Variant report

Variant	nsv1022561
Chromosome Location	chr8:68011159-68129755
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:528)
CpG islands
(count:308)
Chromatin interactive
region (count:74)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:4)

(count:528 , 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	chr8:68032334-68032484	K562	blood:	n/a	n/a
2	ARID3A	chr8:68065780-68065880	K562	blood:	n/a	n/a
3	ARID3A	chr8:68026510-68027171	K562	blood:	n/a	n/a
4	ARID3A	chr8:68022007-68022483	K562	blood:	n/a	n/a
5	ATF1	chr8:68022028-68022347	K562	blood:	n/a	n/a
6	ATF2	chr8:68108339-68108875	GM12878	blood:	n/a	n/a
7	ATF2	chr8:68108470-68108909	GM12878	blood:	n/a	n/a
8	BACH1	chr8:68013863-68013960	H1-hESC	embryonic stem cell:	n/a	n/a
9	BATF	chr8:68071443-68071797	GM12878	blood:	n/a	n/a
10	BATF	chr8:68108487-68108823	GM12878	blood:	n/a	n/a
11	BHLHE40	chr8:68021797-68022409	K562	blood:	n/a	n/a
12	BRCA1	chr8:68107483-68107530	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr8:68021765-68022411	K562	blood:	n/a	n/a
14	CBX3	chr8:68021929-68022308	K562	blood:	n/a	n/a
15	CCNT2	chr8:68026748-68027196	K562	blood:	n/a	n/a
16	CCNT2	chr8:68021959-68022495	K562	blood:	n/a	n/a
17	CEBPB	chr8:68044396-68044716	IMR90	lung:	n/a	chr8:68044543-68044554
18	CEBPB	chr8:68053800-68053928	H1-hESC	embryonic stem cell:	n/a	n/a
19	CEBPB	chr8:68093918-68094118	HepG2	liver:	n/a	chr8:68093982-68093993
20	CEBPB	chr8:68049232-68049274	K562	blood:	n/a	n/a
21	CEBPB	chr8:68057093-68057349	IMR90	lung:	n/a	chr8:68057257-68057268
22	CEBPB	chr8:68124637-68124953	HepG2	liver:	n/a	chr8:68124764-68124775
23	CEBPB	chr8:68044385-68044681	Hela-S3	cervix:	n/a	chr8:68044543-68044554
24	CEBPB	chr8:68053792-68053906	K562	blood:	n/a	n/a
25	CEBPB	chr8:68093857-68094132	A549	lung:	n/a	chr8:68093982-68093993
26	CEBPB	chr8:68124660-68124993	H1-hESC	embryonic stem cell:	n/a	chr8:68124764-68124775
27	CEBPB	chr8:68044365-68044733	HepG2	liver:	n/a	chr8:68044543-68044554
28	CEBPB	chr8:68057085-68057376	H1-hESC	embryonic stem cell:	n/a	chr8:68057257-68057268
29	CEBPB	chr8:68076544-68076875	A549	lung:	n/a	chr8:68076724-68076735
30	CEBPB	chr8:68057084-68057433	K562	blood:	n/a	chr8:68057257-68057268
31	CEBPB	chr8:68021700-68022376	K562	blood:	n/a	n/a
32	CEBPB	chr8:68057094-68057354	Hela-S3	cervix:	n/a	chr8:68057257-68057268
33	CEBPB	chr8:68108158-68108438	HepG2	liver:	n/a	chr8:68108263-68108274
34	CEBPB	chr8:68040311-68040611	IMR90	lung:	n/a	n/a
35	CEBPB	chr8:68044368-68044721	A549	lung:	n/a	chr8:68044543-68044554
36	CEBPB	chr8:68125765-68125766	H1-hESC	embryonic stem cell:	n/a	n/a
37	CEBPB	chr8:68105777-68106006	HepG2	liver:	n/a	n/a
38	CEBPB	chr8:68108163-68108462	Hela-S3	cervix:	n/a	chr8:68108263-68108274
39	CEBPB	chr8:68108138-68108770	IMR90	lung:	n/a	chr8:68108263-68108274
40	CEBPB	chr8:68129493-68129725	A549	lung:	n/a	n/a
41	CEBPB	chr8:68044398-68044717	MCF-7	breast:	n/a	chr8:68044543-68044554
42	CEBPB	chr8:68129459-68129766	HepG2	liver:	n/a	n/a
43	CEBPB	chr8:68021686-68022377	K562	blood:	n/a	n/a
44	CEBPB	chr8:68021723-68021959	K562	blood:	n/a	n/a
45	CEBPB	chr8:68044426-68044629	HepG2	liver:	n/a	chr8:68044543-68044554
46	CEBPB	chr8:68057090-68057352	HepG2	liver:	n/a	chr8:68057257-68057268
47	CEBPB	chr8:68057096-68057354	A549	lung:	n/a	chr8:68057257-68057268
48	CEBPB	chr8:68022022-68022340	K562	blood:	n/a	n/a
49	CEBPB	chr8:68057162-68057407	MCF-7	breast:	n/a	chr8:68057257-68057268
50	CEBPB	chr8:68065864-68065964	K562	blood:	n/a	chr8:68065878-68065891

(count:308 , 50 per page) page: 1 2 3 4 5 6 7

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:68080400-68080450	HepG2	liver:	n/a
2	chr8:68110902-68110952	H1-hESC	embryonic stem cell:	embryo
3	chr8:68125092-68125142	SAEC	small airway:	n/a
4	chr8:68080400-68080450	HepG2	liver:	n/a
5	chr8:68110902-68110952	H1-hESC	embryonic stem cell:	embryo
6	chr8:68125092-68125142	SAEC	small airway:	n/a
7	chr8:68110902-68110952	HCM	heart:	n/a
8	chr8:68107083-68107133	AG09309	skin:	n/a
9	chr8:68022262-68022312	NB4	blood:	n/a
10	chr8:68110902-68110952	SK-N-MC	brain:	n/a
11	chr8:68125092-68125142	HRE	kidney:	n/a
12	chr8:68125092-68125142	AoSMC	blood vessel:	n/a
13	chr8:68022262-68022312	AG04449	skin:	fetal
14	chr8:68080400-68080450	U87	brain:	n/a
15	chr8:68080400-68080450	PFSK-1	brain:	n/a
16	chr8:68107083-68107133	HEEpiC	esophagus:	n/a
17	chr8:68022262-68022312	HAEpiC	amniotic membrane:	n/a
18	chr8:68022262-68022312	PANC-1	pancreas:	n/a
19	chr8:68110902-68110952	HEEpiC	esophagus:	n/a
20	chr8:68080400-68080450	HCF	heart:	n/a
21	chr8:68022262-68022312	LNCaP	prostate:	n/a
22	chr8:68110902-68110952	AG10803	skin:	n/a
23	chr8:68080400-68080450	SK-N-SH_RA	brain:	n/a
24	chr8:68022262-68022312	PrEC	prostate:	n/a
25	chr8:68022262-68022312	AG10803	skin:	n/a
26	chr8:68110902-68110952	ProgFib	skin:	n/a
27	chr8:68125092-68125142	HNPCEpiC	eye:	n/a
28	chr8:68080400-68080450	PrEC	prostate:	n/a
29	chr8:68107083-68107133	SK-N-MC	brain:	n/a
30	chr8:68125092-68125142	SK-N-MC	brain:	n/a
31	chr8:68125092-68125142	HRCEpiC	kidney:	n/a
32	chr8:68125092-68125142	HL-60	blood:	n/a
33	chr8:68022262-68022312	HRCEpiC	kidney:	n/a
34	chr8:68107083-68107133	SAEC	small airway:	n/a
35	chr8:68022262-68022312	K562	blood:	n/a
36	chr8:68080400-68080450	HRE	kidney:	n/a
37	chr8:68107083-68107133	LNCaP	prostate:	n/a
38	chr8:68125092-68125142	HCT-116	colon:	n/a
39	chr8:68125092-68125142	SK-N-SH	brain:	n/a
40	chr8:68110902-68110952	PrEC	prostate:	n/a
41	chr8:68125092-68125142	HMEC	breast:	n/a
42	chr8:68022262-68022312	GM19239	blood:	n/a
43	chr8:68125092-68125142	HAEpiC	amniotic membrane:	n/a
44	chr8:68125092-68125142	LNCaP	prostate:	n/a
45	chr8:68107083-68107133	HL-60	blood:	n/a
46	chr8:68080400-68080450	BE2_C	brain:	n/a
47	chr8:68022262-68022312	SKMC	muscle:	n/a
48	chr8:68107083-68107133	HEK293	kidney:	embryo
49	chr8:68022262-68022312	HCT-116	colon:	n/a
50	chr8:68110902-68110952	AG04449	skin:	fetal

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

No.	Distal block	Cell Line	Cell type
1	chr8:68059036..68061219-chr8:68063581..68066022,2	K562	blood:
2	chr8:68053402..68056915-chr8:68068462..68071572,3	K562	blood:
3	chr8:68059036..68061219-chr8:68063581..68066022,2	K562	blood:
4	chr8:68112732..68114911-chr8:68116863..68119997,3	K562	blood:
5	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
6	chr8:68054368..68056716-chr8:68058153..68060696,2	K562	blood:
7	chr8:68103791..68106483-chr8:68107302..68110332,3	K562	blood:
8	chr8:68049843..68052686-chr8:68057977..68059611,2	K562	blood:
9	chr8:68038512..68041443-chr8:68043392..68045199,2	MCF-7	breast:
10	chr2:88315577..88316138-chr8:68058073..68058573,2	MCF-7	breast:
11	chr8:68049843..68052686-chr8:68057977..68059611,2	K562	blood:
12	chr8:68019882..68024149-chr8:68024565..68029760,5	K562	blood:
13	chr8:67973913..67977272-chr8:68024656..68026462,3	K562	blood:
14	chr8:68086366..68088943-chr8:68089390..68092288,2	K562	blood:
15	chr8:68040930..68042442-chr8:68048471..68050684,2	K562	blood:
16	chr8:68024722..68026418-chr8:68028615..68030810,2	K562	blood:
17	chr8:68040015..68041733-chr8:68043068..68045142,2	MCF-7	breast:
18	chr8:68085116..68087997-chr8:68090501..68093415,2	MCF-7	breast:
19	chr8:68054368..68056716-chr8:68058153..68060696,2	K562	blood:
20	chr8:68106793..68109723-chr8:68110037..68111833,2	K562	blood:
21	chr8:68106563..68108558-chr8:68112555..68114203,2	K562	blood:
22	chr8:68112732..68114911-chr8:68116863..68119997,3	K562	blood:
23	chr8:68019207..68022568-chr8:68026729..68029590,3	K562	blood:
24	chr8:68024722..68026418-chr8:68028615..68030810,2	K562	blood:
25	chr8:68021467..68023804-chr8:68064580..68067516,2	K562	blood:
26	chr8:68098861..68101473-chr8:68104225..68105893,2	MCF-7	breast:
27	chr8:68093632..68095325-chr8:68098007..68100821,2	K562	blood:
28	chr8:68093632..68095325-chr8:68098007..68100821,2	K562	blood:
29	chr8:67972943..67975596-chr8:68018499..68020394,2	MCF-7	breast:
30	chr8:68034598..68037205-chr8:68038455..68041133,2	MCF-7	breast:
31	chr8:67971594..67973615-chr8:68104400..68106393,2	MCF-7	breast:
32	chr8:68127338..68130278-chr8:68135594..68139376,3	K562	blood:
33	chr8:68103451..68106399-chr8:68110061..68112606,2	MCF-7	breast:
34	chr8:68103451..68106399-chr8:68110061..68112606,2	MCF-7	breast:
35	chr8:68068690..68070292-chr8:68071142..68074042,2	K562	blood:
36	chr8:68086366..68088943-chr8:68089390..68092288,2	K562	blood:
37	chr8:67976649..67978941-chr8:68093929..68095807,2	K562	blood:
38	chr8:67833716..67836650-chr8:68108377..68110562,2	K562	blood:
39	chr8:68106793..68109723-chr8:68110037..68111833,2	K562	blood:
40	chr8:68086057..68088943-chr8:68089390..68093675,3	K562	blood:
41	chr8:68040930..68042442-chr8:68048471..68050684,2	K562	blood:
42	chr8:68086057..68088943-chr8:68089390..68093675,3	K562	blood:
43	chr8:68030814..68032510-chr8:68038981..68041972,2	K562	blood:
44	chr8:67835666..67838767-chr8:68102969..68106135,3	K562	blood:
45	chr8:68066129..68069885-chr8:68074156..68076683,4	K562	blood:
46	chr8:68111984..68114620-chr8:68117011..68118931,2	K562	blood:
47	chr8:67973427..67978093-chr8:68011189..68018690,8	K562	blood:
48	chr8:67835610..67837690-chr8:68125017..68126904,2	K562	blood:
49	chr8:68074799..68076714-chr8:68078840..68080441,2	K562	blood:
50	chr8:68103791..68106410-chr8:68107302..68110578,4	K562	blood:

No data

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

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

Variant related genes	Relation type
CSPP1	TF binding region
RNA5SP268	TF binding region
ARFGEF1	TF binding region
ENSG00000250869	TF binding region
CSPP1	CpG island
RNA5SP268	CpG island
ARFGEF1	CpG island
ENSG00000250869	CpG island
ENSG00000104218	chromatin interactions
ENSG00000254341	chromatin interactions
ENSG00000121022	chromatin interactions
ENSG00000066777	chromatin interactions
ENSG00000266491	chromatin interactions
ENSG00000222724	chromatin interactions
ENSG00000245910	chromatin interactions

Extended variants
information (count: 3936 )
Associated
traits (count: 110 )

Variant overlapped rSNPs/rCNVs (count:3936 , 50 per page) page: 1 2 3 4 5 6 7 ... 79

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs74385209	chr8:68011197-68011198	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
2	rs544693498	chr8:68011220-68011221	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
3	rs564293939	chr8:68011222-68011223	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
4	rs533376452	chr8:68011253-68011254	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
5	rs546709949	chr8:68011298-68011299	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
6	rs529286420	chr8:68011322-68011323	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
7	rs531209210	chr8:68011323-68011324	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
8	rs552600736	chr8:68011342-68011343	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
9	rs571183532	chr8:68011362-68011363	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
10	rs186168188	chr8:68011422-68011423	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
11	rs549128065	chr8:68011424-68011425	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
12	rs190641327	chr8:68011453-68011454	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
13	rs151202709	chr8:68011505-68011506	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
14	rs369650973	chr8:68011601-68011602	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
15	rs532003926	chr8:68011621-68011622	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs547036419	chr8:68011723-68011724	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs28368501	chr8:68011779-68011780	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs565415674	chr8:68011836-68011837	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
19	rs570488114	chr8:68011983-68011984	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs374810668	chr8:68012039-68012040	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs539398137	chr8:68012056-68012057	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs184090296	chr8:68012085-68012086	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs188587774	chr8:68012133-68012134	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs573165022	chr8:68012143-68012144	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs535757239	chr8:68012160-68012161	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs535301270	chr8:68012196-68012197	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs192327934	chr8:68012202-68012203	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs564146821	chr8:68012226-68012227	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs575530580	chr8:68012270-68012271	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs544343291	chr8:68012281-68012282	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs141325796	chr8:68012330-68012331	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
32	rs578052976	chr8:68012396-68012397	Weak transcription	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs116784395	chr8:68012403-68012404	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs549455783	chr8:68012424-68012425	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs576446275	chr8:68012473-68012474	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs182990014	chr8:68012492-68012493	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs146973301	chr8:68012558-68012559	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs554308614	chr8:68012647-68012648	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs16933158	chr8:68012703-68012704	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs562709240	chr8:68012778-68012779	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs13278242	chr8:68012836-68012837	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
42	rs551715980	chr8:68012840-68012841	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
43	rs533931209	chr8:68012843-68012844	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
44	rs570523521	chr8:68012895-68012896	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
45	rs539199395	chr8:68012939-68012940	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
46	rs546578808	chr8:68012965-68012966	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
47	rs151195579	chr8:68013024-68013025	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
48	rs566476869	chr8:68013041-68013042	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
49	rs562090907	chr8:68013065-68013066	Weak transcription Enhancers	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
50	rs535717701	chr8:68013133-68013134	Weak transcription Enhancers	Chromatin interactive region	2 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
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:2656 , 50 per page) page: 1 2 3 4 5 6 7 ... 54

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:67977800-68013800	Weak transcription	Primary neutrophils fromperipheralblood	blood
2	chr8:67977800-68021800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
3	chr8:67977800-68044000	Weak transcription	Primary T cells effector/memory enriched fromperipheralblood	blood
4	chr8:67978000-68012200	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
5	chr8:67978200-68012600	Weak transcription	HUVEC	blood vessel
6	chr8:67978200-68074400	Weak transcription	Esophagus	oesophagus
7	chr8:67978400-68044800	Weak transcription	Brain Angular Gyrus	brain
8	chr8:67978400-68045600	Weak transcription	Placenta Amnion	Placenta Amnion
9	chr8:67978600-68031200	Weak transcription	Fetal Heart	heart
10	chr8:67978600-68074200	Weak transcription	Psoas Muscle	Psoas
11	chr8:67978800-68044200	Weak transcription	Colon Smooth Muscle	Colon
12	chr8:67979400-68013200	Weak transcription	Pancreas	Pancrea
13	chr8:67986400-68045400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
14	chr8:67988200-68014000	Weak transcription	Primary T helper memory cells from peripheral blood 2	blood
15	chr8:67988200-68038800	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
16	chr8:67988200-68074800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
17	chr8:67988400-68035000	Weak transcription	Primary T helper naive cells from peripheral blood	blood
18	chr8:67990400-68074400	Weak transcription	Spleen	Spleen
19	chr8:67991000-68021400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr8:67991200-68011400	Weak transcription	Fetal Intestine Small	intestine
21	chr8:67991200-68035000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
22	chr8:67991800-68036800	Weak transcription	Sigmoid Colon	Sigmoid Colon
23	chr8:67993200-68044200	Weak transcription	Skeletal Muscle Male	skeletal muscle
24	chr8:67993400-68020800	Weak transcription	Lung	lung
25	chr8:67993400-68020800	Weak transcription	HSMMtube	muscle
26	chr8:67993400-68027600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
27	chr8:67993400-68044000	Weak transcription	Ovary	ovary
28	chr8:67993400-68085000	Weak transcription	Aorta	Aorta
29	chr8:67994200-68044200	Weak transcription	Stomach Smooth Muscle	stomach
30	chr8:67997000-68036800	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr8:67999800-68031000	Weak transcription	Muscle Satellite Cultured Cells	--
32	chr8:68000400-68022600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
33	chr8:68000400-68031600	Weak transcription	Fetal Brain Female	brain
34	chr8:68000400-68035000	Weak transcription	Brain Inferior Temporal Lobe	brain
35	chr8:68000400-68037600	Weak transcription	Primary T helper naive cells fromperipheralblood	blood
36	chr8:68003800-68038600	Weak transcription	Duodenum Smooth Muscle	Duodenum
37	chr8:68004600-68021000	Weak transcription	Cortex derived primary cultured neurospheres	brain
38	chr8:68004800-68024400	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr8:68005400-68011400	Weak transcription	Fetal Intestine Large	intestine
40	chr8:68005400-68038800	Weak transcription	Primary mononuclear cells fromperipheralblood	Blood
41	chr8:68005800-68011400	Weak transcription	NHEK	skin
42	chr8:68005800-68020400	Weak transcription	HSMM	muscle
43	chr8:68005800-68031200	Weak transcription	Hela-S3	cervix
44	chr8:68005800-68044400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
45	chr8:68006200-68029800	Weak transcription	HMEC	breast
46	chr8:68006400-68039200	Weak transcription	GM12878-XiMat	blood
47	chr8:68007000-68017200	Weak transcription	Fetal Stomach	stomach
48	chr8:68007400-68011400	Weak transcription	Fetal Kidney	kidney
49	chr8:68007400-68028600	Weak transcription	NHDF-Ad	bronchial
50	chr8:68008000-68013200	Weak transcription	Primary hematopoietic stem cells	blood

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