Variant report

Variant	nsv890944
Chromosome Location	chr8:61252500-61307115
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:162)
CpG islands
(count:61)
Chromatin interactive
region (count:44)
LncRNA
region (count:2)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:162 , 50 per page) page: 1 2 3 4

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ATF1	chr8:61297796-61297904	K562	blood:	n/a	n/a
2	ATF3	chr8:61260288-61260522	K562	blood:	n/a	n/a
3	BHLHE40	chr8:61289456-61289467	K562	blood:	n/a	n/a
4	CBX3	chr8:61267993-61268177	K562	blood:	n/a	n/a
5	CBX3	chr8:61267867-61268327	K562	blood:	n/a	n/a
6	CEBPB	chr8:61302213-61302347	K562	blood:	n/a	n/a
7	CEBPB	chr8:61292814-61293091	Hela-S3	cervix:	n/a	n/a
8	CEBPB	chr8:61292899-61293026	HepG2	liver:	n/a	n/a
9	CEBPB	chr8:61283281-61283583	A549	lung:	n/a	chr8:61283409-61283420
10	CEBPB	chr8:61283271-61283580	HepG2	liver:	n/a	chr8:61283409-61283420
11	CEBPB	chr8:61292803-61293103	A549	lung:	n/a	n/a
12	CEBPB	chr8:61305083-61305319	K562	blood:	n/a	n/a
13	CEBPB	chr8:61288025-61288035	H1-hESC	embryonic stem cell:	n/a	n/a
14	CEBPB	chr8:61285977-61286233	HepG2	liver:	n/a	chr8:61286135-61286148 chr8:61286135-61286146
15	CEBPB	chr8:61278372-61278387	K562	blood:	n/a	n/a
16	CEBPB	chr8:61285995-61286218	K562	blood:	n/a	chr8:61286135-61286148 chr8:61286135-61286146
17	CEBPB	chr8:61302193-61302345	HepG2	liver:	n/a	n/a
18	CEBPB	chr8:61283330-61283509	K562	blood:	n/a	chr8:61283409-61283420
19	CEBPB	chr8:61292204-61292375	K562	blood:	n/a	n/a
20	CEBPB	chr8:61257920-61258112	K562	blood:	n/a	n/a
21	CEBPB	chr8:61292929-61293046	K562	blood:	n/a	n/a
22	CEBPB	chr8:61283310-61283559	K562	blood:	n/a	chr8:61283409-61283420
23	CEBPB	chr8:61285997-61286254	A549	lung:	n/a	chr8:61286135-61286148 chr8:61286135-61286146
24	CEBPB	chr8:61283278-61283513	IMR90	lung:	n/a	chr8:61283409-61283420
25	CTCF	chr8:61278184-61278458	K562	blood:	n/a	n/a
26	CTCF	chr8:61304560-61304704	K562	blood:	n/a	n/a
27	CTCF	chr8:61278234-61278330	GM12878	blood:	n/a	n/a
28	CTCF	chr8:61300500-61300650	Hela-S3	cervix:	n/a	n/a
29	CTCF	chr8:61278283-61278325	K562	blood:	n/a	n/a
30	CTCF	chr8:61300499-61300539	NHEK	skin:	n/a	n/a
31	CTCF	chr8:61278240-61278390	RPTEC	kidney:	n/a	n/a
32	CTCF	chr8:61278259-61278319	Hela-S3	cervix:	n/a	n/a
33	CUX1	chr8:61273144-61273254	K562	blood:	n/a	n/a
34	CUX1	chr8:61292330-61292398	K562	blood:	n/a	n/a
35	E2F6	chr8:61260352-61260531	K562	blood:	n/a	n/a
36	ELF1	chr8:61290075-61290421	K562	blood:	n/a	n/a
37	EP300	chr8:61259981-61260112	K562	blood:	n/a	n/a
38	EP300	chr8:61292177-61292374	K562	blood:	n/a	n/a
39	FOS	chr8:61300960-61301129	MCF10A-Er-Src	breast:	n/a	chr8:61301032-61301043
40	FOS	chr8:61257929-61258121	MCF10A-Er-Src	breast:	n/a	n/a
41	FOS	chr8:61258058-61258076	MCF10A-Er-Src	breast:	n/a	n/a
42	FOS	chr8:61300939-61301225	MCF10A-Er-Src	breast:	n/a	chr8:61301032-61301043
43	FOS	chr8:61302338-61302448	MCF10A-Er-Src	breast:	n/a	n/a
44	FOS	chr8:61302285-61302389	MCF10A-Er-Src	breast:	n/a	chr8:61302329-61302338
45	FOS	chr8:61300780-61301330	HUVEC	blood vessel:	n/a	chr8:61301032-61301043
46	FOS	chr8:61301117-61301176	MCF10A-Er-Src	breast:	n/a	n/a
47	FOS	chr8:61283954-61284218	HUVEC	blood vessel:	n/a	chr8:61284096-61284104
48	FOS	chr8:61301734-61301847	MCF10A-Er-Src	breast:	n/a	chr8:61301818-61301828 chr8:61301818-61301828
49	FOS	chr8:61261311-61261861	HUVEC	blood vessel:	n/a	chr8:61261620-61261628 chr8:61261619-61261629 chr8:61261625-61261634 chr8:61261592-61261601 chr8:61261618-61261629
50	FOS	chr8:61273881-61274221	HUVEC	blood vessel:	n/a	chr8:61274128-61274139 chr8:61274046-61274054

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:61287425-61287475	AG10803	skin:	n/a
2	chr8:61287425-61287475	HNPCEpiC	eye:	n/a
3	chr8:61287425-61287475	PrEC	prostate:	n/a
4	chr8:61287425-61287475	Hela-S3	cervix:	n/a
5	chr8:61287425-61287475	BE2_C	brain:	n/a
6	chr8:61287425-61287475	NHBE	bronchial:	n/a
7	chr8:61287425-61287475	Jurkat	blood:	n/a
8	chr8:61287425-61287475	SAEC	small airway:	n/a
9	chr8:61287425-61287475	HCM	heart:	n/a
10	chr8:61287425-61287475	PANC-1	pancreas:	n/a
11	chr8:61287425-61287475	HAEpiC	amniotic membrane:	n/a
12	chr8:61287425-61287475	HEEpiC	esophagus:	n/a
13	chr8:61287425-61287475	GM12892	blood:	n/a
14	chr8:61287425-61287475	HepG2	liver:	n/a
15	chr8:61287425-61287475	HRPEpiC	eye:	n/a
16	chr8:61287425-61287475	NH-A	brain:	n/a
17	chr8:61287425-61287475	GM06990	blood:	n/a
18	chr8:61287425-61287475	HIPEpiC	eye:	n/a
19	chr8:61287425-61287475	NHDF-neo	bronchial:	n/a
20	chr8:61287425-61287475	HCF	heart:	n/a
21	chr8:61287425-61287475	GM12878	blood:	n/a
22	chr8:61287425-61287475	PFSK-1	brain:	n/a
23	chr8:61287425-61287475	HMEC	breast:	n/a
24	chr8:61287425-61287475	AG04450	lung:	fetal
25	chr8:61287425-61287475	SK-N-MC	brain:	n/a
26	chr8:61287425-61287475	NT2-D1	testis:	n/a
27	chr8:61287425-61287475	ovcar-3	ovarian:	n/a
28	chr8:61287425-61287475	HCPEpiC	choroid plexus:	n/a
29	chr8:61287425-61287475	Hepatocyte	liver:	n/a
30	chr8:61287425-61287475	SKMC	muscle:	n/a
31	chr8:61287425-61287475	HRCEpiC	kidney:	n/a
32	chr8:61287425-61287475	A549	lung:	n/a
33	chr8:61287425-61287475	U87	brain:	n/a
34	chr8:61287425-61287475	ECC-1	luminal epithelium:	n/a
35	chr8:61287425-61287475	GM12891	blood:	n/a
36	chr8:61287425-61287475	IMR90	lung:	fetal
37	chr8:61287425-61287475	MCF-7	breast:	n/a
38	chr8:61287425-61287475	RPTEC	kidney:	n/a
39	chr8:61287425-61287475	T-47D	breast:	n/a
40	chr8:61287425-61287475	AoSMC	blood vessel:	n/a
41	chr8:61287425-61287475	BJ	skin:	n/a
42	chr8:61287425-61287475	HCT-116	colon:	n/a
43	chr8:61287425-61287475	HUVEC	blood vessel:	n/a
44	chr8:61287425-61287475	HEK293	kidney:	embryo
45	chr8:61287425-61287475	HPAEpiC	pulmonary alveolar:	n/a
46	chr8:61287425-61287475	HRE	kidney:	n/a
47	chr8:61287425-61287475	ProgFib	skin:	n/a
48	chr8:61287425-61287475	Caco-2	colon:	n/a
49	chr8:61287425-61287475	CMK	blood:	n/a
50	chr8:61287425-61287475	H1-hESC	embryonic stem cell:	embryo

(count:44 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:61251384..61253665-chr8:61258867..61261259,2	K562	blood:
2	chr8:61296490..61298553-chr8:61300202..61301762,2	K562	blood:
3	chr8:61241908..61243740-chr8:61270614..61272294,2	K562	blood:
4	chr8:61300352..61302588-chr8:61303599..61306089,2	K562	blood:
5	chr8:61191611..61196485-chr8:61259734..61262031,5	K562	blood:
6	chr8:61190830..61195522-chr8:61256061..61261664,6	K562	blood:
7	chr8:61193005..61195471-chr8:61301393..61304721,3	K562	blood:
8	chr8:61300352..61302588-chr8:61303599..61306089,2	K562	blood:
9	chr8:61304106..61306671-chr8:61306892..61309869,2	K562	blood:
10	chr8:61179873..61181465-chr8:61258527..61261260,2	K562	blood:
11	chr8:61296490..61298553-chr8:61300202..61301849,3	K562	blood:
12	chr8:61304106..61306671-chr8:61306892..61309869,2	K562	blood:
13	chr8:61259980..61263184-chr8:61267664..61270239,3	K562	blood:
14	chr8:61245428..61247239-chr8:61256258..61259423,3	K562	blood:
15	chr8:61192672..61195405-chr8:61273265..61277207,5	K562	blood:
16	chr8:61266542..61270541-chr8:61272293..61274774,4	K562	blood:
17	chr8:61189033..61190651-chr8:61266545..61268569,2	K562	blood:
18	chr8:61260960..61263184-chr8:61267664..61270239,2	K562	blood:
19	chr8:61256354..61259948-chr8:61262933..61264606,3	K562	blood:
20	chr8:61266542..61270541-chr8:61272293..61274774,4	K562	blood:
21	chr8:61296490..61298553-chr8:61300202..61301762,2	K562	blood:
22	chr8:61287951..61290172-chr8:61291680..61294053,2	K562	blood:
23	chr8:61280699..61283583-chr8:61285097..61287207,2	K562	blood:
24	chr8:61183511..61185456-chr8:61289764..61291425,2	K562	blood:
25	chr8:61193398..61195148-chr8:61271276..61273484,2	K562	blood:
26	chr8:61251384..61253665-chr8:61258867..61261259,2	K562	blood:
27	chr8:61193886..61195404-chr8:61293278..61295181,2	K562	blood:
28	chr8:61191872..61194078-chr8:61288420..61290358,3	K562	blood:
29	chr8:61291623..61293147-chr8:61298971..61301324,2	K562	blood:
30	chr8:61181201..61184970-chr8:61306411..61309605,3	K562	blood:
31	chr8:61191127..61193957-chr8:61268108..61271053,2	K562	blood:
32	chr8:61296490..61298553-chr8:61300202..61301849,3	K562	blood:
33	chr8:61260960..61263184-chr8:61267664..61270239,2	K562	blood:
34	chr8:61192508..61194247-chr8:61259111..61261374,2	MCF-7	breast:
35	chr8:61281417..61283995-chr8:61287741..61289563,2	K562	blood:
36	chr8:61280699..61283583-chr8:61285097..61287207,2	K562	blood:
37	chr8:61185497..61188035-chr8:61257935..61259723,3	K562	blood:
38	chr8:61193047..61196304-chr8:61273740..61277802,5	K562	blood:
39	chr8:61259980..61263184-chr8:61267664..61270239,3	K562	blood:
40	chr8:61287951..61290172-chr8:61291680..61294053,2	K562	blood:
41	chr8:61281417..61283995-chr8:61287741..61289563,2	K562	blood:
42	chr8:61191831..61193372-chr8:61284634..61287151,2	K562	blood:
43	chr8:61191853..61195079-chr8:61287519..61291871,6	K562	blood:
44	chr8:61256354..61259948-chr8:61262933..61264606,3	K562	blood:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CA8-3	chr8:61297147-61297224	ENSG00000251396
2	lnc-CA8-3	chr8:61297766-61297965	ENSG00000251396

No data

Variant related genes	Relation type
PDCL3P1	TF binding region
PDCL3P1	CpG island
ENSG00000178538	chromatin interactions
ENSG00000226301	chromatin interactions
GATA6	miRNA target sites
NLK	miRNA target sites

Extended variants
information (count: 1554 )
Associated
traits (count: 97 )

Variant overlapped rSNPs/rCNVs (count:1554 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568007221	chr8:61256122-61256123	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs549882769	chr8:61256144-61256145	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs527616898	chr8:61256176-61256177	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs571598235	chr8:61256181-61256182	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs538695197	chr8:61256201-61256202	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs527293327	chr8:61256228-61256229	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs372785348	chr8:61256230-61256231	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs549225713	chr8:61256277-61256278	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs566377214	chr8:61256334-61256335	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs536800639	chr8:61256341-61256342	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs555216276	chr8:61256342-61256343	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs540992442	chr8:61256366-61256367	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs187443579	chr8:61256433-61256434	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs140598818	chr8:61256440-61256441	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs116349637	chr8:61256473-61256474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs570372059	chr8:61256504-61256505	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs556019112	chr8:61256568-61256569	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs577557718	chr8:61256579-61256580	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs544725528	chr8:61256589-61256590	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs559970127	chr8:61256625-61256626	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs191469128	chr8:61256651-61256652	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs115139027	chr8:61256666-61256667	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs372945942	chr8:61256669-61256670	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs182652589	chr8:61256673-61256674	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs79614447	chr8:61256776-61256777	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs555992654	chr8:61256806-61256807	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs114147796	chr8:61256807-61256808	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs565279903	chr8:61256810-61256811	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs532487647	chr8:61256902-61256903	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs114588701	chr8:61256905-61256906	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs373225475	chr8:61256984-61256985	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs13279521	chr8:61256999-61257000	Inactive region	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
33	rs79721183	chr8:61257047-61257048	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs530437570	chr8:61257062-61257063	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs373252074	chr8:61257083-61257084	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs142129061	chr8:61257117-61257118	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs548927303	chr8:61257122-61257123	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs570215676	chr8:61257157-61257158	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs555242628	chr8:61257158-61257159	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs35177734	chr8:61257179-61257180	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs201298879	chr8:61257228-61257229	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs556220627	chr8:61257263-61257264	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs571259448	chr8:61257264-61257265	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs187343293	chr8:61257295-61257296	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs553368694	chr8:61257302-61257303	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs146600350	chr8:61257332-61257333	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs112530104	chr8:61257425-61257426	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs112587921	chr8:61257463-61257464	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs375438059	chr8:61257466-61257467	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs150268671	chr8:61257473-61257474	Inactive region	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:97)

Disease	PMID	Source
Cancer	16751803	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
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
Disorders of sex development	21048976	CNVD
Testicular cancer	18059402	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Salivary gland tumor	18059337	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
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
Ewing''s sarcoma	17952124	CNVD
Urothelial carcinoma	21177765	CNVD
small cell lung cancer	20016488	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
Prostate cancer	16461572	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
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Colorectal cancer	21645411	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
Adenocarcinoma	21044232	CNVD
Squamous cell cancer	20885788	CNVD
Schizophrenia	23813976	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:187 , 50 per page) page: 1 2 3 4

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:61257600-61257800	Enhancers	Monocytes-CD14+_RO01746	blood
2	chr8:61257800-61258600	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
3	chr8:61257800-61262400	Enhancers	Primary monocytes fromperipheralblood	blood
4	chr8:61258600-61260200	Enhancers	Monocytes-CD14+_RO01746	blood
5	chr8:61259200-61259400	Enhancers	K562	blood
6	chr8:61259200-61259600	Enhancers	Fetal Stomach	stomach
7	chr8:61259400-61260000	Weak transcription	K562	blood
8	chr8:61259600-61260000	Weak transcription	Fetal Stomach	stomach
9	chr8:61260000-61260600	Enhancers	Fetal Stomach	stomach
10	chr8:61260000-61260800	Enhancers	K562	blood
11	chr8:61260200-61260800	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
12	chr8:61260400-61261000	Enhancers	HUVEC	blood vessel
13	chr8:61260800-61261400	Enhancers	Monocytes-CD14+_RO01746	blood
14	chr8:61261000-61261400	Flanking Active TSS	HUVEC	blood vessel
15	chr8:61261000-61261800	Enhancers	Primary hematopoietic stem cells short term culture	blood
16	chr8:61261400-61262000	Flanking Active TSS	Monocytes-CD14+_RO01746	blood
17	chr8:61261400-61263800	Enhancers	HUVEC	blood vessel
18	chr8:61262000-61262400	Enhancers	Monocytes-CD14+_RO01746	blood
19	chr8:61268000-61268200	Bivalent/Poised TSS	H1 Derived Mesenchymal Stem Cells	ES cell derived
20	chr8:61270400-61270600	Active TSS	ES-UCSF4 Cell Line	embryonic stem cell
21	chr8:61272400-61273400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr8:61272600-61273000	Enhancers	Pancreatic Islets	Pancreatic Islet
23	chr8:61273600-61274400	Enhancers	HUVEC	blood vessel
24	chr8:61281600-61281800	Enhancers	K562	blood
25	chr8:61281800-61282600	Weak transcription	K562	blood
26	chr8:61282600-61282800	Enhancers	K562	blood
27	chr8:61282800-61289200	Weak transcription	K562	blood
28	chr8:61283600-61284200	Enhancers	Primary T cells from cord blood	blood
29	chr8:61283600-61284200	Enhancers	Fetal Thymus	thymus
30	chr8:61284000-61284200	Enhancers	Primary hematopoietic stem cells	blood
31	chr8:61284000-61284400	Enhancers	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
32	chr8:61284200-61284400	Enhancers	ES-I3 Cell Line	embryonic stem cell
33	chr8:61284200-61286800	Weak transcription	Fetal Thymus	thymus
34	chr8:61284400-61285600	Weak transcription	Primary hematopoietic stem cells	blood
35	chr8:61284400-61293600	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
36	chr8:61285600-61286600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
37	chr8:61285600-61286800	Enhancers	Primary hematopoietic stem cells short term culture	blood
38	chr8:61285600-61289400	Enhancers	Primary hematopoietic stem cells	blood
39	chr8:61285800-61286200	Enhancers	HUES6 Cell Line	embryonic stem cell
40	chr8:61285800-61286600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
41	chr8:61286000-61287400	Enhancers	HUVEC	blood vessel
42	chr8:61286200-61286600	Weak transcription	HUES6 Cell Line	embryonic stem cell
43	chr8:61286400-61286800	Weak transcription	ES-I3 Cell Line	embryonic stem cell
44	chr8:61286400-61287400	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr8:61286600-61287000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Female	--
46	chr8:61286600-61287000	Enhancers	Monocytes-CD14+_RO01746	blood
47	chr8:61286600-61287200	Enhancers	HUES6 Cell Line	embryonic stem cell
48	chr8:61286600-61287400	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
49	chr8:61286800-61287000	Flanking Active TSS	Primary hematopoietic stem cells short term culture	blood
50	chr8:61286800-61287000	Enhancers	Spleen	Spleen

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