Variant report

Variant	esv2762189
Chromosome Location	chr1:144945737-145014990
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2026)
CpG islands
(count:1099)
Chromatin interactive
region (count:108)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2026 , 50 per page) page: 1 2 3 4 5 6 7 ... 41

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr1:144997084-144999662	K562	blood:	n/a	n/a
2	ARID3A	chr1:145012025-145018939	K562	blood:	n/a	chr1:145012568-145012584 chr1:145012567-145012583
3	ARID3A	chr1:145000157-145004850	K562	blood:	n/a	chr1:145001553-145001569 chr1:145004748-145004764
4	ARID3A	chr1:145007845-145011203	K562	blood:	n/a	n/a
5	ARID3A	chr1:145005457-145007401	K562	blood:	n/a	n/a
6	ARID3A	chr1:144988785-144990011	HepG2	liver:	n/a	n/a
7	ARID3A	chr1:144991522-144993662	K562	blood:	n/a	n/a
8	ARID3A	chr1:144989106-144991213	K562	blood:	n/a	n/a
9	ARID3A	chr1:144994237-144996744	K562	blood:	n/a	n/a
10	ARID3A	chr1:145014466-145014972	HepG2	liver:	n/a	n/a
11	ATF1	chr1:145014382-145016089	K562	blood:	n/a	n/a
12	ATF1	chr1:144998715-144999351	K562	blood:	n/a	n/a
13	ATF1	chr1:144991677-144992162	K562	blood:	n/a	n/a
14	ATF1	chr1:144994316-144996366	K562	blood:	n/a	n/a
15	ATF1	chr1:144997529-144998431	K562	blood:	n/a	n/a
16	ATF1	chr1:145001703-145004761	K562	blood:	n/a	n/a
17	ATF1	chr1:144988840-144990055	K562	blood:	n/a	n/a
18	ATF1	chr1:145008736-145009963	K562	blood:	n/a	n/a
19	ATF1	chr1:145012108-145014066	K562	blood:	n/a	n/a
20	ATF3	chr1:145009033-145010014	K562	blood:	n/a	n/a
21	ATF3	chr1:145003959-145004695	K562	blood:	n/a	n/a
22	ATF3	chr1:145014931-145015525	K562	blood:	n/a	n/a
23	ATF3	chr1:144997011-144998557	K562	blood:	n/a	n/a
24	BACH1	chr1:144994774-144995705	H1-hESC	embryonic stem cell:	n/a	n/a
25	BACH1	chr1:145008851-145011359	K562	blood:	n/a	n/a
26	BACH1	chr1:145000022-145002759	K562	blood:	n/a	n/a
27	BACH1	chr1:144997213-144999624	K562	blood:	n/a	n/a
28	BACH1	chr1:144994691-144996577	K562	blood:	n/a	n/a
29	BACH1	chr1:144991688-144992152	K562	blood:	n/a	n/a
30	BACH1	chr1:145012286-145016138	K562	blood:	n/a	n/a
31	BACH1	chr1:144994219-144994455	K562	blood:	n/a	n/a
32	BATF	chr1:144965985-144966330	GM12878	blood:	n/a	n/a
33	BATF	chr1:144965596-144965880	GM12878	blood:	n/a	chr1:144965602-144965610 chr1:144965715-144965724
34	BATF	chr1:144954919-144955123	GM12878	blood:	n/a	n/a
35	BATF	chr1:144954925-144955119	GM12878	blood:	n/a	n/a
36	BCL11A	chr1:144965972-144966276	GM12878	blood:	n/a	n/a
37	BCL11A	chr1:144963027-144963277	GM12878	blood:	n/a	n/a
38	BCL11A	chr1:144965672-144966363	GM12878	blood:	n/a	n/a
39	BCLAF1	chr1:144965819-144966130	GM12878	blood:	n/a	n/a
40	BDP1	chr1:145014896-145015168	Hela-S3	cervix:	n/a	n/a
41	BDP1	chr1:145013149-145016951	K562	blood:	n/a	n/a
42	BDP1	chr1:144997413-144997821	Hela-S3	cervix:	n/a	n/a
43	BHLHE40	chr1:144991111-144991271	K562	blood:	n/a	n/a
44	BHLHE40	chr1:144998756-144999486	K562	blood:	n/a	n/a
45	BHLHE40	chr1:144993958-144996487	K562	blood:	n/a	chr1:144994548-144994564
46	BHLHE40	chr1:145008990-145011333	K562	blood:	n/a	n/a
47	BHLHE40	chr1:144999999-145001404	K562	blood:	n/a	n/a
48	BHLHE40	chr1:144966129-144966186	GM12878	blood:	n/a	n/a
49	BHLHE40	chr1:145012116-145016891	K562	blood:	n/a	n/a
50	BHLHE40	chr1:144997167-144998500	K562	blood:	n/a	n/a

(count:1099 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr1:144952173-144952223	AG09309	skin:	n/a
2	chr1:144952173-144952223	AG09309	skin:	n/a
3	chr1:145013480-145013530	HAEpiC	amniotic membrane:	n/a
4	chr1:145003040-145003090	U87	brain:	n/a
5	chr1:144995889-144995939	AoSMC	blood vessel:	n/a
6	chr1:145012822-145012872	NHDF-neo	bronchial:	n/a
7	chr1:144995101-144995151	HMEC	breast:	n/a
8	chr1:144995682-144995732	HNPCEpiC	eye:	n/a
9	chr1:144952173-144952223	HAEpiC	amniotic membrane:	n/a
10	chr1:144995101-144995151	SK-N-SH	brain:	n/a
11	chr1:144995682-144995732	NHDF-neo	bronchial:	n/a
12	chr1:145004305-145004355	AG04449	skin:	fetal
13	chr1:145001340-145001390	K562	blood:	n/a
14	chr1:144998869-144998919	HRPEpiC	eye:	n/a
15	chr1:144994826-144994876	HCPEpiC	choroid plexus:	n/a
16	chr1:144952173-144952223	HL-60	blood:	n/a
17	chr1:145004468-145004518	SKMC	muscle:	n/a
18	chr1:144994715-144994765	HCPEpiC	choroid plexus:	n/a
19	chr1:144994658-144994708	HCF	heart:	n/a
20	chr1:145001340-145001390	HEEpiC	esophagus:	n/a
21	chr1:145003040-145003090	HNPCEpiC	eye:	n/a
22	chr1:145004305-145004355	HAEpiC	amniotic membrane:	n/a
23	chr1:144994542-144994592	NH-A	brain:	n/a
24	chr1:144994715-144994765	NHDF-neo	bronchial:	n/a
25	chr1:144994826-144994876	HEEpiC	esophagus:	n/a
26	chr1:144995101-144995151	AG04449	skin:	fetal
27	chr1:144989624-144989674	PANC-1	pancreas:	n/a
28	chr1:145004468-145004518	HepG2	liver:	n/a
29	chr1:145001340-145001390	ovcar-3	ovarian:	n/a
30	chr1:145004468-145004518	HEK293	kidney:	embryo
31	chr1:144998869-144998919	HEK293	kidney:	embryo
32	chr1:144998869-144998919	HepG2	liver:	n/a
33	chr1:144989624-144989674	A549	lung:	n/a
34	chr1:144994933-144994983	MCF10A-Er-Src	breast:	n/a
35	chr1:145012822-145012872	Hela-S3	cervix:	n/a
36	chr1:144989624-144989674	Jurkat	blood:	n/a
37	chr1:144994658-144994708	CMK	blood:	n/a
38	chr1:144994715-144994765	NHBE	bronchial:	n/a
39	chr1:144994715-144994765	AG09309	skin:	n/a
40	chr1:144952173-144952223	AG09319	gingival:	n/a
41	chr1:145013480-145013530	SK-N-MC	brain:	n/a
42	chr1:144995101-144995151	A549	lung:	n/a
43	chr1:144995682-144995732	NT2-D1	testis:	n/a
44	chr1:144994658-144994708	ProgFib	skin:	n/a
45	chr1:144994658-144994708	AG04449	skin:	fetal
46	chr1:145012822-145012872	HMEC	breast:	n/a
47	chr1:145012822-145012872	GM12878	blood:	n/a
48	chr1:145004305-145004355	SAEC	small airway:	n/a
49	chr1:144995101-144995151	HPAEpiC	pulmonary alveolar:	n/a
50	chr1:145012822-145012872	MCF-7	breast:	n/a

(count:108 , 50 per page) page: 1 2 3

No.	Distal block	Cell Line	Cell type
1	chr1:145012040..145014419-chr1:145052808..145055801,2	K562	blood:
2	chr1:145007566..145009681-chr1:145060269..145062517,2	K562	blood:
3	chr1:145003130..145005875-chr1:149855420..149857105,2	K562	blood:
4	chr1:144989139..144991209-chr8:145724589..145727084,2	MCF-7	breast:
5	chr1:144992139..144994495-chr1:145073891..145076313,2	MCF-7	breast:
6	chr1:144532050..144536421-chr1:145006819..145011373,9	K562	blood:
7	chr1:145006816..145009107-chr1:145057701..145060152,2	K562	blood:
8	chr1:144999173..145001999-chr1:145037688..145039743,3	MCF-7	breast:
9	chr1:145003631..145004191-chr1:145014605..145015136,2	K562	blood:
10	chr1:144992586..144994194-chr1:145030165..145032446,2	MCF-7	breast:
11	chr1:145005888..145007907-chr1:145011945..145014640,3	MCF-7	breast:
12	chr1:145013051..145015770-chr1:145381611..145384530,4	K562	blood:
13	chr1:144708092..144711018-chr1:144989311..144991763,2	K562	blood:
14	chr1:144912685..144914252-chr1:144947438..144950034,2	K562	blood:
15	chr1:144988447..144988982-chr1:145009629..145010133,2	K562	blood:
16	chr1:120510712..120511507-chr1:144989621..144990280,2	MCF-7	breast:
17	chr1:145003631..145004191-chr1:145014605..145015136,2	K562	blood:
18	chr1:145006961..145008693-chr1:145104666..145107384,2	K562	blood:
19	chr1:144989452..144990455-chr1:145058719..145059632,6	K562	blood:
20	chr1:144991648..144993196-chr12:122238579..122241353,2	MCF-7	breast:
21	chr1:145012523..145015160-chr1:145055357..145057301,2	K562	blood:
22	chr1:144610196..144613113-chr1:144999265..145001595,2	K562	blood:
23	chr1:145012787..145014315-chr11:46834339..46836400,2	MCF-7	breast:
24	chr1:145009850..145011713-chr1:145053445..145055856,2	K562	blood:
25	chr1:145013488..145015671-chr1:145056479..145059269,3	MCF-7	breast:
26	chr1:145013724..145015799-chr5:131825406..131827078,2	MCF-7	breast:
27	chr1:144988447..144988982-chr1:145009629..145010133,2	K562	blood:
28	chr1:145006816..145009369-chr1:145057265..145060152,2	K562	blood:
29	chr1:144929950..144932312-chr1:145002420..145004255,2	MCF-7	breast:
30	chr1:145012804..145013720-chr1:145058918..145059629,3	MCF-7	breast:
31	chr1:144989394..144991643-chr1:145383439..145385394,2	K562	blood:
32	chr1:144988088..144989012-chr1:145058100..145059991,5	MCF-7	breast:
33	chr1:144997738..145000659-chr1:145007857..145011011,3	MCF-7	breast:
34	chr1:144989491..144990907-chr1:145058682..145059954,10	MCF-7	breast:
35	chr1:144995928..144998719-chr1:145383813..145386385,2	K562	blood:
36	chr1:145008157..145010957-chr1:145382547..145384620,2	K562	blood:
37	chr1:144932512..144934807-chr1:144998183..145000518,2	MCF-7	breast:
38	chr1:145003720..145005875-chr1:149855605..149858260,2	K562	blood:
39	chr1:144930835..144932990-chr1:145009036..145011761,2	MCF-7	breast:
40	chr1:144988330..144990331-chr1:145096274..145097862,2	MCF-7	breast:
41	chr1:144709036..144711011-chr1:144986149..144988620,2	K562	blood:
42	chr1:145009595..145012188-chr1:145012261..145014678,3	MCF-7	breast:
43	chr1:144993668..144997286-chr1:145038559..145041171,3	MCF-7	breast:
44	chr1:145014334..145015129-chr1:145055872..145056456,2	MCF-7	breast:
45	chr1:145000529..145002356-chr1:145004395..145006145,2	MCF-7	breast:
46	chr1:144929876..144935601-chr1:144987785..144996108,12	MCF-7	breast:
47	chr1:144696978..144697597-chr1:144972550..144973477,2	MCF-7	breast:
48	chr1:144992899..144993435-chr1:145029983..145030524,2	MCF-7	breast:
49	chr1:121484512..121485424-chr1:145014402..145015111,3	MCF-7	breast:
50	chr1:144532979..144535627-chr1:145000792..145004183,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-NBPF9-4	chr1:145013726-145013828	NONHSAT005870
2	lnc-NBPF9-3	chr1:145004781-145005286	NONHSAT005869

No data

Variant related genes	Relation type
ENSG00000272755	TF binding region
PDE4DIP	TF binding region
ENSG00000268172	TF binding region
ENSG00000272755	CpG island
PDE4DIP	CpG island
ENSG00000268172	CpG island
ENSG00000203843	chromatin interactions
ENSG00000233396	chromatin interactions
ENSG00000125347	chromatin interactions
ENSG00000180370	chromatin interactions
ENSG00000160972	chromatin interactions
ENSG00000184260	chromatin interactions
ENSG00000261139	chromatin interactions
ENSG00000268172	chromatin interactions
ENSG00000079335	chromatin interactions
ENSG00000139725	chromatin interactions
ENSG00000201699	chromatin interactions
ENSG00000201558	chromatin interactions
ENSG00000223491	chromatin interactions
ENSG00000212694	chromatin interactions
ENSG00000223380	chromatin interactions
ENSG00000174827	chromatin interactions
ENSG00000255182	chromatin interactions
ENSG00000178104	chromatin interactions
ENSG00000184678	chromatin interactions

Extended variants
information (count: 2536 )
Associated
traits (count: 170 )

Variant overlapped rSNPs/rCNVs (count:2536 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs2996281	chr1:144945737-144945738	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs587701091	chr1:144945740-144945741	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs587758132	chr1:144945792-144945793	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs587633679	chr1:144945801-144945802	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs587670246	chr1:144945838-144945839	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs71664021	chr1:144945870-144945871	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs587723972	chr1:144945873-144945874	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs587626021	chr1:144945885-144945886	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs587679072	chr1:144945895-144945896	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs151127029	chr1:144945912-144945913	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs587765760	chr1:144945919-144945920	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs2500345	chr1:144945941-144945942	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs185928035	chr1:144945951-144945952	Weak transcription Strong transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs587757729	chr1:144946101-144946102	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs587653135	chr1:144946117-144946118	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs587710850	chr1:144946159-144946160	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs2762735	chr1:144946183-144946184	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs587762861	chr1:144946189-144946190	Weak transcription Strong transcription Enhancers Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs587646142	chr1:144946218-144946219	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs587718150	chr1:144946227-144946228	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs113962685	chr1:144946246-144946247	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs587700995	chr1:144946261-144946262	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs587737627	chr1:144946278-144946279	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs587594632	chr1:144946294-144946295	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs185180388	chr1:144946309-144946310	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs587727281	chr1:144946312-144946313	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs587620994	chr1:144946336-144946337	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs587662537	chr1:144946353-144946354	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs587744826	chr1:144946354-144946355	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs112552008	chr1:144946355-144946356	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs368805472	chr1:144946369-144946370	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs587618244	chr1:144946376-144946377	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs2798888	chr1:144946403-144946404	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs2762734	chr1:144946486-144946487	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs587700060	chr1:144946506-144946507	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs2488977	chr1:144946510-144946511	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs587632269	chr1:144946521-144946522	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs587683213	chr1:144946527-144946528	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs587767413	chr1:144946541-144946542	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs587639257	chr1:144946558-144946559	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs587723790	chr1:144946559-144946560	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs201948137	chr1:144946575-144946576	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs587773638	chr1:144946619-144946620	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs140223371	chr1:144946635-144946636	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs371734991	chr1:144946660-144946661	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs144942272	chr1:144946680-144946681	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs77741848	chr1:144946701-144946702	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs141368157	chr1:144946715-144946716	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs587656322	chr1:144946745-144946746	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs587737871	chr1:144946747-144946748	Weak transcription Strong transcription Enhancers Flanking Active TSS Genic enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:170)

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
Cancer	21129771	CNVD
Non-small cell lung cancer	21385341	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
Ewing''s sarcoma	21437220	CNVD
Liposarcoma	21253554	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
Acute lymphoblastic leukemia	17443227	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	17133270	CNVD
small cell lung cancer	20016488	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
Breast cancer	21611746	CNVD
Retinoblastoma	19183342	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21990379	CNVD
Myelofibrosis	22110671	CNVD
Schizophrenia	22499536	CNVD
Schizophrenia	18923514	CNVD
Neuroblastoma	21124317	CNVD
Autism	20970697	CNVD
Bipolar disorder	19114987	CNVD
Epilepsy	20970697	CNVD
Schizophrenia	22118685	CNVD
Schizophrenia	20587603	CNVD
Schizophrenia	21285140	CNVD
Schizophrenia	20553308	CNVD
Schizophrenia	21956041	CNVD
Schizophrenia	20970697	CNVD
Addison''s disease	21851588	CNVD
Heart disease	22199024	CNVD
Mental retardation	19951919	CNVD
Ovarian cancer	20844748	CNVD
Schizophrenia	21399695	CNVD
Prostate cancer	17217626	CNVD
Congenital heart defect	22199024	CNVD
TAR Syndrome	17847015	CNVD
Thrombocytopenia-absent radius syndrome	17236129	CNVD
Autism	18784092	CNVD
Congenital abnormalities	18784092	CNVD
Mental retardation	18784092	CNVD
Schizophrenia	19855392	CNVD
Ovarian cancer	22174824	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
Autism	19521722	CNVD
Mental retardation	19521722	CNVD
Schizophrenia	19521646	CNVD
Neuroblastoma	19536264	CNVD
Epilepsy	20923578	CNVD
Mental retardation	17124404	CNVD
Schizophrenia	19348701	CNVD
Schizophrenia	18668039	CNVD
Schizophrenia	19443537	CNVD
Schizophrenia	19571808	CNVD
Velocardiofacial syndrome	19329560	CNVD
Autism	19955444	CNVD
Autism	20964600	CNVD
Schizophrenia	19955444	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Colorectal cancer	20459617	CNVD
Osteosarcoma	19286668	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
Breast cancer	17142309	CNVD
Acute myeloid leukemia	21251322	CNVD
Multiple myeloma	17550852	CNVD
Prostate cancer	18632612	CNVD
Follicular lymphoma	18703704	CNVD
Lung adenocarcinoma	17982442	CNVD
Breast cancer	21509527	CNVD
Tetralogy of Fallot	22912587	CNVD
Autism	18522746	CNVD
Bladder cancer	21909424	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Acute myeloid leukemia	20729466	CNVD
Schizophrenia	19197363	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Schizophrenia	23813976	CNVD
Lung adenocarcinoma	21935476	CNVD
idiopathic generalized epilepsy	19843651	CNVD
Schizophrenia	19843651	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Non-syndromic sensorineural hearing loss	17289997	CNVD
Autism	20531469	CNVD
Autism	20858243	CNVD
Breast cancer	22522925	CNVD
Autism	22543975	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Epilepsy	20502679	CNVD
Autism	20841430	CNVD

Chromatin state (count:2744 , 50 per page) page: 1 2 3 4 5 6 7 ... 55

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr1:144934000-144949000	Weak transcription	Spleen	Spleen
2	chr1:144936600-144948800	Weak transcription	Pancreas	Pancrea
3	chr1:144937400-144948200	Weak transcription	Primary B cells from cord blood	blood
4	chr1:144937800-144948400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
5	chr1:144939200-144948800	Weak transcription	Colonic Mucosa	Colon
6	chr1:144939800-144952200	Strong transcription	K562	blood
7	chr1:144941000-144946200	Weak transcription	Fetal Intestine Large	intestine
8	chr1:144941200-144946400	Weak transcription	Fetal Intestine Small	intestine
9	chr1:144941400-144946800	Weak transcription	Stomach Mucosa	stomach
10	chr1:144941600-144945800	Weak transcription	Breast Myoepithelial Primary Cells	Breast
11	chr1:144941600-144946800	Strong transcription	Liver	Liver
12	chr1:144941600-144946800	Weak transcription	Ovary	ovary
13	chr1:144941600-144950000	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
14	chr1:144941600-144951000	Strong transcription	Left Ventricle	heart
15	chr1:144942200-144946000	Weak transcription	HMEC	breast
16	chr1:144942200-144949600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
17	chr1:144942200-144960200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
18	chr1:144942400-144949200	Strong transcription	Fetal Muscle Trunk	muscle
19	chr1:144942400-144951400	Strong transcription	Brain Cingulate Gyrus	brain
20	chr1:144942400-144952200	Strong transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
21	chr1:144942600-144948000	Weak transcription	NH-A	brain
22	chr1:144942600-144948400	Weak transcription	Primary T cells from cord blood	blood
23	chr1:144942600-144948800	Weak transcription	Small Intestine	intestine
24	chr1:144942600-144952000	Strong transcription	Osteobl	bone
25	chr1:144942600-144952200	Strong transcription	Placenta	Placenta
26	chr1:144942800-144951800	Strong transcription	HSMM	muscle
27	chr1:144942800-144952200	Strong transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr1:144942800-144952200	Strong transcription	Muscle Satellite Cultured Cells	--
29	chr1:144942800-144952200	Strong transcription	HSMMtube	muscle
30	chr1:144943000-144949000	Strong transcription	Brain Inferior Temporal Lobe	brain
31	chr1:144943200-144946800	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr1:144943200-144948000	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
33	chr1:144943200-144953000	Weak transcription	Fetal Brain Female	brain
34	chr1:144943400-144945800	Weak transcription	Fetal Kidney	kidney
35	chr1:144943400-144947000	Strong transcription	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr1:144943400-144947800	Strong transcription	Aorta	Aorta
37	chr1:144943400-144949200	Strong transcription	Fetal Muscle Leg	muscle
38	chr1:144943400-144961000	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
39	chr1:144943600-144946000	Weak transcription	Duodenum Smooth Muscle	Duodenum
40	chr1:144943800-144946000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr1:144944000-144945800	Weak transcription	Brain Angular Gyrus	brain
42	chr1:144944000-144946000	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
43	chr1:144944000-144946000	Strong transcription	Skeletal Muscle Female	skeletal muscle
44	chr1:144944000-144946400	Strong transcription	Skeletal Muscle Male	skeletal muscle
45	chr1:144944000-144946600	Weak transcription	Gastric	stomach
46	chr1:144944000-144948600	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
47	chr1:144944000-144948600	Weak transcription	Rectal Smooth Muscle	rectum
48	chr1:144944000-144948800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
49	chr1:144944000-144950000	Weak transcription	Fetal Stomach	stomach
50	chr1:144944000-144950000	Weak transcription	Sigmoid Colon	Sigmoid Colon

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