Variant report

Variant	nsv539629
Chromosome Location	chr8:60099776-60539141
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1565)
CpG islands
(count:488)
Chromatin interactive
region (count:38)
LncRNA
region (count:13)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1565 , 50 per page) page: 1 2 3 4 5 6 7 ... 32

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr8:60528040-60528060	K562	blood:	n/a	n/a
2	ARID3A	chr8:60255549-60255738	HepG2	liver:	n/a	n/a
3	ATF1	chr8:60160046-60160228	K562	blood:	n/a	n/a
4	ATF1	chr8:60517318-60517467	K562	blood:	n/a	n/a
5	ATF1	chr8:60173406-60173567	K562	blood:	n/a	n/a
6	ATF1	chr8:60468004-60468241	K562	blood:	n/a	n/a
7	ATF1	chr8:60174335-60174363	K562	blood:	n/a	n/a
8	ATF1	chr8:60131370-60131606	K562	blood:	n/a	n/a
9	ATF1	chr8:60158753-60159120	K562	blood:	n/a	n/a
10	ATF1	chr8:60228000-60228041	K562	blood:	n/a	n/a
11	ATF1	chr8:60522885-60522970	K562	blood:	n/a	n/a
12	ATF2	chr8:60176380-60176861	GM12878	blood:	n/a	n/a
13	ATF2	chr8:60173404-60173807	GM12878	blood:	n/a	n/a
14	ATF2	chr8:60173239-60173820	GM12878	blood:	n/a	n/a
15	ATF2	chr8:60194981-60195604	GM12878	blood:	n/a	n/a
16	ATF2	chr8:60489320-60489706	GM12878	blood:	n/a	n/a
17	ATF2	chr8:60195076-60195620	GM12878	blood:	n/a	n/a
18	ATF2	chr8:60176411-60176842	GM12878	blood:	n/a	n/a
19	ATF3	chr8:60467971-60468280	K562	blood:	n/a	n/a
20	BACH1	chr8:60359389-60359727	H1-hESC	embryonic stem cell:	n/a	n/a
21	BACH1	chr8:60529666-60529970	H1-hESC	embryonic stem cell:	n/a	n/a
22	BACH1	chr8:60359423-60359566	K562	blood:	n/a	n/a
23	BATF	chr8:60489407-60489752	GM12878	blood:	n/a	chr8:60489577-60489588
24	BATF	chr8:60187277-60187610	GM12878	blood:	n/a	chr8:60187462-60187473
25	BATF	chr8:60173369-60173728	GM12878	blood:	n/a	chr8:60173520-60173531 chr8:60173521-60173531
26	BATF	chr8:60195171-60195633	GM12878	blood:	n/a	chr8:60195399-60195410
27	BATF	chr8:60176485-60176759	GM12878	blood:	n/a	n/a
28	BATF	chr8:60217428-60217762	GM12878	blood:	n/a	n/a
29	BATF	chr8:60173363-60173740	GM12878	blood:	n/a	chr8:60173520-60173531 chr8:60173521-60173531
30	BATF	chr8:60187288-60187631	GM12878	blood:	n/a	chr8:60187462-60187473
31	BATF	chr8:60195119-60195554	GM12878	blood:	n/a	chr8:60195399-60195410
32	BATF	chr8:60176465-60176740	GM12878	blood:	n/a	n/a
33	BCL11A	chr8:60176433-60176775	GM12878	blood:	n/a	n/a
34	BCL11A	chr8:60195165-60195481	GM12878	blood:	n/a	n/a
35	BCL11A	chr8:60195111-60195602	GM12878	blood:	n/a	n/a
36	BCL11A	chr8:60173327-60173709	GM12878	blood:	n/a	chr8:60173523-60173532
37	BCL11A	chr8:60169246-60169486	GM12878	blood:	n/a	n/a
38	BCL11A	chr8:60176524-60176726	GM12878	blood:	n/a	n/a
39	BCL3	chr8:60489407-60489652	GM12878	blood:	n/a	n/a
40	BCLAF1	chr8:60173211-60173841	GM12878	blood:	n/a	chr8:60173523-60173532
41	BHLHE40	chr8:60173390-60173942	GM12878	blood:	n/a	n/a
42	BRCA1	chr8:60236380-60236386	H1-hESC	embryonic stem cell:	n/a	n/a
43	BRCA1	chr8:60205674-60205709	GM12878	blood:	n/a	n/a
44	CBX3	chr8:60529603-60530279	HCT-116	colon:	n/a	n/a
45	CBX3	chr8:60133143-60133389	K562	blood:	n/a	n/a
46	CBX3	chr8:60529630-60530309	HCT-116	colon:	n/a	n/a
47	CCNT2	chr8:60468005-60468205	K562	blood:	n/a	chr8:60468068-60468088
48	CCNT2	chr8:60217588-60217788	K562	blood:	n/a	n/a
49	CEBPB	chr8:60167257-60167505	HepG2	liver:	n/a	chr8:60167329-60167340 chr8:60167362-60167373
50	CEBPB	chr8:60152920-60153204	HepG2	liver:	n/a	n/a

(count:488 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr8:60444511-60444561	HRE	kidney:	n/a
2	chr8:60214275-60214325	HepG2	liver:	n/a
3	chr8:60444511-60444561	BJ	skin:	n/a
4	chr8:60218373-60218423	HepG2	liver:	n/a
5	chr8:60214275-60214325	HEEpiC	esophagus:	n/a
6	chr8:60251872-60251922	MCF10A-Er-Src	breast:	n/a
7	chr8:60214275-60214325	SK-N-MC	brain:	n/a
8	chr8:60218373-60218423	A549	lung:	n/a
9	chr8:60444511-60444561	HEEpiC	esophagus:	n/a
10	chr8:60214275-60214325	CMK	blood:	n/a
11	chr8:60537981-60538031	GM12891	blood:	n/a
12	chr8:60197574-60197624	LNCaP	prostate:	n/a
13	chr8:60214275-60214325	SAEC	small airway:	n/a
14	chr8:60224479-60224529	NH-A	brain:	n/a
15	chr8:60537981-60538031	MCF10A-Er-Src	breast:	n/a
16	chr8:60218373-60218423	Hela-S3	cervix:	n/a
17	chr8:60197574-60197624	HUVEC	blood vessel:	n/a
18	chr8:60444511-60444561	PANC-1	pancreas:	n/a
19	chr8:60537981-60538031	IMR90	lung:	fetal
20	chr8:60224479-60224529	ovcar-3	ovarian:	n/a
21	chr8:60218373-60218423	HPAEpiC	pulmonary alveolar:	n/a
22	chr8:60197574-60197624	PANC-1	pancreas:	n/a
23	chr8:60197574-60197624	A549	lung:	n/a
24	chr8:60537981-60538031	BJ	skin:	n/a
25	chr8:60444511-60444561	T-47D	breast:	n/a
26	chr8:60251872-60251922	HPAEpiC	pulmonary alveolar:	n/a
27	chr8:60224479-60224529	SAEC	small airway:	n/a
28	chr8:60218373-60218423	MCF10A-Er-Src	breast:	n/a
29	chr8:60214275-60214325	PANC-1	pancreas:	n/a
30	chr8:60537981-60538031	HRCEpiC	kidney:	n/a
31	chr8:60214275-60214325	GM12891	blood:	n/a
32	chr8:60197574-60197624	Jurkat	blood:	n/a
33	chr8:60214275-60214325	ProgFib	skin:	n/a
34	chr8:60444511-60444561	SK-N-SH	brain:	n/a
35	chr8:60537981-60538031	HCT-116	colon:	n/a
36	chr8:60444511-60444561	Hela-S3	cervix:	n/a
37	chr8:60537981-60538031	LNCaP	prostate:	n/a
38	chr8:60444511-60444561	NT2-D1	testis:	n/a
39	chr8:60214275-60214325	HRPEpiC	eye:	n/a
40	chr8:60197574-60197624	HRE	kidney:	n/a
41	chr8:60251872-60251922	ECC-1	luminal epithelium:	n/a
42	chr8:60214275-60214325	RPTEC	kidney:	n/a
43	chr8:60531025-60531075	H1-hESC	embryonic stem cell:	embryo
44	chr8:60251872-60251922	HCF	heart:	n/a
45	chr8:60214275-60214325	NHDF-neo	bronchial:	n/a
46	chr8:60444511-60444561	HEK293	kidney:	embryo
47	chr8:60197574-60197624	Hela-S3	cervix:	n/a
48	chr8:60197574-60197624	GM06990	blood:	n/a
49	chr8:60537981-60538031	NHDF-neo	bronchial:	n/a
50	chr8:60537981-60538031	NB4	blood:	n/a

(count:38 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr8:60126464..60129437-chr8:60135528..60137372,2	MCF-7	breast:
2	chr8:60236324..60239017-chr8:60241873..60244334,2	MCF-7	breast:
3	chr8:60491495..60494237-chr8:60524811..60527779,2	K562	blood:
4	chr8:60270318..60271875-chr8:60274683..60276592,2	K562	blood:
5	chr8:60535322..60536941-chr8:60538447..60540477,2	K562	blood:
6	chr8:60131223..60133472-chr8:60135461..60137451,2	K562	blood:
7	chr8:60270318..60271875-chr8:60274683..60276592,2	K562	blood:
8	chr8:60349625..60352522-chr8:60358997..60361385,2	K562	blood:
9	chr8:60303688..60306205-chr8:60408820..60411087,2	K562	blood:
10	chr8:60307556..60310133-chr8:60318318..60320436,2	K562	blood:
11	chr8:60111843..60114586-chr8:60116889..60119730,2	K562	blood:
12	chr8:60264224..60266326-chr8:60266427..60268399,2	K562	blood:
13	chr8:60349625..60352522-chr8:60358997..60361385,2	K562	blood:
14	chr8:60353422..60355080-chr8:60359821..60362576,2	K562	blood:
15	chr8:60352662..60355420-chr8:60364405..60366691,2	K562	blood:
16	chr8:60236324..60239017-chr8:60241873..60244334,2	MCF-7	breast:
17	chr8:60126464..60129437-chr8:60135528..60137372,2	MCF-7	breast:
18	chr8:60303688..60306205-chr8:60408820..60411087,2	K562	blood:
19	chr8:60353422..60355080-chr8:60359821..60362576,2	K562	blood:
20	chr8:60264224..60266326-chr8:60266427..60268399,2	K562	blood:
21	chr17:56735699..56736532-chr8:60431326..60431826,2	Hela-S3	cervix:
22	chr8:60485014..60486699-chr8:60491744..60493871,2	K562	blood:
23	chr8:60432149..60433929-chr8:60440083..60443026,2	K562	blood:
24	chr8:60505094..60507330-chr8:60508230..60511083,3	K562	blood:
25	chr8:60432149..60433929-chr8:60440083..60443026,2	K562	blood:
26	chr8:60127735..60128371-chr8:60214631..60215199,2	MCF-7	breast:
27	chr8:60127735..60128371-chr8:60214631..60215199,2	MCF-7	breast:
28	chr8:60491495..60494237-chr8:60524811..60527779,2	K562	blood:
29	chr8:60485014..60486699-chr8:60491744..60493871,2	K562	blood:
30	chr8:60307556..60310133-chr8:60318318..60320436,2	K562	blood:
31	chr8:60536802..60538571-chr8:60542161..60544626,2	K562	blood:
32	chr8:60089336..60092263-chr8:60117316..60119998,2	K562	blood:
33	chr8:60535322..60536941-chr8:60538447..60540477,2	K562	blood:
34	chr8:60352662..60355420-chr8:60364405..60366691,2	K562	blood:
35	chr8:60088819..60090836-chr8:60117316..60119033,2	K562	blood:
36	chr8:60111843..60114586-chr8:60116889..60119730,2	K562	blood:
37	chr8:60131223..60133472-chr8:60135461..60137451,2	K562	blood:
38	chr8:60127615..60128279-chr8:60833868..60834810,2	MCF-7	breast:

(count:13 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-TOX-3	chr8:60104927-60105226	uc_239_-
2	lnc-RAB2A-3	chr8:60513963-60514011	ENSG00000253879
3	lnc-TOX-1	chr8:60473892-60474119	XLOC_007091
4	lnc-TOX-4	chr8:60470087-60470414	NONHSAT126805
5	lnc-RAB2A-3	chr8:60525940-60526334	ENSG00000253879
6	lnc-RAB2A-3	chr8:60525378-60525448	ENSG00000253879
7	lnc-SDCBP-5	chr8:60195449-60196075	l_3606_chr8:60194334-60196450_lymphNode
8	lnc-RAB2A-3	chr8:60519089-60519564	ENSG00000253879
9	lnc-SDCBP-5	chr8:60196083-60196450	l_3606_chr8:60194334-60196450_lymphNode
10	lnc-SDCBP-4	chr8:60104927-60105226	uc_239_+
11	lnc-TOX-1	chr8:60506137-60506377	XLOC_007091
12	lnc-RAB2A-3	chr8:60513937-60514011	ENSG00000253879
13	lnc-SDCBP-5	chr8:60194335-60194398	l_3606_chr8:60194334-60196450_lymphNode

No data

Variant related genes	Relation type
ENSG00000253879	TF binding region
ENSG00000254150	TF binding region
RNA5SP267	TF binding region
ENSG00000253260	TF binding region
ENSG00000253879	CpG island
ENSG00000254150	CpG island
RNA5SP267	CpG island
ENSG00000253260	CpG island
ENSG00000253260	chromatin interactions

Extended variants
information (count: 8904 )
Associated
traits (count: 96 )

Variant overlapped rSNPs/rCNVs (count:8904 , 50 per page) page: 1 2 3 4 5 6 7 ... 179

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs544264462	chr8:60099852-60099853	Enhancers	n/a	n/a	Overlapped CNVs	n/a
2	rs537449537	chr8:60099875-60099876	Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs545322256	chr8:60099882-60099883	Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs529995220	chr8:60099908-60099909	Enhancers	n/a	n/a	Overlapped CNVs	n/a
5	rs192554980	chr8:60100002-60100003	Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs560175589	chr8:60100020-60100021	Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs532391548	chr8:60100023-60100024	Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs143033601	chr8:60100049-60100050	Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs372767633	chr8:60100103-60100104	Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs34352616	chr8:60100184-60100185	Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs569040977	chr8:60100254-60100255	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs368425557	chr8:60100297-60100298	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs146162073	chr8:60100298-60100299	Flanking Active TSS Enhancers	n/a	n/a	Overlapped CNVs	n/a
14	rs140017316	chr8:60100426-60100427	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
15	rs7461272	chr8:60100443-60100444	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
16	rs568057927	chr8:60100457-60100458	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
17	rs184127079	chr8:60100461-60100462	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
18	rs371895865	chr8:60100505-60100506	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
19	rs189549275	chr8:60100560-60100561	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
20	rs375066322	chr8:60100574-60100575	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
21	rs181156552	chr8:60100609-60100610	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
22	rs79368900	chr8:60100658-60100659	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
23	rs558741946	chr8:60100665-60100666	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
24	rs186448760	chr8:60100667-60100668	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
25	rs188656503	chr8:60100684-60100685	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
26	rs376288341	chr8:60100694-60100695	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
27	rs5891712	chr8:60100700-60100701	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
28	rs561183533	chr8:60100738-60100739	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
29	rs181547081	chr8:60100782-60100783	Enhancers Active TSS Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
30	rs5891713	chr8:60100814-60100815	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
31	rs397950292	chr8:60100817-60100818	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
32	rs186020035	chr8:60100818-60100819	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
33	rs540260027	chr8:60100852-60100853	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
34	rs372931184	chr8:60100863-60100864	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
35	rs78252455	chr8:60100866-60100867	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
36	rs544805478	chr8:60100980-60100981	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
37	rs190727975	chr8:60101033-60101034	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
38	rs3110133	chr8:60101068-60101069	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
39	rs562677386	chr8:60101144-60101145	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
40	rs3110132	chr8:60101194-60101195	Enhancers Flanking Active TSS	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs143635534	chr8:60101199-60101200	Enhancers Flanking Active TSS	n/a	n/a	Overlapped CNVs	n/a
42	rs544156772	chr8:60101204-60101205	Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs548306750	chr8:60101205-60101206	Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs77100056	chr8:60101219-60101220	Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs527309726	chr8:60101225-60101226	Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs151274185	chr8:60101235-60101236	Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs377643555	chr8:60101251-60101252	Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs374824971	chr8:60101296-60101297	Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs148616520	chr8:60101319-60101320	Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs150405830	chr8:60101330-60101331	Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:96)

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
Breast cancer	22522925	CNVD
Acute lymphoblastic leukemia	19100363	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:1060 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr8:60098800-60100600	Enhancers	Dnd41	blood
2	chr8:60100000-60100200	Enhancers	Fetal Thymus	thymus
3	chr8:60100000-60100400	Enhancers	Thymus	Thymus
4	chr8:60100200-60100800	Flanking Active TSS	Fetal Thymus	thymus
5	chr8:60100400-60100800	Active TSS	Primary T regulatory cells fromperipheralblood	blood
6	chr8:60100400-60100800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
7	chr8:60100400-60100800	Flanking Active TSS	Thymus	Thymus
8	chr8:60100400-60101200	Enhancers	Primary T cells from cord blood	blood
9	chr8:60100600-60101200	Flanking Active TSS	Dnd41	blood
10	chr8:60100800-60101000	Enhancers	Fetal Thymus	thymus
11	chr8:60100800-60101200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
12	chr8:60100800-60101200	Enhancers	Thymus	Thymus
13	chr8:60101200-60102600	Enhancers	Dnd41	blood
14	chr8:60120600-60121400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
15	chr8:60121600-60122000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
16	chr8:60121600-60125000	Enhancers	Dnd41	blood
17	chr8:60122000-60122800	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
18	chr8:60122000-60122800	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
19	chr8:60122200-60122800	Enhancers	GM12878-XiMat	blood
20	chr8:60122800-60123000	Enhancers	Primary T regulatory cells fromperipheralblood	blood
21	chr8:60123000-60124000	Weak transcription	Primary T regulatory cells fromperipheralblood	blood
22	chr8:60124000-60124200	Enhancers	Primary T regulatory cells fromperipheralblood	blood
23	chr8:60128200-60130000	Enhancers	Dnd41	blood
24	chr8:60130000-60131400	Weak transcription	Dnd41	blood
25	chr8:60131400-60132200	Enhancers	Dnd41	blood
26	chr8:60132200-60133200	ZNF genes & repeats	Dnd41	blood
27	chr8:60132200-60142400	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
28	chr8:60135400-60135600	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
29	chr8:60135400-60136600	Enhancers	Pancreatic Islets	Pancreatic Islet
30	chr8:60135600-60135800	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
31	chr8:60135800-60136000	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
32	chr8:60136000-60136200	Bivalent Enhancer	Rectal Mucosa Donor 29	rectum
33	chr8:60136200-60136400	Flanking Bivalent TSS/Enh	Rectal Mucosa Donor 29	rectum
34	chr8:60139600-60140200	Enhancers	HUVEC	blood vessel
35	chr8:60146200-60146600	Enhancers	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
36	chr8:60147200-60147800	Enhancers	Fetal Heart	heart
37	chr8:60147800-60150000	Weak transcription	Fetal Heart	heart
38	chr8:60148400-60150800	Enhancers	Fetal Intestine Small	intestine
39	chr8:60148600-60149400	Enhancers	Fetal Intestine Large	intestine
40	chr8:60149400-60149800	Enhancers	Stomach Mucosa	stomach
41	chr8:60149400-60150200	Weak transcription	Fetal Intestine Large	intestine
42	chr8:60149800-60150600	Weak transcription	Stomach Mucosa	stomach
43	chr8:60150000-60152200	Enhancers	Fetal Heart	heart
44	chr8:60150200-60150600	Enhancers	Fetal Intestine Large	intestine
45	chr8:60150600-60150800	Weak transcription	Fetal Intestine Large	intestine
46	chr8:60150600-60150800	Enhancers	Stomach Mucosa	stomach
47	chr8:60150800-60151200	Enhancers	Fetal Intestine Large	intestine
48	chr8:60150800-60151600	Weak transcription	Stomach Mucosa	stomach
49	chr8:60150800-60152000	Weak transcription	Fetal Intestine Small	intestine
50	chr8:60151600-60151800	Enhancers	Stomach Mucosa	stomach

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