Variant report

Variant	nsv884510
Chromosome Location	chr6:31873465-31895216
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:567)
CpG islands
(count:366)
Chromatin interactive
region (count:68)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:567 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr6:31887565-31887673	K562	blood:	n/a	n/a
2	ARID3A	chr6:31894926-31895476	HepG2	liver:	n/a	n/a
3	ARID3A	chr6:31878142-31878240	HepG2	liver:	n/a	n/a
4	ARID3A	chr6:31876624-31876971	HepG2	liver:	n/a	n/a
5	ARID3A	chr6:31879193-31879474	K562	blood:	n/a	n/a
6	ARID3A	chr6:31875170-31875461	HepG2	liver:	n/a	n/a
7	ATF2	chr6:31876453-31877059	GM12878	blood:	n/a	n/a
8	ATF2	chr6:31876511-31877051	GM12878	blood:	n/a	n/a
9	ATF3	chr6:31879116-31879438	K562	blood:	n/a	n/a
10	ATF3	chr6:31879212-31879447	K562	blood:	n/a	n/a
11	BATF	chr6:31879156-31879480	GM12878	blood:	n/a	chr6:31879356-31879367 chr6:31879331-31879342
12	BATF	chr6:31879152-31879398	GM12878	blood:	n/a	chr6:31879356-31879367 chr6:31879331-31879342
13	BATF	chr6:31876477-31876959	GM12878	blood:	n/a	n/a
14	BATF	chr6:31876490-31876927	GM12878	blood:	n/a	n/a
15	BCL11A	chr6:31876589-31876925	GM12878	blood:	n/a	n/a
16	BCL11A	chr6:31879171-31879493	GM12878	blood:	n/a	n/a
17	BCL3	chr6:31876527-31876931	GM12878	blood:	n/a	n/a
18	BCLAF1	chr6:31876612-31877015	GM12878	blood:	n/a	n/a
19	BCLAF1	chr6:31876542-31876935	GM12878	blood:	n/a	n/a
20	BHLHE40	chr6:31894964-31895678	HepG2	liver:	n/a	n/a
21	BHLHE40	chr6:31875228-31875331	HepG2	liver:	n/a	n/a
22	BHLHE40	chr6:31894995-31895366	HepG2	liver:	n/a	n/a
23	BHLHE40	chr6:31876632-31876960	GM12878	blood:	n/a	n/a
24	BHLHE40	chr6:31895047-31895374	HepG2	liver:	n/a	n/a
25	CBX3	chr6:31893622-31894124	K562	blood:	n/a	n/a
26	CBX3	chr6:31877890-31878576	HCT-116	colon:	n/a	n/a
27	CBX3	chr6:31883065-31883640	HCT-116	colon:	n/a	n/a
28	CBX3	chr6:31879153-31879556	HCT-116	colon:	n/a	n/a
29	CBX3	chr6:31893700-31894060	K562	blood:	n/a	n/a
30	CEBPB	chr6:31875114-31875485	MCF-7	breast:	n/a	chr6:31875339-31875350
31	CEBPB	chr6:31875147-31875520	HepG2	liver:	n/a	chr6:31875339-31875350
32	CEBPB	chr6:31875145-31875527	HepG2	liver:	n/a	chr6:31875339-31875350
33	CEBPB	chr6:31875133-31875532	Hela-S3	cervix:	n/a	chr6:31875339-31875350
34	CEBPB	chr6:31875146-31875536	K562	blood:	n/a	chr6:31875339-31875350
35	CEBPB	chr6:31888725-31888839	K562	blood:	n/a	chr6:31888811-31888822 chr6:31888810-31888821 chr6:31888810-31888821 chr6:31888810-31888823
36	CEBPB	chr6:31879065-31879499	Hela-S3	cervix:	n/a	n/a
37	CEBPB	chr6:31875155-31875513	H1-hESC	embryonic stem cell:	n/a	chr6:31875339-31875350
38	CEBPB	chr6:31875140-31875483	A549	lung:	n/a	chr6:31875339-31875350
39	CEBPB	chr6:31876347-31876816	IMR90	lung:	n/a	n/a
40	CEBPB	chr6:31875071-31875545	K562	blood:	n/a	chr6:31875339-31875350
41	CEBPB	chr6:31875201-31875473	ECC-1	luminal epithelium:	n/a	chr6:31875339-31875350
42	CEBPB	chr6:31894937-31895235	HepG2	liver:	n/a	chr6:31895090-31895103 chr6:31895090-31895101 chr6:31895090-31895103 chr6:31895091-31895102 chr6:31895090-31895101
43	CEBPB	chr6:31879032-31879457	IMR90	lung:	n/a	n/a
44	CEBPB	chr6:31888656-31888943	A549	lung:	n/a	chr6:31888811-31888822 chr6:31888810-31888821 chr6:31888810-31888821 chr6:31888810-31888823
45	CEBPB	chr6:31888490-31889087	MCF-7	breast:	n/a	chr6:31888811-31888822 chr6:31888810-31888821 chr6:31888810-31888821 chr6:31888810-31888823
46	CEBPB	chr6:31878443-31878571	IMR90	lung:	n/a	n/a
47	CEBPB	chr6:31888598-31888965	HepG2	liver:	n/a	chr6:31888811-31888822 chr6:31888810-31888821 chr6:31888810-31888821 chr6:31888810-31888823
48	CEBPB	chr6:31875154-31875523	A549	lung:	n/a	chr6:31875339-31875350
49	CEBPB	chr6:31875144-31875494	HepG2	liver:	n/a	chr6:31875339-31875350
50	CEBPB	chr6:31875130-31875502	A549	lung:	n/a	chr6:31875339-31875350

(count:366 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr6:31895203-31895253	HNPCEpiC	eye:	n/a
2	chr6:31895203-31895253	HIPEpiC	eye:	n/a
3	chr6:31895203-31895253	NHBE	bronchial:	n/a
4	chr6:31888543-31888593	GM12891	blood:	n/a
5	chr6:31888543-31888593	HL-60	blood:	n/a
6	chr6:31873772-31873822	AG04450	lung:	fetal
7	chr6:31888543-31888593	H1-hESC	embryonic stem cell:	embryo
8	chr6:31893767-31893817	K562	blood:	n/a
9	chr6:31893767-31893817	BE2_C	brain:	n/a
10	chr6:31895179-31895229	HPAEpiC	pulmonary alveolar:	n/a
11	chr6:31895203-31895253	SAEC	small airway:	n/a
12	chr6:31895203-31895253	AG09319	gingival:	n/a
13	chr6:31893767-31893817	NT2-D1	testis:	n/a
14	chr6:31888543-31888593	HRCEpiC	kidney:	n/a
15	chr6:31895179-31895229	SK-N-SH	brain:	n/a
16	chr6:31894990-31895040	Caco-2	colon:	n/a
17	chr6:31893767-31893817	HL-60	blood:	n/a
18	chr6:31873772-31873822	Jurkat	blood:	n/a
19	chr6:31895179-31895229	AG10803	skin:	n/a
20	chr6:31894990-31895040	NHBE	bronchial:	n/a
21	chr6:31895179-31895229	Hepatocyte	liver:	n/a
22	chr6:31895179-31895229	HEEpiC	esophagus:	n/a
23	chr6:31895179-31895229	BJ	skin:	n/a
24	chr6:31888543-31888593	SK-N-SH_RA	brain:	n/a
25	chr6:31895203-31895253	ProgFib	skin:	n/a
26	chr6:31895203-31895253	T-47D	breast:	n/a
27	chr6:31894990-31895040	GM12891	blood:	n/a
28	chr6:31895203-31895253	MCF10A-Er-Src	breast:	n/a
29	chr6:31895179-31895229	NHBE	bronchial:	n/a
30	chr6:31888543-31888593	AG09309	skin:	n/a
31	chr6:31873772-31873822	HRCEpiC	kidney:	n/a
32	chr6:31895203-31895253	HRE	kidney:	n/a
33	chr6:31894990-31895040	HCPEpiC	choroid plexus:	n/a
34	chr6:31894990-31895040	SK-N-SH	brain:	n/a
35	chr6:31895203-31895253	SKMC	muscle:	n/a
36	chr6:31894990-31895040	MCF10A-Er-Src	breast:	n/a
37	chr6:31888543-31888593	ECC-1	luminal epithelium:	n/a
38	chr6:31873772-31873822	NT2-D1	testis:	n/a
39	chr6:31873772-31873822	NH-A	brain:	n/a
40	chr6:31895203-31895253	PFSK-1	brain:	n/a
41	chr6:31895203-31895253	HCT-116	colon:	n/a
42	chr6:31894990-31895040	CMK	blood:	n/a
43	chr6:31895203-31895253	ECC-1	luminal epithelium:	n/a
44	chr6:31895203-31895253	NHDF-neo	bronchial:	n/a
45	chr6:31888543-31888593	HRPEpiC	eye:	n/a
46	chr6:31895179-31895229	HMEC	breast:	n/a
47	chr6:31888543-31888593	BE2_C	brain:	n/a
48	chr6:31894990-31895040	HEK293	kidney:	embryo
49	chr6:31895203-31895253	LNCaP	prostate:	n/a
50	chr6:31894990-31895040	LNCaP	prostate:	n/a

(count:68 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr6:31889287..31890962-chr6:31906834..31909486,2	MCF-7	breast:
2	chr6:31890425..31891402-chr6:31919829..31921030,3	MCF-7	breast:
3	chr6:31887936..31888758-chr6:31920043..31920676,3	MCF-7	breast:
4	chr6:31873514..31876453-chr6:31939524..31941298,2	K562	blood:
5	chr6:31891185..31893588-chr6:31913608..31916229,2	MCF-7	breast:
6	chr6:31882562..31885157-chr6:31886185..31888056,2	K562	blood:
7	chr6:31888751..31890558-chr6:31890630..31892498,2	MCF-7	breast:
8	chr6:31868564..31871785-chr6:31887319..31890291,4	MCF-7	breast:
9	chr6:31782856..31784391-chr6:31887336..31890005,2	MCF-7	breast:
10	chr6:31870028..31871569-chr6:31882046..31884323,2	K562	blood:
11	chr6:31887457..31890235-chr6:31914279..31916150,2	MCF-7	breast:
12	chr6:31871171..31873867-chr6:31879950..31882707,2	K562	blood:
13	chr6:31812130..31814477-chr6:31875072..31877975,2	K562	blood:
14	chr6:31894560..31897888-chr6:31924484..31926934,4	K562	blood:
15	chr6:31586050..31587690-chr6:31877612..31880010,2	K562	blood:
16	chr6:31882959..31885262-chr6:31885767..31888829,3	MCF-7	breast:
17	chr6:31695993..31698251-chr6:31878269..31880269,2	MCF-7	breast:
18	chr6:31863769..31866724-chr6:31879168..31880795,3	K562	blood:
19	chr6:31890740..31892644-chr6:31893823..31895648,2	K562	blood:
20	chr6:31878159..31881890-chr6:31886214..31889355,6	MCF-7	breast:
21	chr6:31883893..31886674-chr6:31911662..31913312,2	MCF-7	breast:
22	chr6:31869193..31873526-chr6:31908186..31911581,4	MCF-7	breast:
23	chr6:31894637..31897740-chr6:31910021..31912431,3	K562	blood:
24	chr6:31829040..31831339-chr6:31870895..31873682,3	K562	blood:
25	chr6:31875081..31878398-chr6:31887360..31892361,5	MCF-7	breast:
26	chr6:31868781..31871119-chr6:31892943..31895660,2	MCF-7	breast:
27	chr6:31866937..31868698-chr6:31878649..31880716,2	K562	blood:
28	chr6:31873514..31876489-chr6:31937601..31941024,3	K562	blood:
29	chr6:31870200..31872258-chr6:31872448..31875801,4	K562	blood:
30	chr6:31878620..31883206-chr6:31886639..31889995,5	K562	blood:
31	chr6:31869602..31872162-chr6:31872448..31875986,6	K562	blood:
32	chr6:31863637..31866359-chr6:31889858..31891387,2	MCF-7	breast:
33	chr6:31869584..31871706-chr6:31883469..31885193,2	MCF-7	breast:
34	chr6:31894560..31897888-chr6:31924484..31928410,3	K562	blood:
35	chr6:31868484..31871109-chr6:31881429..31883570,2	K562	blood:
36	chr6:31885324..31888930-chr6:31894115..31898580,5	MCF-7	breast:
37	chr6:31886651..31888947-chr6:31926731..31929141,2	MCF-7	breast:
38	chr6:31874923..31879806-chr6:31881504..31885897,6	K562	blood:
39	chr6:31804218..31805106-chr6:31890452..31891172,3	MCF-7	breast:
40	chr6:31865470..31869288-chr6:31882804..31884762,3	MCF-7	breast:
41	chr6:31881823..31884670-chr6:31889806..31892160,2	MCF-7	breast:
42	chr6:31890679..31892417-chr6:31910197..31912737,2	MCF-7	breast:
43	chr6:31881823..31884670-chr6:31889806..31892160,2	MCF-7	breast:
44	chr6:31887719..31889549-chr6:31938108..31940067,2	MCF-7	breast:
45	chr6:31885573..31887303-chr6:31888205..31890772,2	K562	blood:
46	chr6:31876714..31878238-chr6:31917519..31919681,2	MCF-7	breast:
47	chr6:31885324..31888930-chr6:31894115..31898580,5	MCF-7	breast:
48	chr6:31889329..31891544-chr6:31924156..31926793,2	K562	blood:
49	chr6:31874923..31879806-chr6:31881504..31885897,6	K562	blood:
50	chr6:31856732..31859729-chr6:31888389..31891218,2	MCF-7	breast:

No data

Variant related genes	Relation type
C2	TF binding region
ZBTB12	TF binding region
CFB	TF binding region
ENSG00000244255	TF binding region
C2	CpG island
ZBTB12	CpG island
CFB	CpG island
ENSG00000244255	CpG island
ENSG00000204389	chromatin interactions
ENSG00000204435	chromatin interactions
ENSG00000204356	chromatin interactions
ENSG00000204344	chromatin interactions
ENSG00000204387	chromatin interactions
ENSG00000204348	chromatin interactions
ENSG00000221267	chromatin interactions
ENSG00000204390	chromatin interactions
ENSG00000204371	chromatin interactions
ENSG00000204351	chromatin interactions
ENSG00000204366	chromatin interactions
ENSG00000204386	chromatin interactions
ENSG00000201754	chromatin interactions
ENSG00000201207	chromatin interactions
ENSG00000244255	chromatin interactions
ENSG00000213722	chromatin interactions
ENSG00000166278	chromatin interactions
ENSG00000204438	chromatin interactions
ENSG00000243649	chromatin interactions

Extended variants
information (count: 552 )
Associated
traits (count: 131 )

Variant overlapped rSNPs/rCNVs (count:552 , 50 per page) page: 1 2 3 4 5 6 7 ... 12

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs56024127	chr6:31873465-31873466	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
2	rs113232348	chr6:31873470-31873471	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
3	rs563690612	chr6:31873474-31873475	Weak transcription Enhancers	TF binding region Chromatin interactive region	5 gene(s)	Overlapped CNVs	n/a
4	rs577039718	chr6:31873541-31873542	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
5	rs138660214	chr6:31873588-31873589	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
6	rs552880475	chr6:31873596-31873597	Weak transcription Enhancers	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
7	rs113939871	chr6:31873612-31873613	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
8	rs181513924	chr6:31873619-31873620	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
9	rs563741769	chr6:31873704-31873705	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
10	rs572247130	chr6:31873705-31873706	Bivalent Enhancer Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
11	rs117731735	chr6:31873797-31873798	Bivalent Enhancer Enhancers Weak transcription	TF binding region CpG island Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs546206815	chr6:31873856-31873857	Enhancers Weak transcription	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs564502952	chr6:31873913-31873914	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
14	rs528780200	chr6:31874038-31874039	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
15	rs547312272	chr6:31874040-31874041	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
16	rs562255580	chr6:31874119-31874120	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
17	rs529442808	chr6:31874125-31874126	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
18	rs148890374	chr6:31874134-31874135	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
19	rs569395190	chr6:31874139-31874140	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
20	rs536778273	chr6:31874140-31874141	Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
21	rs577105358	chr6:31874205-31874206	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
22	rs148083749	chr6:31874303-31874304	Enhancers Weak transcription Bivalent Enhancer Flanking Active TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs553182204	chr6:31874539-31874540	Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
24	rs574663411	chr6:31874775-31874776	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
25	rs535612893	chr6:31874778-31874779	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
26	rs557230612	chr6:31874808-31874809	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
27	rs370931214	chr6:31874820-31874821	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
28	rs142897748	chr6:31874874-31874875	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
29	rs75261372	chr6:31874895-31874896	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
30	rs567901375	chr6:31874917-31874918	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
31	rs374671719	chr6:31874918-31874919	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
32	rs536927869	chr6:31874947-31874948	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
33	rs541435868	chr6:31874976-31874977	Weak transcription Enhancers	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
34	rs146084965	chr6:31875149-31875150	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
35	rs111239985	chr6:31875360-31875361	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
36	rs186167776	chr6:31875494-31875495	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
37	rs576226191	chr6:31875495-31875496	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
38	rs573152387	chr6:31875518-31875519	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
39	rs112057082	chr6:31875523-31875524	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
40	rs9800604	chr6:31875603-31875604	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
41	rs190882360	chr6:31875665-31875666	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
42	rs562788223	chr6:31875748-31875749	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
43	rs532246501	chr6:31875769-31875770	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
44	rs184069776	chr6:31875773-31875774	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
45	rs112647857	chr6:31875780-31875781	Weak transcription Enhancers Active TSS	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
46	rs570455261	chr6:31875885-31875886	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
47	rs9800610	chr6:31875902-31875903	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
48	rs117930498	chr6:31875934-31875935	Weak transcription Enhancers	Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
49	rs568331554	chr6:31876045-31876046	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs377234403	chr6:31876066-31876067	Weak transcription Enhancers	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:131)

Disease	PMID	Source
Follicular lymphoma	20505157	CNVD
Glioblastoma multiforme	21080181	CNVD
Ewing''s sarcoma	21437220	CNVD
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
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
Acute myeloid leukemia	20729466	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Prostate cancer	18632612	CNVD
Breast cancer	21858162	CNVD
Lung cancer	18438408	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
Breast cancer	21552322	CNVD
Immune disease	21076436	CNVD
Autoimmune disease	19135723	CNVD
Systemic lupus erythematosus	17953491	CNVD
Recurrent Infections	22737222	CNVD
Systemic lupus erythematosus	21904924	CNVD
Ovarian cancer	21781307	CNVD
Ependymoma	19289631	CNVD
Breast cancer	22844521	CNVD
Gestational infection	22844521	CNVD
HIV/AIDS	22844521	CNVD
Head circumference	22844521	CNVD
Infertility	22844521	CNVD
Ovarian cancer	22844521	CNVD
Prostate cancer	22844521	CNVD
Psoriasis	22844521	CNVD
Recurrent birth weight diabetes	22844521	CNVD
Rheumatoid arthritis	22844521	CNVD
Sclerosis systemic	22844521	CNVD
Systemic lupus erythematosus	22844521	CNVD
Obesity	22844521	CNVD
Recurrent pregnancy loss	22844521	CNVD
Intellectual disability	21811512	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Congenital anomalies of the kidney and urinary tract	18694510	CNVD
Nasopharyngeal cancer	22815911	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	21115979	CNVD
Acute lymphoblastic leukemia	21339820	CNVD
Autism	22495311	CNVD
Cancer	16790693	CNVD
Cervical cancer	21062161	CNVD
Esophageal adenocarcinoma	18820669	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
Renal cell carcinoma	18765545	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Gastric cancer	17908304	CNVD
Metanephric adenoma	20802469	CNVD
Splenic marginal zone lymphoma	21957467	CNVD
Schizophrenia	19571808	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Neuroblastoma	16790693	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
abnormal development	18461090	CNVD
Melanoma	17363583	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	16397240	CNVD
Retinoblastoma	22278416	CNVD
Non-syndromic sensorineural hearing loss	15273396	CNVD
Systemic lupus erythematosus	20877625	CNVD
Cleidocranial dysplasia	18696259	CNVD
Holoprosencephaly	21359414	CNVD
Liposarcoma	21253554	CNVD
Uveal melanoma	20484589	CNVD
Fibroblasts	20926602	CNVD
Breast cancer	21364760	CNVD
Systemic lupus erythematosus	19279649	CNVD
Retinoblastoma	16790693	CNVD
Acute myocardial infarction	18032375	CNVD
Renal cell carcinoma	19150565	CNVD
Systemic lupus erythematosus	19591781	CNVD
Attention deficit hyperactivity disorder	19287146	CNVD
Autism	19287146	CNVD
Erythema nodosum in leprosy	19287146	CNVD
Henoch-schoenlein purpura	19287146	CNVD
Liver cirrhosis	19287146	CNVD
Systemic lupus erythematosus	19287146	CNVD
Congenital adrenal hyperplasia	18478071	CNVD
Systemic lupus erythematosus	19287147	CNVD
Osteosarcoma	16790693	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Hodgkin''s lymphoma	18641027	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
Urothelial carcinoma	21177765	CNVD
Oral cancer	21386901	CNVD
Cancer	22183965	CNVD
Melanoma	22183965	CNVD
Breast cancer	22522925	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:231 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr6:31870600-31873600	Weak transcription	H1 Cell Line	embryonic stem cell
2	chr6:31870600-31873600	Weak transcription	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
3	chr6:31870600-31873600	Weak transcription	HUES48 Cell Line	embryonic stem cell
4	chr6:31870600-31873800	Weak transcription	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived
5	chr6:31870600-31873800	Weak transcription	iPS-18 Cell Line	embryonic stem cell
6	chr6:31870600-31874000	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
7	chr6:31870600-31874000	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
8	chr6:31870600-31875200	Enhancers	Placenta	Placenta
9	chr6:31870800-31873600	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
10	chr6:31870800-31873600	Weak transcription	HUES64 Cell Line	embryonic stem cell
11	chr6:31870800-31873600	Weak transcription	iPS-20b Cell Line	embryonic stem cell
12	chr6:31870800-31875000	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
13	chr6:31870800-31876400	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
14	chr6:31870800-31877400	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
15	chr6:31870800-31878800	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
16	chr6:31870800-31879200	Weak transcription	HSMM	muscle
17	chr6:31871000-31873600	Weak transcription	H9 Cell Line	embryonic stem cell
18	chr6:31871000-31873600	Weak transcription	iPS-15b Cell Line	embryonic stem cell
19	chr6:31871000-31873800	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
20	chr6:31871000-31874000	Weak transcription	IMR90 fetal lung fibroblasts Cell Line	lung
21	chr6:31871000-31874000	Weak transcription	Primary hematopoietic stem cells short term culture	blood
22	chr6:31871000-31874000	Weak transcription	NHLF	lung
23	chr6:31871000-31874400	Weak transcription	Psoas Muscle	Psoas
24	chr6:31871000-31875000	Weak transcription	Primary Natural Killer cells fromperipheralblood	blood
25	chr6:31871000-31875200	Weak transcription	Adipose Nuclei	Adipose
26	chr6:31871000-31876200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
27	chr6:31871000-31876400	Weak transcription	Bone Marrow Derived Cultured Mesenchymal Stem Cells	Bone marrow
28	chr6:31871000-31876400	Weak transcription	A549	lung
29	chr6:31871000-31876400	Weak transcription	NHDF-Ad	bronchial
30	chr6:31871000-31876600	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
31	chr6:31871400-31874200	Weak transcription	Liver	Liver
32	chr6:31871800-31874800	Weak transcription	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
33	chr6:31872000-31873800	Weak transcription	K562	blood
34	chr6:31872000-31874200	Weak transcription	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
35	chr6:31872800-31874800	Weak transcription	Hela-S3	cervix
36	chr6:31872800-31876200	Weak transcription	Fetal Adrenal Gland	Adrenal Gland
37	chr6:31873000-31873600	Weak transcription	HepG2	liver
38	chr6:31873400-31874600	Enhancers	ES-UCSF4 Cell Line	embryonic stem cell
39	chr6:31873600-31873800	Bivalent Enhancer	ES-I3 Cell Line	embryonic stem cell
40	chr6:31873600-31874200	Enhancers	HepG2	liver
41	chr6:31873600-31874400	Enhancers	H1 Cell Line	embryonic stem cell
42	chr6:31873600-31874400	Enhancers	H9 Cell Line	embryonic stem cell
43	chr6:31873600-31874400	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
44	chr6:31873600-31874400	Enhancers	iPS-15b Cell Line	embryonic stem cell
45	chr6:31873600-31874600	Enhancers	HUES48 Cell Line	embryonic stem cell
46	chr6:31873600-31874600	Enhancers	HUES6 Cell Line	embryonic stem cell
47	chr6:31873600-31874600	Enhancers	HUES64 Cell Line	embryonic stem cell
48	chr6:31873600-31874600	Enhancers	iPS-20b Cell Line	embryonic stem cell
49	chr6:31873600-31875200	Enhancers	hESC Derived CD56+ Ectoderm Cultured Cells	ES cell derived
50	chr6:31873800-31874400	Enhancers	H1 Derived Neuronal Progenitor Cultured Cells	ES cell derived

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