Variant report

Variant	esv3426637
Chromosome Location	chr19:40696137-40698985
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:584)
CpG islands
(count:673)
Chromatin interactive
region (count:10)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:584 , 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	chr19:40696496-40696900	HepG2	liver:	n/a	n/a
2	ATF1	chr19:40697129-40697494	K562	blood:	n/a	n/a
3	ATF2	chr19:40696306-40696953	GM12878	blood:	n/a	n/a
4	ATF3	chr19:40697148-40697419	HepG2	liver:	n/a	chr19:40697328-40697348
5	ATF3	chr19:40696773-40697281	A549	lung:	n/a	n/a
6	ATF3	chr19:40696835-40697440	K562	blood:	n/a	chr19:40697328-40697348
7	ATF3	chr19:40697053-40697456	GM12878	blood:	n/a	chr19:40697328-40697348
8	ATF3	chr19:40697207-40697451	H1-hESC	embryonic stem cell:	n/a	chr19:40697328-40697348
9	BCL3	chr19:40698520-40699332	A549	lung:	n/a	n/a
10	BCL3	chr19:40696378-40697420	A549	lung:	n/a	chr19:40697314-40697323 chr19:40697229-40697242 chr19:40697343-40697356 chr19:40697309-40697322 chr19:40697313-40697326 chr19:40697317-40697326 chr19:40697379-40697392 chr19:40697312-40697325
11	BCLAF1	chr19:40696348-40696956	GM12878	blood:	n/a	n/a
12	BHLHE40	chr19:40696447-40697465	GM12878	blood:	n/a	chr19:40697365-40697381 chr19:40696884-40696900 chr19:40697373-40697389
13	BHLHE40	chr19:40696952-40697383	K562	blood:	n/a	chr19:40697365-40697381
14	BRCA1	chr19:40696938-40697062	H1-hESC	embryonic stem cell:	n/a	n/a
15	BRCA1	chr19:40696556-40697135	GM12878	blood:	n/a	n/a
16	BRCA1	chr19:40697197-40697397	Hela-S3	cervix:	n/a	n/a
17	BRCA1	chr19:40697272-40697307	HepG2	liver:	n/a	n/a
18	CBX3	chr19:40696394-40696997	K562	blood:	n/a	n/a
19	CBX3	chr19:40698651-40699048	K562	blood:	n/a	n/a
20	CCNT2	chr19:40697818-40698093	K562	blood:	n/a	chr19:40697929-40697938 chr19:40697923-40697932
21	CCNT2	chr19:40696754-40697548	K562	blood:	n/a	chr19:40697383-40697392
22	CEBPB	chr19:40696418-40697288	A549	lung:	n/a	n/a
23	CEBPB	chr19:40696420-40696984	Hela-S3	cervix:	n/a	n/a
24	CEBPB	chr19:40696517-40696612	K562	blood:	n/a	n/a
25	CEBPD	chr19:40697801-40698053	HepG2	liver:	n/a	n/a
26	CHD1	chr19:40697874-40698028	GM12878	blood:	n/a	n/a
27	CHD1	chr19:40696592-40697278	GM12878	blood:	n/a	n/a
28	CHD1	chr19:40696999-40697009	H1-hESC	embryonic stem cell:	n/a	n/a
29	CHD2	chr19:40697217-40697229	HepG2	liver:	n/a	n/a
30	CHD2	chr19:40696575-40697447	GM12878	blood:	n/a	n/a
31	CHD2	chr19:40696852-40697014	HepG2	liver:	n/a	n/a
32	CHD2	chr19:40696516-40697505	Hela-S3	cervix:	n/a	n/a
33	CHD2	chr19:40697785-40697973	H1-hESC	embryonic stem cell:	n/a	n/a
34	CHD2	chr19:40697822-40698021	GM12878	blood:	n/a	n/a
35	CHD2	chr19:40696866-40697252	K562	blood:	n/a	n/a
36	CREB1	chr19:40696363-40697843	GM12878	blood:	n/a	n/a
37	CREB1	chr19:40696431-40697455	HepG2	liver:	n/a	n/a
38	CREB1	chr19:40696999-40697599	H1-hESC	embryonic stem cell:	n/a	n/a
39	CREB1	chr19:40697057-40697445	ECC-1	luminal epithelium:	n/a	n/a
40	CREB1	chr19:40697047-40697437	ECC-1	luminal epithelium:	n/a	n/a
41	CREB1	chr19:40696550-40697662	HepG2	liver:	n/a	n/a
42	CREB1	chr19:40696650-40698092	A549	lung:	n/a	n/a
43	CREB1	chr19:40697126-40697519	A549	lung:	n/a	n/a
44	CREB1	chr19:40696878-40697616	K562	blood:	n/a	n/a
45	CREB1	chr19:40696814-40697442	K562	blood:	n/a	n/a
46	CREB1	chr19:40697059-40697457	H1-hESC	embryonic stem cell:	n/a	n/a
47	CTCF	chr19:40697759-40697836	LNCaP	prostate:	n/a	chr19:40697793-40697806
48	CTCF	chr19:40697780-40697930	Hela-S3	cervix:	n/a	chr19:40697793-40697806
49	CTCF	chr19:40697060-40697210	GM12864	blood:	n/a	n/a
50	CTCF	chr19:40697720-40697870	HCM	heart:	n/a	chr19:40697793-40697806

(count:673 , 50 per page) page: 1 2 3 4 5 6 7 ... 14

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr19:40697601-40697651	HMEC	breast:	n/a
2	chr19:40697601-40697651	ECC-1	luminal epithelium:	n/a
3	chr19:40697601-40697651	HMEC	breast:	n/a
4	chr19:40697601-40697651	ECC-1	luminal epithelium:	n/a
5	chr19:40697601-40697651	H1-hESC	embryonic stem cell:	embryo
6	chr19:40697601-40697651	MCF10A-Er-Src	breast:	n/a
7	chr19:40697059-40697109	Caco-2	colon:	n/a
8	chr19:40698551-40698601	HRCEpiC	kidney:	n/a
9	chr19:40697804-40697854	ovcar-3	ovarian:	n/a
10	chr19:40697425-40697475	T-47D	breast:	n/a
11	chr19:40697394-40697444	ECC-1	luminal epithelium:	n/a
12	chr19:40697804-40697854	HepG2	liver:	n/a
13	chr19:40696613-40696663	HUVEC	blood vessel:	n/a
14	chr19:40697059-40697109	MCF-7	breast:	n/a
15	chr19:40697398-40697448	A549	lung:	n/a
16	chr19:40697797-40697847	NHBE	bronchial:	n/a
17	chr19:40697425-40697475	HPAEpiC	pulmonary alveolar:	n/a
18	chr19:40697059-40697109	HEK293	kidney:	embryo
19	chr19:40697398-40697448	MCF10A-Er-Src	breast:	n/a
20	chr19:40697804-40697854	PrEC	prostate:	n/a
21	chr19:40697797-40697847	Jurkat	blood:	n/a
22	chr19:40697804-40697854	SAEC	small airway:	n/a
23	chr19:40697398-40697448	ProgFib	skin:	n/a
24	chr19:40696613-40696663	Caco-2	colon:	n/a
25	chr19:40697059-40697109	GM12878	blood:	n/a
26	chr19:40698192-40698242	AG10803	skin:	n/a
27	chr19:40697797-40697847	LNCaP	prostate:	n/a
28	chr19:40697797-40697847	HRE	kidney:	n/a
29	chr19:40697059-40697109	SKMC	muscle:	n/a
30	chr19:40698551-40698601	BE2_C	brain:	n/a
31	chr19:40697797-40697847	HPAEpiC	pulmonary alveolar:	n/a
32	chr19:40697804-40697854	HIPEpiC	eye:	n/a
33	chr19:40697797-40697847	Caco-2	colon:	n/a
34	chr19:40697425-40697475	NHDF-neo	bronchial:	n/a
35	chr19:40697804-40697854	NT2-D1	testis:	n/a
36	chr19:40697797-40697847	AG04449	skin:	fetal
37	chr19:40697601-40697651	PANC-1	pancreas:	n/a
38	chr19:40698551-40698601	LNCaP	prostate:	n/a
39	chr19:40697804-40697854	HRPEpiC	eye:	n/a
40	chr19:40697601-40697651	NH-A	brain:	n/a
41	chr19:40697797-40697847	HCM	heart:	n/a
42	chr19:40698551-40698601	HepG2	liver:	n/a
43	chr19:40697804-40697854	ECC-1	luminal epithelium:	n/a
44	chr19:40698551-40698601	H1-hESC	embryonic stem cell:	embryo
45	chr19:40697059-40697109	SK-N-MC	brain:	n/a
46	chr19:40696613-40696663	BE2_C	brain:	n/a
47	chr19:40698192-40698242	MCF10A-Er-Src	breast:	n/a
48	chr19:40697256-40697306	ECC-1	luminal epithelium:	n/a
49	chr19:40697601-40697651	CMK	blood:	n/a
50	chr19:40698551-40698601	HL-60	blood:	n/a

(count:10 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr19:40688006..40692388-chr19:40694622..40697525,4	K562	blood:
2	chr19:40697008..40699890-chr19:40723055..40726049,3	MCF-7	breast:
3	chr19:40688598..40690270-chr19:40694622..40697425,2	K562	blood:
4	chr13:111367593..111368509-chr19:40696817..40697667,2	HCT-116	colon:
5	chr19:40476601..40478274-chr19:40696597..40698505,2	MCF-7	breast:
6	chr19:40695427..40698103-chr19:41080992..41083965,2	K562	blood:
7	chr19:40695407..40698481-chr19:40788292..40792778,5	K562	blood:
8	chr19:40696418..40698830-chr19:40709554..40711978,2	K562	blood:
9	chr19:40696492..40699360-chr19:41104510..41106083,2	MCF-7	breast:
10	chr19:40684807..40686349-chr19:40694812..40696838,2	K562	blood:

No data

Variant related genes	Relation type
MAP3K10	TF binding region
MAP3K10	CpG island
ENSG00000130758	chromatin interactions
ENSG00000207631	chromatin interactions
ENSG00000221051	chromatin interactions
ENSG00000090006	chromatin interactions
ENSG00000160410	chromatin interactions
ENSG00000013275	chromatin interactions
ENSG00000153487	chromatin interactions
ENSG00000105221	chromatin interactions
ENSG00000174521	chromatin interactions

Extended variants
information (count: 71 )
Associated
traits (count: 65 )

Variant overlapped rSNPs/rCNVs (count:71 , 50 per page) page: 1 2

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs568659996	chr19:40696138-40696139	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
2	rs535746731	chr19:40696153-40696154	Weak transcription Active TSS Flanking Active TSS Enhancers	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
3	rs369283814	chr19:40696257-40696258	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
4	rs111640276	chr19:40696320-40696321	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
5	rs181076919	chr19:40696344-40696345	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
6	rs79206592	chr19:40696349-40696350	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
7	rs569122549	chr19:40696350-40696351	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
8	rs539117514	chr19:40696373-40696374	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
9	rs184879386	chr19:40696380-40696381	Enhancers Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
10	rs566594675	chr19:40696403-40696404	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
11	rs533543971	chr19:40696421-40696422	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
12	rs555387455	chr19:40696450-40696451	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
13	rs3760917	chr19:40696478-40696479	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
14	rs544534136	chr19:40696486-40696487	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	6 gene(s)	Overlapped CNVs	n/a
15	rs339525	chr19:40696513-40696514	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
16	rs577890511	chr19:40696529-40696530	Bivalent/Poised TSS Enhancers Active TSS Flanking Active TSS Bivalent Enhancer	TF binding region Chromatin interactive region	7 gene(s)	Overlapped CNVs	n/a
17	rs190227837	chr19:40696606-40696607	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
18	rs564417128	chr19:40696634-40696635	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region CpG island Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
19	rs531858331	chr19:40696707-40696708	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
20	rs540217642	chr19:40696722-40696723	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
21	rs561753542	chr19:40696774-40696775	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	8 gene(s)	Overlapped CNVs	n/a
22	rs111977112	chr19:40696879-40696880	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
23	rs529507289	chr19:40696895-40696896	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
24	rs550078240	chr19:40696909-40696910	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
25	rs568340389	chr19:40696946-40696947	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
26	rs376838048	chr19:40696979-40696980	Bivalent/Poised TSS Active TSS Flanking Active TSS Flanking Bivalent TSS/Enh Transcr. at gene 5' and 3'	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
27	rs369682233	chr19:40697002-40697003	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
28	rs569234753	chr19:40697005-40697006	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
29	rs117408195	chr19:40697026-40697027	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
30	rs339526	chr19:40697061-40697062	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
31	rs566440131	chr19:40697094-40697095	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
32	rs533897049	chr19:40697111-40697112	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
33	rs555028879	chr19:40697126-40697127	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
34	rs182412324	chr19:40697156-40697157	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
35	rs537869832	chr19:40697180-40697181	Active TSS Flanking Bivalent TSS/Enh Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
36	rs556483626	chr19:40697218-40697219	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
37	rs578029804	chr19:40697228-40697229	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
38	rs544875736	chr19:40697336-40697337	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
39	rs553938645	chr19:40697351-40697352	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
40	rs186641061	chr19:40697371-40697372	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	mRNA abundance
41	rs192014184	chr19:40697372-40697373	Active TSS Flanking Active TSS Transcr. at gene 5' and 3' Bivalent/Poised TSS Weak transcription	TF binding region Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
42	rs200824781	chr19:40697610-40697611	Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	10 gene(s)	Overlapped CNVs	n/a
43	rs561716797	chr19:40697674-40697675	Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
44	rs529225807	chr19:40697815-40697816	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
45	rs376665121	chr19:40697817-40697818	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region CpG island Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
46	rs544233148	chr19:40697857-40697858	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
47	rs201467895	chr19:40697932-40697933	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
48	rs377356617	chr19:40697996-40697997	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
49	rs370034354	chr19:40697998-40697999	Bivalent/Poised TSS Active TSS Flanking Active TSS Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a
50	rs374398619	chr19:40698100-40698101	Bivalent/Poised TSS Active TSS Flanking Active TSS Enhancers Weak transcription	TF binding region Chromatin interactive region	9 gene(s)	Overlapped CNVs	n/a

Variant related diseases (count:65)

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
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	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
small cell lung cancer	20016488	CNVD
Wilms tumour	21544195	CNVD
Acute lymphoblastic leukemia	20067559	CNVD
Ovarian neoplasms	16753589	CNVD
Malignant fibrous histiocytomas	21085701	CNVD
Metanephric adenoma	20802469	CNVD
Acute myeloid leukemia	16864856	CNVD
Lung cancer	21569311	CNVD
Bladder cancer	21909424	CNVD
Medulloblastoma	16783165	CNVD
Gastric cancer	18160780	CNVD
Hepatocellular carcinoma	16750200	CNVD
Basal cell lymphoma	19029149	CNVD
Breast cancer	20409316	CNVD
Diffuse large b-cell lymphoma	19029149	CNVD
Multiple myeloma	16616336	CNVD
Renal cell carcinoma	18765545	CNVD
Acute myeloid leukemia	20729466	CNVD
Lung cancer	18438408	CNVD
Genital abnormality	22378287	CNVD
Hypospadia	22378287	CNVD
Ovarian clear cell carcinoma	19293255	CNVD
Astrocytoma	22246337	CNVD
Anaplastic thyroid cancer	18753363	CNVD
Breast cancer	22522925	CNVD
Pleomorphic liposarcoma	18784837	CNVD

Chromatin state (count:472 , 50 per page) page: 1 2 3 4 5 6 7 ... 10

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr19:40686000-40696200	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
2	chr19:40691600-40696400	Weak transcription	Skeletal Muscle Male	skeletal muscle
3	chr19:40694800-40696200	Weak transcription	Primary monocytes fromperipheralblood	blood
4	chr19:40694800-40696400	Weak transcription	NHEK	skin
5	chr19:40695000-40696400	Weak transcription	Monocytes-CD14+_RO01746	blood
6	chr19:40695600-40696400	Enhancers	A549	lung
7	chr19:40695600-40696600	Enhancers	Fetal Brain Male	brain
8	chr19:40695800-40696200	Flanking Active TSS	Adipose Derived Mesenchymal Stem Cell Cultured Cells	ES cell derived
9	chr19:40695800-40696200	Enhancers	Foreskin Fibroblast Primary Cells skin01	Skin
10	chr19:40695800-40696200	Enhancers	Foreskin Melanocyte Primary Cells skin03	Skin
11	chr19:40695800-40696200	Enhancers	Brain Hippocampus Middle	brain
12	chr19:40695800-40696200	Enhancers	NHDF-Ad	bronchial
13	chr19:40695800-40696400	Enhancers	Primary B cells from peripheral blood	blood
14	chr19:40695800-40696400	Enhancers	Primary T helper memory cells from peripheral blood 2	blood
15	chr19:40695800-40696400	Enhancers	Ganglion Eminence derived primary cultured neurospheres	brain
16	chr19:40695800-40696400	Enhancers	Brain Cingulate Gyrus	brain
17	chr19:40695800-40696400	Weak transcription	Brain Inferior Temporal Lobe	brain
18	chr19:40695800-40696400	Enhancers	HepG2	liver
19	chr19:40695800-40696400	Enhancers	NHLF	lung
20	chr19:40695800-40698000	Active TSS	GM12878-XiMat	blood
21	chr19:40695800-40698600	Active TSS	Osteobl	bone
22	chr19:40696000-40696200	Enhancers	Adipose Nuclei	Adipose
23	chr19:40696000-40696400	Enhancers	Primary B cells from cord blood	blood
24	chr19:40696000-40696400	Active TSS	Hela-S3	cervix
25	chr19:40696000-40696600	Active TSS	Foreskin Fibroblast Primary Cells skin02	Skin
26	chr19:40696000-40698400	Active TSS	Mesenchymal Stem Cell Derived Adipocyte Cultured Cells	ES cell derived
27	chr19:40696000-40698400	Active TSS	Brain Angular Gyrus	brain
28	chr19:40696200-40696400	Enhancers	Primary T cells fromperipheralblood	blood
29	chr19:40696200-40696400	Enhancers	Primary T helper cells PMA-I stimulated	--
30	chr19:40696200-40696400	Enhancers	Primary T helper cells fromperipheralblood	blood
31	chr19:40696200-40696400	Enhancers	Primary Natural Killer cells fromperipheralblood	blood
32	chr19:40696200-40696400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Female	--
33	chr19:40696200-40696400	Enhancers	Primary hematopoietic stem cells G-CSF-mobilized Male	--
34	chr19:40696200-40696400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
35	chr19:40696200-40696400	Enhancers	Fetal Muscle Leg	muscle
36	chr19:40696200-40696400	Enhancers	Placenta	Placenta
37	chr19:40696200-40696400	Enhancers	Rectal Mucosa Donor 31	rectum
38	chr19:40696200-40696400	Active TSS	Skeletal Muscle Female	skeletal muscle
39	chr19:40696200-40696600	Enhancers	H1 Derived Mesenchymal Stem Cells	ES cell derived
40	chr19:40696200-40696600	Enhancers	Primary monocytes fromperipheralblood	blood
41	chr19:40696200-40696600	Enhancers	Primary T helper memory cells from peripheral blood 1	blood
42	chr19:40696200-40696800	Flanking Active TSS	Foreskin Fibroblast Primary Cells skin01	Skin
43	chr19:40696200-40696800	Active TSS	Foreskin Keratinocyte Primary Cells skin02	Skin
44	chr19:40696200-40696800	Active TSS	Colonic Mucosa	Colon
45	chr19:40696200-40697000	Flanking Active TSS	Adipose Nuclei	Adipose
46	chr19:40696200-40697800	Active TSS	Foreskin Melanocyte Primary Cells skin03	Skin
47	chr19:40696200-40698000	Active TSS	iPS DF 19.11 Cell Line	embryonic stem cell
48	chr19:40696200-40698000	Active TSS	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
49	chr19:40696200-40698000	Active TSS	Brain Anterior Caudate	brain
50	chr19:40696200-40698000	Active TSS	Brain Hippocampus Middle	brain

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