Variant report

Variant	nsv891305
Chromosome Location	chr8:112021630-112171822
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:709)
CpG islands
(count:244)
Chromatin interactive
region (count:74)
LncRNA
region (count:14)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:709 , 50 per page) page: 1 2 3 4 5 6 7 ... 15

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:112055951-112056163	K562	blood:	n/a	n/a
2	ATF1	chr8:112055891-112056208	K562	blood:	n/a	n/a
3	ATF1	chr8:112132480-112132510	K562	blood:	n/a	n/a
4	ATF1	chr8:112052514-112052777	K562	blood:	n/a	n/a
5	ATF2	chr8:112162917-112163564	H1-hESC	embryonic stem cell:	n/a	n/a
6	ATF2	chr8:112162891-112163440	H1-hESC	embryonic stem cell:	n/a	n/a
7	BATF	chr8:112113181-112113447	GM12878	blood:	n/a	n/a
8	BCL11A	chr8:112162999-112163239	H1-hESC	embryonic stem cell:	n/a	n/a
9	BCL11A	chr8:112162971-112163355	H1-hESC	embryonic stem cell:	n/a	n/a
10	BCL3	chr8:112032257-112032818	K562	blood:	n/a	n/a
11	BCLAF1	chr8:112050664-112051080	K562	blood:	n/a	n/a
12	BCLAF1	chr8:112051891-112052761	K562	blood:	n/a	n/a
13	BCLAF1	chr8:112047895-112049222	K562	blood:	n/a	n/a
14	BCLAF1	chr8:112049253-112049676	K562	blood:	n/a	n/a
15	BCLAF1	chr8:112045287-112045677	K562	blood:	n/a	n/a
16	BCLAF1	chr8:112051085-112051725	K562	blood:	n/a	n/a
17	BHLHE40	chr8:112113324-112113447	K562	blood:	n/a	n/a
18	BRCA1	chr8:112152605-112152831	H1-hESC	embryonic stem cell:	n/a	n/a
19	CBX3	chr8:112112808-112113129	K562	blood:	n/a	n/a
20	CBX3	chr8:112052302-112052706	K562	blood:	n/a	n/a
21	CCNT2	chr8:112098454-112098654	K562	blood:	n/a	n/a
22	CCNT2	chr8:112035228-112035538	K562	blood:	n/a	n/a
23	CCNT2	chr8:112053174-112053372	K562	blood:	n/a	n/a
24	CEBPB	chr8:112152585-112152901	H1-hESC	embryonic stem cell:	n/a	n/a
25	CEBPB	chr8:112058029-112058214	K562	blood:	n/a	n/a
26	CEBPB	chr8:112057976-112058248	IMR90	lung:	n/a	n/a
27	CEBPB	chr8:112054727-112055059	HepG2	liver:	n/a	n/a
28	CEBPB	chr8:112054718-112055073	A549	lung:	n/a	n/a
29	CEBPB	chr8:112054708-112055042	IMR90	lung:	n/a	n/a
30	CEBPB	chr8:112101778-112102105	H1-hESC	embryonic stem cell:	n/a	chr8:112101947-112101958
31	CEBPB	chr8:112152567-112153096	MCF-7	breast:	n/a	n/a
32	CEBPB	chr8:112072418-112072646	HepG2	liver:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
33	CEBPB	chr8:112054880-112054909	H1-hESC	embryonic stem cell:	n/a	n/a
34	CEBPB	chr8:112149466-112149680	HepG2	liver:	n/a	chr8:112149616-112149627
35	CEBPB	chr8:112044174-112044499	HepG2	liver:	n/a	chr8:112044333-112044344
36	CEBPB	chr8:112054705-112055080	K562	blood:	n/a	n/a
37	CEBPB	chr8:112101875-112101968	K562	blood:	n/a	chr8:112101947-112101958
38	CEBPB	chr8:112044195-112044491	K562	blood:	n/a	chr8:112044333-112044344
39	CEBPB	chr8:112101790-112102112	HepG2	liver:	n/a	chr8:112101947-112101958
40	CEBPB	chr8:112101702-112102116	A549	lung:	n/a	chr8:112101947-112101958
41	CEBPB	chr8:112072478-112072685	IMR90	lung:	n/a	chr8:112072555-112072566 chr8:112072538-112072549
42	CEBPD	chr8:112052444-112052807	K562	blood:	n/a	n/a
43	CEBPD	chr8:112052015-112052671	K562	blood:	n/a	n/a
44	CHD2	chr8:112044601-112045061	K562	blood:	n/a	n/a
45	CHD2	chr8:112033049-112033225	K562	blood:	n/a	n/a
46	CHD2	chr8:112034744-112034944	K562	blood:	n/a	n/a
47	CHD2	chr8:112052288-112052845	K562	blood:	n/a	n/a
48	CHD2	chr8:112032174-112032753	K562	blood:	n/a	n/a
49	CREB1	chr8:112163049-112163325	H1-hESC	embryonic stem cell:	n/a	n/a
50	CREB1	chr8:112162994-112163540	H1-hESC	embryonic stem cell:	n/a	n/a

(count:244 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:112053139-112053189	NHBE	bronchial:	n/a
2	chr8:112052376-112052426	RPTEC	kidney:	n/a
3	chr8:112053356-112053406	NT2-D1	testis:	n/a
4	chr8:112052376-112052426	T-47D	breast:	n/a
5	chr8:112163550-112163600	HCPEpiC	choroid plexus:	n/a
6	chr8:112052376-112052426	GM12891	blood:	n/a
7	chr8:112053356-112053406	HL-60	blood:	n/a
8	chr8:112052376-112052426	HRPEpiC	eye:	n/a
9	chr8:112052376-112052426	GM12878	blood:	n/a
10	chr8:112163550-112163600	HAEpiC	amniotic membrane:	n/a
11	chr8:112052376-112052426	Jurkat	blood:	n/a
12	chr8:112053356-112053406	AG10803	skin:	n/a
13	chr8:112053356-112053406	HNPCEpiC	eye:	n/a
14	chr8:112052376-112052426	AG09319	gingival:	n/a
15	chr8:112163550-112163600	HNPCEpiC	eye:	n/a
16	chr8:112053139-112053189	HCM	heart:	n/a
17	chr8:112053139-112053189	HCPEpiC	choroid plexus:	n/a
18	chr8:112163550-112163600	GM12878	blood:	n/a
19	chr8:112053356-112053406	MCF10A-Er-Src	breast:	n/a
20	chr8:112052376-112052426	K562	blood:	n/a
21	chr8:112053139-112053189	SK-N-SH_RA	brain:	n/a
22	chr8:112053356-112053406	GM12878	blood:	n/a
23	chr8:112163550-112163600	MCF10A-Er-Src	breast:	n/a
24	chr8:112053139-112053189	GM12891	blood:	n/a
25	chr8:112163550-112163600	AG04449	skin:	fetal
26	chr8:112052376-112052426	HepG2	liver:	n/a
27	chr8:112163550-112163600	AG04450	lung:	fetal
28	chr8:112163550-112163600	RPTEC	kidney:	n/a
29	chr8:112053356-112053406	HAEpiC	amniotic membrane:	n/a
30	chr8:112053139-112053189	HCF	heart:	n/a
31	chr8:112053139-112053189	GM12892	blood:	n/a
32	chr8:112053356-112053406	SK-N-SH	brain:	n/a
33	chr8:112053139-112053189	HEEpiC	esophagus:	n/a
34	chr8:112163550-112163600	PrEC	prostate:	n/a
35	chr8:112053356-112053406	HEEpiC	esophagus:	n/a
36	chr8:112053356-112053406	CMK	blood:	n/a
37	chr8:112053139-112053189	HepG2	liver:	n/a
38	chr8:112053356-112053406	SK-N-SH_RA	brain:	n/a
39	chr8:112163550-112163600	GM12891	blood:	n/a
40	chr8:112053139-112053189	BE2_C	brain:	n/a
41	chr8:112163550-112163600	Hepatocyte	liver:	n/a
42	chr8:112163550-112163600	HCF	heart:	n/a
43	chr8:112163550-112163600	AoSMC	blood vessel:	n/a
44	chr8:112163550-112163600	PANC-1	pancreas:	n/a
45	chr8:112053139-112053189	ProgFib	skin:	n/a
46	chr8:112053139-112053189	Hepatocyte	liver:	n/a
47	chr8:112052376-112052426	NHBE	bronchial:	n/a
48	chr8:112052376-112052426	NHDF-neo	bronchial:	n/a
49	chr8:112053356-112053406	K562	blood:	n/a
50	chr8:112163550-112163600	Hela-S3	cervix:	n/a

(count:74 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:112133641..112134299-chr9:13359583..13360482,2	MCF-7	breast:
2	chr8:112142087..112143993-chr8:112151164..112153566,2	MCF-7	breast:
3	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
4	chr8:112047893..112049980-chr8:112071535..112074858,3	K562	blood:
5	chr8:112073611..112075207-chr8:112079150..112081817,2	MCF-7	breast:
6	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
7	chr8:112040792..112044019-chr8:112049363..112052232,3	K562	blood:
8	chr5:173612522..173613033-chr8:112023628..112024312,2	MCF-7	breast:
9	chr8:112115345..112116966-chr8:112124670..112126786,2	MCF-7	breast:
10	chr8:112121761..112124184-chr8:112126207..112129085,2	K562	blood:
11	chr8:112026713..112028384-chr8:112038537..112040451,2	K562	blood:
12	chr8:112051929..112053704-chr8:112063619..112066974,3	K562	blood:
13	chr8:112123114..112125207-chr8:112128541..112131451,2	K562	blood:
14	chr8:112166075..112166697-chr8:112248498..112249074,2	MCF-7	breast:
15	chr8:111877803..111878653-chr8:112126153..112126716,2	MCF-7	breast:
16	chr8:112046473..112049277-chr8:112050883..112054393,4	K562	blood:
17	chr8:112112298..112113981-chr8:112264995..112266040,10	MCF-7	breast:
18	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
19	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
20	chr5:159495628..159496384-chr8:112067763..112068421,2	MCF-7	breast:
21	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
22	chr8:112049920..112051426-chr8:112052995..112055202,2	K562	blood:
23	chr8:112126432..112126980-chr8:112164515..112165028,2	MCF-7	breast:
24	chr8:112164287..112166378-chr8:112180703..112183075,2	MCF-7	breast:
25	chr8:112154689..112157253-chr8:112157958..112160941,2	MCF-7	breast:
26	chr8:112023343..112027872-chr8:112028215..112031579,4	K562	blood:
27	chr8:112127583..112130124-chr8:112133579..112135146,2	MCF-7	breast:
28	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
29	chr8:112049821..112051426-chr8:112052995..112056257,3	K562	blood:
30	chr8:112048936..112050603-chr8:112056318..112058671,2	K562	blood:
31	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
32	chr8:112112573..112113471-chr8:121617637..121618420,2	MCF-7	breast:
33	chr8:112054463..112057447-chr8:112061238..112063289,2	K562	blood:
34	chr8:112123114..112125207-chr8:112128541..112131451,2	K562	blood:
35	chr8:112020517..112022084-chr8:112022778..112025177,2	K562	blood:
36	chr8:112092554..112095223-chr8:112096856..112098486,2	MCF-7	breast:
37	chr8:111905363..111907255-chr8:112045592..112048412,2	K562	blood:
38	chr8:112113576..112114171-chr8:112248201..112249138,2	MCF-7	breast:
39	chr8:112152245..112153161-chr8:112248220..112248923,2	MCF-7	breast:
40	chr8:112050824..112052774-chr8:112058514..112060198,2	K562	blood:
41	chr8:112045873..112047633-chr8:112047967..112049827,3	K562	blood:
42	chr8:112047893..112049980-chr8:112071535..112074858,3	K562	blood:
43	chr8:112052147..112053672-chr8:112062800..112065119,2	K562	blood:
44	chr8:112139232..112142043-chr8:112142133..112144046,2	MCF-7	breast:
45	chr8:112069491..112071465-chr8:112075168..112076781,2	K562	blood:
46	chr8:112024408..112026830-chr8:112028447..112030493,2	K562	blood:
47	chr8:112152279..112153092-chr8:121617588..121618297,2	MCF-7	breast:
48	chr8:112139232..112142043-chr8:112142133..112144046,2	MCF-7	breast:
49	chr8:112020517..112022084-chr8:112022778..112025177,2	K562	blood:
50	chr8:112037306..112039469-chr8:112041170..112043078,2	K562	blood:

(count:14 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-KCNV1-7	chr8:112096343-112096437	l_3667_chr8:112084787-112108928_brain
2	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
3	lnc-KCNV1-7	chr8:112108711-112108928	l_3667_chr8:112084787-112108928_brain
4	lnc-KCNV1-2	chr8:112027133-112027261	ENSG00000253877
5	lnc-KCNV1-2	chr8:112039535-112039752	XLOC_007182
6	lnc-KCNV1-7	chr8:112086929-112087054	l_3667_chr8:112084787-112108928_brain
7	lnc-CSMD3-3	chr8:112111190-112111368	ENSG00000253103
8	lnc-CSMD3-3	chr8:112128764-112128829	ENSG00000253103
9	lnc-CSMD3-3	chr8:112125661-112125749	ENSG00000253103
10	lnc-KCNV1-7	chr8:112084788-112084855	l_3667_chr8:112084787-112108928_brain
11	lnc-KCNV1-2	chr8:112039535-112039662	ENSG00000253877
12	lnc-KCNV1-7	chr8:112086066-112086174	l_3667_chr8:112084787-112108928_brain
13	lnc-KCNV1-2	chr8:112039535-112039641	XLOC_007182
14	lnc-KCNV1-2	chr8:112039535-112039621	ENSG00000253877

No data

Variant related genes	Relation type
ENSG00000253877	TF binding region
ENSG00000253877	CpG island
ENSG00000253103	chromatin interactions
ENSG00000253877	chromatin interactions
TFRC	miRNA target sites

Extended variants
information (count: 2255 )
Associated
traits (count: 99 )

Variant overlapped rSNPs/rCNVs (count:2255 , 50 per page) page: 1 2 3 4 5 6 7 ... 46

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs4493937	chr8:112021630-112021631	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
2	rs13277392	chr8:112021632-112021633	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs13277619	chr8:112021633-112021634	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs544653604	chr8:112021648-112021649	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs532311218	chr8:112021653-112021654	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs77491743	chr8:112021655-112021656	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs564632739	chr8:112021670-112021671	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs141436918	chr8:112021725-112021726	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs6415456	chr8:112021782-112021783	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs560892928	chr8:112021846-112021847	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs529916351	chr8:112021874-112021875	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs546528495	chr8:112021911-112021912	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs373205693	chr8:112021966-112021967	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs565332348	chr8:112021989-112021990	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs560476690	chr8:112022041-112022042	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs528483109	chr8:112022052-112022053	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs145144438	chr8:112022079-112022080	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs372768032	chr8:112022146-112022147	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs571747224	chr8:112022226-112022227	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs537121607	chr8:112022242-112022243	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs189038682	chr8:112022302-112022303	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs377155515	chr8:112022313-112022314	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs567720230	chr8:112022318-112022319	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs536857645	chr8:112022365-112022366	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs12542466	chr8:112022400-112022401	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs535552821	chr8:112022482-112022483	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs538234758	chr8:112022488-112022489	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs567632808	chr8:112022526-112022527	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs192671335	chr8:112022534-112022535	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs543939540	chr8:112022542-112022543	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs577929157	chr8:112022555-112022556	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs138974893	chr8:112022576-112022577	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs574541355	chr8:112022584-112022585	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs367826039	chr8:112022586-112022587	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs371117658	chr8:112022587-112022588	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs184957897	chr8:112022604-112022605	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs532476377	chr8:112022613-112022614	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs536570372	chr8:112022627-112022628	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs565244226	chr8:112022691-112022692	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs530943079	chr8:112022695-112022696	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs376197358	chr8:112022698-112022699	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs550752599	chr8:112022714-112022715	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs556887084	chr8:112022715-112022716	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs567795509	chr8:112022729-112022730	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs555471055	chr8:112022730-112022731	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs536123647	chr8:112022757-112022758	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs369054938	chr8:112022758-112022759	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs386413679	chr8:112022768-112022769	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs370343878	chr8:112022769-112022770	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs76462702	chr8:112022780-112022781	Weak transcription	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:99)

Disease	PMID	Source
Melanoma	18172304	CNVD
Medulloblastoma	21979893	CNVD
Ewing''s sarcoma	21437220	CNVD
Autism	19415332	CNVD
Malaria	21533027	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Esophageal cancer	21851588	CNVD
Gastric cancer	17908304	CNVD
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Pancreatic cancer	21811587	CNVD
Thyroid cancer	19087340	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	21080181	CNVD
Breast cancer	17603634	CNVD
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Acute myeloid leukemia	20729466	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	CNVD
Cancer	20164919	CNVD
abnormal development	18461090	CNVD
Oral cancer	21386901	CNVD
Uveal melanoma	21693616	CNVD
Langer-Giedion syndrome	22283845	CNVD
Cancer	21637783	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Breast cancer	20632083	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Oral cancer	19627613	CNVD
Prostate cancer	21088497	CNVD
colon cancer	17210682	CNVD
Breast cancer	21264507	CNVD
Breast cancer	22028636	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	16751803	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Gastric cancer	17167181	CNVD
Colorectal cancer	19359472	CNVD
Breast cancer	16461572	CNVD
Human rectal carcinomas	16397240	CNVD
Medulloblastoma	16968546	CNVD
head and neck squamous cell carcinoma	18028549	CNVD
Breast cancer	17001317	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
Lung cancer	18438408	CNVD
Breast cancer	16608533	CNVD
Metanephric adenoma	20802469	CNVD
Hepatocellular carcinoma	18803288	CNVD
Prostate cancer	18632612	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	16461572	CNVD
Breast cancer	21399628	CNVD
High-grade prostatic intraepithelial neoplasia	16573809	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	17393978	CNVD
Burkitt''s lymphoma	18698080	CNVD
Non-syndromic sensorineural hearing loss	20606397	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
lymphocytic leukemia	21291569	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Developmental delay	21147756	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Congenital diaphragmatic hernia	21525063	CNVD
Non-small cell lung cancer	19010865	CNVD
small cell lung cancer	20016488	CNVD
Chronic myeloid leukemia	21384125	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Breast cancer	21364760	CNVD
Neuroticism	17667963	CNVD
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Medulloblastoma	21163964	CNVD
Renal cell carcinoma	21215367	CNVD

Chromatin state (count:143 , 50 per page) page: 1 2 3

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:112011600-112035600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
2	chr8:112022600-112024200	Weak transcription	K562	blood
3	chr8:112023200-112039000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
4	chr8:112024200-112025000	Strong transcription	K562	blood
5	chr8:112025000-112047800	Weak transcription	K562	blood
6	chr8:112025200-112025800	Enhancers	Fetal Heart	heart
7	chr8:112030600-112031200	Enhancers	Brain Angular Gyrus	brain
8	chr8:112031200-112035200	Weak transcription	Brain Angular Gyrus	brain
9	chr8:112032200-112032400	Enhancers	Brain Hippocampus Middle	brain
10	chr8:112032400-112032600	Enhancers	Brain Substantia Nigra	brain
11	chr8:112032400-112033200	Weak transcription	Brain Hippocampus Middle	brain
12	chr8:112032400-112033200	Enhancers	Pancreatic Islets	Pancreatic Islet
13	chr8:112033000-112033200	Enhancers	Brain Inferior Temporal Lobe	brain
14	chr8:112033200-112033400	Enhancers	Brain Hippocampus Middle	brain
15	chr8:112033200-112034600	Weak transcription	Pancreatic Islets	Pancreatic Islet
16	chr8:112033200-112034800	Weak transcription	Brain Inferior Temporal Lobe	brain
17	chr8:112033400-112034000	Weak transcription	Brain Hippocampus Middle	brain
18	chr8:112034000-112035000	Enhancers	Brain Hippocampus Middle	brain
19	chr8:112034600-112034800	Enhancers	Brain Substantia Nigra	brain
20	chr8:112034600-112035200	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
21	chr8:112034600-112036000	Enhancers	Fetal Heart	heart
22	chr8:112034600-112036200	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr8:112034800-112035000	Enhancers	Brain Inferior Temporal Lobe	brain
24	chr8:112035000-112037400	Weak transcription	Brain Hippocampus Middle	brain
25	chr8:112035000-112037400	Weak transcription	Brain Inferior Temporal Lobe	brain
26	chr8:112035200-112035600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
27	chr8:112035200-112035800	Active TSS	Brain Angular Gyrus	brain
28	chr8:112035400-112035800	Active TSS	Brain Cingulate Gyrus	brain
29	chr8:112035600-112036000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
30	chr8:112035600-112036000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr8:112035800-112037400	Weak transcription	Brain Angular Gyrus	brain
32	chr8:112035800-112038800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr8:112036000-112037400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
34	chr8:112036000-112037400	Weak transcription	Fetal Heart	heart
35	chr8:112037400-112037800	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
36	chr8:112037400-112037800	Active TSS	Brain Substantia Nigra	brain
37	chr8:112037400-112037800	Enhancers	Fetal Heart	heart
38	chr8:112037400-112038000	Active TSS	Brain Hippocampus Middle	brain
39	chr8:112037400-112040000	Active TSS	Brain Angular Gyrus	brain
40	chr8:112037400-112040000	Active TSS	Brain Inferior Temporal Lobe	brain
41	chr8:112037400-112040400	Active TSS	Brain Anterior Caudate	brain
42	chr8:112037800-112038800	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
43	chr8:112037800-112039000	Weak transcription	Brain Substantia Nigra	brain
44	chr8:112038000-112038800	Weak transcription	Brain Hippocampus Middle	brain
45	chr8:112038800-112039400	Active TSS	Brain Dorsolateral Prefrontal Cortex	brain
46	chr8:112038800-112039800	Active TSS	Brain Cingulate Gyrus	brain
47	chr8:112038800-112040000	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
48	chr8:112038800-112040000	Active TSS	Brain Hippocampus Middle	brain
49	chr8:112039000-112040000	Active TSS	Foreskin Melanocyte Primary Cells skin01	Skin
50	chr8:112039000-112040000	Active TSS	Brain Substantia Nigra	brain

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