Variant report

Variant	nsv830564
Chromosome Location	chr5:179867394-180010096
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2289)
CpG islands
(count:1588)
Chromatin interactive
region (count:171)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:10)

(count:2289 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr5:179982176-179983500	K562	blood:	n/a	n/a
2	ARID3A	chr5:179989773-179990046	K562	blood:	n/a	n/a
3	ARID3A	chr5:179921098-179921441	K562	blood:	n/a	n/a
4	ARID3A	chr5:179980269-179980947	K562	blood:	n/a	n/a
5	ARID3A	chr5:179942463-179942560	HepG2	liver:	n/a	n/a
6	ARID3A	chr5:179921113-179921482	HepG2	liver:	n/a	n/a
7	ARID3A	chr5:179978584-179978636	K562	blood:	n/a	n/a
8	ARID3A	chr5:179975587-179975877	K562	blood:	n/a	n/a
9	ARID3A	chr5:179920256-179920489	HepG2	liver:	n/a	n/a
10	ATF1	chr5:179980451-179980815	K562	blood:	n/a	n/a
11	ATF1	chr5:179982258-179982960	K562	blood:	n/a	n/a
12	ATF2	chr5:179921005-179921489	GM12878	blood:	n/a	n/a
13	ATF2	chr5:179966866-179967742	GM12878	blood:	n/a	n/a
14	ATF2	chr5:179989676-179990117	GM12878	blood:	n/a	n/a
15	ATF2	chr5:179989638-179990187	GM12878	blood:	n/a	n/a
16	BACH1	chr5:179975564-179975823	K562	blood:	n/a	n/a
17	BACH1	chr5:179921849-179922049	H1-hESC	embryonic stem cell:	n/a	n/a
18	BACH1	chr5:179897963-179898282	H1-hESC	embryonic stem cell:	n/a	n/a
19	BACH1	chr5:179928420-179928427	K562	blood:	n/a	n/a
20	BATF	chr5:179989718-179990055	GM12878	blood:	n/a	n/a
21	BATF	chr5:179989665-179990001	GM12878	blood:	n/a	n/a
22	BATF	chr5:179967271-179967670	GM12878	blood:	n/a	chr5:179967376-179967387
23	BATF	chr5:179920672-179920856	GM12878	blood:	n/a	n/a
24	BATF	chr5:179967060-179967643	GM12878	blood:	n/a	chr5:179967376-179967387
25	BCL11A	chr5:179967330-179967536	GM12878	blood:	n/a	n/a
26	BCL11A	chr5:179967329-179967703	GM12878	blood:	n/a	n/a
27	BCL3	chr5:179989720-179990061	GM12878	blood:	n/a	chr5:179989861-179989868
28	BCL3	chr5:179868437-179868959	A549	lung:	n/a	n/a
29	BCL3	chr5:179920888-179921352	A549	lung:	n/a	n/a
30	BCL3	chr5:179896707-179896968	GM12878	blood:	n/a	n/a
31	BCL3	chr5:179894036-179894564	A549	lung:	n/a	chr5:179894213-179894222
32	BCL3	chr5:179954713-179954975	GM12878	blood:	n/a	n/a
33	BCL3	chr5:179920971-179921485	A549	lung:	n/a	chr5:179921385-179921398
34	BCL3	chr5:179954691-179955054	GM12878	blood:	n/a	n/a
35	BCLAF1	chr5:179920923-179921525	GM12878	blood:	n/a	chr5:179921385-179921398
36	BCLAF1	chr5:179967270-179967735	GM12878	blood:	n/a	n/a
37	BHLHE40	chr5:179921026-179921502	GM12878	blood:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
38	BHLHE40	chr5:179991026-179991295	GM12878	blood:	n/a	n/a
39	BHLHE40	chr5:179989676-179990195	GM12878	blood:	n/a	n/a
40	BHLHE40	chr5:179989714-179990142	K562	blood:	n/a	n/a
41	BHLHE40	chr5:179898034-179898300	K562	blood:	n/a	n/a
42	BHLHE40	chr5:179975767-179975857	K562	blood:	n/a	n/a
43	BHLHE40	chr5:179921021-179921760	HepG2	liver:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
44	BHLHE40	chr5:179971806-179971955	K562	blood:	n/a	n/a
45	BHLHE40	chr5:179921070-179921448	A549	lung:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
46	BHLHE40	chr5:179921030-179921507	K562	blood:	n/a	chr5:179921201-179921217 chr5:179921352-179921368
47	BHLHE40	chr5:179982128-179982802	K562	blood:	n/a	n/a
48	BHLHE40	chr5:179975467-179975475	K562	blood:	n/a	n/a
49	BHLHE40	chr5:179967103-179967608	GM12878	blood:	n/a	n/a
50	BHLHE40	chr5:179891686-179891866	HepG2	liver:	n/a	n/a

(count:1588 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr5:179886241-179886291	U87	brain:	n/a
2	chr5:179918462-179918512	ovcar-3	ovarian:	n/a
3	chr5:179886241-179886291	U87	brain:	n/a
4	chr5:179918462-179918512	ovcar-3	ovarian:	n/a
5	chr5:179921655-179921705	ECC-1	luminal epithelium:	n/a
6	chr5:179922147-179922197	AoSMC	blood vessel:	n/a
7	chr5:179920202-179920252	NH-A	brain:	n/a
8	chr5:179921670-179921720	NT2-D1	testis:	n/a
9	chr5:179886642-179886692	AG09309	skin:	n/a
10	chr5:179921704-179921754	SK-N-SH	brain:	n/a
11	chr5:179924999-179925049	AG09309	skin:	n/a
12	chr5:179950726-179950776	AG10803	skin:	n/a
13	chr5:179961652-179961702	PrEC	prostate:	n/a
14	chr5:179943471-179943521	AG10803	skin:	n/a
15	chr5:179921349-179921399	HPAEpiC	pulmonary alveolar:	n/a
16	chr5:179924999-179925049	Caco-2	colon:	n/a
17	chr5:179921426-179921476	GM12892	blood:	n/a
18	chr5:179961903-179961953	PrEC	prostate:	n/a
19	chr5:179922147-179922197	HCF	heart:	n/a
20	chr5:179886642-179886692	PFSK-1	brain:	n/a
21	chr5:179921286-179921336	NT2-D1	testis:	n/a
22	chr5:179958313-179958363	NT2-D1	testis:	n/a
23	chr5:179961903-179961953	HepG2	liver:	n/a
24	chr5:179868587-179868637	NHDF-neo	bronchial:	n/a
25	chr5:179958313-179958363	ECC-1	luminal epithelium:	n/a
26	chr5:179921670-179921720	T-47D	breast:	n/a
27	chr5:179921349-179921399	Hepatocyte	liver:	n/a
28	chr5:179922339-179922389	HCM	heart:	n/a
29	chr5:179922339-179922389	MCF10A-Er-Src	breast:	n/a
30	chr5:179958313-179958363	PrEC	prostate:	n/a
31	chr5:179962105-179962155	AG09309	skin:	n/a
32	chr5:179920971-179921021	HEEpiC	esophagus:	n/a
33	chr5:179886241-179886291	HAEpiC	amniotic membrane:	n/a
34	chr5:179961903-179961953	Hela-S3	cervix:	n/a
35	chr5:179921704-179921754	MCF-7	breast:	n/a
36	chr5:179961652-179961702	HNPCEpiC	eye:	n/a
37	chr5:179921426-179921476	AG09319	gingival:	n/a
38	chr5:179886642-179886692	LNCaP	prostate:	n/a
39	chr5:179921349-179921399	HCM	heart:	n/a
40	chr5:179920582-179920632	SK-N-SH_RA	brain:	n/a
41	chr5:179958483-179958533	MCF10A-Er-Src	breast:	n/a
42	chr5:179961903-179961953	HEEpiC	esophagus:	n/a
43	chr5:179922147-179922197	SAEC	small airway:	n/a
44	chr5:179920202-179920252	BE2_C	brain:	n/a
45	chr5:179958313-179958363	IMR90	lung:	fetal
46	chr5:179868587-179868637	GM12892	blood:	n/a
47	chr5:179886642-179886692	BE2_C	brain:	n/a
48	chr5:179920971-179921021	AG04449	skin:	fetal
49	chr5:179921426-179921476	HCF	heart:	n/a
50	chr5:179922147-179922197	GM12878	blood:	n/a

(count:171 , 50 per page) page: 1 2 3 4

No.	Distal block	Cell Line	Cell type
1	chr5:179922992..179929395-chr5:179931202..179936163,8	K562	blood:
2	chr5:179992805..179995123-chr5:179996913..179999172,2	K562	blood:
3	chr5:179943961..179945573-chr5:179952586..179955313,2	MCF-7	breast:
4	chr5:179975334..179978058-chr5:179994170..179996114,2	MCF-7	breast:
5	chr5:179949366..179951227-chr5:180284274..180286708,2	K562	blood:
6	chr5:179926836..179929553-chr5:179936130..179939014,2	MCF-7	breast:
7	chr5:179887683..179889324-chr5:179889418..179891911,2	K562	blood:
8	chr5:179991328..179993518-chr5:179994470..179996881,2	K562	blood:
9	chr5:179935454..179937135-chr5:179951603..179954291,2	MCF-7	breast:
10	chr5:179892192..179893698-chr5:179898781..179900873,2	MCF-7	breast:
11	chr5:179986356..179988734-chr5:179996759..179998539,2	K562	blood:
12	chr5:179899433..179901543-chr5:179921321..179923446,2	MCF-7	breast:
13	chr5:179882912..179885325-chr5:179894280..179896586,2	MCF-7	breast:
14	chr5:179933515..179935509-chr5:179936709..179938826,2	K562	blood:
15	chr5:179987845..179991399-chr5:179992538..179995326,4	K562	blood:
16	chr5:179744163..179746642-chr5:179892937..179895669,2	MCF-7	breast:
17	chr5:179738783..179741691-chr5:179897243..179899588,2	MCF-7	breast:
18	chr3:158973363..158973863-chr5:179971569..179972230,2	MCF-7	breast:
19	chr5:179923677..179925323-chr5:179932980..179935315,2	MCF-7	breast:
20	chr5:179982448..179984121-chr5:179987078..179988868,3	K562	blood:
21	chr5:179720197..179721174-chr5:179911166..179912161,9	MCF-7	breast:
22	chr5:179769448..179771276-chr5:179896602..179898870,2	MCF-7	breast:
23	chr5:179918146..179918859-chr5:180033017..180033559,2	MCF-7	breast:
24	chr5:179754405..179760149-chr5:179891592..179897254,9	MCF-7	breast:
25	chr5:179720435..179721221-chr5:179897609..179898164,2	MCF-7	breast:
26	chr5:179910027..179911879-chr5:179947833..179949549,2	MCF-7	breast:
27	chr5:179739299..179743379-chr5:179893176..179898905,6	MCF-7	breast:
28	chr5:179756438..179759576-chr5:179909239..179913349,3	MCF-7	breast:
29	chr5:179985555..179987224-chr5:179991936..179994332,2	MCF-7	breast:
30	chr5:179909233..179911875-chr5:179913971..179916434,2	MCF-7	breast:
31	chr5:179982621..179985082-chr5:179986194..179988848,3	K562	blood:
32	chr5:179805841..179808763-chr5:179880689..179883410,2	MCF-7	breast:
33	chr5:179911143..179913074-chr5:179916683..179919096,2	K562	blood:
34	chr5:179925134..179926691-chr5:179928454..179930583,2	K562	blood:
35	chr5:179897206..179899731-chr5:179901883..179904757,4	K562	blood:
36	chr5:179880821..179884780-chr5:179891609..179894265,3	MCF-7	breast:
37	chr5:179890341..179892861-chr5:179894283..179898100,3	MCF-7	breast:
38	chr5:179720972..179723069-chr5:179918796..179921248,2	MCF-7	breast:
39	chr5:179906997..179909596-chr5:179910031..179912628,2	MCF-7	breast:
40	chr5:179913461..179915433-chr5:179919891..179923348,3	MCF-7	breast:
41	chr5:179922992..179929395-chr5:179931202..179936163,8	K562	blood:
42	chr5:179925282..179927939-chr5:180022784..180024577,2	K562	blood:
43	chr12:120730813..120731447-chr5:179921399..179922129,2	Hela-S3	cervix:
44	chr5:179951729..179953788-chr5:179957919..179959696,2	MCF-7	breast:
45	chr5:179954302..179955834-chr5:179973302..179975583,2	K562	blood:
46	chr5:179901308..179903297-chr5:179907478..179910169,2	MCF-7	breast:
47	chr5:179911143..179913074-chr5:179916683..179919096,2	K562	blood:
48	chr5:179909233..179911875-chr5:179913971..179916434,2	MCF-7	breast:
49	chr5:179924830..179925800-chr7:65958004..65958762,2	NB4	blood:
50	chr5:179933515..179935509-chr5:179936709..179938826,2	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CNOT6-1	chr5:179894886-179895269	XLOC_004680
2	lnc-CNOT6-1	chr5:179910115-179910503	XLOC_004680
3	lnc-CNOT6-6	chr5:180007444-180008867	NONHSAT105687
4	lnc-CNOT6-2	chr5:179868559-179868855	XLOC_004679
5	lnc-CNOT6-2	chr5:179869730-179870238	XLOC_004679

No data

(count:10 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	CNOT6	hsa-miR-130b-3p	chr5:180004720-180004742
2	CNOT6	hsa-miR-106b-5p	chr5:180004230-180004250
3	CNOT6	hsa-miR-130b-3p	chr5:180004226-180004248
4	CNOT6	hsa-miR-183-5p	chr5:180002633-180002657
5	CNOT6	hsa-miR-19b-3p	chr5:180001801-180001822
6	CNOT6	hsa-miR-19b-3p	chr5:180001405-180001426
7	CNOT6	hsa-miR-130b-3p	chr5:180001800-180001823
8	CNOT6	hsa-miR-373-3p	chr5:180004266-180004289
9	CNOT6	hsa-miR-193b-3p	chr5:180001543-180001563
10	CNOT6	hsa-miR-373-3p	chr5:180004227-180004249

Variant related genes	Relation type
CNOT6	TF binding region
ENSG00000250749	TF binding region
RNU6-525P	TF binding region
ENSG00000250509	TF binding region
ENSG00000263759	TF binding region
CNOT6	CpG island
ENSG00000250749	CpG island
RNU6-525P	CpG island
ENSG00000250509	CpG island
ENSG00000263759	CpG island
ENSG00000161055	chromatin interactions
ENSG00000248367	chromatin interactions
ENSG00000128829	chromatin interactions
ENSG00000100084	chromatin interactions
ENSG00000223473	chromatin interactions
ENSG00000037280	chromatin interactions
ENSG00000113300	chromatin interactions
ENSG00000250509	chromatin interactions
ENSG00000242259	chromatin interactions
ENSG00000042753	chromatin interactions
ENSG00000200795	chromatin interactions
ENSG00000237310	chromatin interactions
ENSG00000050748	chromatin interactions
ENSG00000185065	chromatin interactions
ENSG00000263759	chromatin interactions
ENSG00000131459	chromatin interactions
ATXN7	miRNA target sites
ATXN1L	miRNA target sites

Extended variants
information (count: 5591 )
Associated
traits (count: 104 )

Variant overlapped rSNPs/rCNVs (count:5591 , 50 per page) page: 1 2 3 4 5 6 7 ... 112

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs538125809	chr5:179867455-179867456	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
2	rs548895587	chr5:179867458-179867459	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
3	rs532235658	chr5:179867474-179867475	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
4	rs552325279	chr5:179867498-179867499	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
5	rs537517822	chr5:179867500-179867501	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
6	rs181429454	chr5:179867502-179867503	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
7	rs112920119	chr5:179867517-179867518	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
8	rs76142578	chr5:179867530-179867531	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
9	rs60507193	chr5:179867535-179867536	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
10	rs552706690	chr5:179867537-179867538	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
11	rs572966603	chr5:179867569-179867570	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
12	rs185515256	chr5:179867577-179867578	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
13	rs558764927	chr5:179867588-179867589	Enhancers Bivalent Enhancer Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
14	rs575546680	chr5:179867609-179867610	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
15	rs544091433	chr5:179867615-179867616	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
16	rs561208783	chr5:179867621-179867622	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
17	rs574647513	chr5:179867644-179867645	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
18	rs191250863	chr5:179867662-179867663	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
19	rs370636349	chr5:179867724-179867725	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
20	rs147878437	chr5:179867752-179867753	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
21	rs181078548	chr5:179867761-179867762	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
22	rs532466089	chr5:179867797-179867798	Enhancers Weak transcription Bivalent Enhancer	TF binding region	2 gene(s)	Overlapped CNVs	n/a
23	rs12517962	chr5:179867841-179867842	Enhancers Weak transcription	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
24	rs562725404	chr5:179867855-179867856	Enhancers Weak transcription	TF binding region	2 gene(s)	Overlapped CNVs	n/a
25	rs368230119	chr5:179867882-179867883	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs139858923	chr5:179867883-179867884	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs548517095	chr5:179867885-179867886	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs372868919	chr5:179868001-179868002	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
29	rs533982018	chr5:179868031-179868032	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
30	rs2387192	chr5:179868040-179868041	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
31	rs534267840	chr5:179868069-179868070	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
32	rs145694129	chr5:179868171-179868172	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
33	rs566504262	chr5:179868183-179868184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
34	rs570812786	chr5:179868231-179868232	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
35	rs7730474	chr5:179868253-179868254	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
36	rs192073703	chr5:179868259-179868260	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs4498226	chr5:179868288-179868289	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs1848479	chr5:179868339-179868340	Weak transcription Enhancers	TF binding region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs575534796	chr5:179868354-179868355	Weak transcription Enhancers	TF binding region	2 gene(s)	Overlapped CNVs	n/a
40	rs55762317	chr5:179868403-179868404	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
41	rs574665791	chr5:179868408-179868409	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
42	rs375733157	chr5:179868420-179868421	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
43	rs5873696	chr5:179868460-179868461	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
44	rs201142118	chr5:179868466-179868467	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
45	rs373850847	chr5:179868467-179868468	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
46	rs78170033	chr5:179868468-179868469	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
47	rs372801980	chr5:179868469-179868470	Enhancers Weak transcription Flanking Active TSS	TF binding region	2 gene(s)	Overlapped CNVs	n/a
48	rs569491998	chr5:179868564-179868565	Enhancers Weak transcription Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a
49	rs563936694	chr5:179868611-179868612	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region CpG island lncRNA	1 gene(s)	Overlapped CNVs	n/a
50	rs149831392	chr5:179868661-179868662	Enhancers Weak transcription Bivalent/Poised TSS Bivalent Enhancer Flanking Active TSS	TF binding region lncRNA	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:104)

Disease	PMID	Source
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Medulloblastoma	21979893	CNVD
Phyllodes tumor	17334353	CNVD
Malaria	21533027	CNVD
Renal cell carcinoma	19461508	CNVD
Cancer	20164919	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	16751803	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Glioma	20126413	CNVD
Cancer	22429812	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Liposarcoma	21253554	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	17387387	CNVD
Leukemia	17361228	CNVD
Myelodysplastic syndrome	18508791	CNVD
5q-syndrome	17576883	CNVD
Gastric cancer	17908304	CNVD
Lung cancer	16740712	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Urothelial carcinoma	21177765	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Barrett''s syndrome	19417022	CNVD
Thyroid cancer	19087340	CNVD
Acute myeloid leukemia	20729466	CNVD
lymphocytic leukemia	21291569	CNVD
Multiple myeloma	17550852	CNVD
Salivary gland tumor	18059337	CNVD
Renal cell carcinoma	19377443	CNVD
Lung cancer	18438408	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Renal cell carcinoma	18592004	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Prostate cancer	18632612	CNVD
epilepsy	18472482	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Sotos syndrome	21572526	CNVD
T-cell acute lymphoblastic leukemia	20065082	CNVD
Sotos syndrome	17561922	CNVD
Sotos syndrome	16773131	CNVD
Mental retardation	16773131	CNVD
Sotos syndrome	22470819	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Acute myeloid leukemia	18000384	CNVD
Sudden cardiac death	19188705	CNVD
Basal cell lymphoma	16317097	CNVD
Chordoma	18071362	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Olfactory neuroblastoma	18408657	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
abnormal development	18461090	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Lung cancer	17297452	CNVD
Cancer	20164920	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21804112	CNVD
Myelofibrosis	22110671	CNVD
Sotos syndrome	22283845	CNVD
Breast cancer	16272173	CNVD
Sotos syndrome	20503325	CNVD
Lung adenocarcinoma	17086460	CNVD
Congenital Hypertrichosis Syndrome	21636067	CNVD
T-cell acute lymphoblastic leukemia	19406988	CNVD
Breast cancer	19181860	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ehlers-danlos syndrome	17576883	CNVD
Lung cancer	17086460	CNVD
Autism	19246517	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Autism	22543975	CNVD
small cell lung cancer	20016488	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD
Melanoma	20877625	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:3254 , 50 per page) page: 1 2 3 4 5 6 7 ... 66

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr5:179866000-179869800	Enhancers	Placenta	Placenta
2	chr5:179866200-179867400	Enhancers	Pancreas	Pancrea
3	chr5:179866400-179868400	Enhancers	Hela-S3	cervix
4	chr5:179867200-179867400	Enhancers	iPS-15b Cell Line	embryonic stem cell
5	chr5:179867200-179867400	Flanking Bivalent TSS/Enh	NHEK	skin
6	chr5:179867200-179867600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr5:179867200-179867600	Enhancers	Esophagus	oesophagus
8	chr5:179867200-179867600	Enhancers	Spleen	Spleen
9	chr5:179867200-179867600	Enhancers	Monocytes-CD14+_RO01746	blood
10	chr5:179867200-179867800	Enhancers	iPS-18 Cell Line	embryonic stem cell
11	chr5:179867200-179868600	Enhancers	A549	lung
12	chr5:179867400-179867600	Bivalent Enhancer	H1 Derived Mesenchymal Stem Cells	ES cell derived
13	chr5:179867400-179867600	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
14	chr5:179867400-179867600	Bivalent Enhancer	Foreskin Melanocyte Primary Cells skin03	Skin
15	chr5:179867400-179867600	Bivalent Enhancer	Fetal Adrenal Gland	Adrenal Gland
16	chr5:179867400-179867600	Bivalent Enhancer	NHEK	skin
17	chr5:179867400-179867800	Bivalent Enhancer	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
18	chr5:179867400-179867800	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr5:179867400-179867800	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin02	Skin
20	chr5:179867400-179868000	Enhancers	H1 Cell Line	embryonic stem cell
21	chr5:179867400-179868000	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
22	chr5:179867400-179868400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
23	chr5:179867400-179868800	Weak transcription	Pancreas	Pancrea
24	chr5:179867600-179867800	Bivalent Enhancer	Primary hematopoietic stem cells G-CSF-mobilized Male	--
25	chr5:179867600-179868800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
26	chr5:179867600-179868800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
27	chr5:179867600-179869000	Enhancers	HepG2	liver
28	chr5:179868000-179868400	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr5:179868400-179868800	Enhancers	iPS-15b Cell Line	embryonic stem cell
30	chr5:179868400-179869200	Enhancers	H1 Cell Line	embryonic stem cell
31	chr5:179868400-179869200	Flanking Active TSS	Hela-S3	cervix
32	chr5:179868600-179869000	Bivalent/Poised TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
33	chr5:179868600-179869000	Flanking Active TSS	A549	lung
34	chr5:179868600-179869200	Bivalent Enhancer	Foreskin Keratinocyte Primary Cells skin03	Skin
35	chr5:179868800-179869000	ZNF genes & repeats	H1 Derived Mesenchymal Stem Cells	ES cell derived
36	chr5:179868800-179869000	Bivalent Enhancer	Fetal Muscle Trunk	muscle
37	chr5:179868800-179869000	Enhancers	Pancreas	Pancrea
38	chr5:179868800-179869200	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
39	chr5:179869000-179869200	Active TSS	A549	lung
40	chr5:179869000-179869200	Bivalent/Poised TSS	NHEK	skin
41	chr5:179869200-179869400	Enhancers	Hela-S3	cervix
42	chr5:179880800-179882400	Enhancers	Brain Germinal Matrix	brain
43	chr5:179881400-179881800	Enhancers	Fetal Brain Male	brain
44	chr5:179883400-179884200	Enhancers	GM12878-XiMat	blood
45	chr5:179883400-179884200	Enhancers	HepG2	liver
46	chr5:179885200-179885400	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
47	chr5:179885200-179886000	Enhancers	Lung	lung
48	chr5:179885200-179895800	Weak transcription	Right Atrium	heart
49	chr5:179885800-179886800	ZNF genes & repeats	iPS DF 19.11 Cell Line	embryonic stem cell
50	chr5:179886000-179886600	ZNF genes & repeats	H1 Cell Line	embryonic stem cell

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