Variant report

Variant	nsv462940
Chromosome Location	chr6:45532214-45545975
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:84)
CpG islands
(count:61)
Chromatin interactive
region (count:11)
LncRNA
region (count:43)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:84 , 50 per page) page: 1 2

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:45541768-45542056	HepG2	liver:	n/a	n/a
2	CEBPB	chr6:45543354-45543685	HepG2	liver:	n/a	chr6:45543530-45543541 chr6:45543529-45543542
3	CEBPB	chr6:45541649-45542005	HepG2	liver:	n/a	n/a
4	CEBPB	chr6:45542681-45543042	HepG2	liver:	n/a	chr6:45542836-45542847 chr6:45542838-45542849 chr6:45542836-45542849
5	CEBPB	chr6:45542635-45543027	HepG2	liver:	n/a	chr6:45542836-45542847 chr6:45542838-45542849 chr6:45542836-45542849
6	CEBPB	chr6:45542703-45542936	Hela-S3	cervix:	n/a	chr6:45542836-45542847 chr6:45542838-45542849 chr6:45542836-45542849
7	CEBPB	chr6:45542665-45542973	HepG2	liver:	n/a	chr6:45542836-45542847 chr6:45542838-45542849 chr6:45542836-45542849
8	CTCF	chr6:45545690-45545708	Hela-S3	cervix:	n/a	n/a
9	CTCF	chr6:45545660-45545810	AG09319	gingival:	n/a	n/a
10	CTCF	chr6:45545600-45545750	BJ	skin:	n/a	n/a
11	CTCF	chr6:45542820-45542970	HEEpiC	esophagus:	n/a	chr6:45542846-45542854
12	CTCF	chr6:45545620-45545770	AG10803	skin:	n/a	n/a
13	CTCF	chr6:45545600-45545750	AG09319	gingival:	n/a	n/a
14	CTCF	chr6:45545620-45545770	HVMF	connective:	n/a	n/a
15	CTCF	chr6:45545700-45545850	NHDF-neo	bronchial:	n/a	n/a
16	CTCF	chr6:45545600-45545750	HPF	lung:	n/a	n/a
17	CTCF	chr6:45545580-45545730	AG04449	skin:	n/a	n/a
18	CTCF	chr6:45545700-45545850	HFF	foreskin:	n/a	n/a
19	CTCF	chr6:45545640-45545790	HCPEpiC	choroid plexus:	n/a	n/a
20	CTCF	chr6:45545540-45545690	NHDF-neo	bronchial:	n/a	n/a
21	CTCF	chr6:45540739-45540802	GM13976	blood:	n/a	n/a
22	CTCF	chr6:45545580-45545730	BJ	skin:	n/a	n/a
23	CTCF	chr6:45545580-45545730	AG04450	lung:	n/a	n/a
24	CTCF	chr6:45545400-45545550	NHDF-neo	bronchial:	n/a	n/a
25	ELF1	chr6:45544280-45544528	K562	blood:	n/a	chr6:45544401-45544414
26	EP300	chr6:45545602-45546072	SK-N-SH_RA	brain:	n/a	n/a
27	EP300	chr6:45541673-45542033	HepG2	liver:	n/a	n/a
28	EP300	chr6:45534568-45534953	SK-N-SH_RA	brain:	n/a	n/a
29	EP300	chr6:45541615-45542148	HepG2	liver:	n/a	n/a
30	EP300	chr6:45534484-45535188	ECC-1	luminal epithelium:	n/a	n/a
31	EP300	chr6:45545643-45546112	SK-N-SH_RA	brain:	n/a	n/a
32	ESR1	chr6:45544565-45545037	ECC-1	luminal epithelium:	n/a	n/a
33	ESR1	chr6:45544551-45545055	ECC-1	luminal epithelium:	n/a	n/a
34	ESR1	chr6:45544533-45544976	ECC-1	luminal epithelium:	n/a	n/a
35	FOS	chr6:45542639-45542925	MCF10A-Er-Src	breast:	n/a	n/a
36	FOS	chr6:45542669-45542973	MCF10A-Er-Src	breast:	n/a	n/a
37	FOS	chr6:45542782-45542907	MCF10A-Er-Src	breast:	n/a	n/a
38	FOS	chr6:45542654-45542975	MCF10A-Er-Src	breast:	n/a	n/a
39	FOXA1	chr6:45541700-45542131	HepG2	liver:	n/a	n/a
40	FOXA1	chr6:45541703-45542094	HepG2	liver:	n/a	n/a
41	FOXA1	chr6:45541617-45542099	HepG2	liver:	n/a	n/a
42	FOXA2	chr6:45541713-45542035	HepG2	liver:	n/a	n/a
43	GABPA	chr6:45542381-45543247	HL-60	blood:	n/a	n/a
44	GATA3	chr6:45545414-45545709	T-47D	breast:	n/a	n/a
45	GATA3	chr6:45545309-45545957	SK-N-SH	brain:	n/a	chr6:45545391-45545401
46	HNF4A	chr6:45541703-45541920	HepG2	liver:	n/a	n/a
47	HNF4A	chr6:45534558-45534881	HepG2	liver:	n/a	chr6:45534725-45534740 chr6:45534726-45534740
48	HNF4A	chr6:45534604-45534883	HepG2	liver:	n/a	chr6:45534725-45534740 chr6:45534726-45534740
49	JUN	chr6:45534723-45534939	H1-hESC	embryonic stem cell:	n/a	n/a
50	JUN	chr6:45534735-45534880	HepG2	liver:	n/a	n/a

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

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:45545422-45545472	RPTEC	kidney:	n/a
2	chr6:45545422-45545472	SAEC	small airway:	n/a
3	chr6:45545422-45545472	HRCEpiC	kidney:	n/a
4	chr6:45545422-45545472	HNPCEpiC	eye:	n/a
5	chr6:45545422-45545472	AG04449	skin:	fetal
6	chr6:45545422-45545472	Caco-2	colon:	n/a
7	chr6:45545422-45545472	T-47D	breast:	n/a
8	chr6:45545422-45545472	HEEpiC	esophagus:	n/a
9	chr6:45545422-45545472	SK-N-MC	brain:	n/a
10	chr6:45545422-45545472	A549	lung:	n/a
11	chr6:45545422-45545472	NT2-D1	testis:	n/a
12	chr6:45545422-45545472	HEK293	kidney:	embryo
13	chr6:45545422-45545472	PANC-1	pancreas:	n/a
14	chr6:45545422-45545472	HMEC	breast:	n/a
15	chr6:45545422-45545472	AG10803	skin:	n/a
16	chr6:45545422-45545472	SK-N-SH	brain:	n/a
17	chr6:45545422-45545472	NB4	blood:	n/a
18	chr6:45545422-45545472	H1-hESC	embryonic stem cell:	embryo
19	chr6:45545422-45545472	Jurkat	blood:	n/a
20	chr6:45545422-45545472	LNCaP	prostate:	n/a
21	chr6:45545422-45545472	AoSMC	blood vessel:	n/a
22	chr6:45545422-45545472	CMK	blood:	n/a
23	chr6:45545422-45545472	NHDF-neo	bronchial:	n/a
24	chr6:45545422-45545472	ovcar-3	ovarian:	n/a
25	chr6:45545422-45545472	GM12878	blood:	n/a
26	chr6:45545422-45545472	HRPEpiC	eye:	n/a
27	chr6:45545422-45545472	HUVEC	blood vessel:	n/a
28	chr6:45545422-45545472	GM12892	blood:	n/a
29	chr6:45545422-45545472	HPAEpiC	pulmonary alveolar:	n/a
30	chr6:45545422-45545472	PFSK-1	brain:	n/a
31	chr6:45545422-45545472	NHBE	bronchial:	n/a
32	chr6:45545422-45545472	U87	brain:	n/a
33	chr6:45545422-45545472	HL-60	blood:	n/a
34	chr6:45545422-45545472	GM19239	blood:	n/a
35	chr6:45545422-45545472	IMR90	lung:	fetal
36	chr6:45545422-45545472	MCF-7	breast:	n/a
37	chr6:45545422-45545472	ProgFib	skin:	n/a
38	chr6:45545422-45545472	HRE	kidney:	n/a
39	chr6:45545422-45545472	Hela-S3	cervix:	n/a
40	chr6:45545422-45545472	HCM	heart:	n/a
41	chr6:45545422-45545472	HCF	heart:	n/a
42	chr6:45545422-45545472	HCPEpiC	choroid plexus:	n/a
43	chr6:45545422-45545472	BJ	skin:	n/a
44	chr6:45545422-45545472	HAEpiC	amniotic membrane:	n/a
45	chr6:45545422-45545472	HCT-116	colon:	n/a
46	chr6:45545422-45545472	ECC-1	luminal epithelium:	n/a
47	chr6:45545422-45545472	SK-N-SH_RA	brain:	n/a
48	chr6:45545422-45545472	GM12891	blood:	n/a
49	chr6:45545422-45545472	NH-A	brain:	n/a
50	chr6:45545422-45545472	GM06990	blood:	n/a

(count:11 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:45538385..45540491-chr6:45545062..45546957,2	MCF-7	breast:
2	chr6:45545471..45547955-chr6:45549621..45552271,2	K562	blood:
3	chr6:45531563..45533620-chr6:45534711..45536211,2	MCF-7	breast:
4	chr6:45521600..45524007-chr6:45539938..45542034,2	MCF-7	breast:
5	chr6:45538385..45540491-chr6:45545062..45546957,2	MCF-7	breast:
6	chr6:45540470..45542325-chr6:45555218..45557403,2	MCF-7	breast:
7	chr6:45533723..45535563-chr6:45552658..45554257,2	MCF-7	breast:
8	chr6:45533105..45535281-chr6:45537536..45540429,2	MCF-7	breast:
9	chr6:45533105..45535281-chr6:45537536..45540429,2	MCF-7	breast:
10	chr6:45531563..45533620-chr6:45534711..45536211,2	MCF-7	breast:
11	chr6:45525346..45527240-chr6:45531716..45533270,2	MCF-7	breast:

(count:43 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-SUPT3H-1	chr6:45544016-45544508	XLOC_005737
2	lnc-SUPT3H-1	chr6:45543764-45543823	XLOC_005737
3	lnc-SUPT3H-1	chr6:45543764-45544507	ENSG00000261080.1
4	lnc-SUPT3H-1	chr6:45543764-45544507	NONHSAT112989
5	lnc-SUPT3H-1	chr6:45541116-45541851	XLOC_005737
6	lnc-SUPT3H-1	chr6:45533740-45534135	XLOC_005737
7	lnc-SUPT3H-1	chr6:45541116-45542183	XLOC_005737
8	lnc-SUPT3H-1	chr6:45539449-45540445	NONHSAT112989
9	lnc-SUPT3H-1	chr6:45543599-45543823	XLOC_005737
10	lnc-SUPT3H-1	chr6:45534240-45535428	NONHSAT112988
11	lnc-RUNX2-1	chr6:45543599-45545853	XLOC_005302
12	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737
13	lnc-SUPT3H-1	chr6:45544322-45544785	XLOC_005737
14	lnc-SUPT3H-1	chr6:45544322-45544501	XLOC_005737
15	lnc-SUPT3H-1	chr6:45535185-45535428	XLOC_005737
16	lnc-SUPT3H-1	chr6:45541116-45541851	XLOC_005737
17	lnc-SUPT3H-1	chr6:45541083-45541851	ENSG00000261080.1
18	lnc-SUPT3H-1	chr6:45544322-45544501	XLOC_005737
19	lnc-SUPT3H-1	chr6:45533780-45534135	XLOC_005737
20	lnc-SUPT3H-1	chr6:45541083-45541851	NONHSAT112989
21	lnc-SUPT3H-1	chr6:45539456-45540445	ENSG00000251681
22	lnc-SUPT3H-1	chr6:45541116-45541851	NONHSAT112988
23	lnc-SUPT3H-1	chr6:45543764-45543823	XLOC_005737
24	lnc-SUPT3H-1	chr6:45544322-45544501	XLOC_005737
25	lnc-SUPT3H-1	chr6:45541083-45541851	ENSG00000251681
26	lnc-SUPT3H-1	chr6:45544796-45545334	XLOC_005737
27	lnc-SUPT3H-1	chr6:45541116-45541851	XLOC_005737
28	lnc-SUPT3H-1	chr6:45541116-45542183	XLOC_005737
29	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737
30	lnc-SUPT3H-1	chr6:45533780-45534135	XLOC_005737
31	lnc-RUNX2-1	chr6:45540498-45543034	XLOC_005302
32	lnc-SUPT3H-1	chr6:45543764-45543823	XLOC_005737
33	lnc-SUPT3H-1	chr6:45533740-45534135	XLOC_005737
34	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737
35	lnc-SUPT3H-1	chr6:45544322-45544501	XLOC_005737
36	lnc-SUPT3H-1	chr6:45543764-45544507	ENSG00000251681
37	lnc-SUPT3H-1	chr6:45543764-45544495	NONHSAT112988
38	lnc-SUPT3H-1	chr6:45533780-45534135	XLOC_005737
39	lnc-SUPT3H-1	chr6:45535185-45535424	XLOC_005737
40	lnc-SUPT3H-1	chr6:45544322-45544501	XLOC_005737
41	lnc-SUPT3H-1	chr6:45544322-45544501	XLOC_005737
42	lnc-SUPT3H-1	chr6:45541116-45542183	XLOC_005737
43	lnc-SUPT3H-1	chr6:45541116-45542183	XLOC_005737

No data

Variant related genes	Relation type
ENSG00000261080	TF binding region
ENSG00000261080	CpG island
LYST	miRNA target sites
LCA5	miRNA target sites
TTLL3	miRNA target sites
ECE1	miRNA target sites
FAM102A	miRNA target sites
NUB1	miRNA target sites
ILF3	miRNA target sites

Extended variants
information (count: 533 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:533 , 50 per page) page: 1 2 3 4 5 6 7 ... 11

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11969213	chr6:45532214-45532215	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs560949491	chr6:45532219-45532220	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
3	rs572948854	chr6:45532239-45532240	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
4	rs1928532	chr6:45532251-45532252	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
5	rs565267601	chr6:45532315-45532316	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
6	rs556702482	chr6:45532376-45532377	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
7	rs185066523	chr6:45532400-45532401	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
8	rs75209979	chr6:45532401-45532402	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
9	rs530837945	chr6:45532411-45532412	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
10	rs150226230	chr6:45532415-45532416	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
11	rs138821539	chr6:45532501-45532502	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
12	rs565549996	chr6:45532532-45532533	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
13	rs1928531	chr6:45532556-45532557	Weak transcription Enhancers	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
14	rs545376075	chr6:45532567-45532568	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
15	rs571283488	chr6:45532597-45532598	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
16	rs79776396	chr6:45532599-45532600	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
17	rs190708247	chr6:45532606-45532607	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
18	rs575384627	chr6:45532665-45532666	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
19	rs536444268	chr6:45532717-45532718	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
20	rs554883034	chr6:45532728-45532729	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
21	rs113107967	chr6:45532747-45532748	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
22	rs193022782	chr6:45532754-45532755	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
23	rs565252863	chr6:45532781-45532782	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
24	rs577280385	chr6:45532792-45532793	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
25	rs144680942	chr6:45532796-45532797	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
26	rs75784309	chr6:45532806-45532807	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs184494750	chr6:45532828-45532829	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs549193027	chr6:45532829-45532830	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs561201627	chr6:45532831-45532832	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
30	rs528365930	chr6:45532847-45532848	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs546301390	chr6:45532849-45532850	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs571189214	chr6:45532944-45532945	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
33	rs138291786	chr6:45532958-45532959	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs56996542	chr6:45532991-45532992	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs550307052	chr6:45533022-45533023	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs142939373	chr6:45533057-45533058	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs80195280	chr6:45533112-45533113	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
38	rs79966272	chr6:45533122-45533123	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
39	rs188468441	chr6:45533133-45533134	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
40	rs79003723	chr6:45533134-45533135	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
41	rs558688894	chr6:45533139-45533140	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
42	rs16873510	chr6:45533153-45533154	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
43	rs552886599	chr6:45533200-45533201	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
44	rs59803832	chr6:45533231-45533232	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
45	rs147427718	chr6:45533238-45533239	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
46	rs115202835	chr6:45533239-45533240	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
47	rs116646947	chr6:45533241-45533242	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
48	rs116824736	chr6:45533261-45533262	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
49	rs185808443	chr6:45533280-45533281	Weak transcription	n/a	n/a	Overlapped CNVs	n/a
50	rs1041334	chr6:45533289-45533290	Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:91)

Disease	PMID	Source
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Leukemia	21518781	CNVD
Cancer	21637783	CNVD
Facial dysmorphism	22105932	CNVD
Medulloblastoma	21979893	CNVD
Non-syndromic sensorineural hearing loss	18471307	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Glioblastoma multiforme	21080181	CNVD
Hepatocellular carcinoma	22174799	CNVD
Endometrial cancer	22040021	CNVD
Acute myeloid leukemia	16864856	CNVD
Breast cancer	21264507	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Cancer	16751803	CNVD
Bladder cancer	19088036	CNVD
Wilms tumour	21544195	CNVD
Uveal melanoma	21693616	CNVD
Biliary cancer	19435499	CNVD
Malaria	21533027	CNVD
Retinoblastoma	19183342	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Ewing''s sarcoma	17952124	CNVD
Autism	21448237	CNVD
Melanoma	18172304	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Hepatocellular carcinoma	16750200	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Systemic lupus erythematosus	17503323	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Urothelial carcinoma	18382360	CNVD
Cancer	21183584	CNVD
Hodgkin''s lymphoma	17606441	CNVD
small cell lung cancer	20016488	CNVD
Gastric cancer	17908304	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Osteosarcoma	16790693	CNVD
Biliary cancer	20360734	CNVD
Breast cancer	20360734	CNVD
Coronary artery disease	20360734	CNVD
Crohn''s disease	20360734	CNVD
Hypertension	20360734	CNVD
Rheumatoid arthritis	20360734	CNVD
Type 1 diabetes	20360734	CNVD
Type 2 diabetes	20360734	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Lung cancer	18438408	CNVD
Ovarian cancer	21720365	CNVD
Osteosarcoma	21197465	CNVD
Gastric cancer	24379144	CNVD
Neuroblastoma	18923191	CNVD
abnormal development	18461090	CNVD
Breast cancer	17603634	CNVD
Breast cancer	21364760	CNVD
Colorectal cancer	16790693	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Congenital anomalies of the kidney and urinary tract	18316590	CNVD
Systemic lupus erythematosus	19287148	CNVD
Colorectal cancer	19359472	CNVD
Multiple myeloma	16616336	CNVD
Chordoma	18071362	CNVD
Follicular lymphoma	16790693	CNVD
Osteosarcoma	19286668	CNVD
Neurocytoma	17123091	CNVD
lymphocytic leukemia	21291569	CNVD
Gastrointestinal stromal cancer	20818650	CNVD
Myelofibrosis	22110671	CNVD
Heart disease	21282601	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
Breast cancer	16608533	CNVD
Glioblastoma multiforme	21510904	CNVD
Cleidocranial dysplasia	20014132	CNVD
Non-small cell lung cancer	17429853	CNVD
Breast cancer	22522925	CNVD
Cancer	20164919	CNVD
Pancreatic cancer	17952125	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD

Chromatin state (count:234 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:45519600-45532400	Weak transcription	Right Atrium	heart
2	chr6:45522000-45536800	Weak transcription	Primary T helper memory cells from peripheral blood 1	blood
3	chr6:45522200-45533800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:45524800-45537000	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
5	chr6:45525000-45533800	Weak transcription	HSMM	muscle
6	chr6:45525000-45534600	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
7	chr6:45531000-45536200	Weak transcription	Psoas Muscle	Psoas
8	chr6:45531000-45537000	Weak transcription	Ovary	ovary
9	chr6:45531000-45537200	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
10	chr6:45531400-45532400	Enhancers	Fetal Heart	heart
11	chr6:45531600-45532600	Enhancers	Skeletal Muscle Male	skeletal muscle
12	chr6:45532200-45532400	Enhancers	Skeletal Muscle Female	skeletal muscle
13	chr6:45532200-45532400	Enhancers	HSMMtube	muscle
14	chr6:45532200-45532600	Enhancers	Left Ventricle	heart
15	chr6:45532400-45532800	Enhancers	Right Atrium	heart
16	chr6:45532400-45534200	Weak transcription	HSMMtube	muscle
17	chr6:45532400-45537000	Weak transcription	Fetal Heart	heart
18	chr6:45532600-45536200	Weak transcription	Left Ventricle	heart
19	chr6:45532800-45535600	Weak transcription	Right Atrium	heart
20	chr6:45533800-45534000	Enhancers	HSMM	muscle
21	chr6:45533800-45535000	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
22	chr6:45533800-45535400	Enhancers	HUES64 Cell Line	embryonic stem cell
23	chr6:45533800-45537400	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
24	chr6:45534000-45534400	Weak transcription	HSMM	muscle
25	chr6:45534000-45537600	Enhancers	Breast Myoepithelial Primary Cells	Breast
26	chr6:45534200-45534400	Enhancers	HSMMtube	muscle
27	chr6:45534200-45534800	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
28	chr6:45534200-45535400	Enhancers	HepG2	liver
29	chr6:45534200-45535400	Enhancers	NH-A	brain
30	chr6:45534200-45537800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr6:45534200-45538000	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
32	chr6:45534400-45534600	Bivalent Enhancer	iPS-15b Cell Line	embryonic stem cell
33	chr6:45534400-45534600	Bivalent Enhancer	iPS-20b Cell Line	embryonic stem cell
34	chr6:45534400-45534800	Enhancers	Placenta Amnion	Placenta Amnion
35	chr6:45534400-45534800	Flanking Active TSS	HSMMtube	muscle
36	chr6:45534400-45535000	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
37	chr6:45534400-45535000	Bivalent Enhancer	HUES6 Cell Line	embryonic stem cell
38	chr6:45534400-45535000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
39	chr6:45534400-45535200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
40	chr6:45534400-45535200	Enhancers	HSMM	muscle
41	chr6:45534400-45535400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
42	chr6:45534400-45535400	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
43	chr6:45534400-45537600	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
44	chr6:45534400-45538000	Enhancers	HMEC	breast
45	chr6:45534600-45535000	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
46	chr6:45534600-45535000	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
47	chr6:45534600-45535000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:45534600-45535000	Enhancers	Esophagus	oesophagus
49	chr6:45534600-45535200	Enhancers	Cortex derived primary cultured neurospheres	brain
50	chr6:45534600-45535400	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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