Variant report

Variant	nsv1032414
Chromosome Location	chr8:62789246-62861376
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:366)
Chromatin interactive
region (count:36)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:62791305-62791686	K562	blood:	n/a	n/a
2	ARID3A	chr8:62841642-62841850	K562	blood:	n/a	n/a
3	ARID3A	chr8:62826142-62826284	HepG2	liver:	n/a	n/a
4	ATF1	chr8:62852251-62852270	K562	blood:	n/a	n/a
5	ATF1	chr8:62841592-62841841	K562	blood:	n/a	n/a
6	ATF1	chr8:62791337-62791631	K562	blood:	n/a	n/a
7	ATF3	chr8:62826043-62826345	K562	blood:	n/a	n/a
8	BACH1	chr8:62789954-62790048	K562	blood:	n/a	n/a
9	BACH1	chr8:62789298-62789678	H1-hESC	embryonic stem cell:	n/a	chr8:62789501-62789515
10	BACH1	chr8:62789279-62789707	K562	blood:	n/a	chr8:62789501-62789515
11	BACH1	chr8:62841640-62841780	H1-hESC	embryonic stem cell:	n/a	n/a
12	BHLHE40	chr8:62844461-62844494	K562	blood:	n/a	n/a
13	BRCA1	chr8:62826026-62826395	Hela-S3	cervix:	n/a	n/a
14	CCNT2	chr8:62801939-62802180	K562	blood:	n/a	n/a
15	CEBPB	chr8:62789233-62789911	HCT-116	colon:	n/a	chr8:62789825-62789837
16	CEBPB	chr8:62826062-62826435	HepG2	liver:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
17	CEBPB	chr8:62826117-62826311	HepG2	liver:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
18	CEBPB	chr8:62794196-62794428	K562	blood:	n/a	n/a
19	CEBPB	chr8:62826118-62826406	HepG2	liver:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
20	CEBPB	chr8:62826082-62826392	A549	lung:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
21	CEBPB	chr8:62826103-62826449	A549	lung:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
22	CEBPB	chr8:62827072-62827128	HepG2	liver:	n/a	n/a
23	CEBPB	chr8:62826079-62826426	K562	blood:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
24	CEBPB	chr8:62801060-62801173	HepG2	liver:	n/a	chr8:62801132-62801143 chr8:62801134-62801143
25	CEBPB	chr8:62841665-62841729	H1-hESC	embryonic stem cell:	n/a	n/a
26	CEBPB	chr8:62826081-62826354	H1-hESC	embryonic stem cell:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
27	CEBPB	chr8:62826062-62826429	MCF-7	breast:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
28	CEBPB	chr8:62826040-62826449	HepG2	liver:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
29	CEBPB	chr8:62830978-62831066	A549	lung:	n/a	n/a
30	CEBPB	chr8:62826058-62826434	K562	blood:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
31	CEBPB	chr8:62809069-62809099	HepG2	liver:	n/a	chr8:62809082-62809093
32	CEBPB	chr8:62789337-62789694	Hela-S3	cervix:	n/a	n/a
33	CEBPB	chr8:62791277-62791517	K562	blood:	n/a	n/a
34	CEBPB	chr8:62826048-62826471	MCF-7	breast:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
35	CEBPB	chr8:62789235-62789763	HCT-116	colon:	n/a	n/a
36	CEBPB	chr8:62794193-62794409	HepG2	liver:	n/a	n/a
37	CEBPB	chr8:62825950-62826476	Hela-S3	cervix:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
38	CEBPB	chr8:62826006-62826427	K562	blood:	n/a	chr8:62826210-62826221 chr8:62826141-62826153 chr8:62826253-62826264
39	CHD2	chr8:62826022-62826380	Hela-S3	cervix:	n/a	n/a
40	CTCF	chr8:62841620-62841770	GM12867	blood:	n/a	n/a
41	CTCF	chr8:62841636-62841836	LNCaP	prostate:	n/a	n/a
42	CTCF	chr8:62841723-62841792	A549	lung:	n/a	n/a
43	CTCF	chr8:62841546-62841886	MCF-7	breast:	n/a	n/a
44	CTCF	chr8:62841680-62841830	HMF	breast:	n/a	n/a
45	CTCF	chr8:62841458-62842015	MCF-7	breast:	n/a	n/a
46	CTCF	chr8:62841640-62841790	SK-N-SH_RA	brain:	n/a	n/a
47	CTCF	chr8:62832111-62832170	HepG2	liver:	n/a	n/a
48	CTCF	chr8:62841640-62841790	HEK293	kidney:	n/a	n/a
49	CTCF	chr8:62841656-62841837	Gliobla	brain:	n/a	n/a
50	CTCF	chr8:62841640-62841790	HCPEpiC	choroid plexus:	n/a	n/a

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:62825339-62825389	SAEC	small airway:	n/a
2	chr8:62825339-62825389	HRPEpiC	eye:	n/a
3	chr8:62823894-62823944	MCF-7	breast:	n/a
4	chr8:62823815-62823865	HRPEpiC	eye:	n/a
5	chr8:62815595-62815645	HCF	heart:	n/a
6	chr8:62823833-62823883	HAEpiC	amniotic membrane:	n/a
7	chr8:62823833-62823883	A549	lung:	n/a
8	chr8:62823833-62823883	NB4	blood:	n/a
9	chr8:62815650-62815700	ovcar-3	ovarian:	n/a
10	chr8:62823894-62823944	GM12891	blood:	n/a
11	chr8:62823815-62823865	Jurkat	blood:	n/a
12	chr8:62823833-62823883	SK-N-SH_RA	brain:	n/a
13	chr8:62823894-62823944	PFSK-1	brain:	n/a
14	chr8:62825339-62825389	AG04449	skin:	fetal
15	chr8:62815650-62815700	SK-N-SH	brain:	n/a
16	chr8:62823815-62823865	HEEpiC	esophagus:	n/a
17	chr8:62825339-62825389	HEK293	kidney:	embryo
18	chr8:62823815-62823865	ovcar-3	ovarian:	n/a
19	chr8:62823894-62823944	U87	brain:	n/a
20	chr8:62815595-62815645	CMK	blood:	n/a
21	chr8:62825339-62825389	ovcar-3	ovarian:	n/a
22	chr8:62823833-62823883	HCPEpiC	choroid plexus:	n/a
23	chr8:62815650-62815700	ECC-1	luminal epithelium:	n/a
24	chr8:62823894-62823944	GM06990	blood:	n/a
25	chr8:62825339-62825389	HUVEC	blood vessel:	n/a
26	chr8:62823815-62823865	GM19239	blood:	n/a
27	chr8:62823833-62823883	AG09319	gingival:	n/a
28	chr8:62815595-62815645	HUVEC	blood vessel:	n/a
29	chr8:62823815-62823865	AG09309	skin:	n/a
30	chr8:62823833-62823883	Caco-2	colon:	n/a
31	chr8:62825339-62825389	Jurkat	blood:	n/a
32	chr8:62823815-62823865	K562	blood:	n/a
33	chr8:62825339-62825389	A549	lung:	n/a
34	chr8:62823894-62823944	HMEC	breast:	n/a
35	chr8:62823894-62823944	GM19239	blood:	n/a
36	chr8:62823894-62823944	HCT-116	colon:	n/a
37	chr8:62823833-62823883	H1-hESC	embryonic stem cell:	embryo
38	chr8:62815595-62815645	HCM	heart:	n/a
39	chr8:62823894-62823944	HCF	heart:	n/a
40	chr8:62825339-62825389	BJ	skin:	n/a
41	chr8:62823815-62823865	SKMC	muscle:	n/a
42	chr8:62823815-62823865	IMR90	lung:	fetal
43	chr8:62823815-62823865	AG04449	skin:	fetal
44	chr8:62815595-62815645	Jurkat	blood:	n/a
45	chr8:62815595-62815645	GM19239	blood:	n/a
46	chr8:62823833-62823883	K562	blood:	n/a
47	chr8:62825339-62825389	HCPEpiC	choroid plexus:	n/a
48	chr8:62823815-62823865	PrEC	prostate:	n/a
49	chr8:62815650-62815700	BE2_C	brain:	n/a
50	chr8:62815650-62815700	Hepatocyte	liver:	n/a

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

No.	Distal block	Cell Line	Cell type
1	chr8:62817790..62821820-chr8:62830855..62832666,3	K562	blood:
2	chr8:62599050..62601390-chr8:62788513..62790714,2	K562	blood:
3	chr8:62840941..62842961-chr8:62845678..62848368,2	K562	blood:
4	chr8:62800065..62803153-chr8:62804374..62807393,4	K562	blood:
5	chr8:62826515..62828032-chr8:62828299..62830698,2	MCF-7	breast:
6	chr8:62850703..62853092-chr8:62855919..62858366,2	K562	blood:
7	chr8:62799541..62801529-chr8:62809372..62812166,2	MCF-7	breast:
8	chr8:62851196..62853286-chr8:62860071..62862095,2	MCF-7	breast:
9	chr8:62840941..62842961-chr8:62845678..62848368,2	K562	blood:
10	chr8:62770464..62772123-chr8:62826774..62828899,2	K562	blood:
11	chr8:62781573..62783288-chr8:62786712..62789501,2	K562	blood:
12	chr8:62799541..62801529-chr8:62809372..62812166,2	MCF-7	breast:
13	chr8:62815283..62816844-chr8:62823393..62825914,2	K562	blood:
14	chr8:62847070..62849186-chr8:62851343..62853952,2	K562	blood:
15	chr8:62804137..62806853-chr8:62809046..62810581,2	K562	blood:
16	chr8:62830759..62832840-chr8:62836689..62840580,3	K562	blood:
17	chr8:62680044..62682717-chr8:62786976..62789790,2	K562	blood:
18	chr8:62823240..62824957-chr8:62833824..62836674,2	K562	blood:
19	chr8:62860250..62862698-chr8:62867692..62870141,2	K562	blood:
20	chr8:62826515..62828032-chr8:62828299..62830698,2	MCF-7	breast:
21	chr8:62845901..62847507-chr8:62883646..62886616,2	K562	blood:
22	chr8:62861198..62864190-chr8:62867423..62870141,2	K562	blood:
23	chr8:62850703..62853092-chr8:62855919..62858366,2	K562	blood:
24	chr8:62851592..62853559-chr8:62856440..62858366,2	K562	blood:
25	chr8:62851196..62853286-chr8:62860071..62862095,2	MCF-7	breast:
26	chr8:62851592..62853559-chr8:62856440..62858366,2	K562	blood:
27	chr8:62815283..62816844-chr8:62823393..62825914,2	K562	blood:
28	chr8:62678761..62681544-chr8:62788290..62791264,2	K562	blood:
29	chr8:62847070..62849186-chr8:62851343..62853952,2	K562	blood:
30	chr8:62806937..62809503-chr8:62843192..62845966,2	K562	blood:
31	chr8:62830759..62832840-chr8:62836689..62840580,3	K562	blood:
32	chr8:62806937..62809503-chr8:62843192..62845966,2	K562	blood:
33	chr8:62791156..62793257-chr8:62795639..62797220,2	K562	blood:
34	chr8:62817790..62821820-chr8:62830855..62832666,3	K562	blood:
35	chr8:62804137..62806853-chr8:62809046..62810581,2	K562	blood:
36	chr8:62790960..62793781-chr8:62797496..62800114,3	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-CLVS1-3	chr8:62797845-62798121	ENSG00000254119
2	lnc-CLVS1-3	chr8:62807045-62807294	NONHSAT126881
3	lnc-CLVS1-3	chr8:62807045-62807294	ENSG00000254119
4	lnc-ASPH-7	chr8:62841004-62841082	ucscGeneNc_uc003xut_2
5	lnc-ASPH-7	chr8:62834214-62836877	ucscGeneNc_uc003xut_2
6	lnc-NKAIN3-5	chr8:62802398-62802434	ENSG00000254120
7	lnc-CLVS1-3	chr8:62791441-62792336	ENSG00000254119
8	lnc-NKAIN3-5	chr8:62806676-62806765	ENSG00000254120
9	lnc-NKAIN3-5	chr8:62805262-62805400	ENSG00000254120
10	lnc-CLVS1-3	chr8:62797844-62798118	NONHSAT126881
11	lnc-NKAIN3-5	chr8:62805893-62806033	ENSG00000254120
12	lnc-CLVS1-3	chr8:62797845-62798104	XLOC_006817
13	lnc-CLVS1-3	chr8:62851896-62852093	ENSG00000254119
14	lnc-CLVS1-3	chr8:62856698-62856739	ENSG00000254119
15	lnc-CLVS1-3	chr8:62792248-62792336	NONHSAT126881
16	lnc-CLVS1-3	chr8:62797845-62798118	ENSG00000254119
17	lnc-CLVS1-3	chr8:62792248-62792336	ENSG00000254119
18	lnc-CLVS1-3	chr8:62835249-62835382	ENSG00000254119

No data

Variant related genes	Relation type
ENSG00000254120	TF binding region
ENSG00000253544	TF binding region
ENSG00000254119	TF binding region
ENSG00000254120	CpG island
ENSG00000253544	CpG island
ENSG00000254119	CpG island
ENSG00000254119	chromatin interactions
ENSG00000254120	chromatin interactions
ENSG00000253544	chromatin interactions

Extended variants
information (count: 1353 )
Associated
traits (count: 98 )

Variant overlapped rSNPs/rCNVs (count:1353 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs561021602	chr8:62789257-62789258	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
2	rs531717902	chr8:62789280-62789281	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
3	rs575313535	chr8:62789299-62789300	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
4	rs530332757	chr8:62789315-62789316	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
5	rs565125284	chr8:62789382-62789383	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
6	rs548435706	chr8:62789489-62789490	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
7	rs116588400	chr8:62789508-62789509	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
8	rs143803165	chr8:62789513-62789514	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
9	rs80232001	chr8:62789563-62789564	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
10	rs192644424	chr8:62789572-62789573	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
11	rs549219833	chr8:62789585-62789586	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
12	rs567307531	chr8:62789655-62789656	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
13	rs146835475	chr8:62789664-62789665	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
14	rs548604336	chr8:62789683-62789684	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
15	rs184746487	chr8:62789715-62789716	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
16	rs556261829	chr8:62789760-62789761	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
17	rs187601176	chr8:62789778-62789779	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
18	rs538653929	chr8:62789820-62789821	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
19	rs6471975	chr8:62789876-62789877	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
20	rs572428914	chr8:62789891-62789892	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
21	rs542768335	chr8:62789900-62789901	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
22	rs192610730	chr8:62789923-62789924	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
23	rs576617174	chr8:62789936-62789937	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
24	rs16928039	chr8:62789965-62789966	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
25	rs535056842	chr8:62789997-62789998	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
26	rs569956788	chr8:62790017-62790018	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
27	rs184835475	chr8:62790027-62790028	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
28	rs28695290	chr8:62790034-62790035	Enhancers	TF binding region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
29	rs113203133	chr8:62790038-62790039	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
30	rs377102056	chr8:62790044-62790045	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
31	rs189977907	chr8:62790101-62790102	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
32	rs113254100	chr8:62790150-62790151	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
33	rs540307208	chr8:62790192-62790193	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
34	rs56788946	chr8:62790193-62790194	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
35	rs200612811	chr8:62790194-62790195	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
36	rs397784181	chr8:62790219-62790220	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
37	rs538087756	chr8:62790223-62790224	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
38	rs549587903	chr8:62790263-62790264	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
39	rs377426310	chr8:62790289-62790290	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
40	rs571352910	chr8:62790293-62790294	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
41	rs181114616	chr8:62790357-62790358	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
42	rs371243954	chr8:62790407-62790408	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
43	rs140727301	chr8:62790414-62790415	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
44	rs184503789	chr8:62790454-62790455	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
45	rs144478989	chr8:62790500-62790501	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
46	rs145211538	chr8:62790501-62790502	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
47	rs80222413	chr8:62790522-62790523	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
48	rs113875162	chr8:62790529-62790530	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
49	rs544031314	chr8:62790563-62790564	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a
50	rs565202510	chr8:62790566-62790567	Enhancers	TF binding region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:98)

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
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
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
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
Colorectal cancer	21645411	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Gastric cancer	22014070	CNVD
Breast cancer	22522925	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:90 , 50 per page) page: 1 2

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:62787600-62791600	Enhancers	K562	blood
2	chr8:62788600-62790400	Enhancers	Hela-S3	cervix
3	chr8:62788800-62790600	Enhancers	Fetal Adrenal Gland	Adrenal Gland
4	chr8:62789200-62790400	Enhancers	Fetal Brain Male	brain
5	chr8:62789200-62790400	Enhancers	A549	lung
6	chr8:62789800-62791200	Enhancers	Primary hematopoietic stem cells short term culture	blood
7	chr8:62789800-62791800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
8	chr8:62790000-62790600	Enhancers	Primary monocytes fromperipheralblood	blood
9	chr8:62790000-62790600	Enhancers	Primary T helper naive cells fromperipheralblood	blood
10	chr8:62790000-62790600	Enhancers	Primary T helper cells PMA-I stimulated	--
11	chr8:62790000-62790600	Enhancers	Monocytes-CD14+_RO01746	blood
12	chr8:62790000-62790800	Enhancers	Dnd41	blood
13	chr8:62790000-62791400	Enhancers	Primary T helper cells fromperipheralblood	blood
14	chr8:62790000-62791600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
15	chr8:62790000-62792200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr8:62790200-62790600	Enhancers	Primary B cells from peripheral blood	blood
17	chr8:62790400-62790800	Enhancers	Primary T cells from cord blood	blood
18	chr8:62790600-62794000	Weak transcription	Monocytes-CD14+_RO01746	blood
19	chr8:62790600-62794200	Weak transcription	Primary monocytes fromperipheralblood	blood
20	chr8:62790600-62795000	Weak transcription	Primary B cells from peripheral blood	blood
21	chr8:62791200-62792200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr8:62791600-62794400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr8:62791800-62794200	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
24	chr8:62792200-62796000	Enhancers	Primary hematopoietic stem cells short term culture	blood
25	chr8:62794000-62795800	Enhancers	Monocytes-CD14+_RO01746	blood
26	chr8:62794200-62795800	Enhancers	Primary monocytes fromperipheralblood	blood
27	chr8:62794200-62795800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
28	chr8:62794400-62795800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
29	chr8:62794800-62795400	Enhancers	Primary neutrophils fromperipheralblood	blood
30	chr8:62795000-62795400	Enhancers	Primary B cells from peripheral blood	blood
31	chr8:62796000-62797000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
32	chr8:62798800-62799800	ZNF genes & repeats	Pancreas	Pancrea
33	chr8:62800800-62801000	Enhancers	K562	blood
34	chr8:62801000-62801800	Weak transcription	K562	blood
35	chr8:62801800-62802400	Enhancers	K562	blood
36	chr8:62803800-62804400	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
37	chr8:62811200-62812200	Enhancers	GM12878-XiMat	blood
38	chr8:62817800-62818000	Enhancers	Skeletal Muscle Male	skeletal muscle
39	chr8:62818200-62819000	Enhancers	Primary hematopoietic stem cells short term culture	blood
40	chr8:62823800-62824000	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
41	chr8:62823800-62824000	Enhancers	HUES6 Cell Line	embryonic stem cell
42	chr8:62823800-62824000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
43	chr8:62823800-62824600	Enhancers	H1 Cell Line	embryonic stem cell
44	chr8:62823800-62826200	Enhancers	HUES64 Cell Line	embryonic stem cell
45	chr8:62824000-62824200	Enhancers	ES-I3 Cell Line	embryonic stem cell
46	chr8:62824000-62824800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
47	chr8:62824000-62825000	Enhancers	iPS-20b Cell Line	embryonic stem cell
48	chr8:62824000-62826200	Enhancers	iPS-18 Cell Line	embryonic stem cell
49	chr8:62824000-62826400	Enhancers	iPS-15b Cell Line	embryonic stem cell
50	chr8:62824000-62826600	Enhancers	HUES48 Cell Line	embryonic stem cell

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