Variant report

Variant	esv1820434
Chromosome Location	chr6:147518489-147543262
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1059)
CpG islands
(count:795)
Chromatin interactive
region (count:71)
LncRNA
region (count:5)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1059 , 50 per page) page: 1 2 3 4 5 6 7 ... 22

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:147528088-147528191	K562	blood:	n/a	n/a
2	ARID3A	chr6:147526670-147527526	K562	blood:	n/a	chr6:147526834-147526850
3	ARID3A	chr6:147531050-147531310	K562	blood:	n/a	n/a
4	ARID3A	chr6:147539112-147539472	K562	blood:	n/a	n/a
5	ARID3A	chr6:147525839-147525874	HepG2	liver:	n/a	n/a
6	ARID3A	chr6:147524603-147524990	HepG2	liver:	n/a	n/a
7	ARID3A	chr6:147522403-147522536	K562	blood:	n/a	n/a
8	ARID3A	chr6:147521564-147521887	K562	blood:	n/a	n/a
9	ARID3A	chr6:147529694-147529864	K562	blood:	n/a	n/a
10	ARID3A	chr6:147539974-147540745	K562	blood:	n/a	n/a
11	ARID3A	chr6:147528435-147528992	K562	blood:	n/a	n/a
12	ARID3A	chr6:147530188-147530714	K562	blood:	n/a	n/a
13	ARID3A	chr6:147527046-147527225	HepG2	liver:	n/a	n/a
14	ARID3A	chr6:147526065-147526421	K562	blood:	n/a	n/a
15	ARID3A	chr6:147522900-147524003	K562	blood:	n/a	n/a
16	ATF1	chr6:147523058-147524219	K562	blood:	n/a	n/a
17	ATF1	chr6:147526915-147527250	K562	blood:	n/a	n/a
18	ATF2	chr6:147523030-147524633	GM12878	blood:	n/a	n/a
19	ATF3	chr6:147524390-147525050	K562	blood:	n/a	n/a
20	ATF3	chr6:147524738-147525057	HepG2	liver:	n/a	n/a
21	BACH1	chr6:147524935-147524937	K562	blood:	n/a	n/a
22	BACH1	chr6:147526258-147526458	K562	blood:	n/a	n/a
23	BACH1	chr6:147528491-147528686	K562	blood:	n/a	n/a
24	BCLAF1	chr6:147524598-147525209	GM12878	blood:	n/a	chr6:147525120-147525133
25	BCLAF1	chr6:147526825-147527464	K562	blood:	n/a	n/a
26	BCLAF1	chr6:147523614-147525189	K562	blood:	n/a	chr6:147524304-147524317 chr6:147523993-147524002 chr6:147523994-147524003 chr6:147525120-147525133
27	BCLAF1	chr6:147525311-147525800	GM12878	blood:	n/a	chr6:147525385-147525398 chr6:147525386-147525395 chr6:147525389-147525398 chr6:147525381-147525394 chr6:147525426-147525439 chr6:147525387-147525400 chr6:147525391-147525404 chr6:147525392-147525401 chr6:147525388-147525401
28	BCLAF1	chr6:147533572-147534127	K562	blood:	n/a	n/a
29	BCLAF1	chr6:147528369-147529033	K562	blood:	n/a	chr6:147528794-147528803
30	BHLHE40	chr6:147522982-147525150	K562	blood:	n/a	chr6:147525121-147525137
31	BHLHE40	chr6:147525640-147525780	K562	blood:	n/a	n/a
32	BHLHE40	chr6:147524754-147525068	HepG2	liver:	n/a	n/a
33	BHLHE40	chr6:147523423-147525046	GM12878	blood:	n/a	n/a
34	BRCA1	chr6:147523488-147524218	Hela-S3	cervix:	n/a	chr6:147524060-147524069
35	BRCA1	chr6:147523552-147524167	HepG2	liver:	n/a	chr6:147524060-147524069
36	BRCA1	chr6:147524881-147524961	HepG2	liver:	n/a	n/a
37	BRCA1	chr6:147523763-147524185	GM12878	blood:	n/a	chr6:147524060-147524069
38	CBX3	chr6:147522977-147524263	K562	blood:	n/a	n/a
39	CBX3	chr6:147524342-147524946	K562	blood:	n/a	n/a
40	CCNT2	chr6:147523484-147525893	K562	blood:	n/a	chr6:147524779-147524788
41	CCNT2	chr6:147536114-147536383	K562	blood:	n/a	n/a
42	CCNT2	chr6:147529017-147529333	K562	blood:	n/a	n/a
43	CCNT2	chr6:147531066-147531100	K562	blood:	n/a	n/a
44	CCNT2	chr6:147528484-147528732	K562	blood:	n/a	n/a
45	CCNT2	chr6:147539267-147539457	K562	blood:	n/a	n/a
46	CCNT2	chr6:147526769-147527268	K562	blood:	n/a	n/a
47	CCNT2	chr6:147538849-147538940	K562	blood:	n/a	n/a
48	CEBPB	chr6:147521896-147522204	IMR90	lung:	n/a	chr6:147522040-147522051
49	CEBPB	chr6:147522925-147524074	K562	blood:	n/a	n/a
50	CEBPB	chr6:147543148-147543998	K562	blood:	n/a	chr6:147543363-147543374

(count:795 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:147525648-147525698	HCM	heart:	n/a
2	chr6:147524085-147524135	HRE	kidney:	n/a
3	chr6:147525648-147525698	HCM	heart:	n/a
4	chr6:147524085-147524135	HRE	kidney:	n/a
5	chr6:147525648-147525698	HIPEpiC	eye:	n/a
6	chr6:147524841-147524891	BE2_C	brain:	n/a
7	chr6:147525710-147525760	BJ	skin:	n/a
8	chr6:147525477-147525527	PFSK-1	brain:	n/a
9	chr6:147524085-147524135	SKMC	muscle:	n/a
10	chr6:147523659-147523709	HMEC	breast:	n/a
11	chr6:147523200-147523250	MCF-7	breast:	n/a
12	chr6:147525462-147525512	H1-hESC	embryonic stem cell:	embryo
13	chr6:147528521-147528571	AG09319	gingival:	n/a
14	chr6:147525462-147525512	CMK	blood:	n/a
15	chr6:147527113-147527163	HCT-116	colon:	n/a
16	chr6:147527113-147527163	GM12891	blood:	n/a
17	chr6:147524977-147525027	H1-hESC	embryonic stem cell:	embryo
18	chr6:147528521-147528571	NT2-D1	testis:	n/a
19	chr6:147525477-147525527	HMEC	breast:	n/a
20	chr6:147525710-147525760	Hela-S3	cervix:	n/a
21	chr6:147525710-147525760	SKMC	muscle:	n/a
22	chr6:147523200-147523250	SK-N-SH_RA	brain:	n/a
23	chr6:147524977-147525027	RPTEC	kidney:	n/a
24	chr6:147525477-147525527	HIPEpiC	eye:	n/a
25	chr6:147524977-147525027	HRPEpiC	eye:	n/a
26	chr6:147524578-147524628	GM19239	blood:	n/a
27	chr6:147525462-147525512	AoSMC	blood vessel:	n/a
28	chr6:147524977-147525027	PANC-1	pancreas:	n/a
29	chr6:147525648-147525698	LNCaP	prostate:	n/a
30	chr6:147528521-147528571	IMR90	lung:	fetal
31	chr6:147525710-147525760	GM19239	blood:	n/a
32	chr6:147523659-147523709	PANC-1	pancreas:	n/a
33	chr6:147525462-147525512	NT2-D1	testis:	n/a
34	chr6:147525710-147525760	MCF10A-Er-Src	breast:	n/a
35	chr6:147523200-147523250	BJ	skin:	n/a
36	chr6:147525477-147525527	T-47D	breast:	n/a
37	chr6:147527113-147527163	NHBE	bronchial:	n/a
38	chr6:147524841-147524891	K562	blood:	n/a
39	chr6:147527113-147527163	AG09319	gingival:	n/a
40	chr6:147528521-147528571	PANC-1	pancreas:	n/a
41	chr6:147525477-147525527	NHBE	bronchial:	n/a
42	chr6:147528521-147528571	H1-hESC	embryonic stem cell:	embryo
43	chr6:147525462-147525512	PFSK-1	brain:	n/a
44	chr6:147523200-147523250	A549	lung:	n/a
45	chr6:147524272-147524322	Caco-2	colon:	n/a
46	chr6:147525710-147525760	HCF	heart:	n/a
47	chr6:147524841-147524891	HRE	kidney:	n/a
48	chr6:147524578-147524628	IMR90	lung:	fetal
49	chr6:147525710-147525760	H1-hESC	embryonic stem cell:	embryo
50	chr6:147523659-147523709	MCF-7	breast:	n/a

(count:71 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:147224255..147227210-chr6:147538729..147540565,2	K562	blood:
2	chr6:147177851..147181465-chr6:147522179..147525344,4	K562	blood:
3	chr6:147541961..147544233-chr6:147614888..147617069,2	K562	blood:
4	chr6:147518626..147520972-chr6:147541650..147544100,2	MCF-7	breast:
5	chr6:147232346..147237544-chr6:147521050..147527983,13	K562	blood:
6	chr6:147196446..147198870-chr6:147535812..147538207,2	K562	blood:
7	chr6:147231935..147237791-chr6:147522176..147527834,11	MCF-7	breast:
8	chr6:147178857..147181755-chr6:147524235..147526085,2	MCF-7	breast:
9	chr6:147393491..147395235-chr6:147521647..147523275,2	K562	blood:
10	chr6:147475725..147486468-chr6:147521132..147528058,22	K562	blood:
11	chr6:147217369..147219463-chr6:147527173..147529417,2	K562	blood:
12	chr6:147495768..147498501-chr6:147520292..147523233,3	K562	blood:
13	chr6:147516623..147520758-chr6:147522602..147524809,4	MCF-7	breast:
14	chr6:147495613..147497909-chr6:147518076..147519884,2	K562	blood:
15	chr6:147218917..147220717-chr6:147520720..147523033,2	K562	blood:
16	chr6:147476130..147479059-chr6:147530096..147532548,2	K562	blood:
17	chr6:147522872..147525730-chr6:147542858..147544761,2	MCF-7	breast:
18	chr6:147217069..147220905-chr6:147535647..147540121,4	K562	blood:
19	chr6:147223268..147225541-chr6:147530064..147532627,3	K562	blood:
20	chr6:147481284..147483476-chr6:147542253..147543860,2	K562	blood:
21	chr6:147360421..147363039-chr6:147534968..147537211,2	K562	blood:
22	chr6:147532510..147534071-chr6:147598840..147601829,2	K562	blood:
23	chr6:147320535..147323169-chr6:147518851..147520491,2	K562	blood:
24	chr6:147471031..147473027-chr6:147529054..147531179,2	K562	blood:
25	chr6:147537663..147540561-chr6:147542025..147543593,2	MCF-7	breast:
26	chr6:147233166..147237387-chr6:147522685..147525854,6	MCF-7	breast:
27	chr6:147542165..147544877-chr6:147580588..147582503,2	K562	blood:
28	chr6:147221788..147226460-chr6:147542201..147549451,7	K562	blood:
29	chr6:147534848..147537270-chr6:147604730..147607356,2	K562	blood:
30	chr6:147223063..147225142-chr6:147528018..147531876,3	K562	blood:
31	chr6:147177011..147178784-chr6:147528174..147531299,3	K562	blood:
32	chr6:147478214..147481987-chr6:147524471..147526667,3	MCF-7	breast:
33	chr6:147229677..147239083-chr6:147521152..147530893,22	K562	blood:
34	chr6:147524306..147526368-chr6:147531209..147534111,3	MCF-7	breast:
35	chr6:147180477..147182479-chr6:147519593..147522559,2	K562	blood:
36	chr6:147207096..147209923-chr6:147534752..147537140,2	K562	blood:
37	chr6:147523543..147527462-chr6:147538561..147541910,5	MCF-7	breast:
38	chr6:147316468..147318660-chr6:147533860..147536236,2	K562	blood:
39	chr6:147236068..147238038-chr6:147542284..147544825,2	K562	blood:
40	chr6:147513740..147516314-chr6:147536481..147538710,2	K562	blood:
41	chr6:147536981..147538610-chr6:147586523..147588657,2	K562	blood:
42	chr6:147495348..147497909-chr6:147517177..147519884,2	K562	blood:
43	chr6:147524840..147526974-chr6:147542411..147544286,3	MCF-7	breast:
44	chr6:147537663..147540561-chr6:147542025..147543593,2	MCF-7	breast:
45	chr6:147185541..147187437-chr6:147534820..147537621,2	K562	blood:
46	chr6:147176826..147178897-chr6:147521577..147523241,2	K562	blood:
47	chr6:147537757..147539516-chr6:147545815..147547714,2	MCF-7	breast:
48	chr6:147514297..147518572-chr6:147531601..147534869,4	K562	blood:
49	chr6:147201123..147203183-chr6:147520675..147522289,2	K562	blood:
50	chr6:147514297..147518572-chr6:147531601..147534869,4	K562	blood:

(count:5 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-STXBP5-4	chr6:147521754-147521813	NONHSAT115448
2	lnc-SHPRH-2	chr6:147523506-147523603	ENSG00000233452
3	lnc-SHPRH-2	chr6:147525549-147525750	NONHSAT115433
4	lnc-STXBP5-4	chr6:147528560-147528688	NONHSAT115448
5	lnc-SHPRH-2	chr6:147525549-147525676	ENSG00000233452

No data

Variant related genes	Relation type
STXBP5-AS1	TF binding region
STXBP5	TF binding region
STXBP5-AS1	CpG island
STXBP5	CpG island
ENSG00000233452	chromatin interactions
ENSG00000074054	chromatin interactions
ENSG00000196634	chromatin interactions
ENSG00000135541	chromatin interactions
ENSG00000264229	chromatin interactions
ENSG00000227748	chromatin interactions
ENSG00000231028	chromatin interactions
ENSG00000164506	chromatin interactions
DICER1	miRNA target sites
TAB3	miRNA target sites

Extended variants
information (count: 857 )
Associated
traits (count: 75 )

Variant overlapped rSNPs/rCNVs (count:857 , 50 per page) page: 1 2 3 4 5 6 7 ... 18

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs190446392	chr6:147518489-147518490	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs536031420	chr6:147518521-147518522	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs58638359	chr6:147518533-147518534	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
4	rs574508071	chr6:147518565-147518566	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs543140395	chr6:147518579-147518580	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
6	rs182273739	chr6:147518595-147518596	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs114475803	chr6:147518605-147518606	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs545701087	chr6:147518606-147518607	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs559187234	chr6:147518681-147518682	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs528291641	chr6:147518745-147518746	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs548009407	chr6:147518777-147518778	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs4895708	chr6:147518814-147518815	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs186869975	chr6:147518885-147518886	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs550752481	chr6:147518934-147518935	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs570834543	chr6:147518961-147518962	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs539812049	chr6:147518970-147518971	Weak transcription Enhancers	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs138477901	chr6:147519044-147519045	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs567202215	chr6:147519140-147519141	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs191764109	chr6:147519143-147519144	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs556034851	chr6:147519155-147519156	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs547847676	chr6:147519184-147519185	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs575743621	chr6:147519191-147519192	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs9497723	chr6:147519195-147519196	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs567689225	chr6:147519217-147519218	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs576787201	chr6:147519218-147519219	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
26	rs545363888	chr6:147519229-147519230	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs150652350	chr6:147519240-147519241	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs572842859	chr6:147519336-147519337	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs539527397	chr6:147519361-147519362	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs369944365	chr6:147519388-147519389	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs138721211	chr6:147519397-147519398	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
32	rs182669308	chr6:147519403-147519404	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs149358878	chr6:147519455-147519456	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs551072887	chr6:147519478-147519479	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs146268974	chr6:147519487-147519488	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs533445935	chr6:147519518-147519519	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs73580488	chr6:147519554-147519555	Weak transcription	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
38	rs566860849	chr6:147519585-147519586	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs139375824	chr6:147519626-147519627	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
40	rs568766083	chr6:147519645-147519646	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs185451211	chr6:147519686-147519687	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs371906489	chr6:147519793-147519794	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs537759690	chr6:147519802-147519803	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs551425149	chr6:147519816-147519817	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs117813413	chr6:147519826-147519827	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs189954030	chr6:147519877-147519878	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs557041101	chr6:147519882-147519883	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs146250757	chr6:147519895-147519896	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs182258334	chr6:147519909-147519910	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs539130063	chr6:147519936-147519937	Weak transcription	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:75)

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
Autism	22495311	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
lymphocytic leukemia	21291569	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
Zellweger syndrome	21572526	CNVD
Follicular lymphoma	20505157	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
Chondromyxoid Fibroma	20696777	CNVD
Cancer	21183584	CNVD
Developmental delay	19490664	CNVD
Burkitt''s lymphoma	18698080	CNVD
Follicular lymphoma	18703704	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
Renal cell carcinoma	18592004	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Malignant melanoma	17260012	CNVD
Prostate cancer	18632612	CNVD
low-grade B-cell lymphoma tumor	18367492	CNVD
Lung cancer	18438408	CNVD
Endocrine pancreatic tumor	17914106	CNVD
Soft tissue tumor	16732325	CNVD
Burkitt''s lymphoma	19759907	CNVD
Myelofibrosis	22110671	CNVD

Chromatin state (count:928 , 50 per page) page: 1 2 3 4 5 6 7 ... 19

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:147516400-147519000	Enhancers	K562	blood
2	chr6:147516600-147522800	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
3	chr6:147516600-147523000	Weak transcription	Osteobl	bone
4	chr6:147516800-147523000	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
5	chr6:147516800-147523000	Weak transcription	HUVEC	blood vessel
6	chr6:147517000-147518600	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
7	chr6:147517000-147522800	Weak transcription	A549	lung
8	chr6:147517200-147518600	Enhancers	Primary neutrophils fromperipheralblood	blood
9	chr6:147517200-147522800	Weak transcription	Monocytes-CD14+_RO01746	blood
10	chr6:147517400-147522400	Weak transcription	Primary hematopoietic stem cells short term culture	blood
11	chr6:147517400-147522400	Weak transcription	Primary T helper cells PMA-I stimulated	--
12	chr6:147517400-147523000	Weak transcription	Primary monocytes fromperipheralblood	blood
13	chr6:147517400-147523000	Weak transcription	NHDF-Ad	bronchial
14	chr6:147517600-147523000	Weak transcription	Primary T helper 17 cells PMA-I stimulated	--
15	chr6:147517800-147522600	Weak transcription	Primary hematopoietic stem cells	blood
16	chr6:147518000-147522600	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr6:147518000-147522800	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
18	chr6:147518000-147523000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
19	chr6:147518400-147518800	Enhancers	Foreskin Fibroblast Primary Cells skin02	Skin
20	chr6:147518400-147519000	Enhancers	Muscle Satellite Cultured Cells	--
21	chr6:147518400-147519000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
22	chr6:147518600-147522400	Weak transcription	Primary neutrophils fromperipheralblood	blood
23	chr6:147518600-147523000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr6:147519000-147521000	Weak transcription	K562	blood
25	chr6:147519000-147521800	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
26	chr6:147519000-147523200	Weak transcription	Muscle Satellite Cultured Cells	--
27	chr6:147521000-147521400	Flanking Active TSS	K562	blood
28	chr6:147521400-147522600	Enhancers	K562	blood
29	chr6:147521800-147522000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
30	chr6:147522000-147522400	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
31	chr6:147522400-147522800	Enhancers	Primary neutrophils fromperipheralblood	blood
32	chr6:147522400-147522800	Enhancers	Primary hematopoietic stem cells short term culture	blood
33	chr6:147522400-147523000	Active TSS	Primary T helper cells PMA-I stimulated	--
34	chr6:147522400-147523000	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr6:147522600-147522800	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
36	chr6:147522600-147522800	Enhancers	Primary hematopoietic stem cells	blood
37	chr6:147522600-147522800	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
38	chr6:147522600-147522800	Weak transcription	Liver	Liver
39	chr6:147522600-147523000	Bivalent Enhancer	HepG2	liver
40	chr6:147522600-147523200	Flanking Active TSS	K562	blood
41	chr6:147522800-147523000	Enhancers	HUES48 Cell Line	embryonic stem cell
42	chr6:147522800-147523000	Flanking Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
43	chr6:147522800-147523000	Enhancers	Primary B cells from cord blood	blood
44	chr6:147522800-147523000	Enhancers	Primary T cells from cord blood	blood
45	chr6:147522800-147523000	Enhancers	Primary T helper naive cells from peripheral blood	blood
46	chr6:147522800-147523000	Enhancers	Primary T helper naive cells fromperipheralblood	blood
47	chr6:147522800-147523000	Enhancers	Primary T helper cells fromperipheralblood	blood
48	chr6:147522800-147523000	Flanking Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr6:147522800-147523000	Enhancers	Liver	Liver
50	chr6:147522800-147523000	Enhancers	Brain Angular Gyrus	brain

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