Variant report

Variant	nsv1050700
Chromosome Location	chr14:35548276-35639084
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1252)
CpG islands
(count:979)
Chromatin interactive
region (count:113)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:6)

(count:1252 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35615869-35616033	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35628114-35628276	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35591026-35591699	K562	blood:	n/a	chr14:35591480-35591488
5	ARID3A	chr14:35628515-35629631	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:35590633-35592472	HepG2	liver:	n/a	chr14:35591480-35591488
7	ARID3A	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
8	ATF1	chr14:35629215-35629517	K562	blood:	n/a	n/a
9	ATF1	chr14:35590856-35592000	K562	blood:	n/a	n/a
10	ATF2	chr14:35590769-35591863	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr14:35590839-35591575	H1-hESC	embryonic stem cell:	n/a	n/a
12	ATF2	chr14:35590456-35592108	GM12878	blood:	n/a	n/a
13	ATF2	chr14:35591095-35591822	GM12878	blood:	n/a	n/a
14	ATF3	chr14:35591305-35591773	H1-hESC	embryonic stem cell:	n/a	chr14:35591484-35591504
15	ATF3	chr14:35591069-35591891	HepG2	liver:	n/a	chr14:35591484-35591504
16	ATF3	chr14:35629129-35629373	K562	blood:	n/a	n/a
17	ATF3	chr14:35591062-35591829	GM12878	blood:	n/a	chr14:35591484-35591504
18	ATF3	chr14:35591254-35591787	A549	lung:	n/a	chr14:35591484-35591504
19	ATF3	chr14:35590988-35592153	HepG2	liver:	n/a	chr14:35591484-35591504
20	ATF3	chr14:35591368-35591602	GM12878	blood:	n/a	chr14:35591484-35591504
21	ATF3	chr14:35591326-35591632	K562	blood:	n/a	chr14:35591484-35591504
22	BATF	chr14:35629074-35629473	GM12878	blood:	n/a	chr14:35629286-35629297 chr14:35629287-35629297
23	BATF	chr14:35629052-35629485	GM12878	blood:	n/a	chr14:35629286-35629297 chr14:35629287-35629297
24	BATF	chr14:35591663-35591964	GM12878	blood:	n/a	n/a
25	BCL11A	chr14:35629109-35629431	GM12878	blood:	n/a	chr14:35629290-35629299 chr14:35629289-35629298
26	BCL3	chr14:35590607-35591936	A549	lung:	n/a	n/a
27	BCL3	chr14:35590950-35592103	A549	lung:	n/a	n/a
28	BCL3	chr14:35628914-35629626	A549	lung:	n/a	chr14:35629290-35629299 chr14:35629289-35629298
29	BCLAF1	chr14:35590896-35592186	GM12878	blood:	n/a	n/a
30	BCLAF1	chr14:35590870-35592203	GM12878	blood:	n/a	n/a
31	BHLHE40	chr14:35590781-35592288	GM12878	blood:	n/a	n/a
32	BHLHE40	chr14:35590749-35592231	HepG2	liver:	n/a	n/a
33	BHLHE40	chr14:35590665-35592190	K562	blood:	n/a	n/a
34	BHLHE40	chr14:35591280-35591665	A549	lung:	n/a	n/a
35	BHLHE40	chr14:35628362-35628811	HepG2	liver:	n/a	n/a
36	BRCA1	chr14:35613335-35613393	GM12878	blood:	n/a	n/a
37	BRCA1	chr14:35629077-35629584	Hela-S3	cervix:	n/a	n/a
38	BRCA1	chr14:35590603-35591644	H1-hESC	embryonic stem cell:	n/a	n/a
39	BRCA1	chr14:35591074-35592013	HepG2	liver:	n/a	n/a
40	BRCA1	chr14:35590611-35592191	Hela-S3	cervix:	n/a	n/a
41	CBX3	chr14:35590828-35591964	K562	blood:	n/a	n/a
42	CBX3	chr14:35602269-35602685	K562	blood:	n/a	n/a
43	CBX3	chr14:35580846-35581125	K562	blood:	n/a	n/a
44	CBX3	chr14:35580902-35581120	K562	blood:	n/a	n/a
45	CBX3	chr14:35602360-35602546	K562	blood:	n/a	n/a
46	CCNT2	chr14:35590784-35592019	K562	blood:	n/a	n/a
47	CCNT2	chr14:35629331-35629550	K562	blood:	n/a	n/a
48	CEBPB	chr14:35605476-35605702	HepG2	liver:	n/a	n/a
49	CEBPB	chr14:35619064-35619239	HepG2	liver:	n/a	chr14:35619155-35619166
50	CEBPB	chr14:35629119-35629473	IMR90	lung:	n/a	n/a

(count:979 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35589334-35589384	GM12892	blood:	n/a
2	chr14:35591695-35591745	HRPEpiC	eye:	n/a
3	chr14:35589334-35589384	PFSK-1	brain:	n/a
4	chr14:35589334-35589384	GM12892	blood:	n/a
5	chr14:35591695-35591745	HRPEpiC	eye:	n/a
6	chr14:35589334-35589384	PFSK-1	brain:	n/a
7	chr14:35587750-35587800	HepG2	liver:	n/a
8	chr14:35591473-35591523	HPAEpiC	pulmonary alveolar:	n/a
9	chr14:35591523-35591573	Caco-2	colon:	n/a
10	chr14:35591781-35591831	H1-hESC	embryonic stem cell:	embryo
11	chr14:35629311-35629361	HAEpiC	amniotic membrane:	n/a
12	chr14:35591252-35591302	GM19239	blood:	n/a
13	chr14:35592116-35592166	SKMC	muscle:	n/a
14	chr14:35587750-35587800	MCF-7	breast:	n/a
15	chr14:35583718-35583768	IMR90	lung:	fetal
16	chr14:35592116-35592166	Jurkat	blood:	n/a
17	chr14:35587750-35587800	AoSMC	blood vessel:	n/a
18	chr14:35591695-35591745	K562	blood:	n/a
19	chr14:35591779-35591829	HEEpiC	esophagus:	n/a
20	chr14:35591473-35591523	CMK	blood:	n/a
21	chr14:35591252-35591302	SK-N-MC	brain:	n/a
22	chr14:35591625-35591675	T-47D	breast:	n/a
23	chr14:35591252-35591302	HRPEpiC	eye:	n/a
24	chr14:35591840-35591890	ProgFib	skin:	n/a
25	chr14:35583718-35583768	LNCaP	prostate:	n/a
26	chr14:35587750-35587800	AG04449	skin:	fetal
27	chr14:35591695-35591745	HPAEpiC	pulmonary alveolar:	n/a
28	chr14:35591473-35591523	RPTEC	kidney:	n/a
29	chr14:35591572-35591622	NHDF-neo	bronchial:	n/a
30	chr14:35592116-35592166	LNCaP	prostate:	n/a
31	chr14:35589334-35589384	U87	brain:	n/a
32	chr14:35594356-35594406	A549	lung:	n/a
33	chr14:35587750-35587800	HIPEpiC	eye:	n/a
34	chr14:35587750-35587800	SKMC	muscle:	n/a
35	chr14:35591473-35591523	GM12878	blood:	n/a
36	chr14:35591951-35592001	PANC-1	pancreas:	n/a
37	chr14:35594356-35594406	T-47D	breast:	n/a
38	chr14:35591473-35591523	HL-60	blood:	n/a
39	chr14:35591252-35591302	BE2_C	brain:	n/a
40	chr14:35591625-35591675	RPTEC	kidney:	n/a
41	chr14:35591473-35591523	NT2-D1	testis:	n/a
42	chr14:35583718-35583768	HRCEpiC	kidney:	n/a
43	chr14:35591781-35591831	SK-N-SH	brain:	n/a
44	chr14:35594356-35594406	GM06990	blood:	n/a
45	chr14:35591523-35591573	HRCEpiC	kidney:	n/a
46	chr14:35591473-35591523	SKMC	muscle:	n/a
47	chr14:35591951-35592001	BE2_C	brain:	n/a
48	chr14:35587750-35587800	NHBE	bronchial:	n/a
49	chr14:35591951-35592001	IMR90	lung:	fetal
50	chr14:35583718-35583768	Hepatocyte	liver:	n/a

(count:113 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:35571820..35573660-chr14:35580909..35583356,2	MCF-7	breast:
2	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
3	chr14:35592944..35595456-chr14:35809160..35811582,2	K562	blood:
4	chr14:35571820..35573660-chr14:35580909..35583356,2	MCF-7	breast:
5	chr14:35590482..35592799-chr14:35601392..35603277,2	MCF-7	breast:
6	chr14:35560221..35562617-chr14:35563701..35566461,3	MCF-7	breast:
7	chr14:35616325..35618402-chr14:35627328..35629037,2	MCF-7	breast:
8	chr14:35589827..35591407-chr14:35592886..35594751,2	K562	blood:
9	chr14:35582794..35584767-chr14:35585993..35588866,2	MCF-7	breast:
10	chr14:35622836..35624862-chr14:35627590..35631684,4	MCF-7	breast:
11	chr14:35634398..35636898-chr14:35641045..35642555,2	K562	blood:
12	chr14:35636158..35638112-chr14:35872373..35874812,2	MCF-7	breast:
13	chr14:35625114..35628050-chr14:35869275..35871381,2	MCF-7	breast:
14	chr14:35342567..35345567-chr14:35590904..35592504,3	MCF-7	breast:
15	chr14:35565651..35568101-chr14:35571541..35574493,2	K562	blood:
16	chr14:35604150..35607008-chr14:35873146..35874686,2	MCF-7	breast:
17	chr14:35589196..35594400-chr14:35871301..35877730,13	MCF-7	breast:
18	chr14:35568810..35572401-chr14:35587846..35592624,4	MCF-7	breast:
19	chr14:35629587..35631138-chr14:35874069..35875682,2	MCF-7	breast:
20	chr14:35625181..35627591-chr14:35627623..35631343,4	MCF-7	breast:
21	chr14:35591658..35595888-chr14:35872338..35875561,5	K562	blood:
22	chr14:35565651..35568101-chr14:35571541..35574493,2	K562	blood:
23	chr14:35341498..35344850-chr14:35591184..35593267,3	K562	blood:
24	chr14:35342813..35344956-chr14:35595359..35597712,2	K562	blood:
25	chr14:35515621..35517465-chr14:35577132..35579018,2	MCF-7	breast:
26	chr14:35519480..35523190-chr14:35588742..35592990,5	MCF-7	breast:
27	chr14:35552593..35554577-chr14:35554998..35557782,3	MCF-7	breast:
28	chr14:35593618..35595181-chr14:35595674..35598084,2	K562	blood:
29	chr14:35622588..35627460-chr14:35872526..35876521,6	MCF-7	breast:
30	chr14:35557782..35559646-chr14:35560670..35562491,2	MCF-7	breast:
31	chr14:35624804..35627276-chr14:35631634..35634106,2	K562	blood:
32	chr14:35585231..35589339-chr14:35589469..35593386,5	K562	blood:
33	chr14:35575108..35577004-chr14:35580748..35582498,2	MCF-7	breast:
34	chr14:35618961..35620951-chr14:35872636..35874969,2	K562	blood:
35	chr14:35576972..35579105-chr14:35589747..35591526,2	MCF-7	breast:
36	chr14:35589240..35593864-chr14:35869008..35876501,20	MCF-7	breast:
37	chr14:35568012..35571090-chr14:35873276..35876327,3	MCF-7	breast:
38	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
39	chr14:35624804..35627276-chr14:35631634..35634106,2	K562	blood:
40	chr14:35609923..35610592-chr14:35882131..35883118,2	K562	blood:
41	chr14:35513731..35517214-chr14:35589119..35593617,5	MCF-7	breast:
42	chr14:35545880..35548959-chr14:35590371..35593257,4	MCF-7	breast:
43	chr14:35593860..35596443-chr14:35605517..35607732,2	MCF-7	breast:
44	chr14:35607146..35612253-chr14:35870483..35876264,6	MCF-7	breast:
45	chr14:35636279..35638693-chr14:35643286..35645234,2	K562	blood:
46	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
47	chr14:35590489..35591401-chr15:91445904..91446665,2	Hela-S3	cervix:
48	chr14:35556172..35559296-chr14:35562772..35565829,3	MCF-7	breast:
49	chr14:35628320..35630476-chr14:35639523..35641227,2	MCF-7	breast:
50	chr14:35509776..35510382-chr14:35602542..35603513,2	MCF-7	breast:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BAZ1A-3	chr14:35579129-35579835	NONHSAT036363
2	lnc-RP11-173D9.3.1-1	chr14:35579776-35579932	ENSG00000247658
3	lnc-PPP2R3C-2	chr14:35627110-35628305	NONHSAT036367
4	lnc-RP11-173D9.3.1-1	chr14:35579101-35579166	ENSG00000247658
5	lnc-BAZ1A-3	chr14:35585816-35585943	NONHSAT036363
6	lnc-RP11-173D9.3.1-1	chr14:35575573-35575690	ENSG00000247658
7	lnc-RP11-173D9.3.1-1	chr14:35568882-35571935	ENSG00000247658
8	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366
9	lnc-BAZ1A-3	chr14:35591108-35591185	NONHSAT036363

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-124-3p	chr14:35552521-35552538
3	FAM177A1	hsa-miR-155-5p	chr14:35551927-35551947
4	FAM177A1	hsa-miR-142-3p	chr14:35551080-35551101
5	FAM177A1	hsa-miR-186-5p	chr14:35551034-35551055
6	FAM177A1	hsa-miR-124-3p	chr14:35552531-35552538

Variant related genes	Relation type
ENSG00000241052	TF binding region
ENSG00000259090	TF binding region
FAM177A1	TF binding region
KIAA0391	TF binding region
ENSG00000258790	TF binding region
PPP2R3C	TF binding region
ENSG00000241052	CpG island
ENSG00000259090	CpG island
FAM177A1	CpG island
KIAA0391	CpG island
ENSG00000258790	CpG island
PPP2R3C	CpG island
ENSG00000100906	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000151327	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000200169	chromatin interactions
ENSG00000174851	chromatin interactions
ENSG00000165752	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000008130	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000196547	chromatin interactions
ENSG00000094916	chromatin interactions
ENSG00000258738	chromatin interactions
NEFM	miRNA target sites
C2CD4A	miRNA target sites
FNDC3A	miRNA target sites
SAMD4B	miRNA target sites

Extended variants
information (count: 3566 )
Associated
traits (count: 61 )

Variant overlapped rSNPs/rCNVs (count:3566 , 50 per page) page: 1 2 3 4 5 6 7 ... 72

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566651693	chr14:35548305-35548306	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs190706618	chr14:35548323-35548324	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs541185156	chr14:35548324-35548325	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs561310314	chr14:35548325-35548326	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs574771051	chr14:35548335-35548336	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs544080622	chr14:35548359-35548360	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs143699215	chr14:35548380-35548381	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs148123388	chr14:35548390-35548391	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs552306612	chr14:35548403-35548404	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs559531130	chr14:35548432-35548433	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs78142214	chr14:35548512-35548513	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs181989339	chr14:35548590-35548591	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs143924095	chr14:35548620-35548621	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs568214614	chr14:35548696-35548697	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs146318302	chr14:35548792-35548793	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs529221689	chr14:35548797-35548798	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs35813846	chr14:35548816-35548817	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs570010704	chr14:35548887-35548888	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs374982070	chr14:35548889-35548890	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs185605060	chr14:35548897-35548898	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs139039494	chr14:35548899-35548900	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs558742574	chr14:35548951-35548952	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs572172550	chr14:35548956-35548957	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs535098408	chr14:35548960-35548961	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs143275761	chr14:35549042-35549043	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs574769525	chr14:35549065-35549066	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs543458836	chr14:35549069-35549070	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs61989492	chr14:35549073-35549074	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs577082794	chr14:35549116-35549117	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs546104650	chr14:35549146-35549147	Weak transcription Strong transcription Genic enhancers Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs112476925	chr14:35549259-35549260	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs33980744	chr14:35549260-35549261	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs386381102	chr14:35549261-35549262	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs397732891	chr14:35549264-35549265	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs375341293	chr14:35549265-35549266	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs367911419	chr14:35549267-35549268	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs150916090	chr14:35549278-35549279	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs190126676	chr14:35549306-35549307	Weak transcription Strong transcription Genic enhancers Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs138269493	chr14:35549437-35549438	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs181811264	chr14:35549449-35549450	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs371958989	chr14:35549450-35549451	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs560858188	chr14:35549477-35549478	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs36097874	chr14:35549488-35549489	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs529688134	chr14:35549494-35549495	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs549747649	chr14:35549530-35549531	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs569676384	chr14:35549532-35549533	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs532422177	chr14:35549560-35549561	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs74758516	chr14:35549561-35549562	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs565853820	chr14:35549562-35549563	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs530327881	chr14:35549588-35549589	Weak transcription Strong transcription Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:61)

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
Breast cancer	21858162	CNVD
Lung cancer	21569311	CNVD
Lung cancer	21911935	CNVD
Myelofibrosis	22110671	CNVD
abnormal development	18461090	CNVD
Prostate cancer	21298110	CNVD
Metanephric adenoma	20802469	CNVD
Lung adenocarcinoma	17982442	CNVD

Chromatin state (count:3039 , 50 per page) page: 1 2 3 4 5 6 7 ... 61

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35516400-35552600	Weak transcription	Spleen	Spleen
2	chr14:35516800-35551200	Weak transcription	Right Ventricle	heart
3	chr14:35516800-35552200	Weak transcription	H1 Cell Line	embryonic stem cell
4	chr14:35517400-35578800	Weak transcription	Stomach Mucosa	stomach
5	chr14:35517600-35554400	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
6	chr14:35520200-35550800	Weak transcription	NHLF	lung
7	chr14:35521000-35559400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
8	chr14:35526600-35552400	Weak transcription	Brain Substantia Nigra	brain
9	chr14:35528200-35552200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr14:35528200-35559400	Weak transcription	Colonic Mucosa	Colon
11	chr14:35528600-35552400	Weak transcription	Placenta Amnion	Placenta Amnion
12	chr14:35528600-35552800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
13	chr14:35528800-35563200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
14	chr14:35529000-35552000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
15	chr14:35529400-35555800	Weak transcription	Aorta	Aorta
16	chr14:35529400-35590200	Weak transcription	Esophagus	oesophagus
17	chr14:35530400-35550600	Weak transcription	Rectal Smooth Muscle	rectum
18	chr14:35530600-35550200	Weak transcription	iPS-20b Cell Line	embryonic stem cell
19	chr14:35530600-35552400	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr14:35530600-35563600	Weak transcription	Small Intestine	intestine
21	chr14:35530600-35590000	Weak transcription	Fetal Heart	heart
22	chr14:35530800-35552000	Weak transcription	Hela-S3	cervix
23	chr14:35531400-35550800	Weak transcription	HUVEC	blood vessel
24	chr14:35531400-35552600	Weak transcription	Pancreas	Pancrea
25	chr14:35531400-35563400	Weak transcription	Gastric	stomach
26	chr14:35538200-35581000	Weak transcription	Pancreatic Islets	Pancreatic Islet
27	chr14:35538400-35548800	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
28	chr14:35538400-35550800	Weak transcription	Dnd41	blood
29	chr14:35538400-35552600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
30	chr14:35538400-35559800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
31	chr14:35539000-35552400	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr14:35542000-35589600	Weak transcription	Fetal Brain Male	brain
33	chr14:35542400-35554000	Weak transcription	Psoas Muscle	Psoas
34	chr14:35542600-35552600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
35	chr14:35543000-35548400	Weak transcription	Muscle Satellite Cultured Cells	--
36	chr14:35543000-35552600	Weak transcription	Thymus	Thymus
37	chr14:35543200-35549000	Weak transcription	Primary hematopoietic stem cells	blood
38	chr14:35543200-35580800	Weak transcription	K562	blood
39	chr14:35544200-35552600	Weak transcription	Fetal Stomach	stomach
40	chr14:35544600-35548600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
41	chr14:35544600-35550600	Weak transcription	A549	lung
42	chr14:35544600-35554400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr14:35545600-35549200	Strong transcription	Foreskin Melanocyte Primary Cells skin01	Skin
44	chr14:35545600-35559800	Strong transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr14:35545600-35564600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
46	chr14:35545600-35568600	Strong transcription	Duodenum Smooth Muscle	Duodenum
47	chr14:35545600-35569800	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr14:35545600-35580800	Strong transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
49	chr14:35545600-35582800	Strong transcription	Primary T helper cells fromperipheralblood	blood
50	chr14:35545600-35590000	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived

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