Variant report

Variant	nsv1009529
Chromosome Location	chr1:184663898-184731215
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:994)
CpG islands
(count:977)
Chromatin interactive
region (count:81)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:994 , 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	chr1:184723889-184725086	HepG2	liver:	n/a	chr1:184723910-184723918
2	ARID3A	chr1:184721296-184721489	K562	blood:	n/a	n/a
3	ARID3A	chr1:184723938-184725344	K562	blood:	n/a	n/a
4	ARID3A	chr1:184708580-184708874	K562	blood:	n/a	n/a
5	ARID3A	chr1:184723522-184723679	HepG2	liver:	n/a	n/a
6	ARID3A	chr1:184721699-184722664	K562	blood:	n/a	chr1:184721783-184721799 chr1:184721784-184721800
7	ARID3A	chr1:184714297-184714467	K562	blood:	n/a	n/a
8	ARID3A	chr1:184712126-184712865	K562	blood:	n/a	n/a
9	ARID3A	chr1:184718108-184718302	K562	blood:	n/a	n/a
10	ATF1	chr1:184723843-184725135	K562	blood:	n/a	n/a
11	ATF2	chr1:184712195-184712647	GM12878	blood:	n/a	n/a
12	ATF2	chr1:184723276-184724356	GM12878	blood:	n/a	n/a
13	ATF2	chr1:184716336-184716838	GM12878	blood:	n/a	n/a
14	ATF2	chr1:184712054-184712786	GM12878	blood:	n/a	n/a
15	BACH1	chr1:184723587-184723615	K562	blood:	n/a	n/a
16	BACH1	chr1:184711303-184711349	K562	blood:	n/a	n/a
17	BACH1	chr1:184723063-184723968	H1-hESC	embryonic stem cell:	n/a	n/a
18	BATF	chr1:184677461-184677889	GM12878	blood:	n/a	n/a
19	BATF	chr1:184712268-184712529	GM12878	blood:	n/a	chr1:184712498-184712508 chr1:184712502-184712512
20	BCL11A	chr1:184712274-184712562	GM12878	blood:	n/a	n/a
21	BCL3	chr1:184723671-184724389	GM12878	blood:	n/a	chr1:184724141-184724150
22	BCLAF1	chr1:184723711-184724746	GM12878	blood:	n/a	chr1:184724561-184724570 chr1:184724141-184724150
23	BCLAF1	chr1:184723483-184724570	GM12878	blood:	n/a	chr1:184724561-184724570 chr1:184724141-184724150
24	BCLAF1	chr1:184716228-184716855	GM12878	blood:	n/a	n/a
25	BCLAF1	chr1:184712079-184712626	GM12878	blood:	n/a	n/a
26	BHLHE40	chr1:184723187-184723518	GM12878	blood:	n/a	n/a
27	BHLHE40	chr1:184723223-184724627	HepG2	liver:	n/a	n/a
28	BHLHE40	chr1:184723112-184725155	K562	blood:	n/a	n/a
29	BHLHE40	chr1:184715032-184715232	GM12878	blood:	n/a	n/a
30	BHLHE40	chr1:184712199-184712666	GM12878	blood:	n/a	n/a
31	BRCA1	chr1:184724067-184724430	H1-hESC	embryonic stem cell:	n/a	n/a
32	BRCA1	chr1:184723786-184724442	HepG2	liver:	n/a	n/a
33	BRCA1	chr1:184723080-184723385	Hela-S3	cervix:	n/a	n/a
34	BRCA1	chr1:184724072-184724493	GM12878	blood:	n/a	n/a
35	BRCA1	chr1:184723821-184724795	Hela-S3	cervix:	n/a	n/a
36	CBX3	chr1:184723113-184725259	K562	blood:	n/a	n/a
37	CCNT2	chr1:184689528-184689641	K562	blood:	n/a	n/a
38	CCNT2	chr1:184723166-184724570	K562	blood:	n/a	chr1:184724443-184724463
39	CEBPB	chr1:184721712-184722172	K562	blood:	n/a	chr1:184722076-184722088
40	CEBPB	chr1:184723354-184723440	HepG2	liver:	n/a	n/a
41	CEBPB	chr1:184721838-184722215	K562	blood:	n/a	chr1:184722076-184722088
42	CEBPB	chr1:184694981-184695231	HepG2	liver:	n/a	chr1:184695075-184695092
43	CEBPB	chr1:184676121-184676403	HepG2	liver:	n/a	n/a
44	CEBPB	chr1:184717984-184718265	Hela-S3	cervix:	n/a	chr1:184718118-184718129
45	CEBPB	chr1:184671024-184671266	Hela-S3	cervix:	n/a	chr1:184671129-184671140 chr1:184671128-184671141
46	CEBPB	chr1:184713880-184714181	K562	blood:	n/a	n/a
47	CEBPB	chr1:184721280-184721458	IMR90	lung:	n/a	chr1:184721381-184721392 chr1:184721291-184721302 chr1:184721382-184721393 chr1:184721291-184721302
48	CEBPB	chr1:184709806-184710093	A549	lung:	n/a	n/a
49	CEBPB	chr1:184682682-184682779	A549	lung:	n/a	chr1:184682712-184682723 chr1:184682710-184682721 chr1:184682712-184682721
50	CEBPB	chr1:184670989-184671225	K562	blood:	n/a	chr1:184671129-184671140 chr1:184671128-184671141

(count:977 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:184724736-184724786	Jurkat	blood:	n/a
2	chr1:184724736-184724786	Jurkat	blood:	n/a
3	chr1:184724388-184724438	LNCaP	prostate:	n/a
4	chr1:184723524-184723574	HCT-116	colon:	n/a
5	chr1:184724800-184724850	HPAEpiC	pulmonary alveolar:	n/a
6	chr1:184724497-184724547	SAEC	small airway:	n/a
7	chr1:184722970-184723020	AoSMC	blood vessel:	n/a
8	chr1:184724736-184724786	SK-N-SH	brain:	n/a
9	chr1:184724800-184724850	GM12891	blood:	n/a
10	chr1:184723951-184724001	T-47D	breast:	n/a
11	chr1:184724388-184724438	HMEC	breast:	n/a
12	chr1:184724800-184724850	HEEpiC	esophagus:	n/a
13	chr1:184724388-184724438	HRCEpiC	kidney:	n/a
14	chr1:184724009-184724059	NHDF-neo	bronchial:	n/a
15	chr1:184724497-184724547	PrEC	prostate:	n/a
16	chr1:184724388-184724438	AG09309	skin:	n/a
17	chr1:184721222-184721272	NT2-D1	testis:	n/a
18	chr1:184724631-184724681	A549	lung:	n/a
19	chr1:184724009-184724059	ovcar-3	ovarian:	n/a
20	chr1:184722970-184723020	A549	lung:	n/a
21	chr1:184724497-184724547	HIPEpiC	eye:	n/a
22	chr1:184724195-184724245	GM12878	blood:	n/a
23	chr1:184724009-184724059	HCF	heart:	n/a
24	chr1:184715203-184715253	ECC-1	luminal epithelium:	n/a
25	chr1:184724775-184724825	K562	blood:	n/a
26	chr1:184724195-184724245	RPTEC	kidney:	n/a
27	chr1:184722970-184723020	HEK293	kidney:	embryo
28	chr1:184724388-184724438	ProgFib	skin:	n/a
29	chr1:184724208-184724258	CMK	blood:	n/a
30	chr1:184723906-184723956	NHBE	bronchial:	n/a
31	chr1:184721222-184721272	CMK	blood:	n/a
32	chr1:184715203-184715253	MCF10A-Er-Src	breast:	n/a
33	chr1:184724497-184724547	SK-N-MC	brain:	n/a
34	chr1:184724388-184724438	PrEC	prostate:	n/a
35	chr1:184724195-184724245	PANC-1	pancreas:	n/a
36	chr1:184723951-184724001	GM19239	blood:	n/a
37	chr1:184724775-184724825	NB4	blood:	n/a
38	chr1:184724009-184724059	Caco-2	colon:	n/a
39	chr1:184722970-184723020	K562	blood:	n/a
40	chr1:184724208-184724258	AoSMC	blood vessel:	n/a
41	chr1:184722970-184723020	HEEpiC	esophagus:	n/a
42	chr1:184724631-184724681	HEEpiC	esophagus:	n/a
43	chr1:184723906-184723956	HEEpiC	esophagus:	n/a
44	chr1:184724736-184724786	H1-hESC	embryonic stem cell:	embryo
45	chr1:184724775-184724825	Caco-2	colon:	n/a
46	chr1:184721222-184721272	HNPCEpiC	eye:	n/a
47	chr1:184724800-184724850	AG09309	skin:	n/a
48	chr1:184724388-184724438	SAEC	small airway:	n/a
49	chr1:184724631-184724681	Hepatocyte	liver:	n/a
50	chr1:184721222-184721272	HCPEpiC	choroid plexus:	n/a

(count:81 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr1:184708584..184710764-chr1:184716187..184718399,2	MCF-7	breast:
2	chr1:184679455..184682205-chr1:184682828..184685276,2	MCF-7	breast:
3	chr1:184722946..184726170-chr1:184728619..184730766,3	MCF-7	breast:
4	chr1:184694527..184697597-chr1:184706651..184709728,3	K562	blood:
5	chr1:184683195..184685107-chr1:184721891..184724158,3	K562	blood:
6	chr1:184700886..184703045-chr1:184708042..184709740,3	K562	blood:
7	chr1:184682030..184684517-chr1:184685764..184688834,3	K562	blood:
8	chr1:183996674..183999449-chr1:184721278..184723656,2	K562	blood:
9	chr1:184697668..184700399-chr1:184702400..184704230,2	K562	blood:
10	chr1:184705153..184707744-chr1:184942725..184944472,2	K562	blood:
11	chr1:184722993..184726139-chr1:185013897..185016469,4	K562	blood:
12	chr1:184723118..184724888-chr1:185124173..185126460,2	MCF-7	breast:
13	chr1:184689208..184691791-chr1:184942117..184944886,2	K562	blood:
14	chr1:184706332..184708758-chr1:184714030..184715698,2	K562	blood:
15	chr1:184681652..184683327-chr1:184949938..184952588,2	K562	blood:
16	chr1:184697119..184698633-chr1:184706582..184709227,2	MCF-7	breast:
17	chr1:184702525..184704823-chr1:184721375..184723068,2	MCF-7	breast:
18	chr1:184684929..184687575-chr1:184691047..184693770,2	K562	blood:
19	chr1:184687896..184689795-chr1:184715143..184716835,2	MCF-7	breast:
20	chr1:184684929..184687575-chr1:184691047..184694725,3	K562	blood:
21	chr1:184662527..184664515-chr1:184667371..184668893,2	MCF-7	breast:
22	chr1:184660734..184663432-chr1:184719379..184720906,2	MCF-7	breast:
23	chr1:184673163..184675215-chr1:184695509..184697119,2	K562	blood:
24	chr1:184719034..184720835-chr1:184729279..184731046,2	MCF-7	breast:
25	chr1:184669558..184672098-chr1:184694218..184695882,2	K562	blood:
26	chr1:184691631..184695143-chr1:184721197..184724514,4	K562	blood:
27	chr1:184708169..184713415-chr1:184713456..184716461,4	MCF-7	breast:
28	chr1:184702362..184703932-chr1:184704085..184706758,2	K562	blood:
29	chr1:184665706..184667589-chr1:184670259..184672782,2	MCF-7	breast:
30	chr1:184688642..184690448-chr1:184695282..184698252,2	K562	blood:
31	chr1:184708169..184713415-chr1:184713456..184716461,4	MCF-7	breast:
32	chr1:184670636..184673038-chr1:184723688..184726485,2	MCF-7	breast:
33	chr1:184725745..184728657-chr1:184756568..184759148,2	MCF-7	breast:
34	chr1:184687867..184690558-chr1:184692162..184694552,2	MCF-7	breast:
35	chr1:184703854..184706366-chr1:184709752..184714206,4	K562	blood:
36	chr1:184709738..184712321-chr1:184713250..184716697,3	K562	blood:
37	chr1:184697668..184700399-chr1:184702400..184704230,2	K562	blood:
38	chr1:184728189..184730615-chr1:184744000..184745636,2	MCF-7	breast:
39	chr1:184687987..184690948-chr1:184692371..184695173,3	K562	blood:
40	chr1:184664608..184667109-chr1:184680231..184682825,2	K562	blood:
41	chr1:184698326..184700782-chr1:184705878..184708037,2	K562	blood:
42	chr1:184703854..184706366-chr1:184709752..184714206,4	K562	blood:
43	chr1:184687987..184690948-chr1:184692371..184695173,3	K562	blood:
44	chr1:184691316..184693435-chr1:184696792..184698671,2	K562	blood:
45	chr1:184702525..184704823-chr1:184721375..184723068,2	MCF-7	breast:
46	chr1:184694488..184696027-chr1:184706651..184709157,2	K562	blood:
47	chr1:184691316..184693435-chr1:184696792..184698671,2	K562	blood:
48	chr1:184684929..184687575-chr1:184691047..184693770,2	K562	blood:
49	chr1:184708973..184712904-chr1:184713895..184716754,5	K562	blood:
50	chr1:184709738..184712321-chr1:184713250..184716697,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C1orf21-6	chr1:184726198-184726468	NONHSAT008398
2	lnc-C1orf21-7	chr1:184727266-184730133	NONHSAT008399

No data

Variant related genes	Relation type
EDEM3	TF binding region
EDEM3	CpG island
ENSG00000242125	chromatin interactions
ENSG00000158286	chromatin interactions
ENSG00000135842	chromatin interactions
ENSG00000116668	chromatin interactions
ENSG00000121486	chromatin interactions
ENSG00000116406	chromatin interactions
ENSG00000180198	chromatin interactions
ENSG00000121481	chromatin interactions

Extended variants
information (count: 2403 )
Associated
traits (count: 87 )

Variant overlapped rSNPs/rCNVs (count:2403 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9425635	chr1:184663898-184663899	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs552667486	chr1:184663914-184663915	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs114930561	chr1:184664002-184664003	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs538831092	chr1:184664015-184664016	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs556875749	chr1:184664016-184664017	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs575536079	chr1:184664080-184664081	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs542927369	chr1:184664132-184664133	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs527351690	chr1:184664143-184664144	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs574103888	chr1:184664213-184664214	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs367620607	chr1:184664256-184664257	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs548654839	chr1:184664300-184664301	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs369405820	chr1:184664302-184664303	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs145922334	chr1:184664307-184664308	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs531206674	chr1:184664314-184664315	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs559805048	chr1:184664418-184664419	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs74455641	chr1:184664454-184664455	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs377220313	chr1:184664480-184664481	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs186042377	chr1:184664494-184664495	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs563718797	chr1:184664501-184664502	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs369735695	chr1:184664508-184664509	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs188490375	chr1:184664511-184664512	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs143125875	chr1:184664526-184664527	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs376161021	chr1:184664540-184664541	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs181083266	chr1:184664554-184664555	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs538827062	chr1:184664578-184664579	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs76956262	chr1:184664588-184664589	Enhancers Weak transcription Strong transcription Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
27	rs148509152	chr1:184664600-184664601	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	n/a	n/a	Overlapped CNVs	n/a
28	rs538347444	chr1:184664617-184664618	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs76584885	chr1:184664641-184664642	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs141819730	chr1:184664653-184664654	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs576852335	chr1:184664674-184664675	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs555077346	chr1:184664679-184664680	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs576551471	chr1:184664680-184664681	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs554918229	chr1:184664730-184664731	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs150703892	chr1:184664743-184664744	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs185567997	chr1:184664783-184664784	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs371201595	chr1:184664801-184664802	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs140181162	chr1:184664807-184664808	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs578076729	chr1:184664808-184664809	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs545153481	chr1:184664831-184664832	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs563777630	chr1:184664837-184664838	Enhancers Weak transcription Strong transcription Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs10159213	chr1:184665012-184665013	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs143831527	chr1:184665013-184665014	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs539023771	chr1:184665018-184665019	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs537040150	chr1:184665019-184665020	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs561250209	chr1:184665039-184665040	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs146851721	chr1:184665095-184665096	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs139662272	chr1:184665099-184665100	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs577440462	chr1:184665102-184665103	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs78599523	chr1:184665105-184665106	Enhancers Weak transcription Strong transcription Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:87)

Disease	PMID	Source
Breast cancer	17603634	CNVD
Esophageal squamous carcinoma	21637470	CNVD
HIV/AIDS	22032296	CNVD
Schizophrenia	19415332	CNVD
Autism	22495311	CNVD
Liposarcoma	21253554	CNVD
Burkitt''s lymphoma	18698080	CNVD
Melanoma	18172304	CNVD
Rett syndrome	21593744	CNVD
Cancer	20164919	CNVD
Medulloblastoma	21979893	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	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
Ewing''s sarcoma	21437220	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Bladder cancer	19088036	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17002787	CNVD
Breast cancer	21858162	CNVD
Non-small cell lung cancer	21385341	CNVD
Acute lymphoblastic leukemia	21980252	CNVD
Breast cancer	16608533	CNVD
Ewing''s sarcoma	22429812	CNVD
Acute promyelocytic leukemia	19109227	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
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Acute myeloid leukemia	20729466	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Testicular germ cell tumor	18059402	CNVD
Trisomy 5 syndrome	21098271	CNVD
Ependymoma	18628472	CNVD
Leukemia	18628472	CNVD
Neuroblastoma	18923191	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Hepatocellular carcinoma	16750200	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21509527	CNVD
Glioblastoma multiforme	17369134	CNVD
Cancer	17440070	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Metanephric adenoma	20802469	CNVD
Renal cell carcinoma	18765545	CNVD
Nephroblastoma	17189400	CNVD
Melanoma	20688739	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	21611746	CNVD
Myelofibrosis	22110671	CNVD
primary effusion lymphomas	17116491	CNVD
Breast cancer	17393978	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Breast cancer	22522925	CNVD
Barrett''s syndrome	19417022	CNVD

Chromatin state (count:1886 , 50 per page) page: 1 2 3 4 5 6 7 ... 38

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:184641400-184672800	Weak transcription	Gastric	stomach
2	chr1:184653200-184705000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
3	chr1:184654000-184710800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
4	chr1:184654200-184672000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr1:184654200-184701200	Weak transcription	Stomach Mucosa	stomach
6	chr1:184654200-184710000	Weak transcription	Esophagus	oesophagus
7	chr1:184654400-184675400	Weak transcription	Pancreas	Pancrea
8	chr1:184654600-184665800	Weak transcription	HUES6 Cell Line	embryonic stem cell
9	chr1:184654600-184672400	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr1:184654800-184669600	Weak transcription	Fetal Lung	lung
11	chr1:184655000-184664400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
12	chr1:184656000-184672000	Weak transcription	HepG2	liver
13	chr1:184656400-184672800	Weak transcription	Spleen	Spleen
14	chr1:184656600-184670200	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
15	chr1:184656600-184684000	Weak transcription	Fetal Heart	heart
16	chr1:184657000-184672600	Weak transcription	Lung	lung
17	chr1:184657200-184672800	Weak transcription	Fetal Intestine Small	intestine
18	chr1:184657400-184672800	Weak transcription	Fetal Stomach	stomach
19	chr1:184657800-184670200	Weak transcription	HMEC	breast
20	chr1:184658400-184706800	Strong transcription	Primary neutrophils fromperipheralblood	blood
21	chr1:184658600-184665400	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
22	chr1:184659000-184672600	Weak transcription	Aorta	Aorta
23	chr1:184659200-184668400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
24	chr1:184659200-184707000	Strong transcription	Monocytes-CD14+_RO01746	blood
25	chr1:184659400-184676800	Weak transcription	Fetal Brain Male	brain
26	chr1:184660000-184704200	Strong transcription	Primary monocytes fromperipheralblood	blood
27	chr1:184660800-184664400	Weak transcription	Stomach Smooth Muscle	stomach
28	chr1:184660800-184664600	Weak transcription	NHLF	lung
29	chr1:184660800-184669200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
30	chr1:184660800-184680400	Weak transcription	Right Ventricle	heart
31	chr1:184661000-184665800	Strong transcription	K562	blood
32	chr1:184661000-184678600	Weak transcription	Primary T killer memory cells from peripheral blood	blood
33	chr1:184661000-184705600	Strong transcription	Rectal Mucosa Donor 29	rectum
34	chr1:184661200-184665200	Genic enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr1:184661200-184690400	Strong transcription	Primary T cells fromperipheralblood	blood
36	chr1:184661200-184707800	Strong transcription	Primary Natural Killer cells fromperipheralblood	blood
37	chr1:184661400-184666200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
38	chr1:184661400-184671200	Weak transcription	Fetal Kidney	kidney
39	chr1:184661400-184678600	Strong transcription	Liver	Liver
40	chr1:184661400-184690400	Strong transcription	Duodenum Mucosa	Duodenum
41	chr1:184661600-184670800	Weak transcription	A549	lung
42	chr1:184661600-184672800	Weak transcription	Small Intestine	intestine
43	chr1:184661600-184693200	Strong transcription	Dnd41	blood
44	chr1:184661800-184666000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
45	chr1:184662000-184664400	Strong transcription	Primary T regulatory cells fromperipheralblood	blood
46	chr1:184662000-184665800	Strong transcription	Primary B cells from peripheral blood	blood
47	chr1:184662000-184665800	Strong transcription	Primary hematopoietic stem cells	blood
48	chr1:184662000-184666000	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
49	chr1:184662000-184666000	Strong transcription	Duodenum Smooth Muscle	Duodenum
50	chr1:184662000-184666000	Strong transcription	Fetal Thymus	thymus

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