Variant report

Variant	nsv1016128
Chromosome Location	chr8:68019177-68129755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:516)
CpG islands
(count:305)
Chromatin interactive
region (count:72)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:516 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:68022007-68022483	K562	blood:	n/a	n/a
2	ARID3A	chr8:68065780-68065880	K562	blood:	n/a	n/a
3	ARID3A	chr8:68032334-68032484	K562	blood:	n/a	n/a
4	ARID3A	chr8:68026510-68027171	K562	blood:	n/a	n/a
5	ATF1	chr8:68022028-68022347	K562	blood:	n/a	n/a
6	ATF2	chr8:68108470-68108909	GM12878	blood:	n/a	n/a
7	ATF2	chr8:68108339-68108875	GM12878	blood:	n/a	n/a
8	BATF	chr8:68071443-68071797	GM12878	blood:	n/a	n/a
9	BATF	chr8:68108487-68108823	GM12878	blood:	n/a	n/a
10	BHLHE40	chr8:68021797-68022409	K562	blood:	n/a	n/a
11	BRCA1	chr8:68107483-68107530	H1-hESC	embryonic stem cell:	n/a	n/a
12	CBX3	chr8:68021765-68022411	K562	blood:	n/a	n/a
13	CBX3	chr8:68021929-68022308	K562	blood:	n/a	n/a
14	CCNT2	chr8:68021959-68022495	K562	blood:	n/a	n/a
15	CCNT2	chr8:68026748-68027196	K562	blood:	n/a	n/a
16	CEBPB	chr8:68129493-68129725	A549	lung:	n/a	n/a
17	CEBPB	chr8:68076544-68076895	HepG2	liver:	n/a	chr8:68076724-68076735
18	CEBPB	chr8:68108257-68108280	H1-hESC	embryonic stem cell:	n/a	chr8:68108263-68108274
19	CEBPB	chr8:68065864-68065964	K562	blood:	n/a	chr8:68065878-68065891
20	CEBPB	chr8:68057093-68057349	IMR90	lung:	n/a	chr8:68057257-68057268
21	CEBPB	chr8:68057096-68057354	A549	lung:	n/a	chr8:68057257-68057268
22	CEBPB	chr8:68108158-68108438	HepG2	liver:	n/a	chr8:68108263-68108274
23	CEBPB	chr8:68049232-68049274	K562	blood:	n/a	n/a
24	CEBPB	chr8:68053792-68053906	K562	blood:	n/a	n/a
25	CEBPB	chr8:68076544-68076875	A549	lung:	n/a	chr8:68076724-68076735
26	CEBPB	chr8:68044396-68044716	IMR90	lung:	n/a	chr8:68044543-68044554
27	CEBPB	chr8:68057085-68057376	H1-hESC	embryonic stem cell:	n/a	chr8:68057257-68057268
28	CEBPB	chr8:68021700-68022376	K562	blood:	n/a	n/a
29	CEBPB	chr8:68022022-68022340	K562	blood:	n/a	n/a
30	CEBPB	chr8:68053740-68053941	IMR90	lung:	n/a	n/a
31	CEBPB	chr8:68040311-68040611	IMR90	lung:	n/a	n/a
32	CEBPB	chr8:68108127-68108479	A549	lung:	n/a	chr8:68108263-68108274
33	CEBPB	chr8:68044398-68044717	MCF-7	breast:	n/a	chr8:68044543-68044554
34	CEBPB	chr8:68129459-68129766	HepG2	liver:	n/a	n/a
35	CEBPB	chr8:68105777-68106006	HepG2	liver:	n/a	n/a
36	CEBPB	chr8:68053800-68053928	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:68044457-68044696	K562	blood:	n/a	chr8:68044543-68044554
38	CEBPB	chr8:68044368-68044721	A549	lung:	n/a	chr8:68044543-68044554
39	CEBPB	chr8:68093857-68094132	A549	lung:	n/a	chr8:68093982-68093993
40	CEBPB	chr8:68044385-68044681	Hela-S3	cervix:	n/a	chr8:68044543-68044554
41	CEBPB	chr8:68057162-68057407	MCF-7	breast:	n/a	chr8:68057257-68057268
42	CEBPB	chr8:68044365-68044733	HepG2	liver:	n/a	chr8:68044543-68044554
43	CEBPB	chr8:68124637-68124953	HepG2	liver:	n/a	chr8:68124764-68124775
44	CEBPB	chr8:68125765-68125766	H1-hESC	embryonic stem cell:	n/a	n/a
45	CEBPB	chr8:68044426-68044629	HepG2	liver:	n/a	chr8:68044543-68044554
46	CEBPB	chr8:68093918-68094118	HepG2	liver:	n/a	chr8:68093982-68093993
47	CEBPB	chr8:68021723-68021959	K562	blood:	n/a	n/a
48	CEBPB	chr8:68057094-68057354	Hela-S3	cervix:	n/a	chr8:68057257-68057268
49	CEBPB	chr8:68124660-68124993	H1-hESC	embryonic stem cell:	n/a	chr8:68124764-68124775
50	CEBPB	chr8:68057084-68057433	K562	blood:	n/a	chr8:68057257-68057268

(count:305 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:68080400-68080450	HCT-116	colon:	n/a
2	chr8:68110902-68110952	HCPEpiC	choroid plexus:	n/a
3	chr8:68022262-68022312	SKMC	muscle:	n/a
4	chr8:68080400-68080450	CMK	blood:	n/a
5	chr8:68107083-68107133	GM12891	blood:	n/a
6	chr8:68125092-68125142	SK-N-SH_RA	brain:	n/a
7	chr8:68107083-68107133	AoSMC	blood vessel:	n/a
8	chr8:68107083-68107133	IMR90	lung:	fetal
9	chr8:68022262-68022312	T-47D	breast:	n/a
10	chr8:68022262-68022312	HEK293	kidney:	embryo
11	chr8:68125092-68125142	AoSMC	blood vessel:	n/a
12	chr8:68080400-68080450	H1-hESC	embryonic stem cell:	embryo
13	chr8:68125092-68125142	GM06990	blood:	n/a
14	chr8:68080400-68080450	AG10803	skin:	n/a
15	chr8:68110902-68110952	A549	lung:	n/a
16	chr8:68022262-68022312	HCM	heart:	n/a
17	chr8:68125092-68125142	MCF10A-Er-Src	breast:	n/a
18	chr8:68022262-68022312	AoSMC	blood vessel:	n/a
19	chr8:68107083-68107133	HNPCEpiC	eye:	n/a
20	chr8:68022262-68022312	SK-N-SH_RA	brain:	n/a
21	chr8:68107083-68107133	CMK	blood:	n/a
22	chr8:68107083-68107133	Caco-2	colon:	n/a
23	chr8:68125092-68125142	ECC-1	luminal epithelium:	n/a
24	chr8:68107083-68107133	ECC-1	luminal epithelium:	n/a
25	chr8:68080400-68080450	SAEC	small airway:	n/a
26	chr8:68107083-68107133	Hepatocyte	liver:	n/a
27	chr8:68110902-68110952	HMEC	breast:	n/a
28	chr8:68107083-68107133	SKMC	muscle:	n/a
29	chr8:68022262-68022312	HPAEpiC	pulmonary alveolar:	n/a
30	chr8:68110902-68110952	HPAEpiC	pulmonary alveolar:	n/a
31	chr8:68125092-68125142	HL-60	blood:	n/a
32	chr8:68110902-68110952	IMR90	lung:	fetal
33	chr8:68080400-68080450	MCF-7	breast:	n/a
34	chr8:68125092-68125142	BJ	skin:	n/a
35	chr8:68107083-68107133	HCPEpiC	choroid plexus:	n/a
36	chr8:68125092-68125142	Hela-S3	cervix:	n/a
37	chr8:68080400-68080450	GM19239	blood:	n/a
38	chr8:68022262-68022312	LNCaP	prostate:	n/a
39	chr8:68107083-68107133	Hela-S3	cervix:	n/a
40	chr8:68125092-68125142	CMK	blood:	n/a
41	chr8:68080400-68080450	HNPCEpiC	eye:	n/a
42	chr8:68107083-68107133	NHBE	bronchial:	n/a
43	chr8:68080400-68080450	IMR90	lung:	fetal
44	chr8:68022262-68022312	HepG2	liver:	n/a
45	chr8:68080400-68080450	HL-60	blood:	n/a
46	chr8:68125092-68125142	T-47D	breast:	n/a
47	chr8:68080400-68080450	SK-N-MC	brain:	n/a
48	chr8:68110902-68110952	AG04450	lung:	fetal
49	chr8:68125092-68125142	A549	lung:	n/a
50	chr8:68080400-68080450	Hela-S3	cervix:	n/a

(count:72 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr8:68085116..68087997-chr8:68090501..68093415,2	MCF-7	breast:
2	chr8:68040930..68042442-chr8:68048471..68050684,2	K562	blood:
3	chr8:68038512..68041443-chr8:68043392..68045199,2	MCF-7	breast:
4	chr8:68040930..68042442-chr8:68048471..68050684,2	K562	blood:
5	chr8:68086057..68088943-chr8:68089390..68093675,3	K562	blood:
6	chr8:68054368..68056716-chr8:68058153..68060696,2	K562	blood:
7	chr8:68103791..68106483-chr8:68107302..68110332,3	K562	blood:
8	chr8:68112732..68114911-chr8:68116863..68119997,3	K562	blood:
9	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
10	chr8:67976683..67978941-chr8:68094307..68096664,2	K562	blood:
11	chr8:68103791..68106410-chr8:68107302..68110578,4	K562	blood:
12	chr8:68127338..68130278-chr8:68135594..68139376,3	K562	blood:
13	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
14	chr8:68034598..68037205-chr8:68038455..68041133,2	MCF-7	breast:
15	chr8:68111984..68114620-chr8:68117011..68118931,2	K562	blood:
16	chr8:67971594..67973615-chr8:68104400..68106393,2	MCF-7	breast:
17	chr8:68059036..68061219-chr8:68063581..68066022,2	K562	blood:
18	chr8:68040015..68041733-chr8:68043068..68045142,2	MCF-7	breast:
19	chr8:68066129..68069885-chr8:68074156..68076683,4	K562	blood:
20	chr8:68054368..68056716-chr8:68058153..68060696,2	K562	blood:
21	chr2:88315577..88316138-chr8:68058073..68058573,2	MCF-7	breast:
22	chr8:67973913..67977272-chr8:68024656..68026462,3	K562	blood:
23	chr8:68103791..68106410-chr8:68107302..68110578,4	K562	blood:
24	chr8:68034598..68037205-chr8:68038455..68041133,2	MCF-7	breast:
25	chr8:68019313..68021388-chr8:68023240..68024925,2	K562	blood:
26	chr8:68039129..68041953-chr8:68044102..68045625,2	K562	blood:
27	chr8:67974856..67976583-chr8:68088986..68090764,2	MCF-7	breast:
28	chr8:68039129..68041953-chr8:68044102..68045625,2	K562	blood:
29	chr8:68098861..68101473-chr8:68104225..68105893,2	MCF-7	breast:
30	chr8:68074799..68076714-chr8:68078840..68080441,2	K562	blood:
31	chr8:68040015..68041733-chr8:68043068..68045142,2	MCF-7	breast:
32	chr8:68068690..68070292-chr8:68071142..68074042,2	K562	blood:
33	chr8:68049843..68052686-chr8:68057977..68059611,2	K562	blood:
34	chr8:68049843..68052686-chr8:68057977..68059611,2	K562	blood:
35	chr8:68068385..68070863-chr8:68074537..68076964,2	K562	blood:
36	chr8:68085116..68087997-chr8:68090501..68093415,2	MCF-7	breast:
37	chr8:68024722..68026418-chr8:68028615..68030810,2	K562	blood:
38	chr8:68062959..68065035-chr8:68067846..68069927,2	MCF-7	breast:
39	chr8:68103791..68106483-chr8:68107302..68110332,3	K562	blood:
40	chr8:68019207..68022568-chr8:68026729..68029590,3	K562	blood:
41	chr8:68021467..68023804-chr8:68064580..68067516,2	K562	blood:
42	chr8:68086366..68088943-chr8:68089390..68092288,2	K562	blood:
43	chr8:68103451..68106399-chr8:68110061..68112606,2	MCF-7	breast:
44	chr8:67833716..67836650-chr8:68108377..68110562,2	K562	blood:
45	chr8:68019313..68021388-chr8:68023240..68024925,2	K562	blood:
46	chr8:67976649..67978941-chr8:68093929..68095807,2	K562	blood:
47	chr8:67985384..67988219-chr8:68025028..68027428,3	K562	blood:
48	chr8:67835610..67837690-chr8:68125017..68126904,2	K562	blood:
49	chr8:68030814..68032510-chr8:68038981..68041972,2	K562	blood:
50	chr8:68112732..68114911-chr8:68116863..68119997,3	K562	blood:

No data

(count:4 , 50 per page) page: 1

No.	miRNA target gene	miRNA name	Chromosome Location
1	ARFGEF1	hsa-miR-215-5p	chr8:68109929-68109949
2	ARFGEF1	hsa-miR-192-5p	chr8:68109929-68109949
3	ARFGEF1	hsa-miR-192-5p	chr8:68109935-68109928
4	ARFGEF1	hsa-miR-215-5p	chr8:68109935-68109928

Variant related genes	Relation type
ENSG00000250869	TF binding region
CSPP1	TF binding region
ARFGEF1	TF binding region
ENSG00000250869	CpG island
CSPP1	CpG island
ARFGEF1	CpG island
ENSG00000245910	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000266491	chromatin interactions
ENSG00000254341	chromatin interactions
ENSG00000066777	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000104218	chromatin interactions

Extended variants
information (count: 3688 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3688 , 50 per page) page: 1 2 3 4 5 6 7 ... 74

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs192797876	chr8:68019206-68019207	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs7004549	chr8:68019208-68019209	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
3	rs117596307	chr8:68019210-68019211	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs559572119	chr8:68019238-68019239	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs561898713	chr8:68019285-68019286	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs184260676	chr8:68019287-68019288	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs79546222	chr8:68019294-68019295	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs76933427	chr8:68019296-68019297	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs187871848	chr8:68019320-68019321	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs375533803	chr8:68019341-68019342	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs550726329	chr8:68019425-68019426	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs77467522	chr8:68019464-68019465	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs371297844	chr8:68019509-68019510	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs547820562	chr8:68019601-68019602	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs564797999	chr8:68019609-68019610	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs533483915	chr8:68019704-68019705	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs533467738	chr8:68019822-68019823	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs16933160	chr8:68019863-68019864	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
19	rs566725004	chr8:68019905-68019906	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs372887930	chr8:68019927-68019928	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs534383918	chr8:68020038-68020039	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs548254799	chr8:68020048-68020049	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs568093247	chr8:68020049-68020050	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs537049778	chr8:68020052-68020053	Weak transcription Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs116143112	chr8:68020213-68020214	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs34204898	chr8:68020218-68020219	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs56039352	chr8:68020236-68020237	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs200329201	chr8:68020237-68020238	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs36044607	chr8:68020251-68020252	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs577026435	chr8:68020285-68020286	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs539748217	chr8:68020306-68020307	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs78356861	chr8:68020362-68020363	Weak transcription Enhancers Strong transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs553177281	chr8:68020452-68020453	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs573090672	chr8:68020583-68020584	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs192598042	chr8:68020586-68020587	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs376039533	chr8:68020598-68020599	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs562188385	chr8:68020606-68020607	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs78640660	chr8:68020627-68020628	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs75783917	chr8:68020636-68020637	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs536563215	chr8:68020637-68020638	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs78079895	chr8:68020638-68020639	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs368517523	chr8:68020671-68020672	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
43	rs184571406	chr8:68020744-68020745	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs113848668	chr8:68020765-68020766	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs533397247	chr8:68020787-68020788	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs114255721	chr8:68020789-68020790	Weak transcription Enhancers Strong transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs72654945	chr8:68020835-68020836	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
48	rs188970928	chr8:68020872-68020873	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
49	rs181480633	chr8:68020887-68020888	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	Overlapped CNVs	n/a
50	rs568140925	chr8:68020918-68020919	Weak transcription Enhancers Genic enhancers Strong transcription ZNF genes & repeats	n/a	n/a	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
Hodgkin''s lymphoma	17606441	CNVD
Seminomas	18059402	CNVD
Autism	22495311	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
Acute lymphoblastic leukemia	22237106	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
primary effusion lymphomas	17116491	CNVD
Esophageal cancer	20955586	CNVD
Multiple myeloma	16461302	CNVD
abnormal development	18461090	CNVD
Cancer	20164920	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
Salivary gland tumor	18059337	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
Acute myeloid leukemia	21251322	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
Colorectal cancer	16272173	CNVD
Melanoma	22183965	CNVD
Cancer	21949371	CNVD
Non-small cell lung cancer	21829676	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
low-grade B-cell lymphoma tumor	18367492	CNVD
small cell lung cancer	20016488	CNVD
Sezary syndrome	18413736	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Breast cancer	17142309	CNVD
Glioblastoma multiforme	19115005	CNVD
head and neck squamous cell carcinoma	16715129	CNVD
Prostate cancer	16461572	CNVD
Pancreatic cancer	17952125	CNVD
Breast cancer	22522925	CNVD
Ovarian cancer	20844748	CNVD
Breast cancer	21399628	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Gastric cancer	22014070	CNVD
Osteosarcoma	21215367	CNVD

Chromatin state (count:2586 , 50 per page) page: 1 2 3 4 5 6 7 ... 52

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67977800-68021800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
2	chr8:67977800-68044000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
3	chr8:67978200-68074400	Weak transcription	Esophagus	oesophagus
4	chr8:67978400-68044800	Weak transcription	Brain Angular Gyrus	brain
5	chr8:67978400-68045600	Weak transcription	Placenta Amnion	Placenta Amnion
6	chr8:67978600-68031200	Weak transcription	Fetal Heart	heart
7	chr8:67978600-68074200	Weak transcription	Psoas Muscle	Psoas
8	chr8:67978800-68044200	Weak transcription	Colon Smooth Muscle	Colon
9	chr8:67986400-68045400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
10	chr8:67988200-68038800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
11	chr8:67988200-68074800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
12	chr8:67988400-68035000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
13	chr8:67990400-68074400	Weak transcription	Spleen	Spleen
14	chr8:67991000-68021400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr8:67991200-68035000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
16	chr8:67991800-68036800	Weak transcription	Sigmoid Colon	Sigmoid Colon
17	chr8:67993200-68044200	Weak transcription	Skeletal Muscle Male	skeletal muscle
18	chr8:67993400-68020800	Weak transcription	Lung	lung
19	chr8:67993400-68020800	Weak transcription	HSMMtube	muscle
20	chr8:67993400-68027600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
21	chr8:67993400-68044000	Weak transcription	Ovary	ovary
22	chr8:67993400-68085000	Weak transcription	Aorta	Aorta
23	chr8:67994200-68044200	Weak transcription	Stomach Smooth Muscle	stomach
24	chr8:67997000-68036800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
25	chr8:67999800-68031000	Weak transcription	Muscle Satellite Cultured Cells	--
26	chr8:68000400-68022600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
27	chr8:68000400-68031600	Weak transcription	Fetal Brain Female	brain
28	chr8:68000400-68035000	Weak transcription	Brain Inferior Temporal Lobe	brain
29	chr8:68000400-68037600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
30	chr8:68003800-68038600	Weak transcription	Duodenum Smooth Muscle	Duodenum
31	chr8:68004600-68021000	Weak transcription	Cortex derived primary cultured neurospheres	brain
32	chr8:68004800-68024400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
33	chr8:68005400-68038800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
34	chr8:68005800-68020400	Weak transcription	HSMM	muscle
35	chr8:68005800-68031200	Weak transcription	Hela-S3	cervix
36	chr8:68005800-68044400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
37	chr8:68006200-68029800	Weak transcription	HMEC	breast
38	chr8:68006400-68039200	Weak transcription	GM12878-XiMat	blood
39	chr8:68007400-68028600	Weak transcription	NHDF-Ad	bronchial
40	chr8:68008000-68040000	Weak transcription	NHLF	lung
41	chr8:68008000-68045600	Weak transcription	Rectal Smooth Muscle	rectum
42	chr8:68008000-68062400	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
43	chr8:68008200-68045400	Weak transcription	Fetal Brain Male	brain
44	chr8:68008400-68020800	Weak transcription	H1 Cell Line	embryonic stem cell
45	chr8:68008400-68020800	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
46	chr8:68008400-68020800	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
47	chr8:68008400-68021000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
48	chr8:68008400-68024600	Weak transcription	Placenta	Placenta
49	chr8:68008400-68029800	Weak transcription	HUES48 Cell Line	embryonic stem cell
50	chr8:68008400-68030400	Weak transcription	HUES6 Cell Line	embryonic stem cell

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