Variant report

Variant	nsv456205
Chromosome Location	chr14:35772940-35826370
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1522)
CpG islands
(count:305)
Chromatin interactive
region (count:147)
LncRNA
region (count:6)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1522 , 50 per page) page: 1 2 3 4 5 6 7 ... 31

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:35807079-35807330	HepG2	liver:	n/a	n/a
2	ARID3A	chr14:35810902-35811054	HepG2	liver:	n/a	n/a
3	ARID3A	chr14:35816401-35817259	HepG2	liver:	n/a	n/a
4	ARID3A	chr14:35825210-35826108	HepG2	liver:	n/a	n/a
5	ARID3A	chr14:35803380-35803458	HepG2	liver:	n/a	n/a
6	ARID3A	chr14:35825248-35826007	K562	blood:	n/a	n/a
7	ARID3A	chr14:35823045-35823455	HepG2	liver:	n/a	n/a
8	ARID3A	chr14:35805605-35806272	HepG2	liver:	n/a	n/a
9	ARID3A	chr14:35801017-35801023	HepG2	liver:	n/a	n/a
10	ATF1	chr14:35825181-35825633	K562	blood:	n/a	n/a
11	ATF1	chr14:35800839-35801507	K562	blood:	n/a	n/a
12	ATF1	chr14:35805813-35806196	K562	blood:	n/a	n/a
13	ATF2	chr14:35800860-35801427	GM12878	blood:	n/a	n/a
14	ATF3	chr14:35800879-35801137	K562	blood:	n/a	chr14:35801049-35801062 chr14:35801052-35801060 chr14:35801052-35801062 chr14:35801050-35801061 chr14:35801049-35801059 chr14:35801051-35801062 chr14:35801052-35801063 chr14:35801050-35801061 chr14:35801048-35801063 chr14:35801049-35801062 chr14:35801052-35801059
15	ATF3	chr14:35805645-35806364	A549	lung:	n/a	n/a
16	ATF3	chr14:35805536-35806256	A549	lung:	n/a	n/a
17	ATF3	chr14:35825189-35825603	K562	blood:	n/a	n/a
18	BATF	chr14:35800799-35801179	GM12878	blood:	n/a	chr14:35800984-35800995 chr14:35801049-35801062 chr14:35800985-35800995
19	BATF	chr14:35784063-35784375	GM12878	blood:	n/a	n/a
20	BATF	chr14:35825279-35825686	GM12878	blood:	n/a	chr14:35825397-35825407 chr14:35825393-35825403
21	BCL3	chr14:35822061-35822551	GM12878	blood:	n/a	chr14:35822120-35822133
22	BCL3	chr14:35805388-35806455	A549	lung:	n/a	chr14:35806078-35806087
23	BCL3	chr14:35804446-35805297	A549	lung:	n/a	n/a
24	BCL3	chr14:35821923-35822498	GM12878	blood:	n/a	chr14:35822120-35822133 chr14:35821936-35821945
25	BCL3	chr14:35804460-35805352	A549	lung:	n/a	n/a
26	BCL3	chr14:35805525-35806609	A549	lung:	n/a	chr14:35806078-35806087
27	BHLHE40	chr14:35816095-35817186	HepG2	liver:	n/a	n/a
28	BHLHE40	chr14:35805579-35806274	HepG2	liver:	n/a	n/a
29	BHLHE40	chr14:35825458-35826066	GM12878	blood:	n/a	n/a
30	BHLHE40	chr14:35810796-35811188	HepG2	liver:	n/a	n/a
31	BHLHE40	chr14:35805696-35806242	K562	blood:	n/a	n/a
32	BHLHE40	chr14:35825386-35825946	HepG2	liver:	n/a	n/a
33	BHLHE40	chr14:35800890-35801135	K562	blood:	n/a	chr14:35800894-35800910
34	BHLHE40	chr14:35800805-35801137	GM12878	blood:	n/a	chr14:35800894-35800910
35	BHLHE40	chr14:35816962-35817073	K562	blood:	n/a	n/a
36	BHLHE40	chr14:35801346-35801613	GM12878	blood:	n/a	n/a
37	BRCA1	chr14:35806854-35806907	HepG2	liver:	n/a	n/a
38	BRCA1	chr14:35805030-35805172	HepG2	liver:	n/a	n/a
39	BRCA1	chr14:35800955-35801096	HepG2	liver:	n/a	n/a
40	BRCA1	chr14:35805663-35806468	Hela-S3	cervix:	n/a	n/a
41	BRCA1	chr14:35810803-35811180	Hela-S3	cervix:	n/a	chr14:35811082-35811089
42	BRCA1	chr14:35805830-35806408	HepG2	liver:	n/a	n/a
43	BRCA1	chr14:35809052-35809182	GM12878	blood:	n/a	n/a
44	BRCA1	chr14:35804767-35804781	HepG2	liver:	n/a	n/a
45	BRCA1	chr14:35804560-35805181	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr14:35825277-35826138	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr14:35810517-35810563	HepG2	liver:	n/a	n/a
48	BRCA1	chr14:35800898-35801211	Hela-S3	cervix:	n/a	n/a
49	BRCA1	chr14:35816689-35817015	HepG2	liver:	n/a	n/a
50	BRCA1	chr14:35802155-35802268	HepG2	liver:	n/a	n/a

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:35810887-35810937	ovcar-3	ovarian:	n/a
2	chr14:35822554-35822604	NHBE	bronchial:	n/a
3	chr14:35786537-35786587	IMR90	lung:	fetal
4	chr14:35802397-35802447	IMR90	lung:	fetal
5	chr14:35822554-35822604	RPTEC	kidney:	n/a
6	chr14:35822554-35822604	HL-60	blood:	n/a
7	chr14:35802397-35802447	HMEC	breast:	n/a
8	chr14:35822554-35822604	HepG2	liver:	n/a
9	chr14:35810887-35810937	Hela-S3	cervix:	n/a
10	chr14:35810887-35810937	CMK	blood:	n/a
11	chr14:35802397-35802447	SK-N-SH	brain:	n/a
12	chr14:35810887-35810937	HCM	heart:	n/a
13	chr14:35786537-35786587	A549	lung:	n/a
14	chr14:35822554-35822604	BE2_C	brain:	n/a
15	chr14:35802397-35802447	AG04449	skin:	fetal
16	chr14:35786537-35786587	U87	brain:	n/a
17	chr14:35786537-35786587	PrEC	prostate:	n/a
18	chr14:35810887-35810937	HCF	heart:	n/a
19	chr14:35802397-35802447	AG09309	skin:	n/a
20	chr14:35802397-35802447	Hepatocyte	liver:	n/a
21	chr14:35810887-35810937	PrEC	prostate:	n/a
22	chr14:35822554-35822604	AG09319	gingival:	n/a
23	chr14:35786537-35786587	SKMC	muscle:	n/a
24	chr14:35805898-35805948	NHDF-neo	bronchial:	n/a
25	chr14:35802397-35802447	ECC-1	luminal epithelium:	n/a
26	chr14:35805898-35805948	LNCaP	prostate:	n/a
27	chr14:35810887-35810937	HNPCEpiC	eye:	n/a
28	chr14:35810887-35810937	SKMC	muscle:	n/a
29	chr14:35802397-35802447	A549	lung:	n/a
30	chr14:35805898-35805948	K562	blood:	n/a
31	chr14:35810887-35810937	NT2-D1	testis:	n/a
32	chr14:35786537-35786587	SK-N-SH_RA	brain:	n/a
33	chr14:35786537-35786587	HRPEpiC	eye:	n/a
34	chr14:35822554-35822604	SK-N-MC	brain:	n/a
35	chr14:35805898-35805948	NHBE	bronchial:	n/a
36	chr14:35805898-35805948	Caco-2	colon:	n/a
37	chr14:35810887-35810937	SK-N-SH_RA	brain:	n/a
38	chr14:35810887-35810937	NHDF-neo	bronchial:	n/a
39	chr14:35802397-35802447	Caco-2	colon:	n/a
40	chr14:35810887-35810937	GM06990	blood:	n/a
41	chr14:35810887-35810937	HCT-116	colon:	n/a
42	chr14:35805898-35805948	MCF10A-Er-Src	breast:	n/a
43	chr14:35802397-35802447	NB4	blood:	n/a
44	chr14:35802397-35802447	AoSMC	blood vessel:	n/a
45	chr14:35805898-35805948	PANC-1	pancreas:	n/a
46	chr14:35805898-35805948	SAEC	small airway:	n/a
47	chr14:35810887-35810937	IMR90	lung:	fetal
48	chr14:35822554-35822604	AG10803	skin:	n/a
49	chr14:35786537-35786587	NHBE	bronchial:	n/a
50	chr14:35822554-35822604	HAEpiC	amniotic membrane:	n/a

(count:147 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr14:35799325..35802587-chr14:35803466..35807668,8	K562	blood:
2	chr14:35798638..35800955-chr14:35861336..35863044,2	K562	blood:
3	chr14:35792975..35797440-chr14:35798201..35801252,6	MCF-7	breast:
4	chr14:35817047..35819303-chr14:35821094..35823025,2	K562	blood:
5	chr14:35701265..35703150-chr14:35798175..35799719,2	MCF-7	breast:
6	chr14:35787443..35789912-chr14:35792627..35795777,3	MCF-7	breast:
7	chr14:35767852..35773242-chr14:35799435..35804534,8	MCF-7	breast:
8	chr14:35801484..35802301-chr14:35867643..35868601,3	MCF-7	breast:
9	chr14:35793707..35796135-chr14:35808509..35811220,2	MCF-7	breast:
10	chr14:35793722..35795928-chr14:35804588..35807090,2	K562	blood:
11	chr14:35774559..35776882-chr14:35872342..35875113,2	K562	blood:
12	chr14:35702282..35704520-chr14:35800753..35803790,5	MCF-7	breast:
13	chr14:35821200..35823074-chr14:35824484..35827644,3	MCF-7	breast:
14	chr14:35698922..35700571-chr14:35810245..35812248,2	MCF-7	breast:
15	chr14:35778351..35785006-chr14:35799640..35807255,11	MCF-7	breast:
16	chr14:35736271..35738491-chr14:35800943..35803870,2	MCF-7	breast:
17	chr14:35792762..35795033-chr14:35804615..35806413,2	MCF-7	breast:
18	chr14:35759417..35767612-chr14:35799689..35808998,23	MCF-7	breast:
19	chr14:35821200..35823074-chr14:35824484..35827644,3	MCF-7	breast:
20	chr14:35792939..35797188-chr14:35798673..35803214,8	MCF-7	breast:
21	chr14:35778204..35779930-chr14:35870130..35871675,2	MCF-7	breast:
22	chr14:35803428..35804017-chr14:35872984..35873546,2	MCF-7	breast:
23	chr14:35772058..35774272-chr14:35810527..35812254,2	MCF-7	breast:
24	chr14:35805788..35806538-chr14:35873754..35874624,2	MCF-7	breast:
25	chr14:35681682..35685352-chr14:35808762..35812906,3	MCF-7	breast:
26	chr14:35342747..35344772-chr14:35793971..35796787,2	MCF-7	breast:
27	chr14:35792975..35797440-chr14:35798201..35801252,6	MCF-7	breast:
28	chr14:35797442..35799693-chr14:35801625..35803378,2	K562	blood:
29	chr14:35767249..35769056-chr14:35785281..35787174,2	MCF-7	breast:
30	chr14:35801529..35804372-chr14:35808012..35809578,2	K562	blood:
31	chr14:35790365..35792681-chr14:35809651..35811760,2	MCF-7	breast:
32	chr14:35805823..35806650-chr14:35875833..35876360,2	MCF-7	breast:
33	chr14:35589885..35593973-chr14:35809162..35812137,5	MCF-7	breast:
34	chr14:35745755..35748037-chr14:35772284..35774064,2	MCF-7	breast:
35	chr14:35759553..35761751-chr14:35821894..35823859,2	MCF-7	breast:
36	chr14:35800988..35801696-chr14:35872838..35873621,3	MCF-7	breast:
37	chr14:35779341..35784196-chr14:35869353..35875195,7	K562	blood:
38	chr14:35809807..35810560-chr14:35872889..35873456,4	MCF-7	breast:
39	chr14:35779341..35783565-chr14:35868727..35873122,4	K562	blood:
40	chr14:35810790..35811847-chr14:35873610..35874301,3	MCF-7	breast:
41	chr14:35515127..35516753-chr14:35810234..35812265,2	MCF-7	breast:
42	chr14:35698279..35702159-chr14:35801289..35806332,5	MCF-7	breast:
43	chr14:35700471..35702762-chr14:35811850..35814628,2	MCF-7	breast:
44	chr14:35716423..35718490-chr14:35802705..35806298,3	MCF-7	breast:
45	chr14:35801529..35803038-chr14:35808078..35809983,2	K562	blood:
46	chr14:35793722..35795928-chr14:35804588..35807090,2	K562	blood:
47	chr14:35774042..35776362-chr14:35810358..35812429,2	MCF-7	breast:
48	chr14:35799429..35801248-chr14:35836399..35837968,2	K562	blood:
49	chr14:35701570..35704183-chr14:35804617..35807506,4	MCF-7	breast:
50	chr14:35777000..35779255-chr14:35781790..35784953,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-PSMA6-2	chr14:35790963-35791436	NONHSAT036375
2	lnc-NFKBIA-4	chr14:35811376-35812101	l_964_chr14:35808028-35812101_thyroid
3	lnc-PSMA6-4	chr14:35804609-35805475	NONHSAT036376
4	lnc-NFKBIA-4	chr14:35808029-35808268	l_964_chr14:35808028-35812101_thyroid
5	lnc-RP11-173D9.3.1-3	chr14:35774111-35775195	l_963_chr14:35700899-35775195_brain
6	lnc-PSMA6-1	chr14:35789592-35790654	NONHSAT036374

No data

Variant related genes	Relation type
PSMA6	TF binding region
PSMA6	CpG island
ENSG00000151327	chromatin interactions
ENSG00000198604	chromatin interactions
ENSG00000100906	chromatin interactions
ENSG00000234741	chromatin interactions
ENSG00000265530	chromatin interactions
ENSG00000185278	chromatin interactions
ENSG00000240392	chromatin interactions
ENSG00000258738	chromatin interactions
ENSG00000100902	chromatin interactions
ENSG00000258860	chromatin interactions
ENSG00000100890	chromatin interactions
ENSG00000199004	chromatin interactions
ENSG00000100883	chromatin interactions
ENSG00000092020	chromatin interactions
ENSG00000258790	chromatin interactions
ENSG00000256243	chromatin interactions

Extended variants
information (count: 2197 )
Associated
traits (count: 60 )

Variant overlapped rSNPs/rCNVs (count:2197 , 50 per page) page: 1 2 3 4 5 6 7 ... 44

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs10141237	chr14:35772940-35772941	Weak transcription Strong transcription Enhancers Genic enhancers Transcr. at gene 5' and 3'	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs535489644	chr14:35773063-35773064	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs555698100	chr14:35773084-35773085	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs575869432	chr14:35773087-35773088	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs538556025	chr14:35773109-35773110	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs140182729	chr14:35773111-35773112	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs118127067	chr14:35773117-35773118	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs77272828	chr14:35773127-35773128	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs59394747	chr14:35773128-35773129	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs144256238	chr14:35773209-35773210	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs192867737	chr14:35773240-35773241	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs575594475	chr14:35773281-35773282	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs546254782	chr14:35773282-35773283	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs372795651	chr14:35773330-35773331	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs559501626	chr14:35773353-35773354	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
16	rs148796886	chr14:35773369-35773370	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs184986636	chr14:35773370-35773371	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
18	rs541485237	chr14:35773381-35773382	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
19	rs561754964	chr14:35773446-35773447	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs530411059	chr14:35773522-35773523	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
21	rs143932276	chr14:35773602-35773603	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
22	rs146360360	chr14:35773635-35773636	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
23	rs189658597	chr14:35773662-35773663	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
24	rs549978549	chr14:35773664-35773665	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
25	rs117098068	chr14:35773702-35773703	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
26	rs566639937	chr14:35773729-35773730	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
27	rs139662067	chr14:35773791-35773792	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
28	rs569984904	chr14:35773797-35773798	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
29	rs376168285	chr14:35773813-35773814	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
30	rs144400866	chr14:35773862-35773863	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
31	rs569265752	chr14:35773866-35773867	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
32	rs112040033	chr14:35773933-35773934	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
33	rs75825538	chr14:35773934-35773935	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
34	rs397852826	chr14:35773947-35773948	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
35	rs34824477	chr14:35773948-35773949	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
36	rs71445907	chr14:35773965-35773966	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
37	rs552355174	chr14:35774007-35774008	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs537840558	chr14:35774148-35774149	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
39	rs528612904	chr14:35774245-35774246	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
40	rs527720363	chr14:35774255-35774256	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
41	rs114374814	chr14:35774296-35774297	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
42	rs151158145	chr14:35774336-35774337	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
43	rs376940427	chr14:35774352-35774353	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
44	rs57226520	chr14:35774366-35774367	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
45	rs138528267	chr14:35774368-35774369	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region lncRNA	1 gene(s)	Overlapped CNVs	n/a
46	rs56657181	chr14:35774395-35774396	Weak transcription Strong transcription Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
47	rs561079714	chr14:35774418-35774419	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
48	rs578240192	chr14:35774434-35774435	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
49	rs371087857	chr14:35774444-35774445	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
50	rs115438676	chr14:35774481-35774482	Weak transcription Strong transcription ZNF genes & repeats Enhancers Genic enhancers	TF binding region Chromatin interactive region lncRNA	2 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
Cancer	20164920	CNVD

Chromatin state (count:1965 , 50 per page) page: 1 2 3 4 5 6 7 ... 40

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:35762600-35774400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr14:35762600-35778400	Weak transcription	Placenta Amnion	Placenta Amnion
3	chr14:35762800-35778600	Weak transcription	H9 Cell Line	embryonic stem cell
4	chr14:35762800-35778800	Weak transcription	Aorta	Aorta
5	chr14:35763200-35777000	Weak transcription	HUES48 Cell Line	embryonic stem cell
6	chr14:35763200-35778000	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
7	chr14:35763200-35780000	Weak transcription	Fetal Kidney	kidney
8	chr14:35763200-35789600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
9	chr14:35763600-35775000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
10	chr14:35763600-35776800	Weak transcription	Fetal Muscle Trunk	muscle
11	chr14:35763600-35777000	Weak transcription	iPS-18 Cell Line	embryonic stem cell
12	chr14:35763600-35778800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
13	chr14:35763800-35777200	Weak transcription	Placenta	Placenta
14	chr14:35763800-35777600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr14:35763800-35777800	Weak transcription	iPS-20b Cell Line	embryonic stem cell
16	chr14:35763800-35777800	Weak transcription	HSMM	muscle
17	chr14:35763800-35778600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
18	chr14:35763800-35778600	Weak transcription	Colonic Mucosa	Colon
19	chr14:35763800-35778600	Weak transcription	Esophagus	oesophagus
20	chr14:35763800-35778600	Weak transcription	Ovary	ovary
21	chr14:35763800-35779200	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr14:35764000-35778200	Weak transcription	Brain Hippocampus Middle	brain
23	chr14:35764000-35778600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
24	chr14:35764000-35779200	Weak transcription	Cortex derived primary cultured neurospheres	brain
25	chr14:35764200-35777000	Weak transcription	HUES64 Cell Line	embryonic stem cell
26	chr14:35764200-35777200	Weak transcription	Osteobl	bone
27	chr14:35764200-35778200	Weak transcription	Stomach Smooth Muscle	stomach
28	chr14:35764400-35773200	Enhancers	Primary T helper cells fromperipheralblood	blood
29	chr14:35764400-35774000	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
30	chr14:35764400-35777800	Weak transcription	NHLF	lung
31	chr14:35764600-35778600	Weak transcription	Brain Anterior Caudate	brain
32	chr14:35764600-35778600	Weak transcription	Brain Germinal Matrix	brain
33	chr14:35765200-35773200	Weak transcription	Fetal Stomach	stomach
34	chr14:35765200-35774400	Weak transcription	Right Atrium	heart
35	chr14:35765200-35778600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr14:35765200-35778800	Weak transcription	Brain Angular Gyrus	brain
37	chr14:35765200-35779800	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr14:35765400-35773400	Weak transcription	Fetal Intestine Large	intestine
39	chr14:35765400-35777000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
40	chr14:35765400-35778400	Weak transcription	Fetal Brain Female	brain
41	chr14:35765400-35778800	Weak transcription	Gastric	stomach
42	chr14:35765400-35779400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
43	chr14:35765400-35782400	Weak transcription	K562	blood
44	chr14:35765600-35776800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr14:35765800-35773200	Weak transcription	Fetal Intestine Small	intestine
46	chr14:35765800-35778600	Weak transcription	Lung	lung
47	chr14:35766200-35792000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
48	chr14:35766400-35777400	Weak transcription	HUES6 Cell Line	embryonic stem cell
49	chr14:35766400-35777600	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
50	chr14:35767200-35779600	Weak transcription	Brain Substantia Nigra	brain

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