Variant report

Variant	nsv546148
Chromosome Location	chr1:45500294-45627663
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:532)
CpG islands
(count:122)
Chromatin interactive
region (count:65)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:532 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:45569325-45569661	HepG2	liver:	n/a	n/a
2	ARID3A	chr1:45600043-45600639	HepG2	liver:	n/a	n/a
3	ARID3A	chr1:45503170-45503605	K562	blood:	n/a	n/a
4	ARID3A	chr1:45501365-45501700	K562	blood:	n/a	n/a
5	ARID3A	chr1:45574541-45574670	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:45504804-45504866	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:45504649-45505029	K562	blood:	n/a	n/a
8	ATF1	chr1:45503206-45503553	K562	blood:	n/a	n/a
9	ATF1	chr1:45501318-45501749	K562	blood:	n/a	n/a
10	ATF1	chr1:45504683-45504980	K562	blood:	n/a	n/a
11	ATF3	chr1:45504775-45505056	K562	blood:	n/a	n/a
12	ATF3	chr1:45503147-45503527	K562	blood:	n/a	n/a
13	ATF3	chr1:45550237-45550509	K562	blood:	n/a	n/a
14	BACH1	chr1:45503228-45503673	K562	blood:	n/a	n/a
15	BACH1	chr1:45563621-45563992	H1-hESC	embryonic stem cell:	n/a	n/a
16	BACH1	chr1:45563631-45563990	K562	blood:	n/a	n/a
17	BHLHE40	chr1:45550297-45550496	K562	blood:	n/a	n/a
18	BHLHE40	chr1:45518831-45519032	GM12878	blood:	n/a	n/a
19	BHLHE40	chr1:45504624-45505102	K562	blood:	n/a	n/a
20	BHLHE40	chr1:45503235-45503558	K562	blood:	n/a	n/a
21	BHLHE40	chr1:45501370-45501684	K562	blood:	n/a	n/a
22	CBX3	chr1:45504532-45505071	K562	blood:	n/a	n/a
23	CCNT2	chr1:45504641-45505058	K562	blood:	n/a	n/a
24	CCNT2	chr1:45501280-45501728	K562	blood:	n/a	n/a
25	CCNT2	chr1:45503151-45503646	K562	blood:	n/a	n/a
26	CEBPB	chr1:45561246-45561398	HepG2	liver:	n/a	chr1:45561305-45561316
27	CEBPB	chr1:45501321-45501699	K562	blood:	n/a	n/a
28	CEBPB	chr1:45550289-45550537	HepG2	liver:	n/a	chr1:45550418-45550429
29	CEBPB	chr1:45591319-45591494	ECC-1	luminal epithelium:	n/a	chr1:45591385-45591396
30	CEBPB	chr1:45594545-45595028	A549	lung:	n/a	chr1:45594886-45594897
31	CEBPB	chr1:45561175-45561462	IMR90	lung:	n/a	chr1:45561305-45561316
32	CEBPB	chr1:45594684-45595002	K562	blood:	n/a	chr1:45594886-45594897
33	CEBPB	chr1:45582550-45582834	IMR90	lung:	n/a	chr1:45582697-45582708 chr1:45582698-45582709 chr1:45582697-45582710
34	CEBPB	chr1:45508434-45508671	HepG2	liver:	n/a	chr1:45508570-45508581
35	CEBPB	chr1:45591339-45591422	IMR90	lung:	n/a	chr1:45591385-45591396
36	CEBPB	chr1:45594669-45594966	MCF-7	breast:	n/a	chr1:45594886-45594897
37	CEBPB	chr1:45561155-45561465	K562	blood:	n/a	chr1:45561305-45561316
38	CEBPB	chr1:45594709-45595072	IMR90	lung:	n/a	chr1:45594886-45594897
39	CEBPB	chr1:45508416-45508739	K562	blood:	n/a	chr1:45508570-45508581
40	CEBPB	chr1:45561120-45561488	HepG2	liver:	n/a	chr1:45561305-45561316
41	CEBPB	chr1:45594702-45595076	HepG2	liver:	n/a	chr1:45594886-45594897
42	CEBPB	chr1:45508464-45508656	IMR90	lung:	n/a	chr1:45508570-45508581
43	CEBPB	chr1:45594762-45594930	HepG2	liver:	n/a	chr1:45594886-45594897
44	CEBPB	chr1:45594758-45595022	HCT-116	colon:	n/a	chr1:45594886-45594897
45	CEBPB	chr1:45550296-45550567	K562	blood:	n/a	chr1:45550418-45550429
46	CEBPB	chr1:45561151-45561476	H1-hESC	embryonic stem cell:	n/a	chr1:45561305-45561316
47	CEBPB	chr1:45594700-45595073	Hela-S3	cervix:	n/a	chr1:45594886-45594897
48	CEBPB	chr1:45594706-45595072	A549	lung:	n/a	chr1:45594886-45594897
49	CEBPB	chr1:45561154-45561417	K562	blood:	n/a	chr1:45561305-45561316
50	CEBPB	chr1:45591305-45591573	MCF-7	breast:	n/a	chr1:45591385-45591396

(count:122 , 50 per page) page: 1 2 3

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:45572163-45572213	HEEpiC	esophagus:	n/a
2	chr1:45572163-45572213	Jurkat	blood:	n/a
3	chr1:45572163-45572213	MCF-7	breast:	n/a
4	chr1:45572163-45572213	Caco-2	colon:	n/a
5	chr1:45583723-45583773	Hela-S3	cervix:	n/a
6	chr1:45572163-45572213	SK-N-SH_RA	brain:	n/a
7	chr1:45572163-45572213	AG09309	skin:	n/a
8	chr1:45572163-45572213	HNPCEpiC	eye:	n/a
9	chr1:45583723-45583773	HCF	heart:	n/a
10	chr1:45583723-45583773	NB4	blood:	n/a
11	chr1:45572163-45572213	GM06990	blood:	n/a
12	chr1:45583723-45583773	AG09319	gingival:	n/a
13	chr1:45572163-45572213	K562	blood:	n/a
14	chr1:45572163-45572213	AG10803	skin:	n/a
15	chr1:45583723-45583773	SK-N-SH_RA	brain:	n/a
16	chr1:45583723-45583773	HL-60	blood:	n/a
17	chr1:45583723-45583773	A549	lung:	n/a
18	chr1:45572163-45572213	U87	brain:	n/a
19	chr1:45583723-45583773	GM06990	blood:	n/a
20	chr1:45572163-45572213	PANC-1	pancreas:	n/a
21	chr1:45583723-45583773	SK-N-SH	brain:	n/a
22	chr1:45572163-45572213	Hepatocyte	liver:	n/a
23	chr1:45572163-45572213	HepG2	liver:	n/a
24	chr1:45572163-45572213	GM19239	blood:	n/a
25	chr1:45572163-45572213	ProgFib	skin:	n/a
26	chr1:45583723-45583773	HIPEpiC	eye:	n/a
27	chr1:45583723-45583773	NHBE	bronchial:	n/a
28	chr1:45583723-45583773	PANC-1	pancreas:	n/a
29	chr1:45583723-45583773	HMEC	breast:	n/a
30	chr1:45583723-45583773	AG10803	skin:	n/a
31	chr1:45572163-45572213	HCPEpiC	choroid plexus:	n/a
32	chr1:45583723-45583773	SK-N-MC	brain:	n/a
33	chr1:45583723-45583773	HNPCEpiC	eye:	n/a
34	chr1:45572163-45572213	HL-60	blood:	n/a
35	chr1:45583723-45583773	CMK	blood:	n/a
36	chr1:45583723-45583773	Caco-2	colon:	n/a
37	chr1:45572163-45572213	A549	lung:	n/a
38	chr1:45572163-45572213	NB4	blood:	n/a
39	chr1:45583723-45583773	MCF-7	breast:	n/a
40	chr1:45583723-45583773	SKMC	muscle:	n/a
41	chr1:45583723-45583773	AoSMC	blood vessel:	n/a
42	chr1:45572163-45572213	Hela-S3	cervix:	n/a
43	chr1:45572163-45572213	HPAEpiC	pulmonary alveolar:	n/a
44	chr1:45572163-45572213	NHBE	bronchial:	n/a
45	chr1:45572163-45572213	HRE	kidney:	n/a
46	chr1:45572163-45572213	LNCaP	prostate:	n/a
47	chr1:45583723-45583773	RPTEC	kidney:	n/a
48	chr1:45572163-45572213	HCM	heart:	n/a
49	chr1:45583723-45583773	NT2-D1	testis:	n/a
50	chr1:45583723-45583773	HUVEC	blood vessel:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:45612052..45614882-chr1:45615056..45616964,2	K562	blood:
2	chr1:45503364..45509535-chr1:45510898..45517046,6	K562	blood:
3	chr1:45601104..45604532-chr1:45609883..45613262,3	K562	blood:
4	chr1:45483996..45486300-chr1:45594488..45596026,2	K562	blood:
5	chr1:45552821..45555517-chr1:45559008..45561806,2	MCF-7	breast:
6	chr1:45498340..45501082-chr1:45804198..45806208,2	K562	blood:
7	chr1:45478814..45481522-chr1:45521104..45523443,2	K562	blood:
8	chr1:45285200..45288152-chr1:45559027..45562009,2	K562	blood:
9	chr1:45476911..45478907-chr1:45608481..45610800,2	K562	blood:
10	chr1:45450629..45453531-chr1:45573646..45575498,2	K562	blood:
11	chr1:45498340..45501082-chr1:45804198..45806724,3	K562	blood:
12	chr1:45185912..45188809-chr1:45555640..45557709,2	K562	blood:
13	chr1:45285124..45286764-chr1:45554135..45555887,2	K562	blood:
14	chr1:45505490..45509535-chr1:45509540..45512957,3	K562	blood:
15	chr1:45579406..45580975-chr1:45584759..45586410,2	K562	blood:
16	chr1:45185795..45187646-chr1:45502768..45506079,3	K562	blood:
17	chr1:45595180..45597948-chr1:45601398..45603703,2	K562	blood:
18	chr1:45568343..45570582-chr1:45575672..45578540,2	K562	blood:
19	chr1:45595180..45598267-chr1:45601398..45603703,3	K562	blood:
20	chr1:45476938..45479048-chr1:45623410..45625753,2	K562	blood:
21	chr1:45622644..45625122-chr1:45685224..45687808,2	K562	blood:
22	chr1:45607994..45610896-chr1:45671367..45674054,2	MCF-7	breast:
23	chr1:45285124..45287446-chr1:45552897..45556279,3	K562	blood:
24	chr1:45478626..45481172-chr1:45552881..45556060,3	K562	blood:
25	chr1:45477633..45480305-chr1:45514821..45518438,3	K562	blood:
26	chr1:45496126..45498745-chr1:45510128..45512403,2	K562	blood:
27	chr1:45569785..45571943-chr1:45588128..45590653,2	K562	blood:
28	chr1:45187242..45188779-chr1:45607318..45609489,2	K562	blood:
29	chr1:45521218..45524154-chr1:45525277..45526789,2	K562	blood:
30	chr1:45549284..45552082-chr1:45559378..45561289,2	K562	blood:
31	chr1:45293006..45294513-chr1:45507730..45509268,2	K562	blood:
32	chr1:45497167..45499235-chr1:45500803..45502705,2	K562	blood:
33	chr1:45568343..45570582-chr1:45575672..45578540,2	K562	blood:
34	chr1:45551699..45553224-chr1:45605001..45607088,2	K562	blood:
35	chr1:45604686..45606706-chr1:45610501..45612917,2	K562	blood:
36	chr1:45604686..45606706-chr1:45610501..45612917,2	K562	blood:
37	chr1:45524312..45527029-chr1:45527867..45530740,2	K562	blood:
38	chr1:45500321..45502356-chr1:45502649..45504845,2	K562	blood:
39	chr1:45521218..45524154-chr1:45525277..45526789,2	K562	blood:
40	chr1:45492852..45494427-chr1:45515259..45518004,2	K562	blood:
41	chr1:45569785..45571943-chr1:45588128..45590653,2	K562	blood:
42	chr1:45576241..45578269-chr1:45578701..45581051,2	K562	blood:
43	chr1:45612052..45614882-chr1:45615056..45616964,2	K562	blood:
44	chr1:45579406..45580975-chr1:45584759..45586410,2	K562	blood:
45	chr1:45551699..45553224-chr1:45605001..45607088,2	K562	blood:
46	chr1:45607017..45608869-chr1:45636560..45638777,2	MCF-7	breast:
47	chr1:45557417..45559834-chr1:45561786..45564685,2	K562	blood:
48	chr1:45576241..45578269-chr1:45578701..45581051,2	K562	blood:
49	chr1:45450629..45452184-chr1:45572673..45575146,2	K562	blood:
50	chr1:45595180..45598267-chr1:45601398..45603703,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-ZSWIM5-1	chr1:45553747-45553909	NONHSAT002919
2	lnc-UROD-2	chr1:45542169-45543877	refGeneNc_2327_NR_024270

No data

Variant related genes	Relation type
ENSG00000264650	TF binding region
OSTCP5	TF binding region
ENSG00000264650	CpG island
OSTCP5	CpG island
ENSG00000126088	chromatin interactions
ENSG00000132781	chromatin interactions
ENSG00000070785	chromatin interactions
ENSG00000132773	chromatin interactions
ENSG00000126107	chromatin interactions
ENSG00000199377	chromatin interactions
ENSG00000162415	chromatin interactions
ENSG00000202444	chromatin interactions

Extended variants
information (count: 4312 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:4312 , 50 per page) page: 1 2 3 4 5 6 7 ... 87

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs6671633	chr1:45500294-45500295	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs187806580	chr1:45500317-45500318	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs536099598	chr1:45500381-45500382	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs549665435	chr1:45500391-45500392	Strong transcription Weak transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs116506980	chr1:45500403-45500404	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs141533923	chr1:45500434-45500435	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs12043559	chr1:45500466-45500467	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs558604580	chr1:45500479-45500480	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
9	rs552243798	chr1:45500539-45500540	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
10	rs78184567	chr1:45500553-45500554	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
11	rs373997982	chr1:45500556-45500557	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
12	rs151057084	chr1:45500557-45500558	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
13	rs574489185	chr1:45500647-45500648	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
14	rs543316646	chr1:45500652-45500653	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
15	rs12047556	chr1:45500665-45500666	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
16	rs113438923	chr1:45500675-45500676	Weak transcription Strong transcription	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
17	rs372841651	chr1:45500708-45500709	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
18	rs193148926	chr1:45500761-45500762	Weak transcription Strong transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
19	rs565379097	chr1:45500842-45500843	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
20	rs12409676	chr1:45500908-45500909	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
21	rs527824635	chr1:45501002-45501003	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
22	rs573410026	chr1:45501005-45501006	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
23	rs545155808	chr1:45501013-45501014	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
24	rs370147639	chr1:45501024-45501025	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
25	rs150235965	chr1:45501041-45501042	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
26	rs183244203	chr1:45501074-45501075	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
27	rs34814510	chr1:45501091-45501092	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs530057075	chr1:45501178-45501179	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs565346268	chr1:45501191-45501192	Strong transcription Weak transcription Enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs549626691	chr1:45501206-45501207	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs569646038	chr1:45501231-45501232	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs187562517	chr1:45501245-45501246	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs112879989	chr1:45501246-45501247	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs560448958	chr1:45501279-45501280	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs199979191	chr1:45501296-45501297	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs138902614	chr1:45501325-45501326	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs534379315	chr1:45501326-45501327	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs201182804	chr1:45501334-45501335	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs377635919	chr1:45501335-45501336	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs370874222	chr1:45501344-45501345	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs568027451	chr1:45501351-45501352	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs202174580	chr1:45501379-45501380	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs140690848	chr1:45501389-45501390	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs568026294	chr1:45501459-45501460	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs200273650	chr1:45501460-45501461	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs199737437	chr1:45501473-45501474	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs371031471	chr1:45501507-45501508	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs537079715	chr1:45501545-45501546	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs556875321	chr1:45501622-45501623	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs115244315	chr1:45501655-45501656	Strong transcription Weak transcription Enhancers Genic enhancers Flanking Active TSS	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Acute lymphoblastic leukemia	20067559	CNVD
Melanoma	18172304	CNVD
Glioblastoma multiforme	21080181	CNVD
Metanephric adenoma	20802469	CNVD
Breast cancer	17603634	CNVD
Soft tissue tumor	16732325	CNVD
Papillary thyroid carcinoma	21436994	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Colorectal cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Coronary Disease	20032323	CNVD
Prostate cancer	21965145	CNVD
Stargardt''s disease	17277736	CNVD
Neuroblastoma	17897457	CNVD
Uveal melanoma	21693616	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-syndromic sensorineural hearing loss	22290220	CNVD
Liposarcoma	21253554	CNVD
Breast cancer	21264507	CNVD
Acute myeloid leukemia	16864856	CNVD
Astrocytoma	17387387	CNVD
Cancer	21499728	CNVD
Glioblastoma multiforme	17387387	CNVD
Oligodendroglial tumors	17285580	CNVD
Neuroblastoma	17535989	CNVD
Pheochromocytoma	17535989	CNVD
Prostate cancer	16705090	CNVD
Astrocytoma	17934521	CNVD
Colorectal cancer	19359472	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Gastrointestinal stromal cancer	17535989	CNVD
Neuroblastoma	17533364	CNVD
Paraganglioma	17535989	CNVD
Pulmonary chondroma	17535989	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Non-syndromic sensorineural hearing loss	21030649	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Chronic myeloid leukemia	21384125	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Non-small cell lung cancer	21385341	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Chordoma	21602918	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Multiple myeloma	16461302	CNVD
Melanoma	17363583	CNVD
Cancer	21129771	CNVD
Autosomal dominant nocturnal frontal lobe epilepsy	18472482	CNVD
Hirschsprung''s Disease	21712996	CNVD
Non-small cell lung cancer	20864512	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Thrombocytopenia-absent radius syndrome	21933853	CNVD
Psychiatric disorder	22848183	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Hepatocellular carcinoma	16750200	CNVD
Burkitt''s lymphoma	18698080	CNVD
Breast cancer	20409316	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	17393978	CNVD
Cervical cancer	21062161	CNVD
Cancer	21183584	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	22174824	CNVD
Muscle-eye-brain disease	21572526	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21364760	CNVD
Breast cancer	20680643	CNVD
Colorectal cancer	19287155	CNVD
small cell lung cancer	20016488	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Chronic lymphocytic leukemia	21546498	CNVD

Chromatin state (count:669 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:45480800-45500600	Weak transcription	HepG2	liver
2	chr1:45480800-45501200	Weak transcription	Fetal Brain Male	brain
3	chr1:45480800-45510400	Weak transcription	Colon Smooth Muscle	Colon
4	chr1:45481200-45504600	Weak transcription	Colonic Mucosa	Colon
5	chr1:45481200-45510200	Weak transcription	Lung	lung
6	chr1:45481200-45525000	Weak transcription	Rectal Smooth Muscle	rectum
7	chr1:45481200-45527400	Weak transcription	Left Ventricle	heart
8	chr1:45482000-45523800	Weak transcription	Cortex derived primary cultured neurospheres	brain
9	chr1:45485800-45501400	Weak transcription	Ovary	ovary
10	chr1:45491800-45516400	Weak transcription	Spleen	Spleen
11	chr1:45492000-45507600	Weak transcription	Pancreatic Islets	Pancreatic Islet
12	chr1:45494600-45504200	Strong transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
13	chr1:45495000-45506800	Weak transcription	Skeletal Muscle Male	skeletal muscle
14	chr1:45497400-45525400	Weak transcription	Gastric	stomach
15	chr1:45497800-45501000	Weak transcription	Primary T helper cells fromperipheralblood	blood
16	chr1:45497800-45501800	Strong transcription	Breast Myoepithelial Primary Cells	Breast
17	chr1:45498000-45525600	Weak transcription	Pancreas	Pancrea
18	chr1:45498200-45506800	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
19	chr1:45498600-45502000	Strong transcription	Ganglion Eminence derived primary cultured neurospheres	brain
20	chr1:45499200-45502000	Strong transcription	Brain Anterior Caudate	brain
21	chr1:45499200-45502000	Strong transcription	Brain Germinal Matrix	brain
22	chr1:45499200-45502000	Strong transcription	Brain Inferior Temporal Lobe	brain
23	chr1:45499200-45502400	Strong transcription	Stomach Smooth Muscle	stomach
24	chr1:45499200-45516200	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
25	chr1:45499400-45500400	Strong transcription	Sigmoid Colon	Sigmoid Colon
26	chr1:45499400-45501200	Strong transcription	Fetal Intestine Small	intestine
27	chr1:45499400-45501400	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr1:45499400-45502000	Strong transcription	Brain Dorsolateral Prefrontal Cortex	brain
29	chr1:45499400-45502400	Weak transcription	Hela-S3	cervix
30	chr1:45499600-45503200	Weak transcription	GM12878-XiMat	blood
31	chr1:45499800-45501800	Strong transcription	Brain Hippocampus Middle	brain
32	chr1:45499800-45501800	Strong transcription	Brain Substantia Nigra	brain
33	chr1:45499800-45502000	Strong transcription	Brain Angular Gyrus	brain
34	chr1:45499800-45502000	Strong transcription	Brain Cingulate Gyrus	brain
35	chr1:45499800-45502000	Strong transcription	Fetal Adrenal Gland	Adrenal Gland
36	chr1:45499800-45502000	Strong transcription	Fetal Brain Female	brain
37	chr1:45499800-45502000	Strong transcription	Rectal Mucosa Donor 29	rectum
38	chr1:45499800-45502600	Strong transcription	Fetal Stomach	stomach
39	chr1:45500000-45502000	Strong transcription	Duodenum Smooth Muscle	Duodenum
40	chr1:45500000-45502000	Strong transcription	Rectal Mucosa Donor 31	rectum
41	chr1:45500000-45504800	Weak transcription	Primary T cells fromperipheralblood	blood
42	chr1:45500200-45500400	Strong transcription	H9 Derived Neuron Cultured Cells	ES cell derived
43	chr1:45500200-45501000	Weak transcription	Aorta	Aorta
44	chr1:45500200-45501200	Weak transcription	Duodenum Mucosa	Duodenum
45	chr1:45500200-45501600	Weak transcription	Fetal Intestine Large	intestine
46	chr1:45500400-45500800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:45500400-45505200	Weak transcription	Right Ventricle	heart
48	chr1:45500400-45516600	Weak transcription	Sigmoid Colon	Sigmoid Colon
49	chr1:45500600-45502000	Strong transcription	HepG2	liver
50	chr1:45500800-45501200	Enhancers	K562	blood

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