Variant report

Variant	nsv536553
Chromosome Location	chr3:46496775-46546918
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1066)
CpG islands
(count:1467)
Chromatin interactive
region (count:59)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1066 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr3:46538249-46538456	K562	blood:	n/a	n/a
2	ARID3A	chr3:46544482-46544574	K562	blood:	n/a	n/a
3	ARID3A	chr3:46534500-46534911	K562	blood:	n/a	n/a
4	ARID3A	chr3:46530187-46530494	K562	blood:	n/a	n/a
5	ATF1	chr3:46538294-46538577	K562	blood:	n/a	n/a
6	ATF2	chr3:46530156-46530609	GM12878	blood:	n/a	n/a
7	ATF2	chr3:46530151-46530620	H1-hESC	embryonic stem cell:	n/a	n/a
8	ATF2	chr3:46530160-46530603	H1-hESC	embryonic stem cell:	n/a	n/a
9	ATF3	chr3:46530267-46530468	GM12878	blood:	n/a	n/a
10	ATF3	chr3:46530212-46530507	HepG2	liver:	n/a	n/a
11	BACH1	chr3:46530281-46530548	H1-hESC	embryonic stem cell:	n/a	n/a
12	BACH1	chr3:46529520-46529567	K562	blood:	n/a	n/a
13	BATF	chr3:46530183-46530516	GM12878	blood:	n/a	n/a
14	BCL11A	chr3:46530216-46530482	GM12878	blood:	n/a	n/a
15	BCLAF1	chr3:46530139-46530589	GM12878	blood:	n/a	n/a
16	BCLAF1	chr3:46530133-46530574	GM12878	blood:	n/a	n/a
17	BHLHE40	chr3:46546363-46546640	GM12878	blood:	n/a	n/a
18	BHLHE40	chr3:46544278-46544472	K562	blood:	n/a	n/a
19	BHLHE40	chr3:46530221-46530612	GM12878	blood:	n/a	n/a
20	BHLHE40	chr3:46543093-46543691	GM12878	blood:	n/a	chr3:46543520-46543529 chr3:46543519-46543532 chr3:46543515-46543536
21	BHLHE40	chr3:46530177-46530760	K562	blood:	n/a	n/a
22	BHLHE40	chr3:46526575-46526741	K562	blood:	n/a	n/a
23	BHLHE40	chr3:46543423-46543565	HepG2	liver:	n/a	chr3:46543520-46543529 chr3:46543519-46543532 chr3:46543515-46543536
24	BHLHE40	chr3:46538379-46538583	K562	blood:	n/a	n/a
25	BHLHE40	chr3:46542396-46542814	GM12878	blood:	n/a	n/a
26	BHLHE40	chr3:46544686-46544842	K562	blood:	n/a	n/a
27	BHLHE40	chr3:46497566-46497621	K562	blood:	n/a	n/a
28	BRCA1	chr3:46530217-46530533	HepG2	liver:	n/a	n/a
29	BRCA1	chr3:46530172-46530605	Hela-S3	cervix:	n/a	n/a
30	BRCA1	chr3:46530208-46530568	H1-hESC	embryonic stem cell:	n/a	n/a
31	CBX3	chr3:46530128-46530656	K562	blood:	n/a	n/a
32	CBX3	chr3:46530140-46530695	HCT-116	colon:	n/a	n/a
33	CCNT2	chr3:46544283-46544528	K562	blood:	n/a	n/a
34	CCNT2	chr3:46530236-46530802	K562	blood:	n/a	n/a
35	CCNT2	chr3:46540089-46540284	K562	blood:	n/a	n/a
36	CEBPB	chr3:46530208-46530470	K562	blood:	n/a	n/a
37	CEBPB	chr3:46538809-46539124	HepG2	liver:	n/a	chr3:46538963-46538974
38	CEBPB	chr3:46530214-46530556	Hela-S3	cervix:	n/a	n/a
39	CEBPB	chr3:46542321-46542806	K562	blood:	n/a	chr3:46542613-46542624
40	CEBPB	chr3:46542487-46542659	K562	blood:	n/a	chr3:46542613-46542624
41	CEBPB	chr3:46511225-46511456	HepG2	liver:	n/a	chr3:46511372-46511383 chr3:46511370-46511381 chr3:46511370-46511383
42	CEBPB	chr3:46538839-46539115	K562	blood:	n/a	chr3:46538963-46538974
43	CEBPB	chr3:46537470-46537980	Hela-S3	cervix:	n/a	n/a
44	CEBPB	chr3:46506449-46506460	K562	blood:	n/a	n/a
45	CEBPB	chr3:46542217-46542801	IMR90	lung:	n/a	chr3:46542613-46542624
46	CEBPB	chr3:46540715-46541057	K562	blood:	n/a	n/a
47	CEBPB	chr3:46542509-46542804	HepG2	liver:	n/a	chr3:46542613-46542624
48	CEBPB	chr3:46511237-46511317	Hela-S3	cervix:	n/a	n/a
49	CEBPB	chr3:46542429-46542791	K562	blood:	n/a	chr3:46542613-46542624
50	CEBPB	chr3:46506314-46506621	H1-hESC	embryonic stem cell:	n/a	n/a

(count:1467 , 50 per page) page: 1 2 3 4 5 6 7 ... 30

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr3:46538742-46538792	AG04449	skin:	fetal
2	chr3:46530275-46530325	HIPEpiC	eye:	n/a
3	chr3:46506554-46506604	SK-N-SH_RA	brain:	n/a
4	chr3:46538742-46538792	AG04449	skin:	fetal
5	chr3:46530275-46530325	HIPEpiC	eye:	n/a
6	chr3:46506554-46506604	SK-N-SH_RA	brain:	n/a
7	chr3:46509437-46509487	GM12892	blood:	n/a
8	chr3:46506374-46506424	A549	lung:	n/a
9	chr3:46539018-46539068	PANC-1	pancreas:	n/a
10	chr3:46531037-46531087	AG10803	skin:	n/a
11	chr3:46540019-46540069	HRPEpiC	eye:	n/a
12	chr3:46506104-46506154	SK-N-SH	brain:	n/a
13	chr3:46506206-46506256	Hepatocyte	liver:	n/a
14	chr3:46506483-46506533	MCF10A-Er-Src	breast:	n/a
15	chr3:46506519-46506569	GM12891	blood:	n/a
16	chr3:46506483-46506533	HepG2	liver:	n/a
17	chr3:46502652-46502702	SK-N-SH_RA	brain:	n/a
18	chr3:46539013-46539063	BJ	skin:	n/a
19	chr3:46530275-46530325	MCF-7	breast:	n/a
20	chr3:46539013-46539063	HCF	heart:	n/a
21	chr3:46530353-46530403	Jurkat	blood:	n/a
22	chr3:46506206-46506256	HIPEpiC	eye:	n/a
23	chr3:46530275-46530325	T-47D	breast:	n/a
24	chr3:46504469-46504519	NB4	blood:	n/a
25	chr3:46506206-46506256	SK-N-SH	brain:	n/a
26	chr3:46531037-46531087	HCM	heart:	n/a
27	chr3:46538742-46538792	GM12878	blood:	n/a
28	chr3:46502652-46502702	ProgFib	skin:	n/a
29	chr3:46504469-46504519	MCF-7	breast:	n/a
30	chr3:46506206-46506256	LNCaP	prostate:	n/a
31	chr3:46530275-46530325	NT2-D1	testis:	n/a
32	chr3:46535972-46536022	H1-hESC	embryonic stem cell:	embryo
33	chr3:46506374-46506424	PrEC	prostate:	n/a
34	chr3:46535972-46536022	HCT-116	colon:	n/a
35	chr3:46530353-46530403	AG09309	skin:	n/a
36	chr3:46539018-46539068	IMR90	lung:	fetal
37	chr3:46506206-46506256	H1-hESC	embryonic stem cell:	embryo
38	chr3:46530353-46530403	ECC-1	luminal epithelium:	n/a
39	chr3:46506519-46506569	MCF-7	breast:	n/a
40	chr3:46530353-46530403	Hela-S3	cervix:	n/a
41	chr3:46504469-46504519	SK-N-MC	brain:	n/a
42	chr3:46539018-46539068	SK-N-SH	brain:	n/a
43	chr3:46531037-46531087	HCPEpiC	choroid plexus:	n/a
44	chr3:46530353-46530403	HepG2	liver:	n/a
45	chr3:46506404-46506454	ProgFib	skin:	n/a
46	chr3:46506481-46506531	HIPEpiC	eye:	n/a
47	chr3:46506404-46506454	NHBE	bronchial:	n/a
48	chr3:46506483-46506533	HCPEpiC	choroid plexus:	n/a
49	chr3:46506554-46506604	AG09309	skin:	n/a
50	chr3:46509437-46509487	Jurkat	blood:	n/a

(count:59 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr3:46537971..46538930-chr3:46599529..46600154,4	MCF-7	breast:
2	chr2:233835955..233836476-chr3:46529913..46530430,3	MCF-7	breast:
3	chr3:46542254..46545139-chr3:46598522..46600340,2	K562	blood:
4	chr3:46529825..46532011-chr3:46599266..46600570,56	K562	blood:
5	chr3:46489267..46491887-chr3:46498560..46500528,2	K562	blood:
6	chr3:46529904..46530772-chr3:46603076..46604060,2	K562	blood:
7	chr3:46529944..46530794-chr3:46705110..46706015,2	K562	blood:
8	chr3:46530490..46532908-chr3:46536819..46540385,3	K562	blood:
9	chr3:46529871..46530872-chr3:46670590..46672462,23	K562	blood:
10	chr3:46526738..46529447-chr3:46598574..46601375,2	K562	blood:
11	chr3:46508156..46510225-chr3:46511342..46513592,2	K562	blood:
12	chr3:46518251..46521004-chr3:46521282..46522790,2	K562	blood:
13	chr3:46529857..46530830-chr3:46549274..46550154,2	K562	blood:
14	chr3:46491080..46491922-chr3:46530287..46530830,3	MCF-7	breast:
15	chr3:46501096..46502745-chr3:46502800..46504664,2	K562	blood:
16	chr3:46528809..46531447-chr3:46546904..46549677,2	K562	blood:
17	chr3:46508156..46510225-chr3:46511342..46513592,2	K562	blood:
18	chr3:46495712..46498114-chr3:46504861..46507290,2	K562	blood:
19	chr3:46531009..46531629-chr3:46599490..46600081,2	MCF-7	breast:
20	chr3:46539335..46541927-chr3:46542072..46545650,5	K562	blood:
21	chr3:46529884..46530839-chr3:46671105..46672532,19	MCF-7	breast:
22	chr3:46537907..46538428-chr3:46599296..46599996,2	K562	blood:
23	chr3:46518251..46521004-chr3:46521282..46522790,2	K562	blood:
24	chr3:46529686..46530942-chr3:46599020..46600485,46	MCF-7	breast:
25	chr3:46532500..46536089-chr3:46537478..46540838,3	K562	blood:
26	chr3:46530293..46531287-chr3:46600917..46601700,2	K562	blood:
27	chr3:46504252..46506096-chr3:46508837..46511050,2	K562	blood:
28	chr3:46484352..46487691-chr3:46518831..46521127,3	K562	blood:
29	chr3:46539335..46541927-chr3:46542072..46545650,5	K562	blood:
30	chr3:46490983..46491780-chr3:46529871..46530687,2	MCF-7	breast:
31	chr3:46498573..46499197-chr3:46599063..46599998,2	K562	blood:
32	chr3:46537655..46538429-chr3:46599459..46599986,2	MCF-7	breast:
33	chr3:46529979..46530787-chr3:46607787..46608328,2	K562	blood:
34	chr3:46529878..46530429-chr3:46671116..46672037,3	MCF-7	breast:
35	chr3:46503615..46504280-chr3:46671186..46672162,2	MCF-7	breast:
36	chr3:46536326..46539257-chr3:46540337..46542850,3	K562	blood:
37	chr3:46539462..46541927-chr3:46542900..46546171,3	K562	blood:
38	chr3:46528809..46531447-chr3:46546904..46549677,2	K562	blood:
39	chr3:46530210..46534355-chr3:46598500..46601064,4	K562	blood:
40	chr3:46441887..46442673-chr3:46529916..46530717,2	K562	blood:
41	chr1:121484254..121485268-chr3:46529887..46530781,3	MCF-7	breast:
42	chr3:46503439..46504291-chr3:46671319..46672034,3	K562	blood:
43	chr3:46516225..46519087-chr3:46519462..46521207,2	K562	blood:
44	chr3:46499839..46502077-chr3:46515720..46518356,2	K562	blood:
45	chr3:46539462..46541927-chr3:46542900..46546171,3	K562	blood:
46	chr3:46542684..46544753-chr3:46554640..46556935,2	K562	blood:
47	chr3:46531010..46533398-chr3:46589733..46592357,3	K562	blood:
48	chr3:46530992..46532877-chr3:46591442..46593990,2	K562	blood:
49	chr3:46530235..46530934-chr3:46606775..46607619,4	K562	blood:
50	chr3:46495712..46498114-chr3:46504861..46507290,2	K562	blood:

No data

Variant related genes	Relation type
RTP3	TF binding region
LTF	TF binding region
RTP3	CpG island
LTF	CpG island
ENSG00000128683	chromatin interactions
ENSG00000163825	chromatin interactions
ENSG00000264306	chromatin interactions
ENSG00000268324	chromatin interactions
ENSG00000012223	chromatin interactions
ENSG00000163827	chromatin interactions

Extended variants
information (count: 2011 )
Associated
traits (count: 102 )

Variant overlapped rSNPs/rCNVs (count:2011 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs370489762	chr3:46496799-46496800	Weak transcription Enhancers Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs145010128	chr3:46496805-46496806	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs563622677	chr3:46496809-46496810	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs148316288	chr3:46496811-46496812	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs567015734	chr3:46496812-46496813	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs139895902	chr3:46496813-46496814	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs150338070	chr3:46496820-46496821	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs556715067	chr3:46496826-46496827	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs143672113	chr3:46496838-46496839	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs571988865	chr3:46496843-46496844	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs267599844	chr3:46496850-46496851	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs138961010	chr3:46496853-46496854	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs60938611	chr3:46496854-46496855	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs200036445	chr3:46496861-46496862	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs542125560	chr3:46496863-46496864	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs557008950	chr3:46496880-46496881	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs575155077	chr3:46496897-46496898	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs149687900	chr3:46496898-46496899	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs145526650	chr3:46496910-46496911	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs114380478	chr3:46496925-46496926	Weak transcription Enhancers Genic enhancers Strong transcription Bivalent Enhancer	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs540378609	chr3:46497004-46497005	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs561965803	chr3:46497010-46497011	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs529509391	chr3:46497013-46497014	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs551237644	chr3:46497014-46497015	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs113497936	chr3:46497074-46497075	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs188479107	chr3:46497092-46497093	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547641032	chr3:46497110-46497111	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs140978328	chr3:46497153-46497154	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs112099970	chr3:46497160-46497161	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs566926023	chr3:46497180-46497181	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs534312605	chr3:46497181-46497182	Weak transcription Enhancers Genic enhancers Bivalent Enhancer Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs111352033	chr3:46497219-46497220	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs144986893	chr3:46497222-46497223	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs184641990	chr3:46497244-46497245	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs371098365	chr3:46497255-46497256	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs199959753	chr3:46497276-46497277	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs368383905	chr3:46497289-46497290	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs141442902	chr3:46497295-46497296	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs148941436	chr3:46497312-46497313	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs34538438	chr3:46497326-46497327	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs148123129	chr3:46497330-46497331	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs146006710	chr3:46497331-46497332	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs1126479	chr3:46497342-46497343	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs554556520	chr3:46497351-46497352	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs150810057	chr3:46497361-46497362	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs371808586	chr3:46497362-46497363	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs61740465	chr3:46497368-46497369	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs142920270	chr3:46497369-46497370	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs17851991	chr3:46497372-46497373	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs572699872	chr3:46497385-46497386	Weak transcription Genic enhancers Bivalent Enhancer Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:102)

Disease	PMID	Source
Colorectal cancer	21297112	CNVD
Lynch syndrome	18415027	CNVD
Renal cell carcinoma	18592004	CNVD
Acute myeloid leukemia	20729466	CNVD
Urothelial carcinoma	18382360	CNVD
Melanoma	18172304	CNVD
Cervical cancer	21062161	CNVD
Hirschsprung''s Disease	21712996	CNVD
Glioblastoma multiforme	21080181	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Insulin resistance	16721378	CNVD
Neuroblastoma	18664255	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Ewing''s sarcoma	21437220	CNVD
Neuroblastoma	21484798	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Oral cancer	19627613	CNVD
Renal cell carcinoma	19461508	CNVD
Epithelial cancer	22065749	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Acute myeloid leukemia	16864856	CNVD
Liposarcoma	21253554	CNVD
Basal cell lymphoma	21115979	CNVD
Endometrial cancer	22040021	CNVD
Pancreatic endocrine tumor	20981439	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	17387387	CNVD
Oral cancer	21386901	CNVD
Cutaneous squamous cell carcinomas	19131950	CNVD
Medulloblastoma	21979893	CNVD
Basal cell lymphoma	17053054	CNVD
Esophageal cancer	21851588	CNVD
Uveal melanoma	21693616	CNVD
Retinoblastoma	21504564	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Renal cell carcinoma	21668985	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Thoracic aortic aneurysm	21092924	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Intellectual disability	22102821	CNVD
Breast cancer	17603634	CNVD
Esophageal cancer	20955586	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Breast cancer	17133270	CNVD
Uveal melanoma	20484589	CNVD
Autism	22495311	CNVD
Melanoma	20688739	CNVD
Acute myeloid leukemia	21251322	CNVD
Hepatocellular carcinoma	16750200	CNVD
Cancer	21183584	CNVD
Kartagener syndrome	16639409	CNVD
Biliary cancer	19435499	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Bipolar disorder	20877625	CNVD
Bipolar disorder	21956041	CNVD
Bipolar disorder	22241247	CNVD
Biliary cancer	18923514	CNVD
Breast cancer	21509527	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Malignant mesothelioma	18160781	CNVD
Pleural malignant mesothelioma	18160781	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	16397240	CNVD
Breast cancer	22032731	CNVD
Non-small cell lung cancer	20864512	CNVD
Colorectal cancer	16912164	CNVD
Non-small cell lung cancer	19010865	CNVD
Colorectal cancer	16272173	CNVD
Non-muscle invasive bladder neoplasm	19445696	CNVD
Acute myeloid leukemia	17268525	CNVD
Salivary gland tumor	18059337	CNVD
Gastric cancer	16891809	CNVD
Night blindness	17160897	CNVD
Cancer	17160897	CNVD
Breast cancer	20409316	CNVD
Lung cancer	17297452	CNVD
Multiple myeloma	16616336	CNVD
Effusion lymphoma	18079361	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Neuroblastoma	20406844	CNVD
Breast cancer	21785460	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	21045282	CNVD
Urothelial cell carcinoma	18451213	CNVD
Neuroblastoma	17327916	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Melanoma	17363583	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Adrenocortical carcinoma	18281524	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:859 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:46455800-46496800	Strong transcription	Primary neutrophils fromperipheralblood	blood
2	chr3:46480200-46504000	Weak transcription	Lung	lung
3	chr3:46489200-46496800	Weak transcription	Adipose Nuclei	Adipose
4	chr3:46489400-46504000	Weak transcription	Right Atrium	heart
5	chr3:46492200-46501000	Weak transcription	Left Ventricle	heart
6	chr3:46492400-46501000	Weak transcription	Right Ventricle	heart
7	chr3:46492600-46497400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr3:46494800-46497800	Strong transcription	Gastric	stomach
9	chr3:46494800-46498000	Strong transcription	Pancreas	Pancrea
10	chr3:46494800-46499000	Strong transcription	Spleen	Spleen
11	chr3:46495000-46497200	Enhancers	Fetal Intestine Large	intestine
12	chr3:46495000-46497400	Enhancers	Fetal Intestine Small	intestine
13	chr3:46495200-46497400	Enhancers	Dnd41	blood
14	chr3:46495400-46496800	Weak transcription	Skeletal Muscle Male	skeletal muscle
15	chr3:46495800-46497400	Enhancers	Fetal Thymus	thymus
16	chr3:46496600-46497200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr3:46496800-46497200	Bivalent Enhancer	Fetal Muscle Trunk	muscle
18	chr3:46496800-46497400	Strong transcription	Adipose Nuclei	Adipose
19	chr3:46496800-46497800	Strong transcription	Skeletal Muscle Male	skeletal muscle
20	chr3:46496800-46498000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
21	chr3:46497000-46497600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin01	Skin
22	chr3:46497400-46497800	ZNF genes & repeats	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
23	chr3:46497400-46499800	Weak transcription	Adipose Nuclei	Adipose
24	chr3:46497800-46503600	Weak transcription	Gastric	stomach
25	chr3:46497800-46504000	Weak transcription	Skeletal Muscle Male	skeletal muscle
26	chr3:46498000-46499400	Strong transcription	Primary neutrophils fromperipheralblood	blood
27	chr3:46498000-46504800	Weak transcription	Pancreas	Pancrea
28	chr3:46499000-46501000	Weak transcription	Spleen	Spleen
29	chr3:46499400-46499800	Weak transcription	Primary neutrophils fromperipheralblood	blood
30	chr3:46499800-46500000	Genic enhancers	Primary neutrophils fromperipheralblood	blood
31	chr3:46500000-46503800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr3:46501000-46501400	Enhancers	Left Ventricle	heart
33	chr3:46501000-46502200	Genic enhancers	Spleen	Spleen
34	chr3:46501200-46501400	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
35	chr3:46501400-46504000	Weak transcription	Left Ventricle	heart
36	chr3:46502200-46503400	Weak transcription	Spleen	Spleen
37	chr3:46502400-46503000	Weak transcription	Right Ventricle	heart
38	chr3:46503200-46504200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr3:46503200-46504800	Enhancers	Primary B cells from cord blood	blood
40	chr3:46503400-46503600	Enhancers	Stomach Mucosa	stomach
41	chr3:46503400-46504000	Enhancers	Primary monocytes fromperipheralblood	blood
42	chr3:46503400-46504000	Enhancers	Adipose Nuclei	Adipose
43	chr3:46503400-46504400	Enhancers	Spleen	Spleen
44	chr3:46503600-46504200	Enhancers	ES-I3 Cell Line	embryonic stem cell
45	chr3:46503600-46504200	Enhancers	Fetal Intestine Large	intestine
46	chr3:46503600-46504200	Enhancers	Fetal Intestine Small	intestine
47	chr3:46503600-46504400	Enhancers	Gastric	stomach
48	chr3:46503800-46504000	Bivalent Enhancer	Brain Cingulate Gyrus	brain
49	chr3:46503800-46504000	Bivalent Enhancer	Fetal Stomach	stomach
50	chr3:46503800-46504200	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived

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