Variant report

Variant	nsv1038808
Chromosome Location	chr15:34913730-35025496
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:1298)
CpG islands
(count:368)
Chromatin interactive
region (count:82)
LncRNA
region (count:18)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:1298 , 50 per page) page: 1 2 3 4 5 6 7 ... 26

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr15:34929245-34929276	K562	blood:	n/a	n/a
2	ARID3A	chr15:34989159-34989187	K562	blood:	n/a	n/a
3	ARID3A	chr15:34916436-34916602	K562	blood:	n/a	n/a
4	ARID3A	chr15:34954510-34955719	K562	blood:	n/a	n/a
5	ARID3A	chr15:34946314-34948129	K562	blood:	n/a	n/a
6	ARID3A	chr15:34952157-34952158	K562	blood:	n/a	n/a
7	ARID3A	chr15:35000570-35000896	K562	blood:	n/a	n/a
8	ARID3A	chr15:34944080-34945342	K562	blood:	n/a	n/a
9	ARID3A	chr15:34953056-34953951	K562	blood:	n/a	n/a
10	ARID3A	chr15:34949658-34950365	K562	blood:	n/a	n/a
11	ARID3A	chr15:34939172-34940883	K562	blood:	n/a	n/a
12	ARID3A	chr15:34915270-34915290	K562	blood:	n/a	n/a
13	ARID3A	chr15:34913827-34914853	K562	blood:	n/a	chr15:34914367-34914383 chr15:34914368-34914384
14	ARID3A	chr15:34948740-34948973	K562	blood:	n/a	n/a
15	ATF1	chr15:35000572-35001097	K562	blood:	n/a	n/a
16	ATF1	chr15:34944877-34945255	K562	blood:	n/a	n/a
17	ATF1	chr15:34947575-34947975	K562	blood:	n/a	n/a
18	ATF1	chr15:34913992-34914213	K562	blood:	n/a	n/a
19	ATF1	chr15:34940100-34940799	K562	blood:	n/a	n/a
20	ATF1	chr15:35019827-35019831	K562	blood:	n/a	n/a
21	ATF1	chr15:34946741-34947211	K562	blood:	n/a	n/a
22	ATF1	chr15:34985696-34985896	K562	blood:	n/a	n/a
23	ATF1	chr15:34936394-34936711	K562	blood:	n/a	n/a
24	ATF1	chr15:35006704-35007397	K562	blood:	n/a	n/a
25	ATF1	chr15:34949656-34950320	K562	blood:	n/a	n/a
26	ATF2	chr15:34942304-34942739	GM12878	blood:	n/a	n/a
27	ATF2	chr15:34942319-34942566	GM12878	blood:	n/a	n/a
28	BACH1	chr15:34949732-34950003	K562	blood:	n/a	n/a
29	BACH1	chr15:34944497-34944500	K562	blood:	n/a	n/a
30	BATF	chr15:34942288-34942693	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
31	BATF	chr15:34942205-34942724	GM12878	blood:	n/a	chr15:34942439-34942449 chr15:34942438-34942449
32	BCL11A	chr15:34942273-34942696	GM12878	blood:	n/a	n/a
33	BCL11A	chr15:34942342-34942649	GM12878	blood:	n/a	n/a
34	BCLAF1	chr15:34949675-34950412	K562	blood:	n/a	n/a
35	BCLAF1	chr15:34946604-34947084	K562	blood:	n/a	chr15:34946703-34946712
36	BHLHE40	chr15:34944964-34945198	K562	blood:	n/a	n/a
37	BHLHE40	chr15:35000622-35001023	K562	blood:	n/a	n/a
38	BHLHE40	chr15:34957939-34958132	K562	blood:	n/a	n/a
39	BHLHE40	chr15:34949672-34950063	K562	blood:	n/a	n/a
40	BHLHE40	chr15:35006695-35007250	K562	blood:	n/a	n/a
41	BHLHE40	chr15:34985524-34985579	K562	blood:	n/a	n/a
42	BHLHE40	chr15:34942322-34942647	K562	blood:	n/a	n/a
43	BHLHE40	chr15:34947721-34947910	K562	blood:	n/a	n/a
44	BHLHE40	chr15:34952400-34952527	K562	blood:	n/a	n/a
45	BRCA1	chr15:35014096-35015138	Hela-S3	cervix:	n/a	n/a
46	BRCA1	chr15:34971598-34971907	Hela-S3	cervix:	n/a	n/a
47	BRCA1	chr15:35015346-35015372	Hela-S3	cervix:	n/a	n/a
48	BRCA1	chr15:35014429-35014488	H1-hESC	embryonic stem cell:	n/a	n/a
49	BRCA1	chr15:34985718-34985922	Hela-S3	cervix:	n/a	n/a
50	CBX3	chr15:35000583-35000970	K562	blood:	n/a	n/a

(count:368 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr15:35014270-35014320	MCF10A-Er-Src	breast:	n/a
2	chr15:35014229-35014279	HCM	heart:	n/a
3	chr15:35014270-35014320	MCF10A-Er-Src	breast:	n/a
4	chr15:35014229-35014279	HCM	heart:	n/a
5	chr15:35001084-35001134	HL-60	blood:	n/a
6	chr15:35014229-35014279	HIPEpiC	eye:	n/a
7	chr15:35010826-35010876	GM12892	blood:	n/a
8	chr15:35001084-35001134	HRE	kidney:	n/a
9	chr15:34988869-34988919	RPTEC	kidney:	n/a
10	chr15:35010826-35010876	HIPEpiC	eye:	n/a
11	chr15:34988869-34988919	H1-hESC	embryonic stem cell:	embryo
12	chr15:35014229-35014279	GM12891	blood:	n/a
13	chr15:35017944-35017994	HL-60	blood:	n/a
14	chr15:35001084-35001134	AG10803	skin:	n/a
15	chr15:35017944-35017994	HRE	kidney:	n/a
16	chr15:35014270-35014320	AG04450	lung:	fetal
17	chr15:35017944-35017994	HCF	heart:	n/a
18	chr15:34988869-34988919	HCF	heart:	n/a
19	chr15:35014229-35014279	PrEC	prostate:	n/a
20	chr15:35001084-35001134	ovcar-3	ovarian:	n/a
21	chr15:34988869-34988919	HMEC	breast:	n/a
22	chr15:35014270-35014320	SAEC	small airway:	n/a
23	chr15:35010826-35010876	AG09309	skin:	n/a
24	chr15:35010826-35010876	IMR90	lung:	fetal
25	chr15:35001084-35001134	GM06990	blood:	n/a
26	chr15:35014229-35014279	SKMC	muscle:	n/a
27	chr15:35014270-35014320	AG09309	skin:	n/a
28	chr15:35010826-35010876	HAEpiC	amniotic membrane:	n/a
29	chr15:35001084-35001134	Jurkat	blood:	n/a
30	chr15:35017944-35017994	IMR90	lung:	fetal
31	chr15:35010826-35010876	AG04449	skin:	fetal
32	chr15:35014270-35014320	NHDF-neo	bronchial:	n/a
33	chr15:34988869-34988919	NHDF-neo	bronchial:	n/a
34	chr15:35010826-35010876	AG04450	lung:	fetal
35	chr15:35001084-35001134	HCT-116	colon:	n/a
36	chr15:34988869-34988919	SK-N-SH	brain:	n/a
37	chr15:35014229-35014279	SK-N-SH	brain:	n/a
38	chr15:35014229-35014279	HepG2	liver:	n/a
39	chr15:35001084-35001134	HCF	heart:	n/a
40	chr15:35014270-35014320	SK-N-SH	brain:	n/a
41	chr15:35014229-35014279	HRPEpiC	eye:	n/a
42	chr15:35014270-35014320	HCF	heart:	n/a
43	chr15:35010826-35010876	H1-hESC	embryonic stem cell:	embryo
44	chr15:35001084-35001134	AoSMC	blood vessel:	n/a
45	chr15:34988869-34988919	HEEpiC	esophagus:	n/a
46	chr15:35001084-35001134	MCF10A-Er-Src	breast:	n/a
47	chr15:35001084-35001134	MCF-7	breast:	n/a
48	chr15:35014229-35014279	AoSMC	blood vessel:	n/a
49	chr15:35001084-35001134	RPTEC	kidney:	n/a
50	chr15:34988869-34988919	HNPCEpiC	eye:	n/a

(count:82 , 50 per page) page: 1 2

No.	Distal block	Cell Line	Cell type
1	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
2	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
3	chr10:75006642..75007633-chr15:35013735..35014638,2	Hela-S3	cervix:
4	chr15:34980841..34982732-chr15:34984201..34987180,2	K562	blood:
5	chr15:34960285..34962774-chr15:34963252..34966258,4	K562	blood:
6	chr15:35005678..35008340-chr15:35281317..35283659,2	K562	blood:
7	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
8	chr15:34962423..34964134-chr15:34966956..34969710,3	K562	blood:
9	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
10	chr15:34953489..34955951-chr15:35181219..35183157,2	K562	blood:
11	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
12	chr15:34912716..34916752-chr15:34917196..34920581,4	K562	blood:
13	chr15:35001097..35003090-chr15:35007070..35008790,2	K562	blood:
14	chr15:34940940..34942564-chr15:34999108..35001019,2	K562	blood:
15	chr15:34934770..34937620-chr15:34950647..34953239,2	K562	blood:
16	chr15:35014688..35016306-chr15:35021250..35023169,2	K562	blood:
17	chr15:35005516..35008329-chr15:35009732..35011993,2	K562	blood:
18	chr15:35010787..35013754-chr15:35014491..35016542,2	K562	blood:
19	chr15:34960754..34962321-chr15:34966390..34968165,2	K562	blood:
20	chr15:34913694..34916752-chr15:34919011..34920724,3	K562	blood:
21	chr15:34963103..34965254-chr15:34966851..34969218,2	MCF-7	breast:
22	chr15:34983713..34985317-chr6:26197593..26200143,2	K562	blood:
23	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
24	chr15:35010890..35011778-chr17:59321038..59321843,2	MCF-7	breast:
25	chr15:34913751..34914597-chr15:35212096..35212867,7	K562	blood:
26	chr15:35014688..35016306-chr15:35021250..35023169,2	K562	blood:
27	chr15:35001097..35003090-chr15:35007070..35008790,2	K562	blood:
28	chr15:34940257..34942550-chr15:34950335..34951889,2	K562	blood:
29	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
30	chr15:34927785..34933151-chr15:34934497..34941490,8	K562	blood:
31	chr15:34965188..34969119-chr15:34970987..34974956,6	K562	blood:
32	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
33	chr15:34958499..34960200-chr15:34963239..34965401,2	K562	blood:
34	chr15:34989332..34992979-chr15:34995533..34998034,4	K562	blood:
35	chr15:34989332..34992979-chr15:34995533..34998034,4	K562	blood:
36	chr15:34913307..34914991-chr15:34929235..34931577,2	K562	blood:
37	chr15:34907702..34910411-chr15:34952455..34954523,2	K562	blood:
38	chr15:34997005..34998827-chr15:34999088..35001652,2	K562	blood:
39	chr15:34913918..34914531-chr15:35212584..35213285,2	MCF-7	breast:
40	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
41	chr15:34945476..34948299-chr15:35000578..35003258,2	K562	blood:
42	chr15:34934825..34936603-chr15:34945044..34948146,4	K562	blood:
43	chr15:34933035..34934548-chr15:34938251..34939915,2	K562	blood:
44	chr15:34941429..34944034-chr15:34952465..34954233,2	K562	blood:
45	chr15:34965468..34967744-chr15:34968524..34970610,2	K562	blood:
46	chr15:34962434..34964585-chr15:34966364..34969710,3	K562	blood:
47	chr15:34965205..34967093-chr15:34977923..34979811,2	K562	blood:
48	chr15:34953069..34954628-chr15:34955083..34957176,2	K562	blood:
49	chr15:34946410..34947955-chr15:34948303..34950980,2	K562	blood:
50	chr15:34949722..34952645-chr15:34986997..34989606,2	K562	blood:

(count:18 , 50 per page) page: 1

No.	lncRNA name	Chromosome Location	lncRNA alias
1	lnc-GJD2-2	chr15:34972962-34973170	uc_385_-
2	lnc-GJD2-1	chr15:34967556-34967834	XLOC_011422
3	lnc-GOLGA8A-1	chr15:34943336-34943463	ENSG00000261304.1
4	lnc-AC114546.1-4	chr15:35015809-35016397	NONHSAT041604
5	lnc-AC114546.1-4	chr15:35015735-35016108	XLOC_011205
6	lnc-GOLGA8A-1	chr15:34946499-34946618	ENSG00000261304.1
7	lnc-GOLGA8A-1	chr15:34947820-34947978	XLOC_011421
8	lnc-AC114546.1-4	chr15:35014395-35014438	NONHSAT041604
9	lnc-GOLGA8A-1	chr15:34947820-34947965	ENSG00000261304.1
10	lnc-GOLGA8A-1	chr15:34962302-34962370	XLOC_011421
11	lnc-GOLGA8A-1	chr15:34948237-34948332	ucscGeneNc_uc001zji_1
12	lnc-AC114546.1-4	chr15:35014273-35014438	XLOC_011205
13	lnc-GJD2-1	chr15:35012518-35012708	XLOC_011422
14	lnc-GOLGA8A-1	chr15:34943936-34946139	ucscGeneNc_uc001zji_1
15	lnc-AC114546.1-13	chr15:34972962-34973170	uc_385_+
16	lnc-AC114546.1-12	chr15:34982173-34982277	NONHSAT041602
17	lnc-GOLGA8A-1	chr15:34943885-34943977	ENSG00000261304.1
18	lnc-AC114546.1-12	chr15:34988228-34988460	NONHSAT041602

No data

Variant related genes	Relation type
ENSG00000261304	TF binding region
ENSG00000261304	CpG island
ENSG00000197846	chromatin interactions
ENSG00000196866	chromatin interactions
ENSG00000261304	chromatin interactions
ENSG00000197409	chromatin interactions
ENSG00000236756	chromatin interactions
NEK7	miRNA target sites
NEK9	miRNA target sites

Extended variants
information (count: 3882 )
Associated
traits (count: 69 )

Variant overlapped rSNPs/rCNVs (count:3882 , 50 per page) page: 1 2 3 4 5 6 7 ... 78

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs11632867	chr15:34913730-34913731	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs181520972	chr15:34913768-34913769	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
3	rs532123900	chr15:34913778-34913779	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
4	rs375917855	chr15:34913798-34913799	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
5	rs186306071	chr15:34913991-34913992	Enhancers Flanking Active TSS Weak transcription	n/a	n/a	Overlapped CNVs	n/a
6	rs149337625	chr15:34914043-34914044	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
7	rs144152199	chr15:34914064-34914065	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
8	rs536806208	chr15:34914096-34914097	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
9	rs368662654	chr15:34914124-34914125	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
10	rs74921031	chr15:34914132-34914133	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
11	rs567118998	chr15:34914137-34914138	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
12	rs534477534	chr15:34914148-34914149	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
13	rs559019135	chr15:34914158-34914159	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
14	rs375783147	chr15:34914174-34914175	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
15	rs552507419	chr15:34914208-34914209	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
16	rs577304407	chr15:34914223-34914224	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
17	rs574404307	chr15:34914235-34914236	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
18	rs112906698	chr15:34914268-34914269	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
19	rs556578587	chr15:34914288-34914289	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
20	rs59490004	chr15:34914289-34914290	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
21	rs575347026	chr15:34914290-34914291	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
22	rs542775031	chr15:34914291-34914292	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
23	rs560911566	chr15:34914338-34914339	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
24	rs573123509	chr15:34914370-34914371	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
25	rs575368708	chr15:34914383-34914384	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
26	rs367983821	chr15:34914408-34914409	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
27	rs564579909	chr15:34914420-34914421	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
28	rs531940869	chr15:34914450-34914451	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
29	rs4923712	chr15:34914467-34914468	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
30	rs562576321	chr15:34914477-34914478	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
31	rs116801069	chr15:34914494-34914495	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
32	rs4923713	chr15:34914511-34914512	Enhancers Weak transcription	n/a	n/a	LD-proxies of rSNP Overlapped rCNV	n/a
33	rs566930287	chr15:34914515-34914516	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
34	rs189530728	chr15:34914560-34914561	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
35	rs564415550	chr15:34914587-34914588	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
36	rs76911497	chr15:34914588-34914589	Enhancers Weak transcription	n/a	n/a	Overlapped CNVs	n/a
37	rs180763539	chr15:34914635-34914636	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
38	rs373978752	chr15:34914659-34914660	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
39	rs35739810	chr15:34914667-34914668	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
40	rs398043140	chr15:34914671-34914672	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
41	rs187409700	chr15:34914696-34914697	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
42	rs538193455	chr15:34914711-34914712	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
43	rs114928845	chr15:34914713-34914714	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
44	rs574913667	chr15:34914741-34914742	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
45	rs535558385	chr15:34914802-34914803	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
46	rs547023522	chr15:34914818-34914819	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
47	rs190738307	chr15:34914878-34914879	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
48	rs74414633	chr15:34914959-34914960	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
49	rs369004653	chr15:34914973-34914974	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a
50	rs572694838	chr15:34914977-34914978	Weak transcription Enhancers	n/a	n/a	Overlapped CNVs	n/a

Variant related diseases (count:69)

Disease	PMID	Source
HDAC8	0	CNVD
NIPBL	0	CNVD
RAD21	0	CNVD
SMC1A	0	CNVD
SMC3	0	CNVD
Ewing''s sarcoma	21437220	CNVD
Schizophrenia	19415332	CNVD
Breast cancer	22522925	CNVD
Autism	22495311	CNVD
Wilms tumour	21544195	CNVD
Angelman syndrome	16183798	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Testicular germ cell tumor	18059402	CNVD
cataract	16735990	CNVD
Cancer	21637783	CNVD
Colorectal cancer	20709793	CNVD
Medulloblastoma	21979893	CNVD
spastic paraplegia with thinning of corpus callosum	19105190	CNVD
Schizophrenia	21324950	CNVD
Astrocytoma	17387387	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Breast cancer	21264507	CNVD
Disease	21824424	CNVD
Hodgkin''s lymphoma	18641027	CNVD
Melanoma	18172304	CNVD
Colorectal cancer	16774939	CNVD
Gastric cancer	17167181	CNVD
Neuroblastoma	19435921	CNVD
Colorectal cancer	19359472	CNVD
Monoclonal gammopathy of undetermined significance	17077331	CNVD
Multiple myeloma	17077331	CNVD
Colorectal cancer	16272173	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Multiple myeloma	17550852	CNVD
Intellectual disability	22102821	CNVD
Hodgkin''s lymphoma	17606441	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Acute myeloid leukemia	20729466	CNVD
Oral squamous cell carcinoma	17134496	CNVD
Breast cancer	17133270	CNVD
Prostate cancer	16573809	CNVD
Basal cell lymphoma	16317097	CNVD
Diffuse large b-cell lymphoma	16317097	CNVD
Multiple myeloma	20724749	CNVD
Lung cancer	18438408	CNVD
Breast cancer	21858162	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Breast cancer	21785460	CNVD
Abnormal corpus callosum	21572526	CNVD
Gastrointestinal stromal cancer	16982739	CNVD
Autism	19204725	CNVD
Schizophrenia	19204725	CNVD
Schizophrenia	19149910	CNVD
Ovarian cancer	22174824	CNVD
Prostate cancer	18632612	CNVD
small cell lung cancer	20016488	CNVD
Legius syndrome	19443465	CNVD
Holoprosencephaly	21359414	CNVD
Myelofibrosis	22110671	CNVD
Glioblastoma multiforme	22286061	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Prader-willi syndrome	21504564	CNVD
Cancer	17440070	CNVD
Basal cell lymphoma	17053054	CNVD
Pancreatic ductal adenocarcinoma	19077451	CNVD
Acute lymphoblastic leukemia	18458336	CNVD
lymphocytic leukemia	21291569	CNVD
Pancreatic cancer	17952125	CNVD

Chromatin state (count:752 , 50 per page) page: 1 2 3 4 5 6 7 ... 16

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr15:34911800-34915000	Enhancers	HSMMtube	muscle
2	chr15:34912000-34914000	Enhancers	Primary hematopoietic stem cells short term culture	blood
3	chr15:34912000-34914400	Enhancers	HSMM	muscle
4	chr15:34912200-34914000	Enhancers	Adipose Nuclei	Adipose
5	chr15:34912200-34914600	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
6	chr15:34912200-34914600	Enhancers	Muscle Satellite Cultured Cells	--
7	chr15:34912600-34914000	Enhancers	Primary hematopoietic stem cells	blood
8	chr15:34912800-34914000	Enhancers	Hela-S3	cervix
9	chr15:34913000-34914000	Enhancers	Skeletal Muscle Female	skeletal muscle
10	chr15:34913200-34914000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
11	chr15:34913200-34915000	Enhancers	K562	blood
12	chr15:34913400-34917200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
13	chr15:34913600-34914400	Enhancers	HUVEC	blood vessel
14	chr15:34913600-34914600	Enhancers	H9 Derived Neuron Cultured Cells	ES cell derived
15	chr15:34913800-34914400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr15:34914000-34914400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
17	chr15:34914400-34916600	Weak transcription	HUVEC	blood vessel
18	chr15:34914600-34917000	Weak transcription	Muscle Satellite Cultured Cells	--
19	chr15:34914800-34915000	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
20	chr15:34915000-34918800	Weak transcription	K562	blood
21	chr15:34915600-34917000	Weak transcription	Foreskin Melanocyte Primary Cells skin03	Skin
22	chr15:34916600-34918600	Enhancers	HUVEC	blood vessel
23	chr15:34917000-34917400	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
24	chr15:34917000-34918000	Enhancers	Muscle Satellite Cultured Cells	--
25	chr15:34917200-34917600	Enhancers	NHEK	skin
26	chr15:34917200-34917800	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
27	chr15:34917400-34917600	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
28	chr15:34917600-34920000	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
29	chr15:34917600-34920000	Weak transcription	NHEK	skin
30	chr15:34917800-34920200	Weak transcription	Foreskin Keratinocyte Primary Cells skin02	Skin
31	chr15:34918600-34920000	Weak transcription	HUVEC	blood vessel
32	chr15:34919000-34919200	Active TSS	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
33	chr15:34919200-34920200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
34	chr15:34920000-34920400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
35	chr15:34920000-34921600	Enhancers	NHEK	skin
36	chr15:34920000-34922200	Enhancers	Foreskin Keratinocyte Primary Cells skin03	Skin
37	chr15:34920000-34922400	Enhancers	HUVEC	blood vessel
38	chr15:34920200-34921000	Enhancers	HMEC	breast
39	chr15:34920200-34921200	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
40	chr15:34920200-34921600	Enhancers	Muscle Satellite Cultured Cells	--
41	chr15:34920200-34921600	Enhancers	Foreskin Keratinocyte Primary Cells skin02	Skin
42	chr15:34920400-34921200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr15:34920800-34921400	Enhancers	A549	lung
44	chr15:34920800-34921400	Enhancers	NHLF	lung
45	chr15:34921200-34921400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
46	chr15:34921200-34923000	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
47	chr15:34921400-34923200	Weak transcription	Foreskin Fibroblast Primary Cells skin01	Skin
48	chr15:34922200-34923200	Weak transcription	Foreskin Keratinocyte Primary Cells skin03	Skin
49	chr15:34923200-34923400	Enhancers	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
50	chr15:34923200-34923400	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin

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