Variant report

Variant	nsv1018106
Chromosome Location	chr8:130697368-130708333
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:579)
CpG islands
(count:61)
Chromatin interactive
region (count:36)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:579 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:130701435-130702061	K562	blood:	n/a	n/a
2	ARID3A	chr8:130704430-130705462	K562	blood:	n/a	n/a
3	ARID3A	chr8:130697568-130697735	K562	blood:	n/a	n/a
4	ARID3A	chr8:130699624-130700115	K562	blood:	n/a	n/a
5	ATF1	chr8:130701480-130702076	K562	blood:	n/a	n/a
6	ATF1	chr8:130704507-130705519	K562	blood:	n/a	n/a
7	ATF1	chr8:130703204-130703642	K562	blood:	n/a	n/a
8	ATF3	chr8:130697689-130698388	A549	lung:	n/a	n/a
9	ATF3	chr8:130704495-130704908	K562	blood:	n/a	chr8:130704730-130704745 chr8:130704731-130704744
10	BACH1	chr8:130704245-130704377	K562	blood:	n/a	n/a
11	BACH1	chr8:130705205-130705279	K562	blood:	n/a	n/a
12	BHLHE40	chr8:130701543-130702287	K562	blood:	n/a	chr8:130702154-130702175
13	BHLHE40	chr8:130703163-130703576	K562	blood:	n/a	n/a
14	BHLHE40	chr8:130697965-130698035	K562	blood:	n/a	n/a
15	BHLHE40	chr8:130704462-130705619	K562	blood:	n/a	chr8:130705473-130705489
16	BHLHE40	chr8:130702575-130702640	K562	blood:	n/a	n/a
17	BHLHE40	chr8:130699755-130700290	K562	blood:	n/a	n/a
18	CBX3	chr8:130704087-130705480	K562	blood:	n/a	n/a
19	CBX3	chr8:130699588-130700068	K562	blood:	n/a	n/a
20	CBX3	chr8:130703142-130703662	K562	blood:	n/a	n/a
21	CBX3	chr8:130701308-130702021	K562	blood:	n/a	n/a
22	CCNT2	chr8:130704626-130705637	K562	blood:	n/a	n/a
23	CCNT2	chr8:130701341-130702241	K562	blood:	n/a	n/a
24	CCNT2	chr8:130703227-130703528	K562	blood:	n/a	n/a
25	CEBPB	chr8:130704946-130705458	K562	blood:	n/a	n/a
26	CEBPB	chr8:130701673-130701842	K562	blood:	n/a	chr8:130701754-130701767
27	CEBPB	chr8:130697562-130698428	A549	lung:	n/a	n/a
28	CEBPB	chr8:130704504-130705515	K562	blood:	n/a	n/a
29	CEBPB	chr8:130701571-130701958	K562	blood:	n/a	chr8:130701754-130701767
30	CEBPB	chr8:130704160-130704207	K562	blood:	n/a	n/a
31	CEBPD	chr8:130704412-130705488	K562	blood:	n/a	n/a
32	CEBPD	chr8:130704460-130705785	K562	blood:	n/a	n/a
33	CHD2	chr8:130704398-130705362	K562	blood:	n/a	n/a
34	CHD2	chr8:130699902-130699943	K562	blood:	n/a	n/a
35	CREB1	chr8:130702733-130703747	K562	blood:	n/a	n/a
36	CREB1	chr8:130703092-130703607	K562	blood:	n/a	n/a
37	CTCF	chr8:130699568-130700058	HCT-116	colon:	n/a	chr8:130699821-130699839
38	CTCF	chr8:130699740-130699890	HA-sp	spinal cord:	n/a	chr8:130699821-130699839
39	CTCF	chr8:130699735-130699976	GM12892	blood:	n/a	chr8:130699821-130699839
40	CTCF	chr8:130706960-130707110	GM12875	blood:	n/a	n/a
41	CTCF	chr8:130699720-130699870	GM12871	blood:	n/a	chr8:130699821-130699839
42	CTCF	chr8:130699752-130699964	H1-hESC	embryonic stem cell:	n/a	chr8:130699821-130699839
43	CTCF	chr8:130699840-130699990	GM12868	blood:	n/a	n/a
44	CTCF	chr8:130699720-130699870	HUVEC	blood vessel:	n/a	chr8:130699821-130699839
45	CTCF	chr8:130699760-130699910	HCPEpiC	choroid plexus:	n/a	chr8:130699821-130699839
46	CTCF	chr8:130699586-130699926	A549	lung:	n/a	chr8:130699821-130699839
47	CTCF	chr8:130699940-130700090	HEEpiC	esophagus:	n/a	n/a
48	CTCF	chr8:130699758-130699915	GM10248	blood:	n/a	chr8:130699821-130699839
49	CTCF	chr8:130699740-130699890	HPF	lung:	n/a	chr8:130699821-130699839
50	CTCF	chr8:130699622-130700369	K562	blood:	n/a	chr8:130699821-130699839

(count:61 , 50 per page) page: 1 2

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:130698161-130698211	RPTEC	kidney:	n/a
2	chr8:130698161-130698211	PrEC	prostate:	n/a
3	chr8:130698161-130698211	NHBE	bronchial:	n/a
4	chr8:130698161-130698211	GM06990	blood:	n/a
5	chr8:130698161-130698211	LNCaP	prostate:	n/a
6	chr8:130698161-130698211	AG04449	skin:	fetal
7	chr8:130698161-130698211	SK-N-MC	brain:	n/a
8	chr8:130698161-130698211	U87	brain:	n/a
9	chr8:130698161-130698211	BJ	skin:	n/a
10	chr8:130698161-130698211	GM12891	blood:	n/a
11	chr8:130698161-130698211	SK-N-SH	brain:	n/a
12	chr8:130698161-130698211	HRPEpiC	eye:	n/a
13	chr8:130698161-130698211	BE2_C	brain:	n/a
14	chr8:130698161-130698211	ECC-1	luminal epithelium:	n/a
15	chr8:130698161-130698211	HRCEpiC	kidney:	n/a
16	chr8:130698161-130698211	HNPCEpiC	eye:	n/a
17	chr8:130698161-130698211	AoSMC	blood vessel:	n/a
18	chr8:130698161-130698211	HEEpiC	esophagus:	n/a
19	chr8:130698161-130698211	ovcar-3	ovarian:	n/a
20	chr8:130698161-130698211	HAEpiC	amniotic membrane:	n/a
21	chr8:130698161-130698211	Hela-S3	cervix:	n/a
22	chr8:130698161-130698211	NB4	blood:	n/a
23	chr8:130698161-130698211	A549	lung:	n/a
24	chr8:130698161-130698211	SK-N-SH_RA	brain:	n/a
25	chr8:130698161-130698211	ProgFib	skin:	n/a
26	chr8:130698161-130698211	CMK	blood:	n/a
27	chr8:130698161-130698211	HCF	heart:	n/a
28	chr8:130698161-130698211	GM12892	blood:	n/a
29	chr8:130698161-130698211	MCF-7	breast:	n/a
30	chr8:130698161-130698211	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:130698161-130698211	AG09309	skin:	n/a
32	chr8:130698161-130698211	K562	blood:	n/a
33	chr8:130698161-130698211	HIPEpiC	eye:	n/a
34	chr8:130698161-130698211	Caco-2	colon:	n/a
35	chr8:130698161-130698211	HRE	kidney:	n/a
36	chr8:130698161-130698211	GM19239	blood:	n/a
37	chr8:130698161-130698211	SKMC	muscle:	n/a
38	chr8:130698161-130698211	NT2-D1	testis:	n/a
39	chr8:130698161-130698211	GM12878	blood:	n/a
40	chr8:130698161-130698211	H1-hESC	embryonic stem cell:	embryo
41	chr8:130698161-130698211	AG04450	lung:	fetal
42	chr8:130698161-130698211	NH-A	brain:	n/a
43	chr8:130698161-130698211	HCPEpiC	choroid plexus:	n/a
44	chr8:130698161-130698211	PFSK-1	brain:	n/a
45	chr8:130698161-130698211	HMEC	breast:	n/a
46	chr8:130698161-130698211	HCM	heart:	n/a
47	chr8:130698161-130698211	MCF10A-Er-Src	breast:	n/a
48	chr8:130698161-130698211	PANC-1	pancreas:	n/a
49	chr8:130698161-130698211	HEK293	kidney:	embryo
50	chr8:130698161-130698211	IMR90	lung:	fetal

(count:36 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:130698168..130701867-chr8:130706682..130711085,4	MCF-7	breast:
2	chr8:128745097..128750653-chr8:130701645..130707585,8	K562	blood:
3	chr8:130692959..130695780-chr8:130701945..130704433,2	K562	blood:
4	chr8:128747070..128748818-chr8:130703822..130705821,2	K562	blood:
5	chr8:128746816..128749956-chr8:130699107..130701261,3	K562	blood:
6	chr8:130696204..130698352-chr8:130701733..130703322,2	K562	blood:
7	chr8:130699308..130701478-chr8:130717660..130720655,2	K562	blood:
8	chr8:130595589..130597194-chr8:130700231..130702653,2	K562	blood:
9	chr8:128746735..128749301-chr8:130699107..130701549,4	K562	blood:
10	chr8:130707905..130710506-chr8:130721790..130724532,3	K562	blood:
11	chr8:130699958..130701746-chr8:130701931..130704723,3	K562	blood:
12	chr8:130696204..130698352-chr8:130701733..130703322,2	K562	blood:
13	chr8:130700584..130702961-chr8:130710020..130711748,2	MCF-7	breast:
14	chr8:130699541..130700041-chr8:130738268..130738843,2	K562	blood:
15	chr8:130693991..130694498-chr8:130705234..130705963,2	K562	blood:
16	chr8:130700888..130706431-chr8:130718980..130724092,7	K562	blood:
17	chr8:130585350..130587697-chr8:130704130..130706568,2	K562	blood:
18	chr8:130689876..130691516-chr8:130698060..130699622,2	K562	blood:
19	chr8:128806162..128808310-chr8:130696628..130698534,2	MCF-7	breast:
20	chr8:130703853..130706502-chr8:130708490..130712451,4	K562	blood:
21	chr15:70582586..70584161-chr8:130701217..130702945,2	MCF-7	breast:
22	chr8:128752824..128755254-chr8:130703895..130705985,2	K562	blood:
23	chr8:128749024..128750653-chr8:130701645..130703489,2	K562	blood:
24	chr8:130688486..130691516-chr8:130701686..130704518,3	K562	blood:
25	chr8:127888564..127889446-chr8:130699431..130700261,2	K562	blood:
26	chr8:130698168..130701867-chr8:130706682..130711085,4	MCF-7	breast:
27	chr8:130697457..130699780-chr8:130703396..130705887,2	K562	blood:
28	chr8:130697457..130699780-chr8:130703396..130705887,2	K562	blood:
29	chr8:130690016..130691591-chr8:130697534..130699622,2	K562	blood:
30	chr8:130578587..130580098-chr8:130704677..130707267,2	K562	blood:
31	chr8:128805941..128809580-chr8:130703915..130707556,3	MCF-7	breast:
32	chr8:130699826..130701651-chr8:130708566..130712426,4	K562	blood:
33	chr8:130699958..130701746-chr8:130701931..130704723,3	K562	blood:
34	chr8:130701843..130703503-chr8:130719583..130721644,2	K562	blood:
35	chr8:130699941..130700716-chr8:130738329..130738842,2	MCF-7	breast:
36	chr8:130694433..130695997-chr8:130696991..130698919,2	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-MYC-3	chr8:130700133-130700624	NONHSAT129111
2	lnc-GSDMC-4	chr8:130705564-130705921	NONHSAT129128

No data

Variant related genes	Relation type
CCDC26	TF binding region
ENSG00000254223	TF binding region
CCDC26	CpG island
ENSG00000254223	CpG island
ENSG00000249375	chromatin interactions
ENSG00000254223	chromatin interactions
ENSG00000249859	chromatin interactions
ENSG00000136997	chromatin interactions
ENSG00000229140	chromatin interactions

Extended variants
information (count: 419 )
Associated
traits (count: 154 )

Variant overlapped rSNPs/rCNVs (count:419 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs142096799	chr8:130697389-130697390	Weak transcription Enhancers Flanking Active TSS	TF binding region Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
2	rs530402077	chr8:130697598-130697599	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs114757952	chr8:130697605-130697606	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs116663141	chr8:130697608-130697609	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs185003227	chr8:130697617-130697618	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs552600665	chr8:130697618-130697619	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs571369280	chr8:130697619-130697620	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs532306320	chr8:130697620-130697621	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs372056454	chr8:130697626-130697627	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs189092603	chr8:130697628-130697629	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs549819975	chr8:130697659-130697660	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs536133913	chr8:130697695-130697696	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs112101992	chr8:130697747-130697748	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs140303901	chr8:130697762-130697763	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs545007107	chr8:130697817-130697818	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs528838639	chr8:130697819-130697820	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs533665135	chr8:130697860-130697861	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs377087214	chr8:130697898-130697899	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs558590758	chr8:130697922-130697923	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs576839760	chr8:130698004-130698005	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs77715376	chr8:130698018-130698019	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs371096600	chr8:130698034-130698035	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs575785620	chr8:130698035-130698036	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs143980530	chr8:130698041-130698042	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs17182136	chr8:130698050-130698051	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs527990772	chr8:130698090-130698091	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs73401524	chr8:130698127-130698128	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
28	rs181023032	chr8:130698147-130698148	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs140714698	chr8:130698149-130698150	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs564632192	chr8:130698171-130698172	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs567950143	chr8:130698185-130698186	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs550405113	chr8:130698187-130698188	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs566076250	chr8:130698206-130698207	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region CpG island Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs530204124	chr8:130698242-130698243	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs372351799	chr8:130698337-130698338	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs77700672	chr8:130698339-130698340	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs529944111	chr8:130698411-130698412	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs11785932	chr8:130698432-130698433	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs551590712	chr8:130698449-130698450	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs566364479	chr8:130698463-130698464	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs533808976	chr8:130698471-130698472	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
42	rs116434649	chr8:130698493-130698494	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs570568027	chr8:130698494-130698495	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs537935285	chr8:130698497-130698498	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs556797735	chr8:130698513-130698514	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs575046695	chr8:130698559-130698560	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs536172458	chr8:130698574-130698575	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs186309110	chr8:130698581-130698582	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs191599631	chr8:130698582-130698583	Enhancers Weak transcription Flanking Active TSS Genic enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs181222260	chr8:130698633-130698634	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:154)

Disease	PMID	Source
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
Testicular cancer	18059402	CNVD
Breast cancer	17133270	CNVD
Breast cancer	21509527	CNVD
Breast cancer	21858162	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Acute lymphoblastic leukemia	21248843	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	17603634	CNVD
Breast cancer	19602461	CNVD
Cancer	22429812	CNVD
Endometrial cancer	22040021	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	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
Acute myeloid leukemia	20729466	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
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
Endometrioid adenocarcinoma	16974079	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
Papillary thyroid cancer	17515504	CNVD
Basal cell lymphoma	17053054	CNVD
Gastric cancer	21528007	CNVD
Breast cancer	22532251	CNVD
Cervical cancer	21062161	CNVD
Cancer	21129771	CNVD
benign familial neonatal convulsions	18472482	CNVD
Breast cancer	16417655	CNVD
Astrocytoma	17387387	CNVD
Cancer	21183584	CNVD
Follicular lymphoma	20505157	CNVD
T-cell lymphomas	19863542	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	20607354	CNVD
Breast cancer	20814816	CNVD
Colorectal cancer	22486879	CNVD
Breast cancer	17908964	CNVD
Colorectal cancer	20031965	CNVD
Hepatocellular carcinoma	16750200	CNVD
Ovarian cancer	17908964	CNVD
Ovarian cancer	20031965	CNVD
Prostate cancer	20031965	CNVD
Non-small cell lung cancer	17643093	CNVD
Prostate cancer	19242612	CNVD
Colorectal cancer	16774939	CNVD
Malignant melanoma	17260012	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Acute myeloid leukemia	17268525	CNVD
Acute myeloid leukemia	18379011	CNVD
Esophageal squamous carcinoma	18405350	CNVD
Chronic lymphocytic leukemia	20421269	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	22048815	CNVD
Colorectal cancer	16912164	CNVD
Cutaneous T-cell lymphoma	21881587	CNVD
Lung adenocarcinoma	21148746	CNVD
Lung cancer	21911935	CNVD
Breast cancer	20459607	CNVD
Medulloblastoma	19270706	CNVD
Acute myeloid leukemia	19651601	CNVD
Colorectal cancer	21645411	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Colorectal cancer	19455253	CNVD
Glioblastoma multiforme	22286061	CNVD
Colorectal cancer	22860045	CNVD
Esophageal squamous carcinoma	17470683	CNVD
Lung cancer	17925434	CNVD
Non-small cell lung cancer	21829676	CNVD
Prostate cancer	17217626	CNVD
Cancer	17160897	CNVD
Breast cancer	16497871	CNVD
Colorectal cancer	16882699	CNVD
Cystic fibrosis	19273617	CNVD
Chronic stroke	19622162	CNVD
Chordoma	18071362	CNVD
Breast cancer	17850661	CNVD
head and neck squamous cell carcinoma	16740747	CNVD
Gastric cancer	22539939	CNVD
Breast cancer	16272173	CNVD
Uveal melanoma	20484589	CNVD
Ovarian cancer	20844748	CNVD
Multiple myeloma	16616336	CNVD
Breast cancer	16620391	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	21364760	CNVD
Breast cancer	21611746	CNVD
Esophageal adenocarcinoma	18519675	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Schizophrenia	23813976	CNVD

Chromatin state (count:240 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:130689400-130697400	Weak transcription	HMEC	breast
2	chr8:130691800-130697800	Weak transcription	Lung	lung
3	chr8:130692400-130698000	Weak transcription	Psoas Muscle	Psoas
4	chr8:130692600-130698000	Weak transcription	Right Ventricle	heart
5	chr8:130694200-130697400	Weak transcription	HSMM	muscle
6	chr8:130694200-130697400	Weak transcription	HSMMtube	muscle
7	chr8:130694400-130697400	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
8	chr8:130694400-130697400	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr8:130694400-130697400	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
10	chr8:130694400-130697400	Weak transcription	Ovary	ovary
11	chr8:130694400-130697400	Enhancers	A549	lung
12	chr8:130694400-130697600	Weak transcription	Colon Smooth Muscle	Colon
13	chr8:130694400-130697800	Weak transcription	Placenta	Placenta
14	chr8:130694400-130698000	Enhancers	Dnd41	blood
15	chr8:130694600-130697400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
16	chr8:130694600-130697400	Weak transcription	Fetal Stomach	stomach
17	chr8:130694800-130697400	Weak transcription	Primary hematopoietic stem cells	blood
18	chr8:130694800-130697800	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr8:130694800-130703200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
20	chr8:130695000-130697400	Weak transcription	Cortex derived primary cultured neurospheres	brain
21	chr8:130695000-130697400	Weak transcription	Fetal Muscle Leg	muscle
22	chr8:130695000-130697800	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
23	chr8:130696200-130698800	Enhancers	Primary neutrophils fromperipheralblood	blood
24	chr8:130696200-130701400	Weak transcription	Spleen	Spleen
25	chr8:130696200-130703000	Weak transcription	Monocytes-CD14+_RO01746	blood
26	chr8:130696200-130703200	Weak transcription	Pancreas	Pancrea
27	chr8:130696200-130704600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
28	chr8:130696800-130698600	Enhancers	Muscle Satellite Cultured Cells	--
29	chr8:130696800-130698600	Enhancers	NH-A	brain
30	chr8:130696800-130698800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
31	chr8:130696800-130699200	Enhancers	NHDF-Ad	bronchial
32	chr8:130696800-130699400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
33	chr8:130696800-130699600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
34	chr8:130696800-130701600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
35	chr8:130697000-130697400	Enhancers	K562	blood
36	chr8:130697000-130698200	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
37	chr8:130697000-130698200	Enhancers	Primary monocytes fromperipheralblood	blood
38	chr8:130697000-130698400	Enhancers	Primary hematopoietic stem cells short term culture	blood
39	chr8:130697000-130698600	Enhancers	Fetal Thymus	thymus
40	chr8:130697000-130698800	Enhancers	IMR90 fetal lung fibroblasts Cell Line	lung
41	chr8:130697000-130698800	Enhancers	Breast Myoepithelial Primary Cells	Breast
42	chr8:130697000-130698800	Enhancers	Rectal Smooth Muscle	rectum
43	chr8:130697000-130698800	Enhancers	Skeletal Muscle Female	skeletal muscle
44	chr8:130697000-130698800	Enhancers	NHLF	lung
45	chr8:130697000-130699200	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
46	chr8:130697000-130699800	Enhancers	Fetal Lung	lung
47	chr8:130697000-130700200	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
48	chr8:130697000-130700200	Enhancers	Fetal Heart	heart
49	chr8:130697200-130697600	Enhancers	Primary T cells from cord blood	blood
50	chr8:130697200-130697800	Flanking Active TSS	HUVEC	blood vessel

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