Variant report

Variant	nsv539697
Chromosome Location	chr8:100290887-100508952
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1399)
CpG islands
(count:244)
Chromatin interactive
region (count:87)
LncRNA
region (count:7)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1399 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:100416524-100416817	K562	blood:	n/a	n/a
2	ARID3A	chr8:100476490-100476616	HepG2	liver:	n/a	n/a
3	ARID3A	chr8:100370860-100371168	K562	blood:	n/a	n/a
4	ARID3A	chr8:100298952-100299271	HepG2	liver:	n/a	n/a
5	ARID3A	chr8:100370824-100371122	HepG2	liver:	n/a	n/a
6	ARID3A	chr8:100400144-100400181	K562	blood:	n/a	n/a
7	ARID3A	chr8:100445541-100445734	HepG2	liver:	n/a	n/a
8	ATF1	chr8:100416505-100416787	K562	blood:	n/a	n/a
9	ATF1	chr8:100468108-100468135	K562	blood:	n/a	n/a
10	ATF1	chr8:100370807-100371120	K562	blood:	n/a	n/a
11	BACH1	chr8:100395401-100395488	K562	blood:	n/a	n/a
12	BACH1	chr8:100389266-100389270	K562	blood:	n/a	n/a
13	BATF	chr8:100507953-100508207	GM12878	blood:	n/a	n/a
14	BATF	chr8:100508028-100508205	GM12878	blood:	n/a	n/a
15	BATF	chr8:100460738-100460975	GM12878	blood:	n/a	chr8:100460813-100460824
16	BATF	chr8:100460709-100460986	GM12878	blood:	n/a	chr8:100460813-100460824
17	BCL11A	chr8:100305139-100305357	GM12878	blood:	n/a	n/a
18	BCL11A	chr8:100508018-100508319	GM12878	blood:	n/a	n/a
19	BCL11A	chr8:100508034-100508288	H1-hESC	embryonic stem cell:	n/a	n/a
20	BCL11A	chr8:100508036-100508276	GM12878	blood:	n/a	n/a
21	BHLHE40	chr8:100370878-100370919	A549	lung:	n/a	n/a
22	BHLHE40	chr8:100507938-100508318	GM12878	blood:	n/a	n/a
23	BHLHE40	chr8:100404161-100404287	K562	blood:	n/a	n/a
24	BHLHE40	chr8:100507928-100508349	HepG2	liver:	n/a	n/a
25	BHLHE40	chr8:100498996-100499002	K562	blood:	n/a	n/a
26	BRCA1	chr8:100370881-100371042	H1-hESC	embryonic stem cell:	n/a	n/a
27	BRCA1	chr8:100507866-100508321	Hela-S3	cervix:	n/a	chr8:100508029-100508036
28	BRCA1	chr8:100507941-100508318	GM12878	blood:	n/a	chr8:100508029-100508036
29	CBX3	chr8:100389448-100389836	K562	blood:	n/a	n/a
30	CBX3	chr8:100472687-100473201	K562	blood:	n/a	n/a
31	CBX3	chr8:100389428-100389814	K562	blood:	n/a	n/a
32	CBX3	chr8:100445502-100445815	K562	blood:	n/a	n/a
33	CBX3	chr8:100472744-100473154	HCT-116	colon:	n/a	n/a
34	CBX3	chr8:100389390-100389830	HCT-116	colon:	n/a	n/a
35	CBX3	chr8:100445427-100445873	HCT-116	colon:	n/a	n/a
36	CBX3	chr8:100472723-100473116	K562	blood:	n/a	n/a
37	CBX3	chr8:100445421-100445824	K562	blood:	n/a	n/a
38	CCNT2	chr8:100332298-100332498	K562	blood:	n/a	n/a
39	CCNT2	chr8:100334302-100334493	K562	blood:	n/a	n/a
40	CEBPB	chr8:100416519-100416766	A549	lung:	n/a	n/a
41	CEBPB	chr8:100392427-100392937	MCF-7	breast:	n/a	chr8:100392700-100392711
42	CEBPB	chr8:100328445-100328642	K562	blood:	n/a	chr8:100328593-100328604
43	CEBPB	chr8:100309567-100309946	IMR90	lung:	n/a	n/a
44	CEBPB	chr8:100508056-100508190	HepG2	liver:	n/a	n/a
45	CEBPB	chr8:100507939-100508321	Hela-S3	cervix:	n/a	n/a
46	CEBPB	chr8:100392522-100392850	HepG2	liver:	n/a	chr8:100392700-100392711
47	CEBPB	chr8:100373017-100373283	K562	blood:	n/a	chr8:100373128-100373139
48	CEBPB	chr8:100415669-100415852	K562	blood:	n/a	n/a
49	CEBPB	chr8:100416490-100416891	K562	blood:	n/a	n/a
50	CEBPB	chr8:100471518-100472230	IMR90	lung:	n/a	chr8:100472076-100472087

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:100493491-100493541	ProgFib	skin:	n/a
2	chr8:100334620-100334670	HEEpiC	esophagus:	n/a
3	chr8:100464878-100464928	Hela-S3	cervix:	n/a
4	chr8:100297748-100297798	HIPEpiC	eye:	n/a
5	chr8:100493491-100493541	HCT-116	colon:	n/a
6	chr8:100464878-100464928	AG04450	lung:	fetal
7	chr8:100334620-100334670	U87	brain:	n/a
8	chr8:100464878-100464928	SKMC	muscle:	n/a
9	chr8:100297748-100297798	HPAEpiC	pulmonary alveolar:	n/a
10	chr8:100334620-100334670	ovcar-3	ovarian:	n/a
11	chr8:100297748-100297798	NHBE	bronchial:	n/a
12	chr8:100297748-100297798	H1-hESC	embryonic stem cell:	embryo
13	chr8:100493491-100493541	HCM	heart:	n/a
14	chr8:100297748-100297798	AG09319	gingival:	n/a
15	chr8:100493491-100493541	NHDF-neo	bronchial:	n/a
16	chr8:100297748-100297798	GM12892	blood:	n/a
17	chr8:100297748-100297798	HCT-116	colon:	n/a
18	chr8:100297748-100297798	HEEpiC	esophagus:	n/a
19	chr8:100464878-100464928	HUVEC	blood vessel:	n/a
20	chr8:100464878-100464928	HNPCEpiC	eye:	n/a
21	chr8:100297748-100297798	U87	brain:	n/a
22	chr8:100464878-100464928	AG09309	skin:	n/a
23	chr8:100334620-100334670	K562	blood:	n/a
24	chr8:100334620-100334670	CMK	blood:	n/a
25	chr8:100464878-100464928	NB4	blood:	n/a
26	chr8:100493491-100493541	NH-A	brain:	n/a
27	chr8:100493491-100493541	PrEC	prostate:	n/a
28	chr8:100464878-100464928	SK-N-SH	brain:	n/a
29	chr8:100464878-100464928	HRPEpiC	eye:	n/a
30	chr8:100464878-100464928	PANC-1	pancreas:	n/a
31	chr8:100334620-100334670	AG04450	lung:	fetal
32	chr8:100493491-100493541	HEEpiC	esophagus:	n/a
33	chr8:100297748-100297798	HRE	kidney:	n/a
34	chr8:100493491-100493541	HRCEpiC	kidney:	n/a
35	chr8:100493491-100493541	MCF-7	breast:	n/a
36	chr8:100493491-100493541	HAEpiC	amniotic membrane:	n/a
37	chr8:100493491-100493541	AG04450	lung:	fetal
38	chr8:100334620-100334670	GM12891	blood:	n/a
39	chr8:100297748-100297798	CMK	blood:	n/a
40	chr8:100334620-100334670	Hepatocyte	liver:	n/a
41	chr8:100464878-100464928	HIPEpiC	eye:	n/a
42	chr8:100297748-100297798	Hela-S3	cervix:	n/a
43	chr8:100334620-100334670	BJ	skin:	n/a
44	chr8:100297748-100297798	NB4	blood:	n/a
45	chr8:100334620-100334670	SK-N-MC	brain:	n/a
46	chr8:100297748-100297798	MCF10A-Er-Src	breast:	n/a
47	chr8:100334620-100334670	HNPCEpiC	eye:	n/a
48	chr8:100334620-100334670	MCF10A-Er-Src	breast:	n/a
49	chr8:100334620-100334670	NT2-D1	testis:	n/a
50	chr8:100297748-100297798	PANC-1	pancreas:	n/a

(count:87 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:99717161..99717948-chr8:100352640..100353640,2	K562	blood:
2	chr8:100340207..100341801-chr8:100343989..100346691,2	MCF-7	breast:
3	chr8:100450418..100452655-chr8:100468623..100470594,2	K562	blood:
4	chr8:100023786..100025570-chr8:100367969..100370185,3	MCF-7	breast:
5	chr8:100481937..100483971-chr8:100485663..100487345,2	MCF-7	breast:
6	chr8:100360393..100360964-chr8:100816462..100817102,2	MCF-7	breast:
7	chr8:100329098..100330856-chr8:100331177..100332983,2	MCF-7	breast:
8	chr8:100403791..100404673-chr8:100818662..100819568,3	MCF-7	breast:
9	chr8:100485436..100487741-chr8:100494328..100496741,2	K562	blood:
10	chr8:99956540..99958741-chr8:100370642..100372359,2	MCF-7	breast:
11	chr8:100492530..100494149-chr8:100495886..100498811,2	MCF-7	breast:
12	chr16:23607401..23609847-chr8:100473755..100475258,2	MCF-7	breast:
13	chr8:100476013..100478783-chr8:100496071..100498835,2	MCF-7	breast:
14	chr8:100180104..100181200-chr8:100370523..100371154,5	MCF-7	breast:
15	chr8:100024635..100026607-chr8:100339207..100341437,2	MCF-7	breast:
16	chr8:99570015..99570973-chr8:100370433..100371359,3	K562	blood:
17	chr8:100403774..100404566-chr8:100616940..100617627,2	MCF-7	breast:
18	chr8:100459116..100461634-chr8:100473693..100476496,2	MCF-7	breast:
19	chr8:100464584..100466784-chr8:100489016..100491472,2	MCF-7	breast:
20	chr8:100481937..100483971-chr8:100485663..100487345,2	MCF-7	breast:
21	chr8:100440991..100443912-chr8:100444936..100447073,2	K562	blood:
22	chr8:100323481..100327206-chr8:100331154..100333171,3	MCF-7	breast:
23	chr8:100494882..100496542-chr8:100496740..100499297,2	MCF-7	breast:
24	chr8:100474939..100477291-chr8:100497932..100499895,2	MCF-7	breast:
25	chr8:100340207..100341801-chr8:100343989..100346691,2	MCF-7	breast:
26	chr8:100478649..100480256-chr8:100490609..100493235,2	K562	blood:
27	chr8:100283345..100287751-chr8:100288664..100292518,5	K562	blood:
28	chr8:100506206..100508940-chr8:100515378..100517666,2	MCF-7	breast:
29	chr8:100381765..100384655-chr8:100392997..100394529,2	K562	blood:
30	chr8:100433911..100436132-chr8:100443954..100446728,2	MCF-7	breast:
31	chr8:100403279..100404684-chr8:100871403..100872860,7	MCF-7	breast:
32	chr8:99952476..99953694-chr8:100370455..100371470,4	MCF-7	breast:
33	chr8:100180149..100180921-chr8:100370671..100371459,2	MCF-7	breast:
34	chr8:100357228..100359296-chr8:100360534..100362578,2	MCF-7	breast:
35	chr8:100298711..100300024-chr8:100370075..100371268,5	MCF-7	breast:
36	chr8:100476013..100478783-chr8:100496071..100498835,2	MCF-7	breast:
37	chr8:100440991..100443912-chr8:100444936..100447073,2	K562	blood:
38	chr8:100478649..100480256-chr8:100490609..100493235,2	K562	blood:
39	chr8:100343791..100346575-chr8:100348119..100349870,2	MCF-7	breast:
40	chr8:100369443..100371664-chr8:100373746..100375749,2	K562	blood:
41	chr8:100368561..100370943-chr8:100372272..100375246,2	K562	blood:
42	chr8:100459116..100461634-chr8:100473693..100476496,2	MCF-7	breast:
43	chr8:100381765..100384655-chr8:100392997..100394529,2	K562	blood:
44	chr8:100327325..100329198-chr8:100340079..100342358,2	MCF-7	breast:
45	chr8:100403788..100404692-chr8:100799555..100800231,3	MCF-7	breast:
46	chr8:100450418..100452655-chr8:100468623..100470594,2	K562	blood:
47	chr8:99180814..99181617-chr8:100370430..100371368,2	MCF-7	breast:
48	chr8:100323481..100327206-chr8:100331154..100333171,3	MCF-7	breast:
49	chr8:100444521..100447261-chr8:100451811..100454572,2	K562	blood:
50	chr8:100298711..100300024-chr8:100370075..100371268,5	MCF-7	breast:

(count:7 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-OSR2-7	chr8:100401844-100401948	NONHSAT127953
2	lnc-STK3-7	chr8:100358280-100360484	NONHSAT127952
3	lnc-STK3-6	chr8:100352533-100353989	NONHSAT127951
4	lnc-OSR2-7	chr8:100403785-100403932	NONHSAT127953
5	lnc-OSR2-7	chr8:100441798-100441875	NONHSAT127953
6	lnc-OSR2-7	chr8:100443749-100443892	NONHSAT127953
7	lnc-OSR2-7	chr8:100454629-100454639	NONHSAT127953

No data

Variant related genes	Relation type
VPS13B	TF binding region
ENSG00000237704	TF binding region
ENSG00000225017	TF binding region
VPS13B	CpG island
ENSG00000237704	CpG island
ENSG00000225017	CpG island
ENSG00000253948	chromatin interactions
ENSG00000188029	chromatin interactions
ENSG00000004779	chromatin interactions
ENSG00000132549	chromatin interactions
ENSG00000009307	chromatin interactions
ENSG00000225017	chromatin interactions
ENSG00000164920	chromatin interactions
ENSG00000253912	chromatin interactions

Extended variants
information (count: 7444 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:7444 , 50 per page) page: 1 2 3 4 5 6 7 ... 149

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs571244501	chr8:100290939-100290940	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs533523276	chr8:100290962-100290963	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs577360004	chr8:100290983-100290984	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs553843721	chr8:100291049-100291050	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs190768606	chr8:100291059-100291060	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs536104730	chr8:100291159-100291160	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs183112563	chr8:100291175-100291176	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs576040226	chr8:100291222-100291223	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs544866508	chr8:100291232-100291233	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs542012875	chr8:100291327-100291328	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs13268008	chr8:100291406-100291407	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs374384360	chr8:100291408-100291409	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs577981940	chr8:100291424-100291425	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs540219479	chr8:100291520-100291521	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs145912207	chr8:100291538-100291539	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs529341449	chr8:100291544-100291545	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs187705471	chr8:100291571-100291572	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs367832746	chr8:100291628-100291629	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs562322421	chr8:100291634-100291635	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs116663661	chr8:100291635-100291636	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs551672145	chr8:100291654-100291655	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs564994811	chr8:100291675-100291676	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs539938547	chr8:100291734-100291735	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs61301696	chr8:100291755-100291756	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs398009019	chr8:100291756-100291757	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs191072693	chr8:100291791-100291792	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs547074249	chr8:100291967-100291968	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs567410481	chr8:100292036-100292037	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563397265	chr8:100292037-100292038	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs536338047	chr8:100292055-100292056	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs549625543	chr8:100292056-100292057	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182808713	chr8:100292059-100292060	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs111664560	chr8:100292060-100292061	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs187782257	chr8:100292083-100292084	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs34726230	chr8:100292087-100292088	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs558436257	chr8:100292097-100292098	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs10808364	chr8:100292141-100292142	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
38	rs531382150	chr8:100292158-100292159	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs376561494	chr8:100292159-100292160	Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs573828513	chr8:100292203-100292204	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs192875346	chr8:100292219-100292220	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs562610804	chr8:100292232-100292233	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs11985671	chr8:100292254-100292255	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs184925708	chr8:100292277-100292278	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs187080113	chr8:100292279-100292280	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs377086976	chr8:100292301-100292302	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs191960157	chr8:100292320-100292321	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs547404231	chr8:100292351-100292352	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs560844531	chr8:100292383-100292384	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs529684674	chr8:100292400-100292401	ZNF genes & repeats Weak transcription Strong transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:110)

Disease	PMID	Source
Wilms tumour	21544195	CNVD
Gastric cancer	17908304	CNVD
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
Acute promyelocytic leukemia	19109227	CNVD
Breast cancer	21245420	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
lymphocytic leukemia	21291569	CNVD
Liver carcinoma	19366792	CNVD
Seminomas	18059402	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
Hodgkin''s lymphoma	17606441	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
Glioblastoma multiforme	18628472	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	16573809	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	CNVD
Multiple myeloma	16461302	CNVD
Myeloproliferative neoplasm	20015882	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Acute myeloid leukemia	21358987	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
small cell lung cancer	20016488	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
Bladder cancer	19088036	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Breast cancer	17899364	CNVD
Acute myeloid leukemia	21251322	CNVD
head and neck squamous cell carcinoma	19451471	CNVD
Renal cell carcinoma	18765545	CNVD
Basal cell lymphoma	17170743	CNVD
Colorectal cancer	16774939	CNVD
Autosomal-dominant progressive external ophthalmoplegia	19664747	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	17260012	CNVD
Congenital anomalies of the kidney and urinary tract	20467480	CNVD
Colorectal cancer	19455253	CNVD
Sezary syndrome	18413736	CNVD
Breast cancer	21611746	CNVD
Cohen syndrome	20461111	CNVD
Prostate cancer	22341455	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
T-cell lymphomas	22341440	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD

Chromatin state (count:1775 , 50 per page) page: 1 2 3 4 5 6 7 ... 36

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:100214800-100293200	Weak transcription	Primary T cells fromperipheralblood	blood
2	chr8:100253400-100292400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
3	chr8:100268200-100293200	Weak transcription	Aorta	Aorta
4	chr8:100274400-100292200	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
5	chr8:100278800-100302400	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
6	chr8:100280600-100293200	Weak transcription	Left Ventricle	heart
7	chr8:100280800-100292200	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
8	chr8:100280800-100299000	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
9	chr8:100284000-100295000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
10	chr8:100284200-100301200	Weak transcription	GM12878-XiMat	blood
11	chr8:100284600-100292400	Weak transcription	Fetal Intestine Large	intestine
12	chr8:100284600-100298200	Weak transcription	Fetal Stomach	stomach
13	chr8:100284600-100312000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
14	chr8:100284800-100298800	Weak transcription	Fetal Lung	lung
15	chr8:100284800-100307200	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
16	chr8:100285000-100298200	Weak transcription	Adipose Nuclei	Adipose
17	chr8:100285800-100298200	Weak transcription	Lung	lung
18	chr8:100286200-100298000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr8:100286400-100295000	Weak transcription	Duodenum Mucosa	Duodenum
20	chr8:100286600-100295600	Weak transcription	Fetal Muscle Leg	muscle
21	chr8:100286600-100298000	Weak transcription	Rectal Smooth Muscle	rectum
22	chr8:100286600-100298200	Weak transcription	Liver	Liver
23	chr8:100286600-100303000	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
24	chr8:100286600-100306000	Weak transcription	Rectal Mucosa Donor 31	rectum
25	chr8:100286800-100298000	Weak transcription	Colon Smooth Muscle	Colon
26	chr8:100286800-100314000	Weak transcription	HSMM	muscle
27	chr8:100287200-100298000	Weak transcription	K562	blood
28	chr8:100288400-100304400	Weak transcription	Primary hematopoietic stem cells	blood
29	chr8:100288600-100291600	Weak transcription	Breast Myoepithelial Primary Cells	Breast
30	chr8:100288600-100292400	Weak transcription	Monocytes-CD14+_RO01746	blood
31	chr8:100288800-100292600	Weak transcription	Primary B cells from cord blood	blood
32	chr8:100288800-100292800	Weak transcription	Rectal Mucosa Donor 29	rectum
33	chr8:100288800-100298200	Weak transcription	Duodenum Smooth Muscle	Duodenum
34	chr8:100288800-100301600	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
35	chr8:100288800-100302200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
36	chr8:100288800-100309000	Weak transcription	Primary monocytes fromperipheralblood	blood
37	chr8:100289000-100293000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr8:100289000-100301600	Weak transcription	Primary B cells from peripheral blood	blood
39	chr8:100289200-100295600	Weak transcription	HSMMtube	muscle
40	chr8:100290000-100291200	Enhancers	Primary T cells from cord blood	blood
41	chr8:100290000-100291200	Enhancers	Primary T helper cells PMA-I stimulated	--
42	chr8:100290200-100291000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
43	chr8:100290200-100298200	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
44	chr8:100290400-100291000	Enhancers	Primary T killer memory cells from peripheral blood	blood
45	chr8:100290400-100291200	Enhancers	Dnd41	blood
46	chr8:100290400-100291400	Enhancers	Primary neutrophils fromperipheralblood	blood
47	chr8:100290400-100292400	Weak transcription	Muscle Satellite Cultured Cells	--
48	chr8:100290400-100298400	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
49	chr8:100290600-100292400	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
50	chr8:100290800-100292400	Weak transcription	Primary T helper cells fromperipheralblood	blood

The 2.0 version of rSNPBase

Variant report

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