Variant report

Variant	nsv1046680
Chromosome Location	chr14:35608347-35665374
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:429)
CpG islands
(count:63)
Chromatin interactive
region (count:37)
LncRNA
region (count:4)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35628114-35628276	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35628515-35629631	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35658657-35659080	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35613218-35613555	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35609838-35610282	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:35615869-35616033	HepG2	liver:	n/a	n/a
7	ATF1	chr14:35629215-35629517	K562	blood:	n/a	n/a
8	ATF3	chr14:35629129-35629373	K562	blood:	n/a	n/a
9	BATF	chr14:35654077-35654389	GM12878	blood:	n/a	n/a
10	BATF	chr14:35629074-35629473	GM12878	blood:	n/a	chr14:35629286-35629297 chr14:35629287-35629297
11	BATF	chr14:35654130-35654416	GM12878	blood:	n/a	n/a
12	BATF	chr14:35629052-35629485	GM12878	blood:	n/a	chr14:35629286-35629297 chr14:35629287-35629297
13	BCL11A	chr14:35629109-35629431	GM12878	blood:	n/a	chr14:35629290-35629299 chr14:35629289-35629298
14	BCL3	chr14:35628914-35629626	A549	lung:	n/a	chr14:35629290-35629299 chr14:35629289-35629298
15	BHLHE40	chr14:35628362-35628811	HepG2	liver:	n/a	n/a
16	BRCA1	chr14:35629077-35629584	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr14:35613335-35613393	GM12878	blood:	n/a	n/a
18	CCNT2	chr14:35629331-35629550	K562	blood:	n/a	n/a
19	CEBPB	chr14:35629119-35629473	IMR90	lung:	n/a	n/a
20	CEBPB	chr14:35612292-35612467	HepG2	liver:	n/a	chr14:35612414-35612425
21	CEBPB	chr14:35628942-35629670	HCT-116	colon:	n/a	n/a
22	CEBPB	chr14:35612279-35612564	HepG2	liver:	n/a	chr14:35612414-35612425
23	CEBPB	chr14:35613295-35613593	HepG2	liver:	n/a	n/a
24	CEBPB	chr14:35658120-35658257	HepG2	liver:	n/a	chr14:35658171-35658182
25	CEBPB	chr14:35629005-35629607	A549	lung:	n/a	n/a
26	CEBPB	chr14:35629124-35629473	A549	lung:	n/a	n/a
27	CEBPB	chr14:35619064-35619239	HepG2	liver:	n/a	chr14:35619155-35619166
28	CEBPB	chr14:35629121-35629411	HepG2	liver:	n/a	n/a
29	CEBPB	chr14:35655539-35655712	K562	blood:	n/a	n/a
30	CEBPB	chr14:35629053-35629515	Hela-S3	cervix:	n/a	n/a
31	CEBPB	chr14:35625280-35625622	IMR90	lung:	n/a	n/a
32	CEBPB	chr14:35653763-35653855	HepG2	liver:	n/a	chr14:35653812-35653823
33	CEBPB	chr14:35615956-35615976	IMR90	lung:	n/a	n/a
34	CEBPB	chr14:35639135-35639136	HepG2	liver:	n/a	n/a
35	CEBPB	chr14:35629006-35629554	HCT-116	colon:	n/a	n/a
36	CHD2	chr14:35613402-35613558	GM12878	blood:	n/a	n/a
37	CREB1	chr14:35628982-35629516	HepG2	liver:	n/a	chr14:35629381-35629394
38	CTCF	chr14:35610040-35610190	HL-60	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
39	CTCF	chr14:35610100-35610250	HVMF	connective:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
40	CTCF	chr14:35609980-35610130	GM12872	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
41	CTCF	chr14:35663220-35663370	GM12878	blood:	n/a	n/a
42	CTCF	chr14:35609960-35610110	GM12865	blood:	n/a	n/a
43	CTCF	chr14:35610040-35610190	HPF	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
44	CTCF	chr14:35610000-35610150	HEEpiC	esophagus:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
45	CTCF	chr14:35609700-35609850	HMEC	breast:	n/a	n/a
46	CTCF	chr14:35610020-35610170	AG09319	gingival:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
47	CTCF	chr14:35610000-35610150	HPF	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
48	CTCF	chr14:35609977-35610231	Pancreas_OC	pancreas:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
49	CTCF	chr14:35610040-35610190	WI-38	lung:	n/a	chr14:35610106-35610124 chr14:35610108-35610129
50	CTCF	chr14:35610040-35610190	GM12801	blood:	n/a	chr14:35610106-35610124 chr14:35610108-35610129

(count:63 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35629311-35629361	PrEC	prostate:	n/a
2	chr14:35629311-35629361	AoSMC	blood vessel:	n/a
3	chr14:35629311-35629361	PrEC	prostate:	n/a
4	chr14:35629311-35629361	AoSMC	blood vessel:	n/a
5	chr14:35629311-35629361	AG04449	skin:	fetal
6	chr14:35629311-35629361	T-47D	breast:	n/a
7	chr14:35629311-35629361	ProgFib	skin:	n/a
8	chr14:35629311-35629361	MCF10A-Er-Src	breast:	n/a
9	chr14:35629311-35629361	K562	blood:	n/a
10	chr14:35629311-35629361	AG09309	skin:	n/a
11	chr14:35629311-35629361	A549	lung:	n/a
12	chr14:35629311-35629361	ovcar-3	ovarian:	n/a
13	chr14:35629311-35629361	HRE	kidney:	n/a
14	chr14:35629311-35629361	GM12892	blood:	n/a
15	chr14:35629311-35629361	HEK293	kidney:	embryo
16	chr14:35629311-35629361	AG04450	lung:	fetal
17	chr14:35629311-35629361	GM06990	blood:	n/a
18	chr14:35629311-35629361	BE2_C	brain:	n/a
19	chr14:35629311-35629361	Hela-S3	cervix:	n/a
20	chr14:35629311-35629361	ECC-1	luminal epithelium:	n/a
21	chr14:35629311-35629361	HCF	heart:	n/a
22	chr14:35629311-35629361	AG10803	skin:	n/a
23	chr14:35629311-35629361	SAEC	small airway:	n/a
24	chr14:35629311-35629361	PANC-1	pancreas:	n/a
25	chr14:35629311-35629361	NB4	blood:	n/a
26	chr14:35629311-35629361	IMR90	lung:	fetal
27	chr14:35629311-35629361	HCM	heart:	n/a
28	chr14:35629311-35629361	Jurkat	blood:	n/a
29	chr14:35629311-35629361	Caco-2	colon:	n/a
30	chr14:35629311-35629361	CMK	blood:	n/a
31	chr14:35629311-35629361	HRCEpiC	kidney:	n/a
32	chr14:35629311-35629361	GM19239	blood:	n/a
33	chr14:35629311-35629361	HL-60	blood:	n/a
34	chr14:35629311-35629361	MCF-7	breast:	n/a
35	chr14:35629311-35629361	SKMC	muscle:	n/a
36	chr14:35629311-35629361	HCT-116	colon:	n/a
37	chr14:35629311-35629361	BJ	skin:	n/a
38	chr14:35629311-35629361	SK-N-SH_RA	brain:	n/a
39	chr14:35629311-35629361	NH-A	brain:	n/a
40	chr14:35629311-35629361	RPTEC	kidney:	n/a
41	chr14:35629311-35629361	HNPCEpiC	eye:	n/a
42	chr14:35629311-35629361	GM12891	blood:	n/a
43	chr14:35629311-35629361	HIPEpiC	eye:	n/a
44	chr14:35629311-35629361	NT2-D1	testis:	n/a
45	chr14:35629311-35629361	HAEpiC	amniotic membrane:	n/a
46	chr14:35629311-35629361	Hepatocyte	liver:	n/a
47	chr14:35629311-35629361	NHBE	bronchial:	n/a
48	chr14:35629311-35629361	SK-N-SH	brain:	n/a
49	chr14:35629311-35629361	HCPEpiC	choroid plexus:	n/a
50	chr14:35629311-35629361	HEEpiC	esophagus:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr14:35624804..35627276-chr14:35631634..35634106,2	K562	blood:
2	chr14:35664498..35666606-chr14:35871768..35874425,2	MCF-7	breast:
3	chr14:35622836..35624862-chr14:35627590..35631684,4	MCF-7	breast:
4	chr14:35607146..35612253-chr14:35870483..35876264,6	MCF-7	breast:
5	chr14:35627605..35629327-chr14:35631788..35633814,2	MCF-7	breast:
6	chr14:35631921..35634177-chr14:35636642..35638625,2	K562	blood:
7	chr14:35617849..35620759-chr14:35622945..35624771,2	K562	blood:
8	chr14:35609923..35610592-chr14:35882131..35883118,2	K562	blood:
9	chr14:35634398..35636898-chr14:35641045..35642555,2	K562	blood:
10	chr14:35618961..35620951-chr14:35872636..35874969,2	K562	blood:
11	chr14:35617849..35620759-chr14:35622945..35624771,2	K562	blood:
12	chr14:35634398..35636898-chr14:35641045..35642555,2	K562	blood:
13	chr14:35636279..35638693-chr14:35643286..35645234,2	K562	blood:
14	chr14:35624804..35627276-chr14:35631634..35634106,2	K562	blood:
15	chr14:35622588..35627460-chr14:35872526..35876521,6	MCF-7	breast:
16	chr14:35630047..35632589-chr14:35700698..35702553,2	MCF-7	breast:
17	chr14:35628320..35630476-chr14:35639523..35641227,2	MCF-7	breast:
18	chr14:35625114..35628050-chr14:35869275..35871381,2	MCF-7	breast:
19	chr14:35629587..35631138-chr14:35874069..35875682,2	MCF-7	breast:
20	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
21	chr14:35631921..35634177-chr14:35636642..35638625,2	K562	blood:
22	chr14:35590512..35592667-chr14:35626960..35629855,2	MCF-7	breast:
23	chr14:35636158..35638112-chr14:35872373..35874812,2	MCF-7	breast:
24	chr14:35591519..35595247-chr14:35614813..35617284,3	MCF-7	breast:
25	chr14:35616325..35618402-chr14:35627328..35629037,2	MCF-7	breast:
26	chr14:35605217..35606991-chr14:35607370..35609971,2	MCF-7	breast:
27	chr14:35636279..35638693-chr14:35643286..35645234,2	K562	blood:
28	chr14:35450376..35452323-chr14:35627573..35629639,2	K562	blood:
29	chr14:35610882..35612765-chr14:35874078..35876845,2	MCF-7	breast:
30	chr14:35610009..35610550-chr14:36156270..36157192,2	K562	blood:
31	chr14:35604060..35606513-chr14:35608346..35611320,2	K562	blood:
32	chr14:35614979..35617041-chr14:35619996..35622805,3	K562	blood:
33	chr14:35661003..35662833-chr14:35873537..35876182,2	MCF-7	breast:
34	chr14:35625181..35627591-chr14:35627623..35631343,4	MCF-7	breast:
35	chr14:35628567..35630693-chr14:35872213..35874122,2	MCF-7	breast:
36	chr14:35628320..35630476-chr14:35639523..35641227,2	MCF-7	breast:
37	chr14:35628255..35632944-chr14:35633604..35637748,5	MCF-7	breast:

(count:4 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-FAM177A1-4	chr14:35651558-35651951	uc_373_+
2	lnc-PPP2R3C-3	chr14:35651558-35651951	uc_373_-
3	lnc-PPP2R3C-1	chr14:35613227-35613686	NONHSAT036366
4	lnc-PPP2R3C-2	chr14:35627110-35628305	NONHSAT036367

No data

Variant related genes	Relation type
ENSG00000241052	TF binding region
ENSG00000259090	TF binding region
ENSG00000241052	CpG island
ENSG00000259090	CpG island
ENSG00000100906	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000259090	chromatin interactions
ENSG00000258704	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000100883	chromatin interactions

Extended variants
information (count: 2271 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2271 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4982242	chr14:35608347-35608348	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs151091277	chr14:35608382-35608383	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115914922	chr14:35608454-35608455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549300010	chr14:35608461-35608462	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs562817095	chr14:35608545-35608546	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs58964615	chr14:35608617-35608618	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs531806045	chr14:35608680-35608681	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs551916054	chr14:35608685-35608686	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs570461455	chr14:35608686-35608687	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs539570245	chr14:35608689-35608690	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs117480704	chr14:35608731-35608732	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs140156175	chr14:35608767-35608768	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs546370804	chr14:35608768-35608769	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs557036791	chr14:35608828-35608829	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs566499363	chr14:35608868-35608869	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs535421826	chr14:35608872-35608873	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs555722136	chr14:35608896-35608897	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs575575611	chr14:35608946-35608947	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs79137242	chr14:35608997-35608998	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs150940693	chr14:35609063-35609064	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs557888782	chr14:35609158-35609159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs577758429	chr14:35609159-35609160	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs190585096	chr14:35609183-35609184	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs553512626	chr14:35609211-35609212	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs182824538	chr14:35609299-35609300	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs573724764	chr14:35609376-35609377	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs112820744	chr14:35609381-35609382	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542582061	chr14:35609386-35609387	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs187172477	chr14:35609403-35609404	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs139270322	chr14:35609438-35609439	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs61039213	chr14:35609439-35609440	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs368499969	chr14:35609451-35609452	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs531842623	chr14:35609454-35609455	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551785536	chr14:35609470-35609471	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs369616338	chr14:35609510-35609511	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs565516876	chr14:35609518-35609519	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs544035974	chr14:35609520-35609521	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs56293506	chr14:35609585-35609586	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs137907292	chr14:35609603-35609604	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs189877204	chr14:35609610-35609611	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs182411383	chr14:35609681-35609682	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs541396943	chr14:35609718-35609719	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs569176923	chr14:35609730-35609731	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs7157266	chr14:35609769-35609770	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs112031438	chr14:35609805-35609806	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs576827963	chr14:35609950-35609951	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs372689791	chr14:35609958-35609959	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs189132216	chr14:35609966-35609967	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs12888766	chr14:35609980-35609981	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
50	rs571912755	chr14:35609995-35609996	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:60)

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
Cancer	21129771	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Lung cancer	17925434	CNVD
Colorectal cancer	16272173	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
Non-syndromic sensorineural hearing loss	19587683	CNVD

Chromatin state (count:1136 , 50 per page) page: 1 2 3 4 5 6 7 ... 23

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35592600-35625200	Weak transcription	Small Intestine	intestine
2	chr14:35592800-35611000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
3	chr14:35593000-35610200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
4	chr14:35593000-35613400	Weak transcription	Stomach Mucosa	stomach
5	chr14:35593000-35638200	Weak transcription	Fetal Brain Male	brain
6	chr14:35593000-35660400	Weak transcription	Stomach Smooth Muscle	stomach
7	chr14:35593200-35625200	Weak transcription	NH-A	brain
8	chr14:35593200-35625600	Weak transcription	Colon Smooth Muscle	Colon
9	chr14:35593200-35627800	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
10	chr14:35593200-35635400	Weak transcription	Rectal Smooth Muscle	rectum
11	chr14:35593400-35613200	Weak transcription	Osteobl	bone
12	chr14:35593400-35617200	Weak transcription	Muscle Satellite Cultured Cells	--
13	chr14:35594000-35615800	Weak transcription	HUVEC	blood vessel
14	chr14:35594400-35629000	Weak transcription	Rectal Mucosa Donor 31	rectum
15	chr14:35594600-35609600	Weak transcription	Colonic Mucosa	Colon
16	chr14:35595200-35613200	Weak transcription	K562	blood
17	chr14:35596000-35623600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
18	chr14:35597400-35625000	Weak transcription	HUES64 Cell Line	embryonic stem cell
19	chr14:35597600-35625000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
20	chr14:35597800-35615400	Weak transcription	HUES48 Cell Line	embryonic stem cell
21	chr14:35598000-35609800	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
22	chr14:35601400-35609200	Strong transcription	Fetal Thymus	thymus
23	chr14:35601600-35609600	Strong transcription	Primary T helper cells fromperipheralblood	blood
24	chr14:35602000-35609600	Strong transcription	Rectal Mucosa Donor 29	rectum
25	chr14:35602400-35609200	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
26	chr14:35603000-35609400	Strong transcription	HepG2	liver
27	chr14:35603000-35625200	Weak transcription	HSMM	muscle
28	chr14:35603200-35609200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
29	chr14:35603200-35623200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
30	chr14:35603200-35663400	Weak transcription	Fetal Lung	lung
31	chr14:35603400-35625200	Weak transcription	Placenta Amnion	Placenta Amnion
32	chr14:35603600-35621600	Weak transcription	H1 Cell Line	embryonic stem cell
33	chr14:35604000-35609400	Weak transcription	NHLF	lung
34	chr14:35604000-35624400	Weak transcription	NHEK	skin
35	chr14:35604200-35609600	Strong transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
36	chr14:35604200-35611400	Weak transcription	Dnd41	blood
37	chr14:35604200-35613000	Weak transcription	Brain Germinal Matrix	brain
38	chr14:35604200-35613800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
39	chr14:35604200-35615200	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
40	chr14:35604200-35623200	Weak transcription	Primary T helper naive cells from peripheral blood	blood
41	chr14:35604200-35625200	Weak transcription	H9 Cell Line	embryonic stem cell
42	chr14:35604200-35625200	Weak transcription	Duodenum Smooth Muscle	Duodenum
43	chr14:35604200-35628800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
44	chr14:35604200-35651400	Weak transcription	Esophagus	oesophagus
45	chr14:35604400-35611400	Weak transcription	Right Ventricle	heart
46	chr14:35604400-35611600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr14:35604400-35613200	Weak transcription	Gastric	stomach
48	chr14:35604400-35616000	Weak transcription	Pancreas	Pancrea
49	chr14:35604400-35621800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
50	chr14:35604400-35623200	Weak transcription	A549	lung

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