Variant report

Variant	nsv543994
Chromosome Location	chr19:35949892-35984103
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:928)
CpG islands
(count:671)
Chromatin interactive
region (count:39)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

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

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr19:35976462-35976711	HepG2	liver:	n/a	n/a
2	ARID3A	chr19:35977148-35977639	HepG2	liver:	n/a	n/a
3	ARID3A	chr19:35949605-35950533	HepG2	liver:	n/a	n/a
4	ARID3A	chr19:35959632-35959937	HepG2	liver:	n/a	n/a
5	ATF2	chr19:35953134-35954075	GM12878	blood:	n/a	n/a
6	ATF2	chr19:35975346-35976076	GM12878	blood:	n/a	n/a
7	ATF2	chr19:35949710-35950311	GM12878	blood:	n/a	n/a
8	ATF2	chr19:35959404-35960051	GM12878	blood:	n/a	n/a
9	ATF2	chr19:35975451-35975905	GM12878	blood:	n/a	n/a
10	ATF2	chr19:35967038-35967412	H1-hESC	embryonic stem cell:	n/a	n/a
11	ATF2	chr19:35953280-35954068	GM12878	blood:	n/a	n/a
12	ATF2	chr19:35959509-35959930	GM12878	blood:	n/a	n/a
13	BATF	chr19:35953231-35953934	GM12878	blood:	n/a	chr19:35953550-35953561
14	BATF	chr19:35959524-35959868	GM12878	blood:	n/a	chr19:35959686-35959696
15	BATF	chr19:35959523-35959929	GM12878	blood:	n/a	chr19:35959686-35959696
16	BATF	chr19:35975519-35975863	GM12878	blood:	n/a	n/a
17	BATF	chr19:35953335-35953844	GM12878	blood:	n/a	chr19:35953550-35953561
18	BCL11A	chr19:35949875-35950163	GM12878	blood:	n/a	chr19:35950049-35950058 chr19:35949877-35949890
19	BCL11A	chr19:35949804-35950247	GM12878	blood:	n/a	chr19:35949868-35949876 chr19:35950049-35950058 chr19:35949877-35949890
20	BCL11A	chr19:35953366-35953867	GM12878	blood:	n/a	chr19:35953575-35953584
21	BCL11A	chr19:35959568-35959839	GM12878	blood:	n/a	n/a
22	BCL11A	chr19:35959526-35959863	GM12878	blood:	n/a	n/a
23	BCL11A	chr19:35953372-35953919	GM12878	blood:	n/a	chr19:35953575-35953584
24	BCL3	chr19:35953349-35953862	GM12878	blood:	n/a	chr19:35953575-35953584
25	BCL3	chr19:35959500-35959979	GM12878	blood:	n/a	n/a
26	BCL3	chr19:35975487-35975921	GM12878	blood:	n/a	n/a
27	BCLAF1	chr19:35953275-35954053	GM12878	blood:	n/a	chr19:35953575-35953584
28	BCLAF1	chr19:35959497-35959963	GM12878	blood:	n/a	n/a
29	BCLAF1	chr19:35959491-35960038	GM12878	blood:	n/a	n/a
30	BCLAF1	chr19:35953246-35953909	GM12878	blood:	n/a	chr19:35953575-35953584
31	BCLAF1	chr19:35949762-35950218	GM12878	blood:	n/a	chr19:35949868-35949876 chr19:35950049-35950058 chr19:35949877-35949890
32	BHLHE40	chr19:35953321-35954200	GM12878	blood:	n/a	n/a
33	BHLHE40	chr19:35951650-35951908	K562	blood:	n/a	n/a
34	BHLHE40	chr19:35975524-35976013	GM12878	blood:	n/a	n/a
35	BHLHE40	chr19:35951615-35951948	GM12878	blood:	n/a	n/a
36	BHLHE40	chr19:35949717-35950266	GM12878	blood:	n/a	n/a
37	BHLHE40	chr19:35959619-35959914	K562	blood:	n/a	n/a
38	BHLHE40	chr19:35967151-35967344	K562	blood:	n/a	n/a
39	BHLHE40	chr19:35959551-35959956	GM12878	blood:	n/a	n/a
40	CEBPB	chr19:35957991-35958330	H1-hESC	embryonic stem cell:	n/a	chr19:35958150-35958161
41	CEBPB	chr19:35950365-35950481	HepG2	liver:	n/a	n/a
42	CEBPB	chr19:35975213-35975524	A549	lung:	n/a	chr19:35975379-35975390
43	CEBPB	chr19:35958021-35958370	A549	lung:	n/a	chr19:35958150-35958161
44	CEBPB	chr19:35949668-35950048	HepG2	liver:	n/a	n/a
45	CEBPB	chr19:35953511-35953868	GM12878	blood:	n/a	n/a
46	CEBPB	chr19:35949627-35950003	HepG2	liver:	n/a	n/a
47	CEBPB	chr19:35982684-35983082	MCF-7	breast:	n/a	chr19:35982979-35982996
48	CEBPB	chr19:35958039-35958228	HepG2	liver:	n/a	chr19:35958150-35958161
49	CEBPB	chr19:35957931-35958287	MCF-7	breast:	n/a	chr19:35958150-35958161
50	CEBPB	chr19:35957971-35958342	A549	lung:	n/a	chr19:35958150-35958161

(count:671 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:35981347-35981397	K562	blood:	n/a
2	chr19:35981371-35981421	NH-A	brain:	n/a
3	chr19:35981517-35981567	ovcar-3	ovarian:	n/a
4	chr19:35981224-35981274	AG04449	skin:	fetal
5	chr19:35981347-35981397	SKMC	muscle:	n/a
6	chr19:35981224-35981274	U87	brain:	n/a
7	chr19:35981347-35981397	HUVEC	blood vessel:	n/a
8	chr19:35953646-35953696	Jurkat	blood:	n/a
9	chr19:35981531-35981581	AG04450	lung:	fetal
10	chr19:35953646-35953696	HCT-116	colon:	n/a
11	chr19:35982399-35982449	PANC-1	pancreas:	n/a
12	chr19:35981531-35981581	BE2_C	brain:	n/a
13	chr19:35981677-35981727	AoSMC	blood vessel:	n/a
14	chr19:35981517-35981567	MCF-7	breast:	n/a
15	chr19:35953646-35953696	RPTEC	kidney:	n/a
16	chr19:35982442-35982492	AG09309	skin:	n/a
17	chr19:35981517-35981567	SK-N-SH_RA	brain:	n/a
18	chr19:35981531-35981581	HUVEC	blood vessel:	n/a
19	chr19:35981517-35981567	IMR90	lung:	fetal
20	chr19:35981549-35981599	AG09309	skin:	n/a
21	chr19:35981371-35981421	NHBE	bronchial:	n/a
22	chr19:35981531-35981581	ovcar-3	ovarian:	n/a
23	chr19:35981371-35981421	GM06990	blood:	n/a
24	chr19:35982046-35982096	HUVEC	blood vessel:	n/a
25	chr19:35981549-35981599	HPAEpiC	pulmonary alveolar:	n/a
26	chr19:35982442-35982492	PrEC	prostate:	n/a
27	chr19:35982046-35982096	IMR90	lung:	fetal
28	chr19:35982442-35982492	Hela-S3	cervix:	n/a
29	chr19:35981677-35981727	SK-N-MC	brain:	n/a
30	chr19:35981517-35981567	Hela-S3	cervix:	n/a
31	chr19:35982046-35982096	AG04449	skin:	fetal
32	chr19:35981549-35981599	HMEC	breast:	n/a
33	chr19:35981549-35981599	Hepatocyte	liver:	n/a
34	chr19:35981531-35981581	GM12891	blood:	n/a
35	chr19:35981224-35981274	GM12891	blood:	n/a
36	chr19:35982399-35982449	Hepatocyte	liver:	n/a
37	chr19:35981371-35981421	NT2-D1	testis:	n/a
38	chr19:35981677-35981727	HRCEpiC	kidney:	n/a
39	chr19:35981347-35981397	CMK	blood:	n/a
40	chr19:35981549-35981599	GM06990	blood:	n/a
41	chr19:35981549-35981599	U87	brain:	n/a
42	chr19:35981224-35981274	SK-N-SH_RA	brain:	n/a
43	chr19:35981347-35981397	Caco-2	colon:	n/a
44	chr19:35981347-35981397	LNCaP	prostate:	n/a
45	chr19:35981224-35981274	SK-N-MC	brain:	n/a
46	chr19:35981347-35981397	GM12891	blood:	n/a
47	chr19:35981371-35981421	HAEpiC	amniotic membrane:	n/a
48	chr19:35981224-35981274	HIPEpiC	eye:	n/a
49	chr19:35982399-35982449	Caco-2	colon:	n/a
50	chr19:35981517-35981567	T-47D	breast:	n/a

(count:39 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:35966706..35968835-chr19:35977237..35979260,2	MCF-7	breast:
2	chr19:35759087..35760607-chr19:35981790..35983664,2	MCF-7	breast:
3	chr19:35759280..35761933-chr19:35957655..35960513,4	MCF-7	breast:
4	chr19:35907482..35909889-chr19:35957242..35958878,2	K562	blood:
5	chr19:35940497..35942459-chr19:35950134..35952077,2	MCF-7	breast:
6	chr19:35966706..35968835-chr19:35977237..35979260,2	MCF-7	breast:
7	chr19:35980592..35983190-chr19:35983600..35986426,4	K562	blood:
8	chr17:41400494..41402130-chr19:35967654..35969154,2	K562	blood:
9	chr19:35956583..35958942-chr19:35959896..35961677,2	K562	blood:
10	chr19:35842803..35847555-chr19:35958346..35962291,5	MCF-7	breast:
11	chr19:35952414..35955160-chr19:35958571..35960492,2	K562	blood:
12	chr19:35982354..35984301-chr19:36208376..36210128,2	MCF-7	breast:
13	chr19:35910975..35911617-chr19:35959334..35960317,4	MCF-7	breast:
14	chr19:35979822..35982375-chr19:35989666..35992249,2	MCF-7	breast:
15	chr19:35843378..35844331-chr19:35959313..35960316,8	MCF-7	breast:
16	chr19:35843479..35844366-chr19:35970362..35970878,2	MCF-7	breast:
17	chr19:35956583..35958942-chr19:35959896..35961677,2	K562	blood:
18	chr19:35843321..35844375-chr19:35959230..35959949,5	MCF-7	breast:
19	chr19:35953881..35955894-chr19:35965431..35968278,2	K562	blood:
20	chr19:35898850..35901038-chr19:35977233..35979986,2	MCF-7	breast:
21	chr19:35911032..35911903-chr19:35959389..35960277,3	MCF-7	breast:
22	chr19:35952414..35955160-chr19:35958571..35960492,2	K562	blood:
23	chr19:35976705..35979552-chr19:35984108..35985660,2	K562	blood:
24	chr19:35950578..35953125-chr19:35957204..35959006,2	MCF-7	breast:
25	chr19:35843603..35844331-chr19:35959340..35959868,2	K562	blood:
26	chr19:35943873..35946531-chr19:35952558..35955440,2	MCF-7	breast:
27	chr19:35967073..35968739-chr19:36034761..36037590,2	K562	blood:
28	chr19:35940273..35942985-chr19:35948389..35950035,2	MCF-7	breast:
29	chr19:35980525..35983715-chr19:36035506..36037997,3	MCF-7	breast:
30	chr19:35950578..35953125-chr19:35957204..35959006,2	MCF-7	breast:
31	chr19:35843622..35844283-chr19:35963657..35964335,2	MCF-7	breast:
32	chr19:35921074..35922900-chr19:35950996..35953556,2	K562	blood:
33	chr19:35977197..35979552-chr19:35984108..35986237,2	K562	blood:
34	chr19:35959978..35962451-chr19:35964294..35965983,2	MCF-7	breast:
35	chr19:35959978..35962451-chr19:35964294..35965983,2	MCF-7	breast:
36	chr19:35953881..35955894-chr19:35965431..35968278,2	K562	blood:
37	chr19:35924952..35927420-chr19:35951725..35953807,2	K562	blood:
38	chr19:35969956..35970838-chr19:35985954..35986806,5	MCF-7	breast:
39	chr19:35760013..35761636-chr19:35979753..35981551,2	MCF-7	breast:

No data

Variant related genes	Relation type
KRTDAP	TF binding region
KRTDAP	CpG island
ENSG00000272333	chromatin interactions
ENSG00000236144	chromatin interactions
ENSG00000105698	chromatin interactions
ENSG00000105677	chromatin interactions
ENSG00000232680	chromatin interactions
ENSG00000161249	chromatin interactions
ENSG00000188508	chromatin interactions
ENSG00000205786	chromatin interactions
ENSG00000126262	chromatin interactions

Extended variants
information (count: 1400 )
Associated
traits (count: 66 )

Variant overlapped rSNPs/rCNVs (count:1400 , 50 per page) page: 1 2 3 4 5 6 7 ... 28

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs372760300	chr19:35949942-35949943	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
2	rs187549620	chr19:35949954-35949955	Bivalent Enhancer Enhancers Weak transcription Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs573612302	chr19:35950012-35950013	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs549394643	chr19:35950028-35950029	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs531741928	chr19:35950057-35950058	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
6	rs542631852	chr19:35950075-35950076	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
7	rs374691758	chr19:35950118-35950119	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
8	rs142970885	chr19:35950129-35950130	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	n/a	n/a	Overlapped CNVs	n/a
9	rs555627401	chr19:35950144-35950145	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs34536858	chr19:35950174-35950175	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
11	rs147757605	chr19:35950201-35950202	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs368303308	chr19:35950244-35950245	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs541776550	chr19:35950261-35950262	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs371798315	chr19:35950269-35950270	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs374977820	chr19:35950286-35950287	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
16	rs564767052	chr19:35950298-35950299	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
17	rs78036837	chr19:35950306-35950307	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
18	rs550067104	chr19:35950323-35950324	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
19	rs546941640	chr19:35950326-35950327	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
20	rs377533311	chr19:35950336-35950337	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
21	rs563808599	chr19:35950370-35950371	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
22	rs529340714	chr19:35950377-35950378	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
23	rs192948870	chr19:35950415-35950416	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
24	rs565770577	chr19:35950443-35950444	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
25	rs55981709	chr19:35950458-35950459	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
26	rs529822320	chr19:35950469-35950470	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
27	rs374619549	chr19:35950470-35950471	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
28	rs184646415	chr19:35950477-35950478	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
29	rs569727584	chr19:35950483-35950484	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
30	rs537257921	chr19:35950511-35950512	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
31	rs12975762	chr19:35950523-35950524	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs187395181	chr19:35950534-35950535	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
33	rs535999970	chr19:35950536-35950537	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
34	rs191926256	chr19:35950543-35950544	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
35	rs572925307	chr19:35950570-35950571	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
36	rs140664887	chr19:35950571-35950572	Bivalent Enhancer Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
37	rs144630383	chr19:35950610-35950611	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
38	rs147895117	chr19:35950660-35950661	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
39	rs12973353	chr19:35950664-35950665	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
40	rs370030402	chr19:35950741-35950742	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
41	rs140510478	chr19:35950743-35950744	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
42	rs529474955	chr19:35950777-35950778	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
43	rs574131992	chr19:35950785-35950786	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
44	rs542739917	chr19:35950800-35950801	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
45	rs543512515	chr19:35950816-35950817	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
46	rs77555937	chr19:35950817-35950818	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
47	rs551319817	chr19:35950841-35950842	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
48	rs571519206	chr19:35950928-35950929	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
49	rs114608264	chr19:35950934-35950935	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
50	rs541442827	chr19:35950990-35950991	Weak transcription Enhancers Flanking Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:66)

Disease	PMID	Source
Myelodysplastic syndrome	17634407	CNVD
Acute lymphoblastic leukemia	22237106	CNVD
Chordoma	21602918	CNVD
Ewing''s sarcoma	21437220	CNVD
Glioblastoma multiforme	21080181	CNVD
Chronic lymphocytic leukemia	21546498	CNVD
Cancer	21637783	CNVD
Retinoblastoma	21504564	CNVD
Medulloblastoma	21979893	CNVD
Ovarian cancer	21720365	CNVD
Cancer	20164919	CNVD
Thoracic aortic aneurysm	21092924	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
Prostate cancer	18632612	CNVD
Autism	22495311	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Ductal carcinoma	22052326	CNVD
Pleomorphic liposarcoma	18784837	CNVD
Congenital nephrotic syndrome	18421352	CNVD
Astrocytoma	17934521	CNVD
Leukemia	17361228	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Breast cancer	21858162	CNVD
Breast cancer	17603634	CNVD
Glioma	21971842	CNVD
Esophageal squamous carcinoma	21637470	CNVD
Endometrial cancer	22040021	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Oligodendroglial tumors	17285580	CNVD
renal disease	20603712	CNVD
Salivary gland adenoid cystic carcinoma	17545515	CNVD
Ovarian cancer	21397856	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Myelofibrosis	22110671	CNVD
Liver carcinoma	19366792	CNVD
Ovarian cancer	20844748	CNVD
Non-small cell lung cancer	21829676	CNVD
Barrett''s adenocarcinoma	18663352	CNVD
Chronic lymphocytic leukemia	21049055	CNVD
Cancer	21183584	CNVD
Honadal dysgenesis	21048976	CNVD
Neurodevelopmental disorder	22521361	CNVD
Endometrial cancer	23636398	CNVD
Disorders of sex development	21048976	CNVD
Ovarian cancer	22174824	CNVD
Breast cancer	16608533	CNVD
Neuroblastoma	18923191	CNVD
Breast cancer	21364760	CNVD
Invasive pancreatic ductal carcinoma	18765526	CNVD
Rhabdomyosarcoma	16790082	CNVD
Chordoma	18071362	CNVD
Urothelial carcinoma	21177765	CNVD
Gastric cancer	21811585	CNVD
small cell lung cancer	20016488	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Lung cancer	18438408	CNVD
Glioma	17123091	CNVD
Basal cell lymphoma	19029149	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Lung cancer	21569311	CNVD
Non-syndromic sensorineural hearing loss	18451855	CNVD
Non-syndromic sensorineural hearing loss	22037309	CNVD
Glioma	20126413	CNVD
Non-syndromic sensorineural hearing loss	21293372	CNVD

Chromatin state (count:375 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:35941600-35970200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:35943000-35952400	Weak transcription	Primary T helper naive cells from peripheral blood	blood
3	chr19:35943200-35951800	Weak transcription	Primary T killer memory cells from peripheral blood	blood
4	chr19:35946000-35950400	Weak transcription	Brain Anterior Caudate	brain
5	chr19:35946600-35955200	Enhancers	Primary B cells from peripheral blood	blood
6	chr19:35946800-35951800	Weak transcription	Primary T killer naive cells fromperipheralblood	blood
7	chr19:35947200-35952000	Weak transcription	Primary T helper cells fromperipheralblood	blood
8	chr19:35948000-35950200	Enhancers	Pancreatic Islets	Pancreatic Islet
9	chr19:35948000-35952400	Enhancers	Liver	Liver
10	chr19:35948200-35955000	Enhancers	Primary hematopoietic stem cells	blood
11	chr19:35948200-35955000	Enhancers	Fetal Thymus	thymus
12	chr19:35948200-35955600	Enhancers	Primary hematopoietic stem cells short term culture	blood
13	chr19:35948400-35950000	Enhancers	Adipose Nuclei	Adipose
14	chr19:35948600-35951000	Enhancers	Fetal Intestine Large	intestine
15	chr19:35948600-35951200	Enhancers	Fetal Intestine Small	intestine
16	chr19:35948600-35952400	Enhancers	Fetal Stomach	stomach
17	chr19:35948600-35952600	Enhancers	Fetal Lung	lung
18	chr19:35948600-35953000	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
19	chr19:35948600-35955000	Enhancers	Fetal Adrenal Gland	Adrenal Gland
20	chr19:35948800-35950200	Weak transcription	Esophagus	oesophagus
21	chr19:35948800-35951000	Enhancers	Stomach Mucosa	stomach
22	chr19:35948800-35951000	Flanking Active TSS	HepG2	liver
23	chr19:35948800-35951200	Enhancers	Pancreas	Pancrea
24	chr19:35948800-35954600	Enhancers	Placenta	Placenta
25	chr19:35948800-35955000	Enhancers	Primary monocytes fromperipheralblood	blood
26	chr19:35949200-35950400	Weak transcription	Primary T helper cells PMA-I stimulated	--
27	chr19:35949400-35950000	Flanking Active TSS	Primary hematopoietic stem cells G-CSF-mobilized Male	--
28	chr19:35949400-35950800	Enhancers	Small Intestine	intestine
29	chr19:35949400-35951000	Enhancers	Rectal Mucosa Donor 29	rectum
30	chr19:35949400-35951200	Flanking Active TSS	Primary neutrophils fromperipheralblood	blood
31	chr19:35949400-35952000	Enhancers	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
32	chr19:35949600-35950000	Enhancers	Primary T cells fromperipheralblood	blood
33	chr19:35949600-35950000	Enhancers	Duodenum Mucosa	Duodenum
34	chr19:35949600-35950000	Enhancers	Skeletal Muscle Male	skeletal muscle
35	chr19:35949600-35950200	Enhancers	Psoas Muscle	Psoas
36	chr19:35949600-35950400	Enhancers	Primary T cells effector/memory enriched fromperipheralblood	blood
37	chr19:35949600-35950400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr19:35949600-35950600	Enhancers	Duodenum Smooth Muscle	Duodenum
39	chr19:35949600-35950600	Flanking Active TSS	A549	lung
40	chr19:35949600-35950600	Flanking Active TSS	GM12878-XiMat	blood
41	chr19:35949600-35950800	Flanking Active TSS	Primary B cells from cord blood	blood
42	chr19:35949600-35951000	Enhancers	Fetal Kidney	kidney
43	chr19:35949600-35951200	Enhancers	Sigmoid Colon	Sigmoid Colon
44	chr19:35949600-35952200	Enhancers	Skeletal Muscle Female	skeletal muscle
45	chr19:35949600-35952600	Enhancers	Fetal Muscle Leg	muscle
46	chr19:35949600-35953800	Enhancers	Spleen	Spleen
47	chr19:35949600-35955800	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
48	chr19:35949800-35950000	Enhancers	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
49	chr19:35949800-35950000	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
50	chr19:35949800-35950400	Enhancers	Colonic Mucosa	Colon

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