Variant report

Variant	nsv518874
Chromosome Location	chr6:74014468-74041424
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:856)
CpG islands
(count:854)
Chromatin interactive
region (count:30)
LncRNA
region (count:9)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:856 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:74019571-74020071	K562	blood:	n/a	n/a
2	BATF	chr6:74039011-74039240	GM12878	blood:	n/a	chr6:74039112-74039123
3	BCLAF1	chr6:74019300-74019827	GM12878	blood:	n/a	n/a
4	BHLHE40	chr6:74019251-74020293	GM12878	blood:	n/a	n/a
5	BHLHE40	chr6:74017283-74017476	K562	blood:	n/a	n/a
6	BHLHE40	chr6:74018914-74020168	K562	blood:	n/a	n/a
7	BRCA1	chr6:74019497-74020121	GM12878	blood:	n/a	n/a
8	BRCA1	chr6:74018968-74019168	Hela-S3	cervix:	n/a	n/a
9	BRCA1	chr6:74018971-74019069	GM12878	blood:	n/a	n/a
10	BRCA1	chr6:74019456-74020028	Hela-S3	cervix:	n/a	n/a
11	BRCA1	chr6:74019502-74019884	H1-hESC	embryonic stem cell:	n/a	n/a
12	BRCA1	chr6:74036465-74036666	H1-hESC	embryonic stem cell:	n/a	n/a
13	CBX3	chr6:74027786-74028007	K562	blood:	n/a	n/a
14	CBX3	chr6:74019285-74020306	K562	blood:	n/a	n/a
15	CBX3	chr6:74018709-74019100	K562	blood:	n/a	n/a
16	CCNT2	chr6:74019518-74020251	K562	blood:	n/a	chr6:74020180-74020189
17	CHD1	chr6:74019258-74019950	GM12878	blood:	n/a	n/a
18	CHD2	chr6:74019428-74020217	GM12878	blood:	n/a	n/a
19	CHD2	chr6:74019221-74020187	K562	blood:	n/a	n/a
20	CHD2	chr6:74018953-74020259	Hela-S3	cervix:	n/a	n/a
21	CHD2	chr6:74019614-74019629	HepG2	liver:	n/a	n/a
22	CHD2	chr6:74028178-74028372	K562	blood:	n/a	n/a
23	CHD2	chr6:74018891-74018920	K562	blood:	n/a	n/a
24	CREB1	chr6:74019725-74020059	A549	lung:	n/a	n/a
25	CTBP2	chr6:74018884-74020195	H1-hESC	embryonic stem cell:	n/a	n/a
26	CTCF	chr6:74036440-74036590	HEEpiC	esophagus:	n/a	chr6:74036516-74036534 chr6:74036511-74036532 chr6:74036523-74036530
27	CTCF	chr6:74019480-74019630	HCM	heart:	n/a	n/a
28	CTCF	chr6:74019702-74020347	K562	blood:	n/a	chr6:74020150-74020163 chr6:74020153-74020162 chr6:74020147-74020160
29	CTCF	chr6:74036427-74036629	GM10248	blood:	n/a	chr6:74036516-74036534 chr6:74036511-74036532 chr6:74036523-74036530
30	CTCF	chr6:74018900-74019050	AG09309	skin:	n/a	n/a
31	CTCF	chr6:74036440-74036590	NB4	blood:	n/a	chr6:74036516-74036534 chr6:74036511-74036532 chr6:74036523-74036530
32	CTCF	chr6:74018900-74019050	A549	lung:	n/a	n/a
33	CTCF	chr6:74018940-74019090	HMF	breast:	n/a	n/a
34	CTCF	chr6:74018880-74019030	WI-38	lung:	n/a	n/a
35	CTCF	chr6:74036360-74036510	A549	lung:	n/a	n/a
36	CTCF	chr6:74018760-74018910	HCM	heart:	n/a	n/a
37	CTCF	chr6:74018880-74019030	HA-sp	spinal cord:	n/a	n/a
38	CTCF	chr6:74019220-74019370	HCT-116	colon:	n/a	n/a
39	CTCF	chr6:74020009-74020215	SK-N-SH_RA	brain:	n/a	chr6:74020150-74020163 chr6:74020153-74020162 chr6:74020147-74020160
40	CTCF	chr6:74020020-74020170	HL-60	blood:	n/a	chr6:74020150-74020163 chr6:74020153-74020162 chr6:74020147-74020160
41	CTCF	chr6:74018860-74019010	GM12871	blood:	n/a	n/a
42	CTCF	chr6:74018840-74018990	HEEpiC	esophagus:	n/a	n/a
43	CTCF	chr6:74019790-74020289	K562	blood:	n/a	chr6:74020150-74020163 chr6:74020153-74020162 chr6:74020147-74020160
44	CTCF	chr6:74036315-74036696	SK-N-SH_RA	brain:	n/a	chr6:74036516-74036534 chr6:74036511-74036532 chr6:74036523-74036530 chr6:74036649-74036656
45	CTCF	chr6:74018920-74019070	RPTEC	kidney:	n/a	n/a
46	CTCF	chr6:74019967-74019977	MCF-7	breast:	n/a	n/a
47	CTCF	chr6:74020060-74020210	HCM	heart:	n/a	chr6:74020150-74020163 chr6:74020153-74020162 chr6:74020147-74020160
48	CTCF	chr6:74036460-74036610	HUVEC	blood vessel:	n/a	chr6:74036516-74036534 chr6:74036511-74036532 chr6:74036523-74036530
49	CTCF	chr6:74036458-74036625	GM20000	blood:	n/a	chr6:74036516-74036534 chr6:74036511-74036532 chr6:74036523-74036530
50	CTCF	chr6:74020040-74020190	GM12875	blood:	n/a	chr6:74020150-74020163 chr6:74020153-74020162 chr6:74020147-74020160

(count:854 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:74025019-74025069	GM19239	blood:	n/a
2	chr6:74020122-74020172	CMK	blood:	n/a
3	chr6:74021027-74021077	HCT-116	colon:	n/a
4	chr6:74019562-74019612	Caco-2	colon:	n/a
5	chr6:74019653-74019703	HCPEpiC	choroid plexus:	n/a
6	chr6:74019833-74019883	NB4	blood:	n/a
7	chr6:74024628-74024678	HL-60	blood:	n/a
8	chr6:74019833-74019883	HRE	kidney:	n/a
9	chr6:74019833-74019883	HepG2	liver:	n/a
10	chr6:74019562-74019612	PANC-1	pancreas:	n/a
11	chr6:74021027-74021077	H1-hESC	embryonic stem cell:	embryo
12	chr6:74020018-74020068	GM12892	blood:	n/a
13	chr6:74025019-74025069	RPTEC	kidney:	n/a
14	chr6:74024572-74024622	HL-60	blood:	n/a
15	chr6:74020122-74020172	PrEC	prostate:	n/a
16	chr6:74024344-74024394	SK-N-MC	brain:	n/a
17	chr6:74021027-74021077	AoSMC	blood vessel:	n/a
18	chr6:74019653-74019703	SK-N-SH_RA	brain:	n/a
19	chr6:74018889-74018939	NH-A	brain:	n/a
20	chr6:74020018-74020068	U87	brain:	n/a
21	chr6:74020122-74020172	MCF-7	breast:	n/a
22	chr6:74020018-74020068	HCF	heart:	n/a
23	chr6:74024344-74024394	HCM	heart:	n/a
24	chr6:74020122-74020172	NHBE	bronchial:	n/a
25	chr6:74020122-74020172	SK-N-SH	brain:	n/a
26	chr6:74024344-74024394	MCF10A-Er-Src	breast:	n/a
27	chr6:74020122-74020172	HCT-116	colon:	n/a
28	chr6:74019653-74019703	SAEC	small airway:	n/a
29	chr6:74019562-74019612	HepG2	liver:	n/a
30	chr6:74020018-74020068	K562	blood:	n/a
31	chr6:74020018-74020068	BE2_C	brain:	n/a
32	chr6:74024628-74024678	Caco-2	colon:	n/a
33	chr6:74025019-74025069	HEK293	kidney:	embryo
34	chr6:74025019-74025069	SK-N-SH_RA	brain:	n/a
35	chr6:74024628-74024678	BJ	skin:	n/a
36	chr6:74027775-74027825	SK-N-SH	brain:	n/a
37	chr6:74024572-74024622	BJ	skin:	n/a
38	chr6:74027775-74027825	ovcar-3	ovarian:	n/a
39	chr6:74027775-74027825	AG10803	skin:	n/a
40	chr6:74027775-74027825	HRCEpiC	kidney:	n/a
41	chr6:74024628-74024678	HEK293	kidney:	embryo
42	chr6:74019562-74019612	PrEC	prostate:	n/a
43	chr6:74027775-74027825	HUVEC	blood vessel:	n/a
44	chr6:74019833-74019883	AG09319	gingival:	n/a
45	chr6:74025019-74025069	GM12891	blood:	n/a
46	chr6:74019653-74019703	HAEpiC	amniotic membrane:	n/a
47	chr6:74027775-74027825	MCF10A-Er-Src	breast:	n/a
48	chr6:74019653-74019703	ECC-1	luminal epithelium:	n/a
49	chr6:74024628-74024678	MCF-7	breast:	n/a
50	chr6:74025019-74025069	Caco-2	colon:	n/a

(count:30 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr6:73890367..73891378-chr6:74036227..74036958,3	MCF-7	breast:
2	chr6:74018617..74020402-chr6:74229038..74231578,2	K562	blood:
3	chr6:73121726..73122573-chr6:74036126..74036963,2	K562	blood:
4	chr6:74019175..74020751-chr6:74101665..74105754,3	MCF-7	breast:
5	chr6:74017993..74019830-chr6:74023707..74026183,2	K562	blood:
6	6:74039397-74041926..6:74160392-74184826	K562	blood:
7	chr6:74023411..74025387-chr6:74040340..74041969,2	K562	blood:
8	chr6:74016335..74020471-chr6:74023395..74026748,3	MCF-7	breast:
9	chr6:73995073..73995767-chr6:74036342..74037050,3	MCF-7	breast:
10	6:74020790-74026830..6:74078047-74099067	Hela-S3	cervix:
11	chr6:74019132..74021037-chr6:74035102..74038001,2	MCF-7	breast:
12	chr6:74010598..74017256-chr6:74017490..74021575,10	K562	blood:
13	6:74039397-74041926..6:74099986-74112890	H1-hESC	embryonic stem cell:	embryo
14	chr6:74017993..74019830-chr6:74023707..74026183,2	K562	blood:
15	chr6:73121709..73122634-chr6:74035964..74037244,6	MCF-7	breast:
16	6:74012200-74019242..6:74078047-74099067	H1-hESC	embryonic stem cell:	embryo
17	chr6:73995184..73996292-chr6:74036159..74036919,3	MCF-7	breast:
18	chr6:74017750..74019913-chr6:74026260..74028005,2	K562	blood:
19	6:74020790-74026830..6:74099986-74112890	H1-hESC	embryonic stem cell:	embryo
20	chr6:74019132..74021037-chr6:74035102..74038001,2	MCF-7	breast:
21	6:73969782-73974110..6:74020790-74026830	GM12878	blood:
22	6:74039397-74041926..6:74078047-74099067	H1-hESC	embryonic stem cell:	embryo
23	6:74020790-74026830..6:74062967-74076046	Hela-S3	cervix:
24	chr6:74019135..74019848-chr8:134309134..134310019,2	HCT-116	colon:
25	chr6:23741380..23742211-chr6:74038683..74039276,2	MCF-7	breast:
26	chr1:24285827..24286696-chr6:74019562..74020370,2	Hela-S3	cervix:
27	chr6:74023411..74025387-chr6:74040340..74041969,2	K562	blood:
28	6:73927031-73938730..6:74020790-74026830	GM12878	blood:
29	chr6:74036160..74036840-chr6:74098186..74098994,2	MCF-7	breast:
30	6:74012200-74019242..6:74062967-74076046	Hela-S3	cervix:

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

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-C6orf221-4	chr6:74038219-74038740	NONHSAT113552
2	lnc-KHDC1-2	chr6:74024327-74024611	NONHSAT113550
3	lnc-KHDC1-1	chr6:74019275-74019451	NONHSAT113547
4	lnc-KHDC1-1	chr6:74020029-74020088	NONHSAT113544
5	lnc-KHDC1-1	chr6:74020029-74020088	NONHSAT113547
6	lnc-KHDC1-1	chr6:74019275-74019866	NONHSAT113546
7	lnc-C6orf221-4	chr6:74037247-74037892	NONHSAT113552
8	lnc-KHDC1-1	chr6:74019275-74019451	NONHSAT113544
9	lnc-C6orf221-5	chr6:74032560-74033173	NONHSAT113551

No data

Variant related genes	Relation type
KHDC1	TF binding region
SDCBP2P1	TF binding region
PAICSP3	TF binding region
KHDC1	CpG island
SDCBP2P1	CpG island
PAICSP3	CpG island
ENSG00000235174	chromatin interactions
ENSG00000238464	chromatin interactions
ENSG00000263378	chromatin interactions
ENSG00000189266	chromatin interactions
ENSG00000156508	chromatin interactions
ENSG00000203907	chromatin interactions
ENSG00000224221	chromatin interactions
ENSG00000207023	chromatin interactions
ENSG00000229852	chromatin interactions
ENSG00000080007	chromatin interactions
ENSG00000135314	chromatin interactions
ENSG00000231332	chromatin interactions
ENSG00000243501	chromatin interactions
ENSG00000203909	chromatin interactions
ENSG00000104419	chromatin interactions
ENSG00000256980	chromatin interactions
ENSG00000135297	chromatin interactions
ENSG00000164430	chromatin interactions
ENSG00000226840	chromatin interactions
ENSG00000203908	chromatin interactions

Extended variants
information (count: 996 )
Associated
traits (count: 91 )

Variant overlapped rSNPs/rCNVs (count:996 , 50 per page) page: 1 2 3 4 5 6 7 ... 20

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs555779	chr6:74014468-74014469	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
2	rs72945998	chr6:74014522-74014523	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
3	rs542677238	chr6:74014533-74014534	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
4	rs546369323	chr6:74014550-74014551	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
5	rs564571304	chr6:74014688-74014689	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
6	rs573292364	chr6:74014708-74014709	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
7	rs28439447	chr6:74014735-74014736	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
8	rs540713469	chr6:74014798-74014799	Weak transcription Flanking Active TSS Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
9	rs151229414	chr6:74014854-74014855	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs533166757	chr6:74014866-74014867	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs545186033	chr6:74014869-74014870	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs60093179	chr6:74014918-74014919	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
13	rs146988090	chr6:74014948-74014949	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs116116985	chr6:74014950-74014951	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs187638977	chr6:74014965-74014966	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
16	rs12213765	chr6:74014976-74014977	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
17	rs61400658	chr6:74014992-74014993	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
18	rs138356949	chr6:74014994-74014995	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
19	rs538862757	chr6:74015034-74015035	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
20	rs550732749	chr6:74015054-74015055	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
21	rs199769606	chr6:74015062-74015063	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
22	rs199784776	chr6:74015063-74015064	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
23	rs548281188	chr6:74015064-74015065	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
24	rs113993420	chr6:74015138-74015139	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
25	rs536937601	chr6:74015195-74015196	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
26	rs529076155	chr6:74015253-74015254	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
27	rs554708245	chr6:74015256-74015257	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
28	rs548734650	chr6:74015321-74015322	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
29	rs573187205	chr6:74015335-74015336	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
30	rs138716220	chr6:74015374-74015375	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
31	rs565739713	chr6:74015401-74015402	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
32	rs569019199	chr6:74015406-74015407	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
33	rs559105080	chr6:74015412-74015413	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
34	rs375845685	chr6:74015445-74015446	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
35	rs60682661	chr6:74015491-74015492	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
36	rs577380500	chr6:74015527-74015528	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
37	rs192076313	chr6:74015529-74015530	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
38	rs149360573	chr6:74015544-74015545	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
39	rs563454796	chr6:74015585-74015586	Weak transcription Enhancers	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
40	rs575487845	chr6:74015637-74015638	Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
41	rs498674	chr6:74015648-74015649	Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
42	rs532922812	chr6:74015701-74015702	Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
43	rs7769905	chr6:74015765-74015766	Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
44	rs570796785	chr6:74015781-74015782	Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
45	rs148172187	chr6:74015783-74015784	Weak transcription Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
46	rs142918356	chr6:74015852-74015853	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
47	rs564659819	chr6:74015890-74015891	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
48	rs532054778	chr6:74015954-74015955	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
49	rs550798008	chr6:74015991-74015992	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
50	rs569100309	chr6:74016022-74016023	Weak transcription Enhancers Genic enhancers Flanking Active TSS	Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:91)

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
Autism	21448237	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Lung cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Autism	22495311	CNVD
Endometrioid adenocarcinoma	16974079	CNVD
Gastric cancer	17908304	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
Breast cancer	17603634	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Systemic lupus erythematosus	17503323	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Melanoma	18172304	CNVD
Esophageal squamous carcinoma	18350619	CNVD
Cancer	21637783	CNVD
Colorectal cancer	16272173	CNVD
lymphocytic leukemia	21291569	CNVD
Acute lymphoblastic leukemia	17443227	CNVD
T-cell lymphomas	19863542	CNVD
Lung cancer	18438408	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
Ependymoma	16718352	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
Prostate cancer	16573809	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Breast cancer	16272173	CNVD
small cell lung cancer	20016488	CNVD
Prostate cancer	18632612	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Diffuse large b-cell lymphoma	18287131	CNVD
Urothelial carcinoma	18382360	CNVD
Ovarian neoplasms	16753589	CNVD
Hepatocellular carcinoma	16750200	CNVD
Wilms tumour	21544195	CNVD
Breast cancer	21364760	CNVD
Acute lymphoblastic leukemia	21098271	CNVD
Ovarian cancer	17437010	CNVD
Myelofibrosis	22110671	CNVD
Glioma	17123091	CNVD
Mental retardation	17124404	CNVD
Chondromyxoid Fibroma	20696777	CNVD
Multiple myeloma	16616336	CNVD
Acute myeloid leukemia	16864856	CNVD
Follicular lymphoma	17699855	CNVD
Breast cancer	17133270	CNVD
Leukemia	18688285	CNVD
Prostate cancer	19242612	CNVD
Developmental delay	21147756	CNVD
Glioma	21046410	CNVD
Primary central nervous system lymphoma	21088137	CNVD
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	CNVD
Congenital diaphragmatic hernia	21085971	CNVD
Malignant melanoma	18718029	CNVD
Breast cancer	22522925	CNVD

Chromatin state (count:617 , 50 per page) page: 1 2 3 4 5 6 7 ... 13

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:73973600-74018600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
2	chr6:73973600-74018600	Weak transcription	A549	lung
3	chr6:73973600-74018800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
4	chr6:73974000-74018400	Weak transcription	iPS-15b Cell Line	embryonic stem cell
5	chr6:73983800-74018600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
6	chr6:73984400-74018600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
7	chr6:73989000-74017200	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr6:73994200-74018600	Weak transcription	Stomach Mucosa	stomach
9	chr6:73996000-74015800	Weak transcription	Hela-S3	cervix
10	chr6:74001000-74017200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
11	chr6:74005200-74018600	Weak transcription	HUES6 Cell Line	embryonic stem cell
12	chr6:74007800-74017400	Weak transcription	iPS-20b Cell Line	embryonic stem cell
13	chr6:74008800-74018400	Weak transcription	HUES64 Cell Line	embryonic stem cell
14	chr6:74009000-74018400	Weak transcription	H9 Cell Line	embryonic stem cell
15	chr6:74009400-74017200	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:74009400-74017200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
17	chr6:74009400-74017200	Weak transcription	Fetal Thymus	thymus
18	chr6:74009400-74017200	Weak transcription	Pancreas	Pancrea
19	chr6:74009400-74017400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
20	chr6:74009400-74018400	Weak transcription	Fetal Lung	lung
21	chr6:74009400-74019000	Weak transcription	Right Atrium	heart
22	chr6:74009600-74016000	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
23	chr6:74009600-74016000	Weak transcription	Fetal Brain Male	brain
24	chr6:74009600-74017200	Weak transcription	Fetal Muscle Trunk	muscle
25	chr6:74009600-74017400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
26	chr6:74009600-74017400	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
27	chr6:74009600-74017400	Weak transcription	Osteobl	bone
28	chr6:74009600-74018600	Weak transcription	H1 Cell Line	embryonic stem cell
29	chr6:74009600-74018600	Weak transcription	Primary hematopoietic stem cells	blood
30	chr6:74009600-74018600	Weak transcription	Muscle Satellite Cultured Cells	--
31	chr6:74009600-74018600	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
32	chr6:74009600-74018600	Weak transcription	NHLF	lung
33	chr6:74009800-74015800	Weak transcription	Fetal Brain Female	brain
34	chr6:74009800-74015800	Weak transcription	Fetal Muscle Leg	muscle
35	chr6:74009800-74016600	Weak transcription	Brain Germinal Matrix	brain
36	chr6:74009800-74018800	Weak transcription	Ovary	ovary
37	chr6:74009800-74018800	Weak transcription	Spleen	Spleen
38	chr6:74010000-74016000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
39	chr6:74010000-74018400	Weak transcription	ES-I3 Cell Line	embryonic stem cell
40	chr6:74010000-74018600	Weak transcription	Fetal Intestine Small	intestine
41	chr6:74010000-74018800	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
42	chr6:74010000-74018800	Weak transcription	Thymus	Thymus
43	chr6:74010600-74016000	Weak transcription	K562	blood
44	chr6:74010600-74016200	Weak transcription	Primary hematopoietic stem cells short term culture	blood
45	chr6:74010600-74018200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
46	chr6:74011800-74016800	Weak transcription	Fetal Stomach	stomach
47	chr6:74012400-74015800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr6:74012400-74017400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:74012600-74018400	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
50	chr6:74013200-74014800	Enhancers	GM12878-XiMat	blood

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