Variant report

Variant	nsv1015598
Chromosome Location	chr8:19963102-20088510
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2425)
CpG islands
(count:1769)
Chromatin interactive
region (count:65)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:8)

(count:2425 , 50 per page) page: 1 2 3 4 5 6 7 ... 49

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:19981275-19981566	K562	blood:	n/a	n/a
2	ARID3A	chr8:20059810-20060819	K562	blood:	n/a	n/a
3	ARID3A	chr8:20054624-20055100	HepG2	liver:	n/a	n/a
4	ARID3A	chr8:20055631-20056721	K562	blood:	n/a	chr8:20055919-20055935
5	ARID3A	chr8:20061186-20061777	K562	blood:	n/a	n/a
6	ARID3A	chr8:20044734-20045065	HepG2	liver:	n/a	n/a
7	ARID3A	chr8:20056204-20056496	HepG2	liver:	n/a	n/a
8	ARID3A	chr8:20058298-20059045	K562	blood:	n/a	n/a
9	ATF1	chr8:20035931-20036020	K562	blood:	n/a	n/a
10	ATF1	chr8:20061366-20061787	K562	blood:	n/a	n/a
11	ATF1	chr8:20059957-20060262	K562	blood:	n/a	n/a
12	ATF1	chr8:20058346-20058643	K562	blood:	n/a	n/a
13	ATF1	chr8:19983232-19983316	K562	blood:	n/a	n/a
14	ATF2	chr8:20054225-20054645	H1-hESC	embryonic stem cell:	n/a	n/a
15	ATF2	chr8:20054341-20054882	H1-hESC	embryonic stem cell:	n/a	n/a
16	ATF2	chr8:20054801-20055118	GM12878	blood:	n/a	n/a
17	ATF3	chr8:20054627-20055035	K562	blood:	n/a	n/a
18	ATF3	chr8:20058256-20058689	K562	blood:	n/a	n/a
19	BACH1	chr8:20059880-20060390	K562	blood:	n/a	n/a
20	BACH1	chr8:20054460-20054733	H1-hESC	embryonic stem cell:	n/a	n/a
21	BCL3	chr8:19979782-19980139	A549	lung:	n/a	n/a
22	BHLHE40	chr8:20058312-20058656	K562	blood:	n/a	n/a
23	BHLHE40	chr8:20059978-20060366	K562	blood:	n/a	n/a
24	BHLHE40	chr8:20042395-20042574	K562	blood:	n/a	n/a
25	BHLHE40	chr8:20054492-20055157	HepG2	liver:	n/a	chr8:20054690-20054706
26	BHLHE40	chr8:20081331-20081576	GM12878	blood:	n/a	n/a
27	BHLHE40	chr8:20054506-20055286	GM12878	blood:	n/a	chr8:20054690-20054706
28	BHLHE40	chr8:20056219-20056279	HepG2	liver:	n/a	n/a
29	BHLHE40	chr8:20055820-20056414	K562	blood:	n/a	n/a
30	BHLHE40	chr8:20054436-20054743	A549	lung:	n/a	chr8:20054690-20054706
31	BHLHE40	chr8:20058903-20058905	GM12878	blood:	n/a	n/a
32	BHLHE40	chr8:20046719-20047380	K562	blood:	n/a	n/a
33	BHLHE40	chr8:20054427-20055300	K562	blood:	n/a	chr8:20054690-20054706
34	BRCA1	chr8:20042449-20042569	HepG2	liver:	n/a	n/a
35	BRCA1	chr8:20054438-20055283	Hela-S3	cervix:	n/a	n/a
36	BRCA1	chr8:20054859-20055110	GM12878	blood:	n/a	n/a
37	BRCA1	chr8:20081393-20081558	GM12878	blood:	n/a	n/a
38	BRCA1	chr8:19971444-19971736	Hela-S3	cervix:	n/a	n/a
39	CBX3	chr8:20054367-20055106	K562	blood:	n/a	n/a
40	CCNT2	chr8:20054551-20055408	K562	blood:	n/a	chr8:20055306-20055315
41	CCNT2	chr8:20060069-20060269	K562	blood:	n/a	n/a
42	CEBPB	chr8:20054188-20054198	H1-hESC	embryonic stem cell:	n/a	n/a
43	CEBPB	chr8:20042551-20042803	K562	blood:	n/a	chr8:20042677-20042688
44	CEBPB	chr8:20058295-20058678	HepG2	liver:	n/a	chr8:20058442-20058455 chr8:20058442-20058453 chr8:20058503-20058516 chr8:20058442-20058455 chr8:20058443-20058454 chr8:20058475-20058484 chr8:20058473-20058484 chr8:20058475-20058484 chr8:20058504-20058515 chr8:20058503-20058516
45	CEBPB	chr8:20059795-20060194	K562	blood:	n/a	n/a
46	CEBPB	chr8:20058351-20058604	HepG2	liver:	n/a	chr8:20058442-20058455 chr8:20058442-20058453 chr8:20058503-20058516 chr8:20058442-20058455 chr8:20058443-20058454 chr8:20058475-20058484 chr8:20058473-20058484 chr8:20058475-20058484 chr8:20058504-20058515 chr8:20058503-20058516
47	CEBPB	chr8:19963087-19963684	HCT-116	colon:	n/a	chr8:19963393-19963402 chr8:19963391-19963402 chr8:19963391-19963404 chr8:19963393-19963404
48	CEBPB	chr8:20056257-20056983	K562	blood:	n/a	n/a
49	CEBPB	chr8:19969066-19969683	Hela-S3	cervix:	n/a	chr8:19969493-19969506 chr8:19969494-19969505 chr8:19969067-19969080 chr8:19969493-19969504 chr8:19969067-19969078 chr8:19969493-19969506
50	CEBPB	chr8:20058242-20058721	K562	blood:	n/a	chr8:20058442-20058455 chr8:20058442-20058453 chr8:20058503-20058516 chr8:20058442-20058455 chr8:20058443-20058454 chr8:20058475-20058484 chr8:20058473-20058484 chr8:20058475-20058484 chr8:20058504-20058515 chr8:20058503-20058516

(count:1769 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:20054699-20054749	GM12891	blood:	n/a
2	chr8:20054703-20054753	AoSMC	blood vessel:	n/a
3	chr8:20054583-20054633	CMK	blood:	n/a
4	chr8:20002826-20002876	Jurkat	blood:	n/a
5	chr8:20030779-20030829	NHBE	bronchial:	n/a
6	chr8:20038863-20038913	AG09309	skin:	n/a
7	chr8:20060877-20060927	HPAEpiC	pulmonary alveolar:	n/a
8	chr8:20039283-20039333	U87	brain:	n/a
9	chr8:20054703-20054753	HL-60	blood:	n/a
10	chr8:19980910-19980960	BJ	skin:	n/a
11	chr8:20077936-20077986	Jurkat	blood:	n/a
12	chr8:20040654-20040704	NHBE	bronchial:	n/a
13	chr8:20054583-20054633	AG04449	skin:	fetal
14	chr8:19980910-19980960	AG04450	lung:	fetal
15	chr8:20054583-20054633	ProgFib	skin:	n/a
16	chr8:20032030-20032080	SKMC	muscle:	n/a
17	chr8:20031081-20031131	AG04450	lung:	fetal
18	chr8:20060877-20060927	LNCaP	prostate:	n/a
19	chr8:20054583-20054633	IMR90	lung:	fetal
20	chr8:20030779-20030829	Hela-S3	cervix:	n/a
21	chr8:20054595-20054645	Jurkat	blood:	n/a
22	chr8:20038863-20038913	MCF-7	breast:	n/a
23	chr8:20054372-20054422	NHDF-neo	bronchial:	n/a
24	chr8:20048583-20048633	GM12892	blood:	n/a
25	chr8:20054956-20055006	AG04449	skin:	fetal
26	chr8:19980910-19980960	GM06990	blood:	n/a
27	chr8:20060877-20060927	GM12892	blood:	n/a
28	chr8:20054597-20054647	HRPEpiC	eye:	n/a
29	chr8:20054703-20054753	HepG2	liver:	n/a
30	chr8:19980910-19980960	HepG2	liver:	n/a
31	chr8:20055012-20055062	AoSMC	blood vessel:	n/a
32	chr8:20077936-20077986	MCF-7	breast:	n/a
33	chr8:20039283-20039333	HCM	heart:	n/a
34	chr8:20077936-20077986	HMEC	breast:	n/a
35	chr8:20054595-20054645	ECC-1	luminal epithelium:	n/a
36	chr8:20050922-20050972	U87	brain:	n/a
37	chr8:20039283-20039333	SK-N-SH	brain:	n/a
38	chr8:20060877-20060927	Caco-2	colon:	n/a
39	chr8:20039283-20039333	HCT-116	colon:	n/a
40	chr8:20054956-20055006	HCT-116	colon:	n/a
41	chr8:20077936-20077986	HCM	heart:	n/a
42	chr8:20032030-20032080	RPTEC	kidney:	n/a
43	chr8:20055012-20055062	HCT-116	colon:	n/a
44	chr8:20041700-20041750	Hepatocyte	liver:	n/a
45	chr8:20080666-20080716	H1-hESC	embryonic stem cell:	embryo
46	chr8:20050922-20050972	HAEpiC	amniotic membrane:	n/a
47	chr8:20060877-20060927	U87	brain:	n/a
48	chr8:20002826-20002876	AG09309	skin:	n/a
49	chr8:19980910-19980960	IMR90	lung:	fetal
50	chr8:20041853-20041903	HCPEpiC	choroid plexus:	n/a

(count:65 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:20020373..20021951-chr8:20028843..20031840,2	MCF-7	breast:
2	chr8:19614946..19615490-chr8:19990822..19991486,2	MCF-7	breast:
3	chr8:20007650..20009745-chr8:20016355..20018698,2	K562	blood:
4	chr8:19991226..19991903-chr8:20233790..20234437,2	MCF-7	breast:
5	chr8:20052561..20055139-chr8:20062405..20064613,2	K562	blood:
6	chr8:20044765..20048763-chr8:20050929..20055280,7	K562	blood:
7	chr8:20044880..20047796-chr8:20049875..20054274,6	K562	blood:
8	chr8:20078974..20080125-chr8:20233790..20234379,3	MCF-7	breast:
9	chr8:20080837..20081378-chr8:20230451..20231038,2	K562	blood:
10	chr4:775177..775712-chr8:20054759..20055368,2	NB4	blood:
11	chr8:20059849..20062019-chr8:20071866..20073490,2	K562	blood:
12	chr8:20060132..20061783-chr8:20074410..20076344,2	K562	blood:
13	chr8:20054589..20056207-chr8:20061652..20063617,2	MCF-7	breast:
14	chr8:20072689..20074502-chr8:20076708..20078934,2	MCF-7	breast:
15	chr8:19800611..19802825-chr8:20055037..20057972,2	MCF-7	breast:
16	chr8:19674771..19677183-chr8:19988400..19991254,2	K562	blood:
17	chr8:19956033..19958398-chr8:19960107..19963324,3	K562	blood:
18	chr8:19727405..19728444-chr8:19980912..19981476,3	MCF-7	breast:
19	chr8:20059849..20062019-chr8:20071866..20073490,2	K562	blood:
20	chr8:20080893..20081852-chr8:20089441..20090169,2	MCF-7	breast:
21	chr8:20080921..20082306-chr8:20233354..20234450,5	K562	blood:
22	chr16:85454060..85454897-chr8:20080984..20081769,2	MCF-7	breast:
23	chr8:20074199..20078908-chr8:20079233..20083576,5	K562	blood:
24	chr8:20053671..20056309-chr8:20065573..20068336,2	K562	blood:
25	chr8:20007650..20009376-chr8:20017198..20019566,2	K562	blood:
26	chr8:20080349..20082328-chr8:20233127..20234370,21	MCF-7	breast:
27	chr8:20044880..20047796-chr8:20049875..20054274,6	K562	blood:
28	chr8:20054777..20055411-chr9:130185862..130186755,2	Hela-S3	cervix:
29	chr8:20072689..20074502-chr8:20076708..20078934,2	MCF-7	breast:
30	chr8:20049831..20052925-chr8:20057041..20061103,3	K562	blood:
31	chr8:20047045..20049449-chr8:20055849..20058080,2	K562	blood:
32	chr8:19980514..19983511-chr8:19986584..19989159,2	K562	blood:
33	chr8:20042503..20044673-chr8:20052307..20056909,5	K562	blood:
34	chr8:20036475..20038568-chr8:20054692..20056965,2	MCF-7	breast:
35	chr8:20081034..20081913-chr8:20233476..20234485,8	MCF-7	breast:
36	chr8:19229314..19230191-chr8:19990957..19991686,3	K562	blood:
37	chr8:20084830..20086943-chr8:20087821..20089403,2	K562	blood:
38	chr8:20088116..20090278-chr8:20233803..20235473,2	K562	blood:
39	chr8:20036465..20038513-chr8:20041036..20042586,2	K562	blood:
40	chr8:20088088..20089926-chr8:20233248..20234294,12	MCF-7	breast:
41	chr8:19980514..19983511-chr8:19986584..19989159,2	K562	blood:
42	chr8:20076331..20078897-chr8:20084632..20086626,2	K562	blood:
43	chr8:20061426..20067342-chr8:20067355..20071432,7	K562	blood:
44	chr8:20036475..20038568-chr8:20054692..20056965,2	MCF-7	breast:
45	chr8:20081555..20083194-chr8:20086240..20088366,2	K562	blood:
46	chr8:20042078..20043029-chr8:20233107..20233929,2	K562	blood:
47	chr8:20048134..20052055-chr8:20052801..20055810,5	K562	blood:
48	chr8:19797802..19799354-chr8:19971667..19974269,2	K562	blood:
49	chr8:20084830..20086943-chr8:20087821..20089403,2	K562	blood:
50	chr8:20049402..20051451-chr8:20053132..20055967,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SLC18A1-1	chr8:19970854-19971183	NONHSAT125391
2	lnc-ATP6V1B2-2	chr8:19975146-19975953	ENSG00000253775.1

No data

(count:8 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ATP6V1B2	hsa-miR-16-5p	chr8:20077914-20077922
2	ATP6V1B2	hsa-miR-16-5p	chr8:20078405-20078411
3	ATP6V1B2	hsa-miR-30a-5p	chr8:20078743-20078764
4	ATP6V1B2	hsa-miR-1	chr8:20079062-20079068
5	ATP6V1B2	hsa-miR-30a-5p	chr8:20077017-20077039
6	ATP6V1B2	hsa-miR-30a-5p	chr8:20078788-20078809
7	ATP6V1B2	hsa-miR-16-5p	chr8:20078402-20078408
8	ATP6V1B2	hsa-let-7a-5p	chr8:20076433-20076456

Variant related genes	Relation type
ATP6V1B2	TF binding region
RNU6-892P	TF binding region
SLC18A1	TF binding region
RPL30P9	TF binding region
ATP6V1B2	CpG island
RNU6-892P	CpG island
SLC18A1	CpG island
RPL30P9	CpG island
ENSG00000104613	chromatin interactions
ENSG00000196152	chromatin interactions
ENSG00000147408	chromatin interactions
ENSG00000249592	chromatin interactions
ENSG00000222267	chromatin interactions
ENSG00000036565	chromatin interactions
ENSG00000147416	chromatin interactions

Extended variants
information (count: 6396 )
Associated
traits (count: 120 )

Variant overlapped rSNPs/rCNVs (count:6396 , 50 per page) page: 1 2 3 4 5 6 7 ... 128

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs186731819	chr8:19963141-19963142	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
2	rs150841922	chr8:19963158-19963159	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
3	rs191518275	chr8:19963160-19963161	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
4	rs183781039	chr8:19963185-19963186	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
5	rs377064718	chr8:19963198-19963199	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs140542198	chr8:19963203-19963204	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs538126194	chr8:19963227-19963228	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs556209300	chr8:19963234-19963235	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs574568159	chr8:19963235-19963236	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
10	rs144387552	chr8:19963238-19963239	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
11	rs542209882	chr8:19963241-19963242	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
12	rs147863007	chr8:19963258-19963259	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
13	rs186867431	chr8:19963272-19963273	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
14	rs35300709	chr8:19963349-19963350	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs139759960	chr8:19963369-19963370	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs546029426	chr8:19963381-19963382	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs564694266	chr8:19963408-19963409	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs149947363	chr8:19963435-19963436	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs7840262	chr8:19963473-19963474	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs562218723	chr8:19963484-19963485	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs529560997	chr8:19963499-19963500	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs17092016	chr8:19963512-19963513	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
23	rs559722353	chr8:19963523-19963524	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs527374075	chr8:19963525-19963526	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs552018109	chr8:19963546-19963547	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs570601941	chr8:19963561-19963562	Enhancers Weak transcription Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs537613639	chr8:19963694-19963695	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs549963337	chr8:19963710-19963711	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs77976580	chr8:19963720-19963721	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs190908223	chr8:19963742-19963743	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs183409303	chr8:19963743-19963744	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs556395662	chr8:19963752-19963753	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs144895682	chr8:19963786-19963787	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs572514728	chr8:19963796-19963797	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs201591497	chr8:19963799-19963800	Weak transcription Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs539908072	chr8:19963803-19963804	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
37	rs557998800	chr8:19963836-19963837	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs576503472	chr8:19963854-19963855	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs149026492	chr8:19963939-19963940	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs545793903	chr8:19963944-19963945	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs573951091	chr8:19963961-19963962	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs4922124	chr8:19964028-19964029	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
43	rs559700510	chr8:19964032-19964033	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs186622603	chr8:19964048-19964049	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs552169987	chr8:19964055-19964056	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs563991149	chr8:19964072-19964073	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs370608937	chr8:19964075-19964076	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374421726	chr8:19964127-19964128	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs140688428	chr8:19964158-19964159	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs145784676	chr8:19964183-19964184	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:120)

Disease	PMID	Source
Multiple myeloma	16616336	CNVD
Hepatocellular carcinoma	22174799	CNVD
Heart disease	21282601	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Prostate cancer	16573809	CNVD
T-cell lymphomas	19863542	CNVD
Ovarian cancer	22174824	CNVD
Colorectal cancer	21297112	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Salivary gland tumor	18059337	CNVD
Breast cancer	17133270	CNVD
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Chronic lymphocytic leukemia	18922857	CNVD
Breast cancer	17393978	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Breast cancer	20837533	CNVD
Squamous cell cancer	21044232	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Cancer	22429812	CNVD
Non-small cell lung cancer	21044232	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Colorectal cancer	20709793	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Endometrial cancer	22040021	CNVD
Basal cell lymphoma	21115979	CNVD
Breast cancer	21264507	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Oral cancer	21386901	CNVD
Prostate cancer	21088497	CNVD
Prostate cancer	21965145	CNVD
Breast cancer	20940404	CNVD
Colorectal cancer	19359472	CNVD
Embryonal rhabdomyosarcoma	16790082	CNVD
Gastric cancer	17167181	CNVD
Prostate cancer	16705090	CNVD
8p-syndrome	17576883	CNVD
Colorectal cancer	16272173	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
Lung adenocarcinoma	19525976	CNVD
Lung cancer	19525976	CNVD
Prostate cancer	17245344	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Cancer	16751803	CNVD
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Breast cancer	21785460	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21509527	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Breast cancer	16608533	CNVD
Seminomas	18059402	CNVD
Lung cancer	18438408	CNVD
Medulloblastoma	16783165	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Gastrointestinal stromal cancer	19259404	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Myxofibrosarcoma	16751306	CNVD
Immune disease	21572526	CNVD
Non-small cell lung cancer	21829676	CNVD
Ovarian neoplasms	16753589	CNVD
Kallmann Syndrome 2	22470819	CNVD
Autism	22495311	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Ovarian clear cell carcinoma	21343371	CNVD
Epilepsy	22083797	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Myelofibrosis	22110671	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	17603634	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Bladder cancer	21909424	CNVD
Multiple myeloma	17550852	CNVD
Pancreatic cancer	21811587	CNVD
Multiple myeloma	16461302	CNVD
Developmental delay	21373258	CNVD
Thyroid cancer	19087340	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Breast cancer	21364760	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
Pancreatic endocrine tumor	17639061	CNVD
Cancer	18840272	CNVD
Breast cancer	19602461	CNVD
Osteosarcoma	19286668	CNVD
Prostate cancer	19242612	CNVD
Prostate cancer	19258508	CNVD
small cell lung cancer	20016488	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Gastric adenocarcinoma	19115996	CNVD
Colorectal cancer	19455253	CNVD
Melanoma	20688739	CNVD
Esophageal adenocarcinoma	19417022	CNVD
Prostate cancer	22341455	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD
Chordoma	21215367	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:2468 , 50 per page) page: 1 2 3 4 5 6 7 ... 50

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:19956800-19963400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
2	chr8:19957200-19963200	Weak transcription	Monocytes-CD14+_RO01746	blood
3	chr8:19960400-19964600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
4	chr8:19960800-19963800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
5	chr8:19961800-19963600	Enhancers	Lung	lung
6	chr8:19962000-19963800	Enhancers	Right Atrium	heart
7	chr8:19962200-19963600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
8	chr8:19962200-19965400	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
9	chr8:19962600-19963200	Enhancers	HUES64 Cell Line	embryonic stem cell
10	chr8:19962600-19964000	Enhancers	Cortex derived primary cultured neurospheres	brain
11	chr8:19962600-19964200	Enhancers	NHDF-Ad	bronchial
12	chr8:19962600-19964400	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
13	chr8:19962800-19963200	Enhancers	Muscle Satellite Cultured Cells	--
14	chr8:19962800-19963600	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
15	chr8:19962800-19963600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
16	chr8:19962800-19963600	Enhancers	Aorta	Aorta
17	chr8:19962800-19963600	Enhancers	NHLF	lung
18	chr8:19962800-19963800	Enhancers	Primary monocytes fromperipheralblood	blood
19	chr8:19962800-19963800	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
20	chr8:19962800-19963800	Enhancers	Left Ventricle	heart
21	chr8:19962800-19963800	Enhancers	Right Ventricle	heart
22	chr8:19962800-19963800	Enhancers	NH-A	brain
23	chr8:19962800-19963800	Flanking Active TSS	Osteobl	bone
24	chr8:19962800-19964000	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
25	chr8:19962800-19964200	Enhancers	Hela-S3	cervix
26	chr8:19962800-19964400	Enhancers	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
27	chr8:19962800-19964400	Enhancers	HMEC	breast
28	chr8:19962800-19964600	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
29	chr8:19962800-19964600	Enhancers	Adipose Nuclei	Adipose
30	chr8:19962800-19964600	Enhancers	Rectal Smooth Muscle	rectum
31	chr8:19962800-19964600	Enhancers	Skeletal Muscle Male	skeletal muscle
32	chr8:19963000-19963200	Enhancers	iPS-18 Cell Line	embryonic stem cell
33	chr8:19963000-19963200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:19963000-19963400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
35	chr8:19963000-19963400	Flanking Active TSS	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
36	chr8:19963000-19963400	Enhancers	Breast Myoepithelial Primary Cells	Breast
37	chr8:19963000-19963400	Flanking Active TSS	Colon Smooth Muscle	Colon
38	chr8:19963000-19963600	Weak transcription	Fetal Lung	lung
39	chr8:19963000-19963600	Enhancers	Placenta	Placenta
40	chr8:19963000-19963800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
41	chr8:19963000-19963800	Enhancers	HSMMtube	muscle
42	chr8:19963000-19963800	Enhancers	HUVEC	blood vessel
43	chr8:19963000-19964600	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr8:19963200-19963400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
45	chr8:19963200-19963400	Flanking Active TSS	Muscle Satellite Cultured Cells	--
46	chr8:19963200-19963600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
47	chr8:19963200-19963600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
48	chr8:19963200-19963600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
49	chr8:19963200-19963600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
50	chr8:19963200-19963600	Enhancers	Ovary	ovary

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