Variant report

Variant	nsv524207
Chromosome Location	chr2:20448561-20503436
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr2:20490861-20491084	HepG2	liver:	n/a	n/a
2	ATF3	chr2:20490803-20491174	H1-hESC	embryonic stem cell:	n/a	n/a
3	BACH1	chr2:20460156-20460159	K562	blood:	n/a	n/a
4	BHLHE40	chr2:20488765-20489108	K562	blood:	n/a	n/a
5	BHLHE40	chr2:20490870-20491140	HepG2	liver:	n/a	chr2:20491018-20491039
6	BHLHE40	chr2:20488804-20489055	A549	lung:	n/a	n/a
7	BHLHE40	chr2:20490827-20491181	K562	blood:	n/a	chr2:20491018-20491039
8	CBX3	chr2:20490762-20491283	HCT-116	colon:	n/a	n/a
9	CBX3	chr2:20490814-20491206	K562	blood:	n/a	n/a
10	CEBPB	chr2:20466752-20466937	K562	blood:	n/a	n/a
11	CEBPB	chr2:20491592-20491831	HepG2	liver:	n/a	chr2:20491683-20491694
12	CEBPB	chr2:20466780-20466848	A549	lung:	n/a	n/a
13	CEBPB	chr2:20492813-20493078	IMR90	lung:	n/a	chr2:20492914-20492931
14	CEBPB	chr2:20492766-20493106	HepG2	liver:	n/a	chr2:20492914-20492931
15	CEBPB	chr2:20459001-20459261	IMR90	lung:	n/a	chr2:20459108-20459119
16	CEBPB	chr2:20488463-20488693	HepG2	liver:	n/a	chr2:20488551-20488562
17	CEBPB	chr2:20458958-20459288	HepG2	liver:	n/a	chr2:20459108-20459119
18	CEBPB	chr2:20491478-20491678	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr2:20488484-20488736	IMR90	lung:	n/a	chr2:20488551-20488562
20	CEBPB	chr2:20458997-20459433	A549	lung:	n/a	chr2:20459108-20459119
21	CEBPB	chr2:20491523-20491698	K562	blood:	n/a	chr2:20491683-20491694
22	CEBPB	chr2:20488469-20489113	Hela-S3	cervix:	n/a	chr2:20488551-20488562
23	CEBPB	chr2:20458971-20459301	K562	blood:	n/a	chr2:20459108-20459119
24	CEBPB	chr2:20488454-20488711	K562	blood:	n/a	chr2:20488551-20488562
25	CEBPB	chr2:20491545-20491819	A549	lung:	n/a	chr2:20491683-20491694
26	CEBPB	chr2:20486715-20487005	K562	blood:	n/a	n/a
27	CEBPB	chr2:20492781-20493089	A549	lung:	n/a	chr2:20492914-20492931
28	CHD2	chr2:20490801-20491093	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr2:20488773-20488971	Hela-S3	cervix:	n/a	n/a
30	CTCF	chr2:20490940-20491090	GM12867	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
31	CTCF	chr2:20490860-20491010	A549	lung:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
32	CTCF	chr2:20491240-20491390	HCM	heart:	n/a	n/a
33	CTCF	chr2:20490830-20491134	HUVEC	blood vessel:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
34	CTCF	chr2:20490880-20491030	AG04449	skin:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
35	CTCF	chr2:20490852-20491103	Spleen_OC	spleen:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
36	CTCF	chr2:20490940-20491090	NHLF	lung:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
37	CTCF	chr2:20490689-20491184	K562	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
38	CTCF	chr2:20490860-20491010	GM12870	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
39	CTCF	chr2:20490920-20491070	HMEC	breast:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
40	CTCF	chr2:20490900-20491050	HepG2	liver:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
41	CTCF	chr2:20490860-20491010	HCT-116	colon:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
42	CTCF	chr2:20491137-20491169	MCF-7	breast:	n/a	n/a
43	CTCF	chr2:20490854-20491093	Medullo	brain:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
44	CTCF	chr2:20490823-20491105	LNCaP	prostate:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
45	CTCF	chr2:20490829-20491169	Fibrobl	skin:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
46	CTCF	chr2:20490900-20491050	HRPEpiC	eye:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
47	CTCF	chr2:20490920-20491070	K562	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
48	CTCF	chr2:20490860-20491010	AG09319	gingival:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
49	CTCF	chr2:20490722-20491184	A549	lung:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998
50	CTCF	chr2:20490900-20491050	GM12801	blood:	n/a	chr2:20490982-20490995 chr2:20490975-20490996 chr2:20490980-20490998

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr2:20491052-20491102	HUVEC	blood vessel:	n/a
2	chr2:20491052-20491102	Caco-2	colon:	n/a
3	chr2:20491052-20491102	NH-A	brain:	n/a
4	chr2:20491052-20491102	HCF	heart:	n/a
5	chr2:20491052-20491102	NT2-D1	testis:	n/a
6	chr2:20494247-20494297	GM12891	blood:	n/a
7	chr2:20494247-20494297	GM06990	blood:	n/a
8	chr2:20494247-20494297	PANC-1	pancreas:	n/a
9	chr2:20494247-20494297	AG09309	skin:	n/a
10	chr2:20491052-20491102	AG10803	skin:	n/a
11	chr2:20494247-20494297	HCF	heart:	n/a
12	chr2:20491052-20491102	ECC-1	luminal epithelium:	n/a
13	chr2:20449227-20449277	IMR90	lung:	fetal
14	chr2:20449227-20449277	ProgFib	skin:	n/a
15	chr2:20449227-20449277	HCM	heart:	n/a
16	chr2:20491052-20491102	A549	lung:	n/a
17	chr2:20449227-20449277	AG10803	skin:	n/a
18	chr2:20494247-20494297	HRCEpiC	kidney:	n/a
19	chr2:20494247-20494297	PrEC	prostate:	n/a
20	chr2:20449227-20449277	HCT-116	colon:	n/a
21	chr2:20494247-20494297	SKMC	muscle:	n/a
22	chr2:20494247-20494297	ECC-1	luminal epithelium:	n/a
23	chr2:20449227-20449277	AoSMC	blood vessel:	n/a
24	chr2:20491052-20491102	K562	blood:	n/a
25	chr2:20491052-20491102	H1-hESC	embryonic stem cell:	embryo
26	chr2:20449227-20449277	NT2-D1	testis:	n/a
27	chr2:20491052-20491102	NB4	blood:	n/a
28	chr2:20491052-20491102	HepG2	liver:	n/a
29	chr2:20494247-20494297	HIPEpiC	eye:	n/a
30	chr2:20491052-20491102	SK-N-SH	brain:	n/a
31	chr2:20494247-20494297	SAEC	small airway:	n/a
32	chr2:20494247-20494297	BE2_C	brain:	n/a
33	chr2:20494247-20494297	HCPEpiC	choroid plexus:	n/a
34	chr2:20494247-20494297	HRPEpiC	eye:	n/a
35	chr2:20494247-20494297	HUVEC	blood vessel:	n/a
36	chr2:20449227-20449277	PFSK-1	brain:	n/a
37	chr2:20449227-20449277	GM12892	blood:	n/a
38	chr2:20494247-20494297	HL-60	blood:	n/a
39	chr2:20449227-20449277	Jurkat	blood:	n/a
40	chr2:20494247-20494297	ovcar-3	ovarian:	n/a
41	chr2:20491052-20491102	HMEC	breast:	n/a
42	chr2:20491052-20491102	Hela-S3	cervix:	n/a
43	chr2:20494247-20494297	HMEC	breast:	n/a
44	chr2:20494247-20494297	HAEpiC	amniotic membrane:	n/a
45	chr2:20494247-20494297	AG04449	skin:	fetal
46	chr2:20449227-20449277	HEEpiC	esophagus:	n/a
47	chr2:20494247-20494297	SK-N-SH	brain:	n/a
48	chr2:20491052-20491102	SKMC	muscle:	n/a
49	chr2:20449227-20449277	HNPCEpiC	eye:	n/a
50	chr2:20449227-20449277	HL-60	blood:	n/a

No.	Distal block	Cell Line	Cell type
1	chr2:20422501..20424749-chr2:20493123..20495327,2	MCF-7	breast:
2	chr2:20466339..20468775-chr2:20471320..20473308,2	MCF-7	breast:
3	chr2:20297655..20298611-chr2:20490488..20491367,2	MCF-7	breast:
4	chr2:20470435..20474435-chr2:20474599..20476885,4	K562	blood:
5	chr2:20487617..20489634-chr2:20494522..20496628,2	K562	blood:
6	chr2:20445683..20448261-chr2:20451475..20453272,2	MCF-7	breast:
7	chr2:20503412..20505085-chr2:20523282..20524806,2	K562	blood:
8	chr2:20489792..20492036-chr2:20546844..20549353,2	MCF-7	breast:
9	chr2:20444479..20447318-chr2:20451928..20453466,2	MCF-7	breast:
10	chr2:20474838..20476628-chr2:20486157..20488618,2	K562	blood:
11	chr2:20423460..20425374-chr2:20445845..20448782,3	MCF-7	breast:
12	chr2:20481278..20483845-chr2:20486511..20488232,4	MCF-7	breast:
13	chr2:20466339..20468775-chr2:20471320..20473308,2	MCF-7	breast:
14	chr2:20424404..20426434-chr2:20494387..20495933,2	MCF-7	breast:
15	chr2:20475845..20477677-chr2:20489513..20491458,2	K562	blood:
16	chr2:20326769..20329313-chr2:20498796..20501273,2	K562	blood:
17	chr2:20422753..20425256-chr2:20490607..20493628,3	MCF-7	breast:
18	chr2:20478789..20484582-chr2:20484927..20489294,7	K562	blood:
19	chr2:20491737..20495195-chr2:20496209..20497993,3	K562	blood:
20	chr2:20474838..20476628-chr2:20486157..20488618,2	K562	blood:
21	chr2:20473741..20476352-chr2:20478752..20483600,5	MCF-7	breast:
22	chr2:20495005..20497847-chr2:20502307..20504684,2	MCF-7	breast:
23	chr2:20456736..20458629-chr2:20459972..20461571,2	K562	blood:
24	chr2:20490728..20492499-chr2:20498984..20500498,2	MCF-7	breast:
25	chr2:20467246..20470350-chr2:20472212..20474237,3	K562	blood:
26	chr2:20501783..20504502-chr2:20645581..20647102,2	MCF-7	breast:
27	chr2:20469016..20471987-chr2:20480975..20483555,2	MCF-7	breast:
28	chr2:20431635..20433963-chr2:20446751..20449064,2	MCF-7	breast:
29	chr2:20497505..20499547-chr2:20501441..20503193,2	K562	blood:
30	chr2:20503251..20505156-chr2:20505532..20508254,2	K562	blood:
31	chr2:20467246..20470350-chr2:20472212..20474237,3	K562	blood:
32	chr2:20378964..20381641-chr2:20471495..20474271,2	MCF-7	breast:
33	chr2:20477908..20478887-chr2:20491028..20491640,2	K562	blood:
34	chr2:20496655..20499171-chr2:20500184..20502040,2	MCF-7	breast:
35	chr2:20472858..20474518-chr2:20518038..20520813,2	K562	blood:
36	chr2:20500446..20501966-chr6:142366297..142367819,2	MCF-7	breast:
37	chr2:20459796..20461305-chr2:20461411..20463303,2	K562	blood:
38	chr2:20484989..20487523-chr2:20496339..20498014,2	K562	blood:
39	chr2:20473741..20476352-chr2:20478752..20483600,5	MCF-7	breast:
40	chr2:20475766..20478628-chr2:20479027..20481170,2	MCF-7	breast:
41	chr2:20496513..20498388-chr2:20499251..20501283,2	MCF-7	breast:
42	chr2:20484550..20486934-chr2:20490044..20492996,3	MCF-7	breast:
43	chr2:20423075..20426042-chr2:20460120..20462817,2	MCF-7	breast:
44	chr2:20487617..20489634-chr2:20494522..20496628,2	K562	blood:
45	chr2:20463108..20465491-chr2:20466450..20468569,2	K562	blood:
46	chr2:20484989..20487523-chr2:20496339..20498014,2	K562	blood:
47	chr2:20451918..20453855-chr2:20460102..20461929,2	MCF-7	breast:
48	chr2:20425705..20426396-chr2:20447809..20448700,2	MCF-7	breast:
49	chr2:20475845..20477677-chr2:20489513..20491458,2	K562	blood:
50	chr2:20155105..20156071-chr2:20490452..20491074,4	K562	blood:

No.	miRNA target gene	miRNA name	Chromosome Location
1	PUM2	hsa-miR-218-5p	chr2:20451104-20451098
2	PUM2	hsa-miR-10a-5p	chr2:20450216-20450239
3	PUM2	hsa-miR-218-5p	chr2:20451098-20451117

Variant related genes	Relation type
RNU7-113P	TF binding region
RNU7-113P	CpG island
ENSG00000213729	chromatin interactions
ENSG00000068697	chromatin interactions
ENSG00000055917	chromatin interactions
ENSG00000223734	chromatin interactions
ENSG00000223247	chromatin interactions
ENSG00000143878	chromatin interactions
ENSG00000238735	chromatin interactions
ENSG00000115884	chromatin interactions

Extended variants
information (count: 2109 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:2109 , 50 per page) page: 1 2 3 4 5 6 7 ... 43

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs1043419	chr2:20448561-20448562	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs531424590	chr2:20448591-20448592	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
3	rs547948591	chr2:20448594-20448595	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
4	rs115302390	chr2:20448679-20448680	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
5	rs576648794	chr2:20448680-20448681	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
6	rs58368380	chr2:20448741-20448742	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
7	rs533865063	chr2:20448767-20448768	Weak transcription Strong transcription	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
8	rs553347632	chr2:20448817-20448818	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs144272106	chr2:20448835-20448836	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs188545529	chr2:20448884-20448885	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs538617563	chr2:20448888-20448889	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs181045406	chr2:20448889-20448890	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs373634805	chr2:20448890-20448891	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs575612818	chr2:20448937-20448938	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs544699955	chr2:20448981-20448982	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs555228409	chr2:20448995-20448996	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs13394115	chr2:20449068-20449069	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs540967428	chr2:20449074-20449075	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs77031565	chr2:20449081-20449082	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs146566387	chr2:20449083-20449084	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs140995141	chr2:20449085-20449086	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs562618711	chr2:20449086-20449087	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs531340297	chr2:20449091-20449092	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs545718263	chr2:20449108-20449109	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs547860851	chr2:20449127-20449128	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs149918549	chr2:20449149-20449150	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs1043400	chr2:20449174-20449175	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs370467049	chr2:20449227-20449228	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs539036383	chr2:20449228-20449229	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs552320591	chr2:20449250-20449251	Weak transcription Strong transcription	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs569250566	chr2:20449316-20449317	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs538387463	chr2:20449367-20449368	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs555089690	chr2:20449397-20449398	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs575094629	chr2:20449402-20449403	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs534343279	chr2:20449414-20449415	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs111576078	chr2:20449435-20449436	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs554470534	chr2:20449451-20449452	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs35718653	chr2:20449484-20449485	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs577432320	chr2:20449502-20449503	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs546461465	chr2:20449547-20449548	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs562373332	chr2:20449593-20449594	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs35997772	chr2:20449604-20449605	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs575631552	chr2:20449680-20449681	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs569455689	chr2:20449686-20449687	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs541568235	chr2:20449723-20449724	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs561408445	chr2:20449735-20449736	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs74341922	chr2:20449783-20449784	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs76483608	chr2:20449784-20449785	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs78759423	chr2:20449785-20449786	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs74376146	chr2:20449786-20449787	Weak transcription Strong transcription	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

Disease	PMID	Source
Glioblastoma multiforme	21080181	CNVD
Neuroblastoma	21508638	CNVD
Breast cancer	17603634	CNVD
Cancer	16751803	CNVD
Neuroblastoma	16790693	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	17393978	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Medulloblastoma	21979893	CNVD
Lynch syndrome	18415027	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Ovarian neoplasms	16753589	CNVD
Glioblastoma multiforme	17387387	CNVD
Neuroblastoma	17533364	CNVD
Neuroblastoma	18923191	CNVD
Endometrial cancer	22040021	CNVD
Adrenal tumor	17535989	CNVD
Breast cancer	21264507	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	17522785	CNVD
Cancer	23418310	CNVD
Ewing''s sarcoma	21437220	CNVD
Ependymoma	16718352	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Prostate cancer	18632612	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Bladder cancer	21909424	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Intellectual disability	22102821	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Hodgkin''s lymphoma	18641027	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	20505157	CNVD
Autism	17483303	CNVD
Invasive pancreatic ductal carcinoma	16982739	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute myeloid leukemia	21251322	CNVD
Breast cancer	21785460	CNVD
Medulloblastoma	20607354	CNVD
Neuroblastoma	19638189	CNVD
Neuroblastoma	19435921	CNVD
Neuroblastoma	18574593	CNVD
Acute myeloid leukemia	18000384	CNVD
Medulloblastoma	16968546	CNVD
Medulloblastoma	22160402	CNVD
Schizophrenia	22118685	CNVD
Epilepsy	22118685	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	21509527	CNVD
Leukemia	18628472	CNVD
Autism	19521722	CNVD
Autism	18522746	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Ovarian cancer	17908972	CNVD
Neurocytoma	17123091	CNVD
Central neurocytomas	17123091	CNVD
Neuroblastoma	18664255	CNVD
Neuroblastoma	18765546	CNVD
Neuroblastoma	18281664	CNVD
Neuroblastoma	17289879	CNVD
Neuroblastoma	19738985	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	21364760	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1660 , 50 per page) page: 1 2 3 4 5 6 7 ... 34

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr2:20433000-20450200	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
2	chr2:20433000-20451200	Weak transcription	ES-I3 Cell Line	embryonic stem cell
3	chr2:20436600-20452600	Weak transcription	Gastric	stomach
4	chr2:20437000-20453000	Weak transcription	Placenta Amnion	Placenta Amnion
5	chr2:20439800-20450200	Weak transcription	Brain Substantia Nigra	brain
6	chr2:20440600-20451000	Weak transcription	Brain Cingulate Gyrus	brain
7	chr2:20440600-20452600	Weak transcription	Brain Hippocampus Middle	brain
8	chr2:20440800-20452200	Weak transcription	Brain Angular Gyrus	brain
9	chr2:20440800-20452600	Weak transcription	Brain Inferior Temporal Lobe	brain
10	chr2:20441400-20453000	Weak transcription	Pancreatic Islets	Pancreatic Islet
11	chr2:20442000-20448800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
12	chr2:20442000-20449600	Weak transcription	Colon Smooth Muscle	Colon
13	chr2:20442000-20450200	Weak transcription	Primary T killer memory cells from peripheral blood	blood
14	chr2:20442000-20450400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
15	chr2:20442000-20450600	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
16	chr2:20442000-20451000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
17	chr2:20442000-20451200	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
18	chr2:20442000-20452600	Weak transcription	Fetal Heart	heart
19	chr2:20442000-20453400	Weak transcription	Pancreas	Pancrea
20	chr2:20442000-20491000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
21	chr2:20442200-20449000	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
22	chr2:20442200-20451400	Weak transcription	K562	blood
23	chr2:20442200-20452600	Weak transcription	Rectal Smooth Muscle	rectum
24	chr2:20442800-20448600	Weak transcription	Primary hematopoietic stem cells	blood
25	chr2:20442800-20455000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
26	chr2:20442800-20474800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
27	chr2:20443000-20449600	Weak transcription	Skeletal Muscle Female	skeletal muscle
28	chr2:20443000-20451400	Weak transcription	HSMMtube	muscle
29	chr2:20443000-20456800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
30	chr2:20443200-20448600	Weak transcription	H1 Cell Line	embryonic stem cell
31	chr2:20443200-20451600	Weak transcription	H9 Cell Line	embryonic stem cell
32	chr2:20444200-20448800	Weak transcription	HepG2	liver
33	chr2:20444200-20449200	Strong transcription	Fetal Muscle Leg	muscle
34	chr2:20444200-20452600	Weak transcription	Brain Anterior Caudate	brain
35	chr2:20444200-20457200	Strong transcription	A549	lung
36	chr2:20444400-20489000	Weak transcription	Stomach Mucosa	stomach
37	chr2:20444600-20452600	Weak transcription	Skeletal Muscle Male	skeletal muscle
38	chr2:20444800-20452800	Weak transcription	Psoas Muscle	Psoas
39	chr2:20445000-20451400	Weak transcription	Small Intestine	intestine
40	chr2:20445200-20452600	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
41	chr2:20445200-20452800	Weak transcription	Ovary	ovary
42	chr2:20445400-20448800	Weak transcription	Fetal Brain Female	brain
43	chr2:20445400-20450400	Strong transcription	Primary T cells from cord blood	blood
44	chr2:20445400-20457000	Strong transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
45	chr2:20445400-20463600	Strong transcription	Fetal Thymus	thymus
46	chr2:20445400-20473800	Strong transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
47	chr2:20445600-20449600	Strong transcription	Fetal Muscle Trunk	muscle
48	chr2:20445600-20453000	Weak transcription	Aorta	Aorta
49	chr2:20445600-20456600	Strong transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr2:20445800-20450200	Weak transcription	Fetal Brain Male	brain

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