Variant report

Variant	nsv1043470
Chromosome Location	chr14:35398522-35754029
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:4548)
CpG islands
(count:2994)
Chromatin interactive
region (count:409)
LncRNA
region (count:37)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:4548 , 50 per page) page: 1 2 3 4 5 6 7 ... 91

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35628515-35629631	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35519876-35520224	K562	blood:	n/a	n/a
3	ARID3A	chr14:35615869-35616033	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35682775-35683608	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:35519909-35520120	HepG2	liver:	n/a	n/a
7	ARID3A	chr14:35450353-35450528	K562	blood:	n/a	n/a
8	ARID3A	chr14:35456533-35456710	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:35628114-35628276	HepG2	liver:	n/a	n/a
10	ARID3A	chr14:35590633-35592472	HepG2	liver:	n/a	chr14:35591480-35591488
11	ARID3A	chr14:35516133-35516303	HepG2	liver:	n/a	n/a
12	ARID3A	chr14:35591026-35591699	K562	blood:	n/a	chr14:35591480-35591488
13	ARID3A	chr14:35547257-35547542	HepG2	liver:	n/a	n/a
14	ARID3A	chr14:35698749-35699034	HepG2	liver:	n/a	n/a
15	ARID3A	chr14:35514746-35515759	HepG2	liver:	n/a	n/a
16	ARID3A	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
17	ARID3A	chr14:35537558-35537700	HepG2	liver:	n/a	n/a
18	ARID3A	chr14:35521017-35521344	HepG2	liver:	n/a	n/a
19	ARID3A	chr14:35658657-35659080	HepG2	liver:	n/a	n/a
20	ARID3A	chr14:35449799-35452898	HepG2	liver:	n/a	chr14:35452584-35452600
21	ARID3A	chr14:35509539-35510010	HepG2	liver:	n/a	chr14:35509792-35509808
22	ATF1	chr14:35727736-35727930	K562	blood:	n/a	n/a
23	ATF1	chr14:35515122-35515876	K562	blood:	n/a	n/a
24	ATF1	chr14:35451277-35452397	K562	blood:	n/a	chr14:35452182-35452196
25	ATF1	chr14:35629215-35629517	K562	blood:	n/a	n/a
26	ATF1	chr14:35519862-35520172	K562	blood:	n/a	n/a
27	ATF1	chr14:35517147-35517386	K562	blood:	n/a	n/a
28	ATF1	chr14:35590856-35592000	K562	blood:	n/a	n/a
29	ATF2	chr14:35451363-35452438	H1-hESC	embryonic stem cell:	n/a	chr14:35452182-35452196
30	ATF2	chr14:35590769-35591863	H1-hESC	embryonic stem cell:	n/a	n/a
31	ATF2	chr14:35591095-35591822	GM12878	blood:	n/a	n/a
32	ATF2	chr14:35590456-35592108	GM12878	blood:	n/a	n/a
33	ATF2	chr14:35451237-35452526	GM12878	blood:	n/a	chr14:35452182-35452196
34	ATF2	chr14:35451408-35452422	H1-hESC	embryonic stem cell:	n/a	chr14:35452182-35452196
35	ATF2	chr14:35504149-35504484	GM12878	blood:	n/a	n/a
36	ATF2	chr14:35514853-35515586	GM12878	blood:	n/a	n/a
37	ATF2	chr14:35590839-35591575	H1-hESC	embryonic stem cell:	n/a	n/a
38	ATF2	chr14:35723934-35724302	GM12878	blood:	n/a	n/a
39	ATF2	chr14:35515153-35515540	H1-hESC	embryonic stem cell:	n/a	n/a
40	ATF2	chr14:35451431-35452788	GM12878	blood:	n/a	chr14:35452182-35452196
41	ATF2	chr14:35515054-35515466	GM12878	blood:	n/a	n/a
42	ATF2	chr14:35515000-35515488	H1-hESC	embryonic stem cell:	n/a	n/a
43	ATF3	chr14:35451382-35452359	A549	lung:	n/a	n/a
44	ATF3	chr14:35515137-35515513	K562	blood:	n/a	chr14:35515349-35515364 chr14:35515353-35515360 chr14:35515353-35515361 chr14:35515353-35515363 chr14:35515352-35515360 chr14:35515350-35515363 chr14:35515353-35515363
45	ATF3	chr14:35591326-35591632	K562	blood:	n/a	chr14:35591484-35591504
46	ATF3	chr14:35591305-35591773	H1-hESC	embryonic stem cell:	n/a	chr14:35591484-35591504
47	ATF3	chr14:35629129-35629373	K562	blood:	n/a	n/a
48	ATF3	chr14:35591069-35591891	HepG2	liver:	n/a	chr14:35591484-35591504
49	ATF3	chr14:35591062-35591829	GM12878	blood:	n/a	chr14:35591484-35591504
50	ATF3	chr14:35590988-35592153	HepG2	liver:	n/a	chr14:35591484-35591504

(count:2994 , 50 per page) page: 1 2 3 4 5 6 7 ... 60

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35451962-35452012	AoSMC	blood vessel:	n/a
2	chr14:35451984-35452034	SK-N-SH	brain:	n/a
3	chr14:35451935-35451985	NH-A	brain:	n/a
4	chr14:35452420-35452470	GM19239	blood:	n/a
5	chr14:35591951-35592001	IMR90	lung:	fetal
6	chr14:35451962-35452012	AoSMC	blood vessel:	n/a
7	chr14:35451984-35452034	SK-N-SH	brain:	n/a
8	chr14:35451935-35451985	NH-A	brain:	n/a
9	chr14:35452420-35452470	GM19239	blood:	n/a
10	chr14:35591951-35592001	IMR90	lung:	fetal
11	chr14:35591781-35591831	HRPEpiC	eye:	n/a
12	chr14:35451962-35452012	SK-N-SH_RA	brain:	n/a
13	chr14:35452176-35452226	LNCaP	prostate:	n/a
14	chr14:35512367-35512417	SK-N-SH_RA	brain:	n/a
15	chr14:35587750-35587800	HepG2	liver:	n/a
16	chr14:35515356-35515406	BE2_C	brain:	n/a
17	chr14:35591572-35591622	NB4	blood:	n/a
18	chr14:35683834-35683884	RPTEC	kidney:	n/a
19	chr14:35451793-35451843	NB4	blood:	n/a
20	chr14:35447884-35447934	Hela-S3	cervix:	n/a
21	chr14:35408569-35408619	HCF	heart:	n/a
22	chr14:35495536-35495586	T-47D	breast:	n/a
23	chr14:35409083-35409133	NT2-D1	testis:	n/a
24	chr14:35591252-35591302	T-47D	breast:	n/a
25	chr14:35447884-35447934	HMEC	breast:	n/a
26	chr14:35629311-35629361	HepG2	liver:	n/a
27	chr14:35408569-35408619	GM12891	blood:	n/a
28	chr14:35540926-35540976	PANC-1	pancreas:	n/a
29	chr14:35452176-35452226	AoSMC	blood vessel:	n/a
30	chr14:35452441-35452491	GM12892	blood:	n/a
31	chr14:35409083-35409133	LNCaP	prostate:	n/a
32	chr14:35591625-35591675	HEEpiC	esophagus:	n/a
33	chr14:35452110-35452160	GM12878	blood:	n/a
34	chr14:35451962-35452012	BE2_C	brain:	n/a
35	chr14:35408569-35408619	K562	blood:	n/a
36	chr14:35629311-35629361	HPAEpiC	pulmonary alveolar:	n/a
37	chr14:35451935-35451985	H1-hESC	embryonic stem cell:	embryo
38	chr14:35498490-35498540	PANC-1	pancreas:	n/a
39	chr14:35515291-35515341	RPTEC	kidney:	n/a
40	chr14:35447884-35447934	U87	brain:	n/a
41	chr14:35583718-35583768	GM12891	blood:	n/a
42	chr14:35451556-35451606	Hepatocyte	liver:	n/a
43	chr14:35591781-35591831	HRCEpiC	kidney:	n/a
44	chr14:35591840-35591890	BJ	skin:	n/a
45	chr14:35515116-35515166	NB4	blood:	n/a
46	chr14:35591781-35591831	GM06990	blood:	n/a
47	chr14:35592116-35592166	MCF10A-Er-Src	breast:	n/a
48	chr14:35452602-35452652	SKMC	muscle:	n/a
49	chr14:35515116-35515166	SAEC	small airway:	n/a
50	chr14:35452110-35452160	HCT-116	colon:	n/a

(count:409 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Distal block	Cell Line	Cell type
1	chr14:35700495..35703278-chr14:35704050..35706629,2	K562	blood:
2	chr14:35515379..35516132-chr17:56736001..56736995,2	NB4	blood:
3	chr14:35703500..35705028-chr14:35708204..35710934,2	MCF-7	breast:
4	chr14:35726193..35729165-chr14:35868329..35870557,3	MCF-7	breast:
5	chr14:35744140..35746636-chr14:35750906..35752624,2	K562	blood:
6	chr14:35589606..35593451-chr14:35594804..35598522,5	K562	blood:
7	chr14:35680464..35682083-chr14:35684601..35686665,2	MCF-7	breast:
8	chr14:35583281..35585103-chr14:35589464..35591782,2	K562	blood:
9	chr14:35524936..35527808-chr14:35546522..35548065,2	MCF-7	breast:
10	chr14:35512802..35518057-chr14:35589980..35593805,9	MCF-7	breast:
11	chr14:35674645..35676555-chr14:35865462..35867142,2	MCF-7	breast:
12	chr14:35016883..35018423-chr14:35574764..35577501,2	MCF-7	breast:
13	chr14:35681924..35684171-chr14:35710768..35712492,2	MCF-7	breast:
14	chr14:35450146..35454994-chr14:35588530..35593322,8	MCF-7	breast:
15	chr14:35451626..35452173-chr16:74734654..74735645,2	Hela-S3	cervix:
16	chr14:35701570..35704183-chr14:35804617..35807506,4	MCF-7	breast:
17	chr14:35687707..35690246-chr14:35690578..35692404,2	MCF-7	breast:
18	chr14:35455186..35457809-chr14:35509575..35512529,2	K562	blood:
19	chr14:35451620..35453361-chr14:35464939..35467575,2	MCF-7	breast:
20	chr14:35734999..35737663-chr14:35744257..35745770,2	MCF-7	breast:
21	chr14:35698822..35700476-chr14:35705196..35707061,2	MCF-7	breast:
22	chr14:35514347..35516079-chr14:35590063..35591815,2	K562	blood:
23	chr14:35450906..35453739-chr14:35588377..35591005,2	K562	blood:
24	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
25	chr14:35449656..35453109-chr14:35514529..35517063,4	MCF-7	breast:
26	chr14:35737913..35739770-chr14:35744109..35746101,2	K562	blood:
27	chr14:35591181..35592726-chr14:35595848..35598610,3	MCF-7	breast:
28	chr14:35718039..35721234-chr14:35721513..35723379,3	MCF-7	breast:
29	chr14:35424726..35426528-chr14:35427204..35429694,2	K562	blood:
30	chr14:35568810..35572401-chr14:35587846..35592624,4	MCF-7	breast:
31	chr14:35723222..35726200-chr14:35728941..35731510,2	MCF-7	breast:
32	chr14:35579453..35581651-chr14:35585942..35587733,2	K562	blood:
33	chr14:35515172..35516906-chr14:35528396..35530412,2	K562	blood:
34	chr14:35500095..35502926-chr14:35557815..35560264,2	MCF-7	breast:
35	chr14:35590512..35592667-chr14:35626960..35629855,2	MCF-7	breast:
36	chr14:35579884..35582908-chr14:35589580..35593400,4	MCF-7	breast:
37	chr14:35515170..35517585-chr14:35518270..35521794,5	K562	blood:
38	chr14:35450019..35452754-chr14:35591061..35594828,4	K562	blood:
39	chr14:35681343..35684647-chr14:35685694..35689200,4	MCF-7	breast:
40	chr14:35466324..35467917-chr14:35470934..35473111,2	K562	blood:
41	chr14:35450099..35453742-chr14:35513316..35517237,10	K562	blood:
42	chr14:35750207..35752268-chr14:35757042..35759453,2	MCF-7	breast:
43	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
44	chr14:35705860..35707392-chr14:35712096..35713861,2	MCF-7	breast:
45	chr14:35489417..35492128-chr14:35497418..35499039,2	K562	blood:
46	chr14:35514169..35519549-chr14:35872431..35877872,11	MCF-7	breast:
47	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:
48	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
49	chr14:35451408..35453567-chr14:35454171..35458229,4	MCF-7	breast:
50	chr14:35622588..35627460-chr14:35872526..35876521,6	MCF-7	breast:

(count:37 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PPP2R3C-4	chr14:35676137-35676460	l_962_chr14:35668508-35676460_thyroid
2	lnc-PPP2R3C-4	chr14:35714373-35714399	l_962_chr14:35668508-35676460_thyroid
3	lnc-PPP2R3C-4	chr14:35704820-35705215	l_962_chr14:35668508-35676460_thyroid
4	lnc-RP11-173D9.3.1-3	chr14:35704074-35704252	l_963_chr14:35700899-35775195_brain
5	lnc-RP11-173D9.3.1-3	chr14:35704702-35704801	l_963_chr14:35700899-35775195_brain
6	lnc-RP11-173D9.3.1-1	chr14:35579776-35579932	ENSG00000247658
7	lnc-PPP2R3C-4	chr14:35704706-35704801	l_962_chr14:35668508-35676460_thyroid
8	lnc-PPP2R3C-4	chr14:35690827-35691028	l_962_chr14:35668508-35676460_thyroid
9	lnc-RP11-173D9.3.1-3	chr14:35703077-35703223	l_963_chr14:35700899-35775195_brain
10	lnc-PPP2R3C-4	chr14:35668509-35676125	l_962_chr14:35668508-35676460_thyroid
11	lnc-BAZ1A-3	chr14:35591108-35591185	NONHSAT036363
12	lnc-FAM177A1-2	chr14:35487835-35487971	NONHSAT036358
13	lnc-PPP2R3C-4	chr14:35704130-35704256	l_962_chr14:35668508-35676460_thyroid
14	lnc-SRP54-3	chr14:35436212-35436294	NONHSAT036352
15	lnc-RP11-173D9.3.1-3	chr14:35700900-35700969	l_963_chr14:35700899-35775195_brain
16	lnc-FAM177A1-2	chr14:35488172-35488564	NONHSAT036358
17	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366
18	lnc-PPP2R3C-2	chr14:35627110-35628305	NONHSAT036367
19	lnc-RP11-173D9.3.1-1	chr14:35579101-35579166	ENSG00000247658
20	lnc-PPP2R3C-4	chr14:35691819-35692693	l_962_chr14:35668508-35676460_thyroid
21	lnc-BAZ1A-3	chr14:35579129-35579835	NONHSAT036363
22	lnc-SRP54-5	chr14:35409128-35409702	NR_002937
23	lnc-PPP2R3C-3	chr14:35651558-35651951	uc_373_-
24	lnc-SRP54-3	chr14:35438376-35438513	NONHSAT036352
25	lnc-RP11-173D9.3.1-1	chr14:35568882-35571935	ENSG00000247658
26	lnc-FAM177A1-4	chr14:35651558-35651951	uc_373_+
27	lnc-PPP2R3C-4	chr14:35693328-35695629	l_962_chr14:35668508-35676460_thyroid
28	lnc-SRP54-3	chr14:35433120-35433246	NONHSAT036352
29	lnc-BAZ1A-1	chr14:35449441-35452103	NONHSAT036355
30	lnc-SRP54-3	chr14:35435735-35436151	NONHSAT036352
31	lnc-PPP2R3C-4	chr14:35692695-35692853	l_962_chr14:35668508-35676460_thyroid
32	lnc-RP11-173D9.3.1-3	chr14:35751529-35754015	l_963_chr14:35700899-35775195_brain
33	lnc-RP11-173D9.3.1-1	chr14:35575573-35575690	ENSG00000247658
34	lnc-BAZ1A-3	chr14:35585816-35585943	NONHSAT036363
35	lnc-PPP2R3C-4	chr14:35715251-35715712	l_962_chr14:35668508-35676460_thyroid
36	lnc-RP11-173D9.3.1-3	chr14:35750644-35751518	l_963_chr14:35700899-35775195_brain
37	lnc-PPP2R3C-4	chr14:35701581-35701640	l_962_chr14:35668508-35676460_thyroid

No data

(count:6 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	FAM177A1	hsa-miR-186-5p	chr14:35550483-35550504
2	FAM177A1	hsa-miR-142-3p	chr14:35551080-35551101
3	FAM177A1	hsa-miR-155-5p	chr14:35551927-35551947
4	FAM177A1	hsa-miR-186-5p	chr14:35551034-35551055
5	FAM177A1	hsa-miR-124-3p	chr14:35552521-35552538
6	FAM177A1	hsa-miR-124-3p	chr14:35552531-35552538

Variant related genes	Relation type
ENSG00000258704	TF binding region
ENSG00000241052	TF binding region
ENSG00000259090	TF binding region
RPL9P3	TF binding region
SRP54	TF binding region
PSMA6	TF binding region
FAM177A1	TF binding region
KIAA0391	TF binding region
ENSG00000258790	TF binding region
PPP2R3C	TF binding region
IGBP1P1	TF binding region
ENSG00000199980	TF binding region
RPL7AP3	TF binding region
ENSG00000258704	CpG island
ENSG00000241052	CpG island
ENSG00000259090	CpG island
RPL9P3	CpG island
SRP54	CpG island
PSMA6	CpG island
FAM177A1	CpG island
KIAA0391	CpG island
ENSG00000258790	CpG island
PPP2R3C	CpG island
IGBP1P1	CpG island
ENSG00000199980	CpG island
RPL7AP3	CpG island
ENSG00000168246	chromatin interactions
ENSG00000100902	chromatin interactions
ENSG00000272626	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000088888	chromatin interactions
ENSG00000267231	chromatin interactions
ENSG00000118454	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000134294	chromatin interactions
ENSG00000110958	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000129518	chromatin interactions
ENSG00000146834	chromatin interactions
ENSG00000198964	chromatin interactions
ENSG00000078487	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000185634	chromatin interactions
ENSG00000066135	chromatin interactions
ENSG00000097021	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000058262	chromatin interactions
ENSG00000271746	chromatin interactions
ENSG00000202077	chromatin interactions
ENSG00000235883	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000158850	chromatin interactions
ENSG00000126804	chromatin interactions
ENSG00000240392	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000168404	chromatin interactions
ENSG00000089775	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000161091	chromatin interactions
ENSG00000008130	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000249740	chromatin interactions
ENSG00000226200	chromatin interactions
ENSG00000234678	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000115275	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000185347	chromatin interactions
ENSG00000105643	chromatin interactions
ENSG00000163393	chromatin interactions
ENSG00000265530	chromatin interactions
ENSG00000145623	chromatin interactions
ENSG00000153066	chromatin interactions
ENSG00000163435	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000200156	chromatin interactions
ENSG00000141376	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000256243	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000206588	chromatin interactions
ENSG00000255302	chromatin interactions
ENSG00000251562	chromatin interactions
SAMD4B	miRNA target sites
C2CD4A	miRNA target sites
NEFM	miRNA target sites
FNDC3A	miRNA target sites

Extended variants
information (count: 13502 )
Associated
traits (count: 68 )

Variant overlapped rSNPs/rCNVs (count:13502 , 50 per page) page: 1 2 3 4 5 6 7 ... 271

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs539343567	chr14:35398542-35398543	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs116420973	chr14:35398565-35398566	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs571596352	chr14:35398580-35398581	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs191709074	chr14:35398583-35398584	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs547785529	chr14:35398584-35398585	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs182844597	chr14:35398607-35398608	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs536952477	chr14:35398617-35398618	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs371339548	chr14:35398621-35398622	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs556793875	chr14:35398629-35398630	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs576753723	chr14:35398643-35398644	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs537922825	chr14:35398646-35398647	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs140832156	chr14:35398689-35398690	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs557594469	chr14:35398756-35398757	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs566088131	chr14:35398764-35398765	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs57423929	chr14:35398832-35398833	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs398077686	chr14:35398840-35398841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs397697934	chr14:35398841-35398842	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs200478636	chr14:35398842-35398843	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs144622325	chr14:35398849-35398850	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374867046	chr14:35398872-35398873	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs71121244	chr14:35398878-35398879	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539811437	chr14:35398879-35398880	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs147953975	chr14:35398917-35398918	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573552831	chr14:35398981-35398982	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs1738801	chr14:35399035-35399036	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs187172792	chr14:35399048-35399049	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs546567827	chr14:35399062-35399063	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs562328849	chr14:35399067-35399068	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs544320278	chr14:35399129-35399130	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs545211161	chr14:35399189-35399190	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs190095872	chr14:35399190-35399191	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs527798326	chr14:35399204-35399205	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs182214540	chr14:35399251-35399252	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs567700599	chr14:35399295-35399296	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs564128826	chr14:35399397-35399398	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs533212278	chr14:35399413-35399414	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs140227646	chr14:35399429-35399430	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs78172780	chr14:35399479-35399480	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs77986249	chr14:35399480-35399481	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs557255674	chr14:35399484-35399485	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs28505870	chr14:35399505-35399506	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs530576608	chr14:35399511-35399512	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs187467488	chr14:35399513-35399514	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs542946741	chr14:35399595-35399596	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs559118927	chr14:35399661-35399662	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs145629754	chr14:35399710-35399711	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs193270016	chr14:35399719-35399720	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs533889628	chr14:35399743-35399744	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs75712566	chr14:35399748-35399749	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs573341844	chr14:35399785-35399786	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:68)

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
Colorectal cancer	16774939	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
Endometrioid adenocarcinoma	16974079	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
Esophageal cancer	20955586	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Burkitt''s lymphoma	19759907	CNVD
Lung cancer	18438408	CNVD
Urothelial carcinoma	21177765	CNVD
Multiple myeloma	17550852	CNVD
Breast cancer	21785460	CNVD
Breast cancer	21045282	CNVD
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	CNVD
Glioma	24330732	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21364760	CNVD
small cell lung cancer	20016488	CNVD
Cancer	20164919	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD
Cancer	20164920	CNVD

Chromatin state (count:8714 , 50 per page) page: 1 2 3 4 5 6 7 ... 175

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35381000-35398600	Weak transcription	Primary T cells from cord blood	blood
2	chr14:35381400-35412200	Weak transcription	Breast Myoepithelial Primary Cells	Breast
3	chr14:35384800-35398600	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
4	chr14:35389600-35411400	Weak transcription	Aorta	Aorta
5	chr14:35390000-35412600	Weak transcription	Ovary	ovary
6	chr14:35390200-35400600	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
7	chr14:35393000-35404400	Weak transcription	Left Ventricle	heart
8	chr14:35394600-35424000	Weak transcription	Fetal Lung	lung
9	chr14:35395600-35399400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
10	chr14:35396000-35400400	Weak transcription	A549	lung
11	chr14:35396400-35400200	Weak transcription	Muscle Satellite Cultured Cells	--
12	chr14:35396400-35400400	Weak transcription	Osteobl	bone
13	chr14:35396400-35425200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
14	chr14:35396600-35399600	Weak transcription	HUVEC	blood vessel
15	chr14:35396600-35424800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr14:35397200-35412800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
17	chr14:35397800-35399400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr14:35397800-35420600	Weak transcription	Thymus	Thymus
19	chr14:35398000-35408200	Weak transcription	Liver	Liver
20	chr14:35398200-35399200	Enhancers	Primary T helper cells PMA-I stimulated	--
21	chr14:35398200-35399600	Enhancers	Primary T regulatory cells fromperipheralblood	blood
22	chr14:35398200-35399800	Enhancers	Primary T cells fromperipheralblood	blood
23	chr14:35398200-35399800	Enhancers	Primary T helper naive cells fromperipheralblood	blood
24	chr14:35398200-35399800	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
25	chr14:35398200-35399800	Enhancers	Primary T helper cells fromperipheralblood	blood
26	chr14:35398200-35400800	Enhancers	Primary T helper 17 cells PMA-I stimulated	--
27	chr14:35398400-35399000	Enhancers	Primary T helper naive cells from peripheral blood	blood
28	chr14:35398400-35399200	Enhancers	Primary T killer naive cells fromperipheralblood	blood
29	chr14:35398400-35401000	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
30	chr14:35398400-35401200	Enhancers	Primary T killer memory cells from peripheral blood	blood
31	chr14:35398600-35399000	Enhancers	Primary mononuclear cells fromperipheralblood	Blood
32	chr14:35398600-35399800	Enhancers	Primary T cells from cord blood	blood
33	chr14:35398800-35410600	Weak transcription	Fetal Brain Male	brain
34	chr14:35399000-35399400	Flanking Active TSS	Primary T helper naive cells from peripheral blood	blood
35	chr14:35399000-35400000	Enhancers	Primary neutrophils fromperipheralblood	blood
36	chr14:35399000-35412200	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
37	chr14:35399200-35399400	Enhancers	Sigmoid Colon	Sigmoid Colon
38	chr14:35399200-35399600	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
39	chr14:35399200-35399600	Flanking Active TSS	Primary T killer naive cells fromperipheralblood	blood
40	chr14:35399200-35399800	Enhancers	Monocytes-CD14+_RO01746	blood
41	chr14:35399200-35400800	Flanking Active TSS	Primary T helper cells PMA-I stimulated	--
42	chr14:35399400-35399600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
43	chr14:35399400-35399800	Enhancers	Primary T helper naive cells from peripheral blood	blood
44	chr14:35399400-35400600	Flanking Active TSS	Primary T helper memory cells from peripheral blood 2	blood
45	chr14:35399400-35400800	Enhancers	Primary monocytes fromperipheralblood	blood
46	chr14:35399400-35402200	Weak transcription	HepG2	liver
47	chr14:35399400-35406800	Weak transcription	Sigmoid Colon	Sigmoid Colon
48	chr14:35399600-35399800	Enhancers	Primary T killer naive cells fromperipheralblood	blood
49	chr14:35399600-35400000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:35399600-35400400	Flanking Active TSS	Primary T regulatory cells fromperipheralblood	blood

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