a	n/a
33	BCL11A	chr14:31677063-31677802	GM12878	blood:	n/a	chr14:31677127-31677136 chr14:31677128-31677141 chr14:31677735-31677744
34	BCL11A	chr14:31677431-31677721	GM12878	blood:	n/a	n/a
35	BCL3	chr14:31676550-31677764	GM12878	blood:	n/a	chr14:31676793-31676806 chr14:31676657-31676670 chr14:31677127-31677136 chr14:31677128-31677141 chr14:31676658-31676671 chr14:31677735-31677744
36	BCL3	chr14:31632146-31632372	GM12878	blood:	n/a	n/a
37	BCL3	chr14:31591162-31591914	GM12878	blood:	n/a	n/a
38	BCL3	chr14:31591200-31591803	GM12878	blood:	n/a	n/a
39	BCL3	chr14:31676887-31677511	A549	lung:	n/a	chr14:31677127-31677136 chr14:31677128-31677141
40	BCLAF1	chr14:31676731-31677179	K562	blood:	n/a	chr14:31676793-31676806 chr14:31677127-31677136 chr14:31677128-31677141
41	BCLAF1	chr14:31676395-31677778	GM12878	blood:	n/a	chr14:31676793-31676806 chr14:31676657-31676670 chr14:31677127-31677136 chr14:31677128-31677141 chr14:31676658-31676671 chr14:31677735-31677744
42	BCLAF1	chr14:31675817-31677890	GM12878	blood:	n/a	chr14:31676793-31676806 chr14:31676657-31676670 chr14:31677127-31677136 chr14:31677128-31677141 chr14:31676112-31676125 chr14:31676658-31676671 chr14:31677735-31677744
43	BHLHE40	chr14:31676423-31677673	K562	blood:	n/a	chr14:31676458-31676474
44	BHLHE40	chr14:31674857-31675534	HepG2	liver:	n/a	n/a
45	BHLHE40	chr14:31596986-31597291	GM12878	blood:	n/a	n/a
46	BHLHE40	chr14:31553603-31553952	K562	blood:	n/a	chr14:31553795-31553816
47	BHLHE40	chr14:31664389-31664443	A549	lung:	n/a	n/a
48	BHLHE40	chr14:31553571-31554024	GM12878	blood:	n/a	chr14:31553795-31553816
49	BHLHE40	chr14:31676672-31677696	HepG2	liver:	n/a	n/a
50	BHLHE40	chr14:31676948-31677268	A549	lung:	n/a	n/a

(count:1037 , 50 per page) page: 1 2 3 4 5 6 7 ... 21

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:31677716-31677766	Caco-2	colon:	n/a
2	chr14:31676207-31676257	Hela-S3	cervix:	n/a
3	chr14:31673220-31673270	AG10803	skin:	n/a
4	chr14:31554343-31554393	HUVEC	blood vessel:	n/a
5	chr14:31549691-31549741	SKMC	muscle:	n/a
6	chr14:31676811-31676861	AG09319	gingival:	n/a
7	chr14:31607371-31607421	HEK293	kidney:	embryo
8	chr14:31677288-31677338	HUVEC	blood vessel:	n/a
9	chr14:31676811-31676861	HAEpiC	amniotic membrane:	n/a
10	chr14:31677219-31677269	RPTEC	kidney:	n/a
11	chr14:31673220-31673270	MCF10A-Er-Src	breast:	n/a
12	chr14:31607371-31607421	HCPEpiC	choroid plexus:	n/a
13	chr14:31676328-31676378	AG04449	skin:	fetal
14	chr14:31676328-31676378	PFSK-1	brain:	n/a
15	chr14:31677288-31677338	CMK	blood:	n/a
16	chr14:31676815-31676865	T-47D	breast:	n/a
17	chr14:31560529-31560579	HCM	heart:	n/a
18	chr14:31676328-31676378	GM12892	blood:	n/a
19	chr14:31554343-31554393	HRCEpiC	kidney:	n/a
20	chr14:31560529-31560579	LNCaP	prostate:	n/a
21	chr14:31677445-31677495	A549	lung:	n/a
22	chr14:31677219-31677269	ovcar-3	ovarian:	n/a
23	chr14:31677288-31677338	HEEpiC	esophagus:	n/a
24	chr14:31677445-31677495	BE2_C	brain:	n/a
25	chr14:31676207-31676257	CMK	blood:	n/a
26	chr14:31676811-31676861	Jurkat	blood:	n/a
27	chr14:31675363-31675413	ECC-1	luminal epithelium:	n/a
28	chr14:31677288-31677338	GM19239	blood:	n/a
29	chr14:31675363-31675413	Hepatocyte	liver:	n/a
30	chr14:31676207-31676257	LNCaP	prostate:	n/a
31	chr14:31677445-31677495	HRPEpiC	eye:	n/a
32	chr14:31676815-31676865	HepG2	liver:	n/a
33	chr14:31676207-31676257	SK-N-MC	brain:	n/a
34	chr14:31676811-31676861	H1-hESC	embryonic stem cell:	embryo
35	chr14:31677219-31677269	PANC-1	pancreas:	n/a
36	chr14:31549691-31549741	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:31676815-31676865	AG09309	skin:	n/a
38	chr14:31677219-31677269	HMEC	breast:	n/a
39	chr14:31673220-31673270	AG09319	gingival:	n/a
40	chr14:31673220-31673270	SK-N-MC	brain:	n/a
41	chr14:31677716-31677766	HepG2	liver:	n/a
42	chr14:31554343-31554393	AG04449	skin:	fetal
43	chr14:31554343-31554393	NHBE	bronchial:	n/a
44	chr14:31554343-31554393	SAEC	small airway:	n/a
45	chr14:31677288-31677338	HRE	kidney:	n/a
46	chr14:31676811-31676861	MCF10A-Er-Src	breast:	n/a
47	chr14:31676207-31676257	Caco-2	colon:	n/a
48	chr14:31673220-31673270	LNCaP	prostate:	n/a
49	chr14:31677716-31677766	AG09309	skin:	n/a
50	chr14:31676328-31676378	HL-60	blood:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:31654015..31655608-chr14:31658189..31660066,2	K562	blood:
2	chr14:31654015..31655608-chr14:31658189..31660066,2	K562	blood:
3	chr14:31659869..31661727-chr14:31675637..31677459,2	MCF-7	breast:
4	chr14:31566343..31568008-chr14:31570057..31571588,2	K562	blood:
5	chr14:31680131..31682350-chr14:31698979..31700901,2	K562	blood:
6	chr14:31592934..31595654-chr14:31599577..31602427,2	MCF-7	breast:
7	chr14:31662501..31665350-chr14:31676259..31678758,2	MCF-7	breast:
8	chr14:31665590..31668355-chr14:31670115..31671744,2	MCF-7	breast:
9	chr14:31676908..31677885-chr20:25604560..25605123,2	Hela-S3	cervix:
10	chr14:31590905..31593026-chr14:31610871..31613579,2	MCF-7	breast:
11	chr14:31449072..31450058-chr14:31550875..31551908,4	MCF-7	breast:
12	chr14:31642217..31644395-chr14:31650577..31652161,2	MCF-7	breast:
13	chr14:31494347..31495920-chr14:31544461..31546849,2	MCF-7	breast:
14	chr14:31588557..31591164-chr14:31676122..31677690,2	MCF-7	breast:
15	chr14:31621746..31624641-chr14:31675931..31678702,3	MCF-7	breast:
16	chr14:31677097..31678008-chr20:30194510..30195209,2	Hela-S3	cervix:
17	chr14:31577991..31579631-chr14:31580157..31582860,2	K562	blood:
18	chr14:31659369..31661634-chr14:31664053..31665953,2	MCF-7	breast:
19	chr14:31676213..31678874-chr14:31679615..31681870,3	K562	blood:
20	chr14:31344003..31345728-chr14:31604211..31605992,2	K562	blood:
21	chr14:31657985..31659593-chr14:31664052..31666042,2	MCF-7	breast:
22	chr14:31667340..31669101-chr14:31670075..31672615,3	MCF-7	breast:
23	chr14:31676195..31678341-chr2:204101427..204103984,2	MCF-7	breast:
24	chr14:31595755..31597635-chr14:31675471..31677370,2	MCF-7	breast:
25	chr14:31494105..31496790-chr14:31544703..31548574,4	MCF-7	breast:
26	chr14:31605351..31607300-chr14:31607732..31611422,3	MCF-7	breast:
27	chr14:31495967..31497568-chr14:31552055..31553964,3	K562	blood:
28	chr14:31665590..31668355-chr14:31670115..31671744,2	MCF-7	breast:
29	chr14:31450203..31451782-chr14:31545197..31546790,2	K562	blood:
30	chr14:31595755..31597635-chr14:31675471..31677370,2	MCF-7	breast:
31	chr14:31493111..31496047-chr14:31549008..31551334,2	K562	blood:
32	chr14:31677297..31678964-chr14:31721572..31723567,2	K562	blood:
33	chr14:31612683..31614896-chr14:31619951..31622680,2	MCF-7	breast:
34	chr14:31632859..31634674-chr14:31887471..31889887,2	MCF-7	breast:
35	chr14:31677392..31679217-chr14:31684991..31686865,2	MCF-7	breast:
36	chr14:31592934..31595654-chr14:31599577..31602427,2	MCF-7	breast:
37	chr14:31493306..31495804-chr14:31540351..31542443,2	MCF-7	breast:
38	chr14:31504745..31506428-chr14:31545787..31548074,2	K562	blood:
39	chr14:31623239..31625541-chr14:31675591..31677755,2	MCF-7	breast:
40	chr14:31677123..31678687-chr14:31776671..31778228,2	MCF-7	breast:
41	chr14:31677147..31677806-chr7:77167282..77168042,2	NB4	blood:
42	chr14:31632190..31633831-chr14:31674115..31678545,3	MCF-7	breast:
43	chr14:31548388..31550747-chr14:31553010..31555958,3	K562	blood:
44	chr14:31576791..31579720-chr14:31584200..31586773,2	MCF-7	breast:
45	chr14:31675418..31678639-chr14:31811864..31816181,5	MCF-7	breast:
46	chr14:31601478..31601997-chr3:62322077..62322936,2	MCF-7	breast:
47	chr14:31493616..31495498-chr14:31675892..31677511,2	K562	blood:
48	chr14:31494054..31496618-chr14:31538814..31541069,2	MCF-7	breast:
49	chr14:31675912..31678861-chr14:31887661..31889789,2	K562	blood:
50	chr14:31545887..31548153-chr14:31549801..31551382,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STRN3-5	chr14:31580775-31581013	NONHSAT036266
2	lnc-STRN3-5	chr14:31581213-31581445	NONHSAT036266
3	lnc-STRN3-11	chr14:31614377-31615656	l_960_NR_027263

No data

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

No.	miRNA target gene	miRNA name	Chromosome Location	mirBase accession
1	AP4S1	hsa-miR-15b-5p	chr14:31554320-31554342

Variant related genes	Relation type
RPL21P5	TF binding region
RNU6-541P	TF binding region
HECTD1	TF binding region
RPL21P5	CpG island
RNU6-541P	CpG island
HECTD1	CpG island
ENSG00000111412	chromatin interactions
ENSG00000120688	chromatin interactions
ENSG00000143373	chromatin interactions
ENSG00000170191	chromatin interactions
ENSG00000196792	chromatin interactions
ENSG00000127947	chromatin interactions
ENSG00000232671	chromatin interactions
ENSG00000258640	chromatin interactions
ENSG00000168906	chromatin interactions
ENSG00000207440	chromatin interactions
ENSG00000092148	chromatin interactions
ENSG00000075413	chromatin interactions
ENSG00000197006	chromatin interactions
ENSG00000213742	chromatin interactions
ENSG00000264395	chromatin interactions
ENSG00000120690	chromatin interactions
ENSG00000135119	chromatin interactions
ENSG00000129493	chromatin interactions
ENSG00000100478	chromatin interactions
ENSG00000203546	chromatin interactions
ENSG00000119004	chromatin interactions
ENSG00000250365	chromatin interactions
ENSG00000129480	chromatin interactions

Extended variants
information (count: 5780 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:5780 , 50 per page) page: 1 2 3 4 5 6 7 ... 116

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs7155228	chr14:31538984-31538985	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs373580909	chr14:31538992-31538993	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs376103605	chr14:31539000-31539001	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs373434958	chr14:31539005-31539006	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs376464870	chr14:31539007-31539008	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs370458778	chr14:31539028-31539029	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs373657445	chr14:31539039-31539040	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs201008573	chr14:31539058-31539059	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs150801272	chr14:31539064-31539065	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs368658371	chr14:31539070-31539071	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs371132403	chr14:31539078-31539079	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs374522050	chr14:31539081-31539082	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs545328119	chr14:31539088-31539089	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs370582826	chr14:31539089-31539090	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs367967945	chr14:31539100-31539101	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs554442025	chr14:31539132-31539133	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs375129249	chr14:31539145-31539146	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs571747732	chr14:31539230-31539231	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs542199833	chr14:31539275-31539276	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs560677470	chr14:31539308-31539309	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550007298	chr14:31539320-31539321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs543612674	chr14:31539326-31539327	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs564883922	chr14:31539358-31539359	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs146323504	chr14:31539361-31539362	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs186610954	chr14:31539375-31539376	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs573786535	chr14:31539403-31539404	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192400725	chr14:31539440-31539441	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs549372966	chr14:31539487-31539488	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs574053043	chr14:31539502-31539503	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs367811988	chr14:31539505-31539506	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs537910016	chr14:31539508-31539509	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs61976852	chr14:31539558-31539559	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs550351441	chr14:31539559-31539560	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs571793444	chr14:31539605-31539606	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs369267627	chr14:31539632-31539633	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs539212755	chr14:31539739-31539740	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554077621	chr14:31539741-31539742	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs139637934	chr14:31539775-31539776	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs73252178	chr14:31539837-31539838	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs144381246	chr14:31539885-31539886	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs182016296	chr14:31539948-31539949	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs543200833	chr14:31539968-31539969	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs77211541	chr14:31539980-31539981	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs117588309	chr14:31539984-31539985	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541200902	chr14:31539986-31539987	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561787718	chr14:31539989-31539990	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs559708993	chr14:31540028-31540029	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs529984343	chr14:31540054-31540055	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs540150168	chr14:31540055-31540056	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs549404393	chr14:31540086-31540087	Enhancers Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

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
Autism	22495311	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
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
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Chronic myeloid leukemia	20724749	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Cancer	21183584	CNVD
Leukoplakia	24403051	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Chronic myeloid leukemia	16756668	CNVD
Sudden cardiac death	19188705	CNVD
Pilocytic astrocytoma	18670637	CNVD
Multiple myeloma	16616336	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
small cell lung cancer	20016488	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21364760	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:4388 , 50 per page) page: 1 2 3 4 5 6 7 ... 88

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:31497000-31568600	Weak transcription	Fetal Kidney	kidney
2	chr14:31497600-31552800	Weak transcription	Fetal Muscle Trunk	muscle
3	chr14:31501200-31544200	Weak transcription	Primary B cells from cord blood	blood
4	chr14:31501200-31550000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
5	chr14:31507200-31539200	Weak transcription	Fetal Stomach	stomach
6	chr14:31507800-31549600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
7	chr14:31522800-31552800	Weak transcription	Stomach Smooth Muscle	stomach
8	chr14:31522800-31553600	Weak transcription	Lung	lung
9	chr14:31528000-31544000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
10	chr14:31528200-31543200	Weak transcription	Primary B cells from peripheral blood	blood
11	chr14:31528600-31567200	Weak transcription	Primary hematopoietic stem cells	blood
12	chr14:31528800-31541600	Weak transcription	Duodenum Smooth Muscle	Duodenum
13	chr14:31528800-31552800	Weak transcription	Fetal Brain Female	brain
14	chr14:31528800-31559600	Weak transcription	Liver	Liver
15	chr14:31529000-31554400	Weak transcription	Colonic Mucosa	Colon
16	chr14:31529000-31559600	Weak transcription	Skeletal Muscle Male	skeletal muscle
17	chr14:31529000-31559800	Weak transcription	Duodenum Mucosa	Duodenum
18	chr14:31529600-31554000	Weak transcription	Spleen	Spleen
19	chr14:31529800-31539600	Weak transcription	Ovary	ovary
20	chr14:31529800-31548200	Weak transcription	Right Atrium	heart
21	chr14:31529800-31549600	Weak transcription	Esophagus	oesophagus
22	chr14:31529800-31559800	Weak transcription	Small Intestine	intestine
23	chr14:31529800-31566200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
24	chr14:31530000-31539200	Weak transcription	Fetal Intestine Small	intestine
25	chr14:31530000-31539400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
26	chr14:31530000-31539400	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr14:31530000-31539400	Weak transcription	Fetal Muscle Leg	muscle
28	chr14:31530000-31539600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
29	chr14:31530000-31541600	Weak transcription	Pancreas	Pancrea
30	chr14:31530000-31542800	Weak transcription	Fetal Intestine Large	intestine
31	chr14:31530000-31543200	Weak transcription	HUES48 Cell Line	embryonic stem cell
32	chr14:31530000-31544000	Weak transcription	HUES64 Cell Line	embryonic stem cell
33	chr14:31530000-31553000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
34	chr14:31530000-31567000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
35	chr14:31530000-31567200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
36	chr14:31530600-31539400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
37	chr14:31530800-31559400	Weak transcription	Skeletal Muscle Female	skeletal muscle
38	chr14:31533000-31553200	Weak transcription	Brain Anterior Caudate	brain
39	chr14:31533400-31560000	Weak transcription	Left Ventricle	heart
40	chr14:31534200-31566400	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
41	chr14:31534400-31566200	Weak transcription	Fetal Thymus	thymus
42	chr14:31534600-31539200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
43	chr14:31534600-31539600	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
44	chr14:31534600-31572000	Weak transcription	Primary T killer memory cells from peripheral blood	blood
45	chr14:31534800-31543200	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
46	chr14:31534800-31569200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
47	chr14:31535800-31548000	Weak transcription	Hela-S3	cervix
48	chr14:31536200-31559800	Weak transcription	Brain Angular Gyrus	brain
49	chr14:31536400-31566000	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr14:31536600-31559600	Weak transcription	Sigmoid Colon	Sigmoid Colon

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