Variant report

Variant	nsv902027
Chromosome Location	chr14:66975857-67059231
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:463)
CpG islands
(count:244)
Chromatin interactive
region (count:25)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:463 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF2	chr14:66975470-66976275	GM12878	blood:	n/a	n/a
2	BCL11A	chr14:66975710-66975903	GM12878	blood:	n/a	chr14:66975714-66975723
3	BCL3	chr14:66975506-66975904	GM12878	blood:	n/a	chr14:66975714-66975723
4	BCLAF1	chr14:66975385-66976000	GM12878	blood:	n/a	chr14:66975714-66975723
5	BHLHE40	chr14:66973863-66976828	GM12878	blood:	n/a	chr14:66974231-66974244 chr14:66975578-66975594
6	BHLHE40	chr14:66981162-66981258	GM12878	blood:	n/a	n/a
7	BRCA1	chr14:66976123-66976170	GM12878	blood:	n/a	n/a
8	CEBPB	chr14:66980997-66981296	IMR90	lung:	n/a	n/a
9	CEBPB	chr14:67022576-67022783	A549	lung:	n/a	n/a
10	CEBPB	chr14:67032442-67032536	HepG2	liver:	n/a	chr14:67032517-67032530 chr14:67032476-67032493 chr14:67032478-67032489 chr14:67032477-67032490
11	CEBPB	chr14:66980960-66981344	Hela-S3	cervix:	n/a	n/a
12	CEBPB	chr14:66980983-66981296	A549	lung:	n/a	n/a
13	CEBPB	chr14:67008105-67008272	IMR90	lung:	n/a	chr14:67008160-67008171
14	CEBPB	chr14:67009933-67010042	A549	lung:	n/a	n/a
15	CEBPB	chr14:67008036-67008341	HepG2	liver:	n/a	chr14:67008160-67008171
16	CEBPB	chr14:66980971-66981309	HepG2	liver:	n/a	n/a
17	CEBPB	chr14:66981010-66981332	K562	blood:	n/a	n/a
18	CHD1	chr14:66974127-66976039	GM12878	blood:	n/a	chr14:66975315-66975325
19	CHD1	chr14:66976255-66976727	GM12878	blood:	n/a	n/a
20	CHD2	chr14:66974014-66976257	GM12878	blood:	n/a	chr14:66975315-66975325
21	CHD2	chr14:66974064-66975912	K562	blood:	n/a	chr14:66975315-66975325
22	CHD2	chr14:66974037-66976238	Hela-S3	cervix:	n/a	chr14:66975315-66975325
23	CHD2	chr14:66975505-66975960	HepG2	liver:	n/a	n/a
24	CTBP2	chr14:66974142-66976247	H1-hESC	embryonic stem cell:	n/a	n/a
25	CTCF	chr14:66975960-66976110	BJ	skin:	n/a	n/a
26	CTCF	chr14:67016220-67016370	MCF-7	breast:	n/a	n/a
27	CTCF	chr14:66997440-66997590	HepG2	liver:	n/a	n/a
28	CTCF	chr14:67016396-67016466	K562	blood:	n/a	n/a
29	CTCF	chr14:67016232-67016606	GM12878	blood:	n/a	n/a
30	CTCF	chr14:66975712-66975903	GM12878	blood:	n/a	n/a
31	CTCF	chr14:67035080-67035230	RPTEC	kidney:	n/a	chr14:67035128-67035149
32	CTCF	chr14:67035063-67035231	Spleen_OC	spleen:	n/a	chr14:67035128-67035149
33	CTCF	chr14:67016380-67016530	WERI-Rb-1	eye:	n/a	n/a
34	CTCF	chr14:66975960-66976110	HCPEpiC	choroid plexus:	n/a	n/a
35	CTCF	chr14:67035040-67035222	HUVEC	blood vessel:	n/a	chr14:67035128-67035149
36	CTCF	chr14:67035133-67035158	LNCaP	prostate:	n/a	n/a
37	CTCF	chr14:66976040-66976190	SK-N-SH_RA	brain:	n/a	n/a
38	CTCF	chr14:67016304-67016638	MCF-7	breast:	n/a	n/a
39	CTCF	chr14:67034950-67035316	MCF-7	breast:	n/a	chr14:67035128-67035149
40	CTCF	chr14:67016395-67016453	GM12878	blood:	n/a	n/a
41	CTCF	chr14:66991429-66991454	GM13977	blood:	n/a	n/a
42	CTCF	chr14:67035160-67035310	HMEC	breast:	n/a	n/a
43	CTCF	chr14:67035105-67035220	LNCaP	prostate:	n/a	chr14:67035128-67035149
44	CTCF	chr14:66997350-66997457	Fibrobl	skin:	n/a	n/a
45	CTCF	chr14:66975880-66976030	HBMEC	blood vessel:	n/a	n/a
46	CTCF	chr14:67022127-67022182	GM13976	blood:	n/a	n/a
47	CTCF	chr14:67035056-67035192	Hela-S3	cervix:	n/a	chr14:67035128-67035149
48	CTCF	chr14:67016401-67016486	MCF-7	breast:	n/a	n/a
49	CTCF	chr14:67016338-67016465	Spleen_OC	spleen:	n/a	n/a
50	CTCF	chr14:66997445-66997540	MCF-7	breast:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:66980127-66980177	NT2-D1	testis:	n/a
2	chr14:67012668-67012718	AG10803	skin:	n/a
3	chr14:66976062-66976112	NH-A	brain:	n/a
4	chr14:66976062-66976112	HRPEpiC	eye:	n/a
5	chr14:66976276-66976326	HCM	heart:	n/a
6	chr14:66976276-66976326	SKMC	muscle:	n/a
7	chr14:67012668-67012718	ECC-1	luminal epithelium:	n/a
8	chr14:67012668-67012718	HNPCEpiC	eye:	n/a
9	chr14:67012668-67012718	HCM	heart:	n/a
10	chr14:66980127-66980177	NHBE	bronchial:	n/a
11	chr14:66980127-66980177	HEEpiC	esophagus:	n/a
12	chr14:66980127-66980177	Caco-2	colon:	n/a
13	chr14:66980127-66980177	GM12891	blood:	n/a
14	chr14:66976062-66976112	HCF	heart:	n/a
15	chr14:66980127-66980177	LNCaP	prostate:	n/a
16	chr14:66976276-66976326	MCF10A-Er-Src	breast:	n/a
17	chr14:67012668-67012718	SK-N-MC	brain:	n/a
18	chr14:66980127-66980177	HCF	heart:	n/a
19	chr14:66976062-66976112	MCF10A-Er-Src	breast:	n/a
20	chr14:67012668-67012718	NB4	blood:	n/a
21	chr14:66976062-66976112	HRCEpiC	kidney:	n/a
22	chr14:66976276-66976326	A549	lung:	n/a
23	chr14:66980127-66980177	AoSMC	blood vessel:	n/a
24	chr14:66976276-66976326	RPTEC	kidney:	n/a
25	chr14:66976276-66976326	SK-N-MC	brain:	n/a
26	chr14:67012668-67012718	HEEpiC	esophagus:	n/a
27	chr14:66980127-66980177	Hepatocyte	liver:	n/a
28	chr14:66976276-66976326	AG09319	gingival:	n/a
29	chr14:67012668-67012718	AG04449	skin:	fetal
30	chr14:66976062-66976112	AG04449	skin:	fetal
31	chr14:66976062-66976112	PrEC	prostate:	n/a
32	chr14:66976062-66976112	PFSK-1	brain:	n/a
33	chr14:66976276-66976326	Jurkat	blood:	n/a
34	chr14:67012668-67012718	PANC-1	pancreas:	n/a
35	chr14:66980127-66980177	Jurkat	blood:	n/a
36	chr14:66976276-66976326	AoSMC	blood vessel:	n/a
37	chr14:66976276-66976326	HEEpiC	esophagus:	n/a
38	chr14:66980127-66980177	AG04450	lung:	fetal
39	chr14:66980127-66980177	PrEC	prostate:	n/a
40	chr14:66976062-66976112	HCPEpiC	choroid plexus:	n/a
41	chr14:66980127-66980177	HRCEpiC	kidney:	n/a
42	chr14:67012668-67012718	CMK	blood:	n/a
43	chr14:66980127-66980177	GM12878	blood:	n/a
44	chr14:66976062-66976112	GM12878	blood:	n/a
45	chr14:67012668-67012718	AG09309	skin:	n/a
46	chr14:66980127-66980177	HepG2	liver:	n/a
47	chr14:66980127-66980177	Hela-S3	cervix:	n/a
48	chr14:66976276-66976326	HNPCEpiC	eye:	n/a
49	chr14:66980127-66980177	AG04449	skin:	fetal
50	chr14:66976062-66976112	CMK	blood:	n/a

(count:25 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr14:66974580..66976543-chr14:66983199..66985930,3	MCF-7	breast:
2	chr14:67031416..67034033-chr14:67041598..67043348,2	MCF-7	breast:
3	chr14:67013560..67014177-chr16:87123245..87123883,2	MCF-7	breast:
4	chr14:67040072..67042253-chr14:67043564..67045326,2	MCF-7	breast:
5	chr14:66972976..66974827-chr14:67023715..67025851,2	MCF-7	breast:
6	chr14:66974103..66976751-chr14:66998338..67000349,2	MCF-7	breast:
7	chr14:67044325..67045049-chr8:77423954..77424779,2	MCF-7	breast:
8	chr14:66961968..66962547-chr14:67034432..67035854,3	MCF-7	breast:
9	chr14:66998273..67000951-chr14:67001181..67003201,2	MCF-7	breast:
10	chr14:66979852..66981724-chr14:67004183..67006810,2	K562	blood:
11	chr14:66961069..66963949-chr14:66975127..66976775,2	K562	blood:
12	chr14:66979852..66981724-chr14:67004183..67006810,2	K562	blood:
13	chr14:67040072..67042253-chr14:67043564..67045326,2	MCF-7	breast:
14	chr14:66974208..66976195-chr14:67036443..67039003,2	MCF-7	breast:
15	chr14:66972704..66976384-chr14:67000982..67004211,4	MCF-7	breast:
16	chr14:66973238..66976174-chr14:67016237..67019038,2	MCF-7	breast:
17	chr14:66973828..66976621-chr14:66983168..66986678,3	MCF-7	breast:
18	chr14:66974018..66977412-chr14:66988835..66991120,3	MCF-7	breast:
19	chr14:66958930..66964157-chr14:66971787..66977680,8	K562	blood:
20	chr14:67031416..67034033-chr14:67041598..67043348,2	MCF-7	breast:
21	chr14:66975009..66976777-chr14:67006452..67008690,2	MCF-7	breast:
22	chr14:66998273..67000951-chr14:67001181..67003201,2	MCF-7	breast:
23	chr14:66869840..66870579-chr14:67035035..67035552,2	MCF-7	breast:
24	chr14:66974791..66976543-chr14:66986687..66988455,2	MCF-7	breast:
25	chr14:66962226..66964678-chr14:66974039..66976474,4	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CTD-2014B16.3.1-2	chr14:66975792-66976112	ENSG00000258561
2	lnc-CTD-2014B16.3.1-5	chr14:66983554-66984402	ucscGeneNc_uc001xji_1

No data

Variant related genes	Relation type
ENSG00000258561	TF binding region
ENSG00000258561	CpG island
ENSG00000196553	chromatin interactions
ENSG00000171723	chromatin interactions
ENSG00000258561	chromatin interactions

Extended variants
information (count: 3474 )
Associated
traits (count: 67 )

Variant overlapped rSNPs/rCNVs (count:3474 , 50 per page) page: 1 2 3 4 5 6 7 ... 70

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17103571	chr14:66975857-66975858	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs552533833	chr14:66975878-66975879	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
3	rs138132578	chr14:66975880-66975881	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
4	rs535001287	chr14:66975917-66975918	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
5	rs555156499	chr14:66975951-66975952	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
6	rs574902643	chr14:66975962-66975963	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
7	rs142625349	chr14:66975997-66975998	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3'	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
8	rs3840818	chr14:66976019-66976020	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
9	rs397751751	chr14:66976023-66976024	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
10	rs184381280	chr14:66976065-66976066	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	Chromatin interactive region lncRNA	2 gene(s)	Overlapped CNVs	n/a
11	rs375817040	chr14:66976126-66976127	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs567826495	chr14:66976171-66976172	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs188700470	chr14:66976183-66976184	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs181279130	chr14:66976205-66976206	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs185480752	chr14:66976221-66976222	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs572052346	chr14:66976304-66976305	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs528390505	chr14:66976354-66976355	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs190729360	chr14:66976359-66976360	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs561933589	chr14:66976385-66976386	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs146004894	chr14:66976417-66976418	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550339579	chr14:66976475-66976476	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs539136120	chr14:66976500-66976501	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs570245623	chr14:66976505-66976506	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs539136024	chr14:66976518-66976519	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs138649705	chr14:66976534-66976535	Bivalent/Poised TSS Active TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs559481142	chr14:66976687-66976688	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs541282305	chr14:66976789-66976790	Bivalent Enhancer Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Enhancers Weak transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs566306353	chr14:66976810-66976811	Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs8020652	chr14:66976847-66976848	Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
30	rs554939279	chr14:66976855-66976856	Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs17827716	chr14:66976921-66976922	Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
32	rs375383748	chr14:66976953-66976954	Flanking Active TSS Bivalent/Poised TSS Weak transcription Bivalent Enhancer Enhancers Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs557580966	chr14:66977074-66977075	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs577462487	chr14:66977124-66977125	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs182489162	chr14:66977127-66977128	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs543179286	chr14:66977149-66977150	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs573120546	chr14:66977180-66977181	Flanking Active TSS Bivalent/Poised TSS Enhancers Weak transcription Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs141248985	chr14:66977225-66977226	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs566675642	chr14:66977238-66977239	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs17780322	chr14:66977301-66977302	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs550399090	chr14:66977320-66977321	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs113013472	chr14:66977373-66977374	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs568988798	chr14:66977375-66977376	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs17827735	chr14:66977388-66977389	Enhancers Flanking Active TSS Bivalent/Poised TSS Weak transcription Active TSS Flanking Bivalent TSS/Enh	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
45	rs559480664	chr14:66977408-66977409	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs17780334	chr14:66977418-66977419	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
47	rs187298073	chr14:66977425-66977426	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs535135919	chr14:66977478-66977479	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs548950974	chr14:66977498-66977499	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs545421121	chr14:66977506-66977507	Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Weak transcription Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:67)

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
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
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
Gastrointestinal stromal cancer	16982739	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Renal cell carcinoma	21668985	CNVD
Chronic myeloid leukemia	20724749	CNVD
Wilms tumour	21544195	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Urothelial carcinoma	21177765	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Colorectal cancer	16272173	CNVD
Lung cancer	18438408	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Breast cancer	22032731	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Ovarian cancer	21720365	CNVD
Breast cancer	17603634	CNVD
Splenic marginal zone lymphoma	18492102	CNVD
Neuroblastoma	18923191	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Barrett''s syndrome	19417022	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
small cell lung cancer	20016488	CNVD
Myelofibrosis	22110671	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	21364760	CNVD
Breast cancer	17133270	CNVD
Basal cell lymphoma	17053054	CNVD
Cancer	20164920	CNVD
Cancer	17440070	CNVD
Non-syndromic sensorineural hearing loss	21987784	CNVD
Acute myeloid leukemia	21251322	CNVD
early-passage human iPS cells	21368824	CNVD
Breast cancer	22522925	CNVD
cataract	16735990	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD

Chromatin state (count:548 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:66973200-66976000	Active TSS	K562	blood
2	chr14:66973400-66976200	Active TSS	Primary T helper memory cells from peripheral blood 1	blood
3	chr14:66973400-66976800	Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
4	chr14:66973600-66976000	Active TSS	HUES64 Cell Line	embryonic stem cell
5	chr14:66973600-66976000	Active TSS	iPS-15b Cell Line	embryonic stem cell
6	chr14:66973600-66976200	Active TSS	H9 Cell Line	embryonic stem cell
7	chr14:66973600-66976200	Active TSS	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr14:66973600-66976200	Active TSS	Primary T helper memory cells from peripheral blood 2	blood
9	chr14:66973600-66976200	Active TSS	Fetal Adrenal Gland	Adrenal Gland
10	chr14:66973600-66976400	Active TSS	Primary T cells effector/memory enriched fromperipheralblood	blood
11	chr14:66973600-66976400	Active TSS	Ganglion Eminence derived primary cultured neurospheres	brain
12	chr14:66973600-66976400	Active TSS	Pancreatic Islets	Pancreatic Islet
13	chr14:66973600-66976600	Active TSS	Colon Smooth Muscle	Colon
14	chr14:66973600-66976600	Active TSS	Rectal Mucosa Donor 31	rectum
15	chr14:66973600-66976800	Active TSS	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
16	chr14:66973600-66976800	Active TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
17	chr14:66973600-66976800	Active TSS	NHLF	lung
18	chr14:66973600-66977800	Active TSS	GM12878-XiMat	blood
19	chr14:66973800-66976000	Active TSS	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
20	chr14:66973800-66976000	Flanking Active TSS	Primary B cells from cord blood	blood
21	chr14:66973800-66976200	Active TSS	ES-WA7 Cell Line	embryonic stem cell
22	chr14:66973800-66976200	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
23	chr14:66973800-66976200	Active TSS	Fetal Stomach	stomach
24	chr14:66973800-66976400	Active TSS	iPS DF 6.9 Cell Line	embryonic stem cell
25	chr14:66973800-66976400	Active TSS	Primary T killer memory cells from peripheral blood	blood
26	chr14:66973800-66976400	Active TSS	Stomach Mucosa	stomach
27	chr14:66973800-66976600	Active TSS	Brain Cingulate Gyrus	brain
28	chr14:66973800-66976600	Active TSS	Duodenum Smooth Muscle	Duodenum
29	chr14:66973800-66976600	Active TSS	Fetal Intestine Large	intestine
30	chr14:66973800-66976600	Active TSS	Fetal Kidney	kidney
31	chr14:66973800-66976600	Active TSS	Ovary	ovary
32	chr14:66973800-66976600	Active TSS	Rectal Smooth Muscle	rectum
33	chr14:66973800-66976600	Active TSS	HSMM	muscle
34	chr14:66973800-66976800	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
35	chr14:66973800-66976800	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr14:66973800-66976800	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
37	chr14:66973800-66976800	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
38	chr14:66973800-66976800	Active TSS	Fetal Intestine Small	intestine
39	chr14:66973800-66976800	Active TSS	Psoas Muscle	Psoas
40	chr14:66973800-66976800	Active TSS	Right Ventricle	heart
41	chr14:66973800-66976800	Active TSS	HMEC	breast
42	chr14:66973800-66977000	Active TSS	Fetal Brain Female	brain
43	chr14:66974000-66976200	Active TSS	Primary T helper naive cells from peripheral blood	blood
44	chr14:66974000-66976200	Bivalent/Poised TSS	HepG2	liver
45	chr14:66974000-66976400	Active TSS	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
46	chr14:66974000-66976400	Active TSS	Esophagus	oesophagus
47	chr14:66974000-66976400	Active TSS	Left Ventricle	heart
48	chr14:66974000-66976400	Active TSS	Lung	lung
49	chr14:66974000-66976400	Active TSS	Placenta Amnion	Placenta Amnion
50	chr14:66974000-66976400	Active TSS	Sigmoid Colon	Sigmoid Colon

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