Variant report

Variant	nsv605341
Chromosome Location	chr6:167624079-167778498
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:2549)
CpG islands
(count:4033)
Chromatin interactive
region (count:32)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:2549 , 50 per page) page: 1 2 3 4 5 6 7 ... 51

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:167723215-167724601	HepG2	liver:	n/a	n/a
2	ARID3A	chr6:167629887-167630151	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:167637599-167638030	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:167699867-167700232	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:167629415-167629646	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:167655013-167655211	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:167762709-167763005	HepG2	liver:	n/a	n/a
8	ARID3A	chr6:167754780-167756165	HepG2	liver:	n/a	n/a
9	ARID3A	chr6:167645950-167646149	HepG2	liver:	n/a	n/a
10	ARID3A	chr6:167628930-167629130	HepG2	liver:	n/a	n/a
11	ARID3A	chr6:167624462-167624811	HepG2	liver:	n/a	n/a
12	ARID3A	chr6:167632046-167632420	HepG2	liver:	n/a	n/a
13	ARID3A	chr6:167704338-167705733	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:167682223-167682912	HepG2	liver:	n/a	n/a
15	ARID3A	chr6:167722138-167722657	HepG2	liver:	n/a	n/a
16	ARID3A	chr6:167702230-167702578	HepG2	liver:	n/a	n/a
17	ARID3A	chr6:167651727-167651738	HepG2	liver:	n/a	n/a
18	ARID3A	chr6:167633428-167633974	HepG2	liver:	n/a	n/a
19	ARID3A	chr6:167652605-167653007	HepG2	liver:	n/a	n/a
20	ATF1	chr6:167727339-167727444	K562	blood:	n/a	n/a
21	ATF1	chr6:167702337-167702425	K562	blood:	n/a	n/a
22	ATF2	chr6:167626020-167626431	GM12878	blood:	n/a	n/a
23	ATF2	chr6:167764830-167765266	H1-hESC	embryonic stem cell:	n/a	n/a
24	ATF2	chr6:167641353-167641826	H1-hESC	embryonic stem cell:	n/a	n/a
25	ATF2	chr6:167651500-167652487	H1-hESC	embryonic stem cell:	n/a	n/a
26	ATF2	chr6:167641333-167641936	H1-hESC	embryonic stem cell:	n/a	n/a
27	ATF2	chr6:167764810-167765270	H1-hESC	embryonic stem cell:	n/a	n/a
28	ATF2	chr6:167625939-167626508	GM12878	blood:	n/a	n/a
29	BACH1	chr6:167631950-167632087	H1-hESC	embryonic stem cell:	n/a	n/a
30	BACH1	chr6:167754224-167754403	H1-hESC	embryonic stem cell:	n/a	n/a
31	BACH1	chr6:167702257-167702472	H1-hESC	embryonic stem cell:	n/a	n/a
32	BACH1	chr6:167641591-167641850	H1-hESC	embryonic stem cell:	n/a	n/a
33	BACH1	chr6:167764960-167765154	H1-hESC	embryonic stem cell:	n/a	n/a
34	BACH1	chr6:167637370-167637829	H1-hESC	embryonic stem cell:	n/a	n/a
35	BATF	chr6:167726056-167726329	GM12878	blood:	n/a	n/a
36	BATF	chr6:167625959-167626402	GM12878	blood:	n/a	n/a
37	BATF	chr6:167764807-167765183	GM12878	blood:	n/a	n/a
38	BATF	chr6:167726053-167726251	GM12878	blood:	n/a	n/a
39	BATF	chr6:167625794-167626502	GM12878	blood:	n/a	n/a
40	BATF	chr6:167765430-167765771	GM12878	blood:	n/a	n/a
41	BATF	chr6:167765440-167765736	GM12878	blood:	n/a	n/a
42	BATF	chr6:167631870-167632155	GM12878	blood:	n/a	n/a
43	BATF	chr6:167702166-167702414	GM12878	blood:	n/a	n/a
44	BCL11A	chr6:167626130-167626424	GM12878	blood:	n/a	n/a
45	BCL3	chr6:167710341-167710705	GM12878	blood:	n/a	n/a
46	BCLAF1	chr6:167764829-167765189	GM12878	blood:	n/a	chr6:167764879-167764888 chr6:167765036-167765044
47	BHLHE40	chr6:167629860-167630298	HepG2	liver:	n/a	n/a
48	BHLHE40	chr6:167733370-167733629	HepG2	liver:	n/a	n/a
49	BHLHE40	chr6:167755635-167755964	HepG2	liver:	n/a	n/a
50	BHLHE40	chr6:167626013-167626185	GM12878	blood:	n/a	n/a

(count:4033 , 50 per page) page: 1 2 3 4 5 6 7 ... 81

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:167704769-167704819	HRPEpiC	eye:	n/a
2	chr6:167734054-167734104	SK-N-SH_RA	brain:	n/a
3	chr6:167649749-167649799	NT2-D1	testis:	n/a
4	chr6:167762783-167762833	MCF10A-Er-Src	breast:	n/a
5	chr6:167761204-167761254	Jurkat	blood:	n/a
6	chr6:167649336-167649386	BJ	skin:	n/a
7	chr6:167703591-167703641	PrEC	prostate:	n/a
8	chr6:167704769-167704819	HRPEpiC	eye:	n/a
9	chr6:167734054-167734104	SK-N-SH_RA	brain:	n/a
10	chr6:167649749-167649799	NT2-D1	testis:	n/a
11	chr6:167762783-167762833	MCF10A-Er-Src	breast:	n/a
12	chr6:167761204-167761254	Jurkat	blood:	n/a
13	chr6:167649336-167649386	BJ	skin:	n/a
14	chr6:167703591-167703641	PrEC	prostate:	n/a
15	chr6:167739618-167739668	HIPEpiC	eye:	n/a
16	chr6:167738592-167738642	HL-60	blood:	n/a
17	chr6:167762783-167762833	A549	lung:	n/a
18	chr6:167649256-167649306	GM06990	blood:	n/a
19	chr6:167703894-167703944	AG04449	skin:	fetal
20	chr6:167655290-167655340	HIPEpiC	eye:	n/a
21	chr6:167739618-167739668	HCF	heart:	n/a
22	chr6:167655053-167655103	AG10803	skin:	n/a
23	chr6:167680455-167680505	IMR90	lung:	fetal
24	chr6:167761204-167761254	HRE	kidney:	n/a
25	chr6:167649256-167649306	Hela-S3	cervix:	n/a
26	chr6:167705750-167705800	AoSMC	blood vessel:	n/a
27	chr6:167631788-167631838	HCM	heart:	n/a
28	chr6:167737937-167737987	SAEC	small airway:	n/a
29	chr6:167737937-167737987	K562	blood:	n/a
30	chr6:167661905-167661955	NH-A	brain:	n/a
31	chr6:167739618-167739668	HCPEpiC	choroid plexus:	n/a
32	chr6:167718461-167718511	BJ	skin:	n/a
33	chr6:167764523-167764573	HUVEC	blood vessel:	n/a
34	chr6:167661905-167661955	BJ	skin:	n/a
35	chr6:167634139-167634189	RPTEC	kidney:	n/a
36	chr6:167734054-167734104	GM19239	blood:	n/a
37	chr6:167631788-167631838	SK-N-MC	brain:	n/a
38	chr6:167653907-167653957	HepG2	liver:	n/a
39	chr6:167717313-167717363	HRCEpiC	kidney:	n/a
40	chr6:167764146-167764196	AG04449	skin:	fetal
41	chr6:167653982-167654032	SK-N-SH	brain:	n/a
42	chr6:167653907-167653957	Caco-2	colon:	n/a
43	chr6:167717196-167717246	H1-hESC	embryonic stem cell:	embryo
44	chr6:167703591-167703641	Hepatocyte	liver:	n/a
45	chr6:167654977-167655027	T-47D	breast:	n/a
46	chr6:167708827-167708877	GM06990	blood:	n/a
47	chr6:167709237-167709287	HIPEpiC	eye:	n/a
48	chr6:167649256-167649306	SAEC	small airway:	n/a
49	chr6:167708827-167708877	HIPEpiC	eye:	n/a
50	chr6:167708827-167708877	HCM	heart:	n/a

(count:32 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
2	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
3	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
4	chr6:167187967..167188932-chr6:167764453..167765086,2	K562	blood:
5	chr6:167702039..167702568-chr6:167764606..167765474,2	MCF-7	breast:
6	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
7	chr6:167744023..167747282-chr6:167750789..167753119,3	K562	blood:
8	chr6:167734899..167737753-chr6:167743376..167745822,2	MCF-7	breast:
9	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
10	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
11	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
12	chr6:167703616..167705764-chr6:167717598..167719278,2	MCF-7	breast:
13	chr6:167662732..167663315-chr6:167819023..167819880,2	K562	blood:
14	chr6:167636874..167638495-chr6:167694115..167696567,2	K562	blood:
15	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
16	chr6:167623779..167626117-chr6:167629928..167632260,2	MCF-7	breast:
17	chr6:167662535..167665478-chr6:167668701..167671430,2	K562	blood:
18	chr6:167715327..167717333-chr6:167717541..167719931,2	MCF-7	breast:
19	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
20	chr1:28836187..28837925-chr6:167694572..167696254,2	K562	blood:
21	chr6:167615262..167616947-chr6:167733556..167735117,2	MCF-7	breast:
22	chr6:167743283..167745523-chr6:167751106..167753120,2	K562	blood:
23	chr6:167668192..167671777-chr6:167684157..167687082,3	K562	blood:
24	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
25	chr6:167623945..167626187-chr6:168297648..168300373,2	K562	blood:
26	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
27	chr6:167736614..167738249-chr6:167740426..167742938,2	K562	blood:
28	chr6:167620399..167623068-chr6:167623897..167626646,2	K562	blood:
29	chr6:167669951..167671777-chr6:167683631..167687000,3	K562	blood:
30	chr6:167631565..167632072-chr6:167702069..167702692,3	K562	blood:
31	chr6:167631751..167632287-chr6:167701939..167702527,2	MCF-7	breast:
32	chr6:167699179..167702166-chr6:167703091..167705361,2	K562	blood:

(count:9 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GPR31-1	chr6:167653688-167653968	XLOC_005921
2	lnc-GPR31-1	chr6:167650996-167651293	XLOC_005921
3	lnc-UNC93A-3	chr6:167764976-167765446	NONHSAT116095
4	lnc-UNC93A-2	chr6:167760960-167761541	NONHSAT116094
5	lnc-UNC93A-3	chr6:167764293-167764966	NONHSAT116095
6	lnc-UNC93A-1	chr6:167655379-167655453	XLOC_005540
7	lnc-GPR31-1	chr6:167651156-167651293	XLOC_005921
8	lnc-GPR31-1	chr6:167653636-167653833	XLOC_005921
9	lnc-UNC93A-1	chr6:167659275-167659404	XLOC_005540

No data

Variant related genes	Relation type
UNC93A	TF binding region
TTLL2	TF binding region
ENSG00000231720	TF binding region
ENSG00000228648	TF binding region
ENSG00000216966	TF binding region
ENSG00000217447	TF binding region
UNC93A	CpG island
TTLL2	CpG island
ENSG00000231720	CpG island
ENSG00000228648	CpG island
ENSG00000216966	CpG island
ENSG00000217447	CpG island
ENSG00000180198	chromatin interactions
ENSG00000216966	chromatin interactions
ENSG00000112494	chromatin interactions
CYB5R4	miRNA target sites
CYBASC3	miRNA target sites

Extended variants
information (count: 7496 )
Associated
traits (count: 85 )

Variant overlapped rSNPs/rCNVs (count:7496 , 50 per page) page: 1 2 3 4 5 6 7 ... 150

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs9364896	chr6:167624079-167624080	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs574552704	chr6:167624082-167624083	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs115448315	chr6:167624087-167624088	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs563270038	chr6:167624123-167624124	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs372628886	chr6:167624131-167624132	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs368649487	chr6:167624156-167624157	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs551923871	chr6:167624157-167624158	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs564396500	chr6:167624183-167624184	Enhancers Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs535742046	chr6:167624231-167624232	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528760521	chr6:167624261-167624262	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs4709154	chr6:167624266-167624267	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
12	rs568330519	chr6:167624277-167624278	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs184407201	chr6:167624309-167624310	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs535704664	chr6:167624333-167624334	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs573217529	chr6:167624334-167624335	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs4710205	chr6:167624384-167624385	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
17	rs2104841	chr6:167624392-167624393	Enhancers Weak transcription Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs145708732	chr6:167624402-167624403	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs536902810	chr6:167624403-167624404	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs149113267	chr6:167624409-167624410	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs112863318	chr6:167624410-167624411	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs574555323	chr6:167624434-167624435	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs370119766	chr6:167624463-167624464	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs541404376	chr6:167624479-167624480	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs190095143	chr6:167624483-167624484	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs113953756	chr6:167624498-167624499	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs181300740	chr6:167624500-167624501	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs542097136	chr6:167624511-167624512	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs563758716	chr6:167624512-167624513	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs375013081	chr6:167624529-167624530	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs78992030	chr6:167624558-167624559	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs2346143	chr6:167624570-167624571	Enhancers Bivalent Enhancer Weak transcription	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs73267380	chr6:167624748-167624749	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
34	rs558429189	chr6:167624749-167624750	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs529481296	chr6:167624767-167624768	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs57748704	chr6:167624794-167624795	Weak transcription Enhancers Bivalent Enhancer	TF binding region Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
37	rs62439207	chr6:167624803-167624804	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs66530550	chr6:167624808-167624809	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs73787959	chr6:167624818-167624819	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs562610512	chr6:167624819-167624820	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs2346145	chr6:167624820-167624821	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs2346146	chr6:167624821-167624822	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs2346147	chr6:167624822-167624823	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs2346148	chr6:167624823-167624824	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs2346149	chr6:167624824-167624825	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs2346150	chr6:167624825-167624826	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs2346151	chr6:167624826-167624827	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs149220901	chr6:167624840-167624841	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs57615306	chr6:167624842-167624843	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs13216655	chr6:167624845-167624846	Weak transcription Enhancers	TF binding region Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:85)

Disease	PMID	Source
Uveal melanoma	21693616	CNVD
Glioblastoma multiforme	21080181	CNVD
Biliary cancer	19435499	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Ewing''s sarcoma	17952124	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
Neuroblastoma	18923191	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Melanoma	18172304	CNVD
Cancer	21637783	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Follicular lymphoma	19010834	CNVD
Non-small cell lung cancer	21044232	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Glioblastoma multiforme	19960244	CNVD
Hepatocellular carcinoma	22174799	CNVD
Phyllodes tumor	17334353	CNVD
Breast cancer	16608533	CNVD
Non-small cell lung cancer	21385341	CNVD
Prostate cancer	16705090	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Colorectal cancer	16272173	CNVD
Ependymoma	16718352	CNVD
Gastric cancer	17908304	CNVD
High-proliferative meningiomas	17937814	CNVD
Intracranial tumor	16823260	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Breast cancer	16272173	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Acute lymphoblastic leukemia	17690704	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	17603634	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Neurodevelopmental disorder	22521361	CNVD
small cell lung cancer	20016488	CNVD
Adenoid cystic carcinoma	18698036	CNVD
head and neck squamous cell carcinoma	17671120	CNVD
Leukemia	18688285	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Prostate cancer	18632612	CNVD
Lung cancer	18438408	CNVD
Burkitt''s lymphoma	19759907	CNVD
Esophageal cancer	21851588	CNVD
T-cell acute lymphoblastic leukemia	18185524	CNVD
Breast cancer	17133270	CNVD
Testicular germ cell tumor	18059402	CNVD
Chordoma	18071362	CNVD
Glioblastoma multiforme	19435819	CNVD
Developmental delay	21147756	CNVD
Ovarian cancer	21720365	CNVD
abnormal development	18461090	CNVD
Epilepsy	22083797	CNVD
Myelofibrosis	22110671	CNVD
chordoma	19801981	CNVD
Myxofibrosarcoma	16751306	CNVD
Autism	17483303	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Acute myeloid leukemia	19651601	CNVD
Sudden cardiac death	19188705	CNVD
Myofibroblastic sarcoma	19369631	CNVD
Non-syndromic sensorineural hearing loss	17122850	CNVD
Cancer	20164919	CNVD
early-passage human iPS cells	21368824	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:1750 , 50 per page) page: 1 2 3 4 5 6 7 ... 35

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:167615800-167628800	Weak transcription	Right Atrium	heart
2	chr6:167618400-167624400	Weak transcription	Colon Smooth Muscle	Colon
3	chr6:167619000-167624200	Weak transcription	Rectal Smooth Muscle	rectum
4	chr6:167621600-167624400	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:167622200-167624600	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
6	chr6:167622200-167624600	Enhancers	iPS DF 19.11 Cell Line	embryonic stem cell
7	chr6:167622400-167626600	Enhancers	Placenta Amnion	Placenta Amnion
8	chr6:167622400-167627200	Enhancers	HepG2	liver
9	chr6:167622800-167624200	Weak transcription	HUES6 Cell Line	embryonic stem cell
10	chr6:167623000-167629200	Enhancers	Fetal Brain Male	brain
11	chr6:167623200-167624600	Enhancers	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
12	chr6:167623400-167624200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
13	chr6:167623600-167628200	Enhancers	Fetal Brain Female	brain
14	chr6:167623800-167624400	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
15	chr6:167623800-167624600	Enhancers	H1 Cell Line	embryonic stem cell
16	chr6:167624000-167624600	Enhancers	HUES64 Cell Line	embryonic stem cell
17	chr6:167624000-167624800	Enhancers	Brain Germinal Matrix	brain
18	chr6:167624200-167624600	Enhancers	ES-I3 Cell Line	embryonic stem cell
19	chr6:167624200-167624600	Enhancers	HUES6 Cell Line	embryonic stem cell
20	chr6:167624200-167624600	Bivalent Enhancer	Brain Cingulate Gyrus	brain
21	chr6:167624200-167624600	Enhancers	Lung	lung
22	chr6:167624200-167624800	Bivalent Enhancer	Fetal Muscle Trunk	muscle
23	chr6:167624200-167625600	Enhancers	Rectal Smooth Muscle	rectum
24	chr6:167624400-167624600	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
25	chr6:167624400-167624600	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
26	chr6:167624400-167625800	Enhancers	Colon Smooth Muscle	Colon
27	chr6:167624600-167625200	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
28	chr6:167624600-167632800	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
29	chr6:167624800-167627800	Weak transcription	Brain Germinal Matrix	brain
30	chr6:167625000-167625200	Bivalent Enhancer	Stomach Smooth Muscle	stomach
31	chr6:167625600-167630000	Weak transcription	Rectal Smooth Muscle	rectum
32	chr6:167625800-167626000	Enhancers	Lung	lung
33	chr6:167625800-167626000	Bivalent Enhancer	GM12878-XiMat	blood
34	chr6:167625800-167626200	Enhancers	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
35	chr6:167626000-167626200	Enhancers	Brain Inferior Temporal Lobe	brain
36	chr6:167626000-167626800	Enhancers	GM12878-XiMat	blood
37	chr6:167626200-167627800	Weak transcription	Brain Inferior Temporal Lobe	brain
38	chr6:167626200-167635000	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
39	chr6:167626600-167631000	Weak transcription	Placenta Amnion	Placenta Amnion
40	chr6:167626800-167627600	Weak transcription	Brain Cingulate Gyrus	brain
41	chr6:167627200-167627600	Weak transcription	HepG2	liver
42	chr6:167627400-167628000	Enhancers	iPS-20b Cell Line	embryonic stem cell
43	chr6:167627600-167628000	Enhancers	Brain Cingulate Gyrus	brain
44	chr6:167627600-167629000	Enhancers	HepG2	liver
45	chr6:167627800-167628000	Enhancers	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
46	chr6:167627800-167628000	Enhancers	Brain Substantia Nigra	brain
47	chr6:167627800-167628200	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
48	chr6:167627800-167628200	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
49	chr6:167627800-167628200	Bivalent Enhancer	Brain Anterior Caudate	brain
50	chr6:167627800-167628200	Enhancers	Brain Germinal Matrix	brain

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