Variant report

Variant	esv3337768
Chromosome Location	chr14:105639956-105667348
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:992)
CpG islands
(count:1650)
Chromatin interactive
region (count:68)
LncRNA
region (count:1)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:992 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr14:105646970-105647099	K562	blood:	n/a	n/a
2	ATF3	chr14:105647527-105647695	GM12878	blood:	n/a	n/a
3	ATF3	chr14:105647476-105647754	K562	blood:	n/a	n/a
4	ATF3	chr14:105665582-105665772	K562	blood:	n/a	n/a
5	ATF3	chr14:105647408-105647698	GM12878	blood:	n/a	n/a
6	BACH1	chr14:105647431-105647661	H1-hESC	embryonic stem cell:	n/a	n/a
7	BACH1	chr14:105662435-105662753	H1-hESC	embryonic stem cell:	n/a	n/a
8	BACH1	chr14:105650175-105650256	H1-hESC	embryonic stem cell:	n/a	n/a
9	BACH1	chr14:105663077-105663199	H1-hESC	embryonic stem cell:	n/a	n/a
10	BHLHE40	chr14:105641106-105641239	GM12878	blood:	n/a	n/a
11	BHLHE40	chr14:105647471-105647910	GM12878	blood:	n/a	chr14:105647556-105647572
12	BHLHE40	chr14:105647446-105647893	K562	blood:	n/a	chr14:105647556-105647572
13	BRCA1	chr14:105663594-105663903	Hela-S3	cervix:	n/a	n/a
14	CBX3	chr14:105665434-105665804	K562	blood:	n/a	n/a
15	CBX3	chr14:105654397-105654814	K562	blood:	n/a	n/a
16	CBX3	chr14:105654534-105654767	K562	blood:	n/a	n/a
17	CCNT2	chr14:105647484-105647639	K562	blood:	n/a	n/a
18	CCNT2	chr14:105665556-105665715	K562	blood:	n/a	n/a
19	CCNT2	chr14:105662979-105663291	K562	blood:	n/a	n/a
20	CEBPB	chr14:105646836-105646884	K562	blood:	n/a	n/a
21	CEBPB	chr14:105663593-105663880	Hela-S3	cervix:	n/a	n/a
22	CHD2	chr14:105663633-105663886	Hela-S3	cervix:	n/a	n/a
23	CHD2	chr14:105647556-105647857	Hela-S3	cervix:	n/a	n/a
24	CHD2	chr14:105662873-105662997	H1-hESC	embryonic stem cell:	n/a	n/a
25	CREB1	chr14:105647357-105647807	A549	lung:	n/a	n/a
26	CTBP2	chr14:105662423-105663290	H1-hESC	embryonic stem cell:	n/a	n/a
27	CTCF	chr14:105661960-105662110	HCPEpiC	choroid plexus:	n/a	chr14:105662010-105662023
28	CTCF	chr14:105666520-105666668	Hela-S3	cervix:	n/a	chr14:105666577-105666595 chr14:105666578-105666594
29	CTCF	chr14:105666520-105666670	SK-N-SH_RA	brain:	n/a	chr14:105666577-105666595 chr14:105666578-105666594
30	CTCF	chr14:105665020-105665170	GM12868	blood:	n/a	chr14:105665101-105665114 chr14:105665102-105665111
31	CTCF	chr14:105654400-105654550	GM12873	blood:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654465-105654481
32	CTCF	chr14:105654396-105654519	GM13977	blood:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654465-105654481
33	CTCF	chr14:105665071-105665153	Hela-S3	cervix:	n/a	chr14:105665101-105665114 chr14:105665102-105665111
34	CTCF	chr14:105664980-105665130	WERI-Rb-1	eye:	n/a	chr14:105665101-105665114 chr14:105665102-105665111
35	CTCF	chr14:105665040-105665190	GM12873	blood:	n/a	chr14:105665101-105665114 chr14:105665102-105665111
36	CTCF	chr14:105654259-105654649	H1-hESC	embryonic stem cell:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654292-105654300 chr14:105654465-105654481
37	CTCF	chr14:105666540-105666690	WERI-Rb-1	eye:	n/a	chr14:105666577-105666595 chr14:105666578-105666594
38	CTCF	chr14:105666460-105666610	Caco-2	colon:	n/a	chr14:105666577-105666595 chr14:105666578-105666594
39	CTCF	chr14:105666440-105666590	GM12878	blood:	n/a	n/a
40	CTCF	chr14:105654314-105654589	A549	lung:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654465-105654481
41	CTCF	chr14:105666605-105666620	Spleen_OC	spleen:	n/a	n/a
42	CTCF	chr14:105666420-105666570	GM12872	blood:	n/a	n/a
43	CTCF	chr14:105644580-105644730	GM12865	blood:	n/a	n/a
44	CTCF	chr14:105666557-105666648	A549	lung:	n/a	chr14:105666577-105666595 chr14:105666578-105666594
45	CTCF	chr14:105666575-105666641	MCF-7	breast:	n/a	chr14:105666577-105666595 chr14:105666578-105666594
46	CTCF	chr14:105654380-105654530	HUVEC	blood vessel:	n/a	chr14:105654466-105654479 chr14:105654464-105654482 chr14:105654471-105654479 chr14:105654459-105654480 chr14:105654465-105654481
47	CTCF	chr14:105660740-105660890	HUVEC	blood vessel:	n/a	chr14:105660792-105660810 chr14:105660795-105660804
48	CTCF	chr14:105647531-105647611	GM19240	blood:	n/a	n/a
49	CTCF	chr14:105644340-105644490	A549	lung:	n/a	n/a
50	CTCF	chr14:105654300-105654450	GM12868	blood:	n/a	n/a

(count:1650 , 50 per page) page: 1 2 3 4 5 6 7 ... 33

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr14:105648024-105648074	HCT-116	colon:	n/a
2	chr14:105657710-105657760	U87	brain:	n/a
3	chr14:105662805-105662855	HIPEpiC	eye:	n/a
4	chr14:105648024-105648074	HCT-116	colon:	n/a
5	chr14:105657710-105657760	U87	brain:	n/a
6	chr14:105662805-105662855	HIPEpiC	eye:	n/a
7	chr14:105663019-105663069	NHDF-neo	bronchial:	n/a
8	chr14:105647734-105647784	U87	brain:	n/a
9	chr14:105651786-105651836	MCF10A-Er-Src	breast:	n/a
10	chr14:105658685-105658735	HCT-116	colon:	n/a
11	chr14:105655178-105655228	ECC-1	luminal epithelium:	n/a
12	chr14:105648697-105648747	SK-N-SH_RA	brain:	n/a
13	chr14:105651786-105651836	HCPEpiC	choroid plexus:	n/a
14	chr14:105667315-105667365	PrEC	prostate:	n/a
15	chr14:105663402-105663452	PANC-1	pancreas:	n/a
16	chr14:105659225-105659275	GM12878	blood:	n/a
17	chr14:105651786-105651836	SKMC	muscle:	n/a
18	chr14:105660876-105660926	GM12892	blood:	n/a
19	chr14:105659225-105659275	SAEC	small airway:	n/a
20	chr14:105659807-105659857	HNPCEpiC	eye:	n/a
21	chr14:105663478-105663528	NHBE	bronchial:	n/a
22	chr14:105658685-105658735	Hela-S3	cervix:	n/a
23	chr14:105643522-105643572	GM12891	blood:	n/a
24	chr14:105649747-105649797	PFSK-1	brain:	n/a
25	chr14:105647510-105647560	GM06990	blood:	n/a
26	chr14:105648224-105648274	ECC-1	luminal epithelium:	n/a
27	chr14:105662787-105662837	PFSK-1	brain:	n/a
28	chr14:105667315-105667365	GM19239	blood:	n/a
29	chr14:105647507-105647557	T-47D	breast:	n/a
30	chr14:105663019-105663069	PANC-1	pancreas:	n/a
31	chr14:105649097-105649147	HIPEpiC	eye:	n/a
32	chr14:105647510-105647560	H1-hESC	embryonic stem cell:	embryo
33	chr14:105662805-105662855	PANC-1	pancreas:	n/a
34	chr14:105647407-105647457	HRPEpiC	eye:	n/a
35	chr14:105663019-105663069	NT2-D1	testis:	n/a
36	chr14:105658685-105658735	MCF-7	breast:	n/a
37	chr14:105647734-105647784	HCF	heart:	n/a
38	chr14:105647734-105647784	K562	blood:	n/a
39	chr14:105662805-105662855	GM12891	blood:	n/a
40	chr14:105651786-105651836	HPAEpiC	pulmonary alveolar:	n/a
41	chr14:105658949-105658999	LNCaP	prostate:	n/a
42	chr14:105648697-105648747	H1-hESC	embryonic stem cell:	embryo
43	chr14:105655178-105655228	HMEC	breast:	n/a
44	chr14:105663019-105663069	GM12878	blood:	n/a
45	chr14:105660876-105660926	Jurkat	blood:	n/a
46	chr14:105647194-105647244	SK-N-SH_RA	brain:	n/a
47	chr14:105647734-105647784	NB4	blood:	n/a
48	chr14:105663402-105663452	PrEC	prostate:	n/a
49	chr14:105647194-105647244	IMR90	lung:	fetal
50	chr14:105651786-105651836	Hela-S3	cervix:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr14:105614227..105617896-chr14:105637328..105640796,3	K562	blood:
2	chr14:105647226..105648734-chr14:105780236..105782314,2	MCF-7	breast:
3	chr14:105647951..105651045-chr14:105657056..105659475,3	MCF-7	breast:
4	chr14:105433467..105435387-chr14:105640925..105642715,2	MCF-7	breast:
5	chr14:105645461..105647244-chr14:105649629..105652172,2	MCF-7	breast:
6	chr14:105663088..105664783-chr14:105822900..105824850,2	MCF-7	breast:
7	chr14:105644378..105646118-chr14:105647825..105650297,2	MCF-7	breast:
8	chr14:105556806..105557482-chr14:105648408..105649374,2	K562	blood:
9	chr14:105556568..105557626-chr14:105644344..105645020,4	MCF-7	breast:
10	chr14:105667108..105669624-chr14:105818365..105820045,2	K562	blood:
11	chr14:105663948..105665922-chr14:105668555..105670749,2	MCF-7	breast:
12	chr14:105649676..105651978-chr14:105660260..105663010,3	K562	blood:
13	chr14:105646294..105648744-chr14:105860219..105862499,2	MCF-7	breast:
14	chr14:105649547..105651849-chr14:105660128..105661657,2	MCF-7	breast:
15	chr14:105647774..105650762-chr14:105651625..105655733,5	MCF-7	breast:
16	chr14:105647774..105650762-chr14:105651625..105655733,5	MCF-7	breast:
17	chr14:105660777..105662281-chr14:105668696..105670709,2	K562	blood:
18	chr14:105647877..105649605-chr14:105663025..105665566,2	MCF-7	breast:
19	chr14:105662898..105664724-chr14:105766217..105768467,3	MCF-7	breast:
20	chr14:105660449..105662714-chr14:105737778..105740475,2	MCF-7	breast:
21	chr14:105647951..105651045-chr14:105657056..105659475,3	MCF-7	breast:
22	chr14:105638805..105642866-chr14:105643000..105645474,4	K562	blood:
23	chr14:105660748..105662281-chr14:105767050..105768913,2	K562	blood:
24	chr14:105634303..105636398-chr14:105650780..105653428,2	MCF-7	breast:
25	chr14:105647532..105649524-chr14:105654465..105656702,2	MCF-7	breast:
26	chr14:105666418..105671078-chr14:105765699..105768969,5	MCF-7	breast:
27	chr14:105649676..105651978-chr14:105660260..105663010,3	K562	blood:
28	chr14:105642956..105644640-chr14:105647161..105649743,2	MCF-7	breast:
29	chr14:105655523..105657045-chr14:105657884..105660647,2	MCF-7	breast:
30	chr14:105658555..105662273-chr14:105665604..105667749,3	K562	blood:
31	chr14:105649547..105651849-chr14:105660128..105661657,2	MCF-7	breast:
32	chr14:105655523..105657045-chr14:105657884..105660647,2	MCF-7	breast:
33	chr14:105633273..105637288-chr14:105642227..105645314,5	MCF-7	breast:
34	chr14:105512170..105512763-chr14:105653793..105654556,2	MCF-7	breast:
35	chr14:105631465..105635896-chr14:105645452..105649219,9	MCF-7	breast:
36	chr14:105646332..105648438-chr14:105653932..105656621,2	K562	blood:
37	chr14:105638805..105642866-chr14:105643000..105645474,4	K562	blood:
38	chr14:105665162..105667358-chr14:105780436..105782662,2	MCF-7	breast:
39	chr14:105557263..105559202-chr14:105649515..105651192,2	MCF-7	breast:
40	chr14:105644378..105646118-chr14:105647825..105650297,2	MCF-7	breast:
41	chr14:105486956..105489375-chr14:105652100..105655755,4	MCF-7	breast:
42	chr14:105636897..105638962-chr14:105660422..105663007,2	MCF-7	breast:
43	chr14:105568093..105570383-chr14:105666909..105669878,2	K562	blood:
44	chr14:105637173..105640162-chr14:105646187..105648550,3	MCF-7	breast:
45	chr14:105635510..105639334-chr14:105658974..105662269,3	K562	blood:
46	chr14:105637173..105640162-chr14:105646187..105648550,3	MCF-7	breast:
47	chr14:105647019..105649589-chr14:105780411..105782070,2	MCF-7	breast:
48	chr14:105635244..105636129-chr14:105665708..105667054,3	K562	blood:
49	chr14:105557231..105560297-chr14:105661772..105664149,3	MCF-7	breast:
50	chr14:105650402..105652151-chr14:105657349..105659937,3	MCF-7	breast:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-BTBD6-1	chr14:105639787-105640155	ENSG00000257816.1

No data

Variant related genes	Relation type
NUDT14	TF binding region
JAG2	TF binding region
ENSG00000257622	TF binding region
NUDT14	CpG island
JAG2	CpG island
ENSG00000257622	CpG island
ENSG00000183828	chromatin interactions
ENSG00000257622	chromatin interactions
ENSG00000185024	chromatin interactions
ENSG00000256498	chromatin interactions
ENSG00000184916	chromatin interactions
ENSG00000184887	chromatin interactions
ENSG00000204469	chromatin interactions
ENSG00000170779	chromatin interactions
ENSG00000179364	chromatin interactions
ENSG00000257556	chromatin interactions

Extended variants
information (count: 972 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:972 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs187997115	chr14:105640052-105640053	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
2	rs147775456	chr14:105640075-105640076	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
3	rs12894531	chr14:105640076-105640077	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
4	rs370436687	chr14:105640085-105640086	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
5	rs587664195	chr14:105640099-105640100	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
6	rs587720884	chr14:105640117-105640118	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region lncRNA	3 gene(s)	Overlapped CNVs	n/a
7	rs60294316	chr14:105640172-105640173	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs373807400	chr14:105640185-105640186	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs141094344	chr14:105640198-105640199	Weak transcription Genic enhancers Bivalent Enhancer Enhancers Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs113710616	chr14:105640209-105640210	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs11851511	chr14:105640311-105640312	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Bivalent/Poised TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs587611306	chr14:105640404-105640405	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs587669170	chr14:105640439-105640440	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs11844206	chr14:105640460-105640461	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
15	rs11844119	chr14:105640486-105640487	Weak transcription Genic enhancers Enhancers Flanking Active TSS Bivalent/Poised TSS Bivalent Enhancer Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs183001612	chr14:105640630-105640631	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs187577218	chr14:105640644-105640645	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs587620891	chr14:105640645-105640646	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs587683967	chr14:105640664-105640665	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs587674967	chr14:105640746-105640747	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs587774782	chr14:105640761-105640762	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs587637542	chr14:105640863-105640864	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs587707433	chr14:105640955-105640956	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs880404	chr14:105640971-105640972	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs587644132	chr14:105640977-105640978	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs113524219	chr14:105640986-105640987	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Bivalent/Poised TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs145918527	chr14:105641003-105641004	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs587757334	chr14:105641024-105641025	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs184807583	chr14:105641032-105641033	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs186878770	chr14:105641035-105641036	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs587724953	chr14:105641037-105641038	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs74449621	chr14:105641056-105641057	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs79388252	chr14:105641119-105641120	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs140731296	chr14:105641220-105641221	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs587606370	chr14:105641222-105641223	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs111407599	chr14:105641277-105641278	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs587659270	chr14:105641299-105641300	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs192180306	chr14:105641353-105641354	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs587595535	chr14:105641373-105641374	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
40	rs148366383	chr14:105641460-105641461	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
41	rs587724154	chr14:105641469-105641470	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
42	rs75267610	chr14:105641477-105641478	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
43	rs10220575	chr14:105641485-105641486	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
44	rs587754228	chr14:105641510-105641511	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
45	rs587650143	chr14:105641552-105641553	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
46	rs141544278	chr14:105641588-105641589	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
47	rs587766546	chr14:105641589-105641590	Weak transcription Strong transcription Genic enhancers Enhancers Bivalent Enhancer Flanking Active TSS Flanking Bivalent TSS/Enh Active TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
48	rs184265150	chr14:105641604-105641605	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs587700491	chr14:105641646-105641647	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs201305180	chr14:105641738-105641739	Weak transcription Genic enhancers Enhancers Bivalent Enhancer Active TSS Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Retinoblastoma	21504564	CNVD
High-proliferative meningiomas	17937814	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
Lung cancer	18438408	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Colorectal cancer	16774939	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
Neuroblastoma	18923191	CNVD
Barrett''s syndrome	19417022	CNVD
cataract	16735990	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Developmental delay	21147756	CNVD
Cancer	20164920	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Biliary cancer	19435499	CNVD
Follicular lymphoma	20505157	CNVD
Acute lymphoblastic leukemia	20139093	CNVD
Hepatocellular carcinoma	16750200	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Glioblastoma multiforme	21922591	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Ovarian cancer	22174824	CNVD
Non-small cell lung cancer	18320023	CNVD
Melanoma	17363583	CNVD
Prostate cancer	18632612	CNVD
Congenital heart defect	22367666	CNVD
Developmental delay	22367666	CNVD
Genitourinary abnormalities	22367666	CNVD
Intellectual disability	22367666	CNVD
Microcephaly	22367666	CNVD
Muscularhypotonia	22367666	CNVD
Ocular coloboma	22367666	CNVD
Teratozoospermia	22367666	CNVD
Cervical cancer	21062161	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Breast cancer	21990379	CNVD
Breast cancer	16417655	CNVD
22q11 deletion syndrome	22511897	CNVD
Cancer	21129771	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Schizophrenia	21399695	CNVD
Intracranial ependymoma	16609018	CNVD
Lung adenocarcinoma	17086460	CNVD
Gastric adenocarcinoma	19115996	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
14q deletion syndrome	22511897	CNVD
Epilepsy	22083797	CNVD
Ovarian cancer	21720365	CNVD
Cancer	17440070	CNVD
Neurocytoma	17123091	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Central neurocytomas	17123091	CNVD
Acute lymphoblastic leukemia	17315016	CNVD
Lung cancer	17086460	CNVD
Mortal	21835882	CNVD
small cell lung cancer	17426248	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Schizophrenia	20967226	CNVD
early-passage human iPS cells	21368824	CNVD
Williams Syndrome	20824207	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Pancreatic cancer	17952125	CNVD
Schizophrenia	23813976	CNVD
lymphocytic leukemia	21291569	CNVD
Cancer	20164919	CNVD
small cell lung cancer	20016488	CNVD
Recurrent pregnancy loss	19789632	CNVD
Aortic dissecting aneurysms	22263138	CNVD
Stenocardia	21860640	CNVD
Vasospasm	21860640	CNVD
Non-syndromic sensorineural hearing loss	17431168	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	19587683	CNVD

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

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr14:105635200-105642200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
2	chr14:105635600-105641400	Enhancers	Pancreas	Pancrea
3	chr14:105635800-105645000	Genic enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
4	chr14:105635800-105647000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr14:105636200-105642200	Weak transcription	K562	blood
6	chr14:105636600-105641200	Weak transcription	iPS-15b Cell Line	embryonic stem cell
7	chr14:105637000-105640000	Weak transcription	Brain Cingulate Gyrus	brain
8	chr14:105637200-105642400	Weak transcription	Brain Inferior Temporal Lobe	brain
9	chr14:105637400-105640200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
10	chr14:105637400-105640800	Weak transcription	Primary T helper naive cells from peripheral blood	blood
11	chr14:105637400-105640800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
12	chr14:105637400-105642400	Weak transcription	Brain Angular Gyrus	brain
13	chr14:105637400-105646800	Weak transcription	Cortex derived primary cultured neurospheres	brain
14	chr14:105637600-105645800	Enhancers	Fetal Muscle Leg	muscle
15	chr14:105637600-105646000	Weak transcription	Brain Hippocampus Middle	brain
16	chr14:105637800-105640200	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
17	chr14:105637800-105640200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr14:105637800-105640400	Weak transcription	Primary T helper cells PMA-I stimulated	--
19	chr14:105637800-105640400	Weak transcription	Primary T helper cells fromperipheralblood	blood
20	chr14:105637800-105640600	Weak transcription	Primary B cells from cord blood	blood
21	chr14:105637800-105640600	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr14:105637800-105641400	Weak transcription	Psoas Muscle	Psoas
23	chr14:105637800-105641400	Weak transcription	HSMMtube	muscle
24	chr14:105637800-105642200	Weak transcription	Brain Anterior Caudate	brain
25	chr14:105637800-105642200	Weak transcription	A549	lung
26	chr14:105637800-105642200	Weak transcription	Hela-S3	cervix
27	chr14:105637800-105643400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
28	chr14:105637800-105643600	Weak transcription	Liver	Liver
29	chr14:105638000-105640200	Weak transcription	Primary hematopoietic stem cells	blood
30	chr14:105638000-105640400	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
31	chr14:105638000-105640600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
32	chr14:105638000-105640600	Weak transcription	Primary T cells from cord blood	blood
33	chr14:105638000-105640600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
34	chr14:105638000-105641200	Weak transcription	Esophagus	oesophagus
35	chr14:105638000-105641600	Weak transcription	HSMM	muscle
36	chr14:105638000-105646800	Weak transcription	Ovary	ovary
37	chr14:105638200-105640200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
38	chr14:105638200-105640200	Weak transcription	Lung	lung
39	chr14:105638200-105640400	Weak transcription	Adipose Nuclei	Adipose
40	chr14:105638200-105640600	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
41	chr14:105638200-105641200	Weak transcription	Gastric	stomach
42	chr14:105638200-105645800	Weak transcription	Right Ventricle	heart
43	chr14:105638400-105640600	Weak transcription	Skeletal Muscle Female	skeletal muscle
44	chr14:105638400-105641200	Weak transcription	Rectal Mucosa Donor 29	rectum
45	chr14:105638600-105640000	Weak transcription	Spleen	Spleen
46	chr14:105638600-105646600	Weak transcription	Fetal Heart	heart
47	chr14:105639000-105645400	Weak transcription	Fetal Brain Female	brain
48	chr14:105639000-105645800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr14:105639200-105640000	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Female	--
50	chr14:105639400-105640800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood

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