Variant report

Variant	esv3424713
Chromosome Location	chr1:154473153-154475701
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	BACH1	chr1:154474694-154474836	H1-hESC	embryonic stem cell:	n/a	n/a
2	BHLHE40	chr1:154474924-154475153	GM12878	blood:	n/a	chr1:154475043-154475059 chr1:154474975-154474991 chr1:154475094-154475110
3	CEBPB	chr1:154474221-154474356	HepG2	liver:	n/a	chr1:154474300-154474311
4	CEBPB	chr1:154474047-154474519	MCF-7	breast:	n/a	chr1:154474300-154474311
5	CEBPB	chr1:154474124-154474479	ECC-1	luminal epithelium:	n/a	chr1:154474300-154474311
6	CEBPB	chr1:154473971-154474633	A549	lung:	n/a	chr1:154474300-154474311
7	CEBPB	chr1:154474119-154474493	K562	blood:	n/a	chr1:154474300-154474311
8	CEBPB	chr1:154474201-154474450	K562	blood:	n/a	chr1:154474300-154474311
9	CEBPB	chr1:154474069-154474504	H1-hESC	embryonic stem cell:	n/a	chr1:154474300-154474311
10	CEBPB	chr1:154474046-154474595	ECC-1	luminal epithelium:	n/a	chr1:154474300-154474311
11	CEBPB	chr1:154474271-154474320	Hela-S3	cervix:	n/a	chr1:154474300-154474311
12	CEBPB	chr1:154474113-154474492	HepG2	liver:	n/a	chr1:154474300-154474311
13	CEBPB	chr1:154474136-154474472	A549	lung:	n/a	chr1:154474300-154474311
14	CEBPB	chr1:154474183-154474434	HepG2	liver:	n/a	chr1:154474300-154474311
15	CEBPB	chr1:154474120-154474489	IMR90	lung:	n/a	chr1:154474300-154474311
16	CEBPB	chr1:154474207-154474525	A549	lung:	n/a	chr1:154474300-154474311
17	CEBPB	chr1:154474135-154474513	MCF-7	breast:	n/a	chr1:154474300-154474311
18	CEBPB	chr1:154474117-154474492	HepG2	liver:	n/a	chr1:154474300-154474311
19	CHD2	chr1:154475227-154475499	H1-hESC	embryonic stem cell:	n/a	n/a
20	CTCF	chr1:154475567-154475657	H1-hESC	embryonic stem cell:	n/a	n/a
21	CTCF	chr1:154474920-154475070	HUVEC	blood vessel:	n/a	chr1:154474958-154474971 chr1:154474956-154474974
22	CTCF	chr1:154475451-154475510	Fibrobl	skin:	n/a	n/a
23	E2F6	chr1:154474013-154475849	H1-hESC	embryonic stem cell:	n/a	chr1:154475683-154475692 chr1:154474738-154474747 chr1:154475247-154475254 chr1:154474983-154474992 chr1:154475362-154475374 chr1:154475038-154475048
24	E2F6	chr1:154473973-154475840	H1-hESC	embryonic stem cell:	n/a	chr1:154475683-154475692 chr1:154474738-154474747 chr1:154475247-154475254 chr1:154474983-154474992 chr1:154475362-154475374 chr1:154475038-154475048
25	EGR1	chr1:154474220-154474410	K562	blood:	n/a	chr1:154474311-154474325
26	EGR1	chr1:154474189-154474363	K562	blood:	n/a	chr1:154474311-154474325
27	EGR1	chr1:154474464-154474658	GM12878	blood:	n/a	chr1:154474574-154474587 chr1:154474571-154474585 chr1:154474573-154474587 chr1:154474522-154474532 chr1:154474575-154474584 chr1:154474575-154474585
28	EGR1	chr1:154474175-154474487	ECC-1	luminal epithelium:	n/a	chr1:154474311-154474325
29	EGR1	chr1:154474203-154474402	GM12878	blood:	n/a	chr1:154474311-154474325
30	EGR1	chr1:154474701-154474830	GM12878	blood:	n/a	chr1:154474734-154474748 chr1:154474817-154474830 chr1:154474735-154474745
31	GABPA	chr1:154474068-154474427	H1-hESC	embryonic stem cell:	n/a	n/a
32	GTF2F1	chr1:154475046-154475533	H1-hESC	embryonic stem cell:	n/a	n/a
33	HMGN3	chr1:154475062-154475189	K562	blood:	n/a	n/a
34	JUN	chr1:154475060-154475282	H1-hESC	embryonic stem cell:	n/a	n/a
35	JUND	chr1:154474421-154474445	H1-hESC	embryonic stem cell:	n/a	n/a
36	MAX	chr1:154474923-154475703	H1-hESC	embryonic stem cell:	n/a	chr1:154475552-154475562 chr1:154475484-154475493 chr1:154475160-154475179 chr1:154475164-154475175
37	MAX	chr1:154474027-154475856	H1-hESC	embryonic stem cell:	n/a	chr1:154474736-154474746 chr1:154475552-154475562 chr1:154474854-154474864 chr1:154475484-154475493 chr1:154474576-154474585 chr1:154475160-154475179 chr1:154475164-154475175
38	MAX	chr1:154474033-154475830	H1-hESC	embryonic stem cell:	n/a	chr1:154474736-154474746 chr1:154475552-154475562 chr1:154474854-154474864 chr1:154475484-154475493 chr1:154474576-154474585 chr1:154475160-154475179 chr1:154475164-154475175
39	MAX	chr1:154474862-154475636	HUVEC	blood vessel:	n/a	chr1:154475552-154475562 chr1:154475484-154475493 chr1:154475160-154475179 chr1:154475164-154475175
40	MAX	chr1:154475185-154475538	ECC-1	luminal epithelium:	n/a	chr1:154475484-154475493
41	MXI1	chr1:154474997-154475323	H1-hESC	embryonic stem cell:	n/a	n/a
42	MYC	chr1:154474886-154475095	HUVEC	blood vessel:	n/a	n/a
43	MYC	chr1:154475164-154475270	HUVEC	blood vessel:	n/a	chr1:154475164-154475175
44	MYC	chr1:154474193-154474421	H1-hESC	embryonic stem cell:	n/a	n/a
45	MYC	chr1:154475104-154475119	HUVEC	blood vessel:	n/a	n/a
46	MYC	chr1:154475289-154475570	HUVEC	blood vessel:	n/a	chr1:154475552-154475562 chr1:154475484-154475493
47	MYC	chr1:154475282-154475284	HUVEC	blood vessel:	n/a	n/a
48	MYC	chr1:154475028-154475387	H1-hESC	embryonic stem cell:	n/a	chr1:154475160-154475179 chr1:154475164-154475175
49	PAX5	chr1:154474476-154475207	GM12892	blood:	n/a	n/a
50	POLR2A	chr1:154473194-154473522	HUVEC	blood vessel:	n/a	n/a

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:154474108-154474158	K562	blood:	n/a
2	chr1:154474530-154474580	BJ	skin:	n/a
3	chr1:154475139-154475189	HCT-116	colon:	n/a
4	chr1:154475688-154475738	SK-N-MC	brain:	n/a
5	chr1:154474518-154474568	GM06990	blood:	n/a
6	chr1:154475269-154475319	Caco-2	colon:	n/a
7	chr1:154475269-154475319	HNPCEpiC	eye:	n/a
8	chr1:154474344-154474394	NT2-D1	testis:	n/a
9	chr1:154473340-154473390	U87	brain:	n/a
10	chr1:154475139-154475189	BE2_C	brain:	n/a
11	chr1:154475173-154475223	SAEC	small airway:	n/a
12	chr1:154474344-154474394	RPTEC	kidney:	n/a
13	chr1:154474518-154474568	HUVEC	blood vessel:	n/a
14	chr1:154475688-154475738	HCPEpiC	choroid plexus:	n/a
15	chr1:154474528-154474578	Hela-S3	cervix:	n/a
16	chr1:154474344-154474394	SK-N-SH	brain:	n/a
17	chr1:154474528-154474578	ProgFib	skin:	n/a
18	chr1:154475688-154475738	HCT-116	colon:	n/a
19	chr1:154475173-154475223	HMEC	breast:	n/a
20	chr1:154474530-154474580	GM06990	blood:	n/a
21	chr1:154474108-154474158	BJ	skin:	n/a
22	chr1:154474518-154474568	ECC-1	luminal epithelium:	n/a
23	chr1:154475269-154475319	AG04450	lung:	fetal
24	chr1:154475173-154475223	Hela-S3	cervix:	n/a
25	chr1:154475269-154475319	HAEpiC	amniotic membrane:	n/a
26	chr1:154474528-154474578	MCF10A-Er-Src	breast:	n/a
27	chr1:154473340-154473390	SK-N-MC	brain:	n/a
28	chr1:154475688-154475738	GM19239	blood:	n/a
29	chr1:154475068-154475118	HEK293	kidney:	embryo
30	chr1:154475068-154475118	HMEC	breast:	n/a
31	chr1:154474344-154474394	T-47D	breast:	n/a
32	chr1:154475688-154475738	NHDF-neo	bronchial:	n/a
33	chr1:154475173-154475223	HCT-116	colon:	n/a
34	chr1:154474530-154474580	SK-N-MC	brain:	n/a
35	chr1:154474530-154474580	BE2_C	brain:	n/a
36	chr1:154475688-154475738	T-47D	breast:	n/a
37	chr1:154474108-154474158	HRPEpiC	eye:	n/a
38	chr1:154474344-154474394	HPAEpiC	pulmonary alveolar:	n/a
39	chr1:154475139-154475189	AoSMC	blood vessel:	n/a
40	chr1:154474108-154474158	Hepatocyte	liver:	n/a
41	chr1:154475173-154475223	HL-60	blood:	n/a
42	chr1:154475688-154475738	HEK293	kidney:	embryo
43	chr1:154474800-154474850	A549	lung:	n/a
44	chr1:154475068-154475118	H1-hESC	embryonic stem cell:	embryo
45	chr1:154475269-154475319	BJ	skin:	n/a
46	chr1:154475139-154475189	HepG2	liver:	n/a
47	chr1:154474528-154474578	SK-N-SH	brain:	n/a
48	chr1:154474108-154474158	HL-60	blood:	n/a
49	chr1:154473340-154473390	LNCaP	prostate:	n/a
50	chr1:154474344-154474394	Hepatocyte	liver:	n/a

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr1:154191216..154193063-chr1:154472171..154474701,2	K562	blood:
2	chr1:154473384..154476326-chr1:154529885..154532539,2	MCF-7	breast:

Variant related genes	Relation type
TDRD10	TF binding region
SHE	TF binding region
TDRD10	CpG island
SHE	CpG island
ENSG00000143569	chromatin interactions
ENSG00000160714	chromatin interactions
ENSG00000143612	chromatin interactions

Extended variants
information (count: 107 )
Associated
traits (count: 114 )

Variant overlapped rSNPs/rCNVs (count:107 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs566623168	chr1:154473204-154473205	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs534118574	chr1:154473221-154473222	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs558609120	chr1:154473235-154473236	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs570612045	chr1:154473327-154473328	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs537691062	chr1:154473379-154473380	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs138923805	chr1:154473387-154473388	Bivalent/Poised TSS Enhancers Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs574596733	chr1:154473419-154473420	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs183716125	chr1:154473426-154473427	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs190695609	chr1:154473427-154473428	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs572622427	chr1:154473490-154473491	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs546453213	chr1:154473499-154473500	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
12	rs564659575	chr1:154473518-154473519	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
13	rs193045603	chr1:154473549-154473550	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
14	rs545929135	chr1:154473554-154473555	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
15	rs377317608	chr1:154473562-154473563	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
16	rs562519420	chr1:154473567-154473568	Bivalent/Poised TSS Bivalent Enhancer Enhancers Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
17	rs374422571	chr1:154473617-154473618	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs529833759	chr1:154473640-154473641	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs547851276	chr1:154473651-154473652	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs6700296	chr1:154473660-154473661	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
21	rs527333409	chr1:154473667-154473668	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs552438132	chr1:154473715-154473716	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs6683078	chr1:154473726-154473727	Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS Active TSS Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs537602616	chr1:154473819-154473820	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs201817326	chr1:154473841-154473842	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs185291842	chr1:154473859-154473860	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs189824875	chr1:154473866-154473867	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
28	rs572586275	chr1:154473873-154473874	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
29	rs545933242	chr1:154473879-154473880	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
30	rs368651278	chr1:154473895-154473896	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
31	rs554001064	chr1:154473904-154473905	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
32	rs144880846	chr1:154473913-154473914	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
33	rs376792011	chr1:154473939-154473940	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
34	rs375939195	chr1:154473947-154473948	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
35	rs368740035	chr1:154473957-154473958	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
36	rs138829106	chr1:154473961-154473962	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
37	rs371513088	chr1:154473966-154473967	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
38	rs35396239	chr1:154473992-154473993	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
39	rs376607829	chr1:154473996-154473997	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
40	rs35702906	chr1:154473998-154473999	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Flanking Active TSS Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
41	rs267598056	chr1:154474043-154474044	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs138194878	chr1:154474062-154474063	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs199994588	chr1:154474112-154474113	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs4845635	chr1:154474131-154474132	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
45	rs375522819	chr1:154474132-154474133	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs369891189	chr1:154474152-154474153	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs373752177	chr1:154474156-154474157	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region CpG island Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs200876451	chr1:154474189-154474190	Bivalent/Poised TSS Flanking Bivalent TSS/Enh Bivalent Enhancer Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
49	rs202144458	chr1:154474222-154474223	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
50	rs12729294	chr1:154474285-154474286	Bivalent/Poised TSS Bivalent Enhancer Flanking Bivalent TSS/Enh Active TSS Flanking Active TSS	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:114)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	CNVD
Non-small cell lung cancer	21385341	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Breast cancer	20409316	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Glioblastoma multiforme	21080181	CNVD
Cancer	21183584	CNVD
Multiple myeloma	16461302	CNVD
Lung cancer	18438408	CNVD
Rett syndrome	21593744	CNVD
Intellectual disability	22102821	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Systemic lupus erythematosus	21956041	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Non-small cell lung cancer	21829676	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Non-small cell lung cancer	21044232	CNVD
Cervical cancer	21063398	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	20632083	CNVD
Endometrial cancer	22040021	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Medulloblastoma	21292688	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	21264507	CNVD
Multiple myeloma	21628407	CNVD
Cancer	16751803	CNVD
Prostate cancer	16705090	CNVD
Neuroblastoma	19435921	CNVD
Breast cancer	17850661	CNVD
Breast cancer	16461572	CNVD
Intracranial tumor	16823260	CNVD
Medulloblastoma	18056178	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Primary mediastinal b-cell lymphoma	17728785	CNVD
Colorectal cancer	16272173	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Neuroblastoma	21899760	CNVD
Breast cancer	17899364	CNVD
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Retinoblastoma	19183342	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Ewing''s sarcoma	17952124	CNVD
Osteosarcoma	17242211	CNVD
Ovarian cancer	17242211	CNVD
Ovine squamous-cell carcinoma	17599052	CNVD
Schizophrenia	18990708	CNVD
Sudden cardiac death	19188705	CNVD
Plasma-cell dyscrasia	16705089	CNVD
Myeloma	17024118	CNVD
Cancer	17060936	CNVD
Multiple myeloma	16616336	CNVD
Type 2 diabetes	19141583	CNVD
Chordoma	18071362	CNVD
Hepatocellular carcinoma	18803288	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	17001317	CNVD
Urothelial carcinoma	21177765	CNVD
Burkitt''s lymphoma	19759907	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21509527	CNVD
Bladder cancer	21909424	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Gastrointestinal cancer	16790693	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Glioblastoma multiforme	21138945	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21611746	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Myelofibrosis	22110671	CNVD
Follicular lymphoma	20505157	CNVD
Liver carcinoma	19366792	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:283 , 50 per page) page: 1 2 3 4 5 6

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:154461800-154473800	Weak transcription	Pancreas	Pancrea
2	chr1:154471200-154474000	Bivalent Enhancer	Primary neutrophils fromperipheralblood	blood
3	chr1:154471200-154475400	Active TSS	Right Atrium	heart
4	chr1:154471400-154473200	Active TSS	Liver	Liver
5	chr1:154471600-154473600	Enhancers	Breast Myoepithelial Primary Cells	Breast
6	chr1:154471600-154473800	Active TSS	Right Ventricle	heart
7	chr1:154471800-154473400	Flanking Active TSS	HUVEC	blood vessel
8	chr1:154471800-154473800	Bivalent/Poised TSS	Fetal Stomach	stomach
9	chr1:154471800-154473800	Bivalent/Poised TSS	Skeletal Muscle Female	skeletal muscle
10	chr1:154471800-154474200	Bivalent/Poised TSS	Psoas Muscle	Psoas
11	chr1:154472000-154475200	Bivalent/Poised TSS	Left Ventricle	heart
12	chr1:154472200-154473800	Bivalent/Poised TSS	Fetal Muscle Leg	muscle
13	chr1:154472200-154473800	Bivalent/Poised TSS	Stomach Smooth Muscle	stomach
14	chr1:154472200-154475400	Bivalent/Poised TSS	Duodenum Smooth Muscle	Duodenum
15	chr1:154472200-154475400	Bivalent/Poised TSS	Skeletal Muscle Male	skeletal muscle
16	chr1:154472400-154473800	Bivalent/Poised TSS	Fetal Muscle Trunk	muscle
17	chr1:154472400-154474000	Bivalent/Poised TSS	Brain Anterior Caudate	brain
18	chr1:154472400-154474000	Bivalent/Poised TSS	Fetal Intestine Small	intestine
19	chr1:154472400-154474400	Bivalent/Poised TSS	Rectal Mucosa Donor 29	rectum
20	chr1:154472400-154475400	Bivalent/Poised TSS	Duodenum Mucosa	Duodenum
21	chr1:154472600-154473800	Bivalent/Poised TSS	Fetal Intestine Large	intestine
22	chr1:154472600-154474000	Bivalent/Poised TSS	Fetal Kidney	kidney
23	chr1:154472600-154474200	Bivalent/Poised TSS	Fetal Lung	lung
24	chr1:154472800-154473200	Active TSS	Esophagus	oesophagus
25	chr1:154472800-154473800	Bivalent/Poised TSS	Colonic Mucosa	Colon
26	chr1:154472800-154473800	Bivalent/Poised TSS	Fetal Adrenal Gland	Adrenal Gland
27	chr1:154472800-154473800	Bivalent/Poised TSS	Placenta	Placenta
28	chr1:154472800-154473800	Active TSS	Ovary	ovary
29	chr1:154472800-154474800	Bivalent/Poised TSS	Pancreatic Islets	Pancreatic Islet
30	chr1:154472800-154475200	Bivalent/Poised TSS	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
31	chr1:154472800-154475200	Bivalent/Poised TSS	Colon Smooth Muscle	Colon
32	chr1:154472800-154475200	Bivalent/Poised TSS	Rectal Smooth Muscle	rectum
33	chr1:154473000-154473800	Bivalent/Poised TSS	Adipose Nuclei	Adipose
34	chr1:154473000-154474000	Active TSS	Spleen	Spleen
35	chr1:154473000-154474200	Bivalent/Poised TSS	Fetal Thymus	thymus
36	chr1:154473000-154475000	Active TSS	Lung	lung
37	chr1:154473200-154473400	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
38	chr1:154473200-154473400	Bivalent/Poised TSS	Esophagus	oesophagus
39	chr1:154473200-154474400	Flanking Active TSS	Liver	Liver
40	chr1:154473200-154475200	Bivalent/Poised TSS	ES-I3 Cell Line	embryonic stem cell
41	chr1:154473200-154475200	Bivalent/Poised TSS	Rectal Mucosa Donor 31	rectum
42	chr1:154473200-154475600	Bivalent/Poised TSS	Brain Hippocampus Middle	brain
43	chr1:154473200-154475600	Bivalent/Poised TSS	Brain Dorsolateral Prefrontal Cortex	brain
44	chr1:154473400-154473800	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
45	chr1:154473400-154474800	Bivalent/Poised TSS	Aorta	Aorta
46	chr1:154473400-154475000	Bivalent/Poised TSS	Brain Inferior Temporal Lobe	brain
47	chr1:154473400-154475200	Active TSS	HUVEC	blood vessel
48	chr1:154473400-154475400	Bivalent/Poised TSS	Brain Cingulate Gyrus	brain
49	chr1:154473600-154473800	Bivalent/Poised TSS	iPS-15b Cell Line	embryonic stem cell
50	chr1:154473600-154473800	Bivalent Enhancer	Monocytes-CD14+_RO01746	blood

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